| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43182091-43182221 | Rare:37 | ||||
| chr6:43427461-43427572 | Rare:32 | ||||
| chr6:43516791-43517124 | Common:6; Rare:123; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575918-43576234 | Common:2; Rare:126; Clinvar:8 | ||||
| chr6:43635772-43635893 | Common:1; Rare:32 | ||||
| chr6:43687768-43687825 | Common:1; Rare:22 | ||||
| chr6:43770087-43770282 | Common:3; Rare:54 | ||||
| chr6:44127278-44127639 | Common:4; Rare:97 | ||||
| chr6:44223439-44223620 | Common:1; Rare:53 | ||||
| chr6:44246898-44247179 | Common:4; Rare:116 | ||||
| chr6:44387655-44387747 | Common:2; Rare:34 | ||||
| chr6:45377855-45378183 | Common:2; Rare:111 | ||||
| chr6:46129805-46130113 | Common:5; Rare:101 | ||||
| chr6:47477664-47478245 | Common:5; Rare:171; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463186-49463433 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 |