Variant report

Variant	rs160714
Chromosome Location	chr5:98016834-98016835
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs149247	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs150822	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs152980	0.89[ASN][1000 genomes]
rs152981	0.93[ASN][1000 genomes]
rs152982	0.93[ASN][1000 genomes]
rs152983	0.92[ASN][1000 genomes]
rs152986	0.95[ASN][1000 genomes]
rs152987	0.95[ASN][1000 genomes]
rs152990	0.95[ASN][1000 genomes]
rs159162	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1592853	0.94[EUR][1000 genomes]
rs160710	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs160711	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs160713	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs160716	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs160720	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs162674	0.81[ASN][1000 genomes]
rs162675	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs176892	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs184143	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2112421	0.94[EUR][1000 genomes]
rs2545670	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2545692	0.93[EUR][1000 genomes]
rs2547957	0.94[EUR][1000 genomes]
rs2662244	0.88[EUR][1000 genomes]
rs294030	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs29671	0.95[ASN][1000 genomes]
rs29770	0.92[CEU][hapmap];0.82[JPT][hapmap];0.80[TSI][hapmap]
rs29772	0.92[CEU][hapmap];0.82[JPT][hapmap];0.80[TSI][hapmap]
rs316506	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs316508	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs316510	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs373070	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs384863	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs392132	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs403888	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs408005	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs408400	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs423108	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs426515	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs439509	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs442074	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs455749	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs455800	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs456244	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs456367	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs457215	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs458154	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs459865	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs460295	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs461258	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs461548	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs462719	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs463309	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs463872	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs464246	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs465003	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs465427	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67595117	0.93[EUR][1000 genomes]
rs981566	0.81[EUR][1000 genomes]
rs981567	0.86[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	nsv1016611	chr5:97873846-98035559	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
2	nsv537816	chr5:97873846-98035559	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv1029509	chr5:97888644-98040172	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv882413	chr5:97918829-98022320	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv980702	chr5:98015320-98017447	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:98015600-98017000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:98016200-98026000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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