Variant report

Variant	rs7746677
Chromosome Location	chr6:85835116-85835117
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10944065	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10944066	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11752482	0.84[EUR][1000 genomes]
rs12198003	0.83[EUR][1000 genomes]
rs12198648	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1325976	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1332371	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1407163	0.87[EUR][1000 genomes]
rs6925411	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72912229	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7750840	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7751010	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7772456	0.97[EUR][1000 genomes];0.94[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	nsv1017418	chr6:85344786-86259540	Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv538347	chr6:85344786-86259540	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:85833800-85836400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:85834000-85838400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:85834200-85836400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:85834400-85835800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:85834400-85836400	Enhancers	NHDF-Ad	bronchial
6	chr6:85834400-85836600	Enhancers	Osteobl	bone
7	chr6:85834600-85835400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:85834600-85835800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	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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