Variant report

Variant	nsv886148
Chromosome Location	chr6:71623253-71694742
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:523)
CpG islands
(count:1100)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:523 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:71665724-71665822	K562	blood:	n/a	n/a
2	BACH1	chr6:71666632-71667239	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:71665197-71665977	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr6:71665562-71665959	GM12878	blood:	n/a	n/a
5	BCLAF1	chr6:71665543-71665974	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:71665561-71665878	HepG2	liver:	n/a	n/a
7	BHLHE40	chr6:71676879-71677104	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:71665506-71665972	K562	blood:	n/a	n/a
9	BHLHE40	chr6:71665473-71666207	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:71665497-71666133	GM12878	blood:	n/a	n/a
11	BHLHE40	chr6:71690709-71690752	K562	blood:	n/a	n/a
12	BHLHE40	chr6:71665559-71665903	A549	lung:	n/a	n/a
13	BRCA1	chr6:71665685-71665822	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr6:71665698-71665952	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr6:71665615-71665884	K562	blood:	n/a	n/a
16	CCNT2	chr6:71665587-71665988	K562	blood:	n/a	n/a
17	CEBPB	chr6:71676761-71677126	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:71676852-71677116	HepG2	liver:	n/a	n/a
19	CEBPB	chr6:71676786-71677187	HepG2	liver:	n/a	n/a
20	CEBPB	chr6:71676802-71677185	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:71692521-71692773	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:71665743-71665911	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:71665684-71665939	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPD	chr6:71676888-71677077	HepG2	liver:	n/a	n/a
25	CEBPD	chr6:71676861-71677051	HepG2	liver:	n/a	n/a
26	CHD1	chr6:71665757-71665937	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr6:71665649-71665913	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:71665731-71665861	K562	blood:	n/a	n/a
29	CHD2	chr6:71666550-71666719	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:71665706-71665943	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr6:71665637-71665917	GM12878	blood:	n/a	n/a
32	CHD2	chr6:71665713-71666062	HepG2	liver:	n/a	n/a
33	CREB1	chr6:71665490-71665940	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr6:71665597-71665994	A549	lung:	n/a	n/a
35	CTBP2	chr6:71665240-71667308	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr6:71665637-71665966	GM10266	blood:	n/a	n/a
37	CTCF	chr6:71665644-71665971	Spleen_OC	spleen:	n/a	n/a
38	CTCF	chr6:71665740-71665890	GM12874	blood:	n/a	n/a
39	CTCF	chr6:71665720-71665870	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:71665740-71665890	AG04449	skin:	n/a	n/a
41	CTCF	chr6:71665619-71665959	GM13977	blood:	n/a	n/a
42	CTCF	chr6:71665760-71665910	WI-38	lung:	n/a	n/a
43	CTCF	chr6:71665720-71665870	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr6:71665580-71666019	HCT-116	colon:	n/a	n/a
45	CTCF	chr6:71666066-71666120	GM12878	blood:	n/a	n/a
46	CTCF	chr6:71666218-71666276	ProgFib	skin:	n/a	n/a
47	CTCF	chr6:71665674-71665976	A549	lung:	n/a	n/a
48	CTCF	chr6:71665576-71665952	LNCaP	prostate:	n/a	n/a
