| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3157488-3157706 | Common:7; Rare:82 | ||||
| chr6:3258825-3259101 | Rare:107 | ||||
| chr6:4021246-4021423 | Rare:91 | ||||
| chr6:4135216-4135307 | Rare:27 | ||||
| chr6:5003649-5003843 | Common:5; Rare:61 | ||||
| chr6:5004002-5004088 | Common:1; Rare:45 | ||||
| chr6:5260691-5261015 | Common:3; Rare:108; Clinvar (benign):4 | ||||
| chr6:5261428-5261559 | Common:3; Rare:31 | ||||
| chr6:7313083-7313380 | Common:5; Rare:111 | ||||
| chr6:7389718-7389892 | Common:1; Rare:58 | ||||
| chr6:7910610-7910917 | Common:4; Rare:122 | ||||
| chr6:8064307-8064580 | Common:4; Rare:91 | ||||
| chr6:8435354-8435659 | Common:4; Rare:105 | ||||
| chr6:10694603-10694988 | Common:4; Rare:103 | ||||
| chr6:10722823-10723224 | Common:6; Rare:132 |