Variant report

Variant	rs62564597
Chromosome Location	chr9:94610982-94610983
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10820906	0.81[EUR][1000 genomes]
rs10820907	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10820908	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10992123	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10992124	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10992128	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10992129	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10992130	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992131	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10992132	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992135	0.83[EUR][1000 genomes]
rs10992137	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992139	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992140	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10992142	0.82[EUR][1000 genomes]
rs10992143	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10992149	0.82[EUR][1000 genomes]
rs11790144	0.82[AMR][1000 genomes]
rs12376539	0.80[EUR][1000 genomes]
rs12552292	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12552858	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12683797	0.82[EUR][1000 genomes]
rs1534531	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16907887	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1881387	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1881392	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2141368	0.81[EUR][1000 genomes]
rs2841691	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4322068	0.80[EUR][1000 genomes]
rs4639579	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4743857	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4744108	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4744109	0.88[EUR][1000 genomes]
rs4744110	0.88[EUR][1000 genomes]
rs4744113	0.82[EUR][1000 genomes]
rs55663665	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55864279	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56088447	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56308784	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62564595	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62564598	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62564599	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62565674	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6479374	0.81[EUR][1000 genomes]
rs6479375	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6479376	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67944481	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7019210	0.82[EUR][1000 genomes]
rs7031562	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7033819	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7039406	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7045333	0.81[EUR][1000 genomes]
rs7048756	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs72746206	0.81[EUR][1000 genomes]
rs7850636	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7855417	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7856144	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7859331	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7863061	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7867707	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7870902	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7874148	0.81[AMR][1000 genomes];0.81[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	nsv1045332	chr9:94352661-94656016	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv531631	chr9:94373847-94633213	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1036176	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv540171	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94601800-94618400	Weak transcription	K562	blood
2	chr9:94602800-94611200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr9:94602800-94611600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr9:94606600-94616600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr9:94606800-94615000	Weak transcription	Right Atrium	heart
6	chr9:94606800-94619600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:94607200-94619600	Weak transcription	Fetal Intestine Large	intestine
8	chr9:94607600-94619600	Weak transcription	Fetal Intestine Small	intestine
9	chr9:94608400-94619000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr9:94609000-94614400	Weak transcription	Fetal Heart	heart
11	chr9:94609200-94611400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr9:94609600-94611000	Enhancers	Fetal Lung	lung
13	chr9:94609600-94617800	Weak transcription	Colon Smooth Muscle	Colon
14	chr9:94610200-94611000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr9:94610200-94615200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:94610200-94615400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:94610200-94615600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr9:94610200-94616400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr9:94610200-94617400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr9:94610200-94619000	Weak transcription	Ovary	ovary
21	chr9:94610400-94615400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr9:94610400-94617400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:94610400-94618600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr9:94610600-94612600	Weak transcription	Fetal Stomach	stomach
25	chr9:94610600-94618800	Weak transcription	Fetal Kidney	kidney

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