| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137551978-137552155 | Rare:49 | ||||
| chr9:137762510-137762734 | Common:1; Rare:61; Clinvar:1 | ||||
| chr9:137776492-137776678 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:307802-308010 | Common:1; Rare:72 | ||||
| chrX:1356109-1356234 | Common:2; Rare:51 | ||||
| chrX:1395327-1395406 | Common:2; Rare:18 | ||||
| chrX:1401997-1402079 | Common:1; Rare:19 | ||||
| chrX:1406534-1406643 | Common:2; Rare:36 | ||||
| chrX:1407144-1407366 | Rare:62 | ||||
| chrX:1413387-1413682 | Common:4; Rare:92 | ||||
| chrX:1415580-1415780 | Common:5; Rare:51 | ||||
| chrX:1416632-1416883 | Common:11; Rare:119 | ||||
| chrX:1420402-1420461 | Rare:17 | ||||
| chrX:1600520-1600743 | Common:1; Rare:74 | ||||
| chrX:2609154-2609436 | Common:1; Rare:91 |