Variant report

Variant	rs1029436
Chromosome Location	chr7:26668623-26668624
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:26668610..26670470-chr7:26674701..26677216,2	K562	blood:
2	chr7:26663687..26665675-chr7:26667700..26669217,2	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1015857	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10230708	0.86[EUR][1000 genomes]
rs10251530	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10252153	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10276138	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10452789	0.96[ASN][1000 genomes]
rs10486470	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10486471	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11972163	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12668342	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12671270	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17154152	0.99[EUR][1000 genomes]
rs17154189	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2106904	0.84[EUR][1000 genomes]
rs2391305	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2391306	0.94[EUR][1000 genomes]
rs28639403	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35970226	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722627	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs57000259	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs57999903	0.99[EUR][1000 genomes]
rs58317468	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs58394627	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58630663	0.94[EUR][1000 genomes]
rs59304553	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs59446421	0.99[ASN][1000 genomes]
rs59472926	0.99[ASN][1000 genomes]
rs59641892	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs60101479	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60481941	0.99[ASN][1000 genomes]
rs61639217	0.88[ASN][1000 genomes]
rs62446548	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62446549	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62446555	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62447660	0.96[ASN][1000 genomes]
rs62447699	0.94[ASN][1000 genomes]
rs6461960	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6943736	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6944239	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6944318	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6960206	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6962850	0.84[EUR][1000 genomes]
rs6967136	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6967151	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6967592	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6968658	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72595043	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7782588	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7784174	0.86[EUR][1000 genomes]
rs7798139	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7801042	0.86[EUR][1000 genomes]
rs7804935	0.84[EUR][1000 genomes]
rs7807676	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029596	chr7:26302739-26737913	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv538804	chr7:26302739-26737913	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
4	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
5	nsv830929	chr7:26587888-26749735	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1021253	chr7:26653375-26669899	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26667800-26670000	Weak transcription	Placenta	Placenta
2	chr7:26667800-26670800	Weak transcription	Spleen	Spleen
3	chr7:26668000-26669200	Weak transcription	Fetal Stomach	stomach
4	chr7:26668200-26668800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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