Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:31644249-31644481 | Common:1; Rare:52 | ||||
chr1:31644856-31645002 | Common:3; Rare:45 | ||||
chr1:32107949-32108130 | Rare:73 | ||||
chr1:32221888-32222109 | Rare:75 | ||||
chr1:32222326-32222488 | Rare:69 | ||||
chr1:32251185-32251301 | Common:1; Rare:34 | ||||
chr1:32291846-32292200 | Common:1; Rare:102 | ||||
chr1:32362517-32362757 | Common:1; Rare:71 | ||||
chr1:32394406-32394637 | Common:1; Rare:62 | ||||
chr1:32650485-32650637 | Common:1; Rare:71 | ||||
chr1:32650929-32651253 | Common:2; Rare:114 | ||||
chr1:32817270-32817686 | Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
chr1:34985309-34985360 | Common:1; Rare:19 | ||||
chr1:35031663-35031798 | Rare:42 | ||||
chr1:35031892-35031982 | Common:1; Rare:21 |