| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5003641-5003836 | Common:5; Rare:60 | ||||
| chr6:5004006-5004106 | Common:1; Rare:50 | ||||
| chr6:5260675-5261059 | Common:5; Rare:138; Clinvar (benign):4 | ||||
| chr6:5261280-5261554 | Common:9; Rare:65 | ||||
| chr6:6006760-6007055 | Common:1; Rare:64 | ||||
| chr6:6588617-6588787 | Common:1; Rare:55 | ||||
| chr6:7107380-7107801 | Common:1; Rare:134 | ||||
| chr6:7313054-7313298 | Common:5; Rare:96 | ||||
| chr6:7389740-7389881 | Common:1; Rare:41 | ||||
| chr6:7541979-7542056 | Common:2; Rare:33; Clinvar:6; Clinvar (benign):5 | ||||
| chr6:7590075-7590257 | Common:5; Rare:58 | ||||
| chr6:8435491-8435659 | Common:3; Rare:66 | ||||
| chr6:10521219-10521542 | Common:1; Rare:78 | ||||
| chr6:10556152-10556275 | Rare:34; Clinvar:1 | ||||
| chr6:10694607-10694988 | Common:4; Rare:101 |