Variant report

Variant	rs72754436
Chromosome Location	chr9:95285613-95285614
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 133 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:129)

rs_ID	r²[population]
rs17365144	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17366134	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17462606	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17519320	0.81[ASN][1000 genomes]
rs17519397	0.81[ASN][1000 genomes]
rs17519719	0.81[ASN][1000 genomes]
rs17519922	0.81[ASN][1000 genomes]
rs17591372	0.81[ASN][1000 genomes]
rs17591776	0.81[ASN][1000 genomes]
rs17591958	0.81[ASN][1000 genomes]
rs17592026	0.81[ASN][1000 genomes]
rs2277165	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2277167	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2277170	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3780348	0.81[ASN][1000 genomes]
rs3802383	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs41266685	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41273374	0.92[EUR][1000 genomes]
rs41278699	0.81[ASN][1000 genomes]
rs41305495	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs41312236	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72752471	0.81[ASN][1000 genomes]
rs72752472	0.81[ASN][1000 genomes]
rs72752484	0.81[ASN][1000 genomes]
rs72752485	0.81[ASN][1000 genomes]
rs72752486	0.81[ASN][1000 genomes]
rs72752492	0.81[ASN][1000 genomes]
rs72752493	0.81[ASN][1000 genomes]
rs72752497	0.81[ASN][1000 genomes]
rs72752502	0.81[ASN][1000 genomes]
rs72754403	0.81[ASN][1000 genomes]
rs72754404	0.81[ASN][1000 genomes]
rs72754408	0.81[ASN][1000 genomes]
rs72754410	0.81[ASN][1000 genomes]
rs72754411	0.81[ASN][1000 genomes]
rs72754415	0.81[ASN][1000 genomes]
rs72754418	0.81[ASN][1000 genomes]
rs72754420	0.81[ASN][1000 genomes]
rs72754421	0.81[ASN][1000 genomes]
rs72754423	0.81[ASN][1000 genomes]
rs72754425	0.81[ASN][1000 genomes]
rs72754429	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72754430	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72754433	1.00[AMR][1000 genomes]
rs72754434	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754435	1.00[AMR][1000 genomes]
rs72754437	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754440	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754442	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754443	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754444	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754445	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754446	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754447	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72754450	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754452	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754457	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754461	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754463	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754464	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72754465	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754470	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754477	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754480	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72754482	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754483	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754485	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72754487	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72754489	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754491	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754493	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72754496	0.92[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72754499	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72754501	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72756403	0.92[AMR][1000 genomes]
rs72756404	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756405	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756406	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756408	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756410	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756414	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72756415	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72756416	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756418	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72756423	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72756424	0.92[AMR][1000 genomes]
rs72756425	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72756426	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72756427	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72756431	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72756433	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756437	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72756438	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756440	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756441	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756442	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756443	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756444	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72756446	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756447	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756448	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756452	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756455	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756457	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756458	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756459	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756460	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756462	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756464	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756465	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756467	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756468	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756469	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72756471	0.92[EUR][1000 genomes]
rs72756478	0.92[EUR][1000 genomes]
rs72756483	0.92[EUR][1000 genomes]
rs72756486	0.92[EUR][1000 genomes]
rs72756489	0.92[EUR][1000 genomes]
rs72756497	0.92[EUR][1000 genomes]
rs72756498	0.92[EUR][1000 genomes]
rs72756500	0.92[EUR][1000 genomes]
rs72758504	0.92[EUR][1000 genomes]
rs72758505	0.92[EUR][1000 genomes]
rs72758508	0.92[EUR][1000 genomes]
rs72758519	0.92[EUR][1000 genomes]
rs72758524	0.92[EUR][1000 genomes]
rs72758525	0.92[EUR][1000 genomes]
rs72758536	0.88[EUR][1000 genomes]
rs72758539	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1050845	chr9:94687959-95312406	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv893573	chr9:94974188-95355719	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	nsv1047337	chr9:95105638-95347484	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv1822933	chr9:95255176-95293308	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95269800-95298800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr9:95275800-95285800	Weak transcription	Fetal Intestine Small	intestine
3	chr9:95276000-95296600	Weak transcription	Colon Smooth Muscle	Colon
4	chr9:95279600-95290400	Weak transcription	Fetal Muscle Leg	muscle
5	chr9:95280800-95290400	Weak transcription	Aorta	Aorta
6	chr9:95280800-95296400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:95281400-95295800	Weak transcription	Liver	Liver
8	chr9:95281800-95290400	Weak transcription	Adipose Nuclei	Adipose
9	chr9:95283400-95286400	Weak transcription	Fetal Lung	lung
10	chr9:95283600-95286600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr9:95284000-95296400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:95284800-95285800	Enhancers	HepG2	liver
13	chr9:95284800-95286800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr9:95285400-95287000	Enhancers	Fetal Intestine Large	intestine
15	chr9:95285400-95287000	Enhancers	Ovary	ovary
16	chr9:95285600-95286000	Enhancers	Duodenum Mucosa	Duodenum
17	chr9:95285600-95286000	Enhancers	Left Ventricle	heart
18	chr9:95285600-95286400	Flanking Active TSS	K562	blood
19	chr9:95285600-95286600	Enhancers	Fetal Heart	heart

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