Variant report

Variant	nsv934064
Chromosome Location	chr6:146007547-146044233
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	ARID3A	chr6:146012166-146012273	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:146025299-146025674	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:146025333-146025658	K562	blood:	n/a	n/a
4	CEBPB	chr6:146029214-146029500	HepG2	liver:	n/a	chr6:146029348-146029359
5	CEBPB	chr6:146026599-146026702	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr6:146029231-146029481	IMR90	lung:	n/a	chr6:146029348-146029359
7	CEBPB	chr6:146020610-146021139	IMR90	lung:	n/a	chr6:146020752-146020765
8	CEBPB	chr6:146029276-146029423	A549	lung:	n/a	chr6:146029348-146029359
9	CEBPB	chr6:146029226-146029412	K562	blood:	n/a	chr6:146029348-146029359
10	CEBPB	chr6:146029248-146029395	H1-hESC	embryonic stem cell:	n/a	chr6:146029348-146029359
11	CEBPB	chr6:146026533-146027049	IMR90	lung:	n/a	n/a
12	CHD2	chr6:146030526-146030548	K562	blood:	n/a	n/a
13	CTCF	chr6:146025425-146025615	K562	blood:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
14	CTCF	chr6:146025560-146025710	HVMF	connective:	n/a	n/a
15	CTCF	chr6:146025380-146025530	GM12878	blood:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
16	CTCF	chr6:146025340-146025490	HCT-116	colon:	n/a	n/a
17	CTCF	chr6:146025489-146025530	Lung_OC	lung:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
18	CTCF	chr6:146024700-146024850	AG10803	skin:	n/a	n/a
19	CTCF	chr6:146025520-146025670	HCM	heart:	n/a	n/a
20	CTCF	chr6:146025420-146025570	AG09309	skin:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
21	CTCF	chr6:146025400-146025550	GM12874	blood:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
22	CTCF	chr6:146025320-146025470	GM12878	blood:	n/a	n/a
23	CTCF	chr6:146025660-146025810	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr6:146025440-146025590	GM12870	blood:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
25	CTCF	chr6:146025740-146025890	SAEC	small airway:	n/a	n/a
26	CTCF	chr6:146025800-146025950	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr6:146025340-146025490	MCF-7	breast:	n/a	n/a
28	CTCF	chr6:146025380-146025530	K562	blood:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
29	CTCF	chr6:146025420-146025570	GM12875	blood:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
30	CTCF	chr6:146025306-146025346	Medullo	brain:	n/a	n/a
31	CTCF	chr6:146025233-146025780	HCT-116	colon:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
32	CTCF	chr6:146025460-146025610	HPF	lung:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
33	CTCF	chr6:146025754-146025856	K562	blood:	n/a	n/a
34	CTCF	chr6:146025720-146025870	AG04449	skin:	n/a	n/a
35	CTCF	chr6:146025440-146025590	HPF	lung:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
36	CTCF	chr6:146025140-146025290	BJ	skin:	n/a	n/a
37	CTCF	chr6:146025720-146025870	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr6:146025351-146025357	Medullo	brain:	n/a	n/a
39	CTCF	chr6:146025660-146025810	A549	lung:	n/a	n/a
40	CTCF	chr6:146025760-146025910	GM12871	blood:	n/a	n/a
41	CTCF	chr6:146025420-146025570	Caco-2	colon:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
42	CTCF	chr6:146025400-146025550	GM12866	blood:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
43	CTCF	chr6:146025420-146025570	HCM	heart:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
44	CTCF	chr6:146025733-146025871	GM10266	blood:	n/a	n/a
45	CTCF	chr6:146025660-146025810	SAEC	small airway:	n/a	n/a
46	CTCF	chr6:146025426-146025594	LNCaP	prostate:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
47	CTCF	chr6:146025400-146025550	NHEK	skin:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
48	CTCF	chr6:146025420-146025570	HCT-116	colon:	n/a	chr6:146025505-146025523 chr6:146025500-146025521
49	CTCF	chr6:146025667-146025831	Medullo	brain:	n/a	n/a
50	CTCF	chr6:146025760-146025910	GM06990	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:146009877-146009927	PrEC	prostate:	n/a
2	chr6:146009877-146009927	HRE	kidney:	n/a
3	chr6:146009877-146009927	HepG2	liver:	n/a
4	chr6:146009877-146009927	MCF10A-Er-Src	breast:	n/a
5	chr6:146009877-146009927	HL-60	blood:	n/a
6	chr6:146009877-146009927	SK-N-SH_RA	brain:	n/a
7	chr6:146009877-146009927	AG10803	skin:	n/a
8	chr6:146009877-146009927	H1-hESC	embryonic stem cell:	embryo
9	chr6:146009877-146009927	NT2-D1	testis:	n/a
10	chr6:146009877-146009927	HEK293	kidney:	embryo
11	chr6:146009877-146009927	HAEpiC	amniotic membrane:	n/a
12	chr6:146009877-146009927	GM12892	blood:	n/a
13	chr6:146009877-146009927	HMEC	breast:	n/a
14	chr6:146009877-146009927	AG04450	lung:	fetal
15	chr6:146009877-146009927	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:146009877-146009927	HCPEpiC	choroid plexus:	n/a
17	chr6:146009877-146009927	RPTEC	kidney:	n/a
18	chr6:146009877-146009927	CMK	blood:	n/a
19	chr6:146009877-146009927	HUVEC	blood vessel:	n/a
20	chr6:146009877-146009927	SKMC	muscle:	n/a
21	chr6:146009877-146009927	BE2_C	brain:	n/a
22	chr6:146009877-146009927	ovcar-3	ovarian:	n/a
23	chr6:146009877-146009927	AG04449	skin:	fetal
24	chr6:146009877-146009927	NHDF-neo	bronchial:	n/a
25	chr6:146009877-146009927	GM06990	blood:	n/a
26	chr6:146009877-146009927	HRPEpiC	eye:	n/a
27	chr6:146009877-146009927	GM12891	blood:	n/a
