Variant report

Variant	rs4150656
Chromosome Location	chr11:18375368-18375369
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11024610	0.83[AFR][1000 genomes]
rs11024611	0.83[AFR][1000 genomes]
rs11024612	0.83[AFR][1000 genomes]
rs11024615	0.83[AFR][1000 genomes]
rs11024619	0.83[AFR][1000 genomes]
rs11024625	0.86[AFR][1000 genomes]
rs12221676	0.86[AFR][1000 genomes]
rs12224608	0.80[AFR][1000 genomes]
rs1869786	0.83[AFR][1000 genomes]
rs1869787	0.83[AFR][1000 genomes]
rs3781944	0.83[AFR][1000 genomes]
rs4150530	0.85[AFR][1000 genomes]
rs4150572	0.86[AFR][1000 genomes]
rs4150626	0.86[AFR][1000 genomes]
rs4150635	0.85[AFR][1000 genomes]
rs4237721	0.86[AFR][1000 genomes]
rs4344464	0.86[AFR][1000 genomes]
rs4366463	0.83[AFR][1000 genomes]
rs4757642	0.86[AFR][1000 genomes]
rs7113249	0.83[AFR][1000 genomes]
rs7122032	0.83[AFR][1000 genomes]
rs73430881	0.83[AFR][1000 genomes]
rs73430888	0.83[AFR][1000 genomes]
rs73430894	0.83[AFR][1000 genomes]
rs73432712	0.83[AFR][1000 genomes]
rs73434649	0.86[AFR][1000 genomes]
rs9783296	0.91[AFR][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	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats 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 miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv933836	chr11:18300254-18440933	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv553633	chr11:18311701-19058451	Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
4	nsv1047049	chr11:18359702-18520008	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	nsv540955	chr11:18359702-18520008	Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18345000-18383200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:18345000-18405000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:18346800-18382800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:18346800-18390400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr11:18347000-18387400	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr11:18351200-18387000	Weak transcription	Stomach Mucosa	stomach
7	chr11:18352400-18389000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:18354400-18389400	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr11:18357000-18389200	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr11:18357200-18379600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr11:18360000-18382200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr11:18361800-18391600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:18363000-18390200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:18363200-18379400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr11:18363200-18393000	Weak transcription	Fetal Heart	heart
16	chr11:18365800-18381400	Weak transcription	Pancreas	Pancrea
17	chr11:18366600-18381400	Weak transcription	Gastric	stomach
18	chr11:18367200-18375400	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr11:18367600-18390000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr11:18368000-18376000	Weak transcription	Right Ventricle	heart
21	chr11:18368000-18382400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr11:18368200-18375400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:18368200-18379400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr11:18368200-18379800	Weak transcription	Fetal Brain Male	brain
25	chr11:18368600-18381400	Weak transcription	Spleen	Spleen
26	chr11:18369600-18379600	Weak transcription	Colon Smooth Muscle	Colon
27	chr11:18369600-18385800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:18369800-18377000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr11:18369800-18379600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
30	chr11:18369800-18380600	Weak transcription	NHLF	lung
31	chr11:18370000-18377400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr11:18370000-18378600	Weak transcription	HepG2	liver
33	chr11:18370000-18379200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:18370000-18379200	Weak transcription	Rectal Smooth Muscle	rectum
35	chr11:18370200-18379800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr11:18370400-18377400	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr11:18370400-18380000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr11:18370600-18379800	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr11:18371200-18377200	Weak transcription	Brain Cingulate Gyrus	brain
40	chr11:18371400-18376000	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr11:18371400-18376400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:18371400-18377200	Weak transcription	Stomach Smooth Muscle	stomach
43	chr11:18371800-18375600	Weak transcription	NH-A	brain
44	chr11:18371800-18377200	Weak transcription	Fetal Lung	lung
45	chr11:18371800-18377400	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr11:18372800-18387200	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr11:18373200-18376000	Strong transcription	Hela-S3	cervix
48	chr11:18373200-18386000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr11:18373200-18388200	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr11:18373200-18389200	Strong transcription	HUES48 Cell Line	embryonic stem cell

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