Variant report

Variant	rs7976976
Chromosome Location	chr12:30426661-30426662
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10743709	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10771677	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10771683	0.94[ASN][1000 genomes]
rs10771684	0.92[ASN][1000 genomes]
rs10843688	0.93[ASN][1000 genomes]
rs10843691	0.94[ASN][1000 genomes]
rs10843692	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10843693	0.94[ASN][1000 genomes]
rs10843694	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10843695	0.94[ASN][1000 genomes]
rs10843696	0.94[ASN][1000 genomes]
rs10843697	0.81[ASN][1000 genomes]
rs10843698	0.81[ASN][1000 genomes]
rs10843699	0.94[ASN][1000 genomes]
rs10843700	0.94[ASN][1000 genomes]
rs10843701	0.94[ASN][1000 genomes]
rs10843702	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10843712	0.94[EUR][1000 genomes]
rs11050765	0.80[ASN][1000 genomes]
rs11050766	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11050776	0.94[ASN][1000 genomes]
rs11050778	0.94[ASN][1000 genomes]
rs11050779	0.94[ASN][1000 genomes]
rs11050781	0.94[ASN][1000 genomes]
rs11050782	0.92[ASN][1000 genomes]
rs11050783	0.94[ASN][1000 genomes]
rs11050784	0.94[ASN][1000 genomes]
rs11050785	0.94[ASN][1000 genomes]
rs11050786	0.84[ASN][1000 genomes]
rs11050787	0.94[ASN][1000 genomes]
rs11050788	0.94[ASN][1000 genomes]
rs11050789	0.94[ASN][1000 genomes]
rs11050790	0.94[ASN][1000 genomes]
rs11050791	0.94[ASN][1000 genomes]
rs11050792	0.94[ASN][1000 genomes]
rs11050793	0.94[ASN][1000 genomes]
rs11050795	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11050796	0.94[ASN][1000 genomes]
rs12227866	0.94[ASN][1000 genomes]
rs12227878	0.94[ASN][1000 genomes]
rs12227920	0.94[ASN][1000 genomes]
rs12229579	0.90[EUR][1000 genomes]
rs12229601	0.94[EUR][1000 genomes]
rs12423648	0.94[ASN][1000 genomes]
rs1429629	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1429630	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1835250	0.94[ASN][1000 genomes]
rs1896899	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1896900	0.93[ASN][1000 genomes]
rs1896901	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2099146	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2099147	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2195539	0.94[ASN][1000 genomes]
rs2195541	0.94[ASN][1000 genomes]
rs2217388	0.94[ASN][1000 genomes]
rs2217389	0.94[ASN][1000 genomes]
rs3959962	0.94[ASN][1000 genomes]
rs4032096	0.91[ASN][1000 genomes]
rs4143644	0.94[ASN][1000 genomes]
rs4143645	0.94[ASN][1000 genomes]
rs4930915	0.94[ASN][1000 genomes]
rs4930916	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4930919	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4930920	0.94[ASN][1000 genomes]
rs4930921	0.94[ASN][1000 genomes]
rs4931311	0.94[ASN][1000 genomes]
rs4931313	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4931314	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4931315	0.94[ASN][1000 genomes]
rs4931316	0.91[ASN][1000 genomes]
rs57590563	0.94[ASN][1000 genomes]
rs7314953	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs7316460	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7961939	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7963091	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7974311	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7974324	0.80[AMR][1000 genomes];0.99[EUR][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	nsv821695	chr12:30287314-30450174	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv832360	chr12:30393329-30555693	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1042966	chr12:30420183-30439329	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:30424800-30430000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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