Variant report

Variant	esv2830168
Chromosome Location	chr6:87186441-87236867
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:122)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr6:87187567-87187831	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr6:87198812-87199065	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr6:87225876-87226119	GM12878	blood:	n/a	chr6:87225988-87226001 chr6:87225984-87226005 chr6:87225990-87225999 chr6:87225989-87225998 chr6:87225990-87225999 chr6:87225991-87226000
4	CEBPB	chr6:87209815-87210240	MCF-7	breast:	n/a	chr6:87210019-87210030
5	CEBPB	chr6:87209950-87210150	K562	blood:	n/a	chr6:87210019-87210030
6	CEBPB	chr6:87212215-87212561	MCF-7	breast:	n/a	n/a
7	CEBPB	chr6:87201396-87201550	HepG2	liver:	n/a	n/a
8	CEBPB	chr6:87210004-87210060	H1-hESC	embryonic stem cell:	n/a	chr6:87210019-87210030
9	CEBPB	chr6:87209873-87210165	HepG2	liver:	n/a	chr6:87210019-87210030
10	CEBPB	chr6:87209778-87210285	MCF-7	breast:	n/a	chr6:87210019-87210030
11	CEBPB	chr6:87234497-87234764	MCF-7	breast:	n/a	n/a
12	CEBPB	chr6:87209894-87210185	IMR90	lung:	n/a	chr6:87210019-87210030
13	CHD2	chr6:87187373-87187475	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr6:87188340-87188490	GM06990	blood:	n/a	n/a
15	CTCF	chr6:87226040-87226190	WI-38	lung:	n/a	n/a
16	CTCF	chr6:87203528-87203560	GM10266	blood:	n/a	n/a
17	E2F6	chr6:87187348-87187867	H1-hESC	embryonic stem cell:	n/a	n/a
18	EBF1	chr6:87195058-87195352	GM12878	blood:	n/a	n/a
19	EP300	chr6:87212146-87212652	MCF-7	breast:	n/a	chr6:87212625-87212639
20	EP300	chr6:87209705-87210078	SK-N-SH_RA	brain:	n/a	n/a
21	EP300	chr6:87198822-87199072	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr6:87198815-87199105	H1-hESC	embryonic stem cell:	n/a	n/a
23	EP300	chr6:87198053-87199339	SK-N-SH	brain:	n/a	n/a
24	EP300	chr6:87209545-87210342	SK-N-SH	brain:	n/a	n/a
25	EP300	chr6:87221687-87222045	H1-hESC	embryonic stem cell:	n/a	n/a
26	EP300	chr6:87187543-87187835	H1-hESC	embryonic stem cell:	n/a	n/a
27	EP300	chr6:87198832-87199126	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr6:87209648-87210173	SK-N-SH_RA	brain:	n/a	n/a
29	FOS	chr6:87236111-87236203	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr6:87236016-87236247	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr6:87236071-87236299	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr6:87235118-87235318	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr6:87235067-87235254	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr6:87235057-87235352	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr6:87236109-87236204	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr6:87235131-87235331	MCF10A-Er-Src	breast:	n/a	n/a
37	FOXA2	chr6:87207261-87207847	A549	lung:	n/a	n/a
38	FOXA2	chr6:87207266-87207621	A549	lung:	n/a	n/a
39	GATA2	chr6:87209706-87210103	SH-SY5Y	brain:	n/a	n/a
40	GATA2	chr6:87198354-87199280	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr6:87212023-87212697	MCF-7	breast:	n/a	n/a
42	GATA3	chr6:87209738-87210331	MCF-7	breast:	n/a	n/a
43	GATA3	chr6:87209825-87210220	MCF-7	breast:	n/a	n/a
44	GATA3	chr6:87212002-87212721	MCF-7	breast:	n/a	n/a
45	GATA3	chr6:87209728-87210190	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr6:87212198-87212508	MCF-7	breast:	n/a	n/a
47	GATA3	chr6:87198838-87199102	T-47D	breast:	n/a	n/a
48	GATA3	chr6:87198832-87199116	T-47D	breast:	n/a	n/a
49	HDAC2	chr6:87212191-87212574	MCF-7	breast:	n/a	n/a
50	JUND	chr6:87236084-87236321	HepG2	liver:	n/a	chr6:87236141-87236152

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:87196595-87196645	HIPEpiC	eye:	n/a
2	chr6:87196595-87196645	GM12892	blood:	n/a
3	chr6:87196595-87196645	PFSK-1	brain:	n/a
4	chr6:87222174-87222224	HL-60	blood:	n/a
5	chr6:87196595-87196645	HNPCEpiC	eye:	n/a
6	chr6:87222174-87222224	HCM	heart:	n/a
7	chr6:87196595-87196645	BE2_C	brain:	n/a
8	chr6:87196595-87196645	Hela-S3	cervix:	n/a
9	chr6:87222174-87222224	GM12878	blood:	n/a
10	chr6:87196595-87196645	IMR90	lung:	fetal
11	chr6:87222174-87222224	BJ	skin:	n/a
12	chr6:87222174-87222224	GM12891	blood:	n/a
13	chr6:87222174-87222224	NB4	blood:	n/a
14	chr6:87222174-87222224	GM12892	blood:	n/a
15	chr6:87196595-87196645	PrEC	prostate:	n/a
16	chr6:87196595-87196645	HRE	kidney:	n/a
17	chr6:87222174-87222224	CMK	blood:	n/a
18	chr6:87196595-87196645	HCPEpiC	choroid plexus:	n/a
19	chr6:87222174-87222224	MCF-7	breast:	n/a
20	chr6:87222174-87222224	HepG2	liver:	n/a
21	chr6:87222174-87222224	AG09309	skin:	n/a
22	chr6:87196595-87196645	AG10803	skin:	n/a
23	chr6:87222174-87222224	HUVEC	blood vessel:	n/a
24	chr6:87222174-87222224	HIPEpiC	eye:	n/a
25	chr6:87222174-87222224	HRE	kidney:	n/a
26	chr6:87222174-87222224	GM19239	blood:	n/a
27	chr6:87196595-87196645	AG04450	lung:	fetal