28	chr6:146009877-146009927	SK-N-MC	brain:	n/a
29	chr6:146009877-146009927	HEEpiC	esophagus:	n/a
30	chr6:146009877-146009927	HCF	heart:	n/a
31	chr6:146009877-146009927	NHBE	bronchial:	n/a
32	chr6:146009877-146009927	NB4	blood:	n/a
33	chr6:146009877-146009927	AG09319	gingival:	n/a
34	chr6:146009877-146009927	Jurkat	blood:	n/a
35	chr6:146009877-146009927	GM12878	blood:	n/a
36	chr6:146009877-146009927	GM19239	blood:	n/a
37	chr6:146009877-146009927	Caco-2	colon:	n/a
38	chr6:146009877-146009927	U87	brain:	n/a
39	chr6:146009877-146009927	PFSK-1	brain:	n/a
40	chr6:146009877-146009927	Hela-S3	cervix:	n/a
41	chr6:146009877-146009927	K562	blood:	n/a
42	chr6:146009877-146009927	T-47D	breast:	n/a
43	chr6:146009877-146009927	AG09309	skin:	n/a
44	chr6:146009877-146009927	BJ	skin:	n/a
45	chr6:146009877-146009927	AoSMC	blood vessel:	n/a
46	chr6:146009877-146009927	HIPEpiC	eye:	n/a
47	chr6:146009877-146009927	NH-A	brain:	n/a
48	chr6:146009877-146009927	ProgFib	skin:	n/a
49	chr6:146009877-146009927	IMR90	lung:	fetal
50	chr6:146009877-146009927	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:146040825..146042704-chr6:146055386..146057604,2	MCF-7	breast:
2	chr6:146021020..146022840-chr6:146050602..146052412,2	K562	blood:
3	chr6:146042289..146044000-chr6:146051001..146052592,2	MCF-7	breast:
4	chr6:144902617..144903608-chr6:146025327..146026043,2	MCF-7	breast:
5	chr6:146044114..146046476-chr6:146084502..146087117,2	K562	blood:
6	chr6:146041485..146043057-chr6:146133059..146134567,2	K562	blood:
7	chr6:146035079..146038031-chr6:146057257..146059128,2	K562	blood:
8	chr6:146040935..146043789-chr6:146048451..146050573,2	K562	blood:
9	chr6:146042690..146044450-chr6:146054852..146056800,2	MCF-7	breast:
10	chr6:146043919..146045619-chr6:146047459..146050321,2	K562	blood:
11	chr6:146040708..146045667-chr6:146052083..146058701,12	K562	blood:
12	chr6:146023773..146025394-chr6:146054656..146056157,2	K562	blood:
13	chr6:146043150..146050221-chr6:146053202..146058792,11	MCF-7	breast:
14	chr6:146040316..146042577-chr6:146048417..146050382,3	K562	blood:

Variant related genes	Relation type
EPM2A	TF binding region
EPM2A	CpG island
ENSG00000112425	chromatin interactions
ENSG00000270638	chromatin interactions
ENSG00000270828	chromatin interactions

Extended variants
information (count: 1370 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1370 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77139794	chr6:146007565-146007566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537321242	chr6:146007581-146007582	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs552838098	chr6:146007595-146007596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186459243	chr6:146007651-146007652	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535172652	chr6:146007694-146007695	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559697823	chr6:146007734-146007735	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528519723	chr6:146007739-146007740	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553507939	chr6:146007747-146007748	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117906006	chr6:146007754-146007755	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139982530	chr6:146007779-146007780	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs557047478	chr6:146007780-146007781	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201390816	chr6:146007789-146007790	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531735966	chr6:146007790-146007791	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs386706697	chr6:146007791-146007792	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs575525772	chr6:146007822-146007823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76887073	chr6:146007823-146007824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563982186	chr6:146007871-146007872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149438102	chr6:146007884-146007885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539996426	chr6:146007895-146007896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561834743	chr6:146007930-146007931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193274559	chr6:146007932-146007933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550577032	chr6:146007959-146007960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs386706698	chr6:146007967-146007968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562328318	chr6:146008007-146008008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531272250	chr6:146008022-146008023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371496220	chr6:146008023-146008024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571110939	chr6:146008065-146008066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375587260	chr6:146008075-146008076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535241005	chr6:146008099-146008100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550979075	chr6:146008120-146008121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547183129	chr6:146008137-146008138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568564017	chr6:146008157-146008158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571680498	