Variant report

Variant	rs59813207
Chromosome Location	chr4:73813547-73813548
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1303974	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1350777	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16845059	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16848978	1.00[AMR][1000 genomes]
rs16848981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16848984	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16848989	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16848997	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17838980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs41523145	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56131254	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56196459	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57355541	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57601257	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57824486	1.00[AMR][1000 genomes]
rs57833053	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58100751	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58155862	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58205517	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58243508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59508782	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60023650	0.87[AMR][1000 genomes]
rs6828670	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6845896	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6847507	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827143	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827144	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827147	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs73827148	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827149	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827151	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827152	1.00[AMR][1000 genomes]
rs73827153	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73827202	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73830010	0.85[AMR][1000 genomes]
rs73830013	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949371	chr4:73678470-74094500	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1005704	chr4:73708248-73907315	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv829971	chr4:73709753-73880451	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv432611	chr4:73740665-74099265	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv523169	chr4:73752242-74120910	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv998707	chr4:73753922-74044843	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv537136	chr4:73753922-74044843	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv917017	chr4:73754127-74044830	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
9	nsv1013174	chr4:73785324-74031884	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv537137	chr4:73785324-74031884	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 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	chr4:73809800-73816800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:73812000-73818000	Weak transcription	Aorta	Aorta

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