| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51499954-51500306 | Common:1; Rare:74 | ||||
| chr3:51975051-51975171 | Common:1; Rare:45 | ||||
| chr3:52198031-52198165 | Rare:60 | ||||
| chr3:52239075-52239255 | Common:2; Rare:65 | ||||
| chr3:52278627-52278791 | Rare:56 | ||||
| chr3:52455464-52455643 | Common:2; Rare:64 | ||||
| chr3:52536333-52536697 | Common:2; Rare:114 | ||||
| chr3:52685952-52686049 | Common:1; Rare:35 | ||||
| chr3:52705576-52706223 | Common:4; Rare:207 | ||||
| chr3:53130411-53130545 | Common:1; Rare:40; Clinvar (benign):2 | ||||
| chr3:53255992-53256169 | Common:2; Rare:70 | ||||
| chr3:53347510-53347776 | Common:2; Rare:85 | ||||
| chr3:53891807-53892040 | Common:2; Rare:72 | ||||
| chr3:54123413-54123579 | Rare:47 | ||||
| chr3:56557086-56557238 | Common:2; Rare:60 |