| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75979088-75979283 | Rare:53; Clinvar:4 | ||||
| chr17:75979443-75979470 | Rare:8 | ||||
| chr17:76725754-76726085 | Common:1; Rare:92 | ||||
| chr17:76726491-76727004 | Common:5; Rare:192 | ||||
| chr17:76737325-76737530 | Common:2; Rare:77 | ||||
| chr17:77140635-77141040 | Common:3; Rare:143 | ||||
| chr17:77287855-77288007 | Rare:23 | ||||
| chr17:77319681-77319961 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr17:77320077-77320317 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78187018-78187364 | Common:3; Rare:116 | ||||
| chr17:78840758-78841114 | Common:2; Rare:137 | ||||
| chr17:78979872-78980201 | Common:2; Rare:66 | ||||
| chr17:79009717-79009930 | Common:9; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:80220329-80220453 | Rare:48; Clinvar:1 | ||||
| chr17:80415115-80415189 | Common:1; Rare:48 |