Table 4.
The information of the 9 fetus hypermethylation DNA markers (FH) and 12 fetus hypomethylation DNA markers (FL)
| Marker ID | Chromosomal locition | Associated gene |
|---|---|---|
| FH1 |
ChrM:1-542 |
Mitochondrial DNA D-loop |
| FH2 |
ChrM:16,025-16,571 |
Mitochondrial DNA D-loop |
| FH3 |
Chr19:40,628,281-40,629,300 |
Free fatty acid receptor 2 (FFAR2) |
| FH4 |
Chr21:38,791,600-38,792,000 |
Erythroblastosis virus E26 oncogene onmcogene homolog (ERG) |
| FH5 |
Chr7:2,411,800-2,412,100 |
Carbohydrate (chondroitin 4) Sulfotransferase 12 (CHST12) |
| FH6 |
Chr12:6,528,400-6,528,750 |
Intermediate filament family orphan 1 (IFFO1) |
| FH7 |
Chr9:129,579,800-129,580,000 |
SH2 domain containing 3C (SH2D3C) |
| FH8 |
Chr17:36,717,500-36,717,900 |
Keratin associated protein 16-1 (KRTAP16-1) |
| FH9 |
Chr19:1,019,900-1,020,200 |
Histocompatibility (minor) HA-1 (HMHA1) |
| FL1 |
Chr7:27,130,100-27,130,600 |
Homeobox A3 (HOXA3) |
| FL2 |
Chr11:62127350-62127700 |
Echinoderm microtubule associated protein like 3 (EML3) |
| FL3 |
Chr3:32,835,500-32,835,800 |
Tripartite motif containing 71, E3 ubiquitin protein ligase (TRIM71) |
| FL4 |
Chr7:27,185,300-27,185,650 |
Homo sapiens homeobox A11 (HOXA11) |
| FL5 |
Chr6:10,664,250-10,664,600 |
Homo sapiens glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (GCNT2) |
| FL6 |
Chr7:27,113,100-27,113,300 |
Homo sapiens homeobox A2 (HOXA2) |
| FL7 |
Chr7:27,148,050-27,148,400 |
Homeobox A5 (HOXA5) |
| FL8 |
Chr19:12,997,300-12,997,450 |
Nuclear factor I/X (NFIX) (CCAAT-binding transcription factor) |
| FL9 |
Chr8:116,753,900-116,754,200 |
Homo sapiens trichorhinophalangeal syndrome I (TRPS1) |
| FL10 |
Chr5:95,321,600-95,321,800 |
Elongation factor, RNA polymerase II, 2 (ELL2) |
| FL11 |
Chr7:32,213,400-32,213,600 |
Phosphodiesterase 1C, calmodulin-dependent (PDE1C) |
| FL12 | Chr8:82,066,300-82,066,500 | Phosphoprotein associated with glycosphingolipid microdomains 1 (PAG1) |