Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:149587312-149587400 | Rare:15 | ||||
chr2:152717902-152717970 | Rare:30 | ||||
chr2:159712393-159712541 | Common:2; Rare:65 | ||||
chr2:162073526-162073690 | Rare:45 | ||||
chr2:162318635-162318840 | Common:1; Rare:42 | ||||
chr2:162318843-162319084 | Rare:46 | ||||
chr2:169584751-169584844 | Rare:28 | ||||
chr2:169694364-169694565 | Common:5; Rare:63 | ||||
chr2:171433977-171434267 | Common:2; Rare:75 | ||||
chr2:171999837-171999983 | Common:1; Rare:59 | ||||
chr2:174395642-174395812 | Common:1; Rare:58 | ||||
chr2:176002191-176002414 | Common:4; Rare:94 | ||||
chr2:177392651-177392829 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr2:177392929-177393062 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr2:178451083-178451387 | Common:6; Rare:89; Clinvar:4; Clinvar (benign):3 |