Variant report

Variant	rs7330392
Chromosome Location	chr13:50329800-50329801
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10492591	0.90[AMR][1000 genomes]
rs1127021	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1198315	0.81[AMR][1000 genomes]
rs1198319	0.86[AMR][1000 genomes]
rs1198320	0.86[AMR][1000 genomes]
rs1198322	0.86[AMR][1000 genomes]
rs1198324	0.86[AMR][1000 genomes]
rs1201716	0.86[AMR][1000 genomes]
rs1211304	0.86[AMR][1000 genomes]
rs1407440	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1407441	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1547623	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1570353	0.86[AMR][1000 genomes]
rs1581745	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2025263	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2181185	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2407804	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2897770	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3851162	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4942863	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61961491	0.83[AMR][1000 genomes]
rs7983303	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7984061	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9316474	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9526591	0.89[EUR][1000 genomes]
rs9526593	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9535305	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9535307	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9535310	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9535316	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9535330	0.80[AFR][1000 genomes]
rs9535340	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9535341	0.86[AMR][1000 genomes]
rs9562927	0.86[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7330392	TRIM13	Cis_1M	lymphoblastoid	RTeQTL
rs7330392	KPNA3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50266400-50349000	Weak transcription	Esophagus	oesophagus
2	chr13:50273200-50333800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr13:50290000-50334000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr13:50294400-50333000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr13:50296200-50330400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:50296600-50330400	Weak transcription	Small Intestine	intestine
7	chr13:50296600-50338600	Weak transcription	Ovary	ovary
8	chr13:50300600-50345600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr13:50302800-50333800	Weak transcription	Thymus	Thymus
10	chr13:50303200-50334000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr13:50306000-50351600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr13:50306200-50334200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr13:50306200-50336200	Weak transcription	Adipose Nuclei	Adipose
14	chr13:50306800-50333800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr13:50308000-50356000	Weak transcription	Fetal Kidney	kidney
16	chr13:50315200-50336000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr13:50317600-50343600	Weak transcription	Primary T cells from cord blood	blood
18	chr13:50318800-50333800	Weak transcription	NH-A	brain
19	chr13:50319600-50333600	Weak transcription	Primary hematopoietic stem cells	blood
20	chr13:50319600-50334800	Weak transcription	Fetal Lung	lung
21	chr13:50320000-50333600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr13:50320000-50333600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr13:50320000-50333600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr13:50320400-50336800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr13:50320600-50332200	Weak transcription	Fetal Muscle Leg	muscle
26	chr13:50320600-50332600	Weak transcription	Fetal Brain Female	brain
27	chr13:50320600-50333000	Weak transcription	Fetal Intestine Large	intestine
28	chr13:50320600-50333600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr13:50320600-50333600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr13:50320600-50333600	Weak transcription	Fetal Intestine Small	intestine
31	chr13:50320600-50333800	Weak transcription	Brain Hippocampus Middle	brain
32	chr13:50320600-50333800	Weak transcription	Fetal Stomach	stomach
33	chr13:50320600-50334800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr13:50320600-50334800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr13:50320600-50337400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr13:50320600-50337800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr13:50320800-50333400	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr13:50320800-50333800	Weak transcription	Primary B cells from cord blood	blood
39	chr13:50320800-50333800	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr13:50320800-50340400	Weak transcription	HUVEC	blood vessel
41	chr13:50321000-50331800	Weak transcription	Primary T helper cells fromperipheralblood	blood
42	chr13:50321000-50333400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr13:50321000-50363800	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr13:50321200-50333400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr13:50321200-50333600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr13:50321200-50333800	Weak transcription	Fetal Thymus	thymus
47	chr13:50321200-50333800	Weak transcription	Dnd41	blood
48	chr13:50324400-50333400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr13:50324400-50340400	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr13:50324600-50333400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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