Variant report

Variant	esv1796319
Chromosome Location	chr6:81034505-81058025
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	BACH1	chr6:81047978-81048274	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr6:81047866-81047969	K562	blood:	n/a	n/a
3	CEBPB	chr6:81051052-81051360	IMR90	lung:	n/a	chr6:81051065-81051076
4	CHD2	chr6:81047983-81048302	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr6:81052649-81052770	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr6:81048060-81048210	GM12866	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
7	CTCF	chr6:81047796-81047899	GM10248	blood:	n/a	n/a
8	CTCF	chr6:81048018-81048275	GM12891	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
9	CTCF	chr6:81048120-81048270	HCM	heart:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
10	CTCF	chr6:81039931-81040063	Hela-S3	cervix:	n/a	chr6:81039964-81039985
11	CTCF	chr6:81048000-81048150	HFF-Myc	foreskin:	n/a	n/a
12	CTCF	chr6:81048020-81048170	HUVEC	blood vessel:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
13	CTCF	chr6:81039809-81040202	K562	blood:	n/a	chr6:81039964-81039985
14	CTCF	chr6:81039972-81039995	Gliobla	brain:	n/a	n/a
15	CTCF	chr6:81047981-81048254	T-47D	breast:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
16	CTCF	chr6:81048020-81048170	GM12878	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
17	CTCF	chr6:81047980-81048130	HCT-116	colon:	n/a	n/a
18	CTCF	chr6:81044620-81044770	AG10803	skin:	n/a	n/a
19	CTCF	chr6:81048080-81048230	HEK293	kidney:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
20	CTCF	chr6:81048108-81048283	A549	lung:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
21	CTCF	chr6:81048010-81048294	GM19238	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
22	CTCF	chr6:81048080-81048230	GM12871	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
23	CTCF	chr6:81048060-81048210	GM12872	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
24	CTCF	chr6:81048120-81048270	RPTEC	kidney:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
25	CTCF	chr6:81048120-81048270	GM12872	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
26	CTCF	chr6:81048080-81048230	HVMF	connective:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
27	CTCF	chr6:81048000-81048150	WI-38	lung:	n/a	n/a
28	CTCF	chr6:81048049-81048283	HepG2	liver:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
29	CTCF	chr6:81048080-81048230	HFF-Myc	foreskin:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
30	CTCF	chr6:81048100-81048250	GM12873	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
31	CTCF	chr6:81048032-81048263	Fibrobl	skin:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
32	CTCF	chr6:81048024-81048280	Hela-S3	cervix:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
33	CTCF	chr6:81048060-81048210	A549	lung:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
34	CTCF	chr6:81048018-81048312	Medullo	brain:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
35	CTCF	chr6:81048180-81048330	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr6:81048019-81048282	H1-hESC	embryonic stem cell:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
37	CTCF	chr6:81048120-81048270	GM12871	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
38	CTCF	chr6:81048043-81048260	HepG2	liver:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
39	CTCF	chr6:81048003-81048297	MCF-7	breast:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
40	CTCF	chr6:81048060-81048210	GM12867	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
41	CTCF	chr6:81048060-81048210	K562	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
42	CTCF	chr6:81047872-81048436	K562	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
43	CTCF	chr6:81048021-81048282	Spleen_OC	spleen:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
44	CTCF	chr6:81048100-81048250	GM12866	blood:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
45	CTCF	chr6:81048032-81048238	A549	lung:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
46	CTCF	chr6:81047980-81048270	NHLF	lung:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
47	CTCF	chr6:81048080-81048230	HMEC	breast:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
48	CTCF	chr6:81044680-81044830	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr6:81048040-81048190	AG09309	skin:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170
50	CTCF	chr6:81048040-81048190	HBMEC	blood vessel:	n/a	chr6:81048147-81048165 chr6:81048150-81048163 chr6:81048150-81048159 chr6:81048152-81048162 chr6:81048149-81048170

No.	Distal block	Cell Line	Cell type
1	chr6:81032325..81034991-chr6:81050067..81051684,2	K562	blood:
2	chr6:80923846..80924785-chr6:81039854..81040458,2	MCF-7	breast:
3	chr6:81047806..81048624-chr6:81314824..81315362,2	MCF-7	breast:
4	chr6:81047724..81048347-chr6:82463313..82464141,2	MCF-7	breast:
5	chr6:81032325..81034991-chr6:81050067..81051684,2	K562	blood:
6	chr6:81047988..81048553-chr6:81186140..81186935,2	MCF-7	breast:
7	chr6:80842428..80843336-chr6:81048460..81049369,2	MCF-7	breast:
8	chr6:81048632..81050136-chr6:81059450..81061569,2	K562	blood:
9	chr6:81047941..81048548-chr6:82463318..82463845,3	K562	blood:
10	chr6:81047651..81048631-chr6:81237581..81238534,2	MCF-7	breast:
11	chr6:81029449..81030983-chr6:81039020..81041203,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BCKDHB	hsa-miR-1	chr6:81055812-81055831
2	BCKDHB	hsa-miR-1	chr6:81054571-81054592

