Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:36999254-36999413 | Rare:69 | ||||
chr13:39038102-39038406 | Common:1; Rare:75 | ||||
chr13:40771128-40771436 | Common:3; Rare:92 | ||||
chr13:40789370-40789617 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):2 | ||||
chr13:41061387-41061586 | Common:2; Rare:54 | ||||
chr13:41311168-41311292 | Rare:51 | ||||
chr13:44989419-44989597 | Rare:72 | ||||
chr13:45120402-45120648 | Common:1; Rare:85 | ||||
chr13:45341042-45341442 | Common:4; Rare:188 | ||||
chr13:48001225-48001405 | Common:1; Rare:82; Clinvar:3; Clinvar (benign):6 | ||||
chr13:48037520-48037824 | Common:2; Rare:129; Clinvar:2 | ||||
chr13:49247852-49247967 | Rare:35 | ||||
chr13:49585527-49585624 | Common:1; Rare:30 | ||||
chr13:50081980-50082298 | Common:1; Rare:87 | ||||
chr13:50910020-50910074 | Rare:15 |