| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140691276-140691620 | Common:2; Rare:127; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320750-141320902 | Common:1; Rare:47 | ||||
| chr5:141636800-141636982 | Common:2; Rare:86 | ||||
| chr5:141637329-141637452 | Common:1; Rare:29 | ||||
| chr5:141682191-141682328 | Common:1; Rare:45 | ||||
| chr5:141923568-141923910 | Common:1; Rare:96 | ||||
| chr5:141968989-141969272 | Common:3; Rare:88 | ||||
| chr5:142324940-142325218 | Rare:100 | ||||
| chr5:143434663-143434818 | Rare:25 | ||||
| chr5:144170546-144170720 | Common:1; Rare:69 | ||||
| chr5:146182489-146182916 | Common:4; Rare:130 | ||||
| chr5:146203338-146203649 | Common:2; Rare:90 | ||||
| chr5:148383763-148384022 | Rare:74 | ||||
| chr5:149142464-149142625 | Rare:33 | ||||
| chr5:149345332-149345540 | Common:1; Rare:71 |