Variant report

Variant	rs10763031
Chromosome Location	chr10:55704495-55704496
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10763029	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.81[YRI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10825139	0.85[CEU][hapmap]
rs10825150	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs10825154	0.85[CEU][hapmap];0.88[YRI][hapmap];0.87[EUR][1000 genomes]
rs10825158	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10825164	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10825166	0.87[CHB][hapmap];0.90[JPT][hapmap]
rs10825169	1.00[CEU][hapmap]
rs11003917	0.85[CEU][hapmap]
rs11003929	0.85[ASN][1000 genomes]
rs11003941	0.86[ASN][1000 genomes]
rs11003969	0.81[CEU][hapmap]
rs1900414	0.93[CEU][hapmap];0.96[YRI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1900438	1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap]
rs2121524	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2384337	1.00[CEU][hapmap];0.83[CHB][hapmap];0.90[JPT][hapmap];0.96[YRI][hapmap]
rs2593126	0.81[JPT][hapmap]
rs2921922	0.93[CEU][hapmap];0.83[YRI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2921923	0.92[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2926411	0.93[CEU][hapmap];0.85[YRI][hapmap]
rs34989793	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4628594	0.88[CEU][hapmap]
rs7067725	0.93[CEU][hapmap];0.81[JPT][hapmap];0.88[YRI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7088140	0.96[CEU][hapmap];0.93[EUR][1000 genomes]
rs7089225	0.93[EUR][1000 genomes]
rs7090681	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7101001	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7894095	0.91[EUR][1000 genomes]
rs7898068	0.93[CEU][hapmap];0.96[YRI][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7907348	0.90[EUR][1000 genomes]
rs7908973	0.93[ASN][1000 genomes]
rs7910613	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1842975	chr10:55378668-55736655	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv949692	chr10:55502542-55893206	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv895429	chr10:55564355-55736655	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv895430	chr10:55645953-55736655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1052939	chr10:55654719-55769239	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv550948	chr10:55662089-55714355	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv467213	chr10:55662089-55725234	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv550949	chr10:55662089-55725234	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv550950	chr10:55662156-55714355	ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv3389944	chr10:55703946-55708744	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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