Variant report

Variant	rs1813049
Chromosome Location	chr2:213318790-213318791
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10153722	0.88[EUR][1000 genomes]
rs10165364	0.89[EUR][1000 genomes]
rs10172512	0.89[EUR][1000 genomes]
rs10178298	0.88[EUR][1000 genomes]
rs10190653	0.88[EUR][1000 genomes]
rs10196652	0.91[EUR][1000 genomes]
rs10207963	0.97[ASN][1000 genomes]
rs10497976	0.92[EUR][1000 genomes]
rs11689233	0.95[EUR][1000 genomes]
rs11695241	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13382605	0.86[EUR][1000 genomes]
rs13388843	0.92[EUR][1000 genomes]
rs13392407	0.89[EUR][1000 genomes]
rs13394464	0.88[EUR][1000 genomes]
rs13401008	0.91[EUR][1000 genomes]
rs13411815	0.88[EUR][1000 genomes]
rs13420607	0.90[EUR][1000 genomes]
rs13422427	0.87[EUR][1000 genomes]
rs13422701	0.94[ASN][1000 genomes]
rs1482381	0.88[EUR][1000 genomes]
rs1552161	0.88[EUR][1000 genomes]
rs1586045	0.92[EUR][1000 genomes]
rs16848583	0.97[ASN][1000 genomes]
rs16848584	0.97[ASN][1000 genomes]
rs16848611	0.91[EUR][1000 genomes]
rs16848707	0.88[EUR][1000 genomes]
rs16848787	0.89[EUR][1000 genomes]
rs17260933	0.88[EUR][1000 genomes]
rs17325381	0.95[EUR][1000 genomes]
rs1813050	0.95[EUR][1000 genomes]
rs1882352	0.95[EUR][1000 genomes]
rs1921630	0.91[EUR][1000 genomes]
rs1997470	0.88[EUR][1000 genomes]
rs2086612	0.92[EUR][1000 genomes]
rs2101151	0.92[EUR][1000 genomes]
rs2170530	0.97[ASN][1000 genomes]
rs2204853	0.95[EUR][1000 genomes]
rs57473409	0.95[EUR][1000 genomes]
rs57921759	0.95[EUR][1000 genomes]
rs6435706	0.97[ASN][1000 genomes]
rs6710782	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6715328	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6733009	0.91[EUR][1000 genomes]
rs6752016	0.97[ASN][1000 genomes]
rs6760968	0.97[ASN][1000 genomes]
rs73989006	0.97[ASN][1000 genomes]
rs73989011	0.97[ASN][1000 genomes]
rs73989012	0.97[ASN][1000 genomes]
rs73989013	0.97[ASN][1000 genomes]
rs7568763	0.88[EUR][1000 genomes]
rs7570124	0.97[ASN][1000 genomes]
rs7593163	0.97[ASN][1000 genomes]
rs7603379	0.97[ASN][1000 genomes]
rs972488	0.95[EUR][1000 genomes]
rs972489	0.95[EUR][1000 genomes]
rs9808433	0.92[EUR][1000 genomes]
rs999946	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834527	chr2:213115966-213334308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1004573	chr2:213186537-213365252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv875811	chr2:213200920-213347104	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv432024	chr2:213314899-213446726	Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:213312200-213320400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr2:213318200-213319800	Weak transcription	Fetal Heart	heart

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