| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129439852-129440247 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893585-129893887 | Rare:129 | ||||
| chr3:131026734-131026951 | Common:2; Rare:55 | ||||
| chr3:131381507-131381801 | Common:2; Rare:69 | ||||
| chr3:131502809-131502995 | Common:1; Rare:89 | ||||
| chr3:132659799-132659921 | Common:3; Rare:26 | ||||
| chr3:133661856-133662021 | Rare:38 | ||||
| chr3:134483176-134483349 | Rare:31 | ||||
| chr3:134485437-134485791 | Rare:91 | ||||
| chr3:134485957-134486260 | Common:3; Rare:107 | ||||
| chr3:136862014-136862295 | Common:1; Rare:90 | ||||
| chr3:138187209-138187569 | Rare:107 | ||||
| chr3:138594209-138594442 | Rare:65 | ||||
| chr3:139389568-139389864 | Common:1; Rare:96 | ||||
| chr3:141368260-141368575 | Rare:70 |