Variant report

Variant	rs728323
Chromosome Location	chr1:102374280-102374281
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1008809	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1008810	0.96[ASN][1000 genomes]
rs10493968	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10493969	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10782858	0.96[ASN][1000 genomes]
rs10782859	0.92[ASN][1000 genomes]
rs10874527	0.94[ASN][1000 genomes]
rs11164323	0.82[ASN][1000 genomes]
rs11164332	0.96[ASN][1000 genomes]
rs11164334	0.96[ASN][1000 genomes]
rs11164335	0.96[ASN][1000 genomes]
rs11809591	0.81[ASN][1000 genomes]
rs12061071	0.96[ASN][1000 genomes]
rs12748614	0.84[ASN][1000 genomes]
rs1336800	0.96[ASN][1000 genomes]
rs1360998	0.96[ASN][1000 genomes]
rs1360999	0.96[ASN][1000 genomes]
rs1891123	0.96[ASN][1000 genomes]
rs1891125	0.96[ASN][1000 genomes]
rs1981274	0.96[ASN][1000 genomes]
rs1981275	0.96[ASN][1000 genomes]
rs1998978	0.96[ASN][1000 genomes]
rs1999795	0.86[ASN][1000 genomes]
rs2000149	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2000150	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2000151	0.96[ASN][1000 genomes]
rs2211297	0.91[JPT][hapmap]
rs2339117	0.86[ASN][1000 genomes]
rs2339119	0.96[ASN][1000 genomes]
rs2879348	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs2879349	0.96[ASN][1000 genomes]
rs3748653	0.82[ASN][1000 genomes]
rs4908198	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4908199	0.96[ASN][1000 genomes]
rs4908200	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4908201	0.96[ASN][1000 genomes]
rs6577281	0.90[ASN][1000 genomes]
rs6577283	0.96[ASN][1000 genomes]
rs6577285	0.96[ASN][1000 genomes]
rs6577286	0.96[ASN][1000 genomes]
rs6662872	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6668325	0.96[ASN][1000 genomes]
rs6697587	0.96[ASN][1000 genomes]
rs7521861	0.96[ASN][1000 genomes]
rs7523948	0.96[ASN][1000 genomes]
rs7524443	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7526689	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7531673	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7543735	0.94[ASN][1000 genomes]
rs943556	0.94[ASN][1000 genomes]
rs943557	0.96[ASN][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	nsv522921	chr1:102170295-102876392	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv522156	chr1:102309649-102421714	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1004240	chr1:102360610-102428344	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1012856	chr1:102360610-102438432	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv520768	chr1:102366140-102435130	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv2756852	chr1:102372339-102417093	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv2758953	chr1:102372339-102417093	Weak transcription Enhancers	TF binding region 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	chr1:102373200-102377000	Weak transcription	Fetal Heart	heart
2	chr1:102373400-102374400	Weak transcription	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links