| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12584610-12584818 | Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:14125732-14125906 | Common:1; Rare:44 | ||||
| chr3:14943925-14944025 | Common:1; Rare:21 | ||||
| chr3:15242922-15243053 | Rare:26 | ||||
| chr3:15271893-15272181 | Common:3; Rare:68 | ||||
| chr3:15738350-15738527 | Common:2; Rare:41 | ||||
| chr3:21645697-21645815 | Common:1; Rare:25 | ||||
| chr3:21646001-21646038 | Rare:6 | ||||
| chr3:28347645-28347763 | Common:1; Rare:21 | ||||
| chr3:30696754-30696895 | Rare:20 | ||||
| chr3:39143917-39144217 | Rare:82 | ||||
| chr3:40453175-40453417 | Common:4; Rare:53 | ||||
| chr3:41225468-41225700 | Rare:48; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:42632306-42632652 | Common:2; Rare:72 | ||||
| chr3:42652681-42652928 | Rare:40 |