Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40161151-40161402 | Common:1; Rare:66 | ||||
chr1:40257880-40258282 | Common:4; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40508626-40508828 | Common:6; Rare:61 | ||||
chr1:40531497-40531733 | Common:1; Rare:65 | ||||
chr1:40691495-40691810 | Common:3; Rare:155 | ||||
chr1:40692051-40692247 | Common:1; Rare:62 | ||||
chr1:40979583-40979797 | Common:3; Rare:79 | ||||
chr1:41242101-41242364 | Rare:76 | ||||
chr1:42335149-42335353 | Common:3; Rare:107 | ||||
chr1:42456258-42456583 | Common:1; Rare:100 | ||||
chr1:42682158-42682448 | Common:2; Rare:71 | ||||
chr1:42683229-42683465 | Common:3; Rare:106 | ||||
chr1:42766976-42767309 | Common:4; Rare:113; Clinvar (benign):1 | ||||
chr1:42817009-42817136 | Common:1; Rare:32 | ||||
chr1:42846387-42846642 | Common:1; Rare:75 |