Variant report

Variant	rs56102366
Chromosome Location	chr6:37374324-37374325
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10947683	1.00[EUR][1000 genomes]
rs56830331	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57466008	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61282104	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73730769	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73730779	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73730786	1.00[EUR][1000 genomes]
rs73730789	1.00[EUR][1000 genomes]
rs7755939	1.00[EUR][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	nsv520294	chr6:37360557-37380324	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	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	chr6:37373600-37374800	Enhancers	Placenta	Placenta
2	chr6:37373800-37375400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr6:37374000-37374400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:37374000-37374400	Enhancers	NHEK	skin
5	chr6:37374000-37375200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:37374200-37375400	Enhancers	HMEC	breast

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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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