Variant report

Variant	rs964222
Chromosome Location	chr9:8139013-8139014
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10733540	0.80[EUR][1000 genomes]
rs10739148	0.81[EUR][1000 genomes]
rs1159842	0.86[EUR][1000 genomes]
rs1339291	0.84[EUR][1000 genomes]
rs1339292	0.84[EUR][1000 genomes]
rs1361317	0.84[EUR][1000 genomes]
rs16927158	0.89[EUR][1000 genomes]
rs16927160	0.90[EUR][1000 genomes]
rs2181151	0.87[EUR][1000 genomes]
rs2224578	0.83[EUR][1000 genomes]
rs2381707	0.86[EUR][1000 genomes]
rs6477265	0.84[EUR][1000 genomes]
rs7024972	0.81[EUR][1000 genomes]
rs7040383	0.83[EUR][1000 genomes]
rs747437	0.86[EUR][1000 genomes]
rs911764	0.82[EUR][1000 genomes]
rs911765	0.81[EUR][1000 genomes]
rs986195	0.80[EUR][1000 genomes]
rs989723	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1024456	chr9:7887727-8157591	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv539979	chr9:7887727-8157591	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1027699	chr9:8094833-8144973	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv613283	chr9:8102278-8141003	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv1018671	chr9:8102490-8163549	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv523627	chr9:8106282-8161572	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv1030904	chr9:8108480-8163549	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
9	nsv1015783	chr9:8117601-8148244	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8134400-8140600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:8138600-8141600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr9:8138600-8141600	Enhancers	Fetal Heart	heart
4	chr9:8138600-8141800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr9:8138800-8139600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr9:8138800-8139800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr9:8138800-8141400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr9:8139000-8139200	Enhancers	iPS-15b 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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