| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42050347-42050534 | Common:1; Rare:52 | ||||
| chr6:42142604-42142722 | Common:1; Rare:35 | ||||
| chr6:42564124-42564210 | Rare:19 | ||||
| chr6:42564380-42564394 | Rare:3 | ||||
| chr6:42746074-42746340 | Rare:73 | ||||
| chr6:42879577-42879940 | Rare:106 | ||||
| chr6:42929226-42929566 | Common:3; Rare:98 | ||||
| chr6:42984284-42984609 | Rare:80 | ||||
| chr6:43013878-43014305 | Common:2; Rare:96 | ||||
| chr6:43059812-43059890 | Rare:26 | ||||
| chr6:43076180-43076464 | Rare:86 | ||||
| chr6:43182110-43182228 | Rare:33 | ||||
| chr6:43516869-43517127 | Common:4; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576197 | Rare:97; Clinvar:4 | ||||
| chr6:43629143-43629484 | Common:2; Rare:96 |