| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:157981625-157981902 | Common:3; Rare:72 | ||||
| chr6:158168191-158168421 | Common:2; Rare:82; Clinvar:1 | ||||
| chr6:158644683-158644945 | Common:3; Rare:106 | ||||
| chr6:158818227-158818339 | Common:1; Rare:42 | ||||
| chr6:158819336-158819452 | Common:2; Rare:37 | ||||
| chr6:158999729-158999975 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:159000185-159000261 | Rare:20 | ||||
| chr6:159693150-159693612 | Common:6; Rare:141 | ||||
| chr6:159726878-159727176 | Common:1; Rare:128 | ||||
| chr6:159727276-159727703 | Common:6; Rare:168 | ||||
| chr6:159779660-159779951 | Common:1; Rare:89 | ||||
| chr6:159788185-159788478 | Common:1; Rare:70 | ||||
| chr6:159789407-159789990 | Common:4; Rare:207 | ||||
| chr6:159790257-159790564 | Common:8; Rare:111 | ||||
| chr6:159968952-159969168 | Common:1; Rare:82 |