Variant report

Variant	rs371675604
Chromosome Location	chr8:91515769-91515770
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2408826	chr8:91515233-91515898	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
2	esv3479615	chr8:91515295-91515789	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	esv3497933	chr8:91515312-91515782	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
4	esv3497935	chr8:91515326-91515791	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
5	esv2621133	chr8:91515761-91517085	Weak transcription Enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91510000-91516600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:91514200-91516400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr8:91515400-91516600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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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