Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208266063-208266302 | Common:8; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210477553-210477685 | Rare:38 | ||||
chr2:215311871-215312102 | Common:6; Rare:86 | ||||
chr2:215409556-215410142 | Rare:157 | ||||
chr2:215435648-215436136 | Common:3; Rare:122 | ||||
chr2:216081771-216081865 | Rare:30 | ||||
chr2:216412665-216412786 | Rare:14 | ||||
chr2:216498740-216499035 | Common:11; Rare:115 | ||||
chr2:218217076-218217246 | Common:1; Rare:60 | ||||
chr2:218270089-218270541 | Common:5; Rare:142; Clinvar:3; Clinvar (benign):1 | ||||
chr2:218568307-218568659 | Common:3; Rare:93 | ||||
chr2:218659616-218659738 | Rare:30 | ||||
chr2:218671971-218672348 | Common:2; Rare:95 | ||||
chr2:219176911-219177083 | Common:4; Rare:51 | ||||
chr2:219229577-219229891 | Common:2; Rare:95 |