Variant report

Variant	rs11103937
Chromosome Location	chr12:86746044-86746045
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10160933	1.00[YRI][hapmap]
rs11103901	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11103902	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11103905	1.00[AFR][1000 genomes]
rs11103906	1.00[AFR][1000 genomes]
rs11103907	1.00[AFR][1000 genomes]
rs11103910	1.00[YRI][hapmap]
rs11103922	0.87[YRI][hapmap]
rs11103956	1.00[YRI][hapmap]
rs11103959	0.88[YRI][hapmap]
rs11103986	0.88[YRI][hapmap]
rs12296316	0.88[YRI][hapmap]
rs12298208	1.00[AFR][1000 genomes]
rs12298422	1.00[AFR][1000 genomes]
rs12299772	1.00[AFR][1000 genomes]
rs12299950	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs12300410	0.84[AFR][1000 genomes]
rs12303146	0.88[AFR][1000 genomes]
rs12304625	1.00[YRI][hapmap]
rs12305480	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs12306070	1.00[YRI][hapmap]
rs12306455	1.00[AFR][1000 genomes]
rs12306583	0.94[AFR][1000 genomes]
rs12306726	1.00[YRI][hapmap]
rs12308711	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs12309297	1.00[AFR][1000 genomes]
rs12311208	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs12311647	1.00[YRI][hapmap]
rs12315031	1.00[AFR][1000 genomes]
rs12316205	0.88[AFR][1000 genomes]
rs12316480	1.00[YRI][hapmap]
rs12318124	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs12318366	1.00[YRI][hapmap]
rs12318727	0.88[AFR][1000 genomes]
rs12318998	1.00[YRI][hapmap]
rs12319070	0.88[YRI][hapmap]
rs12321412	1.00[YRI][hapmap]
rs12321594	1.00[YRI][hapmap]
rs12321784	0.87[YRI][hapmap]
rs4842468	1.00[YRI][hapmap]
rs9971936	0.87[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761759	chr12:86415936-86747726	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv518059	chr12:86416212-86747726	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1037003	chr12:86610040-86798121	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1053234	chr12:86701070-86774957	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	esv2754127	chr12:86723232-87576932	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1041126	chr12:86736601-86774957	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
8	nsv1051494	chr12:86736601-86776021	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	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
a single nucleotide as 0-based coordinates: chr1:12345
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