| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89829614-89829914 | Rare:70 | ||||
| chr6:90586992-90587334 | Common:3; Rare:94 | ||||
| chr6:95577408-95577571 | Common:4; Rare:45 | ||||
| chr6:96521497-96521876 | Common:10; Rare:154 | ||||
| chr6:96897797-96898012 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:97283168-97283318 | Common:2; Rare:50 | ||||
| chr6:99425253-99425506 | Common:2; Rare:69 | ||||
| chr6:99515400-99515595 | Common:1; Rare:63 | ||||
| chr6:100881245-100881498 | Common:5; Rare:97 | ||||
| chr6:106325403-106325514 | Common:1; Rare:22 | ||||
| chr6:106325551-106325892 | Common:1; Rare:112 | ||||
| chr6:106629443-106629675 | Common:3; Rare:56 | ||||
| chr6:106975287-106975397 | Rare:34 | ||||
| chr6:107459528-107459676 | Common:1; Rare:35 | ||||
| chr6:107958106-107958428 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):2 |