| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32838212-32838362 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr6:32843979-32844130 | Rare:35; Clinvar:1 | ||||
| chr6:32844346-32844447 | Rare:27 | ||||
| chr6:32844565-32844861 | Common:1; Rare:59 | ||||
| chr6:32853664-32853796 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853979-32854250 | Common:2; Rare:64 | ||||
| chr6:32940915-32941204 | Common:1; Rare:51 | ||||
| chr6:32968502-32968600 | Common:1; Rare:26 | ||||
| chr6:33075775-33076015 | Common:3; Rare:28 | ||||
| chr6:33200656-33200921 | Common:2; Rare:82 | ||||
| chr6:33208452-33208530 | Rare:21 | ||||
| chr6:33271836-33272130 | Common:2; Rare:121 | ||||
| chr6:33272335-33272739 | Common:2; Rare:77 | ||||
| chr6:33298937-33299042 | Rare:28 | ||||
| chr6:33322891-33323246 | Common:5; Rare:116 |