Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92029929-92030052 | Rare:33 | ||||
chr1:92298958-92299090 | Common:1; Rare:68; Clinvar:1 | ||||
chr1:93079089-93079299 | Common:2; Rare:88 | ||||
chr1:93180067-93180216 | Rare:57 | ||||
chr1:93180220-93180762 | Common:2; Rare:214 | ||||
chr1:93345831-93345953 | Common:2; Rare:43 | ||||
chr1:93448007-93448170 | Common:2; Rare:60 | ||||
chr1:93847220-93847286 | Common:1; Rare:14 | ||||
chr1:93879117-93879285 | Common:2; Rare:64 | ||||
chr1:94237454-94237744 | Rare:103 | ||||
chr1:94418131-94418470 | Common:2; Rare:121 | ||||
chr1:94903141-94903509 | Common:1; Rare:74 | ||||
chr1:94926900-94927192 | Common:3; Rare:94 | ||||
chr1:95072863-95073020 | Common:1; Rare:61; Clinvar (benign):1 | ||||
chr1:95233955-95234236 | Common:5; Rare:85 |