Variant report

Variant	rs10059739
Chromosome Location	chr5:15347072-15347073
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	chr5:15345890..15347410-chr5:15350054..15351833,2	K562	blood:

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10062499	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10069717	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10074605	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10077161	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1447278	1.00[EUR][1000 genomes]
rs1457155	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1457156	1.00[EUR][1000 genomes]
rs2085469	1.00[EUR][1000 genomes]
rs2166687	1.00[EUR][1000 genomes]
rs28505727	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4348213	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4499832	1.00[EUR][1000 genomes]
rs56775717	1.00[EUR][1000 genomes]
rs57117756	1.00[EUR][1000 genomes]
rs57224947	1.00[EUR][1000 genomes]
rs57276081	1.00[EUR][1000 genomes]
rs58297994	0.86[EUR][1000 genomes]
rs59276260	1.00[EUR][1000 genomes]
rs59697153	1.00[EUR][1000 genomes]
rs60410514	1.00[EUR][1000 genomes]
rs61058493	1.00[EUR][1000 genomes]
rs61122680	1.00[EUR][1000 genomes]
rs61446556	1.00[EUR][1000 genomes]
rs6859257	1.00[EUR][1000 genomes]
rs6859415	1.00[EUR][1000 genomes]
rs6860738	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6863823	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6865211	1.00[EUR][1000 genomes]
rs6865337	1.00[EUR][1000 genomes]
rs6876033	1.00[EUR][1000 genomes]
rs6876400	1.00[EUR][1000 genomes]
rs6876826	1.00[EUR][1000 genomes]
rs6879327	1.00[EUR][1000 genomes]
rs6879460	1.00[EUR][1000 genomes]
rs6880299	1.00[EUR][1000 genomes]
rs6880827	1.00[EUR][1000 genomes]
rs6886201	1.00[EUR][1000 genomes]
rs6897946	1.00[EUR][1000 genomes]
rs6898871	1.00[EUR][1000 genomes]
rs6899293	1.00[EUR][1000 genomes]
rs73053365	1.00[EUR][1000 genomes]
rs73053366	1.00[EUR][1000 genomes]
rs73053369	1.00[EUR][1000 genomes]
rs73053370	1.00[EUR][1000 genomes]
rs73053371	1.00[EUR][1000 genomes]
rs73053373	1.00[EUR][1000 genomes]
rs73053376	1.00[EUR][1000 genomes]
rs73053377	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73053378	1.00[EUR][1000 genomes]
rs73053385	1.00[EUR][1000 genomes]
rs73053386	1.00[EUR][1000 genomes]
rs73053388	1.00[EUR][1000 genomes]
rs73053391	1.00[EUR][1000 genomes]
rs73053392	1.00[EUR][1000 genomes]
rs73055304	1.00[EUR][1000 genomes]
rs73055307	1.00[EUR][1000 genomes]
rs73055310	1.00[EUR][1000 genomes]
rs73055314	1.00[EUR][1000 genomes]
rs73055315	1.00[EUR][1000 genomes]
rs73055316	1.00[EUR][1000 genomes]
rs73055317	1.00[EUR][1000 genomes]
rs73055318	1.00[EUR][1000 genomes]
rs73060985	1.00[EUR][1000 genomes]
rs73064098	1.00[EUR][1000 genomes]
rs73064099	1.00[EUR][1000 genomes]
rs73066012	1.00[EUR][1000 genomes]
rs73066014	1.00[EUR][1000 genomes]
rs73066018	1.00[EUR][1000 genomes]
rs73066022	1.00[EUR][1000 genomes]
rs73068095	1.00[EUR][1000 genomes]
rs73068101	1.00[EUR][1000 genomes]
rs73070003	1.00[EUR][1000 genomes]
rs73070004	0.86[EUR][1000 genomes]
rs73070006	1.00[EUR][1000 genomes]
rs73070008	1.00[EUR][1000 genomes]
rs73070013	1.00[EUR][1000 genomes]
rs73070014	1.00[EUR][1000 genomes]
rs73070017	1.00[EUR][1000 genomes]
rs73070018	1.00[EUR][1000 genomes]
rs73070020	1.00[EUR][1000 genomes]
rs73070021	1.00[EUR][1000 genomes]
rs753329	1.00[EUR][1000 genomes]
rs7713358	1.00[EUR][1000 genomes]
rs7713373	1.00[EUR][1000 genomes]
rs7713578	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7717253	1.00[EUR][1000 genomes]
rs7717350	1.00[EUR][1000 genomes]
rs7717373	1.00[EUR][1000 genomes]
rs7717382	1.00[EUR][1000 genomes]
rs7719232	1.00[EUR][1000 genomes]
rs7730925	1.00[EUR][1000 genomes]
rs7731144	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7734588	1.00[EUR][1000 genomes]
rs7736162	0.86[EUR][1000 genomes]
rs897816	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530221	chr5:14859687-15364470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv516929	chr5:15087791-15870300	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1023068	chr5:15095221-15863583	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv869040	chr5:15097602-15866117	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv530222	chr5:15151662-15851485	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv881558	chr5:15291398-15420775	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr5:15344800-15350600	Weak transcription	Dnd41	blood
2	chr5:15346600-15347600	Enhancers	HUVEC	blood vessel

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