Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:107716960-107717192 | Common:1; Rare:27 | ||||
chrX:107775553-107775914 | Rare:61 | ||||
chrX:108091521-108091818 | Rare:79 | ||||
chrX:110002340-110002452 | Rare:19 | ||||
chrX:110318077-110318271 | Rare:47 | ||||
chrX:111096143-111096275 | Rare:19 | ||||
chrX:111681112-111681298 | Rare:54; Clinvar (benign):7 | ||||
chrX:118345877-118346155 | Common:3; Rare:47 | ||||
chrX:118975218-118975381 | Rare:34 | ||||
chrX:119468191-119468552 | Common:3; Rare:113 | ||||
chrX:119574372-119574581 | Rare:47 | ||||
chrX:119791584-119791721 | Rare:58 | ||||
chrX:119871634-119871904 | Common:1; Rare:59; Clinvar (benign):2 | ||||
chrX:119943607-119943852 | Rare:44 | ||||
chrX:120560617-120560859 | Rare:36 |