| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161416558-161416771 | Rare:47 | ||||
| chr2:161624159-161624512 | Common:1; Rare:67 | ||||
| chr2:162838525-162838685 | Rare:43 | ||||
| chr2:162838702-162839142 | Common:1; Rare:89 | ||||
| chr2:164841805-164841984 | Common:1; Rare:52 | ||||
| chr2:164955523-164955630 | Rare:29 | ||||
| chr2:165469534-165469722 | Rare:36 | ||||
| chr2:166375799-166376094 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:169584290-169584622 | Common:1; Rare:127 | ||||
| chr2:169584744-169584809 | Rare:15 | ||||
| chr2:169694360-169694590 | Common:5; Rare:75 | ||||
| chr2:170816465-170816924 | Common:4; Rare:100; Clinvar:4 | ||||
| chr2:170928902-170929324 | Common:5; Rare:120 | ||||
| chr2:171433941-171434234 | Common:3; Rare:76 | ||||
| chr2:171894210-171894369 | Rare:65; Clinvar:1 |