| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:159263191-159263357 | Common:1; Rare:54 | ||||
| chr5:160419031-160419171 | Common:2; Rare:46 | ||||
| chr5:163437287-163437641 | Rare:104 | ||||
| chr5:163460331-163460675 | Common:5; Rare:81 | ||||
| chr5:163505444-163505755 | Common:1; Rare:107 | ||||
| chr5:168579267-168579476 | Common:1; Rare:54 | ||||
| chr5:169583592-169583801 | Common:6; Rare:65 | ||||
| chr5:169637021-169637308 | Common:3; Rare:56 | ||||
| chr5:170297716-170297941 | Common:1; Rare:44 | ||||
| chr5:170389280-170389492 | Common:4; Rare:38 | ||||
| chr5:170772411-170772566 | Common:4; Rare:28 | ||||
| chr5:171387580-171388006 | Rare:206; Clinvar:1 | ||||
| chr5:172006503-172006930 | Common:2; Rare:118 | ||||
| chr5:172454340-172454655 | Common:10; Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:172770639-172770931 | Common:3; Rare:72 |