| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42746039-42746340 | Common:1; Rare:97 | ||||
| chr6:42746672-42747012 | Rare:74 | ||||
| chr6:42781887-42782080 | Common:8; Rare:45 | ||||
| chr6:42879594-42879950 | Rare:105 | ||||
| chr6:42929138-42929205 | Rare:21 | ||||
| chr6:42929209-42929406 | Common:3; Rare:46 | ||||
| chr6:42929409-42929786 | Common:2; Rare:150 | ||||
| chr6:42984284-42984660 | Rare:106 | ||||
| chr6:43013784-43014305 | Common:2; Rare:136 | ||||
| chr6:43053782-43054082 | Common:1; Rare:82; Clinvar:5 | ||||
| chr6:43059812-43059890 | Rare:26 | ||||
| chr6:43171630-43171945 | Common:1; Rare:59 | ||||
| chr6:43182053-43182223 | Rare:49 | ||||
| chr6:43516750-43517119 | Common:6; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575903-43576240 | Common:2; Rare:137; Clinvar:8 |