| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:39725397-39725544 | Common:2; Rare:31 | ||||
| chr6:39934431-39934568 | Common:2; Rare:75 | ||||
| chr6:41072312-41072513 | Rare:60 | ||||
| chr6:41921109-41921239 | Rare:34 | ||||
| chr6:42050369-42050534 | Common:1; Rare:50 | ||||
| chr6:42217846-42217962 | Common:2; Rare:30 | ||||
| chr6:42746069-42746258 | Rare:54 | ||||
| chr6:42890803-42890885 | Rare:34 | ||||
| chr6:42929240-42929556 | Common:3; Rare:85 | ||||
| chr6:42984284-42984609 | Rare:80 | ||||
| chr6:43013869-43014287 | Common:2; Rare:92 | ||||
| chr6:43427468-43427580 | Rare:36 | ||||
| chr6:43477488-43477589 | Rare:20 | ||||
| chr6:43516846-43517109 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576175 | Rare:87; Clinvar:4 |