Variant report

Variant	rs62527116
Chromosome Location	chr8:104935937-104935938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:104935888..104938011-chr8:104940420..104943081,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10100545	0.82[AMR][1000 genomes]
rs1116623	0.81[AMR][1000 genomes]
rs1176672	0.81[AMR][1000 genomes]
rs1176675	0.81[AMR][1000 genomes]
rs1176676	0.81[AMR][1000 genomes]
rs1176678	0.81[AMR][1000 genomes]
rs11776873	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11782932	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11784781	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12114518	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12114906	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13251060	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13258713	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13259052	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13261271	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13262019	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13264010	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13265186	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13268881	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13270856	0.82[ASN][1000 genomes]
rs13278444	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1390847	0.83[ASN][1000 genomes]
rs2029934	0.86[ASN][1000 genomes]
rs3104249	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3104251	0.83[ASN][1000 genomes]
rs3104253	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3107465	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs3110455	0.81[AMR][1000 genomes]
rs3110458	0.82[AMR][1000 genomes]
rs3110466	0.83[ASN][1000 genomes]
rs3110473	0.81[AMR][1000 genomes]
rs35761468	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35964420	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62527103	0.82[ASN][1000 genomes]
rs62527117	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62527123	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7004037	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72681344	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7826043	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7837796	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs924163	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs924165	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752692	chr8:104520824-105123824	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1031195	chr8:104601231-105194208	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv831415	chr8:104907757-105115320	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104919600-104938600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:104924200-104938600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr8:104929400-104949600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:104930000-104949400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr8:104933600-104943800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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