Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:102394511-102394668 | Common:1; Rare:62 | ||||
chr13:110307828-110307867 | Rare:13 | ||||
chr14:49633938-49634064 | Common:1; Rare:51; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862635-49863036 | Common:1; Rare:182 | ||||
chr14:69886136-69886462 | Rare:36 | ||||
chr14:81170407-81170484 | Rare:19 | ||||
chr14:81219345-81219504 | Rare:35 | ||||
chr14:95516614-95516773 | Common:2; Rare:37 | ||||
chr14:96039076-96039380 | Common:2; Rare:77 | ||||
chr14:100825971-100826179 | Rare:51 | ||||
chr14:100828505-100828749 | Common:2; Rare:32 | ||||
chr15:29730386-29730611 | Rare:46 | ||||
chr15:38254681-38254790 | Common:1; Rare:23 | ||||
chr15:73927695-73927851 | Common:1; Rare:46 | ||||
chr15:82372895-82373124 | Common:1; Rare:32 |