| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:102736856-102736932 | Common:1; Rare:26 | ||||
| chr2:105337473-105337606 | Common:1; Rare:64 | ||||
| chr2:105396950-105397213 | Common:6; Rare:70 | ||||
| chr2:105398973-105399204 | Rare:84 | ||||
| chr2:108449098-108449271 | Rare:68 | ||||
| chr2:108534158-108534557 | Common:8; Rare:155 | ||||
| chr2:108719352-108719586 | Common:3; Rare:104; Clinvar (benign):2 | ||||
| chr2:111884151-111884255 | Rare:30 | ||||
| chr2:112542139-112542493 | Common:1; Rare:111 | ||||
| chr2:112584293-112584639 | Common:2; Rare:95 | ||||
| chr2:112645655-112645981 | Common:2; Rare:119 | ||||
| chr2:112764578-112764773 | Common:1; Rare:64; Clinvar (pathogenic):1 | ||||
| chr2:113627041-113627279 | Common:1; Rare:70 | ||||
| chr2:113756484-113756771 | Common:4; Rare:91 | ||||
| chr2:113889765-113890321 | Common:9; Rare:169 |