Variant report

Variant	esv3473873
Chromosome Location	chr6:29650420-29651090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:29637497..29639601-chr6:29651008..29653048,2	K562	blood:

Variant related genes	Relation type
ENSG00000204655	chromatin interactions

Extended variants
information (count: 32 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372498418	chr6:29650426-29650427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189302335	chr6:29650434-29650435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546042792	chr6:29650437-29650438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113822137	chr6:29650461-29650462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs2474100	chr6:29650462-29650463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs28370966	chr6:29650465-29650466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368412678	chr6:29650466-29650467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11758488	chr6:29650471-29650472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571761788	chr6:29650478-29650479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559760970	chr6:29650532-29650533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527419416	chr6:29650566-29650567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144157432	chr6:29650569-29650570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs28866836	chr6:29650646-29650647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371737449	chr6:29650678-29650679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371604063	chr6:29650679-29650680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11758534	chr6:29650681-29650682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs148925268	chr6:29650693-29650694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528582891	chr6:29650734-29650735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs9257975	chr6:29650754-29650755	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs3129050	chr6:29650763-29650764	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs9257976	chr6:29650764-29650765	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs3129049	chr6:29650803-29650804	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
23	rs3131844	chr6:29650837-29650838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2894112	chr6:29650842-29650843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs182148249	chr6:29650896-29650897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs3117291	chr6:29650905-29650906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs187269856	chr6:29650910-29650911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541410355	chr6:29650968-29650969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557185609	chr6:29650988-29650989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115775459	chr6:29650994-29650995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549944118	chr6:29651037-29651038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2535237	chr6:29651073-29651074	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:107)

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
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29625000-29663600	Weak transcription	Right Atrium	heart
2	chr6:29646000-29651400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr6:29646200-29651400	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr6:29646200-29651400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr6:29646800-29651400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:29647000-29651400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr6:29647000-29651400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:29647400-29651600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:29648000-29651400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:29648200-29651400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr6:29648800-29651400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:29648800-29662600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:29649000-29651200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:29649200-29652000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr6:29649200-29655000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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