Variant report

Variant	rs73120779
Chromosome Location	chr2:234893082-234893083
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11563207	1.00[EUR][1000 genomes]
rs11898669	1.00[EUR][1000 genomes]
rs1395838	1.00[EUR][1000 genomes]
rs28901874	1.00[EUR][1000 genomes]
rs28901883	1.00[EUR][1000 genomes]
rs28902186	1.00[AMR][1000 genomes]
rs28902221	1.00[EUR][1000 genomes]
rs28902241	1.00[EUR][1000 genomes]
rs28903977	1.00[AMR][1000 genomes]
rs28948675	1.00[EUR][1000 genomes]
rs6756537	1.00[EUR][1000 genomes]
rs7594792	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv532476	chr2:234595695-235134381	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234886200-234898000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:234886200-234898200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr2:234886400-234901200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:234891800-234893400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr2:234892000-234893200	Weak transcription	Fetal Brain Male	brain
6	chr2:234892200-234897200	Weak transcription	NHLF	lung
7	chr2:234892400-234901000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:234892600-234893400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:234892800-234894000	Weak transcription	Liver	Liver
10	chr2:234892800-234897400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr2:234893000-234901200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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Input of quick search could be:

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

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