| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:142324973-142325243 | Rare:89 | ||||
| chr5:143404422-143404611 | Common:2; Rare:43 | ||||
| chr5:144170557-144170874 | Common:2; Rare:103 | ||||
| chr5:144205182-144205445 | Rare:55 | ||||
| chr5:146182489-146182857 | Common:3; Rare:100 | ||||
| chr5:146203286-146203674 | Common:2; Rare:123 | ||||
| chr5:146878051-146878310 | Rare:76 | ||||
| chr5:146878580-146878864 | Common:3; Rare:65; Clinvar (benign):1 | ||||
| chr5:147056125-147056422 | Rare:62 | ||||
| chr5:147453911-147454062 | Common:1; Rare:36 | ||||
| chr5:147454094-147454226 | Common:1; Rare:41 | ||||
| chr5:147509895-147510016 | Rare:33 | ||||
| chr5:147782502-147782887 | Common:4; Rare:87 | ||||
| chr5:148383715-148384021 | Rare:81 | ||||
| chr5:149345332-149345619 | Common:1; Rare:110 |