Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225880679-225880820 | Rare:27 | ||||
chr1:228506000-228506278 | Common:8; Rare:55 | ||||
chr1:228513266-228513592 | Common:1; Rare:57 | ||||
chr1:230725366-230725644 | Rare:39 | ||||
chr1:231421037-231421249 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr1:234600053-234600259 | Common:7; Rare:91 | ||||
chr1:234611362-234611485 | Common:1; Rare:40 | ||||
chr1:234716463-234716631 | Common:2; Rare:34 | ||||
chr1:234772769-234772875 | Common:7; Rare:21 | ||||
chr1:234817403-234817627 | Rare:31 | ||||
chr1:234960750-234960939 | Common:2; Rare:31 | ||||
chr1:234971178-234971365 | Common:1; Rare:30 | ||||
chr1:235068418-235068643 | Common:2; Rare:43 | ||||
chr1:235069662-235069939 | Common:3; Rare:52 | ||||
chr1:235073576-235073825 | Common:1; Rare:49 |