Variant report

Variant	nsv1033419
Chromosome Location	chr6:86474368-86550030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr6:86538698-86539019	K562	blood:	n/a	n/a
2	CBX3	chr6:86538752-86539012	K562	blood:	n/a	n/a
3	CEBPB	chr6:86508692-86508914	IMR90	lung:	n/a	chr6:86508772-86508783 chr6:86508773-86508784 chr6:86508774-86508783 chr6:86508772-86508785
4	CEBPB	chr6:86508621-86508921	HepG2	liver:	n/a	chr6:86508772-86508783 chr6:86508773-86508784 chr6:86508774-86508783 chr6:86508772-86508785
5	CEBPB	chr6:86508616-86509014	MCF-7	breast:	n/a	chr6:86508772-86508783 chr6:86508773-86508784 chr6:86508774-86508783 chr6:86508772-86508785
6	CEBPB	chr6:86508609-86509001	MCF-7	breast:	n/a	chr6:86508772-86508783 chr6:86508773-86508784 chr6:86508774-86508783 chr6:86508772-86508785
7	CEBPB	chr6:86508664-86508854	K562	blood:	n/a	chr6:86508772-86508783 chr6:86508773-86508784 chr6:86508774-86508783 chr6:86508772-86508785
8	CEBPB	chr6:86508630-86508937	A549	lung:	n/a	chr6:86508772-86508783 chr6:86508773-86508784 chr6:86508774-86508783 chr6:86508772-86508785
9	CHD2	chr6:86481883-86481934	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr6:86485715-86485897	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr6:86482720-86482774	GM19238	blood:	n/a	n/a
12	CTCF	chr6:86536340-86536490	HEK293	kidney:	n/a	n/a
13	CTCF	chr6:86549758-86549882	MCF-7	breast:	n/a	n/a
14	CTCF	chr6:86485744-86485853	MCF-7	breast:	n/a	n/a
15	CTCF	chr6:86485720-86485870	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:86509119-86509134	HepG2	liver:	n/a	n/a
17	CTCF	chr6:86549778-86549861	GM12878	blood:	n/a	n/a
18	CTCF	chr6:86509040-86509190	BE2_C	brain:	n/a	n/a
19	CTCF	chr6:86534140-86534290	RPTEC	kidney:	n/a	n/a
20	CTCF	chr6:86545025-86545028	GM10266	blood:	n/a	n/a
21	CTCF	chr6:86482704-86482790	GM19240	blood:	n/a	n/a
22	CTCF	chr6:86536160-86536310	K562	blood:	n/a	n/a
23	CTCF	chr6:86534200-86534201	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr6:86549741-86549880	MCF-7	breast:	n/a	n/a
25	CTCF	chr6:86485752-86485838	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr6:86482700-86482850	GM12871	blood:	n/a	n/a
27	CTCF	chr6:86534192-86534301	NHEK	skin:	n/a	n/a
28	CTCF	chr6:86485740-86485890	BE2_C	brain:	n/a	n/a
29	CTCF	chr6:86534120-86534366	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:86534169-86534312	HepG2	liver:	n/a	n/a
31	CTCF	chr6:86534160-86534310	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr6:86485746-86485871	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:86534203-86534307	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr6:86534176-86534306	HepG2	liver:	n/a	n/a
35	CTCF	chr6:86485733-86485879	HepG2	liver:	n/a	n/a
36	CTCF	chr6:86534117-86534381	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:86482712-86482780	GM19239	blood:	n/a	n/a
38	CTCF	chr6:86485729-86485930	LNCaP	prostate:	n/a	n/a
39	CTCF	chr6:86485756-86485876	Medullo	brain:	n/a	n/a
40	CTCF	chr6:86536595-86536715	ProgFib	skin:	n/a	n/a
41	CTCF	chr6:86534153-86534330	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:86482689-86482785	GM12892	blood:	n/a	n/a
43	CTCF	chr6:86519380-86519530	HEK293	kidney:	n/a	n/a
44	CTCF	chr6:86534100-86534250	SAEC	small airway:	n/a	n/a
