Variant report

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

rs_ID	r²[population]
rs149247	0.84[EUR][1000 genomes]
rs150822	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs160710	0.83[EUR][1000 genomes]
rs160711	0.84[EUR][1000 genomes]
rs160713	0.80[EUR][1000 genomes]
rs160714	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs160716	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs160720	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs162675	0.86[EUR][1000 genomes]
rs176892	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs184143	0.84[EUR][1000 genomes]
rs2545670	0.80[EUR][1000 genomes]
rs294030	0.83[EUR][1000 genomes]
rs316506	0.84[EUR][1000 genomes]
rs316508	0.84[EUR][1000 genomes]
rs316510	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs373070	0.84[EUR][1000 genomes]
rs384863	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs392132	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs403888	0.83[EUR][1000 genomes]
rs408005	0.81[EUR][1000 genomes]
rs408400	0.83[EUR][1000 genomes]
rs439509	0.80[EUR][1000 genomes]
rs455749	0.83[EUR][1000 genomes]
rs455800	0.81[EUR][1000 genomes]
rs456244	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs456367	0.83[EUR][1000 genomes]
rs458154	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs459865	0.88[EUR][1000 genomes]
rs460295	0.83[EUR][1000 genomes]
rs461258	0.83[EUR][1000 genomes]
rs461548	0.83[EUR][1000 genomes]
rs463309	0.84[EUR][1000 genomes]
rs463872	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs464246	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs465003	0.83[EUR][1000 genomes]
rs465427	0.83[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	nsv4929	chr5:97988331-98005486	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97992400-97999400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:97993000-98000000	Weak transcription	Gastric	stomach
3	chr5:97993600-97999600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr5:97995600-97999000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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