| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:136807243-136807393 | Rare:18 | ||||
| chrX:136875084-136875327 | Rare:62 | ||||
| chrX:136909293-136909474 | Rare:46 | ||||
| chrX:137563132-137563435 | Common:1; Rare:40 | ||||
| chrX:137564025-137564321 | Common:1; Rare:21 | ||||
| chrX:137564482-137564561 | Rare:12 | ||||
| chrX:137564946-137565076 | Rare:17 | ||||
| chrX:137567393-137567749 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chrX:137573850-137574045 | Common:3; Rare:34 | ||||
| chrX:138266909-138266963 | Rare:11 | ||||
| chrX:139448658-139448864 | Rare:27 | ||||
| chrX:139932165-139932425 | Common:1; Rare:47 | ||||
| chrX:140503033-140503214 | Common:1; Rare:21 | ||||
| chrX:142423398-142423488 | Common:1; Rare:14 | ||||
| chrX:150903207-150903332 | Common:1; Rare:19 |