Variant report

Variant	rs2163370
Chromosome Location	chr15:57190683-57190684
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1015967	0.81[AMR][1000 genomes]
rs10438332	0.81[AMR][1000 genomes]
rs11632502	0.81[AMR][1000 genomes]
rs11632526	0.81[AMR][1000 genomes]
rs11856338	0.91[ASN][1000 genomes]
rs12437976	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12440219	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12595644	0.81[AMR][1000 genomes]
rs12902058	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12906025	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1625176	0.81[AMR][1000 genomes]
rs1628974	0.81[AMR][1000 genomes]
rs1631079	0.81[AMR][1000 genomes]
rs1642925	0.84[AMR][1000 genomes]
rs1642928	0.81[AMR][1000 genomes]
rs1642935	0.81[AMR][1000 genomes]
rs1642936	0.84[AMR][1000 genomes]
rs1642937	0.81[AMR][1000 genomes]
rs1652732	0.84[AMR][1000 genomes]
rs1652737	0.82[AMR][1000 genomes]
rs1652738	0.81[AMR][1000 genomes]
rs1652739	0.81[AMR][1000 genomes]
rs1657926	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs169893	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1963831	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1968399	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1975092	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2111890	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2116067	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2116068	0.91[EUR][1000 genomes]
rs213148	0.84[AMR][1000 genomes]
rs213152	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs213155	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs213160	0.89[AMR][1000 genomes]
rs213163	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs213166	0.89[AMR][1000 genomes]
rs213168	0.86[AMR][1000 genomes]
rs2439921	0.84[AMR][1000 genomes]
rs2543675	0.82[EUR][1000 genomes]
rs2566840	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2566846	0.81[AMR][1000 genomes]
rs2585076	0.81[AMR][1000 genomes]
rs2585116	0.81[AMR][1000 genomes]
rs28637136	0.91[ASN][1000 genomes]
rs34373044	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4581646	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4774246	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4774247	0.92[ASN][1000 genomes]
rs4774900	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7162730	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7168945	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs72749491	0.81[AMR][1000 genomes]
rs8031788	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9806712	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3422474	chr15:56867190-57244330	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv833020	chr15:57055947-57216068	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv457162	chr15:57083006-57225766	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv569577	chr15:57083006-57225766	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv1042486	chr15:57094598-57505992	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv542393	chr15:57115116-57341363	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 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	chr15:57180200-57208000	Weak transcription	Fetal Muscle Trunk	muscle
2	chr15:57180400-57196000	Weak transcription	Fetal Brain Female	brain
3	chr15:57181000-57190800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr15:57181000-57191400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:57181200-57192600	Weak transcription	Brain Hippocampus Middle	brain
6	chr15:57181600-57204000	Weak transcription	Thymus	Thymus
7	chr15:57182000-57209200	Weak transcription	Fetal Stomach	stomach
8	chr15:57182600-57204200	Weak transcription	Fetal Thymus	thymus

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