Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:48331354-48331463 | Rare:37 | ||||
chr15:48645704-48645923 | Common:2; Rare:71; Clinvar (benign):1 | ||||
chr15:48878017-48878394 | Rare:139 | ||||
chr15:48963863-48964070 | Rare:34 | ||||
chr15:49046280-49046659 | Common:2; Rare:136 | ||||
chr15:49155558-49155846 | Common:2; Rare:98 | ||||
chr15:49170148-49170264 | Rare:23 | ||||
chr15:49620810-49621121 | Common:6; Rare:119 | ||||
chr15:50354890-50355061 | Rare:45 | ||||
chr15:50355106-50355309 | Common:3; Rare:79 | ||||
chr15:50355397-50355513 | Rare:51 | ||||
chr15:50424307-50424500 | Common:1; Rare:79 | ||||
chr15:50686721-50686937 | Common:5; Rare:91 | ||||
chr15:50765625-50765790 | Common:2; Rare:58 | ||||
chr15:50908569-50908766 | Common:2; Rare:82; Clinvar (benign):2 |