45	CTCF	chr6:86533983-86534455	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:86485701-86485902	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:86485700-86485850	BE2_C	brain:	n/a	n/a
48	CTCF	chr6:86534206-86534238	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:86534103-86534371	GM12878	blood:	n/a	n/a
50	CTCF	chr6:86534166-86534307	HUVEC	blood vessel:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:86548232-86548282	HMEC	breast:	n/a
2	chr6:86548232-86548282	SK-N-MC	brain:	n/a
3	chr6:86547801-86547851	GM12878	blood:	n/a
4	chr6:86547801-86547851	RPTEC	kidney:	n/a
5	chr6:86548232-86548282	CMK	blood:	n/a
6	chr6:86548232-86548282	SKMC	muscle:	n/a
7	chr6:86548232-86548282	Hepatocyte	liver:	n/a
8	chr6:86548232-86548282	AG10803	skin:	n/a
9	chr6:86548232-86548282	NHDF-neo	bronchial:	n/a
10	chr6:86547801-86547851	PFSK-1	brain:	n/a
11	chr6:86548232-86548282	ovcar-3	ovarian:	n/a
12	chr6:86547801-86547851	Jurkat	blood:	n/a
13	chr6:86548232-86548282	NB4	blood:	n/a
14	chr6:86548232-86548282	GM12891	blood:	n/a
15	chr6:86548232-86548282	HUVEC	blood vessel:	n/a
16	chr6:86548232-86548282	Hela-S3	cervix:	n/a
17	chr6:86547801-86547851	AG09319	gingival:	n/a
18	chr6:86547801-86547851	AG04449	skin:	fetal
19	chr6:86547801-86547851	HepG2	liver:	n/a
20	chr6:86548232-86548282	HRE	kidney:	n/a
21	chr6:86547801-86547851	HMEC	breast:	n/a
22	chr6:86548232-86548282	HIPEpiC	eye:	n/a
23	chr6:86548232-86548282	HAEpiC	amniotic membrane:	n/a
24	chr6:86548232-86548282	SK-N-SH_RA	brain:	n/a
25	chr6:86547801-86547851	Caco-2	colon:	n/a
26	chr6:86547801-86547851	IMR90	lung:	fetal
27	chr6:86547801-86547851	BJ	skin:	n/a
28	chr6:86548232-86548282	ProgFib	skin:	n/a
29	chr6:86548232-86548282	HCM	heart:	n/a
30	chr6:86547801-86547851	AG10803	skin:	n/a
31	chr6:86547801-86547851	AG04450	lung:	fetal
32	chr6:86547801-86547851	NH-A	brain:	n/a
33	chr6:86547801-86547851	HNPCEpiC	eye:	n/a
34	chr6:86548232-86548282	GM06990	blood:	n/a
35	chr6:86547801-86547851	NHDF-neo	bronchial:	n/a
36	chr6:86548232-86548282	PFSK-1	brain:	n/a
37	chr6:86548232-86548282	AG04450	lung:	fetal
38	chr6:86548232-86548282	U87	brain:	n/a
39	chr6:86548232-86548282	K562	blood:	n/a
40	chr6:86547801-86547851	H1-hESC	embryonic stem cell:	embryo
41	chr6:86548232-86548282	Caco-2	colon:	n/a
42	chr6:86547801-86547851	A549	lung:	n/a
43	chr6:86547801-86547851	HL-60	blood:	n/a
44	chr6:86548232-86548282	AoSMC	blood vessel:	n/a
45	chr6:86548232-86548282	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:86547801-86547851	ovcar-3	ovarian:	n/a
47	chr6:86548232-86548282	MCF10A-Er-Src	breast:	n/a
48	chr6:86547801-86547851	LNCaP	prostate:	n/a
49	chr6:86547801-86547851	Hela-S3	cervix:	n/a
50	chr6:86548232-86548282	NT2-D1	testis:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:86501351..86504380-chr6:86507013..86510023,3	K562	blood:
2	chr6:86386922..86388666-chr6:86473238..86475490,2	K562	blood:
3	chr6:86387321..86388934-chr6:86506201..86508595,2	MCF-7	breast:
4	chr6:86534169..86534685-chr6:86574198..86574815,2	MCF-7	breast:
5	chr6:86501351..86504380-chr6:86507013..86510023,3	K562	blood:
6	chr6:86389006..86390560-chr6:86474592..86476523,2	K562	blood:
7	chr6:86351778..86354255-chr6:86511973..86513723,2	MCF-7	breast:
8	chr6:86387054..86388677-chr6:86473658..86476590,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM165A-2	chr6:86482026-86482088	NONHSAT113871

