| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76726471-76726895 | Common:5; Rare:162 | ||||
| chr17:76737306-76737698 | Common:4; Rare:142 | ||||
| chr17:76737887-76738043 | Common:3; Rare:44 | ||||
| chr17:77140630-77141034 | Common:3; Rare:144 | ||||
| chr17:77450533-77450841 | Rare:58 | ||||
| chr17:78168510-78168619 | Rare:31 | ||||
| chr17:78187052-78187386 | Common:3; Rare:105 | ||||
| chr17:78378465-78378689 | Common:1; Rare:77 | ||||
| chr17:78782240-78782555 | Common:9; Rare:102 | ||||
| chr17:78840747-78841082 | Common:2; Rare:125 | ||||
| chr17:78979916-78980043 | Common:2; Rare:30 | ||||
| chr17:79009753-79009943 | Common:8; Rare:52; Clinvar (benign):1 | ||||
| chr17:79797029-79797398 | Common:1; Rare:121 | ||||
| chr17:80035849-80035983 | Common:1; Rare:49 | ||||
| chr17:80036608-80036665 | Common:2; Rare:13; Clinvar (benign):2 |