Variant report

Variant	rs71427842
Chromosome Location	chr2:183231500-183231501
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs13035314	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34758055	1.00[AMR][1000 genomes]
rs35764937	1.00[AMR][1000 genomes]
rs35852909	1.00[AMR][1000 genomes]
rs71427838	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583913	chr2:183043563-183243313	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv533782	chr2:183059730-183500040	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv834481	chr2:183189758-183339577	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183224400-183233800	Weak transcription	Fetal Kidney	kidney
2	chr2:183225600-183235000	Weak transcription	NHLF	lung
3	chr2:183225600-183237400	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr2:183226400-183237200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:183226600-183236800	Weak transcription	Colon Smooth Muscle	Colon
6	chr2:183229200-183237400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:183230400-183234000	Enhancers	Hela-S3	cervix
8	chr2:183230800-183232000	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr2:183231000-183235200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr2:183231200-183231800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr2:183231400-183231600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:183231400-183231800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:183231400-183231800	Flanking Active TSS	A549	lung
14	chr2:183231400-183231800	Enhancers	NHDF-Ad	bronchial

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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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