| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35088240-35088640 | Common:1; Rare:67 | ||||
| chr17:35088745-35089145 | Common:2; Rare:101 | ||||
| chr17:35089050-35089586 | Common:32; Rare:535 | ||||
| chr17:35119017-35119417 | Common:1; Rare:106; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr17:35119611-35120084 | Common:2; Rare:344; Clinvar:14; Clinvar (benign):13 | ||||
| chr17:35141553-35142263 | Common:4; Rare:248 | ||||
| chr17:35142276-35142486 | Common:2; Rare:76 | ||||
| chr17:35242800-35243200 | Rare:312 | ||||
| chr17:35373482-35373882 | Common:10; Rare:127 | ||||
| chr17:35448264-35448666 | Common:3; Rare:166 | ||||
| chr17:35487070-35487370 | Common:1; Rare:57 | ||||
| chr17:35537569-35537971 | Common:17; Rare:155 | ||||
| chr17:35577094-35578338 | Common:10; Rare:449; Clinvar:25; Clinvar (benign):3; Clinvar (pathogenic):16 | ||||
| chr17:35578244-35579554 | Common:21; Rare:840; Clinvar:17; Clinvar (benign):10 | ||||
| chr17:35586615-35586978 | Common:2; Rare:75 |