| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76353579-76353659 | Rare:30 | ||||
| chr17:76537900-76538242 | Common:1; Rare:103 | ||||
| chr17:76688673-76688767 | Common:1; Rare:22 | ||||
| chr17:76726456-76726893 | Common:5; Rare:168 | ||||
| chr17:76737291-76737691 | Common:4; Rare:153 | ||||
| chr17:76737901-76738070 | Common:2; Rare:48 | ||||
| chr17:77319702-77319935 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr17:77320097-77320329 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78186540-78186727 | Common:7; Rare:38 | ||||
| chr17:78187035-78187386 | Common:3; Rare:115 | ||||
| chr17:78378619-78378701 | Common:1; Rare:39 | ||||
| chr17:78840740-78841047 | Common:2; Rare:110 | ||||
| chr17:78924960-78925020 | Rare:7 | ||||
| chr17:79009744-79009935 | Common:8; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:79024130-79024290 | Common:1; Rare:31 |