Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151165840-151166171 | Common:3; Rare:93 | ||||
chr1:151190129-151190321 | Rare:53 | ||||
chr1:151198343-151198609 | Common:1; Rare:89 | ||||
chr1:151254624-151254785 | Rare:40 | ||||
chr1:151281662-151281782 | Rare:18 | ||||
chr1:151281924-151282318 | Rare:115 | ||||
chr1:151327598-151327820 | Common:2; Rare:43 | ||||
chr1:151346852-151347029 | Rare:51 | ||||
chr1:151347233-151347538 | Rare:72 | ||||
chr1:151399484-151399635 | Common:2; Rare:59; Clinvar (pathogenic):2 | ||||
chr1:151763429-151763573 | Common:2; Rare:55 | ||||
chr1:151790446-151790837 | Common:2; Rare:92 | ||||
chr1:151909397-151909593 | Common:1; Rare:76 | ||||
chr1:151992569-151992778 | Common:1; Rare:47 | ||||
chr1:152036912-152037090 | Common:2; Rare:48 |