Variant report

Variant	nsv970341
Chromosome Location	chr6:87567573-87616057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr6:87582634-87582782	HepG2	liver:	n/a	chr6:87582731-87582742
2	CEBPB	chr6:87582620-87582898	HepG2	liver:	n/a	chr6:87582731-87582742
3	CEBPB	chr6:87582556-87582895	MCF-7	breast:	n/a	chr6:87582731-87582742
4	CTCF	chr6:87569320-87569470	HepG2	liver:	n/a	n/a
5	CTCF	chr6:87569433-87569460	GM13976	blood:	n/a	n/a
6	CTCF	chr6:87569329-87569540	MCF-7	breast:	n/a	n/a
7	CTCF	chr6:87569408-87569477	GM13977	blood:	n/a	n/a
8	CTCF	chr6:87569357-87569461	MCF-7	breast:	n/a	n/a
9	CTCF	chr6:87601726-87601818	MCF-7	breast:	n/a	n/a
10	CTCF	chr6:87600540-87600690	K562	blood:	n/a	n/a
11	CTCF	chr6:87601740-87601890	GM06990	blood:	n/a	n/a
12	CTCF	chr6:87569360-87569510	HEK293	kidney:	n/a	n/a
13	CTCF	chr6:87569280-87569430	HEK293	kidney:	n/a	n/a
14	CTCF	chr6:87569376-87569494	MCF-7	breast:	n/a	n/a
15	CTCF	chr6:87569403-87569484	LNCaP	prostate:	n/a	n/a
16	CTCF	chr6:87601640-87601790	GM12864	blood:	n/a	n/a
17	CTCF	chr6:87569320-87569470	NHEK	skin:	n/a	n/a
18	CTCF	chr6:87601798-87601825	GM12878	blood:	n/a	n/a
19	CTCF	chr6:87571153-87571304	MCF-7	breast:	n/a	n/a
20	CTCF	chr6:87601900-87602050	MCF-7	breast:	n/a	n/a
21	CTCF	chr6:87601700-87601850	NB4	blood:	n/a	n/a
22	CTCF	chr6:87569380-87569530	BE2_C	brain:	n/a	n/a
23	CTCF	chr6:87569380-87569530	GM12873	blood:	n/a	n/a
24	CTCF	chr6:87608120-87608193	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr6:87601738-87601837	GM19238	blood:	n/a	n/a
26	CTCF	chr6:87569380-87569530	GM12865	blood:	n/a	n/a
27	CTCF	chr6:87601700-87601850	GM12864	blood:	n/a	n/a
28	CTCF	chr6:87569415-87569486	GM10266	blood:	n/a	n/a
29	CTCF	chr6:87601700-87601850	GM12872	blood:	n/a	n/a
30	CTCF	chr6:87569360-87569510	HepG2	liver:	n/a	n/a
31	CTCF	chr6:87569380-87569530	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:87569360-87569510	GM12873	blood:	n/a	n/a
33	CTCF	chr6:87569408-87569443	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr6:87601600-87601750	GM12864	blood:	n/a	n/a
35	CTCF	chr6:87569374-87569530	HepG2	liver:	n/a	n/a
36	CTCF	chr6:87569243-87569500	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr6:87601765-87601826	HepG2	liver:	n/a	n/a
38	CTCF	chr6:87569220-87569370	GM12873	blood:	n/a	n/a
39	CTCF	chr6:87569445-87569453	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr6:87569283-87569590	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr6:87601720-87601870	HEK293	kidney:	n/a	n/a
42	CTCF	chr6:87569360-87569510	HMEC	breast:	n/a	n/a
43	CTCF	chr6:87569380-87569530	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr6:87569405-87569472	Gliobla	brain:	n/a	n/a
45	CTCF	chr6:87601747-87601856	GM13977	blood:	n/a	n/a
46	CTCF	chr6:87569380-87569530	NB4	blood:	n/a	n/a
47	CTCF	chr6:87569435-87569495	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr6:87569194-87569649	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:87569360-87569510	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr6:87569340-87569490	GM12874	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:87607161-87607211	HRPEpiC	eye:	n/a
2	chr6:87607195-87607245	AG04449	skin:	fetal
3	chr6:87607161-87607211	GM12892	blood:	n/a
4	chr6:87607655-87607705	HRPEpiC	eye:	n/a
5	chr6:87607195-87607245	NB4	blood:	n/a
6	chr6:87607744-87607794	AoSMC	blood vessel:	n/a
7	chr6:87607178-87607228	PANC-1	pancreas:	n/a
8	chr6:87607195-87607245	AG09319	gingival:	n/a
9	chr6:87607195-87607245	GM12891	blood:	n/a
10	chr6:87607195-87607245	GM19239	blood:	n/a
11	chr6:87607161-87607211	AG04450	lung:	fetal
12	chr6:87607161-87607211	CMK	blood:	n/a
13	chr6:87607655-87607705	HNPCEpiC	eye:	n/a
14	chr6:87607178-87607228	IMR90	lung:	fetal
15	chr6:87607161-87607211	ovcar-3	ovarian:	n/a
16	chr6:87607161-87607211	HL-60	blood:	n/a
17	chr6:87607655-87607705	HEK293	kidney:	embryo
18	chr6:87607178-87607228	H1-hESC	embryonic stem cell:	embryo
19	chr6:87607178-87607228	GM12891	blood:	n/a
20	chr6:87607744-87607794	AG04449	skin:	fetal
21	chr6:87607195-87607245	AG10803	skin:	n/a
22	chr6:87607744-87607794	HEK293	kidney:	embryo
23	chr6:87607161-87607211	HIPEpiC	eye:	n/a
24	chr6:87607744-87607794	HRPEpiC	eye:	n/a
25	chr6:87607195-87607245	HMEC	breast:	n/a
26	chr6:87607178-87607228	SK-N-SH	brain:	n/a
27	chr6:87607744-87607794	Hepatocyte	liver:	n/a
28	chr6:87607161-87607211	Caco-2	colon:	n/a
29	chr6:87607161-87607211	MCF10A-Er-Src	breast:	n/a
30	chr6:87607744-87607794	HCT-116	colon:	n/a
31	chr6:87607195-87607245	SK-N-SH_RA	brain:	n/a
32	chr6:87607178-87607228	GM06990	blood:	n/a
33	chr6:87607655-87607705	HCPEpiC	choroid plexus:	n/a
34	chr6:87607655-87607705	SK-N-MC	brain:	n/a
35	chr6:87607195-87607245	PFSK-1	brain:	n/a
36	chr6:87607161-87607211	AG09319	gingival:	n/a
37	chr6:87607655-87607705	AG04449	skin:	fetal
38	chr6:87607178-87607228	PFSK-1	brain:	n/a
