Variant report

Variant	rs614046
Chromosome Location	chr7:83948401-83948402
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10081337	0.86[ASN][1000 genomes]
rs10085599	0.86[ASN][1000 genomes]
rs1015629	0.82[ASN][1000 genomes]
rs10231889	0.86[ASN][1000 genomes]
rs10260152	0.86[ASN][1000 genomes]
rs10263842	0.86[ASN][1000 genomes]
rs11971807	0.84[ASN][1000 genomes]
rs11979170	0.94[JPT][hapmap]
rs12539919	0.89[JPT][hapmap]
rs1808204	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2040696	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2214503	0.88[ASN][1000 genomes]
rs2372167	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2372168	0.81[ASN][1000 genomes]
rs4607535	0.86[ASN][1000 genomes]
rs471152	0.88[ASN][1000 genomes]
rs471477	0.88[ASN][1000 genomes]
rs488333	0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs489440	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs501229	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs512896	0.89[ASN][1000 genomes]
rs514083	0.88[ASN][1000 genomes]
rs521401	0.88[ASN][1000 genomes]
rs537358	0.88[ASN][1000 genomes]
rs562475	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs569493	0.88[ASN][1000 genomes]
rs584566	0.88[ASN][1000 genomes]
rs585661	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs589077	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs592778	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs600346	0.88[ASN][1000 genomes]
rs600642	0.85[EUR][1000 genomes]
rs645226	0.88[ASN][1000 genomes]
rs6467990	0.85[EUR][1000 genomes]
rs671711	0.88[ASN][1000 genomes]
rs6946162	0.86[ASN][1000 genomes]
rs6964607	0.86[ASN][1000 genomes]
rs6969121	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs726978	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs727784	0.88[ASN][1000 genomes]
rs7787024	0.83[ASN][1000 genomes]
rs7799452	0.86[ASN][1000 genomes]
rs811622	0.86[ASN][1000 genomes]
rs812780	0.88[ASN][1000 genomes]
rs9642175	0.89[JPT][hapmap]
rs996033	0.89[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1017884	chr7:83724138-83972995	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv538995	chr7:83724138-83972995	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	esv2754468	chr7:83851249-84166749	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv1793815	chr7:83909503-83997755	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv888631	chr7:83911271-84010005	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv981810	chr7:83946250-83952505	Active TSS Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83930800-83950000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:83947200-83966800	Weak transcription	NHDF-Ad	bronchial

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