Variant report

Variant	rs34480545
Chromosome Location	chr12:41266377-41266378
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1028949	0.97[ASN][1000 genomes]
rs11178978	0.87[ASN][1000 genomes]
rs12578583	0.86[ASN][1000 genomes]
rs12578762	0.97[ASN][1000 genomes]
rs12579682	0.95[ASN][1000 genomes]
rs12580909	0.86[ASN][1000 genomes]
rs12581257	0.85[ASN][1000 genomes]
rs12581462	0.88[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12582450	0.97[ASN][1000 genomes]
rs12582480	0.97[ASN][1000 genomes]
rs12582790	0.85[ASN][1000 genomes]
rs12582806	0.97[ASN][1000 genomes]
rs12810195	0.85[ASN][1000 genomes]
rs12824161	0.85[ASN][1000 genomes]
rs34409157	0.85[ASN][1000 genomes]
rs34435345	0.85[ASN][1000 genomes]
rs34588792	0.85[ASN][1000 genomes]
rs35067046	0.85[ASN][1000 genomes]
rs35640051	0.85[ASN][1000 genomes]
rs35840550	0.85[ASN][1000 genomes]
rs56928815	0.85[ASN][1000 genomes]
rs59969287	0.85[ASN][1000 genomes]
rs7303594	0.97[ASN][1000 genomes]
rs7307211	0.95[ASN][1000 genomes]
rs7310770	0.85[ASN][1000 genomes]
rs7311456	0.85[ASN][1000 genomes]
rs73118754	0.85[ASN][1000 genomes]
rs73118756	0.85[ASN][1000 genomes]
rs7312428	0.97[ASN][1000 genomes]
rs7314477	0.97[ASN][1000 genomes]
rs7960431	0.89[ASN][1000 genomes]
rs7969238	0.95[ASN][1000 genomes]

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	nsv427909	chr12:41054306-41322257	Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv832380	chr12:41132306-41323961	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41226800-41266400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	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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