Variant report

Variant	rs72940050
Chromosome Location	chr3:112269208-112269209
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:112267834..112269856-chr3:112273355..112275580,2	MCF-7	breast:
2	chr3:112268324..112269882-chr3:112359880..112361529,2	MCF-7	breast:
3	chr3:112267679..112269481-chr3:112276502..112278431,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000091986	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs13070342	0.94[AFR][1000 genomes]
rs57937078	1.00[AMR][1000 genomes]
rs59090018	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938420	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938422	1.00[AMR][1000 genomes]
rs72938432	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938438	1.00[AMR][1000 genomes]
rs72938454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938457	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938461	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938469	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938470	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938475	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938476	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938477	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938478	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72938498	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940020	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940024	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940078	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940083	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940091	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72940099	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942032	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942055	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942057	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942068	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942074	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942077	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942080	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72942089	1.00[AMR][1000 genomes]
rs72943904	1.00[AMR][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	nsv1003936	chr3:112125931-112274613	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv998309	chr3:112130290-112278804	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv591300	chr3:112144026-112270857	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv1006065	chr3:112147080-112276983	Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1005323	chr3:112171990-112274613	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv877342	chr3:112185025-112332629	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
7	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
8	nsv591301	chr3:112252532-112332629	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112227400-112269800	Weak transcription	Small Intestine	intestine
2	chr3:112234200-112272000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr3:112239600-112272200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:112243000-112271600	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr3:112244400-112274200	Weak transcription	Stomach Mucosa	stomach
6	chr3:112244400-112278200	Weak transcription	K562	blood
7	chr3:112244400-112278400	Weak transcription	HSMMtube	muscle
8	chr3:112245200-112273200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr3:112245800-112279600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:112247600-112279600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr3:112248400-112274200	Weak transcription	Brain Cingulate Gyrus	brain
12	chr3:112249200-112269800	Weak transcription	Psoas Muscle	Psoas
13	chr3:112249200-112275800	Weak transcription	Fetal Stomach	stomach
14	chr3:112249200-112276000	Weak transcription	Spleen	Spleen
15	chr3:112249200-112278200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr3:112249200-112278400	Weak transcription	Aorta	Aorta
17	chr3:112249200-112279600	Weak transcription	Esophagus	oesophagus
18	chr3:112249200-112279600	Weak transcription	Gastric	stomach
19	chr3:112249200-112279800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr3:112249400-112270000	Weak transcription	Fetal Intestine Small	intestine
21	chr3:112249400-112276200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:112249400-112279600	Weak transcription	Lung	lung
23	chr3:112251000-112274200	Weak transcription	Brain Angular Gyrus	brain
24	chr3:112252200-112270200	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr3:112252400-112269800	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr3:112252600-112278400	Weak transcription	Fetal Kidney	kidney
27	chr3:112253000-112273400	Weak transcription	Brain Substantia Nigra	brain
28	chr3:112253200-112278600	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr3:112254200-112273600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr3:112257600-112274000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr3:112259200-112270400	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr3:112260000-112271200	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr3:112260000-112278200	Weak transcription	Fetal Brain Male	brain
34	chr3:112260400-112279600	Weak transcription	Pancreas	Pancrea
35	chr3:112261200-112269800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
36	chr3:112261400-112270200	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr3:112262200-112270200	Strong transcription	GM12878-XiMat	blood
38	chr3:112262400-112270200	Strong transcription	Primary B cells from peripheral blood	blood
39	chr3:112263200-112270400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:112264200-112270600	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr3:112264600-112269400	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr3:112265000-112276000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr3:112266000-112274200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr3:112266200-112270000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr3:112266200-112270400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr3:112266200-112278200	Weak transcription	Fetal Heart	heart
47	chr3:112266200-112278200	Weak transcription	NHLF	lung
48	chr3:112266200-112278400	Weak transcription	Colonic Mucosa	Colon
49	chr3:112266400-112269800	Weak transcription	HepG2	liver
50	chr3:112266400-112278200	Weak transcription	NHEK	skin

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