| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:6825249-6825396 | Common:1; Rare:27 | ||||
| chr6:7543246-7543523 | Common:1; Rare:52 | ||||
| chr6:7545859-7546128 | Common:1; Rare:47 | ||||
| chr6:7553811-7553858 | Rare:4 | ||||
| chr6:7558001-7558264 | Common:1; Rare:65; Clinvar:6; Clinvar (benign):3 | ||||
| chr6:7567765-7568012 | Rare:52; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr6:16436665-16436786 | Common:1; Rare:24 | ||||
| chr6:21595840-21596016 | Rare:68 | ||||
| chr6:25006535-25006827 | Common:3; Rare:51 | ||||
| chr6:26122991-26123193 | Common:2; Rare:56 | ||||
| chr6:26126246-26126537 | Common:3; Rare:48 | ||||
| chr6:28161722-28161781 | Rare:6 | ||||
| chr6:29749009-29749186 | Common:7; Rare:31 | ||||
| chr6:29752581-29752639 | Common:1; Rare:7 | ||||
| chr6:29888414-29888665 | Common:19; Rare:105 |