Variant report

Variant	rs456367
Chromosome Location	chr5:98035618-98035619
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:98034269..98036713-chr5:98038711..98041425,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs149247	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs150822	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs159162	0.89[EUR][1000 genomes]
rs1592853	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs160710	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs160711	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs160713	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs160714	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs160716	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs160720	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs162675	0.93[EUR][1000 genomes]
rs176892	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs184143	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2112421	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2545670	0.95[EUR][1000 genomes]
rs2545692	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2547957	0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2662244	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs294030	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs29770	0.93[CEU][hapmap];0.82[GIH][hapmap]
rs29772	0.93[CEU][hapmap];0.82[GIH][hapmap]
rs316506	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs316508	1.00[CEU][hapmap];0.95[GIH][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs316510	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs373070	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs384863	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs392132	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs403888	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs408005	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs408400	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs423108	0.83[EUR][1000 genomes]
rs426515	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs439509	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs442074	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs455749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs455800	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs456244	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs457215	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs458154	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs459865	0.94[EUR][1000 genomes]
rs460295	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs461258	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs461548	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs462719	0.84[EUR][1000 genomes]
rs463309	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs463872	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs464246	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs465003	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs465427	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67595117	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs981566	0.83[EUR][1000 genomes]
rs981567	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv1032060	chr5:98022226-98093492	Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv537817	chr5:98022226-98093492	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:98026000-98040000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:98034800-98036200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:98034800-98036400	Weak transcription	Osteobl	bone

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