| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:4021209-4021454 | Rare:109 | ||||
| chr6:5004007-5004126 | Common:1; Rare:53 | ||||
| chr6:5260691-5261059 | Common:5; Rare:130; Clinvar (benign):4 | ||||
| chr6:5261238-5261578 | Common:9; Rare:88 | ||||
| chr6:7108381-7108686 | Common:1; Rare:91 | ||||
| chr6:7313042-7313383 | Common:5; Rare:126 | ||||
| chr6:7541349-7542096 | Common:5; Rare:247; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr6:8102524-8102756 | Common:1; Rare:77 | ||||
| chr6:8435452-8435662 | Common:4; Rare:79 | ||||
| chr6:10694620-10695015 | Common:4; Rare:102 | ||||
| chr6:10722947-10723224 | Common:5; Rare:102 | ||||
| chr6:10747582-10747855 | Common:3; Rare:106 | ||||
| chr6:11232612-11232820 | Rare:44 | ||||
| chr6:13615303-13615550 | Common:1; Rare:92 | ||||
| chr6:15245675-15245976 | Common:2; Rare:82 |