Variant report

Variant	rs72710141
Chromosome Location	chr4:172079085-172079086
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10003589	0.87[EUR][1000 genomes]
rs10016739	0.87[EUR][1000 genomes]
rs10024424	0.87[EUR][1000 genomes]
rs10026424	0.87[EUR][1000 genomes]
rs10028706	0.88[EUR][1000 genomes]
rs10084957	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1038813	0.90[EUR][1000 genomes]
rs11722373	0.86[EUR][1000 genomes]
rs13111056	0.86[EUR][1000 genomes]
rs13120288	0.86[EUR][1000 genomes]
rs13133591	0.82[EUR][1000 genomes]
rs1491336	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1491337	0.87[EUR][1000 genomes]
rs1491338	0.87[EUR][1000 genomes]
rs1491339	0.87[EUR][1000 genomes]
rs1491340	0.87[EUR][1000 genomes]
rs1491341	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1491342	0.87[EUR][1000 genomes]
rs1491345	0.87[EUR][1000 genomes]
rs17195349	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17195384	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1907495	0.87[EUR][1000 genomes]
rs1907496	0.86[EUR][1000 genomes]
rs2035825	0.87[EUR][1000 genomes]
rs2130915	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2130916	0.87[EUR][1000 genomes]
rs2172147	0.87[EUR][1000 genomes]
rs4413369	0.87[EUR][1000 genomes]
rs4692874	0.87[EUR][1000 genomes]
rs6811352	0.86[EUR][1000 genomes]
rs6836611	1.00[EUR][1000 genomes]
rs6841957	1.00[EUR][1000 genomes]
rs72710147	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72710158	0.99[EUR][1000 genomes]
rs72710159	1.00[EUR][1000 genomes]
rs7654686	0.90[EUR][1000 genomes]
rs7657554	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7660351	0.87[EUR][1000 genomes]
rs7660725	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7665382	0.90[EUR][1000 genomes]
rs7667994	0.87[EUR][1000 genomes]
rs7669971	0.87[EUR][1000 genomes]
rs7670769	0.87[EUR][1000 genomes]
rs7675758	0.87[EUR][1000 genomes]
rs7676981	0.87[EUR][1000 genomes]
rs7690912	0.90[EUR][1000 genomes]
rs7695786	0.87[EUR][1000 genomes]
rs9312499	0.87[EUR][1000 genomes]
rs958355	0.90[EUR][1000 genomes]
rs958357	0.90[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	nsv881345	chr4:171673765-172228547	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1018793	chr4:171808272-172395180	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv461836	chr4:171963233-172494233	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv596169	chr4:171963233-172494233	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1016836	chr4:171982072-172496279	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
6	nsv537355	chr4:171982072-172496279	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1020886	chr4:171993828-172140098	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:172077800-172079600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:172078400-172079200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr4:172078400-172079200	Enhancers	Small Intestine	intestine
4	chr4:172078400-172079400	Enhancers	Fetal Intestine Large	intestine
5	chr4:172078600-172079200	Enhancers	Pancreas	Pancrea
6	chr4:172078800-172080000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:172079000-172079400	Active TSS	Fetal Intestine Small	intestine

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