Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:49307027-49307227 | Common:2; Rare:51 | ||||
chr2:63615158-63615305 | Common:1; Rare:35 | ||||
chr2:70086269-70086485 | Common:4; Rare:86 | ||||
chr2:70088036-70088477 | Common:1; Rare:119 | ||||
chr2:73902224-73902482 | Common:2; Rare:53; Clinvar:2 | ||||
chr2:73908713-73909139 | Common:1; Rare:88; Clinvar (pathogenic):3 | ||||
chr2:74120183-74120377 | Rare:71 | ||||
chr2:74120562-74120631 | Common:1; Rare:21 | ||||
chr2:78542037-78542156 | Common:1; Rare:37 | ||||
chr2:88016548-88016817 | Common:8; Rare:109 | ||||
chr2:91659912-91660021 | Rare:18 | ||||
chr2:94947301-94947554 | Common:1; Rare:72 | ||||
chr2:95526681-95526826 | Common:1; Rare:50 | ||||
chr2:96010464-96010574 | Rare:30 | ||||
chr2:113584068-113584117 | Rare:12 |