| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48508870-48509027 | Rare:29 | ||||
| chrX:48574869-48575219 | Common:3; Rare:86 | ||||
| chrX:48696584-48696777 | Rare:43 | ||||
| chrX:48801674-48802099 | Common:1; Rare:77 | ||||
| chrX:48911637-48911715 | Rare:19; Clinvar (benign):3 | ||||
| chrX:48919013-48919207 | Rare:30 | ||||
| chrX:48958355-48958675 | Rare:61 | ||||
| chrX:49079831-49079946 | Rare:16 | ||||
| chrX:49171759-49171992 | Common:3; Rare:29 | ||||
| chrX:49922344-49922656 | Common:1; Rare:74 | ||||
| chrX:53225175-53225504 | Common:2; Rare:106 | ||||
| chrX:53422624-53422971 | Common:1; Rare:82 | ||||
| chrX:53434335-53434625 | Common:2; Rare:57 | ||||
| chrX:54043903-54044049 | Rare:29 | ||||
| chrX:54357866-54357893 | Rare:9 |