Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9630928-9631316 | Common:3; Rare:125 | ||||
chr2:9843254-9843533 | Common:6; Rare:83 | ||||
chr2:10689910-10690038 | Common:2; Rare:42 | ||||
chr2:11466127-11466181 | Rare:13 | ||||
chr2:11746422-11746671 | Common:2; Rare:73; Clinvar:4 | ||||
chr2:12716627-12716965 | Common:3; Rare:102 | ||||
chr2:15561309-15561407 | Rare:39 | ||||
chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 | ||||
chr2:19901642-19901746 | Common:1; Rare:51 | ||||
chr2:19990079-19990211 | Rare:34 | ||||
chr2:20350835-20351092 | Common:2; Rare:111 | ||||
chr2:20446887-20447074 | Common:2; Rare:62 | ||||
chr2:20651059-20651211 | Rare:44 | ||||
chr2:20823056-20823159 | Rare:41 | ||||
chr2:23940379-23940529 | Common:3; Rare:56 |