Variant report

Variant	rs72729013
Chromosome Location	chr9:93578780-93578781
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:93563428..93565399-chr9:93578384..93582187,4	MCF-7	breast:
2	chr9:93566333..93568000-chr9:93577767..93579301,2	MCF-7	breast:
3	chr9:93560904..93565448-chr9:93577288..93580605,5	K562	blood:
4	chr9:93569272..93571391-chr9:93577022..93579806,2	K562	blood:
5	chr9:93561901..93563996-chr9:93577117..93579715,2	MCF-7	breast:
6	chr9:93560904..93565448-chr9:93577148..93580132,4	K562	blood:
7	chr9:93564315..93567256-chr9:93578660..93580228,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165025	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10821508	0.88[ASN][1000 genomes]
rs10993696	0.89[ASN][1000 genomes]
rs10993697	1.00[ASN][1000 genomes]
rs10993698	1.00[ASN][1000 genomes]
rs11788207	0.88[ASN][1000 genomes]
rs12551275	0.88[ASN][1000 genomes]
rs12553524	0.88[ASN][1000 genomes]
rs1460834	0.88[ASN][1000 genomes]
rs1460835	0.88[ASN][1000 genomes]
rs16906825	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16906859	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17488335	0.85[ASN][1000 genomes]
rs2042983	0.87[ASN][1000 genomes]
rs2042984	0.88[ASN][1000 genomes]
rs2115484	0.88[ASN][1000 genomes]
rs2115485	0.88[ASN][1000 genomes]
rs2126051	0.88[ASN][1000 genomes]
rs2162977	0.88[ASN][1000 genomes]
rs290233	0.96[ASN][1000 genomes]
rs290240	0.87[ASN][1000 genomes]
rs290241	0.87[ASN][1000 genomes]
rs3789890	0.88[ASN][1000 genomes]
rs3789891	0.88[ASN][1000 genomes]
rs3789892	0.88[ASN][1000 genomes]
rs3789893	0.99[ASN][1000 genomes]
rs4002564	0.85[ASN][1000 genomes]
rs4002565	0.85[ASN][1000 genomes]
rs4002566	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4501705	0.88[ASN][1000 genomes]
rs58668584	0.88[ASN][1000 genomes]
rs61495376	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62554850	0.88[ASN][1000 genomes]
rs7020331	0.88[ASN][1000 genomes]
rs7032733	0.88[ASN][1000 genomes]
rs7046173	0.88[ASN][1000 genomes]
rs7046193	0.88[ASN][1000 genomes]
rs7046316	0.88[ASN][1000 genomes]
rs72729008	0.99[ASN][1000 genomes]
rs72729009	0.99[ASN][1000 genomes]
rs72729010	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs72729020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72729022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72729024	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72729025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72729026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72742789	1.00[AFR][1000 genomes]
rs72746350	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][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	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

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93565000-93609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr9:93567800-93584800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:93567800-93584800	Weak transcription	Fetal Intestine Large	intestine
4	chr9:93567800-93597400	Weak transcription	Gastric	stomach
5	chr9:93572600-93591000	Weak transcription	Lung	lung
6	chr9:93572800-93584800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr9:93573200-93589600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr9:93574600-93578800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr9:93574800-93580200	Weak transcription	Pancreas	Pancrea
10	chr9:93575000-93580600	Weak transcription	Stomach Mucosa	stomach
11	chr9:93575200-93580400	Weak transcription	Fetal Intestine Small	intestine
12	chr9:93576200-93579000	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr9:93576400-93580200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr9:93576600-93578800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:93576800-93582400	Weak transcription	Small Intestine	intestine
16	chr9:93577000-93585800	Genic enhancers	Primary B cells from peripheral blood	blood
17	chr9:93577000-93598800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr9:93577200-93589000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr9:93577600-93578800	Enhancers	Fetal Kidney	kidney
20	chr9:93577800-93582200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr9:93577800-93584000	Weak transcription	HMEC	breast
22	chr9:93577800-93584800	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr9:93577800-93585000	Weak transcription	Spleen	Spleen
24	chr9:93577800-93606200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr9:93578000-93578800	Enhancers	Dnd41	blood
26	chr9:93578000-93585000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr9:93578200-93578800	Enhancers	Fetal Thymus	thymus
28	chr9:93578200-93578800	Enhancers	Thymus	Thymus
29	chr9:93578200-93582400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr9:93578200-93585000	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr9:93578400-93578800	Enhancers	Primary B cells from cord blood	blood
32	chr9:93578400-93578800	Enhancers	GM12878-XiMat	blood
33	chr9:93578400-93578800	Enhancers	K562	blood
34	chr9:93578400-93579000	Enhancers	Primary hematopoietic stem cells	blood
35	chr9:93578400-93579400	Genic enhancers	Monocytes-CD14+_RO01746	blood
36	chr9:93578400-93580400	Weak transcription	Fetal Stomach	stomach
37	chr9:93578600-93579000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr9:93578600-93579200	Genic enhancers	Primary neutrophils fromperipheralblood	blood
39	chr9:93578600-93579800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr9:93578600-93584800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:93578600-93592400	Weak transcription	Esophagus	oesophagus

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