| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179698671-179699095 | Common:4; Rare:135 | ||||
| chr5:179806321-179806448 | Rare:41 | ||||
| chr5:180810102-180810292 | Common:5; Rare:57 | ||||
| chr5:181223224-181223315 | Rare:28 | ||||
| chr5:181261083-181261213 | Rare:38 | ||||
| chr6:693054-693188 | Rare:45 | ||||
| chr6:2245585-2245817 | Rare:76 | ||||
| chr6:2765920-2765995 | Rare:26 | ||||
| chr6:4021161-4021440 | Rare:115 | ||||
| chr6:5003644-5003825 | Common:5; Rare:53 | ||||
| chr6:5260681-5261654 | Common:21; Rare:303; Clinvar (benign):4 | ||||
| chr6:7910777-7910917 | Rare:50 | ||||
| chr6:10412247-10412309 | Rare:12 | ||||
| chr6:10412351-10412556 | Common:2; Rare:36 | ||||
| chr6:10747582-10747869 | Common:3; Rare:110 |