| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32130175-32130389 | Common:2; Rare:39 | ||||
| chr6:32154376-32154648 | Common:1; Rare:51 | ||||
| chr6:32176049-32176276 | Common:1; Rare:49 | ||||
| chr6:32177047-32177407 | Common:1; Rare:61 | ||||
| chr6:32178125-32178666 | Common:2; Rare:113 | ||||
| chr6:32190146-32190322 | Rare:35 | ||||
| chr6:32192487-32192712 | Rare:39 | ||||
| chr6:32439712-32439938 | Common:2; Rare:42 | ||||
| chr6:32843973-32844156 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32844564-32844848 | Common:1; Rare:57 | ||||
| chr6:32853664-32853783 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854024-32854242 | Common:2; Rare:56 | ||||
| chr6:32953021-32953248 | Rare:45 | ||||
| chr6:32968454-32968616 | Common:3; Rare:43 | ||||
| chr6:32969128-32969360 | Common:4; Rare:69 |