Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:45341040-45341525 | Common:4; Rare:233 | ||||
chr13:46052681-46052877 | Common:2; Rare:56 | ||||
chr13:46553069-46553291 | Common:2; Rare:65 | ||||
chr13:46797121-46797355 | Common:3; Rare:81 | ||||
chr13:46896824-46897083 | Rare:58 | ||||
chr13:48001235-48001385 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):4 | ||||
chr13:48975782-48975923 | Common:1; Rare:51 | ||||
chr13:49247844-49247977 | Rare:43 | ||||
chr13:49443997-49444241 | Common:1; Rare:83 | ||||
chr13:49585520-49585633 | Common:1; Rare:37 | ||||
chr13:49936241-49936586 | Common:1; Rare:104 | ||||
chr13:49996790-49997095 | Common:1; Rare:57 | ||||
chr13:50081980-50082251 | Common:1; Rare:76 | ||||
chr13:50909738-50910074 | Common:1; Rare:76; Clinvar:5; Clinvar (benign):1 | ||||
chr13:51453026-51453381 | Rare:137 |