Variant report

Variant	rs7081265
Chromosome Location	chr10:96125649-96125650
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:96125181..96128659-chr10:96161307..96164992,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000108239	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10509670	0.85[MEX][hapmap]
rs10509671	0.86[MEX][hapmap]
rs10509672	1.00[CHB][hapmap];0.82[JPT][hapmap];0.95[ASN][1000 genomes]
rs10786161	0.84[EUR][1000 genomes]
rs10882416	0.81[TSI][hapmap]
rs10882422	0.86[MEX][hapmap]
rs10882424	0.86[MEX][hapmap];0.85[TSI][hapmap];0.82[EUR][1000 genomes]
rs10882430	0.81[EUR][1000 genomes]
rs10882435	0.95[CEU][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10882436	0.93[CEU][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10882437	0.93[MEX][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs10882442	0.81[CEU][hapmap]
rs11187850	0.86[MEX][hapmap]
rs11187869	0.91[EUR][1000 genomes]
rs11187876	0.82[EUR][1000 genomes]
rs11187881	0.81[EUR][1000 genomes]
rs11187893	0.95[CEU][hapmap];0.93[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11187894	0.90[CEU][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11187899	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11187900	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11187901	0.93[MEX][hapmap];0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs11187906	0.97[ASN][1000 genomes]
rs11187907	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11558740	0.91[EUR][1000 genomes]
rs12217597	0.85[CEU][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12219063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12255683	0.80[GIH][hapmap]
rs12263737	0.86[MEX][hapmap];0.81[TSI][hapmap]
rs12773229	0.84[EUR][1000 genomes]
rs12780491	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[JPT][hapmap];0.93[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12781451	0.95[CEU][hapmap];0.91[EUR][1000 genomes]
rs2274223	0.86[MEX][hapmap]
rs34032820	0.81[AFR][1000 genomes]
rs3765524	0.86[MEX][hapmap];0.81[TSI][hapmap]
rs3781264	0.86[MEX][hapmap]
rs3818432	0.86[MEX][hapmap];0.81[TSI][hapmap]
rs6583937	0.82[EUR][1000 genomes]
rs6583940	0.85[EUR][1000 genomes]
rs7074125	0.81[EUR][1000 genomes]
rs7077192	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7084339	0.85[MEX][hapmap]
rs7084988	0.85[EUR][1000 genomes]
rs7085378	0.85[EUR][1000 genomes]
rs7092226	0.86[MEX][hapmap];0.80[TSI][hapmap]
rs7096037	0.82[EUR][1000 genomes]
rs7100430	0.93[MEX][hapmap];0.91[TSI][hapmap];0.86[EUR][1000 genomes]
rs7100870	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7101207	0.95[ASN][1000 genomes]

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	esv2761616	chr10:95966768-96303701	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv831946	chr10:96055190-96226438	Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	esv1819509	chr10:96064300-96361776	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7081265	NOC3L	cis	parietal	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96123200-96128000	Weak transcription	Brain Angular Gyrus	brain
2	chr10:96123400-96128200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr10:96123400-96128400	Weak transcription	Brain Anterior Caudate	brain
4	chr10:96125600-96126600	Enhancers	Brain Hippocampus Middle	brain
5	chr10:96125600-96126600	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr10:96125600-96126600	Enhancers	Brain Substantia Nigra	brain
7	chr10:96125600-96126800	Enhancers	Brain Cingulate Gyrus	brain

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