| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75493900-75493917 | Rare:3 | ||||
| chr6:75749094-75749246 | Common:3; Rare:46; Clinvar:1 | ||||
| chr6:78867470-78867621 | Rare:73 | ||||
| chr6:79078245-79078590 | Common:1; Rare:148 | ||||
| chr6:79234585-79234771 | Common:2; Rare:48 | ||||
| chr6:79537148-79537222 | Rare:19; Clinvar:1 | ||||
| chr6:79537351-79537676 | Common:2; Rare:104; Clinvar:4 | ||||
| chr6:79631156-79631358 | Common:2; Rare:51 | ||||
| chr6:80004511-80004697 | Common:3; Rare:38 | ||||
| chr6:83193191-83193407 | Common:3; Rare:72 | ||||
| chr6:84763442-84763647 | Rare:48 | ||||
| chr6:85593714-85593975 | Common:1; Rare:88 | ||||
| chr6:85643812-85643957 | Common:2; Rare:43 | ||||
| chr6:87155248-87155606 | Rare:94 | ||||
| chr6:87589915-87590169 | Common:3; Rare:130; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 |