Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:112840822-112841004 | Rare:39 | ||||
chrX:118345792-118346114 | Common:3; Rare:54 | ||||
chrX:118346359-118346506 | Rare:31 | ||||
chrX:119236556-119236618 | Rare:17 | ||||
chrX:119468216-119468456 | Common:3; Rare:68 | ||||
chrX:119574382-119574603 | Rare:49 | ||||
chrX:119791590-119791978 | Common:2; Rare:102 | ||||
chrX:119871638-119871905 | Common:1; Rare:59; Clinvar (benign):2 | ||||
chrX:120560795-120560860 | Rare:8 | ||||
chrX:123961270-123961432 | Common:2; Rare:22 | ||||
chrX:123961553-123961850 | Rare:43 | ||||
chrX:129779817-129779975 | Rare:22 | ||||
chrX:129906041-129906191 | Rare:42 | ||||
chrX:130401862-130402019 | Common:3; Rare:47 | ||||
chrX:131058136-131058389 | Common:1; Rare:37 |