Variant report

Variant	rs73822691
Chromosome Location	chr4:62470247-62470248
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs2088113	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55636236	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55773246	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55939610	0.83[EUR][1000 genomes]
rs56338474	0.83[EUR][1000 genomes]
rs59130415	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs60293956	0.83[AMR][1000 genomes]
rs60655392	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61483832	0.83[AMR][1000 genomes]
rs73822609	0.83[EUR][1000 genomes]
rs73822610	0.83[EUR][1000 genomes]
rs73822617	0.83[EUR][1000 genomes]
rs73822619	0.83[EUR][1000 genomes]
rs73822621	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73822622	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73822651	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73822652	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73822654	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73822688	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73822690	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73822692	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73822695	0.89[AMR][1000 genomes]
rs73823214	0.83[AMR][1000 genomes]
rs73823219	0.83[AMR][1000 genomes]
rs73825906	0.85[AMR][1000 genomes]
rs73825907	0.89[AMR][1000 genomes]
rs73825913	0.84[AMR][1000 genomes]
rs7660587	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9917973	0.83[EUR][1000 genomes]
rs9918049	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv868844	chr4:62241702-62497248	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv461377	chr4:62368762-62883431	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv594328	chr4:62368762-62883431	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1004815	chr4:62398737-62553769	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv537110	chr4:62398737-62553769	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv594329	chr4:62416593-62478230	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv879077	chr4:62419426-62545435	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 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	chr4:62460400-62473400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr4:62461200-62478000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:62461600-62473600	Weak transcription	Fetal Stomach	stomach
4	chr4:62468400-62476800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:62469200-62473400	Weak transcription	Fetal Lung	lung
6	chr4:62469600-62472800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr4:62470000-62485000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:62470200-62472400	Enhancers	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links