| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103686685-103687028 | Common:4; Rare:45 | ||||
| chrX:103832225-103832495 | Common:2; Rare:44 | ||||
| chrX:104156923-104157058 | Common:1; Rare:25 | ||||
| chrX:108091521-108091815 | Rare:79 | ||||
| chrX:119468216-119468456 | Common:3; Rare:68 | ||||
| chrX:119574374-119574575 | Rare:45 | ||||
| chrX:119791590-119791743 | Common:2; Rare:62 | ||||
| chrX:119871673-119871891 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chrX:120560634-120560858 | Rare:36 | ||||
| chrX:123733025-123733086 | Rare:13 | ||||
| chrX:123961264-123961432 | Common:2; Rare:22 | ||||
| chrX:123961563-123961812 | Rare:34 | ||||
| chrX:129906052-129906176 | Rare:35 | ||||
| chrX:130171819-130171972 | Common:1; Rare:40 | ||||
| chrX:135022507-135022754 | Rare:47 |