Variant report

Variant	rs73140814
Chromosome Location	chr3:21789920-21789921
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs7636784	0.83[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	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1010460	chr3:21516810-21839871	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1007048	chr3:21666807-21865229	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv536516	chr3:21666807-21865229	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1007665	chr3:21781727-21809266	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1011725	chr3:21786893-21804428	Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv2751992	chr3:21786893-22212357	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv948555	chr3:21786893-22212357	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21778200-21791400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:21780600-21791400	Weak transcription	Fetal Heart	heart
3	chr3:21784200-21790600	Weak transcription	Fetal Muscle Trunk	muscle
4	chr3:21786400-21793600	Active TSS	Aorta	Aorta
5	chr3:21786600-21790000	Enhancers	Fetal Lung	lung
6	chr3:21787200-21791400	Weak transcription	HSMM	muscle
7	chr3:21788000-21791200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr3:21788200-21790200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:21788200-21791800	Active TSS	Adipose Nuclei	Adipose
10	chr3:21788400-21790400	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr3:21788600-21790000	Enhancers	Right Ventricle	heart
12	chr3:21788800-21790000	Enhancers	Fetal Muscle Leg	muscle
13	chr3:21788800-21790000	Enhancers	HMEC	breast
14	chr3:21788800-21790400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr3:21788800-21790400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:21788800-21790400	Enhancers	Left Ventricle	heart
17	chr3:21788800-21791800	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr3:21788800-21793200	Active TSS	Duodenum Smooth Muscle	Duodenum
19	chr3:21789000-21790400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:21789000-21791600	Active TSS	Psoas Muscle	Psoas
21	chr3:21789000-21791800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
22	chr3:21789200-21790200	Enhancers	Right Atrium	heart
23	chr3:21789200-21790600	Enhancers	Brain Germinal Matrix	brain
24	chr3:21789200-21791400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr3:21789200-21791600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr3:21789200-21791800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr3:21789200-21793200	Active TSS	Fetal Brain Female	brain
28	chr3:21789400-21790200	Flanking Active TSS	Fetal Stomach	stomach
29	chr3:21789400-21791400	Weak transcription	HSMMtube	muscle
30	chr3:21789400-21793200	Active TSS	NHDF-Ad	bronchial
31	chr3:21789600-21790000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr3:21789600-21790600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr3:21789600-21792600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr3:21789800-21790200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:21789800-21790200	Active TSS	Fetal Kidney	kidney
36	chr3:21789800-21790200	Flanking Active TSS	NH-A	brain
37	chr3:21789800-21790400	Flanking Active TSS	Fetal Brain Male	brain
38	chr3:21789800-21791600	Active TSS	Brain Angular Gyrus	brain
39	chr3:21789800-21791600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr3:21789800-21793200	Active TSS	Stomach Smooth Muscle	stomach

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