| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78717025-78717090 | Rare:11 | ||||
| chr17:78782216-78782577 | Common:9; Rare:118 | ||||
| chr17:78840740-78841124 | Common:2; Rare:142 | ||||
| chr17:78873883-78874318 | Common:4; Rare:90 | ||||
| chr17:78976029-78976414 | Common:4; Rare:99 | ||||
| chr17:78979839-78980057 | Common:2; Rare:49 | ||||
| chr17:79009687-79009938 | Common:9; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:79074617-79074907 | Common:3; Rare:68 | ||||
| chr17:79796815-79796860 | Rare:5 | ||||
| chr17:79796999-79797420 | Common:1; Rare:148 | ||||
| chr17:79950611-79950993 | Common:3; Rare:75 | ||||
| chr17:79951572-79951650 | Common:1; Rare:29 | ||||
| chr17:79952122-79952333 | Common:3; Rare:50 | ||||
| chr17:79993689-79993806 | Common:1; Rare:23 | ||||
| chr17:80035840-80036044 | Common:1; Rare:71 |