| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:101219935-101220154 | Rare:19 | ||||
| chrX:101407893-101408274 | Common:5; Rare:71; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:101408284-101408487 | Rare:42 | ||||
| chrX:101418141-101418295 | Common:1; Rare:30 | ||||
| chrX:101485283-101485473 | Rare:27 | ||||
| chrX:101622985-101623215 | Common:1; Rare:38 | ||||
| chrX:103214951-103215164 | Common:2; Rare:46 | ||||
| chrX:103585454-103585608 | Common:3; Rare:34 | ||||
| chrX:103607790-103608010 | Rare:40 | ||||
| chrX:103629443-103629525 | Rare:24 | ||||
| chrX:103686629-103686895 | Common:1; Rare:43 | ||||
| chrX:104156942-104157069 | Common:1; Rare:22 | ||||
| chrX:106802535-106802778 | Rare:49 | ||||
| chrX:107628219-107628529 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chrX:107716279-107716623 | Common:1; Rare:47 |