Variant report

Variant	rs10169078
Chromosome Location	chr2:190975545-190975546
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10804032	1.00[ASN][1000 genomes]
rs11687019	1.00[EUR][1000 genomes]
rs12617421	1.00[ASN][1000 genomes]
rs13411862	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1357722	1.00[ASN][1000 genomes]
rs4241289	1.00[EUR][1000 genomes]
rs55680126	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55867429	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58093950	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60577390	1.00[EUR][1000 genomes]
rs73978912	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73978915	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73978917	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73978921	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73978923	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73978929	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73978930	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73978935	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs785227	1.00[EUR][1000 genomes]
rs785249	1.00[EUR][1000 genomes]
rs785269	1.00[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	esv3439178	chr2:190877215-191124499	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:190966200-190975600	Weak transcription	Psoas Muscle	Psoas
2	chr2:190970800-190985400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:190974200-190976400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr2:190974200-190976600	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr2:190974400-190975600	Enhancers	NH-A	brain
6	chr2:190974400-190975800	Enhancers	Osteobl	bone
7	chr2:190974400-190976400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:190974400-190976400	Enhancers	Brain Cingulate Gyrus	brain
9	chr2:190974400-190976400	Enhancers	Brain Hippocampus Middle	brain
10	chr2:190974600-190975600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr2:190974600-190975800	Weak transcription	Brain Angular Gyrus	brain
12	chr2:190974800-190975600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr2:190975200-190976400	Enhancers	Brain Substantia Nigra	brain
14	chr2:190975400-190975600	Enhancers	Brain Anterior Caudate	brain
15	chr2:190975400-190976000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr2:190975400-190976200	Active TSS	Skeletal Muscle Female	skeletal muscle

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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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