| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:73963201-73963355 | Common:1; Rare:23 | ||||
| chrX:73984461-73984492 | Rare:8 | ||||
| chrX:74221056-74221373 | Rare:27 | ||||
| chrX:74292497-74292745 | Rare:44 | ||||
| chrX:74420561-74420866 | Common:1; Rare:86 | ||||
| chrX:77278835-77279021 | Common:1; Rare:42 | ||||
| chrX:80808926-80809001 | Rare:15 | ||||
| chrX:85293744-85293780 | Common:1; Rare:5 | ||||
| chrX:103357012-103357157 | Rare:20 | ||||
| chrX:107676934-107677165 | Rare:29 | ||||
| chrX:107712909-107712925 | Common:1; Rare:3 | ||||
| chrX:125204303-125204527 | Rare:25 | ||||
| chrX:130131752-130131955 | Rare:40; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:132382203-132382535 | Common:1; Rare:56 | ||||
| chrX:136208392-136208530 | Rare:21; Clinvar:1; Clinvar (benign):2 |