| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31897574-31897786 | Rare:49 | ||||
| chr6:31958369-31958657 | Common:1; Rare:66 | ||||
| chr6:31958877-31959206 | Rare:112; Clinvar:8 | ||||
| chr6:32130149-32130395 | Common:2; Rare:40 | ||||
| chr6:32151875-32151942 | Rare:22 | ||||
| chr6:32154305-32154487 | Rare:25 | ||||
| chr6:32176020-32176258 | Common:1; Rare:49 | ||||
| chr6:32178084-32178469 | Common:3; Rare:61 | ||||
| chr6:32190170-32190248 | Rare:15 | ||||
| chr6:32838237-32838460 | Common:1; Rare:37 | ||||
| chr6:32843998-32844083 | Rare:24; Clinvar:1 | ||||
| chr6:32844585-32844814 | Common:1; Rare:45 | ||||
| chr6:32853660-32853810 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:32854010-32854241 | Common:2; Rare:57 | ||||
| chr6:32968362-32968668 | Common:6; Rare:90 |