Variant report

Variant rs73738717
Chromosome Location chr6:27251932-27251933
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:27248600-27255800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr6:27249400-27255200 Weak transcription HMEC breast
3 chr6:27249400-27255600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:27250600-27252000 Active TSS H9 Cell Line embryonic stem cell
5 chr6:27250600-27252200 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
6 chr6:27250600-27252200 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
7 chr6:27250800-27252600 Bivalent/Poised TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr6:27251000-27252400 ZNF genes & repeats Pancreatic Islets Pancreatic Islet
9 chr6:27251800-27252000 Bivalent/Poised TSS NHEK skin
10 chr6:27251800-27252400 Bivalent/Poised TSS Primary T cells from cord blood blood

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