| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42050778-42050928 | Common:1; Rare:31 | ||||
| chr6:42155258-42155457 | Common:1; Rare:25 | ||||
| chr6:42217813-42217978 | Common:5; Rare:53 | ||||
| chr6:42451884-42452329 | Common:4; Rare:82 | ||||
| chr6:42563807-42564109 | Common:1; Rare:73 | ||||
| chr6:42564110-42564206 | Rare:21 | ||||
| chr6:42746039-42746348 | Common:1; Rare:99 | ||||
| chr6:42746840-42747003 | Rare:35 | ||||
| chr6:42781929-42782080 | Common:3; Rare:35 | ||||
| chr6:42879577-42879940 | Rare:106 | ||||
| chr6:42890789-42890864 | Rare:38 | ||||
| chr6:42929096-42929205 | Rare:30 | ||||
| chr6:42929211-42929440 | Common:3; Rare:56 | ||||
| chr6:42929446-42929578 | Rare:51 | ||||
| chr6:42979162-42979324 | Common:3; Rare:51; Clinvar:4; Clinvar (benign):1 |