Variant report

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs149247	0.82[EUR][1000 genomes]
rs1592853	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs160710	0.81[EUR][1000 genomes]
rs160711	0.82[EUR][1000 genomes]
rs160714	0.81[EUR][1000 genomes]
rs160720	0.82[EUR][1000 genomes]
rs176892	0.81[EUR][1000 genomes]
rs184143	0.82[EUR][1000 genomes]
rs2112421	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2545670	0.86[EUR][1000 genomes]
rs2545692	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2547957	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2662244	0.82[EUR][1000 genomes]
rs294030	0.82[EUR][1000 genomes]
rs316510	0.81[EUR][1000 genomes]
rs373070	0.82[EUR][1000 genomes]
rs392132	0.83[EUR][1000 genomes]
rs403888	0.83[EUR][1000 genomes]
rs408400	0.83[EUR][1000 genomes]
rs439509	0.81[EUR][1000 genomes]
rs442074	0.81[EUR][1000 genomes]
rs455749	0.83[EUR][1000 genomes]
rs455800	0.82[EUR][1000 genomes]
rs456367	0.83[EUR][1000 genomes]
rs460295	0.83[EUR][1000 genomes]
rs461258	0.83[EUR][1000 genomes]
rs461548	0.83[EUR][1000 genomes]
rs463309	0.82[EUR][1000 genomes]
rs463872	0.81[EUR][1000 genomes]
rs464246	0.81[EUR][1000 genomes]
rs465003	0.83[EUR][1000 genomes]
rs465427	0.83[EUR][1000 genomes]
rs67595117	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs981567	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][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	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
2	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:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:98059200-98065600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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