Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:43595946-43596203 | Common:1; Rare:93 | ||||
chr2:43995960-43996289 | Common:4; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
chr2:44361437-44362007 | Common:3; Rare:187 | ||||
chr2:46617023-46617275 | Common:7; Rare:110 | ||||
chr2:46915722-46915908 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
chr2:46916033-46916168 | Common:2; Rare:45 | ||||
chr2:47402925-47403180 | Common:1; Rare:114; Clinvar:36; Clinvar (benign):23 | ||||
chr2:48314884-48315046 | Common:1; Rare:70 | ||||
chr2:48440631-48440851 | Common:7; Rare:108 | ||||
chr2:53786851-53787090 | Rare:83 | ||||
chr2:53970755-53971168 | Common:12; Rare:153 | ||||
chr2:54115493-54115701 | Rare:76 | ||||
chr2:55050432-55050818 | Common:4; Rare:119 | ||||
chr2:55112594-55112727 | Rare:31 | ||||
chr2:55232242-55232719 | Common:3; Rare:131 |