Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:148679690-148679944 | Rare:23 | ||||
chr1:148952058-148952153 | Common:3; Rare:23 | ||||
chr1:148952264-148952637 | Common:5; Rare:103 | ||||
chr1:149082385-149082518 | Common:1; Rare:32 | ||||
chr1:149103499-149103866 | Common:7; Rare:134 | ||||
chr1:149390400-149390634 | Rare:32 | ||||
chr1:149812171-149812235 | Rare:26 | ||||
chr1:149812364-149812532 | Rare:51 | ||||
chr1:149813682-149813919 | Common:3; Rare:70 | ||||
chr1:149886454-149886489 | Rare:13 | ||||
chr1:149886637-149886994 | Common:2; Rare:135 | ||||
chr1:149887952-149888215 | Rare:57 | ||||
chr1:149927748-149927855 | Rare:45; Clinvar (benign):4 | ||||
chr1:149936811-149936922 | Common:1; Rare:20 | ||||
chr1:150010464-150010484 | Rare:3 |