| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5003609-5003843 | Common:6; Rare:73 | ||||
| chr6:5003998-5004121 | Common:2; Rare:56 | ||||
| chr6:5260648-5261060 | Common:6; Rare:150; Clinvar (benign):4 | ||||
| chr6:5261268-5261585 | Common:9; Rare:86 | ||||
| chr6:6002900-6003039 | Common:1; Rare:30 | ||||
| chr6:6006695-6007115 | Common:3; Rare:98 | ||||
| chr6:6007369-6007428 | Common:1; Rare:18 | ||||
| chr6:6007450-6007642 | Common:3; Rare:57 | ||||
| chr6:7313062-7313404 | Common:5; Rare:127 | ||||
| chr6:7389740-7389976 | Common:1; Rare:61 | ||||
| chr6:7590111-7590254 | Common:3; Rare:45 | ||||
| chr6:8064288-8064434 | Common:1; Rare:65 | ||||
| chr6:8102435-8102706 | Common:1; Rare:98 | ||||
| chr6:8435354-8435721 | Common:7; Rare:127 | ||||
| chr6:10555919-10556291 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 |