| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:40172251-40172733 | Rare:138 | ||||
| chrX:40175505-40176113 | Common:4; Rare:158 | ||||
| chrX:47129060-47129460 | Common:2; Rare:138 | ||||
| chrX:47129450-47130080 | Common:4; Rare:89 | ||||
| chrX:48713080-48713420 | Rare:45 | ||||
| chrX:48737150-48737400 | Rare:57 | ||||
| chrX:48737490-48737800 | Common:2; Rare:54 | ||||
| chrX:49877360-49877720 | Common:2; Rare:70 | ||||
| chrX:49878830-49879128 | Common:2; Rare:98 | ||||
| chrX:50154441-50154800 | Common:2; Rare:65 | ||||
| chrX:50431546-50431970 | Common:6; Rare:99 | ||||
| chrX:52934980-52935370 | Common:4; Rare:258 | ||||
| chrX:53412910-53413310 | Rare:50; Clinvar (benign):2 | ||||
| chrX:54639280-54639600 | Common:6; Rare:87 | ||||
| chrX:65529251-65530020 | Common:5; Rare:176; Clinvar:3; Clinvar (benign):2 |