| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:93419546-93419822 | Common:1; Rare:75 | ||||
| chr6:95577374-95577560 | Common:4; Rare:51 | ||||
| chr6:96521674-96521887 | Common:8; Rare:103 | ||||
| chr6:96897771-96898012 | Common:2; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:99424793-99424963 | Rare:58 | ||||
| chr6:99425259-99425611 | Common:2; Rare:87 | ||||
| chr6:100881207-100881495 | Common:5; Rare:107 | ||||
| chr6:105137021-105137299 | Common:1; Rare:95 | ||||
| chr6:105179907-105180054 | Common:4; Rare:38 | ||||
| chr6:106629448-106629669 | Common:3; Rare:54 | ||||
| chr6:107459490-107459738 | Common:2; Rare:64; Clinvar:1 | ||||
| chr6:107490451-107490575 | Common:2; Rare:44 | ||||
| chr6:107958075-107958374 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108260764-108260815 | Rare:14 | ||||
| chr6:108560730-108560971 | Rare:99 |