Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93180199-93180350 | Rare:47 | ||||
chr1:93180355-93180721 | Common:1; Rare:161 | ||||
chr1:93345624-93345962 | Common:5; Rare:113 | ||||
chr1:93448012-93448149 | Common:2; Rare:54 | ||||
chr1:93847211-93847286 | Common:1; Rare:19 | ||||
chr1:94541730-94541994 | Rare:78 | ||||
chr1:94820186-94820382 | Common:3; Rare:50 | ||||
chr1:94903169-94903444 | Common:1; Rare:52 | ||||
chr1:94926854-94926933 | Rare:22 | ||||
chr1:94926934-94927456 | Common:4; Rare:166 | ||||
chr1:95233924-95234241 | Common:5; Rare:95 | ||||
chr1:96721582-96721867 | Common:2; Rare:134 | ||||
chr1:98661616-98661869 | Common:2; Rare:92 | ||||
chr1:99646235-99646320 | Rare:23 | ||||
chr1:99850319-99850409 | Rare:28; Clinvar:1; Clinvar (benign):1 |