| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151080879-151081220 | Common:2; Rare:106 | ||||
| chr5:151087099-151087223 | Common:1; Rare:20 | ||||
| chr5:154038878-154039015 | Common:1; Rare:49 | ||||
| chr5:154857815-154857889 | Rare:18 | ||||
| chr5:154858422-154858723 | Common:1; Rare:94 | ||||
| chr5:157266016-157266183 | Common:1; Rare:48 | ||||
| chr5:157460086-157460269 | Common:2; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:157731392-157731454 | Common:2; Rare:28 | ||||
| chr5:157858936-157859250 | Common:2; Rare:99 | ||||
| chr5:159262969-159263090 | Common:2; Rare:21 | ||||
| chr5:159263201-159263354 | Common:1; Rare:53 | ||||
| chr5:160419049-160419260 | Common:4; Rare:80 | ||||
| chr5:163437292-163437628 | Rare:99 | ||||
| chr5:163505444-163505697 | Common:1; Rare:88 | ||||
| chr5:169583592-169583889 | Common:7; Rare:88 |