Variant report

Variant	rs4886270
Chromosome Location	chr13:53780054-53780055
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1016829	0.94[ASN][1000 genomes]
rs1322939	0.87[EUR][1000 genomes]
rs1322949	1.00[CHB][hapmap];0.85[JPT][hapmap];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1322951	1.00[CHB][hapmap];0.85[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1322952	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1322955	0.90[ASN][1000 genomes]
rs1322956	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1322958	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1322961	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1322962	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1407686	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1853369	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1909648	0.93[ASN][1000 genomes]
rs1923771	1.00[CHB][hapmap];0.85[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2015677	0.93[ASN][1000 genomes]
rs2038649	0.92[ASN][1000 genomes]
rs2093599	0.86[ASN][1000 genomes]
rs2491124	0.94[ASN][1000 genomes]
rs2759706	0.94[ASN][1000 genomes]
rs2759708	0.92[ASN][1000 genomes]
rs2759709	0.85[ASN][1000 genomes]
rs2759712	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2759716	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2806936	0.84[ASN][1000 genomes]
rs2806939	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2806941	0.86[ASN][1000 genomes]
rs2806956	0.94[ASN][1000 genomes]
rs2806960	0.94[ASN][1000 genomes]
rs2806963	0.94[ASN][1000 genomes]
rs2806964	0.95[ASN][1000 genomes]
rs2806966	0.95[ASN][1000 genomes]
rs7318473	0.82[EUR][1000 genomes]
rs7984963	0.90[ASN][1000 genomes]
rs7994915	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8002513	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs912052	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs912054	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs927518	0.95[CHB][hapmap];0.90[JPT][hapmap];0.94[ASN][1000 genomes]
rs9527057	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9536364	0.87[EUR][1000 genomes]
rs9536378	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs9568808	0.83[EUR][1000 genomes]
rs9568813	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9568826	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs959222	0.94[ASN][1000 genomes]
rs980186	0.80[EUR][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:2 , 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

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