Variant report

Variant	rs2328060
Chromosome Location	chr6:140653927-140653928
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1113096	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11965946	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11966793	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11967431	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11969633	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12524727	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12525793	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12526277	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12529188	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12529620	0.83[ASN][1000 genomes]
rs12529729	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1390500	0.84[ASN][1000 genomes]
rs1496114	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1580734	0.84[ASN][1000 genomes]
rs17069805	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17069893	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17069935	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17069970	0.90[ASN][1000 genomes]
rs1879097	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2328026	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57789174	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59447713	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62429779	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62429786	0.95[ASN][1000 genomes]
rs62429787	0.95[ASN][1000 genomes]
rs62429788	0.95[ASN][1000 genomes]
rs62429789	0.95[ASN][1000 genomes]
rs62429831	0.84[ASN][1000 genomes]
rs62431098	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62431099	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62431110	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62431142	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6914407	0.95[ASN][1000 genomes]
rs732015	0.82[EUR][1000 genomes];0.84[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	nsv1016532	chr6:140174639-141029988	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1015293	chr6:140544956-140798437	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv817390	chr6:140558103-141166039	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 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	chr6:140641400-140658000	Weak transcription	K562	blood

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