| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79537131-79537184 | Rare:12; Clinvar:1 | ||||
| chr6:79537344-79537858 | Common:2; Rare:148; Clinvar:4 | ||||
| chr6:79631245-79631304 | Rare:13 | ||||
| chr6:80106434-80106722 | Common:1; Rare:101; Clinvar (pathogenic):1 | ||||
| chr6:82364174-82364337 | Common:2; Rare:47 | ||||
| chr6:83193183-83193413 | Common:3; Rare:76 | ||||
| chr6:85449570-85449749 | Common:2; Rare:46 | ||||
| chr6:87155248-87155597 | Rare:90 | ||||
| chr6:87589921-87590183 | Common:3; Rare:136; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87701857-87702002 | Common:1; Rare:47 | ||||
| chr6:87702213-87702504 | Common:1; Rare:89 | ||||
| chr6:88963579-88963875 | Common:2; Rare:103 | ||||
| chr6:89145932-89146096 | Rare:44 | ||||
| chr6:89638404-89638541 | Common:1; Rare:31 | ||||
| chr6:89638685-89638832 | Common:5; Rare:56 |