Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:109733158-109733479 | Common:1; Rare:75 | ||||
chrX:110317922-110318262 | Rare:89 | ||||
chrX:111681028-111681294 | Rare:69; Clinvar (benign):7 | ||||
chrX:111681530-111681630 | Rare:38 | ||||
chrX:118345861-118346155 | Common:3; Rare:49 | ||||
chrX:119236575-119236658 | Rare:21 | ||||
chrX:119468238-119468456 | Common:3; Rare:64 | ||||
chrX:119574401-119574586 | Rare:39 | ||||
chrX:119791590-119791978 | Common:2; Rare:102 | ||||
chrX:119852938-119853237 | Common:3; Rare:49; Clinvar (benign):3 | ||||
chrX:119871614-119871911 | Common:2; Rare:61; Clinvar (benign):3 | ||||
chrX:120560475-120560863 | Rare:63; Clinvar:2 | ||||
chrX:120560923-120561230 | Rare:64 | ||||
chrX:120561411-120561709 | Common:1; Rare:45 | ||||
chrX:120629924-120630260 | Common:4; Rare:66 |