Variant report

Variant	rs12154477
Chromosome Location	chr7:14563565-14563566
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10231750	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10244094	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10245171	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10245903	0.88[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap]
rs10256038	0.88[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10260659	0.82[CEU][hapmap]
rs10270441	0.88[CEU][hapmap]
rs1030578	0.96[CEU][hapmap];0.87[CHB][hapmap];0.84[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11762226	0.80[CEU][hapmap];0.88[CHB][hapmap];0.90[JPT][hapmap]
rs11767969	1.00[YRI][hapmap]
rs11768166	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11771951	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11982590	1.00[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap]
rs12666867	0.85[CEU][hapmap]
rs12670458	0.92[CEU][hapmap]
rs12699618	0.80[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12699619	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs12699621	0.88[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12699623	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12699624	1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs12699625	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.88[YRI][hapmap]
rs12699626	1.00[YRI][hapmap]
rs12699627	0.80[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699628	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699629	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs12699635	1.00[YRI][hapmap]
rs12699636	0.81[CHB][hapmap]
rs12699637	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs12699645	0.81[CEU][hapmap]
rs13243691	0.80[CEU][hapmap];0.88[CHB][hapmap];0.90[JPT][hapmap]
rs13438642	0.87[CEU][hapmap];0.85[CHB][hapmap];0.88[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1367780	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1367781	0.83[EUR][1000 genomes]
rs1367783	0.88[CEU][hapmap];0.87[CHB][hapmap];0.94[JPT][hapmap]
rs1431513	0.89[JPT][hapmap]
rs1431526	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs1431527	0.80[CEU][hapmap]
rs1431532	0.83[CEU][hapmap]
rs1431538	1.00[CEU][hapmap];0.88[CHB][hapmap];0.90[JPT][hapmap]
rs1541874	0.80[CEU][hapmap]
rs1560479	0.85[YRI][hapmap]
rs1583184	0.81[CHB][hapmap]
rs1978671	1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[ASN][1000 genomes]
rs2116314	0.96[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2116315	0.89[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2116319	0.92[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];0.86[YRI][hapmap]
rs2163507	0.85[CEU][hapmap]
rs2884348	1.00[CHB][hapmap];0.90[JPT][hapmap]
rs34862028	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34919207	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4607508	0.81[EUR][1000 genomes]
rs4719407	0.80[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4719409	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4721342	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6461102	0.80[CEU][hapmap]
rs6943928	0.80[CEU][hapmap];0.88[CHB][hapmap];0.90[JPT][hapmap]
rs6959924	0.81[CEU][hapmap]
rs6975021	0.88[CEU][hapmap]
rs7777868	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7782805	0.83[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs7793372	0.89[JPT][hapmap];0.81[EUR][1000 genomes]
rs7794554	0.80[ASN][1000 genomes]
rs7806743	0.85[JPT][hapmap]
rs9639203	0.81[CEU][hapmap]
rs9690425	0.88[CHB][hapmap];0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv887708	chr7:14494508-14617982	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1800100	chr7:14511454-14564068	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv606282	chr7:14542836-14579801	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
8	nsv1022267	chr7:14551894-14607627	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv887709	chr7:14562957-14604898	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14561600-14563600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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