chr6:146008183-146008184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535558442	chr6:146008184-146008185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537556059	chr6:146008195-146008196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557362011	chr6:146008218-146008219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs575543221	chr6:146008242-146008243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs702323	chr6:146008274-146008275	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs116081577	chr6:146008298-146008299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567469876	chr6:146008305-146008306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs540057556	chr6:146008332-146008333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371256320	chr6:146008368-146008369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185421003	chr6:146008420-146008421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573713105	chr6:146008476-146008477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs367812162	chr6:146008501-146008502	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs144778017	chr6:146008520-146008521	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs562549797	chr6:146008586-146008587	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs532960355	chr6:146008618-146008619	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs373867670	chr6:146008630-146008631	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs376188123	chr6:146008635-146008636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	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	chr6:145980600-146010800	Weak transcription	Right Ventricle	heart
2	chr6:145991200-146008800	Weak transcription	Brain Angular Gyrus	brain
3	chr6:145991800-146009200	Weak transcription	NHDF-Ad	bronchial
4	chr6:145994800-146008400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:145995000-146010800	Weak transcription	Left Ventricle	heart
6	chr6:145995200-146013200	Weak transcription	Pancreas	Pancrea
7	chr6:145998800-146010800	Weak transcription	HSMMtube	muscle
8	chr6:145999000-146010800	Weak transcription	Psoas Muscle	Psoas
9	chr6:145999600-146008600	Weak transcription	Fetal Intestine Large	intestine
10	chr6:146000600-146010600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr6:146001600-146008800	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr6:146001800-146012200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr6:146002200-146007800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr6:146002400-146009400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:146003200-146008200	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr6:146003200-146008800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr6:146003400-146007800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:146003400-146008600	Weak transcription	Fetal Thymus	thymus
19	chr6:146003400-146009000	Weak transcription	Colon Smooth Muscle	Colon
20	chr6:146003400-146009400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr6:146003400-146010800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:146003400-146011600	Weak transcription	Brain Substantia Nigra	brain
23	chr6:146003400-146033600	Weak transcription	Brain Hippocampus Middle	brain
24	chr6:146003600-146008400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:146003600-146008400	Weak transcription	Dnd41	blood
26	chr6:146003600-146008600	Weak transcription	Fetal Brain Male	brain
27	chr6:146003600-146009400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:146003600-146009600	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr6:146003600-146009600	Weak transcription	Primary hematopoietic stem cells	blood
30	chr6:146003600-146010800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr6:146003600-146010800	Weak transcription	Aorta	Aorta
32	chr6:146003600-146020600	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr6:146003600-146029400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:146003800-146007600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr6:146003800-146008000	Weak transcription	Primary T cells from cord blood	blood
36	chr6:146003800-146008000	Weak transcription	Brain Anterior Caudate	brain
37	chr6:146003800-146009200	Weak transcription	Thymus	Thymus
38	chr6:146003800-146009800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:146003800-146012200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr6:146003800-146012400	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr6:146003800-146026600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:146003800-146029600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr6:146003800-146029600	Weak transcription	Ovary	ovary
44	chr6:146004000-146009000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:146004000-146009400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr6:146006000-146008000	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr6:146006000-146009600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr6:146006400-146008400	Enhancers	Fetal Heart	heart
49	chr6:146006800-146014800	Weak transcription	Adipose Nuclei	Adipose
50	chr6:146006800-146050000	Weak transcription	Brain Cingulate Gyrus	brain

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