| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161308378-161308566 | Common:2; Rare:43 | ||||
| chr2:161415978-161416758 | Common:1; Rare:146; Clinvar (benign):1 | ||||
| chr2:161417182-161417404 | Common:1; Rare:44 | ||||
| chr2:162838714-162838855 | Common:1; Rare:26 | ||||
| chr2:164955523-164955578 | Rare:20 | ||||
| chr2:165203851-165204166 | Common:2; Rare:41 | ||||
| chr2:165469569-165469716 | Rare:29 | ||||
| chr2:165574197-165574307 | Rare:23 | ||||
| chr2:166375899-166376299 | Common:5; Rare:105; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:169584734-169584809 | Rare:17 | ||||
| chr2:169694333-169694597 | Common:5; Rare:92 | ||||
| chr2:170816460-170816753 | Common:4; Rare:66; Clinvar:1 | ||||
| chr2:170817189-170817286 | Common:5; Rare:22 | ||||
| chr2:170928970-170929318 | Common:4; Rare:108 | ||||
| chr2:171433991-171434248 | Common:1; Rare:66 |