49	CTCF	chr6:71689570-71689670	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr6:71665740-71665890	HMEC	breast:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:71666282-71666332	Hepatocyte	liver:	n/a
2	chr6:71667105-71667155	HEK293	kidney:	embryo
3	chr6:71666282-71666332	Hepatocyte	liver:	n/a
4	chr6:71667105-71667155	HEK293	kidney:	embryo
5	chr6:71665936-71665986	H1-hESC	embryonic stem cell:	embryo
6	chr6:71666063-71666113	H1-hESC	embryonic stem cell:	embryo
7	chr6:71669827-71669877	ProgFib	skin:	n/a
8	chr6:71665522-71665572	AoSMC	blood vessel:	n/a
9	chr6:71665936-71665986	HNPCEpiC	eye:	n/a
10	chr6:71665574-71665624	NT2-D1	testis:	n/a
11	chr6:71665522-71665572	AG09309	skin:	n/a
12	chr6:71666063-71666113	HL-60	blood:	n/a
13	chr6:71665522-71665572	PrEC	prostate:	n/a
14	chr6:71668029-71668079	AG04449	skin:	fetal
15	chr6:71666063-71666113	HUVEC	blood vessel:	n/a
16	chr6:71666824-71666874	ovcar-3	ovarian:	n/a
17	chr6:71666803-71666853	HMEC	breast:	n/a
18	chr6:71667105-71667155	T-47D	breast:	n/a
19	chr6:71666121-71666171	HCF	heart:	n/a
20	chr6:71666682-71666732	SK-N-MC	brain:	n/a
21	chr6:71666803-71666853	PrEC	prostate:	n/a
22	chr6:71666682-71666732	HepG2	liver:	n/a
23	chr6:71662998-71663048	HNPCEpiC	eye:	n/a
24	chr6:71666809-71666859	NT2-D1	testis:	n/a
25	chr6:71666282-71666332	AG10803	skin:	n/a
26	chr6:71668029-71668079	HRE	kidney:	n/a
27	chr6:71666282-71666332	HepG2	liver:	n/a
28	chr6:71666809-71666859	LNCaP	prostate:	n/a
29	chr6:71666803-71666853	HepG2	liver:	n/a
30	chr6:71667067-71667117	HCPEpiC	choroid plexus:	n/a
31	chr6:71664559-71664609	HRE	kidney:	n/a
32	chr6:71666824-71666874	T-47D	breast:	n/a
33	chr6:71666809-71666859	HUVEC	blood vessel:	n/a
34	chr6:71666803-71666853	RPTEC	kidney:	n/a
35	chr6:71667067-71667117	GM12878	blood:	n/a
36	chr6:71665395-71665445	HCF	heart:	n/a
37	chr6:71664559-71664609	RPTEC	kidney:	n/a
38	chr6:71667067-71667117	AG09319	gingival:	n/a
39	chr6:71666858-71666908	HEK293	kidney:	embryo
40	chr6:71664559-71664609	AG04449	skin:	fetal
41	chr6:71665936-71665986	NB4	blood:	n/a
42	chr6:71665936-71665986	CMK	blood:	n/a
43	chr6:71669827-71669877	H1-hESC	embryonic stem cell:	embryo
44	chr6:71667067-71667117	T-47D	breast:	n/a
45	chr6:71665522-71665572	HCT-116	colon:	n/a
46	chr6:71667105-71667155	HIPEpiC	eye:	n/a
47	chr6:71666858-71666908	GM19239	blood:	n/a
48	chr6:71666809-71666859	HCF	heart:	n/a
49	chr6:71666809-71666859	SK-N-MC	brain:	n/a
50	chr6:71666063-71666113	ECC-1	luminal epithelium:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:71415956..71416839-chr6:71665369..71665919,2	K562	blood:
2	chr6:71665737..71667966-chr6:71669230..71671989,2	K562	blood:
3	chr6:71660383..71662410-chr6:71669635..71671756,2	K562	blood:
4	chr6:71594169..71594842-chr6:71665262..71666233,2	MCF-7	breast:
5	chr6:71594143..71594787-chr6:71662346..71663077,2	K562	blood:
6	chr6:71660383..71662410-chr6:71669635..71671756,2	K562	blood:
7	chr6:71256857..71257781-chr6:71665609..71666111,2	MCF-7	breast:
8	chr6:71415810..71416633-chr6:71665559..71666663,3	MCF-7	breast:
9	chr6:71230031..71231237-chr6:71665008..71666316,7	MCF-7	breast:
10	chr6:71416313..71416967-chr6:71665219..71666338,4	MCF-7	breast:

