Variant report

Variant	rs66916621
Chromosome Location	chr9:18274410-18274411
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs13286848	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13287745	0.96[EUR][1000 genomes]
rs13288027	0.96[EUR][1000 genomes]
rs13288253	0.86[EUR][1000 genomes]
rs13289416	0.86[EUR][1000 genomes]
rs13292897	0.84[EUR][1000 genomes]
rs13294282	0.84[EUR][1000 genomes]
rs13299234	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13299428	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13301672	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13301677	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936500	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16936525	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16936527	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16936553	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2585578	0.96[EUR][1000 genomes]
rs34106751	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34154171	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34201861	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34263413	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34263679	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34308902	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34536464	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35046976	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35124487	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35132372	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35289513	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35622845	0.83[EUR][1000 genomes]
rs35641978	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35762648	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs36073480	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4512483	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55928170	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56391525	0.90[EUR][1000 genomes]
rs71506866	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72684978	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72684982	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72684987	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7862758	0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831522	chr9:18231982-18459492	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv2764161	chr9:18247433-18443060	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv892684	chr9:18261485-18401585	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1020662	chr9:18270455-18295314	Weak transcription ZNF genes & repeats Enhancers Active TSS	lncRNA	n/a	inside rSNPs	diseases
6	nsv1015972	chr9:18272700-18299446	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	lncRNA	n/a	inside rSNPs	diseases
7	nsv892685	chr9:18273100-18302439	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	lncRNA	n/a	inside rSNPs	diseases
8	nsv892686	chr9:18273100-18328341	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18273000-18274600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:18273800-18275200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr9:18274200-18275200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr9:18274400-18275600	Enhancers	HUVEC	blood vessel
5	chr9:18274400-18276200	Enhancers	NHEK	skin
6	chr9:18274400-18276400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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