| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149481122-149481187 | Rare:10 | ||||
| chr6:150456529-150456613 | Rare:28 | ||||
| chr6:150632827-150633056 | Common:1; Rare:34 | ||||
| chr6:150684743-150685047 | Rare:55 | ||||
| chr6:150827232-150827455 | Common:2; Rare:39 | ||||
| chr6:152428253-152428577 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):5 | ||||
| chr6:152992856-152993167 | Common:1; Rare:77 | ||||
| chr6:155221087-155221256 | Common:14; Rare:35 | ||||
| chr6:155222516-155222687 | Common:17; Rare:28 | ||||
| chr6:157022134-157022355 | Common:2; Rare:72 | ||||
| chr6:157189744-157190086 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:158770772-158770980 | Rare:67 | ||||
| chr6:158771256-158771597 | Common:1; Rare:98 | ||||
| chr6:159694384-159694476 | Common:2; Rare:18 | ||||
| chr6:159761240-159761456 | Common:1; Rare:37 |