39	chr6:87607195-87607245	NHDF-neo	bronchial:	n/a
40	chr6:87607195-87607245	A549	lung:	n/a
41	chr6:87607195-87607245	T-47D	breast:	n/a
42	chr6:87607161-87607211	HCT-116	colon:	n/a
43	chr6:87607161-87607211	NT2-D1	testis:	n/a
44	chr6:87607161-87607211	NB4	blood:	n/a
45	chr6:87607655-87607705	GM12892	blood:	n/a
46	chr6:87607161-87607211	HEK293	kidney:	embryo
47	chr6:87607161-87607211	MCF-7	breast:	n/a
48	chr6:87607744-87607794	LNCaP	prostate:	n/a
49	chr6:87607195-87607245	NT2-D1	testis:	n/a
50	chr6:87607195-87607245	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:87569230..87570355-chr6:87738909..87740054,4	MCF-7	breast:
2	chr6:87569023..87569900-chr6:87646597..87647139,2	MCF-7	breast:
3	chr6:87570712..87571662-chr6:87646445..87647351,6	MCF-7	breast:
4	chr6:87570969..87571590-chr6:87646510..87647169,2	MCF-7	breast:
5	chr6:87569382..87569938-chr6:87739160..87740006,3	MCF-7	breast:
6	chr6:87569162..87570137-chr6:87646249..87647415,7	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000217769	TF binding region
ENSG00000220240	TF binding region
ENSG00000217769	CpG island
ENSG00000220240	CpG island
ENSG00000168830	chromatin interactions

Extended variants
information (count: 862 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:862 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs578202950	chr6:87567585-87567586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575658106	chr6:87569040-87569041	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536742710	chr6:87569064-87569065	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs539827354	chr6:87569096-87569097	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558381348	chr6:87569098-87569099	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs55982849	chr6:87569105-87569106	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs540892750	chr6:87569145-87569146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553200196	chr6:87569211-87569212	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574770170	chr6:87569240-87569241	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576617679	chr6:87569253-87569254	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369518427	chr6:87569260-87569261	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542174802	chr6:87569264-87569265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187965378	chr6:87569327-87569328	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs35360309	chr6:87569333-87569334	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs531780590	chr6:87569352-87569353	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs372964033	chr6:87569364-87569365	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs12525091	chr6:87569383-87569384	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551938352	chr6:87569439-87569440	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs567689450	chr6:87569480-87569481	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142969315	chr6:87569482-87569483	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs12525105	chr6:87569507-87569508	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs547686945	chr6:87569526-87569527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4544880	chr6:87569562-87569563	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530305847	chr6:87569591-87569592	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs369821573	chr6:87569608-87569609	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569272244	chr6:87569614-87569615	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs536648891	chr6:87569615-87569616	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs191108947	chr6:87569628-87569629	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372655417	chr6:87569666-87569667	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376458842	chr6:87569714-87569715	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs9444442	chr6:87569725-87569726	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs184023406	chr6:87569759-87569760	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574733780	chr6:87569808-87569809	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs150174333	chr6:87569811-87569812	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs557302187	chr6:87569815-87569816	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188713315	chr6:87569829-87569830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114096747	chr6:87569842-87569843	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565344398	chr6:87569865-87569866	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs532482865	chr6:87569879-87569880	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs559619350	chr6:87569887-87569888	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs72910598	chr6:87569912-87569913	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs559514788	