Variant report

Variant	rs62156265
Chromosome Location	chr2:98964651-98964652
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1010387	1.00[AFR][1000 genomes]
rs11684812	1.00[AFR][1000 genomes]
rs11684899	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11691306	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs17427608	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17427825	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17428745	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17428990	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17429379	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17500406	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17501094	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62155312	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62155317	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62155347	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62155354	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62155355	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62155358	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156266	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156268	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156305	0.82[EUR][1000 genomes]
rs62156346	1.00[AFR][1000 genomes]
rs62156686	1.00[AFR][1000 genomes]
rs62156724	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62156744	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62157892	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62157901	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62157907	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62157908	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62157916	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72817785	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72817792	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72817793	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs72819903	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72819917	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72819919	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72819921	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72819925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72819927	1.00[AMR][1000 genomes];1.00[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	nsv518056	chr2:98586842-99156296	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh 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
2	nsv1004082	chr2:98792256-98967681	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv535833	chr2:98792256-98967681	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1008645	chr2:98915767-99010743	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1010466	chr2:98938886-98998109	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv1013617	chr2:98943377-99004173	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:98962400-98964800	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr2:98962600-98965000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
3	chr2:98962600-98965200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:98962600-98965200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
5	chr2:98962800-98964800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
6	chr2:98962800-98964800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
7	chr2:98962800-98964800	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
8	chr2:98962800-98964800	Bivalent Enhancer	Spleen	Spleen
9	chr2:98962800-98965000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
10	chr2:98962800-98965000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
11	chr2:98962800-98965200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
12	chr2:98963200-98964800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
13	chr2:98963200-98964800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:98963400-98964800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
15	chr2:98963400-98965000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr2:98963400-98965600	Enhancers	Fetal Brain Male	brain
17	chr2:98963800-98964800	Bivalent Enhancer	Fetal Stomach	stomach
18	chr2:98964000-98964800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:98964000-98964800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr2:98964000-98964800	Bivalent Enhancer	Brain Angular Gyrus	brain
21	chr2:98964000-98964800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
22	chr2:98964200-98964800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
23	chr2:98964200-98964800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr2:98964200-98964800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
25	chr2:98964200-98964800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
26	chr2:98964200-98964800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr2:98964200-98964800	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
28	chr2:98964200-98964800	Bivalent Enhancer	Brain Substantia Nigra	brain
29	chr2:98964200-98965200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
30	chr2:98964200-98965400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
31	chr2:98964200-98965600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:98964400-98964800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
33	chr2:98964400-98964800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
34	chr2:98964400-98964800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
35	chr2:98964400-98964800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
36	chr2:98964400-98964800	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
37	chr2:98964400-98965000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
38	chr2:98964400-98965200	Flanking Active TSS	Fetal Brain Female	brain
39	chr2:98964600-98964800	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:98964600-98964800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:98964600-98964800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
42	chr2:98964600-98964800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr2:98964600-98964800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr2:98964600-98964800	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
45	chr2:98964600-98964800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
46	chr2:98964600-98965000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:98964600-98965200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell

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