Variant report

Variant	rs11032478
Chromosome Location	chr11:34013031-34013032
allele	A/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	chr11:34006400-34018200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:34012800-34013200	Enhancers	Primary T cells fromperipheralblood	blood
3	chr11:34012800-34013200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr11:34012800-34013400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr11:34012800-34013600	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr11:34012800-34013600	Enhancers	Fetal Thymus	thymus
7	chr11:34013000-34013400	Active TSS	Primary T cells from cord blood	blood
8	chr11:34013000-34013400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
9	chr11:34013000-34013400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr11:34013000-34013400	Enhancers	Dnd41	blood

Quick Search:

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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