Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231040040-231040680 | Common:2; Rare:197 | ||||
chr1:231161720-231162170 | Common:4; Rare:93 | ||||
chr1:231241109-231241292 | Rare:100; Clinvar:3 | ||||
chr1:231337795-231338077 | Common:3; Rare:101 | ||||
chr1:231338220-231338394 | Rare:49 | ||||
chr1:231338476-231338908 | Common:3; Rare:188 | ||||
chr1:231528537-231528805 | Common:2; Rare:97 | ||||
chr1:231626530-231626860 | Common:4; Rare:77 | ||||
chr1:232950390-232950664 | Common:4; Rare:100 | ||||
chr1:233294982-233295382 | Common:7; Rare:147 | ||||
chr1:233295707-233295829 | Common:1; Rare:36 | ||||
chr1:234373276-234373679 | Common:1; Rare:180; Clinvar (benign):5 | ||||
chr1:234478410-234479030 | Common:8; Rare:198 | ||||
chr1:234479098-234479238 | Common:5; Rare:55 | ||||
chr1:234607376-234607804 | Common:4; Rare:201; Clinvar (benign):1 |