Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9423457-9423669 | Rare:70 | ||||
chr2:24123282-24123469 | Common:1; Rare:46 | ||||
chr2:26033788-26034159 | Common:3; Rare:132 | ||||
chr2:26244602-26244931 | Common:2; Rare:117; Clinvar:5; Clinvar (benign):6 | ||||
chr2:27212242-27212367 | Common:1; Rare:65 | ||||
chr2:27370317-27370644 | Common:1; Rare:129 | ||||
chr2:27583002-27583045 | Rare:12 | ||||
chr2:27628998-27629051 | Rare:23 | ||||
chr2:27663607-27663896 | Rare:103 | ||||
chr2:37084346-37084544 | Common:3; Rare:73 | ||||
chr2:37231572-37231674 | Common:3; Rare:49; Clinvar (benign):3 | ||||
chr2:38875877-38876010 | Common:2; Rare:42 | ||||
chr2:39437078-39437439 | Common:4; Rare:128 | ||||
chr2:46617037-46617197 | Common:5; Rare:45 | ||||
chr2:46915738-46915862 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 |