Variant report

Variant	nsv830699
Chromosome Location	chr6:77111857-77291223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:77272270-77272992	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr6:77151494-77151955	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr6:77151557-77151935	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:77271069-77271494	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr6:77151504-77151916	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr6:77151627-77151935	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:77113127-77113151	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:77148487-77148871	H1-hESC	embryonic stem cell:	n/a	chr6:77148663-77148677
9	BACH1	chr6:77228168-77228521	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:77283185-77283204	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr6:77176105-77176301	GM12878	blood:	n/a	chr6:77176197-77176208
12	BATF	chr6:77176056-77176337	GM12878	blood:	n/a	chr6:77176197-77176208
13	BATF	chr6:77219241-77219437	GM12878	blood:	n/a	chr6:77219332-77219343
14	BHLHE40	chr6:77129899-77130121	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:77176053-77176331	GM12878	blood:	n/a	n/a
16	BRCA1	chr6:77271283-77271621	H1-hESC	embryonic stem cell:	n/a	n/a
17	CBX3	chr6:77205617-77206052	HCT-116	colon:	n/a	n/a
18	CEBPB	chr6:77151408-77151975	H1-hESC	embryonic stem cell:	n/a	chr6:77151746-77151757
19	CEBPB	chr6:77273322-77273624	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:77113927-77114148	H1-hESC	embryonic stem cell:	n/a	chr6:77114059-77114070 chr6:77114060-77114071
21	CEBPB	chr6:77126531-77126964	MCF-7	breast:	n/a	n/a
22	CEBPB	chr6:77222375-77222632	IMR90	lung:	n/a	chr6:77222528-77222539
23	CEBPB	chr6:77128203-77128588	MCF-7	breast:	n/a	n/a
24	CEBPB	chr6:77270671-77271457	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:77113908-77114114	A549	lung:	n/a	chr6:77114059-77114070 chr6:77114060-77114071
26	CEBPB	chr6:77151495-77151928	HepG2	liver:	n/a	chr6:77151746-77151757
27	CEBPB	chr6:77273334-77273659	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:77151585-77151889	IMR90	lung:	n/a	chr6:77151746-77151757
29	CEBPB	chr6:77113907-77114221	HepG2	liver:	n/a	chr6:77114059-77114070 chr6:77114060-77114071
30	CEBPB	chr6:77258211-77258468	HepG2	liver:	n/a	chr6:77258347-77258360 chr6:77258347-77258358 chr6:77258349-77258360
31	CEBPB	chr6:77140360-77140810	HepG2	liver:	n/a	chr6:77140653-77140666 chr6:77140654-77140665 chr6:77140653-77140664
32	CEBPB	chr6:77133008-77133190	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr6:77273332-77273682	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:77225453-77225545	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr6:77222364-77222689	HepG2	liver:	n/a	chr6:77222528-77222539
36	CEBPB	chr6:77140266-77140742	IMR90	lung:	n/a	chr6:77140653-77140666 chr6:77140654-77140665 chr6:77140653-77140664
37	CHD1	chr6:77274462-77275324	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD1	chr6:77271046-77273553	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD1	chr6:77151523-77151703	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr6:77129951-77130049	GM12878	blood:	n/a	n/a
41	CHD2	chr6:77271136-77271457	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr6:77151555-77152013	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:77148127-77148152	ProgFib	skin:	n/a	n/a
44	CTCF	chr6:77128620-77128770	MCF-7	breast:	n/a	chr6:77128659-77128680
45	CTCF	chr6:77243008-77243025	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:77128700-77128850	AG04449	skin:	n/a	n/a
47	CTCF	chr6:77235924-77235938	Fibrobl	skin:	n/a	n/a
48	CTCF	chr6:77211495-77211569	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:77161980-77161989	Fibrobl	skin:	n/a	n/a
50	CTCF	chr6:77205051-77205114	GM13976	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:77265160-77265210	T-47D	breast:	n/a
2	chr6:77265160-77265210	AoSMC	blood vessel:	n/a
3	chr6:77265160-77265210	BJ	skin:	n/a
4	chr6:77265160-77265210	BE2_C	brain:	n/a
5	chr6:77265160-77265210	HAEpiC	amniotic membrane:	n/a
6	chr6:77265160-77265210	LNCaP	prostate:	n/a
7	chr6:77265160-77265210	HepG2	liver:	n/a
8	chr6:77265160-77265210	GM12878	blood:	n/a
9	chr6:77265160-77265210	HRCEpiC	kidney:	n/a
10	chr6:77265160-77265210	RPTEC	kidney:	n/a
11	chr6:77265160-77265210	HPAEpiC	pulmonary alveolar:	n/a
12	chr6:77265160-77265210	Hela-S3	cervix:	n/a
13	chr6:77265160-77265210	AG09309	skin:	n/a
14	chr6:77265160-77265210	K562	blood:	n/a
15	chr6:77265160-77265210	NHBE	bronchial:	n/a
16	chr6:77265160-77265210	NB4	blood:	n/a
17	chr6:77265160-77265210	AG10803	skin:	n/a
18	chr6:77265160-77265210	HCF	heart:	n/a
19	chr6:77265160-77265210	HRE	kidney:	n/a
20	chr6:77265160-77265210	SAEC	small airway:	n/a
21	chr6:77265160-77265210	Caco-2	colon:	n/a
22	chr6:77265160-77265210	HEEpiC	esophagus:	n/a
23	chr6:77265160-77265210	AG04449	skin:	fetal
24	chr6:77265160-77265210	ECC-1	luminal epithelium:	n/a
25	chr6:77265160-77265210	HCM	heart:	n/a
26	chr6:77265160-77265210	SKMC	muscle:	n/a
