| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33420043-33420282 | Rare:50 | ||||
| chr6:33580243-33580376 | Common:2; Rare:34 | ||||
| chr6:33711687-33711795 | Rare:43; Clinvar (benign):1 | ||||
| chr6:34248981-34249242 | Common:1; Rare:58 | ||||
| chr6:34392162-34392676 | Common:1; Rare:198 | ||||
| chr6:34426000-34426158 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34514625-34514829 | Common:1; Rare:56 | ||||
| chr6:34696717-34696975 | Common:1; Rare:59 | ||||
| chr6:34757337-34757541 | Common:1; Rare:61 | ||||
| chr6:34887947-34888124 | Common:1; Rare:45 | ||||
| chr6:35921042-35921241 | Common:1; Rare:82 | ||||
| chr6:36442900-36443070 | Common:2; Rare:69 | ||||
| chr6:36547417-36547559 | Rare:68 | ||||
| chr6:36594167-36594381 | Common:3; Rare:79 | ||||
| chr6:36874785-36875142 | Common:1; Rare:74 |