Variant report

Variant	rs60905342
Chromosome Location	chr5:108611923-108611924
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11739672	0.83[ASN][1000 genomes]
rs11741980	0.84[ASN][1000 genomes]
rs11743452	0.83[ASN][1000 genomes]
rs11744353	0.83[ASN][1000 genomes]
rs11746207	0.83[ASN][1000 genomes]
rs11748450	0.83[ASN][1000 genomes]
rs1363212	0.81[ASN][1000 genomes]
rs1363213	0.83[ASN][1000 genomes]
rs1592807	0.83[ASN][1000 genomes]
rs1592811	0.83[ASN][1000 genomes]
rs17161665	0.83[ASN][1000 genomes]
rs17161674	0.83[ASN][1000 genomes]
rs1833567	0.83[ASN][1000 genomes]
rs1833568	0.83[ASN][1000 genomes]
rs1833569	0.83[ASN][1000 genomes]
rs1862201	0.83[ASN][1000 genomes]
rs1862202	0.83[ASN][1000 genomes]
rs1862203	0.83[ASN][1000 genomes]
rs1895200	0.83[ASN][1000 genomes]
rs36123121	0.83[ASN][1000 genomes]
rs4388251	0.83[ASN][1000 genomes]
rs4392675	0.83[ASN][1000 genomes]
rs57629433	0.83[ASN][1000 genomes]
rs60335509	0.83[ASN][1000 genomes]
rs60878839	0.83[ASN][1000 genomes]
rs6594365	0.83[ASN][1000 genomes]
rs6863688	0.83[ASN][1000 genomes]
rs6863893	0.83[ASN][1000 genomes]
rs6879134	0.83[ASN][1000 genomes]
rs7700458	0.83[ASN][1000 genomes]
rs7704359	0.83[ASN][1000 genomes]
rs7705919	0.83[ASN][1000 genomes]
rs7721272	0.83[ASN][1000 genomes]
rs7721427	0.83[ASN][1000 genomes]
rs7721730	0.83[ASN][1000 genomes]
rs7721870	0.83[ASN][1000 genomes]
rs7722100	0.83[ASN][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	nsv1027163	chr5:108445447-108839913	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv599338	chr5:108528729-108675737	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv508375	chr5:108587628-108624046	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2763481	chr5:108605390-108693696	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:108601800-108615000	Weak transcription	Pancreas	Pancrea
2	chr5:108611800-108612200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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