Variant report

Variant	rs371403419
Chromosome Location	chr6:44494699-44494700
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv969300	chr6:44493755-44494845	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44492400-44496600	Enhancers	Fetal Thymus	thymus
2	chr6:44492400-44509800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:44493200-44498000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:44493400-44494800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:44493600-44495600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:44494400-44495800	Enhancers	Dnd41	blood
7	chr6:44494400-44495800	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr6:44494600-44495200	Enhancers	Thymus	Thymus
9	chr6:44494600-44495600	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr6:44494600-44496000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr6:44494600-44496200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr6:44494600-44496200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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