Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:203014676-203014945 | Common:1; Rare:81 | ||||
chr2:203238836-203239050 | Common:1; Rare:84 | ||||
chr2:203239226-203239281 | Rare:18 | ||||
chr2:203535231-203535546 | Common:3; Rare:132 | ||||
chr2:205682356-205682608 | Rare:47 | ||||
chr2:205682817-205683090 | Common:2; Rare:38 | ||||
chr2:206085919-206085981 | Rare:19 | ||||
chr2:206086085-206086209 | Rare:16 | ||||
chr2:206086272-206086303 | Rare:3 | ||||
chr2:206159389-206160057 | Common:3; Rare:206 | ||||
chr2:206765255-206765645 | Common:3; Rare:111; Clinvar:4; Clinvar (benign):4 | ||||
chr2:207165928-207166094 | Rare:30 | ||||
chr2:207166170-207166380 | Common:3; Rare:90 | ||||
chr2:207529684-207530110 | Common:3; Rare:122 | ||||
chr2:207625183-207625616 | Common:1; Rare:121 |