Variant report

Variant	rs9535340
Chromosome Location	chr13:50357873-50357874
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:50356308..50362290-chr13:50362376..50368273,10	K562	blood:
2	chr13:50352653..50354938-chr13:50357340..50359158,2	MCF-7	breast:
3	chr13:50351267..50358317-chr13:50361760..50368621,11	MCF-7	breast:

Variant related genes	Relation type
ENSG00000102753	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1009333	0.82[EUR][1000 genomes]
rs10492591	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1127021	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1198315	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1198319	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1198320	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1198322	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1198324	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1201716	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1211304	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1407440	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1407441	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1547623	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1570353	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1581745	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1885724	0.83[AFR][1000 genomes]
rs2025263	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2181185	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2407804	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2897770	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3851162	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4942863	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4942866	0.81[AMR][1000 genomes]
rs61961491	0.81[AMR][1000 genomes]
rs7330392	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7983303	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7984061	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9316474	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9526591	0.91[EUR][1000 genomes]
rs9526593	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9535305	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9535307	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9535310	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9535316	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9535330	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs9535341	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9562927	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[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:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9535340	TRIM13	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50321000-50363800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr13:50336200-50364800	Weak transcription	Fetal Intestine Small	intestine
3	chr13:50336800-50364600	Weak transcription	NHLF	lung
4	chr13:50339200-50358800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr13:50339800-50358800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr13:50341200-50359400	Weak transcription	Primary hematopoietic stem cells	blood
7	chr13:50349600-50365400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr13:50349600-50365400	Weak transcription	Lung	lung
9	chr13:50350600-50358600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr13:50351200-50364200	Weak transcription	HSMM	muscle
11	chr13:50351200-50364600	Weak transcription	HSMMtube	muscle
12	chr13:50351400-50362600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr13:50351400-50363000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr13:50351600-50359200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:50351600-50359200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr13:50351600-50360800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr13:50351600-50363800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr13:50351800-50359400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr13:50351800-50363800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr13:50351800-50364000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr13:50352000-50365200	Weak transcription	Fetal Thymus	thymus
22	chr13:50352400-50364400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr13:50352600-50358200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr13:50352600-50363800	Weak transcription	Pancreas	Pancrea
25	chr13:50352600-50363800	Weak transcription	Thymus	Thymus
26	chr13:50352600-50364800	Weak transcription	A549	lung
27	chr13:50353000-50358000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr13:50353000-50359200	Weak transcription	Liver	Liver
29	chr13:50353000-50359800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr13:50353000-50360400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr13:50353000-50363800	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr13:50353000-50363800	Weak transcription	Small Intestine	intestine
33	chr13:50353200-50360800	Weak transcription	Primary T cells from cord blood	blood
34	chr13:50353800-50363800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr13:50354200-50363800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr13:50354200-50363800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr13:50354200-50364400	Weak transcription	Right Atrium	heart
38	chr13:50354200-50365400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr13:50354400-50361200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr13:50354400-50362600	Weak transcription	Dnd41	blood
41	chr13:50354400-50363200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr13:50354400-50363600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr13:50354400-50365400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr13:50354600-50360400	Weak transcription	Primary T helper cells fromperipheralblood	blood
45	chr13:50354800-50359200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr13:50354800-50362400	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr13:50355000-50361200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr13:50355200-50361200	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr13:50355600-50360800	Weak transcription	Fetal Lung	lung
50	chr13:50355800-50358600	Weak transcription	Colon Smooth Muscle	Colon

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