Variant report

Variant	rs7071258
Chromosome Location	chr10:91574624-91574625
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10881718	1.00[CHB][hapmap]
rs11593819	1.00[ASN][1000 genomes]
rs11593892	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11594682	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11595126	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11597847	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs11598015	1.00[ASN][1000 genomes]
rs11598257	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12413697	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12414269	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12414849	1.00[ASN][1000 genomes]
rs12415422	1.00[ASN][1000 genomes]
rs1326195	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17484219	0.95[CEU][hapmap];1.00[ASN][1000 genomes]
rs2026553	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs34354493	1.00[ASN][1000 genomes]
rs35059516	1.00[ASN][1000 genomes]
rs4426060	1.00[ASN][1000 genomes]
rs4933167	1.00[CHB][hapmap]
rs56318555	1.00[ASN][1000 genomes]
rs6583667	1.00[CHB][hapmap]
rs72818732	1.00[ASN][1000 genomes]
rs72818736	1.00[ASN][1000 genomes]
rs72818740	1.00[ASN][1000 genomes]
rs72818744	1.00[ASN][1000 genomes]
rs72818750	1.00[ASN][1000 genomes]
rs72818751	1.00[ASN][1000 genomes]
rs72818757	1.00[ASN][1000 genomes]
rs72818758	1.00[ASN][1000 genomes]
rs72818759	1.00[ASN][1000 genomes]
rs72818766	1.00[ASN][1000 genomes]
rs72818768	1.00[ASN][1000 genomes]
rs72818770	1.00[ASN][1000 genomes]
rs72818773	1.00[ASN][1000 genomes]
rs72818774	1.00[ASN][1000 genomes]
rs72818781	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72818783	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72818786	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72818790	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72818792	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs728852	1.00[ASN][1000 genomes]
rs997456	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046241	chr10:91478562-91614437	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv869080	chr10:91498641-91712834	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1036581	chr10:91526705-91691536	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv1043571	chr10:91568555-92036154	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv551874	chr10:91570211-92036154	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91573400-91574800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr10:91574200-91574800	Enhancers	Fetal Muscle Leg	muscle
3	chr10:91574200-91576400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:91574400-91575200	Flanking Active TSS	HepG2	liver
5	chr10:91574600-91575200	Enhancers	Fetal Intestine Large	intestine

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