Variant report

Variant	rs72680965
Chromosome Location	chr4:120651906-120651907
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs11098535	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098536	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11098537	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17005547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17005814	0.86[EUR][1000 genomes]
rs55922435	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56085109	0.83[AMR][1000 genomes]
rs56199127	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56296554	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56324051	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678594	0.83[AMR][1000 genomes]
rs72678595	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678596	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678597	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678599	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678601	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678602	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680932	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680933	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680934	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680935	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680936	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680937	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680938	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680941	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680944	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680945	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680949	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680951	0.83[AMR][1000 genomes]
rs72680953	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680958	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680959	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680962	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680964	0.83[AMR][1000 genomes]
rs72680967	0.83[AMR][1000 genomes]
rs72680968	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680969	0.83[AMR][1000 genomes]
rs72680972	0.96[EUR][1000 genomes]
rs72680973	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680974	0.83[AMR][1000 genomes]
rs72680975	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72680976	0.83[AMR][1000 genomes]
rs72680978	0.83[AMR][1000 genomes]
rs72680980	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680982	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680985	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680987	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680989	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680990	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72680995	0.83[AMR][1000 genomes]
rs72681002	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72682804	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72682807	0.86[EUR][1000 genomes]
rs7659472	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7682717	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1010753	chr4:120429028-120684310	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537233	chr4:120429028-120684310	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1006572	chr4:120432494-120694243	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1802546	chr4:120558608-120675026	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1010638	chr4:120586178-120671835	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1009771	chr4:120590902-120665812	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv1803992	chr4:120649398-120665812	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120647800-120652200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:120649400-120653000	Enhancers	Hela-S3	cervix
3	chr4:120649600-120658200	Enhancers	NHLF	lung
4	chr4:120649800-120653200	Enhancers	Osteobl	bone
5	chr4:120650000-120653000	Enhancers	NH-A	brain
6	chr4:120650000-120653400	Enhancers	HSMM	muscle
7	chr4:120650200-120652400	Enhancers	HMEC	breast
8	chr4:120650200-120652400	Enhancers	HUVEC	blood vessel
9	chr4:120650200-120653000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:120650200-120653200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:120650200-120653400	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr4:120650200-120653600	Enhancers	Fetal Lung	lung
13	chr4:120650200-120658000	Enhancers	HSMMtube	muscle
14	chr4:120650200-120658400	Enhancers	NHDF-Ad	bronchial
15	chr4:120650400-120653600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr4:120650400-120653600	Enhancers	Stomach Mucosa	stomach
17	chr4:120650400-120657200	Weak transcription	Psoas Muscle	Psoas
18	chr4:120650800-120652400	Enhancers	Fetal Stomach	stomach
19	chr4:120650800-120652800	Weak transcription	Small Intestine	intestine
20	chr4:120651000-120652400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr4:120651000-120652600	Enhancers	Colon Smooth Muscle	Colon
22	chr4:120651000-120653000	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr4:120651000-120653200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:120651000-120653200	Enhancers	Liver	Liver
25	chr4:120651200-120652000	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr4:120651200-120652200	Enhancers	A549	lung
27	chr4:120651200-120652400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr4:120651200-120653600	Enhancers	Adipose Nuclei	Adipose
29	chr4:120651200-120656000	Weak transcription	Stomach Smooth Muscle	stomach
30	chr4:120651400-120652000	Enhancers	Pancreas	Pancrea
31	chr4:120651400-120652000	Enhancers	HepG2	liver
32	chr4:120651400-120652200	Enhancers	Left Ventricle	heart
33	chr4:120651400-120652200	Enhancers	Rectal Smooth Muscle	rectum
34	chr4:120651400-120652800	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr4:120651400-120653200	Enhancers	Right Atrium	heart
36	chr4:120651400-120653400	Enhancers	Ovary	ovary
37	chr4:120651400-120654000	Enhancers	Placenta	Placenta
38	chr4:120651600-120652000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:120651600-120652000	Enhancers	Colonic Mucosa	Colon
40	chr4:120651600-120652000	Enhancers	Fetal Heart	heart
41	chr4:120651600-120652200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr4:120651600-120652600	Weak transcription	Fetal Kidney	kidney
43	chr4:120651600-120652800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr4:120651600-120652800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr4:120651600-120656000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:120651600-120658000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:120651800-120652000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:120651800-120652000	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr4:120651800-120652400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:120651800-120652600	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links