Variant report

Variant	rs11767969
Chromosome Location	chr7:14562108-14562109
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10231750	0.80[YRI][hapmap]
rs10235540	0.84[CEU][hapmap]
rs10237359	0.85[EUR][1000 genomes]
rs10244094	0.80[YRI][hapmap]
rs10245171	0.80[YRI][hapmap]
rs10245826	0.80[EUR][1000 genomes]
rs10247453	0.84[CEU][hapmap]
rs10260522	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10260659	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10263131	0.85[CEU][hapmap]
rs10266998	0.81[EUR][1000 genomes]
rs10274270	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10274418	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10499441	0.84[CEU][hapmap]
rs10499442	0.85[CEU][hapmap];0.94[CHB][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10950530	0.82[EUR][1000 genomes]
rs11505395	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11505396	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11762226	0.85[CEU][hapmap]
rs11767890	0.88[CEU][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11771647	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11982590	0.81[CEU][hapmap]
rs12154477	1.00[YRI][hapmap]
rs12666867	0.92[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs12669548	0.80[CEU][hapmap]
rs12670458	0.81[CEU][hapmap]
rs12674261	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs12699617	0.88[CEU][hapmap]
rs12699618	0.85[CEU][hapmap]
rs12699619	0.84[CEU][hapmap]
rs12699622	0.84[CEU][hapmap];0.93[CHB][hapmap];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12699626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699629	0.80[YRI][hapmap]
rs12699635	0.96[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap]
rs12699641	0.81[CEU][hapmap]
rs13232496	0.82[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs13236153	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13243691	0.85[CEU][hapmap]
rs1367780	0.80[CEU][hapmap]
rs1431520	0.80[CEU][hapmap]
rs1431521	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs1431525	0.84[CEU][hapmap]
rs1431526	0.83[CEU][hapmap]
rs1431527	0.85[CEU][hapmap]
rs1431528	0.80[CEU][hapmap]
rs1431532	0.88[CEU][hapmap]
rs1541874	0.85[CEU][hapmap]
rs1560479	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs1897300	0.81[CEU][hapmap]
rs196751	0.80[CEU][hapmap]
rs1991685	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs2116319	0.81[CEU][hapmap]
rs2163508	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2357960	0.84[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2884348	0.84[CEU][hapmap]
rs3823843	0.84[CEU][hapmap];0.86[EUR][1000 genomes]
rs4370419	0.85[CEU][hapmap]
rs4719406	0.82[CEU][hapmap]
rs4719407	0.80[YRI][hapmap]
rs4719409	0.89[YRI][hapmap]
rs4721335	0.87[CEU][hapmap]
rs4721338	0.84[CEU][hapmap]
rs4721345	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6461102	0.85[CEU][hapmap]
rs6461104	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs6943928	0.85[CEU][hapmap]
rs6958607	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6958691	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6959924	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6979012	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6979330	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6980167	0.82[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs7782805	0.84[CEU][hapmap]
rs7783571	0.89[EUR][1000 genomes]
rs7800703	0.80[EUR][1000 genomes]
rs7801624	0.83[EUR][1000 genomes]
rs7807072	0.84[CEU][hapmap];0.82[EUR][1000 genomes]
rs9639203	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.80[YRI][hapmap];0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9639204	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9690425	0.88[CEU][hapmap]
rs987448	0.80[CEU][hapmap]
rs987449	0.84[CEU][hapmap]

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	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

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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