28	chr6:87196595-87196645	Jurkat	blood:	n/a
29	chr6:87196595-87196645	ECC-1	luminal epithelium:	n/a
30	chr6:87196595-87196645	SAEC	small airway:	n/a
31	chr6:87222174-87222224	H1-hESC	embryonic stem cell:	embryo
32	chr6:87222174-87222224	HNPCEpiC	eye:	n/a
33	chr6:87196595-87196645	RPTEC	kidney:	n/a
34	chr6:87196595-87196645	HEEpiC	esophagus:	n/a
35	chr6:87222174-87222224	HAEpiC	amniotic membrane:	n/a
36	chr6:87196595-87196645	HRPEpiC	eye:	n/a
37	chr6:87196595-87196645	GM19239	blood:	n/a
38	chr6:87196595-87196645	CMK	blood:	n/a
39	chr6:87222174-87222224	MCF10A-Er-Src	breast:	n/a
40	chr6:87222174-87222224	HEK293	kidney:	embryo
41	chr6:87196595-87196645	HCM	heart:	n/a
42	chr6:87196595-87196645	NHBE	bronchial:	n/a
43	chr6:87222174-87222224	U87	brain:	n/a
44	chr6:87222174-87222224	AoSMC	blood vessel:	n/a
45	chr6:87196595-87196645	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:87196595-87196645	HCF	heart:	n/a
47	chr6:87222174-87222224	SK-N-SH	brain:	n/a
48	chr6:87196595-87196645	AG04449	skin:	fetal
49	chr6:87196595-87196645	LNCaP	prostate:	n/a
50	chr6:87196595-87196645	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:87225517..87227389-chr6:87237269..87238777,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000221101	TF binding region
ENSG00000221101	CpG island

Extended variants
information (count: 2140 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:2140 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9450463	chr6:87186441-87186442	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182363058	chr6:87186463-87186464	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs544476777	chr6:87186475-87186476	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs35782874	chr6:87186506-87186507	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs187904054	chr6:87186511-87186512	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs192587495	chr6:87186522-87186523	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs559774480	chr6:87186523-87186524	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184261432	chr6:87186532-87186533	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567275243	chr6:87186558-87186559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527292644	chr6:87186561-87186562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151095091	chr6:87186572-87186573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs187453270	chr6:87186603-87186604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531939445	chr6:87186647-87186648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142487023	chr6:87186654-87186655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs550421158	chr6:87186671-87186672	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565355762	chr6:87186695-87186696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368996002	chr6:87186698-87186699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192301972	chr6:87186719-87186720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538295782	chr6:87186720-87186721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536732922	chr6:87186735-87186736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548326241	chr6:87186752-87186753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570009030	chr6:87186771-87186772	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372312742	chr6:87186783-87186784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575119200	chr6:87186784-87186785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574846859	chr6:87186794-87186795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139129624	chr6:87186815-87186816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540806302	chr6:87186841-87186842	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554495468	chr6:87186843-87186844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12202175	chr6:87186844-87186845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184890318	chr6:87186855-87186856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111261783	chr6:87186861-87186862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538398290	chr6:87186903-87186904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12202283	chr6:87186922-87186923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553542412	chr6:87186956-87186957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571844663	chr6:87186987-87186988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs542686852	chr6:87186992-87186993	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560744092	chr6:87186998-87186999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575960932	chr6:87187008-87187009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543771835	