Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:47803367-47803490 | Rare:59; Clinvar:21; Clinvar (benign):12 | ||||
chr2:47906467-47906815 | Common:2; Rare:127 | ||||
chr2:54560438-54560588 | Common:2; Rare:45 | ||||
chr2:55282248-55282362 | Common:5; Rare:36 | ||||
chr2:65435790-65435950 | Common:2; Rare:44 | ||||
chr2:70086222-70086565 | Common:5; Rare:157 | ||||
chr2:70125291-70125491 | Rare:52 | ||||
chr2:70142704-70142993 | Common:2; Rare:126 | ||||
chr2:70552602-70552709 | Common:1; Rare:24 | ||||
chr2:74120123-74120387 | Common:1; Rare:88 | ||||
chr2:74120551-74120608 | Common:1; Rare:13 | ||||
chr2:88016540-88016827 | Common:10; Rare:122 | ||||
chr2:91659912-91660138 | Rare:61 | ||||
chr2:96010450-96010618 | Rare:42 | ||||
chr2:104843464-104843551 | Rare:17 |