Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:98661620-98661885 | Common:2; Rare:94 | ||||
chr1:99645874-99645929 | Rare:11 | ||||
chr1:99849997-99850130 | Common:1; Rare:49 | ||||
chr1:99969878-99970074 | Rare:46 | ||||
chr1:100038001-100038189 | Common:1; Rare:74 | ||||
chr1:100132887-100133210 | Common:2; Rare:116 | ||||
chr1:100249812-100250045 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
chr1:100266107-100266332 | Common:3; Rare:82 | ||||
chr1:100894631-100894923 | Common:2; Rare:69 | ||||
chr1:100895896-100896155 | Rare:67 | ||||
chr1:101025754-101025923 | Common:1; Rare:52 | ||||
chr1:101236611-101237025 | Common:4; Rare:82 | ||||
chr1:103525455-103525747 | Rare:85 | ||||
chr1:103525922-103526018 | Rare:24 | ||||
chr1:107056587-107056718 | Common:1; Rare:50 |