Variant report

Variant	rs4707907
Chromosome Location	chr6:71993336-71993337
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71988200-71997400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:71988200-71997400	Weak transcription	Left Ventricle	heart
3	chr6:71988400-71997800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:71991600-71997800	Weak transcription	Lung	lung
5	chr6:71991800-71997200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr6:71992000-71997800	Weak transcription	Esophagus	oesophagus
7	chr6:71992800-71993600	Enhancers	Primary B cells from cord blood	blood
8	chr6:71993000-71993400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:71993000-71993400	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:71993200-71993400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:71993200-71993400	Weak transcription	Primary T helper cells PMA-I stimulated	--

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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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