| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:88963549-88963850 | Common:2; Rare:103 | ||||
| chr6:89080610-89080808 | Common:1; Rare:88 | ||||
| chr6:89117937-89118093 | Common:1; Rare:61 | ||||
| chr6:89352627-89353039 | Common:2; Rare:98 | ||||
| chr6:89638443-89638522 | Common:1; Rare:15 | ||||
| chr6:89638721-89638824 | Common:3; Rare:36 | ||||
| chr6:89819732-89819917 | Rare:62 | ||||
| chr6:89829592-89829962 | Rare:98 | ||||
| chr6:90587012-90587203 | Common:3; Rare:63 | ||||
| chr6:93419538-93419744 | Common:1; Rare:62 | ||||
| chr6:95577424-95577582 | Common:5; Rare:47 | ||||
| chr6:96521583-96521871 | Common:9; Rare:128 | ||||
| chr6:96897803-96898086 | Common:4; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283101-97283416 | Common:3; Rare:87 | ||||
| chr6:99424627-99424980 | Rare:95 |