| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32189786-32189927 | Common:3; Rare:48 | ||||
| chr6:32838219-32838256 | Rare:14; Clinvar (benign):1 | ||||
| chr6:32843906-32844130 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32844294-32844795 | Common:1; Rare:106 | ||||
| chr6:32853682-32853856 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853986-32854224 | Common:2; Rare:57 | ||||
| chr6:32968491-32968652 | Common:1; Rare:52 | ||||
| chr6:33200346-33200440 | Rare:24 | ||||
| chr6:33200649-33200976 | Common:3; Rare:94 | ||||
| chr6:33202081-33202301 | Common:2; Rare:68 | ||||
| chr6:33271827-33272127 | Common:1; Rare:121 | ||||
| chr6:33288966-33289106 | Rare:56 | ||||
| chr6:33289133-33289157 | Rare:8 | ||||
| chr6:33289163-33289693 | Common:4; Rare:124 | ||||
| chr6:33299417-33299510 | Common:1; Rare:22 |