Variant report

Variant	rs2806963
Chromosome Location	chr13:53781644-53781645
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1016829	0.98[ASN][1000 genomes]
rs1322938	0.83[EUR][1000 genomes]
rs1322949	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1322951	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1322952	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1322955	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1322956	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1322961	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1322962	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1407686	0.85[ASN][1000 genomes]
rs1853369	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1909648	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1909650	0.81[EUR][1000 genomes]
rs1923770	0.80[EUR][1000 genomes]
rs1923771	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2015677	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2038649	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2093599	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2491124	0.98[ASN][1000 genomes]
rs2759675	0.86[EUR][1000 genomes]
rs2759706	0.88[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2759708	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2759709	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2759712	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2759716	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2806936	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2806939	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2806941	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2806956	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2806960	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2806964	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2806966	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4886270	0.94[ASN][1000 genomes]
rs7984963	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7994915	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8002513	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs912051	0.85[EUR][1000 genomes]
rs912052	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs912054	0.85[ASN][1000 genomes]
rs927518	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9527057	0.88[ASN][1000 genomes]
rs9568813	0.82[ASN][1000 genomes]
rs9568826	0.87[ASN][1000 genomes]
rs959222	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050969	chr13:53665927-54064861	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv1834091	chr13:53774627-53784083	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv1838050	chr13:53774627-53784083	Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv1835986	chr13:53774627-53786026	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv1840677	chr13:53774627-53791895	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53776200-53781800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:53778600-53781800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:53780800-53782200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:53781600-53782000	Enhancers	Brain Hippocampus Middle	brain

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