| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140647594-140647889 | Common:5; Rare:118; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664773-140664943 | Common:2; Rare:50 | ||||
| chr5:140691322-140691460 | Common:1; Rare:45; Clinvar:4 | ||||
| chr5:140700231-140700469 | Rare:78 | ||||
| chr5:141320762-141320889 | Common:1; Rare:35 | ||||
| chr5:141618917-141619275 | Common:1; Rare:115; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636810-141636982 | Common:2; Rare:76 | ||||
| chr5:141869532-141869841 | Common:1; Rare:70 | ||||
| chr5:141923744-141923875 | Common:1; Rare:26 | ||||
| chr5:142012994-142013114 | Rare:37 | ||||
| chr5:142324973-142325219 | Rare:85 | ||||
| chr5:145835276-145835472 | Common:1; Rare:49 | ||||
| chr5:146182505-146182912 | Common:4; Rare:126 | ||||
| chr5:149063043-149063353 | Rare:65; Clinvar:1 | ||||
| chr5:149345337-149345524 | Common:1; Rare:57 |