Drosophila |
Domain-restricted analysis for anterior–posterior patterning of blastoderm to identify accessible regions |
[30] |
Tissue-specific accessibility during three embryonic stages with germ-layer enhancer validation |
[44] |
Zebrafish |
Chromatin accessibility atlas of embryonic and adult tissues |
[43] |
Identification of key elements during zygotic genome activation |
[45] |
Neural crest and melanoma development |
[53,56] |
Heart regeneration |
[64,67] |
Liver development and response to injury |
[68] |
Fin regeneration |
[69] |
Endothelial enhancers |
[29] |
Xenopus |
Wnt signalling in dorsal–ventral patterning in comparison with mesoderm and neural crest development |
[47] |
Mesendoderm specification |
[48] |
Chicken |
Neural crest development, GRN reconstruction and identification of specific enhancers |
[27,28] |
Anterior–posterior axis elongation and paraxial mesoderm development, differential TF occupancy and in vivo enhancer validation |
[16] |
Mouse |
Chromatin accessibility atlas of adult tissues |
[42] |
Sex-specific accessibility of in vivo and IVF inner cell mass |
[50] |
Chromatin accessibility preconfigures region-specific neural fates along anterior–posterior axis |
[52] |
Sinoatrial node development |
[65] |
Heart development of key developmental stages |
[66] |
Mouse/Pig |
Limb development and digit adaptation |
[63] |
Bovine |
Chromatin accessibility in oocytes and early embryos, and comparison of in vivo and in vitro blastocysts |
[49] |
Human |
Chromatin accessibility of inner cell mass and trophectoderm of blastocysts |
[51] |
Human ESC differentiation into neural crest identifies disease enhancer |
[5] |