Variant report

Variant	rs10122293
Chromosome Location	chr9:10334664-10334665
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10114902	0.95[CEU][hapmap];0.80[EUR][1000 genomes]
rs10118721	0.80[EUR][1000 genomes]
rs10123946	0.95[CEU][hapmap];0.82[EUR][1000 genomes]
rs10123985	0.90[CEU][hapmap];0.80[EUR][1000 genomes]
rs10125573	0.86[ASN][1000 genomes]
rs10959014	0.83[JPT][hapmap]
rs10959026	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs10959049	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs10959050	0.95[CEU][hapmap];0.82[EUR][1000 genomes]
rs10959051	0.95[CEU][hapmap]
rs12344926	0.83[JPT][hapmap]
rs1323498	0.83[JPT][hapmap]
rs1407925	0.87[CHB][hapmap];0.94[JPT][hapmap]
rs1535663	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1544056	0.83[JPT][hapmap]
rs616040	0.89[JPT][hapmap]
rs694201	0.89[JPT][hapmap]
rs694209	0.82[CHB][hapmap];0.89[JPT][hapmap]
rs7849722	0.95[CEU][hapmap]
rs942158	0.83[JPT][hapmap]
rs9987891	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034731	chr9:9776126-10481262	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv892295	chr9:9832245-10380406	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1030657	chr9:10002355-10481262	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1033178	chr9:10169848-10428731	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2758179	chr9:10188450-10370398	Enhancers Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv2759666	chr9:10188450-10370398	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10325800-10335800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr9:10331600-10338200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr9:10331600-10338200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr9:10333400-10338000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr9:10333600-10339400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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