Variant report

Variant	rs35928894
Chromosome Location	chr12:11363767-11363768
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10743945	0.86[EUR][1000 genomes]
rs10743946	0.86[EUR][1000 genomes]
rs10772426	0.83[EUR][1000 genomes]
rs10772427	0.86[EUR][1000 genomes]
rs10772429	0.86[EUR][1000 genomes]
rs10772431	0.86[EUR][1000 genomes]
rs11054183	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11054212	0.86[EUR][1000 genomes]
rs11507725	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1344667	0.86[EUR][1000 genomes]
rs1344668	0.86[EUR][1000 genomes]
rs1366027	0.86[EUR][1000 genomes]
rs1366028	0.86[EUR][1000 genomes]
rs1427755	0.86[EUR][1000 genomes]
rs1427756	0.86[EUR][1000 genomes]
rs1451771	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1469376	0.83[EUR][1000 genomes]
rs1816224	0.86[EUR][1000 genomes]
rs1863850	0.86[EUR][1000 genomes]
rs1896550	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1896551	0.86[EUR][1000 genomes]
rs1965071	0.86[EUR][1000 genomes]
rs1968355	0.86[EUR][1000 genomes]
rs1972420	0.86[EUR][1000 genomes]
rs2008542	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2042847	0.86[EUR][1000 genomes]
rs2416551	0.80[EUR][1000 genomes]
rs35518946	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3899746	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4237931	0.86[EUR][1000 genomes]
rs4332603	0.86[EUR][1000 genomes]
rs4763243	0.86[EUR][1000 genomes]
rs4763639	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4763649	0.86[EUR][1000 genomes]
rs4763650	0.86[EUR][1000 genomes]
rs4763651	0.86[EUR][1000 genomes]
rs4763652	0.86[EUR][1000 genomes]
rs4763653	0.86[EUR][1000 genomes]
rs4763654	0.86[EUR][1000 genomes]
rs4763656	0.86[EUR][1000 genomes]
rs4763659	0.86[EUR][1000 genomes]
rs4763660	0.86[EUR][1000 genomes]
rs6488360	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6488361	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6488362	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7133045	0.86[EUR][1000 genomes]
rs7307066	0.86[EUR][1000 genomes]
rs7307412	0.86[EUR][1000 genomes]
rs7307651	0.86[EUR][1000 genomes]
rs7307932	0.86[EUR][1000 genomes]
rs7308141	0.86[EUR][1000 genomes]
rs7308391	0.86[EUR][1000 genomes]
rs7309064	0.86[EUR][1000 genomes]
rs7955473	0.86[EUR][1000 genomes]
rs7961670	0.87[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs7966713	0.86[EUR][1000 genomes]
rs7967923	0.86[EUR][1000 genomes]
rs7968635	0.86[EUR][1000 genomes]
rs7971604	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7971884	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7978976	0.86[EUR][1000 genomes]
rs7980324	0.86[EUR][1000 genomes]
rs838965	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]

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	esv2758294	chr12:10969620-11714921	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
2	esv2759879	chr12:10969620-11714921	Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
3	nsv1038277	chr12:11060978-11504091	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
4	nsv428272	chr12:11069845-11714921	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
5	nsv1050050	chr12:11192046-11436359	Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	nsv1053783	chr12:11203509-11495584	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
7	esv1807067	chr12:11214215-11568895	Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
8	nsv976532	chr12:11351537-11368813	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11330600-11365400	Weak transcription	Primary T cells from cord blood	blood
2	chr12:11362200-11371800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:11362400-11366000	Weak transcription	Liver	Liver

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