| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48476080-48476247 | Rare:34 | ||||
| chrX:48508861-48509040 | Rare:35 | ||||
| chrX:48521541-48521889 | Common:1; Rare:56 | ||||
| chrX:48574880-48575211 | Common:3; Rare:83 | ||||
| chrX:48597423-48597543 | Rare:19 | ||||
| chrX:48918962-48919265 | Rare:59 | ||||
| chrX:48958374-48958472 | Rare:22 | ||||
| chrX:49079858-49079939 | Rare:13 | ||||
| chrX:49101166-49101407 | Common:1; Rare:50 | ||||
| chrX:49186371-49186478 | Common:1; Rare:20 | ||||
| chrX:53422596-53422927 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:53434342-53434610 | Common:2; Rare:53 | ||||
| chrX:53536223-53536511 | Common:3; Rare:52; Clinvar (benign):1 | ||||
| chrX:53686693-53686990 | Common:2; Rare:59 | ||||
| chrX:54357939-54358252 | Common:1; Rare:55 |