Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1971908-1972103 | Common:1; Rare:54 | ||||
chr16:2047795-2048058 | Rare:129; Clinvar:2; Clinvar (benign):5 | ||||
chr16:2682366-2682598 | Rare:105 | ||||
chr16:2777235-2777392 | Common:1; Rare:65 | ||||
chr16:2964071-2964328 | Common:2; Rare:66 | ||||
chr16:2980410-2980619 | Common:2; Rare:73 | ||||
chr16:3020222-3020377 | Rare:58 | ||||
chr16:3134852-3135125 | Common:2; Rare:67 | ||||
chr16:3263665-3263829 | Common:1; Rare:44 | ||||
chr16:3305382-3305534 | Common:1; Rare:55 | ||||
chr16:3400974-3401226 | Common:6; Rare:92 | ||||
chr16:3443452-3443737 | Common:3; Rare:95 | ||||
chr16:3611578-3611762 | Rare:75 | ||||
chr16:4425773-4425884 | Common:1; Rare:51 | ||||
chr16:4476273-4476483 | Common:3; Rare:79 |