Variant report

Variant	rs72746350
Chromosome Location	chr9:93570343-93570344
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:93569248..93572925-chr9:93585588..93587867,3	K562	blood:
2	chr9:93562623..93567761-chr9:93568030..93571323,5	K562	blood:
3	chr9:93561656..93565893-chr9:93566155..93575937,12	MCF-7	breast:
4	chr9:93569272..93571391-chr9:93577022..93579806,2	K562	blood:

Variant related genes	Relation type
ENSG00000165025	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10821508	0.99[ASN][1000 genomes]
rs10993696	1.00[ASN][1000 genomes]
rs10993697	0.89[ASN][1000 genomes]
rs10993698	0.89[ASN][1000 genomes]
rs11788207	0.99[ASN][1000 genomes]
rs12551275	0.99[ASN][1000 genomes]
rs12553524	0.99[ASN][1000 genomes]
rs1460834	0.99[ASN][1000 genomes]
rs1460835	0.99[ASN][1000 genomes]
rs16906825	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16906859	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17488335	0.96[ASN][1000 genomes]
rs2042983	0.98[ASN][1000 genomes]
rs2042984	0.99[ASN][1000 genomes]
rs2115484	0.99[ASN][1000 genomes]
rs2115485	0.99[ASN][1000 genomes]
rs2126051	0.99[ASN][1000 genomes]
rs2162977	0.99[ASN][1000 genomes]
rs290233	0.88[ASN][1000 genomes]
rs290239	0.89[ASN][1000 genomes]
rs290240	0.98[ASN][1000 genomes]
rs290241	0.98[ASN][1000 genomes]
rs3789890	0.99[ASN][1000 genomes]
rs3789891	0.99[ASN][1000 genomes]
rs3789892	0.99[ASN][1000 genomes]
rs3789893	0.90[ASN][1000 genomes]
rs4002564	0.96[ASN][1000 genomes]
rs4002565	0.96[ASN][1000 genomes]
rs4002566	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4501705	0.99[ASN][1000 genomes]
rs56955255	0.90[ASN][1000 genomes]
rs58668584	0.99[ASN][1000 genomes]
rs61495376	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62554850	0.99[ASN][1000 genomes]
rs7020331	0.99[ASN][1000 genomes]
rs7032733	0.99[ASN][1000 genomes]
rs7046173	0.99[ASN][1000 genomes]
rs7046193	0.99[ASN][1000 genomes]
rs7046316	0.99[ASN][1000 genomes]
rs72729008	0.90[ASN][1000 genomes]
rs72729009	0.90[ASN][1000 genomes]
rs72729010	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs72729013	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72729020	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72729022	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72729024	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72729025	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72729026	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72742789	0.82[ASN][1000 genomes]
rs72742798	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893567	chr9:93519280-93609668	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831652	chr9:93527411-93696923	Bivalent Enhancer Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv893569	chr9:93552550-93587089	Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1038685	chr9:93556174-93685729	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv1813758	chr9:93557698-93573095	Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv275555	chr9:93565999-93570451	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93564600-93572000	Weak transcription	Lung	lung
2	chr9:93565000-93609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr9:93565400-93570600	Weak transcription	HMEC	breast
4	chr9:93565400-93570800	Weak transcription	Placenta	Placenta
5	chr9:93565400-93577000	Weak transcription	Colonic Mucosa	Colon
6	chr9:93567000-93572800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr9:93567600-93571000	Weak transcription	Fetal Intestine Small	intestine
8	chr9:93567600-93573000	Weak transcription	NHEK	skin
9	chr9:93567800-93570800	Weak transcription	Pancreas	Pancrea
10	chr9:93567800-93570800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr9:93567800-93572000	Weak transcription	Esophagus	oesophagus
12	chr9:93567800-93572000	Weak transcription	K562	blood
13	chr9:93567800-93572400	Weak transcription	Stomach Mucosa	stomach
14	chr9:93567800-93584800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:93567800-93584800	Weak transcription	Fetal Intestine Large	intestine
16	chr9:93567800-93597400	Weak transcription	Gastric	stomach
17	chr9:93568400-93575000	Enhancers	Fetal Thymus	thymus
18	chr9:93568400-93576600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr9:93568600-93573600	Genic enhancers	Primary B cells from peripheral blood	blood
20	chr9:93569200-93570400	Genic enhancers	Primary B cells from cord blood	blood
21	chr9:93569200-93570400	Genic enhancers	Primary hematopoietic stem cells	blood
22	chr9:93569200-93570600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr9:93569200-93570800	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr9:93569200-93571200	Enhancers	Spleen	Spleen
25	chr9:93569400-93570400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:93569400-93570400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
27	chr9:93569400-93571400	Enhancers	Primary T cells from cord blood	blood
28	chr9:93569400-93573200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr9:93569600-93570600	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr9:93569600-93574600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr9:93569800-93571800	Enhancers	Fetal Kidney	kidney
32	chr9:93570000-93570800	Weak transcription	Fetal Stomach	stomach
33	chr9:93570000-93571000	Weak transcription	Small Intestine	intestine
34	chr9:93570000-93571600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr9:93570200-93570600	Enhancers	Thymus	Thymus
36	chr9:93570200-93570600	Enhancers	GM12878-XiMat	blood
37	chr9:93570200-93571000	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr9:93570200-93571600	Genic enhancers	Duodenum Mucosa	Duodenum
39	chr9:93570200-93571600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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