chr6:87187042-87187043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2089521	chr6:87187070-87187071	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532853856	chr6:87187080-87187081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548048607	chr6:87187103-87187104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559968969	chr6:87187144-87187145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141592627	chr6:87187194-87187195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376292643	chr6:87187201-87187202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150396717	chr6:87187236-87187237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569965778	chr6:87187313-87187314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537411451	chr6:87187322-87187323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138667123	chr6:87187325-87187326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112470850	chr6:87187344-87187345	Enhancers	n/a	n/a	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
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Developmental delay	19490664	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:87176400-87186600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:87186000-87188200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr6:87186400-87186600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:87186600-87187000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:87186600-87187600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:87187000-87187800	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr6:87187000-87188200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:87187000-87188200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:87187000-87188400	Enhancers	Fetal Intestine Large	intestine
10	chr6:87187200-87187600	Enhancers	Fetal Kidney	kidney
11	chr6:87187200-87187800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:87187200-87187800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr6:87187200-87188200	Enhancers	H1 Cell Line	embryonic stem cell
14	chr6:87187200-87188200	Enhancers	Fetal Intestine Small	intestine
15	chr6:87187200-87188400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:87187400-87188000	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr6:87187600-87189800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:87188200-87188600	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr6:87189800-87190600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:87190600-87191400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr6:87191400-87201600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:87195800-87196600	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr6:87196000-87196800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:87196400-87197000	Enhancers	H1 Cell Line	embryonic stem cell
25	chr6:87199000-87199600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:87199800-87200000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr6:87200000-87201600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:87201600-87201800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr6:87201800-87207000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr6:87206600-87208600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
31	chr6:87207000-87208000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:87207600-87210400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr6:87209400-87213000	Enhancers	Fetal Intestine Small	intestine
34	chr6:87209400-87213400	Enhancers	Fetal Intestine Large	intestine
35	chr6:87209800-87212400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:87211800-87212200	Enhancers	Placenta	Placenta
37	chr6:87212400-87213000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr6:87218000-87218600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:87218600-87222000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:87220400-87222600	Enhancers	Fetal Intestine Large	intestine
41	chr6:87220400-87222600	Enhancers	Fetal Intestine Small	intestine
42	chr6:87221000-87222600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:87221200-87222600	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr6:87221200-87222600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr6:87221400-87222400	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr6:87221400-87222600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr6:87221600-87221800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr6:87221600-87222200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:87221600-87222600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr6:87221600-87222800	Enhancers	HUES64 Cell Line	embryonic stem cell

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