| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47209829-47209988 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chrX:47214218-47214387 | Common:2; Rare:36; Clinvar:1 | ||||
| chrX:47224496-47224699 | Common:1; Rare:31 | ||||
| chrX:47224724-47224837 | Rare:28 | ||||
| chrX:48522496-48522510 | Rare:1 | ||||
| chrX:48937096-48937410 | Rare:42 | ||||
| chrX:49156245-49156429 | Common:1; Rare:40 | ||||
| chrX:49230943-49231232 | Common:1; Rare:50 | ||||
| chrX:53093930-53094212 | Rare:51 | ||||
| chrX:53193296-53193451 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:55908044-55908502 | Rare:75 | ||||
| chrX:55908866-55908991 | Rare:17 | ||||
| chrX:57453730-57453966 | Common:1; Rare:43 | ||||
| chrX:66018853-66018960 | Rare:23 | ||||
| chrX:66027483-66027711 | Common:3; Rare:43 |