Variant report

Variant	rs73022301
Chromosome Location	chr2:177694207-177694208
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11903983	1.00[AMR][1000 genomes]
rs57320252	1.00[AMR][1000 genomes]
rs58991591	1.00[AMR][1000 genomes]
rs60999786	1.00[AMR][1000 genomes]
rs61615763	1.00[AMR][1000 genomes]
rs73023523	1.00[AMR][1000 genomes]
rs73039150	1.00[AMR][1000 genomes]
rs73041481	1.00[AMR][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	nsv1006500	chr2:177548521-177707097	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:177692200-177695000	Weak transcription	Fetal Thymus	thymus
2	chr2:177692800-177695000	Weak transcription	Fetal Kidney	kidney
3	chr2:177693600-177695400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr2:177693600-177695400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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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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