Variant report

Variant	rs35736349
Chromosome Location	chr4:56939138-56939139
allele	A/C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1108947	0.84[EUR][1000 genomes]
rs1108948	0.84[EUR][1000 genomes]
rs11934389	0.85[EUR][1000 genomes]
rs11938852	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13102087	0.85[EUR][1000 genomes]
rs13113844	0.85[EUR][1000 genomes]
rs13121092	0.82[EUR][1000 genomes]
rs13139132	0.82[EUR][1000 genomes]
rs13147381	0.84[EUR][1000 genomes]
rs17086249	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2412717	0.85[EUR][1000 genomes]
rs2412718	0.85[EUR][1000 genomes]
rs2412719	0.83[EUR][1000 genomes]
rs2412721	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2412726	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2412728	0.81[EUR][1000 genomes]
rs2702332	0.80[EUR][1000 genomes]
rs2899054	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34181414	0.85[EUR][1000 genomes]
rs34546346	0.87[ASN][1000 genomes]
rs34683632	0.84[EUR][1000 genomes]
rs34796075	0.85[EUR][1000 genomes]
rs35400594	0.85[EUR][1000 genomes]
rs35770075	0.84[EUR][1000 genomes]
rs35786306	0.85[EUR][1000 genomes]
rs35786805	0.85[EUR][1000 genomes]
rs35976456	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36092812	0.86[ASN][1000 genomes]
rs4364320	0.85[EUR][1000 genomes]
rs58795379	0.85[EUR][1000 genomes]
rs59838410	0.87[ASN][1000 genomes]
rs60296378	0.87[ASN][1000 genomes]
rs6554328	0.85[EUR][1000 genomes]
rs6819574	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6836376	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6839220	0.86[EUR][1000 genomes]
rs6839870	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71601617	0.83[EUR][1000 genomes]
rs73162701	0.84[ASN][1000 genomes]
rs7657181	0.84[EUR][1000 genomes]
rs7659694	0.85[EUR][1000 genomes]
rs7663270	0.82[EUR][1000 genomes]
rs7672541	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7676365	0.85[EUR][1000 genomes]
rs7685766	0.83[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	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
2	nsv1005845	chr4:56522075-56980357	Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 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	chr4:56927200-56939800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr4:56931200-56943600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:56935400-56942800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:56935400-56945000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:56935800-56942800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:56936000-56943800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:56937400-56941800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr4:56939000-56941800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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