Variant report

Variant	rs72905000
Chromosome Location	chr4:100392644-100392645
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs12499297	0.82[ASN][1000 genomes]
rs12499621	0.92[ASN][1000 genomes]
rs12499625	0.92[ASN][1000 genomes]
rs12499683	0.92[ASN][1000 genomes]
rs12501931	0.95[ASN][1000 genomes]
rs12502381	0.91[ASN][1000 genomes]
rs12503219	0.92[ASN][1000 genomes]
rs12504511	0.93[ASN][1000 genomes]
rs12505135	1.00[ASN][1000 genomes]
rs12505224	0.93[ASN][1000 genomes]
rs12509265	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12509626	0.95[ASN][1000 genomes]
rs12510523	0.95[ASN][1000 genomes]
rs12510823	0.93[ASN][1000 genomes]
rs12510825	0.93[ASN][1000 genomes]
rs12510954	0.92[ASN][1000 genomes]
rs12512792	1.00[ASN][1000 genomes]
rs1354367	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1442477	0.93[ASN][1000 genomes]
rs1503775	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1969097	0.85[EUR][1000 genomes]
rs2083685	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2903200	0.93[ASN][1000 genomes]
rs4147549	0.93[ASN][1000 genomes]
rs4699750	0.95[ASN][1000 genomes]
rs57441592	0.93[ASN][1000 genomes]
rs58440244	0.93[ASN][1000 genomes]
rs60003800	0.93[ASN][1000 genomes]
rs60156573	0.93[ASN][1000 genomes]
rs6831961	0.93[ASN][1000 genomes]
rs6853853	0.93[ASN][1000 genomes]
rs72904927	0.92[ASN][1000 genomes]
rs72904928	0.93[ASN][1000 genomes]
rs72904929	0.93[ASN][1000 genomes]
rs72906741	0.80[EUR][1000 genomes]
rs7669241	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7670511	0.90[ASN][1000 genomes]
rs7678920	0.93[ASN][1000 genomes]
rs7690269	0.93[ASN][1000 genomes]
rs7692423	0.86[ASN][1000 genomes]
rs930478	0.92[ASN][1000 genomes]
rs971074	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009017	chr4:99669441-100406394	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
2	nsv879656	chr4:99976646-100533722	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1010988	chr4:100105463-100444445	Weak transcription Strong transcription Enhancers Flanking Active TSS 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	10 gene(s)	inside rSNPs	diseases
4	nsv1000659	chr4:100117276-100444445	Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3353320	chr4:100147870-100425701	Genic enhancers ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv3394995	chr4:100147890-100425671	Enhancers Genic enhancers Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	esv1847619	chr4:100321443-100430924	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3584519	chr4:100323870-100477462	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	esv3584520	chr4:100324071-100400696	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100390200-100394200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:100390600-100393000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:100392600-100394600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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