Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:32627929-32628143 | Rare:66 | ||||
chr2:33599258-33599432 | Common:1; Rare:61 | ||||
chr2:36561496-36561850 | Common:2; Rare:74 | ||||
chr2:37084319-37084559 | Common:3; Rare:91 | ||||
chr2:37231551-37231703 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr2:37671614-37671908 | Common:11; Rare:114 | ||||
chr2:38751339-38751474 | Rare:70 | ||||
chr2:38875892-38876055 | Common:1; Rare:60 | ||||
chr2:39437104-39437453 | Common:4; Rare:122 | ||||
chr2:42169182-42169429 | Common:1; Rare:129 | ||||
chr2:43595957-43596178 | Common:1; Rare:72 | ||||
chr2:44361490-44361986 | Common:3; Rare:155 | ||||
chr2:46073674-46073873 | Common:1; Rare:35 | ||||
chr2:46617019-46617257 | Common:6; Rare:102 | ||||
chr2:46698986-46699347 | Common:1; Rare:111 |