| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33299152-33299532 | Common:3; Rare:83 | ||||
| chr6:33322891-33323265 | Common:5; Rare:117 | ||||
| chr6:33391696-33391888 | Common:1; Rare:49 | ||||
| chr6:33410920-33411058 | Rare:26 | ||||
| chr6:33418015-33418493 | Common:3; Rare:116 | ||||
| chr6:33419976-33420301 | Rare:65; Clinvar (benign):1 | ||||
| chr6:33454406-33454601 | Rare:55 | ||||
| chr6:33580237-33580371 | Common:2; Rare:34 | ||||
| chr6:33711666-33711795 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr6:34236823-34236873 | Rare:21 | ||||
| chr6:34248981-34249239 | Common:1; Rare:58 | ||||
| chr6:34392162-34392512 | Common:1; Rare:140 | ||||
| chr6:34426010-34426155 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696768-34696980 | Common:1; Rare:48 | ||||
| chr6:34757335-34757579 | Common:1; Rare:74 |