| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:161546639-161547041 | Common:1; Rare:81; Clinvar (benign):3 | ||||
| chr5:161548088-161548363 | Common:1; Rare:61 | ||||
| chr5:161548379-161548455 | Rare:20 | ||||
| chr5:161847939-161848207 | Rare:49; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:161848497-161848603 | Common:2; Rare:32 | ||||
| chr5:162067415-162067809 | Common:1; Rare:101; Clinvar:2 | ||||
| chr5:163437316-163437623 | Rare:92 | ||||
| chr5:163505281-163505674 | Common:1; Rare:109 | ||||
| chr5:168291405-168291606 | Common:1; Rare:50 | ||||
| chr5:168486337-168486497 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr5:168529228-168529304 | Common:1; Rare:19 | ||||
| chr5:169583609-169583889 | Common:7; Rare:83 | ||||
| chr5:171387491-171388006 | Common:1; Rare:240; Clinvar:1 | ||||
| chr5:172006491-172006916 | Common:2; Rare:121 | ||||
| chr5:172454366-172454655 | Common:10; Rare:76; Clinvar:1; Clinvar (benign):3 |