Variant report

Variant	rs2770337
Chromosome Location	chr6:101577043-101577044
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10782325	0.81[ASN][1000 genomes]
rs4133169	0.83[ASN][1000 genomes]
rs4329122	0.82[ASN][1000 genomes]
rs4376359	0.81[ASN][1000 genomes]
rs4598083	0.81[ASN][1000 genomes]
rs61647432	0.82[ASN][1000 genomes]
rs6905979	0.81[ASN][1000 genomes]
rs6915514	0.81[ASN][1000 genomes]
rs6927027	0.80[CHB][hapmap]
rs72610831	0.82[ASN][1000 genomes]
rs72610833	0.83[ASN][1000 genomes]
rs72610834	0.83[ASN][1000 genomes]
rs72610835	0.82[ASN][1000 genomes]
rs7747415	0.98[ASN][1000 genomes]
rs7749035	0.81[ASN][1000 genomes]
rs7753454	0.81[ASN][1000 genomes]
rs7753811	0.81[ASN][1000 genomes]
rs7754468	0.82[ASN][1000 genomes]
rs7762966	0.95[ASN][1000 genomes]
rs7768876	0.82[ASN][1000 genomes]
rs7773911	0.80[ASN][1000 genomes]
rs9322380	0.81[ASN][1000 genomes]
rs9322394	0.95[ASN][1000 genomes]
rs9377262	0.83[ASN][1000 genomes]
rs9386270	0.81[ASN][1000 genomes]
rs9390720	0.82[ASN][1000 genomes]
rs9390722	0.82[ASN][1000 genomes]
rs9390723	0.82[ASN][1000 genomes]
rs9390729	0.95[ASN][1000 genomes]
rs9390731	0.83[ASN][1000 genomes]
rs9390732	0.83[ASN][1000 genomes]
rs9399705	0.81[ASN][1000 genomes]
rs9399706	0.81[ASN][1000 genomes]
rs9399710	0.95[ASN][1000 genomes]
rs9399711	0.98[ASN][1000 genomes]
rs9399712	0.85[ASN][1000 genomes]
rs9404081	0.95[ASN][1000 genomes]
rs9404083	0.82[ASN][1000 genomes]
rs9404085	0.83[ASN][1000 genomes]
rs9404089	0.84[JPT][hapmap]
rs9485452	0.82[ASN][1000 genomes]
rs9485453	0.82[ASN][1000 genomes]
rs9485455	0.81[ASN][1000 genomes]
rs9498474	0.82[ASN][1000 genomes]
rs9498478	0.81[ASN][1000 genomes]
rs9498484	0.81[ASN][1000 genomes]
rs9498485	0.81[ASN][1000 genomes]
rs9498488	0.81[ASN][1000 genomes]
rs9498509	0.95[ASN][1000 genomes]
rs9498510	0.95[ASN][1000 genomes]
rs9498511	0.96[ASN][1000 genomes]
rs9498515	0.98[ASN][1000 genomes]
rs9498520	0.98[ASN][1000 genomes]
rs9498521	0.98[ASN][1000 genomes]
rs9498522	0.98[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	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr6:101577000-101578600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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