Variant report

Variant	nsv981124
Chromosome Location	chr6:29384962-29385549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUND	chr6:29385433-29385490	K562	blood:	n/a	n/a

Variant related genes	Relation type
OR12D1	TF binding region

Extended variants
information (count: 27 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150639548	chr6:29384966-29384967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143768233	chr6:29385015-29385016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs566716172	chr6:29385031-29385032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs386698369	chr6:29385054-29385055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114824035	chr6:29385056-29385057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575461671	chr6:29385092-29385093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs116564057	chr6:29385123-29385124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200934193	chr6:29385134-29385135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201775217	chr6:29385174-29385175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554412673	chr6:29385190-29385191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17839876	chr6:29385198-29385199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs146371483	chr6:29385226-29385227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs3131024	chr6:29385237-29385238	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs139721570	chr6:29385245-29385246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs17177563	chr6:29385275-29385276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562754464	chr6:29385276-29385277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531578945	chr6:29385278-29385279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145430702	chr6:29385329-29385330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148823399	chr6:29385342-29385343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115669706	chr6:29385350-29385351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76142796	chr6:29385388-29385389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577494892	chr6:29385441-29385442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142512628	chr6:29385442-29385443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114550211	chr6:29385446-29385447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371086776	chr6:29385485-29385486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552487089	chr6:29385514-29385515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs118172403	chr6:29385547-29385548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	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
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
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	19571809	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	21509527	CNVD
Schizophrenia	23813976	CNVD
Melanoma	17363583	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29381600-29386600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:29385200-29385600	Enhancers	Pancreas	Pancrea

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