Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:44536886-44537192 | Common:1; Rare:109 | ||||
chr15:44711314-44711539 | Rare:59 | ||||
chr15:45114135-45114329 | Common:2; Rare:41 | ||||
chr15:45587123-45587237 | Rare:17 | ||||
chr15:45587281-45587461 | Common:1; Rare:53; Clinvar:6; Clinvar (benign):1 | ||||
chr15:48645710-48645903 | Common:2; Rare:63; Clinvar (benign):1 | ||||
chr15:49155570-49155819 | Common:2; Rare:83 | ||||
chr15:49620810-49621093 | Common:6; Rare:110 | ||||
chr15:50355106-50355504 | Common:3; Rare:158 | ||||
chr15:50686723-50686894 | Common:4; Rare:75 | ||||
chr15:50765571-50765750 | Common:2; Rare:60 | ||||
chr15:51971738-51971831 | Rare:45 | ||||
chr15:52019032-52019282 | Common:1; Rare:130 | ||||
chr15:52179918-52179997 | Common:1; Rare:31 | ||||
chr15:55319089-55319229 | Common:1; Rare:35 |