Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177022635-177022743 | Rare:39 | ||||
chr5:177303665-177303816 | Common:4; Rare:69 | ||||
chr5:177496733-177496922 | Rare:44 | ||||
chr5:179698635-179699096 | Common:4; Rare:159 | ||||
chr5:179806279-179806423 | Rare:40 | ||||
chr5:179824082-179824313 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
chr6:693096-693206 | Rare:31 | ||||
chr6:5260696-5261059 | Common:5; Rare:127; Clinvar (benign):4 | ||||
chr6:5261250-5261612 | Common:9; Rare:104 | ||||
chr6:8435467-8435648 | Common:3; Rare:69 | ||||
chr6:13574391-13574601 | Common:1; Rare:50 | ||||
chr6:13615170-13615494 | Common:2; Rare:136 | ||||
chr6:18122607-18122753 | Common:1; Rare:37; Clinvar (benign):3 | ||||
chr6:24666861-24667200 | Common:3; Rare:140 | ||||
chr6:26204445-26204610 | Common:1; Rare:70 |