Variant related genes	Relation type
BCKDHB	TF binding region

Extended variants
information (count: 920 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:920 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16891673	chr6:81034505-81034506	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568314600	chr6:81034509-81034510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370030035	chr6:81034547-81034548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533793062	chr6:81034566-81034567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77843574	chr6:81034568-81034569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs806848	chr6:81034583-81034584	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs140585470	chr6:81034591-81034592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs555809556	chr6:81034658-81034659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs569323754	chr6:81034725-81034726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs806847	chr6:81034730-81034731	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs150404954	chr6:81034746-81034747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs806846	chr6:81034777-81034778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541299126	chr6:81034781-81034782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1535075	chr6:81034806-81034807	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs578089955	chr6:81034851-81034852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10214467	chr6:81034854-81034855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375033544	chr6:81034866-81034867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574424338	chr6:81034880-81034881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73748794	chr6:81034902-81034903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138116364	chr6:81034920-81034921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182252187	chr6:81034935-81034936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs372983239	chr6:81034964-81034965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143830226	chr6:81035028-81035029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527565990	chr6:81035063-81035064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543237003	chr6:81035075-81035076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs3805872	chr6:81035102-81035103	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs570645026	chr6:81035108-81035109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532946857	chr6:81035111-81035112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs806845	chr6:81035173-81035174	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs552004267	chr6:81035235-81035236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116030655	chr6:81035267-81035268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147282518	chr6:81035270-81035271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554929926	chr6:81035304-81035305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs79479028	chr6:81035335-81035336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111327242	chr6:81035449-81035450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558134398	chr6:81035486-81035487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs578131584	chr6:81035493-81035494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs543987394	chr6:81035515-81035516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs806844	chr6:81035547-81035548	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs374542083	chr6:81035602-81035603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs574172078	chr6:81035625-81035626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs537494411	chr6:81035633-81035634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186962374	chr6:81035634-81035635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555476249	chr6:81035639-81035640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs7747016	chr6:81035737-81035738	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs528445592	chr6:81035743-81035744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541331065	chr6:81035771-81035772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs7747327	chr6:81035774-81035775	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567222088	chr6:81035838-81035839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192356665	chr6:81035871-81035872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:81005200-81056200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:81015600-81036400	Weak transcription	Ovary	ovary
3	chr6:81015600-81037400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:81026800-81037400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:81027000-81044600	Weak transcription	Aorta	Aorta
6	chr6:81029400-81038200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr6:81029400-81038600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:81029400-81079600	Weak transcription	HSMM	muscle
9	chr6:81032000-81037600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:81033800-81070200	Weak transcription	Left Ventricle	heart
11	chr6:81034000-81039200	Weak transcription	Esophagus	oesophagus
12	chr6:81035000-81035600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr6:81035200-81036200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:81035200-81039200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr6:81035400-81035600	Enhancers	Fetal Lung	lung
16	chr6:81035400-81035800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:81035400-81035800	Enhancers	NHDF-Ad	bronchial
18	chr6:81035600-81035800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:81035600-81037400	Weak transcription	Fetal Lung	lung
20	chr6:81035600-81037600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:81035800-81036800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:81035800-81037200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:81036200-81037400	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr6:81036600-81041000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr6:81036800-81044600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:81037000-81038400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:81037200-81041000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr6:81037200-81041200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:81037200-81041200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:81037400-81037800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:81037400-81038200	Enhancers	Fetal Lung	lung
32	chr6:81037400-81038600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:81037400-81039600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:81037400-81044800	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr6:81037600-81038200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:81037600-81040600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:81037600-81042000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr6:81037600-81044400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:81037800-81038200	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr6:81037800-81038200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr6:81037800-81038200	Enhancers	Brain Substantia Nigra	brain
42	chr6:81037800-81039800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr6:81038000-81038200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr6:81038000-81038200	Enhancers	Brain Anterior Caudate	brain
45	chr6:81038200-81038600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:81038200-81038800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr6:81038200-81039200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr6:81038200-81039200	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr6:81038200-81039200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr6:81038200-81039200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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