| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31777134-31777182 | Rare:12 | ||||
| chr6:31815340-31815550 | Common:1; Rare:67 | ||||
| chr6:31834596-31834924 | Common:3; Rare:75 | ||||
| chr6:31897673-31897782 | Rare:20 | ||||
| chr6:31958892-31959195 | Rare:100; Clinvar:8 | ||||
| chr6:32154749-32155072 | Rare:65 | ||||
| chr6:32177042-32177442 | Common:2; Rare:67 | ||||
| chr6:32190142-32190311 | Rare:36 | ||||
| chr6:32844002-32844144 | Rare:31; Clinvar:1 | ||||
| chr6:32844616-32844848 | Common:1; Rare:50 | ||||
| chr6:32853670-32853884 | Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854019-32854250 | Common:2; Rare:58 | ||||
| chr6:32968795-32968933 | Common:4; Rare:45 | ||||
| chr6:33200356-33200449 | Rare:24 | ||||
| chr6:33200652-33200976 | Common:3; Rare:93 |