Variant report

Variant	rs11886780
Chromosome Location	chr2:37112799-37112800
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:37112041..37114418-chr22:37594275..37597076,2	MCF-7	breast:
2	chr2:37112252..37114608-chr2:37115570..37119781,3	MCF-7	breast:
3	chr2:37111890..37113424-chr2:37118017..37119870,2	K562	blood:

Variant related genes	Relation type
ENSG00000133466	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11904027	1.00[EUR][1000 genomes]
rs13421441	1.00[EUR][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	nsv1004483	chr2:36875235-37356812	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv535644	chr2:36875235-37356812	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv428395	chr2:36990348-37300352	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv456363	chr2:37109281-37235324	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
5	nsv581470	chr2:37109281-37235324	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37067600-37146200	Weak transcription	Psoas Muscle	Psoas
2	chr2:37075600-37139200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:37077000-37116200	Weak transcription	Hela-S3	cervix
4	chr2:37077000-37116200	Weak transcription	NHLF	lung
5	chr2:37077200-37144400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr2:37077400-37136600	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:37078200-37118400	Weak transcription	Fetal Brain Male	brain
8	chr2:37082200-37115600	Weak transcription	Stomach Mucosa	stomach
9	chr2:37087400-37146200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:37090800-37114200	Strong transcription	Primary B cells from peripheral blood	blood
11	chr2:37091000-37114000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:37091200-37114400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr2:37092800-37115600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:37094200-37113400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr2:37094400-37154200	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr2:37096400-37117000	Weak transcription	K562	blood
17	chr2:37096400-37143800	Weak transcription	Fetal Kidney	kidney
18	chr2:37096800-37154400	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr2:37099000-37116800	Weak transcription	A549	lung
20	chr2:37099200-37140200	Weak transcription	Colonic Mucosa	Colon
21	chr2:37100400-37116800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr2:37101800-37119200	Weak transcription	GM12878-XiMat	blood
23	chr2:37102400-37114200	Weak transcription	NHDF-Ad	bronchial
24	chr2:37103800-37113400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr2:37103800-37117200	Weak transcription	HSMMtube	muscle
26	chr2:37103800-37121400	Weak transcription	Small Intestine	intestine
27	chr2:37103800-37146200	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr2:37104200-37117800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr2:37105000-37152600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr2:37105000-37164600	Weak transcription	Lung	lung
31	chr2:37105200-37115200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr2:37105200-37116600	Weak transcription	NHEK	skin
33	chr2:37105200-37117000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr2:37105200-37117200	Weak transcription	HMEC	breast
35	chr2:37105200-37118400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr2:37105200-37125400	Weak transcription	Brain Hippocampus Middle	brain
37	chr2:37105200-37136200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:37105200-37139200	Weak transcription	Aorta	Aorta
39	chr2:37105200-37141200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr2:37105200-37144000	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr2:37105200-37154400	Weak transcription	Esophagus	oesophagus
42	chr2:37105200-37157800	Weak transcription	Pancreas	Pancrea
43	chr2:37105200-37164600	Weak transcription	Spleen	Spleen
44	chr2:37105800-37116800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:37105800-37146400	Weak transcription	Right Ventricle	heart
46	chr2:37106800-37113800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr2:37107200-37114000	Strong transcription	Primary neutrophils fromperipheralblood	blood
48	chr2:37107200-37115800	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr2:37107400-37114000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:37107400-37114200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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