| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44246036-44246313 | Rare:73 | ||||
| chr6:44246880-44247193 | Common:4; Rare:132 | ||||
| chr6:44387439-44387868 | Common:4; Rare:115 | ||||
| chr6:45377805-45378198 | Common:2; Rare:130 | ||||
| chr6:45421974-45422115 | Common:1; Rare:46 | ||||
| chr6:46129762-46130176 | Common:5; Rare:129 | ||||
| chr6:46170846-46171173 | Common:3; Rare:83 | ||||
| chr6:46491941-46491982 | Rare:11 | ||||
| chr6:46652684-46653022 | Rare:82 | ||||
| chr6:46921819-46922086 | Common:3; Rare:70 | ||||
| chr6:47029050-47029336 | Rare:57 | ||||
| chr6:47477610-47478252 | Common:5; Rare:186; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463143-49463412 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:49636830-49637036 | Rare:50 | ||||
| chr6:50818836-50818932 | Common:1; Rare:25; Clinvar (benign):1 |