| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154379231-154380089 | Common:1; Rare:216; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chrX:154398796-154399071 | Common:4; Rare:61 | ||||
| chrX:154399269-154399331 | Rare:27 | ||||
| chrX:154409152-154409461 | Rare:47 | ||||
| chrX:154411430-154411603 | Rare:35 | ||||
| chrX:154428448-154428730 | Common:2; Rare:54 | ||||
| chrX:154437152-154437263 | Rare:46 | ||||
| chrX:154438354-154438628 | Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:154450262-154450551 | Common:2; Rare:76 | ||||
| chrX:154468535-154468837 | Common:1; Rare:73 | ||||
| chrX:154485601-154485856 | Common:3; Rare:77 | ||||
| chrX:154486547-154486772 | Rare:34 | ||||
| chrX:154490618-154490926 | Common:2; Rare:62 | ||||
| chrX:154516099-154516536 | Common:4; Rare:86 | ||||
| chrX:154532567-154533161 | Common:2; Rare:137; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):4 |