| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:29792500-29792570 | Common:1; Rare:22 | ||||
| chr6:29888100-29888209 | Common:10; Rare:59 | ||||
| chr6:29889716-29889806 | Common:8; Rare:25 | ||||
| chr6:29927067-29927320 | Common:19; Rare:33 | ||||
| chr6:29944139-29944616 | Common:36; Rare:121 | ||||
| chr6:30191064-30191188 | Common:1; Rare:13 | ||||
| chr6:30491188-30491653 | Common:1; Rare:124 | ||||
| chr6:30601504-30601807 | Common:1; Rare:72 | ||||
| chr6:30815527-30815686 | Common:3; Rare:43 | ||||
| chr6:30916991-30917252 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr6:30998749-30998829 | Rare:15 | ||||
| chr6:31001139-31001301 | Common:4; Rare:33 | ||||
| chr6:31055501-31055971 | Common:4; Rare:54 | ||||
| chr6:31067780-31067825 | Common:2; Rare:8 | ||||
| chr6:31186046-31186179 | Common:5; Rare:27 |