| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31739708-31740020 | Common:3; Rare:80 | ||||
| chr6:31806788-31807064 | Common:1; Rare:109 | ||||
| chr6:31815312-31815546 | Common:1; Rare:71 | ||||
| chr6:31827456-31827746 | Common:2; Rare:84 | ||||
| chr6:31834621-31834929 | Common:3; Rare:68 | ||||
| chr6:31958902-31959184 | Rare:87; Clinvar:8 | ||||
| chr6:32127767-32127910 | Rare:36 | ||||
| chr6:32128203-32128451 | Common:2; Rare:58 | ||||
| chr6:32838209-32838338 | Rare:33; Clinvar (benign):1 | ||||
| chr6:32844002-32844086 | Rare:22; Clinvar:1 | ||||
| chr6:32844631-32844792 | Common:1; Rare:32 | ||||
| chr6:32853686-32853777 | Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32854023-32854216 | Common:2; Rare:49 | ||||
| chr6:33200656-33200925 | Common:2; Rare:82 | ||||
| chr6:33208439-33208524 | Rare:22 |