Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91021963-91022152 | Rare:54 | ||||
chr1:91500751-91500901 | Common:2; Rare:49 | ||||
chr1:92298923-92299076 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
chr1:93079056-93079314 | Common:4; Rare:111 | ||||
chr1:93180355-93180694 | Common:1; Rare:142 | ||||
chr1:93345787-93345953 | Common:3; Rare:65 | ||||
chr1:93448007-93448269 | Common:3; Rare:88 | ||||
chr1:93846618-93846768 | Common:1; Rare:49 | ||||
chr1:93879144-93879308 | Common:3; Rare:58 | ||||
chr1:94418175-94418470 | Common:2; Rare:108 | ||||
chr1:94541751-94541969 | Rare:69 | ||||
chr1:94820212-94820416 | Common:2; Rare:57 | ||||
chr1:95072857-95073041 | Common:2; Rare:73; Clinvar (benign):2 | ||||
chr1:95233973-95234228 | Common:5; Rare:77 | ||||
chr1:96721550-96721879 | Common:2; Rare:149 |