| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:161848323-161848583 | Common:4; Rare:75; Clinvar (benign):4 | ||||
| chr5:162067390-162067493 | Rare:33 | ||||
| chr5:163437272-163437607 | Rare:91 | ||||
| chr5:167573420-167573721 | Common:4; Rare:50 | ||||
| chr5:168529219-168529346 | Common:1; Rare:31 | ||||
| chr5:169583592-169583889 | Common:7; Rare:88 | ||||
| chr5:170297768-170297905 | Rare:26 | ||||
| chr5:171387512-171387998 | Rare:231; Clinvar:1 | ||||
| chr5:172454365-172454655 | Common:10; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172771189-172771489 | Common:5; Rare:114 | ||||
| chr5:172834163-172834416 | Common:1; Rare:61 | ||||
| chr5:172958791-172958876 | Rare:20 | ||||
| chr5:172959136-172959475 | Common:5; Rare:84 | ||||
| chr5:173056132-173056407 | Common:1; Rare:76 | ||||
| chr5:174045651-174045843 | Common:2; Rare:48 |