| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3157530-3157648 | Common:6; Rare:45 | ||||
| chr6:4021201-4021454 | Rare:111 | ||||
| chr6:5004007-5004126 | Common:1; Rare:53 | ||||
| chr6:5260651-5261025 | Common:3; Rare:130; Clinvar (benign):4 | ||||
| chr6:5261274-5261559 | Common:9; Rare:72 | ||||
| chr6:7108553-7108656 | Common:1; Rare:35 | ||||
| chr6:7313052-7313361 | Common:5; Rare:117 | ||||
| chr6:7389740-7389969 | Common:1; Rare:61 | ||||
| chr6:7541305-7541866 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:7590075-7590252 | Common:5; Rare:54 | ||||
| chr6:8064323-8064576 | Common:4; Rare:83 | ||||
| chr6:8102517-8102693 | Common:1; Rare:59 | ||||
| chr6:8435431-8435687 | Common:5; Rare:94 | ||||
| chr6:10521182-10521575 | Common:1; Rare:98 | ||||
| chr6:10585626-10585778 | Common:2; Rare:33 |