No data

Variant related genes	Relation type
ENSG00000200427	TF binding region
ENSG00000200427	CpG island
ENSG00000135316	chromatin interactions
ENSG00000203875	chromatin interactions

Extended variants
information (count: 1759 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1759 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9294338	chr6:86474368-86474369	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs562845470	chr6:86474498-86474499	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs533383250	chr6:86474506-86474507	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551892539	chr6:86474579-86474580	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139940930	chr6:86474582-86474583	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs9362242	chr6:86474606-86474607	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192986957	chr6:86474616-86474617	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs114464459	chr6:86474625-86474626	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568430572	chr6:86474705-86474706	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568172464	chr6:86474714-86474715	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114697259	chr6:86474720-86474721	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs556858333	chr6:86474721-86474722	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574858328	chr6:86474746-86474747	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs539080272	chr6:86474770-86474771	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141703371	chr6:86474786-86474787	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185632871	chr6:86474864-86474865	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs117050030	chr6:86474867-86474868	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562265183	chr6:86474920-86474921	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559873439	chr6:86474938-86474939	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs541167949	chr6:86474939-86474940	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs368404732	chr6:86474944-86474945	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544888552	chr6:86474966-86474967	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372894812	chr6:86474984-86474985	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563211392	chr6:86475026-86475027	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs150746721	chr6:86475066-86475067	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs66526504	chr6:86475104-86475105	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs10566286	chr6:86475105-86475106	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs202235054	chr6:86475106-86475107	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs397783168	chr6:86475108-86475109	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs577866037	chr6:86475124-86475125	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs11961241	chr6:86475133-86475134	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs190508491	chr6:86475136-86475137	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560374840	chr6:86475165-86475166	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs527745734	chr6:86475183-86475184	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181959665	chr6:86475210-86475211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549831816	chr6:86475214-86475215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs567886359	chr6:86475234-86475235	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs116755536	chr6:86475243-86475244	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563401253	chr6:86475279-86475280	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs117985235	chr6:86475282-86475283	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529220254	chr6:86475309-86475310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568839800	chr6:86475326-86475327	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs377466537	chr6:86475351-86475352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542634228	chr6:86475374-86475375	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539042070	chr6:86475409-86475410	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs386703433	chr6:86475410-86475411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184946164	chr6:86475411-86475412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs549237897	chr6:86475413-86475414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs149882990	chr6:86475419-86475420	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534217267	chr6:86475466-86475467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	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
Lung adenocarcinoma	21935476	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
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
craniofacial dysmorphism	21918468	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86473800-86475600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr6:86474000-86475200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:86474200-86475800	Enhancers	Ovary	ovary
4	chr6:86474400-86475600	Enhancers	Adipose Nuclei	Adipose
5	chr6:86474600-86475200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr6:86474600-86475200	Enhancers	Aorta	Aorta
7	chr6:86474600-86475200	Enhancers	HepG2	liver
8	chr6:86474800-86475200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr6:86475200-86478200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr6:86475200-86485600	Weak transcription	Aorta	Aorta
11	chr6:86481400-86481600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr6:86481400-86482200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:86481400-86482200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:86481400-86482400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:86481600-86481800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr6:86481600-86482200	Enhancers	H1 Cell Line	embryonic stem cell
17	chr6:86481600-86482200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr6:86481600-86482200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:86481600-86482600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:86481800-86482000	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr6:86481800-86482200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:86481800-86482400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:86481800-86482600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:86482200-86482600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:86482600-86482800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:86485600-86486400	Enhancers	Aorta	Aorta
27	chr6:86505400-86505600	Enhancers	Psoas Muscle	Psoas
28	chr6:86505600-86506200	Enhancers	Brain Germinal Matrix	brain
29	chr6:86505600-86512000	Weak transcription	Psoas Muscle	Psoas
30	chr6:86507800-86508000	Enhancers	Brain Germinal Matrix	brain
31	chr6:86507800-86508400	Enhancers	Esophagus	oesophagus
32	chr6:86508000-86509400	Enhancers	Fetal Lung	lung
33	chr6:86508200-86508600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:86508400-86509200	Enhancers	Adipose Nuclei	Adipose
35	chr6:86512000-86512200	Enhancers	Psoas Muscle	Psoas
36	chr6:86513400-86513800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:86517000-86517600	Weak transcription	Aorta	Aorta
38	chr6:86518000-86518200	ZNF genes & repeats	Aorta	Aorta
39	chr6:86525600-86526000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:86534400-86534800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr6:86537600-86537800	ZNF genes & repeats	Ovary	ovary
42	chr6:86537800-86550000	Weak transcription	Ovary	ovary
43	chr6:86546800-86556800	Weak transcription	Right Atrium	heart
44	chr6:86550000-86550400	ZNF genes & repeats	Ovary	ovary

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