27	chr6:77265160-77265210	PrEC	prostate:	n/a
28	chr6:77265160-77265210	HUVEC	blood vessel:	n/a
29	chr6:77265160-77265210	GM12892	blood:	n/a
30	chr6:77265160-77265210	MCF-7	breast:	n/a
31	chr6:77265160-77265210	GM06990	blood:	n/a
32	chr6:77265160-77265210	HEK293	kidney:	embryo
33	chr6:77265160-77265210	PFSK-1	brain:	n/a
34	chr6:77265160-77265210	HIPEpiC	eye:	n/a
35	chr6:77265160-77265210	HCPEpiC	choroid plexus:	n/a
36	chr6:77265160-77265210	HL-60	blood:	n/a
37	chr6:77265160-77265210	SK-N-SH_RA	brain:	n/a
38	chr6:77265160-77265210	ProgFib	skin:	n/a
39	chr6:77265160-77265210	GM12891	blood:	n/a
40	chr6:77265160-77265210	AG04450	lung:	fetal
41	chr6:77265160-77265210	HNPCEpiC	eye:	n/a
42	chr6:77265160-77265210	ovcar-3	ovarian:	n/a
43	chr6:77265160-77265210	Hepatocyte	liver:	n/a
44	chr6:77265160-77265210	HCT-116	colon:	n/a
45	chr6:77265160-77265210	IMR90	lung:	fetal
46	chr6:77265160-77265210	H1-hESC	embryonic stem cell:	embryo
47	chr6:77265160-77265210	PANC-1	pancreas:	n/a
48	chr6:77265160-77265210	SK-N-SH	brain:	n/a
49	chr6:77265160-77265210	AG09319	gingival:	n/a
50	chr6:77265160-77265210	NH-A	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:77172267..77174922-chr6:77177230..77180103,2	K562	blood:
2	chr6:77241082..77243411-chr6:77248684..77250256,2	K562	blood:
3	chr6:77258609..77260545-chr6:77270279..77272860,2	K562	blood:
4	chr6:77241082..77243411-chr6:77248684..77250256,2	K562	blood:
5	chr6:77258609..77260545-chr6:77270279..77272860,2	K562	blood:
6	chr6:77172267..77174922-chr6:77177230..77180103,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO6-8	chr6:77288887-77289240	NONHSAT113643
2	lnc-IMPG1-1	chr6:77232168-77232521	ENSG00000236635.2
3	lnc-MYO6-2	chr6:77232168-77232521	ENSG00000236635

No data

Variant related genes	Relation type
ENSG00000272445	TF binding region
RNU6-261P	TF binding region
ENSG00000272445	CpG island
RNU6-261P	CpG island

Extended variants
information (count: 4280 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:4280 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191362521	chr6:77126603-77126604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs546617369	chr6:77126648-77126649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112120500	chr6:77126651-77126652	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375021538	chr6:77126689-77126690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73467814	chr6:77126699-77126700	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538616158	chr6:77126733-77126734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550686586	chr6:77126740-77126741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73467819	chr6:77126741-77126742	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs536069466	chr6:77126781-77126782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141588672	chr6:77126841-77126842	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs573081611	chr6:77126882-77126883	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs150402461	chr6:77126962-77126963	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs183117215	chr6:77126963-77126964	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs576935043	chr6:77126972-77126973	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs112924649	chr6:77127000-77127001	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs9343437	chr6:77127010-77127011	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs188658436	chr6:77127055-77127056	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs192269634	chr6:77127073-77127074	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs112424638	chr6:77127137-77127138	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs114829237	chr6:77127149-77127150	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs115266567	chr6:77127167-77127168	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs115835908	chr6:77127168-77127169	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs565211678	chr6:77127169-77127170	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs532376430	chr6:77127223-77127224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564624719	chr6:77127233-77127234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569297776	chr6:77127238-77127239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536727126	chr6:77127252-77127253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548116401	chr6:77127292-77127293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145409746	chr6:77127293-77127294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533946736	chr6:77127294-77127295	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558893991	chr6:77127327-77127328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs149207853	chr6:77127331-77127332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537880129	chr6:77127373-77127374	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187553319	chr6:77127376-77127377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373272631	