Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1019873-1020173 | Common:1; Rare:97 | ||||
chr1:1020261-1020339 | Rare:19 | ||||
chr1:1020580-1020933 | Common:7; Rare:105 | ||||
chr1:1050083-1050151 | Common:1; Rare:19 | ||||
chr1:1115876-1116528 | Common:3; Rare:199 | ||||
chr1:1231471-1231676 | Common:1; Rare:59 | ||||
chr1:1231714-1232361 | Rare:215; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:1273770-1273906 | Common:1; Rare:58 | ||||
chr1:1273928-1274125 | Common:2; Rare:64 | ||||
chr1:1274170-1274262 | Common:1; Rare:24 | ||||
chr1:1304562-1304906 | Common:3; Rare:101 | ||||
chr1:1305072-1305131 | Common:1; Rare:14 | ||||
chr1:1305656-1305871 | Rare:72 | ||||
chr1:1307801-1308281 | Common:1; Rare:131 | ||||
chr1:1308383-1308852 | Common:10; Rare:197 |