Variant report

Variant	rs9362805
Chromosome Location	chr6:91743780-91743781
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11970222	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1368761	0.96[ASN][1000 genomes]
rs1897706	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2217724	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62417785	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6454834	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6917243	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6936812	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6937386	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6937466	0.84[ASN][1000 genomes]
rs7751490	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7752240	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9294473	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9294477	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9294478	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9345074	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9345075	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9362804	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9451556	0.82[EUR][1000 genomes];0.88[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	nsv523939	chr6:91067623-91790493	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv463946	chr6:91710872-91769607	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2752130	chr6:91740447-92196479	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr6:91742000-91743800	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr6:91743400-91744600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr6:91743400-91744800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:91743400-91745000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:91743600-91744600	Enhancers	HUES64 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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