Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:88992583-88992988 | Common:3; Rare:105 | ||||
chr1:89022764-89022811 | Rare:9 | ||||
chr1:89022829-89022888 | Rare:7 | ||||
chr1:89125977-89126153 | Rare:43 | ||||
chr1:89198579-89198612 | Common:2; Rare:6 | ||||
chr1:89198846-89199019 | Common:1; Rare:28 | ||||
chr1:89272746-89272908 | Common:1; Rare:42 | ||||
chr1:89525331-89525486 | Common:3; Rare:53 | ||||
chr1:89632905-89633227 | Common:3; Rare:91 | ||||
chr1:89820910-89821202 | Common:1; Rare:90 | ||||
chr1:89994981-89995193 | Common:2; Rare:80 | ||||
chr1:91021967-91022399 | Rare:107 | ||||
chr1:91886018-91886334 | Rare:128 | ||||
chr1:92298945-92299090 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92784618-92784879 | Common:2; Rare:73 |