| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:133953020-133953233 | Common:2; Rare:62 | ||||
| chr6:134174800-134175066 | Common:1; Rare:145 | ||||
| chr6:134175676-134175734 | Rare:17 | ||||
| chr6:134317780-134317981 | Common:1; Rare:42 | ||||
| chr6:135054741-135054937 | Common:6; Rare:59 | ||||
| chr6:135497578-135497975 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136250272-136250483 | Common:2; Rare:59 | ||||
| chr6:136289322-136289485 | Rare:81 | ||||
| chr6:136289774-136290040 | Common:1; Rare:116 | ||||
| chr6:136550346-136550691 | Common:2; Rare:105 | ||||
| chr6:136551313-136551593 | Common:3; Rare:31 | ||||
| chr6:136793002-136793088 | Rare:17 | ||||
| chr6:137044710-137044754 | Rare:6 | ||||
| chr6:137044900-137045063 | Common:2; Rare:40 | ||||
| chr6:137219075-137219197 | Rare:29 |