Variant report

Variant	rs56050669
Chromosome Location	chr12:83868414-83868415
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11829151	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11832298	1.00[AMR][1000 genomes]
rs11835525	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11838305	1.00[AMR][1000 genomes]
rs55793072	1.00[AMR][1000 genomes]
rs57189980	1.00[AMR][1000 genomes]
rs58825414	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61482473	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74106449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74106450	1.00[AMR][1000 genomes]
rs74106452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74106456	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74106462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74106463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74106476	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74107103	1.00[AMR][1000 genomes]
rs74107165	1.00[AMR][1000 genomes]
rs74107166	1.00[AMR][1000 genomes]
rs74107921	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv1042674	chr12:83620899-83942628	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1037194	chr12:83859925-83910630	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases
4	nsv1041589	chr12:83861093-83890080	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83866800-83871400	Enhancers	Fetal Heart	heart
2	chr12:83867800-83872000	Enhancers	Liver	Liver

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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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