Variant report

Variant	rs73232931
Chromosome Location	chr3:140957177-140957178
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1871278	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2291040	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55655840	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55839795	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55877951	0.84[EUR][1000 genomes]
rs56293064	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73232934	0.92[EUR][1000 genomes]
rs73236512	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73236514	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73236515	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73236516	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73236517	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs73236521	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460870	chr3:140938546-141005574	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv591892	chr3:140938546-141005574	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140951600-140959000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:140951600-140979000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:140951800-140958800	Weak transcription	Osteobl	bone
4	chr3:140951800-140959000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:140951800-140960200	Weak transcription	Esophagus	oesophagus
6	chr3:140951800-140960400	Weak transcription	Brain Substantia Nigra	brain
7	chr3:140951800-140962000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:140951800-140962200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:140952000-140958400	Weak transcription	Fetal Kidney	kidney
10	chr3:140952000-140959000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr3:140952000-140959000	Weak transcription	Placenta	Placenta
12	chr3:140952000-140959600	Weak transcription	Rectal Smooth Muscle	rectum
13	chr3:140952000-140962000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr3:140952200-140958000	Weak transcription	Right Ventricle	heart
15	chr3:140952400-140959600	Weak transcription	Colon Smooth Muscle	Colon
16	chr3:140952600-140957800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:140953000-140958800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr3:140953200-140959200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:140953400-140958800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr3:140953600-140959600	Genic enhancers	Fetal Thymus	thymus
21	chr3:140953600-140960200	Weak transcription	Spleen	Spleen
22	chr3:140953800-140958400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr3:140954000-140959200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr3:140954200-140959200	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr3:140954800-140957200	Genic enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr3:140954800-140957200	Enhancers	Primary hematopoietic stem cells	blood
27	chr3:140954800-140958600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr3:140955000-140959400	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr3:140955000-140959600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:140955000-140960200	Weak transcription	Adipose Nuclei	Adipose
31	chr3:140955000-140960600	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr3:140955000-140961800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr3:140955200-140958200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr3:140955200-140958200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:140955200-140959000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr3:140955200-140962000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr3:140955200-140980600	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr3:140955400-140957400	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr3:140955400-140959000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:140955400-140968400	Genic enhancers	Dnd41	blood
41	chr3:140955400-140985800	Weak transcription	Duodenum Mucosa	Duodenum
42	chr3:140955600-140959800	Weak transcription	Fetal Intestine Large	intestine
43	chr3:140956000-140957600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr3:140956000-140957800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr3:140956000-140959400	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr3:140956200-140957800	Enhancers	Brain Cingulate Gyrus	brain
47	chr3:140956200-140962600	Enhancers	Fetal Brain Male	brain
48	chr3:140956400-140957200	Flanking Active TSS	Primary T cells from cord blood	blood
49	chr3:140956400-140957200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr3:140956400-140957200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle

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