Variant report

Variant	rs73832874
Chromosome Location	chr4:86522651-86522652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1026871	1.00[AMR][1000 genomes]
rs10516752	1.00[AMR][1000 genomes]
rs12108201	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17010532	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55914555	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55962316	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57062765	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58048238	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6811202	0.82[AFR][1000 genomes]
rs72979969	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72982048	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72982049	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833370	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833375	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833384	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833388	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73833389	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73835232	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519588	chr4:85762385-86591202	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv461566	chr4:85988032-86725502	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv594747	chr4:85988032-86725502	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv470048	chr4:85998783-86720838	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	esv3450999	chr4:86485840-86773745	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
6	nsv829999	chr4:86500257-86666019	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:86517800-86542200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:86518000-86524400	Weak transcription	HSMM	muscle
3	chr4:86518600-86524800	Weak transcription	Fetal Heart	heart
4	chr4:86520400-86525200	Weak transcription	Gastric	stomach
5	chr4:86520400-86525200	Weak transcription	Left Ventricle	heart
6	chr4:86521400-86523800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr4:86521800-86524800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:86522600-86523600	ZNF genes & repeats	Primary B cells from cord blood	blood

Quick Search:

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

what's new

Quick links