| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32153338-32153564 | Rare:33 | ||||
| chr6:32154364-32154492 | Rare:15 | ||||
| chr6:32176069-32176216 | Common:1; Rare:27 | ||||
| chr6:32177063-32177250 | Rare:30 | ||||
| chr6:32178110-32178462 | Common:2; Rare:53 | ||||
| chr6:32190127-32190351 | Rare:45 | ||||
| chr6:32530220-32530489 | Common:19; Rare:31 | ||||
| chr6:32589733-32589826 | Common:9; Rare:24 | ||||
| chr6:32637254-32637439 | Common:18; Rare:13 | ||||
| chr6:32666636-32666966 | Common:49; Rare:28 | ||||
| chr6:32838219-32838345 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr6:32843993-32844136 | Rare:33; Clinvar:1 | ||||
| chr6:32844616-32844848 | Common:1; Rare:50 | ||||
| chr6:32853670-32854216 | Common:3; Rare:160; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32968509-32968602 | Common:1; Rare:26 |