Variant report

Variant	rs553973636
Chromosome Location	chr3:82604029-82604030
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013820	chr3:82175705-82968181	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv965384	chr3:82603863-82608331	Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:82603400-82604200	Enhancers	H9 Cell Line	embryonic stem cell
2	chr3:82603400-82604200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr3:82603600-82604200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr3:82603600-82604400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr3:82603600-82604600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:82603800-82607200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr3:82604000-82604200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr3:82604000-82606600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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