Variant report

Variant	esv3386877
Chromosome Location	chr6:15073957-15074339
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:15065231..15078374-chr6:15243362..15252213,26	MCF-7	breast:
2	chr6:15065449..15068780-chr6:15072645..15074662,4	K562	blood:
3	chr6:15071613..15074171-chr6:15076318..15078190,2	K562	blood:
4	chr6:15069299..15075541-chr6:15075577..15080851,9	K562	blood:
5	chr6:15062551..15066335-chr6:15072410..15076511,4	MCF-7	breast:
6	chr6:15070915..15075463-chr6:15246209..15249841,5	MCF-7	breast:
7	chr6:15070190..15074230-chr6:15074491..15076843,3	MCF-7	breast:
8	chr6:15069314..15074049-chr6:15088016..15092585,9	MCF-7	breast:
9	chr6:15072178..15075145-chr6:15244379..15247154,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000271888	chromatin interactions
ENSG00000234261	chromatin interactions
ENSG00000008083	chromatin interactions
ENSG00000235488	chromatin interactions

Extended variants
information (count: 16 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561856088	chr6:15073960-15073961	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs375192445	chr6:15073988-15073989	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs530793562	chr6:15074017-15074018	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs371819632	chr6:15074067-15074068	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs116592480	chr6:15074094-15074095	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs539624981	chr6:15074095-15074096	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs77475493	chr6:15074162-15074163	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs552690772	chr6:15074171-15074172	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs9383016	chr6:15074186-15074187	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs534931007	chr6:15074195-15074196	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs551272142	chr6:15074219-15074220	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs556045709	chr6:15074227-15074228	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs568666328	chr6:15074286-15074287	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs139592535	chr6:15074317-15074318	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs55999893	chr6:15074319-15074320	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs144278451	chr6:15074320-15074321	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Cancer	16790693	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15043800-15077400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:15058200-15074400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:15067200-15076600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:15067400-15076600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:15067600-15076200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:15068800-15077200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:15069200-15076400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:15072600-15075600	Weak transcription	K562	blood
9	chr6:15073000-15074400	Enhancers	GM12878-XiMat	blood
10	chr6:15073200-15074000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:15073200-15074200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:15073200-15074400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr6:15073200-15075600	Enhancers	Brain Cingulate Gyrus	brain
14	chr6:15073400-15074200	Enhancers	Brain Substantia Nigra	brain
15	chr6:15073600-15074000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr6:15073600-15074000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr6:15073600-15074000	Enhancers	Placenta	Placenta
18	chr6:15073600-15074200	Enhancers	Brain Angular Gyrus	brain
19	chr6:15073600-15074200	Enhancers	Brain Hippocampus Middle	brain
20	chr6:15073600-15074200	Enhancers	HSMMtube	muscle
21	chr6:15073600-15074600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr6:15073600-15074800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:15073600-15075400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr6:15073600-15075400	Enhancers	Brain Anterior Caudate	brain
25	chr6:15073600-15076600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:15073800-15075000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:15073800-15079600	Weak transcription	Stomach Mucosa	stomach
28	chr6:15074000-15075200	Weak transcription	Placenta	Placenta
29	chr6:15074000-15076600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:15074000-15076800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:15074000-15077400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr6:15074200-15075600	Weak transcription	Brain Hippocampus Middle	brain

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