| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:236167330-236167454 | Common:1; Rare:56 | ||||
| chr2:237085719-237085955 | Common:2; Rare:81 | ||||
| chr2:237966728-237967039 | Common:3; Rare:91 | ||||
| chr2:238203616-238203797 | Common:3; Rare:76 | ||||
| chr2:240025291-240025455 | Common:1; Rare:66; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136264-240136376 | Rare:43 | ||||
| chr2:241102274-241102357 | Common:2; Rare:31 | ||||
| chr2:241315146-241315347 | Common:4; Rare:72 | ||||
| chr2:241315649-241316002 | Common:5; Rare:134 | ||||
| chr2:241508539-241508921 | Common:2; Rare:122 | ||||
| chr2:241637515-241637704 | Common:1; Rare:103 | ||||
| chr2:241686740-241687013 | Common:1; Rare:85 | ||||
| chr20:1118468-1118654 | Common:3; Rare:56 | ||||
| chr20:1393009-1393036 | Rare:13 | ||||
| chr20:2652455-2652655 | Common:8; Rare:66 |