Variant report

Variant	rs66539130
Chromosome Location	chr9:110072388-110072389
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:110066546..110068820-chr9:110070099..110072888,2	K562	blood:
2	chr9:110069222..110072456-chr9:110073619..110076462,3	MCF-7	breast:
3	chr9:110044300..110048942-chr9:110067094..110074281,11	MCF-7	breast:
4	chr9:110044399..110049612-chr9:110071012..110080286,12	K562	blood:
5	chr9:110070129..110072488-chr9:110081712..110083415,2	K562	blood:
6	chr9:110070353..110073170-chr9:110078217..110082315,4	MCF-7	breast:
7	chr9:110049581..110051989-chr9:110070046..110072937,2	MCF-7	breast:
8	chr9:110070283..110073210-chr9:110082560..110084216,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000119318	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10868	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11573607	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11573662	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11573665	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11573703	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11573709	1.00[ASN][1000 genomes]
rs11573711	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11573721	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12379885	1.00[ASN][1000 genomes]
rs12379895	1.00[ASN][1000 genomes]
rs13287251	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1805331	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34593991	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34731486	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34745099	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35218924	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35494237	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35626978	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35827173	1.00[ASN][1000 genomes]
rs35865856	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35967129	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36016101	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36089467	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56161943	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66495692	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67630898	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71495992	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs716004	1.00[ASN][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	nsv869351	chr9:109593212-110191170	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv530948	chr9:109760752-110413602	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	nsv831682	chr9:109937181-110075453	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv519266	chr9:110049477-110085255	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:110051600-110079200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:110057200-110079200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr9:110057400-110074600	Weak transcription	Spleen	Spleen
4	chr9:110057400-110074800	Weak transcription	Psoas Muscle	Psoas
5	chr9:110058600-110074800	Weak transcription	Right Atrium	heart
6	chr9:110058600-110098600	Weak transcription	Small Intestine	intestine
7	chr9:110061400-110094600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr9:110061600-110073400	Strong transcription	K562	blood
9	chr9:110062000-110076000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:110062000-110078000	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr9:110062400-110077800	Strong transcription	HUES48 Cell Line	embryonic stem cell
12	chr9:110062400-110078600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr9:110062600-110078800	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr9:110062800-110077600	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr9:110063000-110073200	Strong transcription	GM12878-XiMat	blood
16	chr9:110063000-110077200	Strong transcription	A549	lung
17	chr9:110063000-110078200	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr9:110063000-110079200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:110063200-110077400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
20	chr9:110063200-110077400	Strong transcription	Primary B cells from peripheral blood	blood
21	chr9:110063200-110077800	Strong transcription	Placenta	Placenta
22	chr9:110063400-110077800	Strong transcription	Fetal Lung	lung
23	chr9:110063600-110078600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr9:110063800-110073200	Strong transcription	NHLF	lung
25	chr9:110063800-110079200	Strong transcription	Osteobl	bone
26	chr9:110063800-110079400	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr9:110064000-110073000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr9:110064000-110074400	Strong transcription	HSMM	muscle
29	chr9:110064000-110074600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:110064000-110074600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:110064000-110085000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:110065200-110089200	Strong transcription	Fetal Thymus	thymus
33	chr9:110065400-110077800	Strong transcription	Primary B cells from cord blood	blood
34	chr9:110065600-110098600	Strong transcription	Dnd41	blood
35	chr9:110066000-110072600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr9:110066800-110072400	Strong transcription	Fetal Muscle Trunk	muscle
37	chr9:110067000-110077800	Strong transcription	Rectal Mucosa Donor 31	rectum
38	chr9:110067400-110076600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr9:110068400-110077200	Strong transcription	Duodenum Mucosa	Duodenum
40	chr9:110068600-110073000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
41	chr9:110068600-110074400	Strong transcription	Adipose Nuclei	Adipose
42	chr9:110068600-110077400	Strong transcription	HUVEC	blood vessel
43	chr9:110069000-110072600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr9:110069000-110074400	Weak transcription	Pancreas	Pancrea
45	chr9:110069000-110074600	Weak transcription	Gastric	stomach
46	chr9:110069000-110074800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr9:110069800-110074600	Weak transcription	Aorta	Aorta
48	chr9:110069800-110074600	Weak transcription	Fetal Stomach	stomach
49	chr9:110070000-110074200	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr9:110070000-110074200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links