| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43076149-43076468 | Rare:100 | ||||
| chr6:43516794-43517115 | Common:5; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575939-43576339 | Common:1; Rare:142; Clinvar:10 | ||||
| chr6:43770538-43770782 | Common:1; Rare:55; Clinvar:1 | ||||
| chr6:43777649-43777989 | Common:1; Rare:72 | ||||
| chr6:44126799-44126929 | Rare:38 | ||||
| chr6:44127334-44127677 | Common:4; Rare:100 | ||||
| chr6:45377424-45377514 | Common:2; Rare:28 | ||||
| chr6:45421991-45422338 | Common:1; Rare:96 | ||||
| chr6:49463174-49463418 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420101-52420376 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576812-52577327 | Common:7; Rare:185 | ||||
| chr6:52577363-52577470 | Rare:37 | ||||
| chr6:53544635-53544691 | Rare:21 | ||||
| chr6:56541842-56542176 | Rare:48 |