Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:32004770-32005160 | Common:4; Rare:89 | ||||
chr9:32550860-32551220 | Common:1; Rare:247; Clinvar:3; Clinvar (benign):2 | ||||
chr9:33165800-33166030 | Common:2; Rare:77 | ||||
chr9:34380480-34381010 | Common:4; Rare:249 | ||||
chr9:35603994-35604193 | Common:6; Rare:101 | ||||
chr9:35604220-35604520 | Common:1; Rare:120 | ||||
chr9:37079563-37080037 | Common:8; Rare:191 | ||||
chr9:38047745-38048151 | Common:4; Rare:127 | ||||
chr9:38059423-38059770 | Rare:96 | ||||
chr9:38376310-38376587 | Common:6; Rare:108 | ||||
chr9:38437615-38437749 | Common:4; Rare:60 | ||||
chr9:40105830-40106310 | Common:12; Rare:60 | ||||
chr9:40583960-40584510 | Rare:4 | ||||
chr9:40991931-40992379 | Common:14; Rare:59 | ||||
chr9:41354207-41354690 | Common:4; Rare:88 |