Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:159712402-159712584 | Common:2; Rare:75 | ||||
chr2:160493412-160493596 | Common:1; Rare:60 | ||||
chr2:160493796-160494061 | Common:1; Rare:63 | ||||
chr2:161160870-161161131 | Common:1; Rare:54 | ||||
chr2:161308334-161308498 | Common:2; Rare:41 | ||||
chr2:162073502-162073706 | Rare:61 | ||||
chr2:162073974-162074014 | Rare:16 | ||||
chr2:164841817-164841977 | Common:1; Rare:49 | ||||
chr2:166375885-166376127 | Common:4; Rare:73; Clinvar:1; Clinvar (benign):5 | ||||
chr2:169584542-169584624 | Rare:16 | ||||
chr2:169584709-169584811 | Rare:26 | ||||
chr2:169694376-169694571 | Common:5; Rare:57 | ||||
chr2:169824855-169825044 | Common:3; Rare:59 | ||||
chr2:170928902-170929338 | Common:5; Rare:128 | ||||
chr2:171433955-171434239 | Common:2; Rare:72 |