Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42658262-42658463 | Common:2; Rare:58 | ||||
chr1:42658467-42658747 | Common:1; Rare:65 | ||||
chr1:42659011-42659261 | Common:2; Rare:55 | ||||
chr1:42682117-42682201 | Rare:29 | ||||
chr1:42682205-42682731 | Common:3; Rare:167 | ||||
chr1:42683191-42683465 | Common:3; Rare:123 | ||||
chr1:42766976-42767502 | Common:8; Rare:182; Clinvar (benign):1 | ||||
chr1:42817004-42817136 | Common:1; Rare:32 | ||||
chr1:42817193-42817455 | Rare:93 | ||||
chr1:42846392-42846646 | Common:1; Rare:71 | ||||
chr1:42958813-42959063 | Common:3; Rare:70; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43147767-43147952 | Common:3; Rare:47 | ||||
chr1:43171911-43172414 | Common:3; Rare:190 | ||||
chr1:43172537-43172743 | Common:6; Rare:53 | ||||
chr1:43184946-43185213 | Common:1; Rare:57 |