Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:119574396-119574603 | Rare:44 | ||||
chrX:119791584-119791978 | Common:2; Rare:107 | ||||
chrX:119871622-119871904 | Common:2; Rare:59; Clinvar (benign):2 | ||||
chrX:120560654-120560858 | Rare:32 | ||||
chrX:120560951-120561281 | Rare:71 | ||||
chrX:120603872-120604164 | Rare:59 | ||||
chrX:123960389-123960734 | Rare:22 | ||||
chrX:123961289-123961432 | Common:2; Rare:21 | ||||
chrX:135052104-135052342 | Common:2; Rare:64 | ||||
chrX:135344632-135344823 | Common:1; Rare:36 | ||||
chrX:135973671-135973850 | Rare:63 | ||||
chrX:139933051-139933211 | Rare:31 | ||||
chrX:149540827-149541065 | Common:4; Rare:45 | ||||
chrX:149938437-149938612 | Common:1; Rare:46 | ||||
chrX:151396957-151397276 | Common:5; Rare:144 |