| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76725969-76726116 | Common:1; Rare:39 | ||||
| chr17:76726453-76726865 | Common:5; Rare:148 | ||||
| chr17:76737295-76737493 | Common:3; Rare:88 | ||||
| chr17:76737855-76738127 | Common:4; Rare:79 | ||||
| chr17:77127731-77127895 | Rare:29 | ||||
| chr17:77129905-77130110 | Common:1; Rare:30 | ||||
| chr17:77140756-77141080 | Rare:107 | ||||
| chr17:78041013-78041078 | Rare:17 | ||||
| chr17:78187018-78187391 | Common:3; Rare:130 | ||||
| chr17:78782196-78782577 | Common:9; Rare:124 | ||||
| chr17:78840751-78841047 | Common:2; Rare:106 | ||||
| chr17:78979833-78980076 | Common:2; Rare:51 | ||||
| chr17:79009732-79009922 | Common:8; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:79023896-79024342 | Common:3; Rare:96 | ||||
| chr17:79993689-79993813 | Common:1; Rare:24 |