Variant report

Variant	rs10950297
Chromosome Location	chr7:71574128-71574129
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10215588	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10225060	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10231333	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10240685	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10243717	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10248170	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10251441	0.92[JPT][hapmap]
rs10252717	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.81[ASN][1000 genomes]
rs10254309	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10255136	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10256017	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10259034	0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10260183	0.95[GIH][hapmap];1.00[JPT][hapmap]
rs10260420	0.95[GIH][hapmap];1.00[JPT][hapmap]
rs10260767	0.95[GIH][hapmap];1.00[JPT][hapmap]
rs10268010	0.88[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs10281262	1.00[JPT][hapmap]
rs10807742	0.91[JPT][hapmap]
rs10807744	0.91[JPT][hapmap]
rs10950291	0.90[JPT][hapmap]
rs10950294	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10950295	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs10950298	1.00[JPT][hapmap]
rs11772246	0.91[JPT][hapmap]
rs11972568	1.00[JPT][hapmap]
rs11982267	0.91[JPT][hapmap]
rs11983124	0.91[JPT][hapmap]
rs12535265	0.86[ASN][1000 genomes]
rs12538529	0.82[JPT][hapmap]
rs12666578	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.81[YRI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12668623	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12668647	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12673109	0.92[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs13224539	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs13231587	0.88[AMR][1000 genomes]
rs13231944	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13239589	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs17144357	0.82[JPT][hapmap]
rs17144373	0.83[GIH][hapmap];0.84[JPT][hapmap];0.84[MEX][hapmap]
rs1852088	0.80[ASN][1000 genomes]
rs1852089	0.80[ASN][1000 genomes]
rs2040869	1.00[JPT][hapmap]
rs28411695	0.88[AMR][1000 genomes]
rs2867567	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[ASN][1000 genomes]
rs33986788	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs34518405	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34655504	0.83[CHB][hapmap];0.95[GIH][hapmap];0.92[JPT][hapmap]
rs34801868	0.83[GIH][hapmap];0.92[JPT][hapmap];0.84[MEX][hapmap]
rs34862805	0.81[ASN][1000 genomes]
rs35401350	0.86[ASN][1000 genomes]
rs35509687	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35897134	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4457209	0.89[GIH][hapmap];1.00[JPT][hapmap]
rs4717628	0.82[JPT][hapmap]
rs4719207	0.83[CHD][hapmap];0.91[JPT][hapmap]
rs4719209	0.91[JPT][hapmap]
rs4719216	0.91[JPT][hapmap]
rs59086558	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs59738349	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs60902167	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs61193914	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6952558	0.91[JPT][hapmap]
rs6959686	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs6963114	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.82[ASN][1000 genomes]
rs71551247	0.81[ASN][1000 genomes]
rs73124391	0.86[ASN][1000 genomes]
rs73124394	0.86[ASN][1000 genomes]
rs73124396	0.82[ASN][1000 genomes]
rs7796985	0.81[ASN][1000 genomes]
rs7797796	0.91[JPT][hapmap]
rs7799436	0.92[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 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	nsv491610	chr7:71422560-71803630	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv831023	chr7:71443549-71588033	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv531373	chr7:71487076-71765613	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv817506	chr7:71488542-71935721	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv1034282	chr7:71531113-71876617	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1015848	chr7:71552185-71736068	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv538942	chr7:71552185-71736068	ZNF genes & repeats Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv831024	chr7:71569349-71735250	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:71571400-71574600	Weak transcription	Thymus	Thymus
2	chr7:71572600-71575400	ZNF genes & repeats	Fetal Thymus	thymus
3	chr7:71572800-71574200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:71572800-71574800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:71573400-71578200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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