| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77088591-77088810 | Common:1; Rare:63 | ||||
| chr17:77140630-77140908 | Common:3; Rare:105 | ||||
| chr17:77450280-77450567 | Common:2; Rare:61 | ||||
| chr17:77450594-77450768 | Rare:34 | ||||
| chr17:78040924-78041068 | Common:2; Rare:42 | ||||
| chr17:78168456-78168619 | Rare:45 | ||||
| chr17:78187045-78187380 | Common:3; Rare:108 | ||||
| chr17:78723494-78723710 | Rare:64 | ||||
| chr17:78782224-78782525 | Common:5; Rare:91 | ||||
| chr17:78840745-78841127 | Common:2; Rare:141 | ||||
| chr17:78979916-78980145 | Common:2; Rare:46 | ||||
| chr17:79009732-79009943 | Common:8; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:80036552-80036668 | Common:2; Rare:30; Clinvar (benign):2 | ||||
| chr17:80220320-80220469 | Common:1; Rare:57; Clinvar:1 | ||||
| chr17:80415005-80415509 | Common:6; Rare:253 |