Variant report

Variant	rs7962980
Chromosome Location	chr12:43208244-43208245
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 117 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs1009431	0.90[ASN][1000 genomes]
rs11181692	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11181693	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11181694	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11181695	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11181696	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12227600	0.81[EUR][1000 genomes]
rs1400811	0.90[ASN][1000 genomes]
rs1400814	0.90[ASN][1000 genomes]
rs1517666	0.90[ASN][1000 genomes]
rs1517667	0.93[ASN][1000 genomes]
rs1517670	0.90[ASN][1000 genomes]
rs1517671	0.90[ASN][1000 genomes]
rs1517672	0.90[ASN][1000 genomes]
rs1554248	0.89[ASN][1000 genomes]
rs1554249	0.89[ASN][1000 genomes]
rs1554250	0.90[ASN][1000 genomes]
rs1554251	0.90[ASN][1000 genomes]
rs1554252	0.90[ASN][1000 genomes]
rs1607249	0.93[ASN][1000 genomes]
rs17091970	0.90[ASN][1000 genomes]
rs17092061	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1878577	0.89[ASN][1000 genomes]
rs1878579	0.89[ASN][1000 genomes]
rs1878580	0.89[ASN][1000 genomes]
rs2037238	0.90[ASN][1000 genomes]
rs2056192	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2056196	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2252131	0.89[ASN][1000 genomes]
rs2255231	0.89[ASN][1000 genomes]
rs2255712	0.90[ASN][1000 genomes]
rs2255713	0.90[ASN][1000 genomes]
rs2407112	0.89[ASN][1000 genomes]
rs2407113	0.89[ASN][1000 genomes]
rs2459736	0.90[ASN][1000 genomes]
rs2459741	0.93[ASN][1000 genomes]
rs2459742	0.92[ASN][1000 genomes]
rs2468321	0.93[ASN][1000 genomes]
rs2468322	0.92[ASN][1000 genomes]
rs2468324	0.89[ASN][1000 genomes]
rs2468325	0.90[ASN][1000 genomes]
rs2468326	0.90[ASN][1000 genomes]
rs2468327	0.90[ASN][1000 genomes]
rs2678102	0.90[ASN][1000 genomes]
rs2678103	0.89[ASN][1000 genomes]
rs2678104	0.89[ASN][1000 genomes]
rs2678105	0.89[ASN][1000 genomes]
rs2678108	0.89[ASN][1000 genomes]
rs2678109	0.89[ASN][1000 genomes]
rs2678110	0.89[ASN][1000 genomes]
rs2678111	0.89[ASN][1000 genomes]
rs2678112	0.89[ASN][1000 genomes]
rs2678113	0.89[ASN][1000 genomes]
rs2678114	0.89[ASN][1000 genomes]
rs2678115	0.89[ASN][1000 genomes]
rs2678116	0.89[ASN][1000 genomes]
rs2678118	0.89[ASN][1000 genomes]
rs2678132	0.90[ASN][1000 genomes]
rs2678134	0.92[ASN][1000 genomes]
rs2678135	0.93[ASN][1000 genomes]
rs2678136	0.93[ASN][1000 genomes]
rs2678137	0.93[ASN][1000 genomes]
rs2678141	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2678143	0.93[ASN][1000 genomes]
rs2678144	0.93[ASN][1000 genomes]
rs2678145	0.90[ASN][1000 genomes]
rs2678146	0.90[ASN][1000 genomes]
rs2678147	0.90[ASN][1000 genomes]
rs2678149	0.90[ASN][1000 genomes]
rs2678151	0.90[ASN][1000 genomes]
rs2678153	0.90[ASN][1000 genomes]
rs2730965	0.90[ASN][1000 genomes]
rs2730967	0.90[ASN][1000 genomes]
rs2730968	0.93[ASN][1000 genomes]
rs2730969	0.93[ASN][1000 genomes]
rs2730970	0.92[ASN][1000 genomes]
rs2730976	0.89[ASN][1000 genomes]
rs2730977	0.90[ASN][1000 genomes]
rs2730980	0.93[ASN][1000 genomes]
rs2730997	0.90[ASN][1000 genomes]
rs2730998	0.88[ASN][1000 genomes]
rs2730999	0.90[ASN][1000 genomes]
rs2731002	0.90[ASN][1000 genomes]
rs2731003	0.90[ASN][1000 genomes]
rs2731004	0.92[ASN][1000 genomes]
rs2731005	0.89[ASN][1000 genomes]
rs2731007	0.89[ASN][1000 genomes]
rs2731008	0.89[ASN][1000 genomes]
rs2731010	0.88[ASN][1000 genomes]
rs2731015	0.89[ASN][1000 genomes]
rs2731016	0.89[ASN][1000 genomes]
rs2731017	0.89[ASN][1000 genomes]
rs2956457	0.89[ASN][1000 genomes]
rs35204519	0.89[ASN][1000 genomes]
rs73130905	0.81[EUR][1000 genomes]
rs7314719	0.93[ASN][1000 genomes]
rs7962735	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7976494	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7976690	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs908656	0.90[ASN][1000 genomes]
rs908657	0.90[ASN][1000 genomes]
rs908658	0.90[ASN][1000 genomes]
rs908660	0.90[ASN][1000 genomes]
rs908661	0.90[ASN][1000 genomes]
rs908662	0.90[ASN][1000 genomes]
rs908663	0.90[ASN][1000 genomes]
rs908666	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs952054	0.90[ASN][1000 genomes]
rs952056	0.90[ASN][1000 genomes]
rs9651992	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs973001	0.89[ASN][1000 genomes]
rs9788178	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs981248	0.89[ASN][1000 genomes]
rs991703	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044790	chr12:42672255-43344184	Enhancers Bivalent Enhancer Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
2	nsv541483	chr12:42672255-43344184	Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	29 gene(s)	inside rSNPs	diseases
3	nsv558749	chr12:43180190-43275097	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43204000-43208800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:43204200-43209000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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