| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7573904-7573976 | Rare:25 | ||||
| chr17:7579413-7579675 | Common:1; Rare:85 | ||||
| chr17:7583508-7583916 | Common:1; Rare:161; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:7584070-7584129 | Rare:11 | ||||
| chr17:7614512-7614757 | Rare:56 | ||||
| chr17:7686613-7686728 | Rare:31 | ||||
| chr17:7687457-7687576 | Rare:30; Clinvar:1 | ||||
| chr17:7688145-7688486 | Common:5; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7843643-7843733 | Rare:32 | ||||
| chr17:7857100-7857345 | Common:1; Rare:121 | ||||
| chr17:7857382-7857758 | Common:3; Rare:124 | ||||
| chr17:7857868-7858283 | Common:1; Rare:153 | ||||
| chr17:7885172-7885365 | Rare:62 | ||||
| chr17:7885517-7885565 | Rare:9 | ||||
| chr17:7888715-7888819 | Rare:28 |