Variant report

Variant	rs13093776
Chromosome Location	chr3:99842140-99842141
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:99840756..99842324-chr3:99842654..99845217,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1017968	0.85[EUR][1000 genomes]
rs1021341	0.83[EUR][1000 genomes]
rs11537816	0.81[AMR][1000 genomes]
rs13064704	0.84[EUR][1000 genomes]
rs13069311	0.84[EUR][1000 genomes]
rs13323143	0.87[EUR][1000 genomes]
rs1489816	0.84[EUR][1000 genomes]
rs17393059	0.81[EUR][1000 genomes]
rs2291494	0.84[EUR][1000 genomes]
rs2291495	0.84[EUR][1000 genomes]
rs28503408	0.83[EUR][1000 genomes]
rs34922392	0.83[EUR][1000 genomes]
rs35669453	0.84[EUR][1000 genomes]
rs35844878	0.85[EUR][1000 genomes]
rs35885423	0.88[EUR][1000 genomes]
rs62285461	0.83[EUR][1000 genomes]
rs62285462	0.84[EUR][1000 genomes]
rs62285471	0.88[EUR][1000 genomes]
rs62285473	0.88[EUR][1000 genomes]
rs62285478	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6790535	0.85[EUR][1000 genomes]
rs6790877	0.84[EUR][1000 genomes]
rs6799379	0.81[EUR][1000 genomes]
rs6802422	0.84[EUR][1000 genomes]
rs6806178	0.81[EUR][1000 genomes]
rs71313585	0.81[EUR][1000 genomes]
rs7620228	0.85[EUR][1000 genomes]
rs7627991	0.88[EUR][1000 genomes]
rs923470	0.81[EUR][1000 genomes]
rs923471	0.81[EUR][1000 genomes]
rs9289985	0.81[AMR][1000 genomes]
rs9814359	0.83[EUR][1000 genomes]
rs9815439	0.83[EUR][1000 genomes]
rs9823908	0.85[EUR][1000 genomes]
rs9828079	0.86[EUR][1000 genomes]
rs9833980	0.84[EUR][1000 genomes]
rs9837602	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9841186	0.85[EUR][1000 genomes]
rs9851645	0.83[EUR][1000 genomes]
rs9854260	0.81[AMR][1000 genomes]
rs9864437	0.84[EUR][1000 genomes]
rs9875878	0.81[AMR][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:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:99795800-99866600	Weak transcription	Primary T cells from cord blood	blood
2	chr3:99825200-99844000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:99825200-99844200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr3:99826600-99862600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:99839000-99842800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:99839400-99842400	Weak transcription	Fetal Heart	heart
7	chr3:99839800-99842200	Weak transcription	Ovary	ovary
8	chr3:99839800-99842400	Weak transcription	Left Ventricle	heart
9	chr3:99839800-99843200	Weak transcription	Lung	lung
10	chr3:99840000-99842400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr3:99840400-99844600	Enhancers	Fetal Muscle Leg	muscle
12	chr3:99840600-99843200	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr3:99840800-99842200	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:99841000-99843800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:99841200-99842200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr3:99841200-99842400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr3:99841200-99842600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr3:99841200-99843200	Weak transcription	Spleen	Spleen
19	chr3:99841200-99843400	Enhancers	Brain Cingulate Gyrus	brain
20	chr3:99841200-99843600	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr3:99841200-99846000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:99841200-99846800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:99841400-99842400	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr3:99841400-99842400	Weak transcription	Aorta	Aorta
25	chr3:99841400-99842600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr3:99841400-99843000	Weak transcription	Fetal Intestine Small	intestine
27	chr3:99841600-99842600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr3:99841800-99842200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr3:99841800-99842400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr3:99842000-99842400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:99842000-99842400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr3:99842000-99844000	Enhancers	Right Atrium	heart
33	chr3:99842000-99844200	Enhancers	Right Ventricle	heart
34	chr3:99842000-99844600	Enhancers	Psoas Muscle	Psoas

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