Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:190343961-190344025 | Rare:12 | ||||
chr2:190534681-190534853 | Common:1; Rare:58 | ||||
chr2:190649420-190649584 | Common:1; Rare:48 | ||||
chr2:190880623-190880834 | Common:3; Rare:66 | ||||
chr2:191014133-191014333 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677856-191678191 | Common:4; Rare:96 | ||||
chr2:191846708-191846935 | Common:1; Rare:64 | ||||
chr2:196926728-196926799 | Common:1; Rare:21 | ||||
chr2:196927483-196927696 | Rare:45 | ||||
chr2:197434973-197435186 | Rare:73 | ||||
chr2:197499807-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515913-197516101 | Rare:74 | ||||
chr2:197675688-197675958 | Rare:46 | ||||
chr2:197705228-197705424 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
chr2:200510040-200510084 | Rare:15 |