Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89198837-89199004 | Common:1; Rare:29 | ||||
chr1:89632894-89633211 | Common:1; Rare:90 | ||||
chr1:89994981-89995193 | Common:2; Rare:80 | ||||
chr1:91021967-91022418 | Common:1; Rare:112 | ||||
chr1:91500568-91500890 | Common:3; Rare:79 | ||||
chr1:91885878-91886330 | Common:1; Rare:178 | ||||
chr1:92029921-92030002 | Rare:25 | ||||
chr1:92298923-92299076 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92961430-92961567 | Rare:52 | ||||
chr1:93180072-93180164 | Rare:34 | ||||
chr1:93180166-93180690 | Common:1; Rare:197 | ||||
chr1:93345774-93345979 | Common:4; Rare:83 | ||||
chr1:93447876-93448158 | Common:2; Rare:97 | ||||
chr1:93847181-93847284 | Common:1; Rare:31 | ||||
chr1:93879128-93879274 | Common:1; Rare:53 |