Variant report

Variant	rs11829881
Chromosome Location	chr12:44322395-44322396
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10506232	0.90[EUR][1000 genomes]
rs10748379	0.90[EUR][1000 genomes]
rs10748380	0.90[EUR][1000 genomes]
rs10785470	0.90[EUR][1000 genomes]
rs10785471	0.90[EUR][1000 genomes]
rs10785472	0.90[EUR][1000 genomes]
rs10785473	0.90[EUR][1000 genomes]
rs10785474	0.90[EUR][1000 genomes]
rs10785476	0.83[EUR][1000 genomes]
rs10785477	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs10785478	0.91[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs10785479	0.90[EUR][1000 genomes]
rs10785482	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs10880586	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs10880588	0.90[EUR][1000 genomes]
rs10880589	0.90[EUR][1000 genomes]
rs10880591	0.90[EUR][1000 genomes]
rs10880597	0.90[EUR][1000 genomes]
rs10880598	0.90[EUR][1000 genomes]
rs10880599	0.88[EUR][1000 genomes]
rs10880600	0.84[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs10880601	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs10880604	0.86[EUR][1000 genomes]
rs10880605	0.86[EUR][1000 genomes]
rs11182326	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11182327	0.88[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs11182328	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182329	0.90[EUR][1000 genomes]
rs11182332	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182337	0.90[EUR][1000 genomes]
rs11182339	0.88[EUR][1000 genomes]
rs11182341	0.90[EUR][1000 genomes]
rs11182345	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11182346	0.84[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs12301015	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12303804	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12305959	0.90[EUR][1000 genomes]
rs12309681	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12315094	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12318365	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12369569	0.90[EUR][1000 genomes]
rs12578394	0.89[ASN][1000 genomes]
rs1675786	0.83[EUR][1000 genomes]
rs17093971	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2031056	0.90[EUR][1000 genomes]
rs3925072	0.88[EUR][1000 genomes]
rs3925073	0.90[EUR][1000 genomes]
rs4238092	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4238093	0.90[EUR][1000 genomes]
rs4417371	0.90[EUR][1000 genomes]
rs4768544	0.85[EUR][1000 genomes]
rs59709721	0.97[ASN][1000 genomes]
rs73085705	0.93[ASN][1000 genomes]
rs7308588	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73100931	0.90[EUR][1000 genomes]
rs73100975	0.90[EUR][1000 genomes]
rs7312373	0.91[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs7956825	0.90[EUR][1000 genomes]
rs7957074	0.90[EUR][1000 genomes]
rs7957146	0.83[EUR][1000 genomes]
rs7958314	0.83[EUR][1000 genomes]
rs7964465	0.90[EUR][1000 genomes]
rs7966024	0.83[EUR][1000 genomes]
rs7969641	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7971487	0.90[EUR][1000 genomes]
rs7974501	0.90[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832390	chr12:44318071-44512114	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 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	chr12:44311400-44324600	Weak transcription	Left Ventricle	heart
3	chr12:44315200-44324200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:44317600-44325400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr12:44319000-44324200	Weak transcription	Aorta	Aorta
6	chr12:44319000-44325600	Weak transcription	Esophagus	oesophagus
7	chr12:44319600-44324200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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