chr6:77127382-77127383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34742967	chr6:77127397-77127398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574477815	chr6:77127442-77127443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs377260229	chr6:77127447-77127448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530453407	chr6:77127448-77127449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs541894278	chr6:77127469-77127470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112825260	chr6:77127489-77127490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192584230	chr6:77127515-77127516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184298134	chr6:77127526-77127527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs565247879	chr6:77127569-77127570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138940325	chr6:77127592-77127593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs73467821	chr6:77127613-77127614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs540573423	chr6:77127645-77127646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189298496	chr6:77127666-77127667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs565473840	chr6:77127680-77127681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548682137	chr6:77127683-77127684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
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
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77126600-77126800	Enhancers	Fetal Heart	heart
2	chr6:77126600-77127200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr6:77126600-77127200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:77126800-77127000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr6:77126800-77127200	Flanking Active TSS	Fetal Heart	heart
6	chr6:77127000-77127200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr6:77127200-77128000	Enhancers	Fetal Heart	heart
8	chr6:77127200-77128200	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr6:77128200-77128600	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr6:77130800-77131000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
11	chr6:77131000-77131200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
12	chr6:77131400-77131600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chr6:77131400-77131800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr6:77131800-77132600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
15	chr6:77132000-77133600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
16	chr6:77132200-77133000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
17	chr6:77132200-77133000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:77132200-77133400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr6:77132400-77132600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
20	chr6:77132400-77132600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr6:77132400-77133000	Enhancers	Fetal Lung	lung
22	chr6:77132400-77133200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
23	chr6:77132400-77133200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
24	chr6:77132600-77134800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:77133000-77133200	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
26	chr6:77133800-77134200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
27	chr6:77134000-77134200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr6:77134000-77134200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:77134200-77134400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
30	chr6:77135000-77135600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr6:77135200-77135400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
32	chr6:77135200-77135400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:77135200-77135400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:77135200-77135400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr6:77135200-77135600	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr6:77135400-77135600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr6:77140400-77140800	Enhancers	Fetal Lung	lung
38	chr6:77144600-77145200	Enhancers	Adipose Nuclei	Adipose
39	chr6:77144600-77145200	Enhancers	Fetal Heart	heart
40	chr6:77144800-77145200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr6:77144800-77145200	Enhancers	Brain Hippocampus Middle	brain
42	chr6:77145000-77145200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr6:77145200-77149200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:77145200-77149200	Weak transcription	Fetal Heart	heart
45	chr6:77145200-77151600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr6:77148000-77148200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr6:77148000-77148200	Enhancers	H9 Cell Line	embryonic stem cell
48	chr6:77148000-77148200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:77148200-77149200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr6:77148200-77149400	Weak transcription	H9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links