| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31620065-31620162 | Common:2; Rare:33 | ||||
| chr6:31683287-31683469 | Common:2; Rare:35 | ||||
| chr6:31821814-31822143 | Common:2; Rare:54 | ||||
| chr6:32302607-32302683 | Rare:10 | ||||
| chr6:32348014-32348017 | |||||
| chr6:32459997-32460064 | Common:1; Rare:28 | ||||
| chr6:32717909-32718096 | Common:2; Rare:29 | ||||
| chr6:32820673-32820817 | Common:4; Rare:12 | ||||
| chr6:32879637-32879829 | Common:1; Rare:35 | ||||
| chr6:32894614-32894832 | Common:6; Rare:62 | ||||
| chr6:33185631-33185809 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:33203392-33203557 | Common:1; Rare:34 | ||||
| chr6:33249208-33249361 | Common:2; Rare:42 | ||||
| chr6:33425388-33425427 | Rare:5 | ||||
| chr6:33425665-33425878 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 |