| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206086281-206086407 | Rare:22 | ||||
| chr2:206159347-206160070 | Common:4; Rare:217; Clinvar (benign):1 | ||||
| chr2:206274504-206274794 | Common:1; Rare:89 | ||||
| chr2:206274909-206275041 | Rare:49 | ||||
| chr2:206765276-206765668 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166088 | Rare:29 | ||||
| chr2:207166166-207166380 | Common:3; Rare:92 | ||||
| chr2:207529553-207530116 | Common:3; Rare:145 | ||||
| chr2:207624565-207624693 | Rare:31 | ||||
| chr2:207625216-207625565 | Common:1; Rare:97 | ||||
| chr2:207711585-207711923 | Rare:104 | ||||
| chr2:208254094-208254372 | Common:1; Rare:57 | ||||
| chr2:208254997-208255255 | Common:2; Rare:67 | ||||
| chr2:208266038-208266341 | Common:9; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423876-209424115 | Common:1; Rare:80 |