Variant report

Variant	rs9373441
Chromosome Location	chr6:145311927-145311928
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:145311761..145313363-chr6:145317514..145320282,2	MCF-7	breast:
2	chr6:145310133..145312483-chr6:145315397..145316971,2	MCF-7	breast:
3	chr6:145310448..145311952-chr6:145321899..145324314,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs1011291	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1111809	0.90[EUR][1000 genomes]
rs11752326	0.86[EUR][1000 genomes]
rs12175554	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13200093	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13213543	0.93[EUR][1000 genomes]
rs13216473	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1338704	0.90[EUR][1000 genomes]
rs1338705	0.91[EUR][1000 genomes]
rs1572675	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17074550	0.93[EUR][1000 genomes]
rs2050719	0.91[EUR][1000 genomes]
rs2328623	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6932709	0.86[EUR][1000 genomes]
rs7742978	0.81[AMR][1000 genomes]
rs7768827	0.94[EUR][1000 genomes]
rs7769009	0.93[EUR][1000 genomes]
rs9322016	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9322017	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9373439	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9373440	0.84[AMR][1000 genomes]
rs9376883	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9376884	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9376885	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9376886	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9376887	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9376888	0.85[ASN][1000 genomes]
rs9386096	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9386097	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9390263	0.93[EUR][1000 genomes]
rs9390268	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9390269	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9390270	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9390271	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9390272	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9399523	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9399524	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9399525	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9399526	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9399527	0.86[ASN][1000 genomes]
rs9403645	0.93[EUR][1000 genomes]
rs9403649	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403650	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9403652	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9403653	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9403655	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS 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 miRNA target site	8 gene(s)	inside rSNPs	diseases
2	esv1850377	chr6:145199259-145319640	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv886742	chr6:145269757-145376903	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145311000-145314600	Weak transcription	HUVEC	blood vessel
2	chr6:145311000-145315000	Weak transcription	NHDF-Ad	bronchial
3	chr6:145311200-145312200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr6:145311200-145312600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:145311400-145312600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr6:145311400-145315000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:145311800-145312400	Enhancers	Stomach Mucosa	stomach
8	chr6:145311800-145312600	Enhancers	Fetal Intestine Large	intestine

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