Table 1. Translocation datasets and permutation results.

Dataset	Mean Hi-C Score (Translocations)*	Mean Hi-C Score (Permutations)*	Permutation P-Value	Rank-Sum P-Value	Individual Significant Translocations	Total Unique Translocations	% Genome Covered	% Interactions Covered**	Source
Mitelman Database	0.17±0.03	0.052±0.001	<0.001	6.42E-23	7	577	79.7%	1.12%	Mitelman et al. 2011
Blood	0.19±0.03	0.063±0.001	<0.001	2.13E-20	6	440	72.4%	0.87%
Non-Blood	0.10±0.05	0.018±0.001	<0.001	1.78E-04	1	137	45.2%	0.27%
Multiple Myeloma	0.17±0.09	0.039±0.002	<0.001	7.27E-03	2	89	22.9%	0.03%	Chapman et al. 2011
Prostate Cancer	0.07±0.04	0.002±0.001	<0.001	7.92E-04	0	89	21.9%	0.03%	Berger et al. 2011
Mendelian	0.04±0.02	0.006±0.001	<0.001	4.05E-03	1	779	91.5%	0.79%	https://www1.hgu.mrc.ac.uk/Softdata/Translocation/

^*Bounds represent a 95% confidence interval.

^**Percentage of inter-chromosomal 1-Mb bins that are covered by translocations.