| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5003998-5004112 | Common:2; Rare:55 | ||||
| chr6:5260691-5261017 | Common:3; Rare:109; Clinvar (benign):4 | ||||
| chr6:7313052-7313298 | Common:5; Rare:97 | ||||
| chr6:7389740-7389820 | Rare:24 | ||||
| chr6:8102517-8102706 | Common:1; Rare:62 | ||||
| chr6:8435440-8435670 | Common:5; Rare:83 | ||||
| chr6:10555675-10555873 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:10555996-10556328 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:10585625-10585815 | Common:2; Rare:43 | ||||
| chr6:10694629-10695051 | Common:4; Rare:112 | ||||
| chr6:10722860-10723233 | Common:6; Rare:129 | ||||
| chr6:10747575-10747869 | Common:3; Rare:115 | ||||
| chr6:10886979-10887108 | Common:3; Rare:41 | ||||
| chr6:13328503-13328629 | Common:3; Rare:51 | ||||
| chr6:13615159-13615744 | Common:3; Rare:245 |