Variant report

Variant	rs10096465
Chromosome Location	chr8:121284829-121284830
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10087151	1.00[YRI][hapmap]
rs10090895	1.00[AMR][1000 genomes]
rs10093240	1.00[AMR][1000 genomes]
rs10093254	1.00[AMR][1000 genomes]
rs10101208	1.00[AMR][1000 genomes]
rs10103126	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10108141	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10108255	1.00[AMR][1000 genomes]
rs11774123	1.00[YRI][hapmap]
rs12334294	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13439158	1.00[AMR][1000 genomes]
rs1519814	1.00[YRI][hapmap]
rs1989004	1.00[AMR][1000 genomes]
rs28382363	1.00[AMR][1000 genomes]
rs28488443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28500675	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28591198	1.00[AMR][1000 genomes]
rs28669978	1.00[AMR][1000 genomes]
rs28728283	1.00[AMR][1000 genomes]
rs28801706	1.00[AMR][1000 genomes]
rs28848832	1.00[AMR][1000 genomes]
rs28892927	1.00[AMR][1000 genomes]
rs4133251	1.00[YRI][hapmap]
rs4271006	1.00[YRI][hapmap]
rs4369033	1.00[YRI][hapmap]
rs4504680	1.00[YRI][hapmap]
rs4588897	1.00[YRI][hapmap]
rs4871037	1.00[YRI][hapmap]
rs4871041	1.00[YRI][hapmap]
rs6469900	1.00[YRI][hapmap]
rs6469902	1.00[YRI][hapmap]
rs6983133	1.00[YRI][hapmap]
rs6992410	1.00[YRI][hapmap]
rs6995843	1.00[YRI][hapmap]
rs7000103	1.00[YRI][hapmap]
rs7000609	1.00[YRI][hapmap]
rs9297620	1.00[AMR][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	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv891420	chr8:121194900-121561369	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv612112	chr8:121234298-121385167	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121275600-121293400	Weak transcription	Fetal Stomach	stomach
2	chr8:121282400-121285400	ZNF genes & repeats	Fetal Lung	lung
3	chr8:121283000-121290800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr8:121283800-121285200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
5	chr8:121284000-121285000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:121284200-121292000	Weak transcription	Ovary	ovary
7	chr8:121284400-121295000	Weak transcription	Aorta	Aorta
8	chr8:121284400-121295800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:121284800-121289400	Weak transcription	Placenta	Placenta
10	chr8:121284800-121347800	Weak transcription	Duodenum Smooth Muscle	Duodenum

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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