| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31958891-31959191 | Rare:97; Clinvar:8 | ||||
| chr6:32176056-32176238 | Common:1; Rare:38 | ||||
| chr6:32192583-32192753 | Rare:27 | ||||
| chr6:32843993-32844119 | Rare:29; Clinvar:1 | ||||
| chr6:32844374-32844840 | Common:1; Rare:103 | ||||
| chr6:32853640-32854242 | Common:4; Rare:180; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:33200656-33200925 | Common:2; Rare:82 | ||||
| chr6:33208441-33208522 | Rare:22 | ||||
| chr6:33271664-33272138 | Common:3; Rare:167 | ||||
| chr6:33289186-33289357 | Common:1; Rare:44 | ||||
| chr6:33298882-33299052 | Rare:42 | ||||
| chr6:33313979-33314109 | Common:2; Rare:51 | ||||
| chr6:33417864-33417959 | Rare:40 | ||||
| chr6:33418028-33418455 | Common:2; Rare:102 | ||||
| chr6:33454446-33454607 | Rare:39 |