Variant report

Variant	rs73270368
Chromosome Location	chr8:69515522-69515523
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11998496	0.95[ASN][1000 genomes]
rs1347381	0.88[ASN][1000 genomes]
rs1369224	0.88[ASN][1000 genomes]
rs1434923	0.88[ASN][1000 genomes]
rs1469788	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1473266	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1473267	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1529831	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16934777	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2164202	0.93[ASN][1000 genomes]
rs2380484	0.88[ASN][1000 genomes]
rs35583718	0.95[ASN][1000 genomes]
rs4421338	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4477005	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs60779448	0.93[ASN][1000 genomes]
rs6472409	0.93[ASN][1000 genomes]
rs6472410	0.92[ASN][1000 genomes]
rs6472411	0.88[ASN][1000 genomes]
rs6980767	0.88[ASN][1000 genomes]
rs6981539	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6982437	0.95[ASN][1000 genomes]
rs6986162	0.95[ASN][1000 genomes]
rs7013043	0.88[ASN][1000 genomes]
rs7013431	0.88[ASN][1000 genomes]
rs7825855	0.88[ASN][1000 genomes]
rs7831265	0.95[ASN][1000 genomes]
rs7831621	0.95[ASN][1000 genomes]
rs7845972	0.88[ASN][1000 genomes]
rs892704	0.88[ASN][1000 genomes]
rs9692888	0.95[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	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv890981	chr8:69413110-69534542	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv890984	chr8:69482825-69556111	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69512600-69522400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:69514600-69519800	Weak transcription	Aorta	Aorta
3	chr8:69515200-69516000	Weak transcription	HUES6 Cell Line	embryonic stem cell

Quick Search:

Input of quick search could be:

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

what's new

Quick links