Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94925764-94925777 | Rare:1 | ||||
chr1:94926817-94927509 | Common:4; Rare:217 | ||||
chr1:95072804-95073037 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
chr1:95117253-95117391 | Rare:42 | ||||
chr1:95233938-95234242 | Common:5; Rare:92 | ||||
chr1:98661581-98661879 | Common:2; Rare:105 | ||||
chr1:99645951-99646407 | Common:1; Rare:91 | ||||
chr1:99766607-99766727 | Rare:24 | ||||
chr1:99850287-99850392 | Rare:22; Clinvar:1 | ||||
chr1:99969872-99970087 | Rare:47 | ||||
chr1:100038006-100038199 | Common:1; Rare:79 | ||||
chr1:100132902-100133206 | Common:2; Rare:108 | ||||
chr1:100266097-100266418 | Common:4; Rare:113 | ||||
chr1:100894639-100894914 | Common:2; Rare:67 | ||||
chr1:100895139-100895237 | Common:1; Rare:17 |