No data

Variant related genes	Relation type
B3GAT2	TF binding region
B3GAT2	CpG island
ENSG00000112309	chromatin interactions

Extended variants
information (count: 380 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146459231	chr6:71650632-71650633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs115316554	chr6:71650635-71650636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532439543	chr6:71650639-71650640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140876819	chr6:71650640-71650641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548625349	chr6:71650711-71650712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189340043	chr6:71650742-71650743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181717429	chr6:71650757-71650758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75515967	chr6:71650794-71650795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577369748	chr6:71650804-71650805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567145366	chr6:71650818-71650819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534235637	chr6:71650821-71650822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368357576	chr6:71650856-71650857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144783603	chr6:71650888-71650889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577737576	chr6:71650934-71650935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs34063587	chr6:71650966-71650967	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs557079548	chr6:71651015-71651016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115595101	chr6:71651036-71651037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs4707868	chr6:71651039-71651040	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs34377250	chr6:71651068-71651069	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs187146151	chr6:71651069-71651070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs573044531	chr6:71651070-71651071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540177426	chr6:71651071-71651072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564900681	chr6:71651136-71651137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10945273	chr6:71661866-71661867	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573827063	chr6:71661944-71661945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73489548	chr6:71661958-71661959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7774025	chr6:71662002-71662003	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs74742266	chr6:71662035-71662036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373572733	chr6:71662047-71662048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376384010	chr6:71662053-71662054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539787361	chr6:71662120-71662121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563628628	chr6:71662149-71662150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35966846	chr6:71662203-71662204	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs397887830	chr6:71662208-71662209	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139836712	chr6:71662230-71662231	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78983701	chr6:71662282-71662283	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143138012	chr6:71662284-71662285	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7749568	chr6:71662286-71662287	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528566357	chr6:71662321-71662322	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs71538454	chr6:71662326-71662327	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs10945274	chr6:71662329-71662330	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551313792	chr6:71662362-71662363	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145529722	chr6:71662378-71662379	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537788142	chr6:71662386-71662387	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532772558	chr6:71662404-71662405	Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs180870252	chr6:71662408-71662409	Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs61596019	chr6:71662541-71662542	Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs549646856	chr6:71662544-71662545	Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs61107972	chr6:71662580-71662581	Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs148841311	chr6:71662584-71662585	Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Cancer	20164919	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71650600-71651200	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr6:71661800-71662400	Enhancers	Fetal Brain Female	brain
3	chr6:71662000-71662800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr6:71662200-71662600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
5	chr6:71662200-71662600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr6:71662200-71662600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:71662200-71662800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr6:71662200-71663400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr6:71662400-71662600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:71662400-71662600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
11	chr6:71662400-71662800	Flanking Active TSS	Fetal Brain Female	brain
12	chr6:71662800-71663000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
13	chr6:71662800-71663000	Active TSS	Fetal Brain Female	brain
14	chr6:71662800-71663200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:71663000-71663200	Flanking Active TSS	Fetal Brain Female	brain
16	chr6:71663200-71663600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:71663200-71664000	Active TSS	Fetal Brain Female	brain
18	chr6:71663400-71665800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr6:71663600-71664200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:71663600-71664200	Enhancers	Fetal Brain Male	brain
21	chr6:71663600-71667000	Active TSS	Brain Cingulate Gyrus	brain
22	chr6:71663800-71667200	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr6:71663800-71667600	Active TSS	Brain Anterior Caudate	brain
24	chr6:71664000-71665000	Flanking Active TSS	Fetal Brain Female	brain
25	chr6:71664200-71664400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr6:71664200-71664400	Flanking Active TSS	Fetal Brain Male	brain
27	chr6:71664200-71664600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr6:71664200-71664600	Active TSS	Brain Hippocampus Middle	brain
29	chr6:71664200-71665200	Enhancers	Brain Substantia Nigra	brain
30	chr6:71664200-71667600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr6:71664400-71664600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr6:71664400-71664600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:71664400-71664600	Bivalent Enhancer	Thymus	Thymus
34	chr6:71664400-71664800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
35	chr6:71664400-71664800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
36	chr6:71664400-71664800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
37	chr6:71664400-71664800	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
38	chr6:71664400-71665000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr6:71664400-71665200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr6:71664400-71665200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
41	chr6:71664600-71664800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
42	chr6:71664600-71664800	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
43	chr6:71664600-71664800	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr6:71664600-71665000	Bivalent Enhancer	Primary B cells from cord blood	blood
45	chr6:71664600-71665000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr6:71664600-71665200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr6:71664600-71665200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr6:71664600-71665200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
49	chr6:71664600-71665200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
50	chr6:71664600-71665200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood

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