Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70088922-70088936 | Rare:3 | ||||
chr2:70089010-70089091 | Rare:23 | ||||
chr2:70948558-70948735 | Common:2; Rare:42 | ||||
chr2:74503939-74504248 | Common:2; Rare:62 | ||||
chr2:86136818-86137141 | Common:1; Rare:69 | ||||
chr2:95526701-95526838 | Common:1; Rare:50 | ||||
chr2:99363585-99363657 | Rare:13 | ||||
chr2:104853187-104853297 | Rare:22 | ||||
chr2:112022166-112022352 | Rare:44; Clinvar:3 | ||||
chr2:113584028-113584098 | Rare:17 | ||||
chr2:131682429-131682524 | Common:2; Rare:30 | ||||
chr2:162318052-162318125 | Rare:25; Clinvar:1 | ||||
chr2:170770759-170771044 | Common:1; Rare:47 | ||||
chr2:190997858-190998245 | Common:5; Rare:63; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:197400119-197400254 | Common:1; Rare:30 |