| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:180810108-180810289 | Common:5; Rare:55 | ||||
| chr6:693077-693182 | Rare:33 | ||||
| chr6:2765880-2765995 | Common:2; Rare:50 | ||||
| chr6:3456064-3456181 | Rare:40 | ||||
| chr6:5260675-5261052 | Common:5; Rare:136; Clinvar (benign):4 | ||||
| chr6:7910768-7910938 | Common:1; Rare:63 | ||||
| chr6:11094106-11094264 | Rare:47 | ||||
| chr6:13487565-13487932 | Common:2; Rare:86 | ||||
| chr6:13615165-13615474 | Common:3; Rare:133 | ||||
| chr6:24666862-24667193 | Common:3; Rare:139 | ||||
| chr6:27132791-27133042 | Common:3; Rare:81 | ||||
| chr6:27814775-27815022 | Common:2; Rare:68 | ||||
| chr6:28923664-28924060 | Common:5; Rare:115 | ||||
| chr6:30061149-30061363 | Common:1; Rare:40 | ||||
| chr6:30326380-30326469 | Common:1; Rare:12 |