| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87589946-87590177 | Common:3; Rare:109; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702213-87702298 | Rare:42 | ||||
| chr6:88963540-88963830 | Common:2; Rare:96 | ||||
| chr6:89080610-89080869 | Common:2; Rare:111 | ||||
| chr6:89117943-89118133 | Common:4; Rare:79 | ||||
| chr6:89352634-89352714 | Rare:17 | ||||
| chr6:89638443-89638845 | Common:6; Rare:124 | ||||
| chr6:89819720-89819877 | Rare:54 | ||||
| chr6:89829595-89829962 | Rare:98 | ||||
| chr6:90586964-90587366 | Common:5; Rare:109 | ||||
| chr6:93419525-93419824 | Common:1; Rare:79 | ||||
| chr6:95577398-95577608 | Common:5; Rare:60 | ||||
| chr6:96521723-96521871 | Common:3; Rare:69 | ||||
| chr6:96897771-96898040 | Common:4; Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:96924356-96924702 | Common:4; Rare:95 |