Variant report

Variant	rs1782629
Chromosome Location	chr6:161195866-161195867
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10455783	0.90[ASN][1000 genomes]
rs10455784	0.90[ASN][1000 genomes]
rs1084653	0.91[ASN][1000 genomes]
rs12194271	0.92[ASN][1000 genomes]
rs12206847	0.80[ASN][1000 genomes]
rs12214254	0.92[ASN][1000 genomes]
rs1247559	0.99[ASN][1000 genomes]
rs1247560	0.99[ASN][1000 genomes]
rs1247564	0.99[ASN][1000 genomes]
rs1247565	0.99[ASN][1000 genomes]
rs1247567	0.95[ASN][1000 genomes]
rs1247572	0.84[ASN][1000 genomes]
rs12526591	0.92[ASN][1000 genomes]
rs1271391	0.99[ASN][1000 genomes]
rs13203571	0.89[ASN][1000 genomes]
rs13216458	0.92[ASN][1000 genomes]
rs1344729	0.91[ASN][1000 genomes]
rs1344730	0.91[ASN][1000 genomes]
rs1344731	0.92[ASN][1000 genomes]
rs1358755	0.81[ASN][1000 genomes]
rs1367216	0.96[ASN][1000 genomes]
rs1549741	0.92[ASN][1000 genomes]
rs1611873	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1620969	0.99[ASN][1000 genomes]
rs1652456	0.95[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs1652481	0.99[ASN][1000 genomes]
rs1652498	0.99[ASN][1000 genomes]
rs1652501	0.99[ASN][1000 genomes]
rs1740430	0.84[ASN][1000 genomes]
rs1740431	0.85[ASN][1000 genomes]
rs1740445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1740447	0.96[ASN][1000 genomes]
rs1740466	0.80[ASN][1000 genomes]
rs1782627	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1782628	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1965092	0.92[ASN][1000 genomes]
rs1991598	0.92[ASN][1000 genomes]
rs1991599	0.88[ASN][1000 genomes]
rs2115869	0.91[ASN][1000 genomes]
rs2115870	0.90[ASN][1000 genomes]
rs2115871	0.90[ASN][1000 genomes]
rs2144727	0.91[ASN][1000 genomes]
rs2465835	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2465836	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs34797199	0.92[ASN][1000 genomes]
rs4440440	0.84[ASN][1000 genomes]
rs4708878	0.92[ASN][1000 genomes]
rs4708881	0.92[ASN][1000 genomes]
rs4708882	0.92[ASN][1000 genomes]
rs4708884	0.89[ASN][1000 genomes]
rs4708886	0.88[ASN][1000 genomes]
rs4708887	0.91[ASN][1000 genomes]
rs4708888	0.92[ASN][1000 genomes]
rs4708889	0.89[ASN][1000 genomes]
rs4708891	0.89[ASN][1000 genomes]
rs4708892	0.89[ASN][1000 genomes]
rs4708893	0.89[ASN][1000 genomes]
rs4709466	0.92[ASN][1000 genomes]
rs4709467	0.92[ASN][1000 genomes]
rs4709469	0.92[ASN][1000 genomes]
rs7450979	0.84[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs783176	0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs9456586	0.92[ASN][1000 genomes]
rs9456588	0.81[ASN][1000 genomes]
rs9456589	0.81[ASN][1000 genomes]
rs9458023	0.87[ASN][1000 genomes]
rs9458025	0.92[ASN][1000 genomes]
rs9458026	0.92[ASN][1000 genomes]
rs9458030	0.86[ASN][1000 genomes]
rs9458031	0.87[ASN][1000 genomes]
rs9458036	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758089	chr6:160372244-161234665	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2759484	chr6:160372244-161234665	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv1019113	chr6:161127584-161197558	Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv3352911	chr6:161140543-161324358	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv830853	chr6:161180005-161376481	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv981309	chr6:161193505-161211503	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161195600-161196400	Weak transcription	Fetal Lung	lung

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