| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:88963561-88963888 | Common:2; Rare:115 | ||||
| chr6:89145972-89146094 | Rare:35 | ||||
| chr6:89352694-89353005 | Common:1; Rare:69 | ||||
| chr6:89638434-89638542 | Common:1; Rare:24 | ||||
| chr6:89638712-89638953 | Common:4; Rare:79 | ||||
| chr6:89819705-89819879 | Rare:58 | ||||
| chr6:89829609-89829974 | Common:1; Rare:92 | ||||
| chr6:90587012-90587357 | Common:4; Rare:98 | ||||
| chr6:95577403-95577595 | Common:5; Rare:55 | ||||
| chr6:96521695-96521866 | Common:5; Rare:80 | ||||
| chr6:96897702-96898077 | Common:4; Rare:141; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:97283120-97283416 | Common:3; Rare:84 | ||||
| chr6:99402505-99402824 | Rare:82 | ||||
| chr6:99424857-99424952 | Rare:38 | ||||
| chr6:99425215-99425496 | Common:2; Rare:84 |