Variant report

Variant	rs12464763
Chromosome Location	chr2:76695140-76695141
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10196661	0.85[ASN][1000 genomes]
rs11688462	0.96[ASN][1000 genomes]
rs12463620	0.93[ASN][1000 genomes]
rs12476072	0.95[ASN][1000 genomes]
rs12477015	0.80[ASN][1000 genomes]
rs12477049	0.80[ASN][1000 genomes]
rs12477122	0.80[ASN][1000 genomes]
rs12613882	0.94[ASN][1000 genomes]
rs12618802	0.93[ASN][1000 genomes]
rs12621334	0.95[ASN][1000 genomes]
rs12624158	0.91[ASN][1000 genomes]
rs12991135	0.80[ASN][1000 genomes]
rs13020282	0.80[ASN][1000 genomes]
rs13020905	0.80[ASN][1000 genomes]
rs17012789	0.93[ASN][1000 genomes]
rs17516461	0.85[ASN][1000 genomes]
rs1921241	0.96[ASN][1000 genomes]
rs1921242	0.93[ASN][1000 genomes]
rs1921249	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1997450	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2178518	0.93[ASN][1000 genomes]
rs28884919	0.94[ASN][1000 genomes]
rs34486900	0.95[ASN][1000 genomes]
rs3923527	0.85[ASN][1000 genomes]
rs4264582	0.86[ASN][1000 genomes]
rs4853245	0.88[ASN][1000 genomes]
rs4853246	0.95[ASN][1000 genomes]
rs4853247	0.95[ASN][1000 genomes]
rs60185714	0.95[ASN][1000 genomes]
rs61331198	0.95[ASN][1000 genomes]
rs72809051	0.85[ASN][1000 genomes]
rs7422743	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7559351	0.85[ASN][1000 genomes]
rs7563300	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757809	chr2:76541920-76705354	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv2759064	chr2:76541920-76705354	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv874317	chr2:76554077-76890567	Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1013614	chr2:76624220-76715121	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv582227	chr2:76662404-76712789	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76694800-76696600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr2:76694800-76705800	Weak transcription	H1 Cell Line	embryonic stem cell

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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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