Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49491486-49491758 | Common:1; Rare:86 | ||||
chr19:50491103-50491349 | Common:4; Rare:45 | ||||
chr19:55133828-55134125 | Common:3; Rare:112; Clinvar:4; Clinvar (benign):5 | ||||
chr2:8545085-8545350 | Rare:55 | ||||
chr2:13523377-13523521 | Rare:25 | ||||
chr2:20447729-20447988 | Rare:81 | ||||
chr2:70086269-70086484 | Common:4; Rare:86 | ||||
chr2:74120562-74120608 | Common:1; Rare:12 | ||||
chr2:88016540-88016817 | Common:10; Rare:118 | ||||
chr2:96010505-96010596 | Rare:21 | ||||
chr2:127103602-127103935 | Common:2; Rare:75 | ||||
chr2:151492385-151492595 | Common:2; Rare:68; Clinvar (benign):1 | ||||
chr2:151553482-151553798 | Rare:72 | ||||
chr2:159764612-159764873 | Common:1; Rare:51 | ||||
chr2:176637574-176637762 | Common:3; Rare:68 |