Variant report

Variant	rs3934734
Chromosome Location	chr8:49093540-49093541
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 124 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs10086138	0.86[AFR][1000 genomes]
rs10086728	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10095363	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10099232	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10099601	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10103627	0.87[AFR][1000 genomes]
rs10104502	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10105954	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10107062	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10107500	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10107531	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10109229	0.81[ASN][1000 genomes]
rs10110043	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10112655	0.83[ASN][1000 genomes]
rs10216490	0.83[AMR][1000 genomes]
rs10958494	0.93[YRI][hapmap]
rs11778279	0.82[AFR][1000 genomes]
rs11783647	0.86[AFR][1000 genomes]
rs11783734	0.87[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs12544623	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12708172	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12708173	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12708174	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13248162	0.81[ASN][1000 genomes]
rs13250861	0.81[ASN][1000 genomes]
rs13251473	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs13252104	0.85[AFR][1000 genomes]
rs13263949	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs13265298	0.86[AFR][1000 genomes]
rs13270721	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs13276357	0.81[ASN][1000 genomes]
rs13277100	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs13281542	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28421609	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28459674	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs28489005	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs28539823	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28678298	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs28678847	0.96[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs34075137	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34172095	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34568428	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34608684	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34850099	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35040443	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35088698	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs35578152	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs35637385	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35748311	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs36004689	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs3923232	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3934732	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3934733	0.88[AFR][1000 genomes]
rs4130803	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4242483	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4242484	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4242485	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4263791	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4329299	0.86[AFR][1000 genomes]
rs4373544	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4375031	0.89[AFR][1000 genomes]
rs4380968	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4397430	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4475511	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4489344	0.80[AFR][1000 genomes]
rs4526384	0.86[AFR][1000 genomes]
rs4527898	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4534147	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4543570	0.81[AMR][1000 genomes]
rs4610781	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4873781	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4873782	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4873783	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4873784	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4873785	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4873788	0.93[YRI][hapmap]
rs60275259	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs61146557	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6474074	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6986825	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6990698	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6994417	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6994790	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6998272	0.97[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7004442	0.81[ASN][1000 genomes]
rs7004828	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7009463	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7011426	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7014393	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7815183	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7820720	0.89[AFR][1000 genomes]
rs7822672	0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7827365	0.81[AMR][1000 genomes]
rs7831644	0.81[AMR][1000 genomes]
rs7838513	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs9657169	0.91[AFR][1000 genomes]
rs9792196	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9792312	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs9792353	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831310	chr8:49080177-49256440	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv611307	chr8:49081709-49093889	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3366505	chr8:49092649-49094997	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	nsv824618	chr8:49092729-49093849	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
5	nsv824619	chr8:49092774-49093849	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv12953	chr8:49092986-49093961	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv819150	chr8:49093138-49095727	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	nsv824621	chr8:49093223-49093849	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
9	nsv821514	chr8:49093223-49093961	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3481169	chr8:49093250-49094089	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv21261	chr8:49093271-49093961	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3508436	chr8:49093276-49094090	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3339241	chr8:49093285-49094060	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3508437	chr8:49093294-49094021	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3479176	chr8:49093295-49093865	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3479177	chr8:49093295-49093865	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
17	esv3508439	chr8:49093323-49094029	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	esv3508438	chr8:49093328-49094029	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3428594	chr8:49093348-49093999	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
20	esv3481170	chr8:49093372-49093983	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
21	esv3508435	chr8:49093382-49093982	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
22	esv3481171	chr8:49093386-49093980	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
23	esv3508440	chr8:49093386-49093980	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
24	nsv611308	chr8:49093467-49093889	Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv1841988	chr8:49093467-49156411	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49085200-49098400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:49089600-49094000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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