Variant report

Variant	rs73144473
Chromosome Location	chr3:99871036-99871037
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs56273975	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs56313042	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73138669	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73148388	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817478	chr3:99474086-99955548	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv916476	chr3:99478229-100124625	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv869848	chr3:99652246-99904276	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv932634	chr3:99660690-99888854	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1010579	chr3:99660754-99901817	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1008483	chr3:99660754-99903769	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1010897	chr3:99660754-99904783	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1001529	chr3:99661758-99892654	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
9	nsv536665	chr3:99661758-99892654	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
10	nsv591148	chr3:99774720-99905803	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99856000-99877800	Weak transcription	Ovary	ovary
2	chr3:99858600-99877200	Weak transcription	HSMM	muscle
3	chr3:99860200-99874000	Weak transcription	A549	lung
4	chr3:99862200-99874200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:99863400-99872200	Weak transcription	Primary B cells from peripheral blood	blood
6	chr3:99863400-99873800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr3:99863400-99874000	Weak transcription	NHEK	skin
8	chr3:99863600-99874000	Weak transcription	GM12878-XiMat	blood
9	chr3:99863800-99873000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:99863800-99873600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr3:99863800-99874000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr3:99864000-99873400	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr3:99864400-99886600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr3:99864600-99873600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr3:99865000-99873400	Weak transcription	Fetal Intestine Small	intestine
16	chr3:99865000-99894600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:99865400-99873800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:99865600-99898400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr3:99866000-99874000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr3:99866400-99871200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:99866400-99874200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr3:99866600-99871400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr3:99866600-99872600	Strong transcription	Primary T cells from cord blood	blood
24	chr3:99867200-99874000	Weak transcription	K562	blood
25	chr3:99867400-99874000	Weak transcription	Brain Hippocampus Middle	brain
26	chr3:99867600-99874000	Weak transcription	Dnd41	blood
27	chr3:99868000-99897000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr3:99868200-99873200	Weak transcription	Duodenum Mucosa	Duodenum
29	chr3:99868400-99874000	Weak transcription	HepG2	liver
30	chr3:99868800-99873600	Weak transcription	Primary B cells from cord blood	blood
31	chr3:99869000-99871200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:99869000-99873400	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr3:99869000-99873600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr3:99869000-99873600	Weak transcription	Fetal Muscle Trunk	muscle
35	chr3:99869000-99874000	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr3:99869000-99874800	Weak transcription	Thymus	Thymus
37	chr3:99869000-99876400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr3:99869000-99895400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:99869000-99897800	Weak transcription	Pancreas	Pancrea
40	chr3:99869400-99874000	Weak transcription	Fetal Lung	lung
41	chr3:99869600-99871400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr3:99869800-99871800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:99869800-99874200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr3:99870000-99872000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr3:99870200-99871400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr3:99870200-99871400	Enhancers	Psoas Muscle	Psoas
47	chr3:99870200-99871600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr3:99870200-99873600	Weak transcription	NHDF-Ad	bronchial
49	chr3:99870200-99873800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:99870400-99871200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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