Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:174248454-174248731 | Common:1; Rare:83 | ||||
chr2:174395637-174395800 | Common:1; Rare:55 | ||||
chr2:174487061-174487409 | Common:2; Rare:80 | ||||
chr2:176002229-176002384 | Common:2; Rare:66 | ||||
chr2:177212414-177212825 | Common:4; Rare:165 | ||||
chr2:177263419-177263741 | Common:2; Rare:78 | ||||
chr2:177264630-177264959 | Common:2; Rare:100 | ||||
chr2:177392672-177393070 | Common:2; Rare:139; Clinvar:6; Clinvar (benign):4 | ||||
chr2:178478503-178478659 | Common:1; Rare:48 | ||||
chr2:180980246-180980545 | Common:1; Rare:94 | ||||
chr2:186486039-186486354 | Common:3; Rare:91 | ||||
chr2:186590193-186590349 | Rare:43 | ||||
chr2:188291822-188292078 | Common:3; Rare:87 | ||||
chr2:188292737-188292869 | Common:1; Rare:34 | ||||
chr2:188292985-188293026 | Rare:7 |