Variant report

Variant	rs2188440
Chromosome Location	chr7:108922486-108922487
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10234165	0.85[EUR][1000 genomes]
rs1023506	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10953602	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11983931	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12705552	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12705553	0.84[AMR][1000 genomes]
rs12705576	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13308920	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1858893	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1858894	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1987422	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2012783	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2015731	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2015789	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2078861	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2106442	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2106443	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2106445	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2188433	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2214061	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2396074	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2396075	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2396076	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2396095	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4727722	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4730365	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs756842	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs756843	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs766705	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs766706	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7779745	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7786274	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7800005	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7800571	0.93[EUR][1000 genomes]
rs7801136	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7809205	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs848835	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831091	chr7:108756218-108923644	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv1018586	chr7:108759240-109034145	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv429794	chr7:108763098-109003574	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1016803	chr7:108786402-109013227	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv539054	chr7:108786402-109013227	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv831094	chr7:108806619-108981593	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv532176	chr7:108905368-109024846	Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv888949	chr7:108918561-108987486	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108922200-108924000	Enhancers	Fetal Heart	heart
2	chr7:108922400-108922600	Enhancers	Fetal Brain Male	brain

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