| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:239309376-239309412 | Rare:5 | ||||
| chr2:239400998-239401280 | Common:3; Rare:83 | ||||
| chr2:239401637-239401750 | Rare:56 | ||||
| chr2:240025225-240025477 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560873 | Common:1; Rare:49 | ||||
| chr2:241102271-241102517 | Common:2; Rare:73 | ||||
| chr2:241315140-241315359 | Common:4; Rare:79 | ||||
| chr2:241315633-241315991 | Common:5; Rare:137 | ||||
| chr2:241637527-241637714 | Common:1; Rare:104 | ||||
| chr2:241701890-241702065 | Common:1; Rare:72 | ||||
| chr2:241808994-241809145 | Common:2; Rare:53 | ||||
| chr20:1118461-1118695 | Common:4; Rare:73 | ||||
| chr20:1325869-1325925 | Common:1; Rare:9 | ||||
| chr20:1329137-1329277 | Rare:26 | ||||
| chr20:2652430-2652655 | Common:8; Rare:75 |