| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49918284-49918733 | Common:4; Rare:160; Clinvar (benign):3 | ||||
| chr22:50278284-50278505 | Rare:70 | ||||
| chr22:50582371-50582712 | Common:1; Rare:162; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr22:50582779-50583153 | Common:8; Rare:131; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50783598-50783822 | Common:2; Rare:73 | ||||
| chr3:8501641-8501944 | Common:2; Rare:110 | ||||
| chr3:8768414-8768815 | Common:5; Rare:61 | ||||
| chr3:8769331-8769653 | Common:3; Rare:67 | ||||
| chr3:9362986-9363098 | Rare:43 | ||||
| chr3:9792369-9792583 | Rare:61 | ||||
| chr3:9792699-9793127 | Common:3; Rare:150 | ||||
| chr3:9933544-9933863 | Common:2; Rare:128; Clinvar:2 | ||||
| chr3:9986752-9987172 | Common:4; Rare:121 | ||||
| chr3:10026281-10026477 | Common:1; Rare:64 | ||||
| chr3:11154300-11154533 | Common:4; Rare:63 |