| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78979905-78980076 | Common:2; Rare:36 | ||||
| chr17:79009717-79009932 | Common:9; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:80035861-80036067 | Common:1; Rare:70 | ||||
| chr17:80147095-80147331 | Common:5; Rare:92 | ||||
| chr17:80220317-80220453 | Rare:53; Clinvar:1 | ||||
| chr17:80415115-80415189 | Common:1; Rare:48 | ||||
| chr17:80991806-80991888 | Common:1; Rare:33 | ||||
| chr17:81295297-81295413 | Common:1; Rare:25 | ||||
| chr17:81512679-81513144 | Common:9; Rare:242; Clinvar (benign):14 | ||||
| chr17:81552335-81552453 | Common:1; Rare:47 | ||||
| chr17:81666558-81666763 | Common:1; Rare:90 | ||||
| chr17:81683696-81684057 | Common:4; Rare:181 | ||||
| chr17:81703298-81703510 | Common:2; Rare:60; Clinvar (benign):2 | ||||
| chr17:81833243-81833411 | Rare:76 | ||||
| chr17:81860946-81861116 | Common:1; Rare:52 |