Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10507656	0.90[EUR][1000 genomes]
rs12861751	0.92[EUR][1000 genomes]
rs12875061	0.92[EUR][1000 genomes]
rs1514165	0.88[EUR][1000 genomes]
rs1548176	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1572023	0.98[EUR][1000 genomes]
rs17058733	0.88[EUR][1000 genomes]
rs17058789	0.92[EUR][1000 genomes]
rs17331929	0.88[EUR][1000 genomes]
rs2175869	0.98[EUR][1000 genomes]
rs3127034	0.98[EUR][1000 genomes]
rs35252142	0.92[EUR][1000 genomes]
rs71434967	0.98[EUR][1000 genomes]
rs7317718	0.98[EUR][1000 genomes]
rs7338113	0.98[EUR][1000 genomes]
rs7982093	0.94[EUR][1000 genomes]
rs7985854	0.98[EUR][1000 genomes]
rs884318	0.92[EUR][1000 genomes]
rs884319	0.92[EUR][1000 genomes]
rs9528209	0.92[EUR][1000 genomes]
rs9528210	0.90[EUR][1000 genomes]
rs9538891	0.85[EUR][1000 genomes]
rs9538901	0.92[EUR][1000 genomes]
rs9538907	0.94[EUR][1000 genomes]
rs9538920	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9538923	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9538937	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817223	chr13:60623429-61453435	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv832623	chr13:61303818-61468576	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1037954	chr13:61319533-61395907	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv561866	chr13:61328813-61388794	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr13:61372000-61372800	Enhancers	Fetal Intestine Small	intestine

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