| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43770076-43770254 | Common:3; Rare:54 | ||||
| chr6:43771923-43772055 | Rare:23 | ||||
| chr6:44126898-44127010 | Common:1; Rare:30 | ||||
| chr6:44127278-44127669 | Common:4; Rare:108 | ||||
| chr6:44219496-44219651 | Common:1; Rare:39 | ||||
| chr6:44246898-44247192 | Common:4; Rare:122 | ||||
| chr6:44387447-44387753 | Common:4; Rare:81 | ||||
| chr6:45377790-45378183 | Common:2; Rare:126 | ||||
| chr6:46129804-46130071 | Common:5; Rare:82 | ||||
| chr6:46170875-46171150 | Common:3; Rare:74 | ||||
| chr6:47477589-47478077 | Common:3; Rare:127; Clinvar:5; Clinvar (benign):4 | ||||
| chr6:49463186-49463434 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284713-52285085 | Common:2; Rare:120 | ||||
| chr6:52420150-52420376 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995267-52995817 | Common:4; Rare:228 |