| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85643812-85643931 | Common:2; Rare:37 | ||||
| chr6:87155268-87155594 | Rare:87 | ||||
| chr6:87589920-87590190 | Common:3; Rare:139; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87702223-87702526 | Common:1; Rare:91 | ||||
| chr6:89081048-89081360 | Common:2; Rare:123 | ||||
| chr6:89352627-89353008 | Common:2; Rare:85 | ||||
| chr6:89638443-89638845 | Common:6; Rare:124 | ||||
| chr6:89819732-89819813 | Rare:32 | ||||
| chr6:89829592-89829955 | Rare:96 | ||||
| chr6:90586992-90587334 | Common:3; Rare:94 | ||||
| chr6:93419552-93419824 | Common:1; Rare:73 | ||||
| chr6:95577325-95577578 | Common:6; Rare:69 | ||||
| chr6:96521719-96521887 | Common:3; Rare:80 | ||||
| chr6:96897805-96898083 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283174-97283302 | Common:1; Rare:47 |