Variant report

Variant	rs11182332
Chromosome Location	chr12:44317599-44317600
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:44311824..44313734-chr12:44316196..44317780,2	MCF-7	breast:
2	chr12:44311484..44313107-chr12:44314992..44317607,2	K562	blood:
3	chr12:44310016..44313786-chr12:44314229..44318943,4	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11182326	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11182328	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182345	0.93[ASN][1000 genomes]
rs11182348	0.87[CEU][hapmap];0.81[AMR][1000 genomes]
rs11182353	0.87[CEU][hapmap];0.81[AMR][1000 genomes]
rs11182354	0.87[CEU][hapmap];0.81[AMR][1000 genomes]
rs11182355	0.87[CEU][hapmap];0.81[AMR][1000 genomes]
rs11182359	0.81[AMR][1000 genomes]
rs11829881	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12301015	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12303804	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12309681	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12315094	0.90[ASN][1000 genomes]
rs12318365	0.91[ASN][1000 genomes]
rs12371940	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs12578394	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17093971	0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4238092	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59709721	0.89[ASN][1000 genomes]
rs73085705	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7308588	0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs73100979	0.81[AMR][1000 genomes]
rs7969641	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7976722	1.00[CEU][hapmap];0.81[AMR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:44307400-44324000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:44308400-44318400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr12:44311400-44324600	Weak transcription	Left Ventricle	heart
4	chr12:44315200-44324200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr12:44316000-44321200	Weak transcription	HSMMtube	muscle
6	chr12:44317400-44321200	Weak transcription	Fetal Intestine Large	intestine

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