Variant report

Variant	rs35158352
Chromosome Location	chr2:46953763-46953764
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1058157	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1109380	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11676737	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11680875	0.88[ASN][1000 genomes]
rs11695058	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12474201	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12998753	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12998762	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12999586	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13012099	0.82[EUR][1000 genomes]
rs13025595	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13025984	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13031872	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13429704	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17822019	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17822294	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2346878	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2346882	0.81[EUR][1000 genomes]
rs2346883	0.81[EUR][1000 genomes]
rs34401107	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35722922	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs35825831	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3829835	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4356702	0.81[EUR][1000 genomes]
rs4952842	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4952843	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4953419	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4953423	0.82[EUR][1000 genomes]
rs62134772	0.81[EUR][1000 genomes]
rs62134773	0.81[EUR][1000 genomes]
rs6738426	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7562173	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7584870	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7594523	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs897530	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014425	chr2:46670179-47033417	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv535678	chr2:46670179-47033417	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv873996	chr2:46670941-47065227	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv533112	chr2:46800828-46959977	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
6	nsv873997	chr2:46821640-46984627	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1013079	chr2:46949337-46998417	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46945400-46985400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr2:46947000-46954600	Weak transcription	HUVEC	blood vessel
3	chr2:46947000-46954800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr2:46947600-46975600	Weak transcription	HSMM	muscle
5	chr2:46948000-46954600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr2:46948000-46954600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr2:46948000-46954600	Weak transcription	Thymus	Thymus
8	chr2:46948200-46954400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:46948200-46954600	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr2:46948200-46954600	Weak transcription	Left Ventricle	heart
11	chr2:46948200-46954600	Weak transcription	Right Ventricle	heart
12	chr2:46948200-46954800	Weak transcription	Pancreas	Pancrea
13	chr2:46948200-46955000	Weak transcription	Ovary	ovary
14	chr2:46948200-46955800	Weak transcription	Lung	lung
15	chr2:46948200-46956600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:46948200-46962000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:46948200-46964400	Weak transcription	NHEK	skin
18	chr2:46948200-46967400	Weak transcription	Esophagus	oesophagus
19	chr2:46948200-46974600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr2:46948200-46977200	Weak transcription	Aorta	Aorta
21	chr2:46948400-46954600	Weak transcription	Stomach Smooth Muscle	stomach
22	chr2:46948400-46954800	Weak transcription	Primary B cells from peripheral blood	blood
23	chr2:46948400-46961600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr2:46948600-46954600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr2:46948600-46964200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:46948600-46964400	Weak transcription	NH-A	brain
27	chr2:46948600-46974400	Weak transcription	Fetal Stomach	stomach
28	chr2:46948800-46955200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:46949000-46954600	Weak transcription	Psoas Muscle	Psoas
30	chr2:46949000-46954600	Weak transcription	Small Intestine	intestine
31	chr2:46949000-46954800	Weak transcription	Brain Hippocampus Middle	brain
32	chr2:46949400-46953800	Enhancers	HepG2	liver
33	chr2:46949600-46958400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr2:46949800-46954600	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr2:46950000-46954600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr2:46950800-46954600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr2:46950800-46958200	Weak transcription	NHLF	lung
38	chr2:46950800-46975400	Weak transcription	Fetal Lung	lung
39	chr2:46951400-46954600	Weak transcription	Fetal Heart	heart
40	chr2:46951400-46962200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr2:46951600-46954600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr2:46951600-46954600	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr2:46951800-46954600	Weak transcription	Colon Smooth Muscle	Colon
44	chr2:46951800-46959000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:46952000-46954400	Weak transcription	Osteobl	bone
46	chr2:46952000-46954600	Weak transcription	Primary T cells from cord blood	blood
47	chr2:46952000-46954600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr2:46952000-46955200	Weak transcription	Primary B cells from cord blood	blood
49	chr2:46952000-46961800	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr2:46952200-46954200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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