| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:8435361-8435678 | Common:5; Rare:115 | ||||
| chr6:10694614-10695024 | Common:4; Rare:111 | ||||
| chr6:10722808-10723220 | Common:6; Rare:138 | ||||
| chr6:10747470-10747869 | Common:4; Rare:138 | ||||
| chr6:11232511-11232850 | Rare:89 | ||||
| chr6:13328490-13328615 | Common:4; Rare:56 | ||||
| chr6:13487569-13487886 | Common:2; Rare:80 | ||||
| chr6:13574389-13574639 | Common:1; Rare:67 | ||||
| chr6:13615180-13615624 | Common:2; Rare:174 | ||||
| chr6:13814109-13814289 | Common:1; Rare:61 | ||||
| chr6:17706388-17706495 | Rare:53 | ||||
| chr6:17706730-17706938 | Common:1; Rare:57 | ||||
| chr6:18155128-18155504 | Common:10; Rare:100 | ||||
| chr6:24495092-24495246 | Common:1; Rare:55; Clinvar:10; Clinvar (benign):4 | ||||
| chr6:24666759-24666935 | Common:1; Rare:82 |