| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:153131215-153131521 | Rare:137 | ||||
| chr6:155314456-155314635 | Common:2; Rare:61 | ||||
| chr6:157323473-157323593 | Common:2; Rare:52 | ||||
| chr6:157715771-157716120 | Rare:53 | ||||
| chr6:158168201-158168388 | Common:2; Rare:66 | ||||
| chr6:158644704-158644930 | Common:2; Rare:89 | ||||
| chr6:158649852-158650070 | Common:1; Rare:38 | ||||
| chr6:158818109-158818345 | Common:4; Rare:92 | ||||
| chr6:158819322-158819435 | Common:2; Rare:44 | ||||
| chr6:158999752-158999886 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159000172-159000305 | Rare:33 | ||||
| chr6:159693144-159693587 | Common:6; Rare:131 | ||||
| chr6:159726911-159727029 | Common:1; Rare:52 | ||||
| chr6:159727057-159727235 | Rare:56 | ||||
| chr6:159727325-159727673 | Common:5; Rare:141 |