Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:203014516-203014649 | Rare:45 | ||||
chr2:203014672-203014931 | Common:1; Rare:78 | ||||
chr2:203238852-203239054 | Common:1; Rare:82 | ||||
chr2:203239212-203239331 | Rare:37 | ||||
chr2:203328022-203328532 | Common:2; Rare:176 | ||||
chr2:203328882-203328916 | Rare:11 | ||||
chr2:203535131-203535557 | Common:3; Rare:158 | ||||
chr2:205682226-205682563 | Rare:70 | ||||
chr2:206085765-206085981 | Common:1; Rare:62 | ||||
chr2:206086141-206086319 | Rare:19 | ||||
chr2:206159178-206159982 | Common:6; Rare:224; Clinvar (benign):2 | ||||
chr2:206274916-206275041 | Rare:47 | ||||
chr2:206443724-206443957 | Rare:63 | ||||
chr2:206765273-206765668 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165766-207166099 | Rare:64 |