| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140647548-140647887 | Common:10; Rare:263; Clinvar:8; Clinvar (benign):7 | ||||
| chr5:140664737-140664926 | Common:3; Rare:52 | ||||
| chr5:140691282-140691667 | Common:3; Rare:277; Clinvar:24; Clinvar (benign):5 | ||||
| chr5:141320724-141320933 | Common:6; Rare:141 | ||||
| chr5:141618010-141618460 | Common:2; Rare:97 | ||||
| chr5:141618897-141619275 | Common:1; Rare:120; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636794-141637014 | Common:4; Rare:193 | ||||
| chr5:141637328-141637501 | Common:2; Rare:72 | ||||
| chr5:141923744-141923958 | Common:2; Rare:106 | ||||
| chr5:141968938-141969275 | Common:3; Rare:104 | ||||
| chr5:142012967-142013161 | Common:3; Rare:106 | ||||
| chr5:142108646-142108870 | Common:6; Rare:134 | ||||
| chr5:142324871-142325313 | Common:1; Rare:280 | ||||
| chr5:142770173-142770563 | Common:2; Rare:207 | ||||
| chr5:143402872-143403590 | Common:7; Rare:239 |