Variant report

Variant	rs9535330
Chromosome Location	chr13:50336020-50336021
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 2 )

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

rs_ID	r²[population]
rs1547623	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs1581745	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs2181185	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs2407804	0.85[AFR][1000 genomes]
rs2897770	0.80[EUR][1000 genomes]
rs3851162	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs4942863	0.83[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs7330392	0.80[AFR][1000 genomes]
rs7983303	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs7984061	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs9316474	0.85[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs9535316	0.84[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs9535340	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900072	chr13:50266109-50381016	Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv900073	chr13:50286218-50381016	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv1818134	chr13:50306897-50374102	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv900074	chr13:50317104-50381016	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv1038	chr13:50324773-50359990	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv900075	chr13:50331992-50376858	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs9535330	TRIM13	Cis_1M	lymphoblastoid	RTeQTL
rs9535330	KPNA3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50266400-50349000	Weak transcription	Esophagus	oesophagus
2	chr13:50296600-50338600	Weak transcription	Ovary	ovary
3	chr13:50300600-50345600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr13:50306000-50351600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr13:50306200-50336200	Weak transcription	Adipose Nuclei	Adipose
6	chr13:50308000-50356000	Weak transcription	Fetal Kidney	kidney
7	chr13:50317600-50343600	Weak transcription	Primary T cells from cord blood	blood
8	chr13:50320400-50336800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr13:50320600-50337400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:50320600-50337800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr13:50320800-50340400	Weak transcription	HUVEC	blood vessel
12	chr13:50321000-50363800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr13:50324400-50340400	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr13:50324600-50350800	Weak transcription	HSMM	muscle
15	chr13:50324600-50351000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr13:50324800-50338600	Weak transcription	Right Atrium	heart
17	chr13:50326200-50349000	Weak transcription	Left Ventricle	heart
18	chr13:50328200-50338600	Weak transcription	Right Ventricle	heart
19	chr13:50328400-50338600	Weak transcription	Pancreas	Pancrea
20	chr13:50328400-50349000	Weak transcription	Lung	lung
21	chr13:50328600-50349000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr13:50330800-50349000	Weak transcription	HepG2	liver
23	chr13:50333400-50338800	Weak transcription	Fetal Heart	heart
24	chr13:50333600-50336200	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr13:50333800-50336600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
26	chr13:50334000-50338000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:50334000-50352200	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr13:50334200-50351200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:50334400-50337400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr13:50334400-50350800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr13:50334400-50351400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr13:50334600-50336600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:50334600-50350200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr13:50334800-50336400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr13:50334800-50336600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr13:50334800-50337600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr13:50335000-50336200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr13:50335000-50336600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
39	chr13:50335000-50356400	Weak transcription	Primary B cells from cord blood	blood
40	chr13:50335200-50337800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr13:50335200-50339800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:50335200-50341800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr13:50335200-50342800	Weak transcription	GM12878-XiMat	blood
44	chr13:50335200-50347200	Weak transcription	Primary B cells from peripheral blood	blood
45	chr13:50335200-50349400	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr13:50335400-50337200	Weak transcription	Dnd41	blood
47	chr13:50335400-50339800	Weak transcription	Primary hematopoietic stem cells	blood
48	chr13:50335400-50339800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr13:50335400-50340000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr13:50335400-50343000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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