Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:44350823-44351147 | Common:3; Rare:61 | ||||
chr13:44405711-44406030 | Common:1; Rare:53 | ||||
chr13:48413064-48413193 | Rare:18 | ||||
chr13:52194392-52194505 | Rare:35 | ||||
chr13:52617316-52617551 | Common:1; Rare:58 | ||||
chr13:102394500-102394660 | Common:1; Rare:59 | ||||
chr13:110424793-110424989 | Common:4; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110503656-110503920 | Common:6; Rare:64; Clinvar (benign):2 | ||||
chr14:32203267-32203667 | Common:13; Rare:169 | ||||
chr14:34874125-34874191 | Rare:17 | ||||
chr14:49633956-49634047 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49802669-49802828 | Rare:46 | ||||
chr14:49862639-49862989 | Common:1; Rare:165 | ||||
chr14:49868143-49868456 | Common:3; Rare:67 | ||||
chr14:55103191-55103412 | Common:1; Rare:58 |