Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:47659071-47659189 | Rare:36 | ||||
chrX:48003959-48004137 | Rare:49 | ||||
chrX:48468300-48468471 | Common:1; Rare:23 | ||||
chrX:48508887-48509026 | Rare:27 | ||||
chrX:48521664-48521889 | Rare:40 | ||||
chrX:48574113-48574528 | Common:3; Rare:96 | ||||
chrX:48574861-48575015 | Rare:44 | ||||
chrX:48597372-48597546 | Rare:28 | ||||
chrX:48597666-48597877 | Common:1; Rare:24 | ||||
chrX:48898113-48898277 | Common:1; Rare:25 | ||||
chrX:48911626-48911679 | Rare:16; Clinvar (benign):3 | ||||
chrX:48958296-48958406 | Rare:34 | ||||
chrX:49079842-49079983 | Rare:24 | ||||
chrX:49171827-49172091 | Common:1; Rare:44 | ||||
chrX:49186298-49186466 | Common:1; Rare:30 |