Variant report

Variant	rs11835141
Chromosome Location	chr12:12688788-12688789
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:12684001..12705444-chr12:12707828..12718639,50	MCF-7	breast:
2	chr12:12602118..12604673-chr12:12687247..12689420,2	MCF-7	breast:
3	chr12:12685312..12688917-chr12:12690468..12693651,8	MCF-7	breast:
4	chr12:12688605..12691536-chr12:12762054..12764846,3	MCF-7	breast:
5	chr12:12681668..12683344-chr12:12686468..12688798,2	MCF-7	breast:
6	chr12:12676154..12677988-chr12:12685954..12688802,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111269	Chromatin interaction
ENSG00000111266	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11834653	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11835684	1.00[AMR][1000 genomes]
rs59272770	1.00[AMR][1000 genomes]
rs60014612	1.00[AMR][1000 genomes]
rs60117219	1.00[AMR][1000 genomes]
rs60402543	1.00[AMR][1000 genomes]
rs61082937	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758295	chr12:12620654-12783124	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv2759880	chr12:12620654-12783124	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv898811	chr12:12655443-12928295	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12664000-12690400	Weak transcription	NHLF	lung
2	chr12:12672800-12691200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr12:12673000-12690200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:12674200-12691200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr12:12681400-12693600	Weak transcription	Lung	lung
6	chr12:12682200-12691400	Weak transcription	Adipose Nuclei	Adipose
7	chr12:12682200-12693000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr12:12682400-12689000	Enhancers	Fetal Intestine Small	intestine
9	chr12:12683400-12693600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:12683800-12688800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr12:12685000-12692600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr12:12685400-12689000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr12:12685400-12689600	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr12:12685600-12688800	Enhancers	Fetal Muscle Leg	muscle
15	chr12:12685800-12689200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr12:12686200-12689000	Enhancers	Primary T helper cells PMA-I stimulated	--
17	chr12:12686200-12689600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr12:12686600-12692200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr12:12686600-12693600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr12:12686600-12701000	Weak transcription	HSMM	muscle
21	chr12:12686600-12703200	Weak transcription	NH-A	brain
22	chr12:12686600-12708000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr12:12686600-12711400	Weak transcription	Esophagus	oesophagus
24	chr12:12686800-12691000	Weak transcription	Brain Cingulate Gyrus	brain
25	chr12:12686800-12712200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:12686800-12712600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:12687000-12691000	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr12:12687000-12691200	Weak transcription	Brain Anterior Caudate	brain
29	chr12:12687200-12688800	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:12687200-12689000	Enhancers	Fetal Heart	heart
31	chr12:12687200-12689200	Enhancers	Liver	Liver
32	chr12:12687200-12692000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr12:12687200-12693800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr12:12687200-12698400	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr12:12687200-12708000	Weak transcription	Right Ventricle	heart
36	chr12:12687200-12711600	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr12:12687200-12712600	Weak transcription	Aorta	Aorta
38	chr12:12687400-12689400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr12:12687400-12691000	Weak transcription	Psoas Muscle	Psoas
40	chr12:12687400-12691000	Weak transcription	Thymus	Thymus
41	chr12:12687400-12691200	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:12687400-12691400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr12:12687400-12691600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr12:12687400-12691600	Weak transcription	Stomach Smooth Muscle	stomach
45	chr12:12687400-12692800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr12:12687400-12694000	Weak transcription	Fetal Stomach	stomach
47	chr12:12687400-12694200	Weak transcription	Placenta	Placenta
48	chr12:12687400-12706400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr12:12687400-12708000	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr12:12687400-12708000	Weak transcription	H9 Cell Line	embryonic stem cell

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