Variant report

Variant	rs9396465
Chromosome Location	chr6:14034986-14034987
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14027800-14037400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:14032200-14035000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:14032200-14035800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:14033800-14035400	Enhancers	Pancreas	Pancrea
5	chr6:14034200-14036200	Enhancers	Placenta	Placenta
6	chr6:14034200-14036800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:14034600-14035600	Enhancers	Adipose Nuclei	Adipose
8	chr6:14034800-14035400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:14034800-14035800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:14034800-14038400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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