| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:161547531-161547587 | Rare:15 | ||||
| chr5:163437292-163437697 | Common:1; Rare:119 | ||||
| chr5:163460047-163460165 | Common:2; Rare:49 | ||||
| chr5:163505442-163505674 | Common:1; Rare:76 | ||||
| chr5:169583580-169583810 | Common:6; Rare:81 | ||||
| chr5:170266873-170267014 | Rare:50 | ||||
| chr5:170297681-170297897 | Common:1; Rare:41 | ||||
| chr5:171387500-171388006 | Common:1; Rare:239; Clinvar:1 | ||||
| chr5:172006503-172006950 | Common:2; Rare:122 | ||||
| chr5:172454354-172454699 | Common:12; Rare:94; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172641099-172641312 | Common:3; Rare:57 | ||||
| chr5:172770653-172770935 | Common:3; Rare:68 | ||||
| chr5:172771141-172771553 | Common:7; Rare:159 | ||||
| chr5:172834162-172834451 | Common:1; Rare:70 | ||||
| chr5:172904576-172904868 | Common:2; Rare:49 |