| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103919053-103919164 | Common:3; Rare:25 | ||||
| chrX:104156902-104157069 | Common:1; Rare:28 | ||||
| chrX:107118777-107118889 | Common:2; Rare:23 | ||||
| chrX:107716960-107717182 | Common:1; Rare:27 | ||||
| chrX:108091516-108091805 | Rare:75 | ||||
| chrX:109733177-109733502 | Common:1; Rare:77 | ||||
| chrX:110318077-110318308 | Rare:66 | ||||
| chrX:118345875-118346137 | Common:2; Rare:45 | ||||
| chrX:119468216-119468506 | Common:3; Rare:97 | ||||
| chrX:119574401-119574586 | Rare:39 | ||||
| chrX:119791572-119791729 | Rare:61 | ||||
| chrX:119871629-119871969 | Common:1; Rare:70; Clinvar (benign):3 | ||||
| chrX:120250825-120250942 | Rare:19 | ||||
| chrX:120559879-120560114 | Rare:38 | ||||
| chrX:120603831-120604147 | Rare:60 |