Variant report

Variant	rs10982726
Chromosome Location	chr9:118165644-118165645
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 4 )

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

rs_ID	r²[population]
rs10124685	0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10817756	0.86[CEU][hapmap];0.94[JPT][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10817758	0.89[JPT][hapmap];0.80[EUR][1000 genomes]
rs10982719	0.89[JPT][hapmap];0.80[EUR][1000 genomes]
rs10982722	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10982724	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10982725	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10982743	0.82[EUR][1000 genomes]
rs10982755	0.81[EUR][1000 genomes]
rs10982757	0.81[AMR][1000 genomes]
rs10982764	0.80[EUR][1000 genomes]
rs11791418	0.86[EUR][1000 genomes]
rs12336386	0.81[EUR][1000 genomes]
rs2067094	0.82[EUR][1000 genomes]
rs3750505	0.93[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7018671	0.86[CEU][hapmap];0.94[JPT][hapmap];1.00[TSI][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7029620	0.83[EUR][1000 genomes]
rs7040283	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7040762	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7871775	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9408863	0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9408864	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9408865	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9409148	0.92[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9409149	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9409150	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9409155	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9409159	0.81[EUR][1000 genomes]
rs976734	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs981911	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv615251	chr9:117975864-118514444	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv948346	chr9:118107565-118718197	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1042957	chr9:118153824-118313540	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv2761245	chr9:118157164-118171298	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs10982726	DNAJC25	cis	parietal	SCAN
rs10982726	C9orf29	cis	parietal	SCAN
rs10982726	DEC1	cis	cerebellum	SCAN
rs10982726	ZNF618	cis	parietal	SCAN

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:118159000-118170600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr9:118160400-118173600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr9:118162200-118166000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:118162200-118174000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr9:118164000-118169000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:118164200-118170000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:118164600-118169600	Weak transcription	NHDF-Ad	bronchial
8	chr9:118165000-118166200	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr9:118165000-118166200	Weak transcription	Fetal Lung	lung
10	chr9:118165000-118166400	Weak transcription	Fetal Kidney	kidney
11	chr9:118165400-118166000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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