| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103687990-103688348 | Common:1; Rare:44 | ||||
| chrX:103918721-103918850 | Common:1; Rare:20 | ||||
| chrX:103919045-103919221 | Common:4; Rare:36 | ||||
| chrX:104112363-104112578 | Rare:50 | ||||
| chrX:104156906-104157089 | Common:1; Rare:34 | ||||
| chrX:107118772-107118910 | Common:2; Rare:31 | ||||
| chrX:108091408-108091825 | Rare:109 | ||||
| chrX:109733148-109733436 | Common:1; Rare:64 | ||||
| chrX:110002635-110002740 | Rare:19 | ||||
| chrX:111681014-111681244 | Rare:61; Clinvar (benign):5 | ||||
| chrX:111681546-111681678 | Rare:54 | ||||
| chrX:112840822-112840944 | Rare:28 | ||||
| chrX:118346135-118346180 | Common:1; Rare:9 | ||||
| chrX:118545909-118546066 | Rare:27 | ||||
| chrX:118727458-118727724 | Rare:53 |