chr6:87569928-87569929	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs191671696	chr6:87569977-87569978	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548429650	chr6:87570005-87570006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs138635841	chr6:87570030-87570031	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs149308169	chr6:87570036-87570037	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547795287	chr6:87570080-87570081	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551871953	chr6:87570083-87570084	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570712887	chr6:87570104-87570105	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184455304	chr6:87570125-87570126	Inactive region	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
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
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
Myelodysplastic syndrome	18508791	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	21364760	CNVD
Developmental delay	19490664	CNVD
Schizophrenia	23813976	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:87567000-87567600	Enhancers	Fetal Lung	lung
2	chr6:87567200-87567600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr6:87577600-87577800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:87578000-87582600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:87582600-87582800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:87597200-87598000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr6:87597200-87599200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:87597400-87597600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:87597400-87597800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr6:87597400-87597800	Enhancers	H9 Cell Line	embryonic stem cell
11	chr6:87597400-87598200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr6:87597400-87598400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:87597400-87598400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:87597400-87599000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr6:87597600-87598000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr6:87597600-87599200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr6:87597600-87599200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:87597800-87599000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr6:87597800-87599200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr6:87598000-87598400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr6:87598200-87599400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr6:87598400-87599400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr6:87598800-87599000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr6:87599000-87599200	Enhancers	H9 Cell Line	embryonic stem cell
25	chr6:87599200-87599400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr6:87599400-87599600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr6:87599400-87604600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr6:87604600-87604800	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr6:87604600-87604800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr6:87604800-87605200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr6:87605000-87605200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr6:87607200-87607400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
33	chr6:87607200-87607400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
34	chr6:87607200-87607400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
35	chr6:87607200-87607400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
36	chr6:87607200-87607600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
37	chr6:87607200-87607600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
38	chr6:87607200-87607600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
39	chr6:87607200-87607800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
40	chr6:87607400-87607600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr6:87607400-87607600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr6:87607400-87607600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
43	chr6:87607400-87607600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr6:87607400-87608000	Active TSS	H9 Cell Line	embryonic stem cell
45	chr6:87607400-87608000	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr6:87607400-87608400	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr6:87607600-87607800	Active TSS	H1 Cell Line	embryonic stem cell
48	chr6:87607600-87608000	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr6:87607600-87608200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr6:87607600-87608200	Active TSS	HUES48 Cell Line	embryonic stem cell

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