| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:108736373-108736553 | Rare:26 | ||||
| chrX:109733177-109733502 | Common:1; Rare:77 | ||||
| chrX:118345875-118346150 | Common:3; Rare:47 | ||||
| chrX:119235964-119236289 | Rare:71 | ||||
| chrX:119468205-119468456 | Common:3; Rare:70 | ||||
| chrX:119574381-119574592 | Rare:45 | ||||
| chrX:119791592-119791978 | Common:2; Rare:102 | ||||
| chrX:119871622-119871933 | Common:2; Rare:65; Clinvar (benign):3 | ||||
| chrX:119943606-119943862 | Rare:45 | ||||
| chrX:120560726-120560860 | Rare:20 | ||||
| chrX:120560910-120561158 | Rare:49 | ||||
| chrX:120604086-120604150 | Rare:17 | ||||
| chrX:123733021-123733155 | Rare:22 | ||||
| chrX:123960350-123960732 | Rare:28 | ||||
| chrX:123961511-123961812 | Rare:42 |