Variant report

Variant	rs11182562
Chromosome Location	chr12:45009887-45009888
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1037433	0.92[YRI][hapmap]
rs10785513	0.81[CEU][hapmap];0.80[EUR][1000 genomes]
rs10880658	0.91[YRI][hapmap]
rs10880659	0.87[YRI][hapmap]
rs11182552	0.85[CEU][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs12302273	0.82[ASN][1000 genomes]
rs12314678	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12815257	0.91[YRI][hapmap]
rs12829763	0.89[ASN][1000 genomes]
rs1450540	0.87[CHB][hapmap];0.91[JPT][hapmap]
rs1470803	0.87[ASN][1000 genomes]
rs1545496	0.89[CEU][hapmap];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1563043	0.86[YRI][hapmap]
rs17094865	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17094882	0.91[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2060839	0.86[CEU][hapmap];0.82[JPT][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2060841	0.85[CEU][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2060842	0.86[CEU][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2060895	0.89[CEU][hapmap];0.91[YRI][hapmap];0.94[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2060896	0.84[CEU][hapmap];0.91[YRI][hapmap];0.94[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2060899	0.81[CHB][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs2084614	0.87[CHB][hapmap]
rs2218943	0.91[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs2408047	0.85[CHB][hapmap]
rs4544065	0.86[YRI][hapmap]
rs4641544	0.90[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4768066	0.87[YRI][hapmap]
rs4768067	0.98[ASN][1000 genomes]
rs4768562	0.88[CEU][hapmap];0.81[CHB][hapmap];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4768564	0.91[YRI][hapmap]
rs586188	0.81[ASN][1000 genomes]
rs590905	0.85[CHB][hapmap]
rs617006	0.87[CHB][hapmap]
rs625691	0.87[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs632893	0.81[ASN][1000 genomes]
rs633526	0.86[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs641782	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs655191	0.80[ASN][1000 genomes]
rs6582508	0.94[AFR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6582509	0.89[CEU][hapmap];0.82[CHB][hapmap];0.81[JPT][hapmap];0.91[YRI][hapmap];0.86[AFR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs683285	0.91[CHB][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs686110	0.86[CHB][hapmap];0.91[JPT][hapmap]
rs7134952	0.86[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7299592	0.82[ASN][1000 genomes]
rs7304431	0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs7308509	0.86[YRI][hapmap]
rs7958608	0.89[CEU][hapmap];0.91[YRI][hapmap];0.95[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7966743	0.83[CEU][hapmap];0.82[EUR][1000 genomes]
rs7966744	0.82[EUR][1000 genomes]
rs7968076	0.85[YRI][hapmap]
rs838975	0.81[ASN][1000 genomes]
rs966383	0.87[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049818	chr12:44486312-45133783	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3378050	chr12:44963059-45264289	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv430506	chr12:45003342-45072343	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv983484	chr12:45007736-45010626	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44986800-45015800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:44998200-45024400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:44998800-45018200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr12:45003200-45014200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:45004600-45012600	Weak transcription	Brain Germinal Matrix	brain
6	chr12:45004800-45020800	Weak transcription	Fetal Brain Female	brain
7	chr12:45004800-45034800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr12:45004800-45043200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr12:45005000-45023200	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr12:45005000-45031200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:45005000-45044200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr12:45005400-45010400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:45005600-45011600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr12:45009800-45010000	Enhancers	Brain Angular Gyrus	brain
15	chr12:45009800-45010400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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