Variant report

Variant	rs13160481
Chromosome Location	chr5:44447093-44447094
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:44445601..44447763-chr5:44448741..44451445,2	K562	blood:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1004720	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10512853	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10512855	0.85[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13158765	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs13160899	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13166702	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13169538	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13171351	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13176611	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13176804	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13182739	0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13184756	0.85[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13188583	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13189872	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1482676	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16901855	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16901879	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16901889	0.85[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16901892	0.85[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2062140	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2128437	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34031522	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34057718	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs34110145	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34180349	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34277429	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34414216	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34439572	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34462071	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34512854	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34611602	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34617631	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34640244	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34810292	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35074718	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35108601	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35262233	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35321661	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35391530	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35483918	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35517954	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35530450	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35544349	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35805621	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35947880	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55880927	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66479031	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66570818	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs66704172	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66815332	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs67771916	1.00[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72748094	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830277	chr5:44383402-44566881	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1024923	chr5:44439853-44528314	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:44395200-44447400	Weak transcription	Fetal Lung	lung
2	chr5:44443800-44452200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr5:44444000-44447800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:44445000-44453800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:44447000-44448000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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