| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42564368-42564394 | Rare:4 | ||||
| chr6:42746062-42746335 | Rare:80 | ||||
| chr6:42879583-42879934 | Rare:102 | ||||
| chr6:42929230-42929609 | Common:3; Rare:111 | ||||
| chr6:42929673-42929774 | Rare:40 | ||||
| chr6:42960626-42960755 | Common:1; Rare:29 | ||||
| chr6:42979162-42979324 | Common:3; Rare:51; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:42984312-42984649 | Rare:95 | ||||
| chr6:43013891-43014270 | Common:2; Rare:81 | ||||
| chr6:43060207-43060585 | Common:1; Rare:98 | ||||
| chr6:43072959-43073274 | Rare:62 | ||||
| chr6:43427783-43427893 | Rare:23 | ||||
| chr6:43516846-43517109 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575933-43576240 | Common:2; Rare:124; Clinvar:8 | ||||
| chr6:43629126-43629464 | Common:2; Rare:99 |