Variant report

Variant	rs4841430
Chromosome Location	chr8:10578801-10578802
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:10549207..10552160-chr8:10577938..10579847,2	K562	blood:
2	chr8:10561879..10564186-chr8:10576793..10578956,2	K562	blood:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10090558	0.94[EUR][1000 genomes]
rs10103202	0.94[EUR][1000 genomes]
rs10794714	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11250060	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12056524	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12056623	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12547475	0.85[AFR][1000 genomes]
rs13277080	0.84[AFR][1000 genomes]
rs4841425	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4841426	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4841427	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4841428	0.86[ASN][1000 genomes]
rs4841429	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57949601	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs60270701	0.90[EUR][1000 genomes]
rs60837490	0.95[EUR][1000 genomes]
rs6601505	0.90[EUR][1000 genomes]
rs6601506	0.95[EUR][1000 genomes]
rs6601507	0.92[EUR][1000 genomes]
rs6601508	0.90[EUR][1000 genomes]
rs6601509	1.00[CEU][hapmap];0.86[CHB][hapmap];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6999206	1.00[CEU][hapmap];0.82[CHB][hapmap];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73536579	0.89[EUR][1000 genomes]
rs7815136	0.81[ASN][1000 genomes]
rs7818747	0.81[ASN][1000 genomes]
rs7822666	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs7827595	0.94[EUR][1000 genomes]
rs7836972	0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7840510	0.94[EUR][1000 genomes]
rs7844805	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1015932	chr8:10357101-10597856	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1021048	chr8:10504395-10591896	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
6	nsv527184	chr8:10530037-10589913	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1028266	chr8:10537081-10586112	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	nsv1034829	chr8:10537081-10591896	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1032725	chr8:10561962-10585683	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1022582	chr8:10571218-10636162	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv539468	chr8:10571218-10636162	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
13	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10572000-10583000	Weak transcription	Liver	Liver
2	chr8:10574200-10579400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr8:10574200-10579600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:10574200-10579600	Weak transcription	NHEK	skin
5	chr8:10574400-10579600	Weak transcription	Esophagus	oesophagus
6	chr8:10574400-10579800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:10574800-10584200	Weak transcription	Hela-S3	cervix
8	chr8:10575000-10581800	Weak transcription	Adipose Nuclei	Adipose
9	chr8:10575200-10583000	Weak transcription	Spleen	Spleen
10	chr8:10575400-10580000	Weak transcription	HUVEC	blood vessel
11	chr8:10575600-10583600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:10575800-10580000	Weak transcription	Lung	lung
13	chr8:10576800-10587200	Weak transcription	Gastric	stomach
14	chr8:10577000-10586000	Weak transcription	Right Atrium	heart
15	chr8:10578800-10579000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland

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