Variant report

Variant	rs10009045
Chromosome Location	chr4:7780024-7780025
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10018256	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2067842	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3934540	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4234831	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4443285	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4447865	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4579115	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4689860	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4689865	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4689875	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6446624	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6446625	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6828858	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6829710	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6856371	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6856795	0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71612280	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7654361	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7682611	0.80[EUR][1000 genomes]
rs7684718	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9996019	0.89[EUR][1000 genomes];0.98[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	nsv878570	chr4:7534603-7836835	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv491712	chr4:7582506-8155069	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1007319	chr4:7705550-7832097	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv537018	chr4:7705550-7832097	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7758000-7780800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr4:7758200-7783200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:7758400-7795400	Weak transcription	Hela-S3	cervix
4	chr4:7758600-7780600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:7759400-7790400	Weak transcription	Psoas Muscle	Psoas
6	chr4:7760000-7783000	Strong transcription	HSMMtube	muscle
7	chr4:7760000-7783200	Strong transcription	HSMM	muscle
8	chr4:7760400-7780400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:7761000-7780400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:7761200-7781000	Strong transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:7761400-7784400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:7762000-7788000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:7762000-7805800	Weak transcription	Stomach Mucosa	stomach
14	chr4:7766000-7780600	Strong transcription	Osteobl	bone
15	chr4:7766800-7781200	Strong transcription	HUVEC	blood vessel
16	chr4:7767200-7780800	Strong transcription	NH-A	brain
17	chr4:7767600-7781000	Strong transcription	Muscle Satellite Cultured Cells	--
18	chr4:7769000-7780200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr4:7770800-7828400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr4:7771600-7780800	Strong transcription	Pancreas	Pancrea
21	chr4:7771800-7780200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr4:7772000-7783000	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr4:7772800-7780400	Weak transcription	Brain Angular Gyrus	brain
24	chr4:7773600-7782800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr4:7773600-7783000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr4:7773600-7783600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr4:7773800-7783400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:7774000-7782800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr4:7774000-7783400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr4:7774200-7781600	Strong transcription	A549	lung
31	chr4:7774400-7780600	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr4:7774400-7781000	Weak transcription	Fetal Heart	heart
33	chr4:7774600-7780200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr4:7774600-7783000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:7774600-7783400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:7775000-7780600	Strong transcription	Adipose Nuclei	Adipose
37	chr4:7775200-7782400	Strong transcription	Placenta	Placenta
38	chr4:7775400-7780400	Strong transcription	Fetal Muscle Leg	muscle
39	chr4:7775400-7780800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr4:7775400-7783400	Weak transcription	Small Intestine	intestine
41	chr4:7775800-7780400	Strong transcription	Fetal Muscle Trunk	muscle
42	chr4:7775800-7780800	Strong transcription	NHDF-Ad	bronchial
43	chr4:7776000-7780800	Strong transcription	Fetal Intestine Large	intestine
44	chr4:7776000-7784400	Strong transcription	Fetal Intestine Small	intestine
45	chr4:7776200-7781000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:7776400-7780800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:7776400-7787200	Weak transcription	Fetal Brain Male	brain
48	chr4:7776400-7790000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr4:7776400-7799000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr4:7776400-7800000	Weak transcription	H1 Cell Line	embryonic stem cell

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