Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:15686504-15686848 | Common:3; Rare:103 | ||||
chr7:15686850-15686934 | Rare:20 | ||||
chr7:16645649-16646205 | Common:3; Rare:192 | ||||
chr7:17298434-17298761 | Common:3; Rare:85 | ||||
chr7:17940412-17940582 | Common:1; Rare:88 | ||||
chr7:19708986-19709217 | Common:4; Rare:86 | ||||
chr7:20330404-20331077 | Common:4; Rare:174 | ||||
chr7:20331377-20331545 | Common:1; Rare:39 | ||||
chr7:20331739-20331974 | Common:1; Rare:93 | ||||
chr7:21427900-21428241 | Common:4; Rare:139 | ||||
chr7:23105673-23105963 | Common:3; Rare:133; Clinvar:3; Clinvar (benign):3 | ||||
chr7:23181919-23182128 | Rare:91 | ||||
chr7:24980153-24980425 | Common:8; Rare:111 | ||||
chr7:25125209-25125443 | Rare:103; Clinvar:3 | ||||
chr7:26200558-26201435 | Common:3; Rare:389 |