| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3751290-3751583 | Common:2; Rare:128 | ||||
| chr6:4021187-4021445 | Rare:113 | ||||
| chr6:5003656-5003843 | Common:5; Rare:58 | ||||
| chr6:5004007-5004106 | Common:1; Rare:49 | ||||
| chr6:5260671-5261597 | Common:20; Rare:298; Clinvar (benign):4 | ||||
| chr6:6004017-6004241 | Rare:54 | ||||
| chr6:7108338-7108523 | Rare:54 | ||||
| chr6:7108557-7108686 | Common:1; Rare:44 | ||||
| chr6:7313052-7313380 | Common:5; Rare:124 | ||||
| chr6:7389740-7389980 | Common:1; Rare:63 | ||||
| chr6:7541467-7541701 | Rare:70; Clinvar (benign):1 | ||||
| chr6:8435440-8435665 | Common:4; Rare:82 | ||||
| chr6:10521213-10521488 | Common:1; Rare:70 | ||||
| chr6:10555962-10556291 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:10694607-10694991 | Common:4; Rare:102 |