| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200864530-200864806 | Common:1; Rare:97 | ||||
| chr2:200889005-200889445 | Common:3; Rare:142 | ||||
| chr2:200963443-200963516 | Rare:14 | ||||
| chr2:200963536-200963871 | Common:1; Rare:92 | ||||
| chr2:201071586-201072052 | Rare:102 | ||||
| chr2:201115949-201116436 | Common:2; Rare:90 | ||||
| chr2:201117399-201117605 | Rare:24 | ||||
| chr2:201118346-201118531 | Rare:32 | ||||
| chr2:201118605-201118857 | Rare:38 | ||||
| chr2:201122374-201122674 | Common:1; Rare:54 | ||||
| chr2:201257979-201258216 | Common:1; Rare:46 | ||||
| chr2:201260420-201260585 | Rare:35 | ||||
| chr2:201451416-201451832 | Common:2; Rare:111 | ||||
| chr2:201642633-201642775 | Rare:70 | ||||
| chr2:201780890-201781075 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 |