Variant report

Variant	rs34050956
Chromosome Location	chr17:63310483-63310484
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12943735	1.00[AFR][1000 genomes]
rs34239840	1.00[AFR][1000 genomes]
rs35763069	1.00[AFR][1000 genomes]
rs71379928	1.00[AFR][1000 genomes]

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	nsv482610	chr17:63214370-63372334	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:63308600-63313200	Weak transcription	Lung	lung
2	chr17:63310000-63310600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
3	chr17:63310200-63310600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
4	chr17:63310200-63310600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr17:63310200-63310600	Bivalent Enhancer	Dnd41	blood
6	chr17:63310400-63310800	Bivalent Enhancer	Fetal Thymus	thymus

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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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