| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:4135210-4135426 | Common:1; Rare:56 | ||||
| chr6:5003656-5003843 | Common:5; Rare:58 | ||||
| chr6:5004000-5004126 | Common:2; Rare:57 | ||||
| chr6:5260651-5261059 | Common:5; Rare:149; Clinvar (benign):4 | ||||
| chr6:5261275-5261610 | Common:9; Rare:95 | ||||
| chr6:7107527-7108037 | Common:2; Rare:155 | ||||
| chr6:7108272-7108519 | Rare:75 | ||||
| chr6:7313049-7313383 | Common:5; Rare:125 | ||||
| chr6:7389400-7389488 | Rare:18 | ||||
| chr6:7389753-7389966 | Common:1; Rare:53 | ||||
| chr6:7541288-7542040 | Common:5; Rare:238; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr6:7590075-7590281 | Common:5; Rare:74 | ||||
| chr6:7910606-7910910 | Common:4; Rare:118 | ||||
| chr6:8064314-8064581 | Common:4; Rare:91 | ||||
| chr6:8102484-8102757 | Common:1; Rare:94 |