| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42600422-42600485 | Common:1; Rare:20 | ||||
| chr3:42600525-42600749 | Common:1; Rare:89 | ||||
| chr3:42600801-42601009 | Rare:72 | ||||
| chr3:42653553-42653725 | Rare:38 | ||||
| chr3:42804212-42804663 | Common:2; Rare:130 | ||||
| chr3:42979209-42979355 | Rare:42 | ||||
| chr3:43286459-43286654 | Common:2; Rare:86 | ||||
| chr3:43690817-43690995 | Common:3; Rare:96; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338387-44338518 | Common:1; Rare:48 | ||||
| chr3:44338714-44338807 | Common:3; Rare:30 | ||||
| chr3:44477625-44477751 | Common:1; Rare:28 | ||||
| chr3:44624905-44625095 | Common:2; Rare:55 | ||||
| chr3:44761577-44761695 | Common:3; Rare:60 | ||||
| chr3:44861796-44861918 | Common:2; Rare:56 | ||||
| chr3:44976120-44976272 | Common:2; Rare:63 |