Variant report

Variant	rs10950286
Chromosome Location	chr7:71381825-71381826
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10447536	0.94[GIH][hapmap];0.84[TSI][hapmap]
rs11766067	0.82[CEU][hapmap];0.88[CHB][hapmap];0.86[CHD][hapmap];0.88[GIH][hapmap];0.84[TSI][hapmap];0.87[ASN][1000 genomes]
rs11769248	0.84[CEU][hapmap];0.88[CHB][hapmap];0.87[ASN][1000 genomes]
rs11772460	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12537492	0.85[JPT][hapmap]
rs16869589	0.84[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17144059	0.85[JPT][hapmap]
rs17340451	0.94[GIH][hapmap];0.87[TSI][hapmap]
rs17340639	0.88[GIH][hapmap];0.87[TSI][hapmap]
rs17424992	0.94[GIH][hapmap];0.84[TSI][hapmap]
rs17425888	0.82[CEU][hapmap];0.88[CHB][hapmap];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2051883	0.83[ASN][1000 genomes]
rs2051884	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2107880	0.84[AMR][1000 genomes]
rs2158656	1.00[CEU][hapmap];0.88[CHB][hapmap]
rs2214747	0.82[AMR][1000 genomes]
rs2867559	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2867560	0.84[AMR][1000 genomes]
rs4717619	0.84[AMR][1000 genomes]
rs59392444	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66607901	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs67172404	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6944606	0.82[CEU][hapmap];0.88[CHB][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6946044	0.95[CEU][hapmap];0.88[CHB][hapmap];0.88[GIH][hapmap];0.92[TSI][hapmap];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6956808	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6956922	0.91[ASN][1000 genomes]
rs6959613	0.85[AMR][1000 genomes]
rs6965098	1.00[CEU][hapmap];0.88[CHB][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6966229	0.84[AMR][1000 genomes]
rs6967264	0.83[ASN][1000 genomes]
rs6969870	0.85[JPT][hapmap]
rs6976024	0.82[AMR][1000 genomes]
rs726469	0.82[CEU][hapmap];0.88[CHB][hapmap];0.86[CHD][hapmap];0.94[GIH][hapmap];0.84[TSI][hapmap]
rs733909	0.82[CEU][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7349979	0.88[GIH][hapmap];0.85[JPT][hapmap];0.87[TSI][hapmap]
rs769022	0.82[CEU][hapmap];0.88[CHB][hapmap];0.86[CHD][hapmap];0.94[GIH][hapmap];0.84[TSI][hapmap];0.83[ASN][1000 genomes]
rs7776793	0.84[CEU][hapmap];0.86[CHB][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026896	chr7:71003462-71721516	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1027496	chr7:71162362-71575116	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv916220	chr7:71200006-71708048	Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv531372	chr7:71300090-71909517	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
5	nsv1017367	chr7:71339782-71476575	ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10950286	CLIP2	cis	parietal	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71380400-71387600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:71381000-71382000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr7:71381600-71395200	Weak transcription	Thymus	Thymus
4	chr7:71381800-71382200	Strong transcription	Fetal Thymus	thymus

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