Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrM:15937-16000 | |||||
chrX:1123791-1124031 | Common:2; Rare:49 | ||||
chrX:3271317-3271637 | Rare:37 | ||||
chrX:3271694-3271826 | Rare:16 | ||||
chrX:15165981-15166176 | Rare:25 | ||||
chrX:15675305-15675475 | Common:5; Rare:30 | ||||
chrX:15675606-15675761 | Common:1; Rare:35 | ||||
chrX:21738565-21738803 | Rare:21 | ||||
chrX:34884778-34884928 | Rare:29 | ||||
chrX:40243815-40244141 | Common:1; Rare:45 | ||||
chrX:49977649-49977961 | Rare:47 | ||||
chrX:53093870-53094189 | Rare:60 | ||||
chrX:67545583-67545739 | Rare:34; Clinvar (pathogenic):1 | ||||
chrX:73944114-73944375 | Common:1; Rare:71 | ||||
chrX:74292581-74292745 | Rare:25 |