Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10492504	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17426071	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1888545	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2148521	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2182533	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2209651	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4281579	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4771854	0.90[EUR][1000 genomes]
rs57786284	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs59410447	0.91[EUR][1000 genomes]
rs72636830	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72636831	0.80[EUR][1000 genomes]
rs72636832	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72636834	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72636840	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7489550	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7987741	0.90[EUR][1000 genomes]
rs9523535	0.90[EUR][1000 genomes]
rs9560983	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9560984	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9560985	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9560986	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9589454	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv456066	chr13:92694581-92884370	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv562723	chr13:92694581-92884370	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1035365	chr13:92805325-92926114	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1053468	chr13:92814581-92893231	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92863800-92870800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr13:92864000-92870600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr13:92864000-92871200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:92865200-92867200	Enhancers	Fetal Lung	lung
5	chr13:92866000-92868200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr13:92866600-92867200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr13:92866800-92867200	Enhancers	Ovary	ovary
8	chr13:92867000-92873600	Weak transcription	Fetal Intestine Large	intestine

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