Variant report

Variant	nsv5385
Chromosome Location	chr6:87781015-87803663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:87797762-87798194	GM12878	blood:	n/a	n/a
2	ATF2	chr6:87797755-87798253	GM12878	blood:	n/a	n/a
3	BACH1	chr6:87788747-87789058	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:87797746-87798075	GM12878	blood:	n/a	n/a
5	BATF	chr6:87791902-87792351	GM12878	blood:	n/a	n/a
6	BATF	chr6:87797786-87798113	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:87797775-87798107	GM12878	blood:	n/a	n/a
8	BCL3	chr6:87797793-87798126	GM12878	blood:	n/a	n/a
9	BCLAF1	chr6:87797660-87798172	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:87784199-87784212	GM12878	blood:	n/a	n/a
11	CEBPB	chr6:87803639-87804125	IMR90	lung:	n/a	n/a
12	CHD2	chr6:87783954-87784206	GM12878	blood:	n/a	n/a
13	CTCF	chr6:87788880-87789030	GM12865	blood:	n/a	chr6:87788918-87788931
14	CTCF	chr6:87788840-87788990	AG09319	gingival:	n/a	chr6:87788918-87788931
15	CTCF	chr6:87788752-87789097	Gliobla	brain:	n/a	chr6:87788918-87788931
16	CTCF	chr6:87788840-87788990	AoAF	blood vessel:	n/a	chr6:87788918-87788931
17	CTCF	chr6:87788759-87789089	Fibrobl	skin:	n/a	chr6:87788918-87788931
18	CTCF	chr6:87788860-87789010	GM12871	blood:	n/a	chr6:87788918-87788931
19	CTCF	chr6:87788785-87789045	Hela-S3	cervix:	n/a	chr6:87788918-87788931
20	CTCF	chr6:87788840-87788990	HPF	lung:	n/a	chr6:87788918-87788931
21	CTCF	chr6:87788860-87789010	GM12872	blood:	n/a	chr6:87788918-87788931
22	CTCF	chr6:87788840-87788990	HUVEC	blood vessel:	n/a	chr6:87788918-87788931
23	CTCF	chr6:87788860-87789010	Hela-S3	cervix:	n/a	chr6:87788918-87788931
24	CTCF	chr6:87788860-87789010	GM12868	blood:	n/a	chr6:87788918-87788931
25	CTCF	chr6:87788784-87789051	H1-hESC	embryonic stem cell:	n/a	chr6:87788918-87788931
26	CTCF	chr6:87788840-87788990	A549	lung:	n/a	chr6:87788918-87788931
27	CTCF	chr6:87788716-87789165	H1-hESC	embryonic stem cell:	n/a	chr6:87788918-87788931
28	CTCF	chr6:87788940-87789090	HAc	cerebellar:	n/a	n/a
29	CTCF	chr6:87788840-87788990	HMEC	breast:	n/a	chr6:87788918-87788931
30	CTCF	chr6:87788880-87789030	GM12870	blood:	n/a	chr6:87788918-87788931
31	CTCF	chr6:87788860-87789010	GM12865	blood:	n/a	chr6:87788918-87788931
32	CTCF	chr6:87788763-87789087	GM12891	blood:	n/a	chr6:87788918-87788931
33	CTCF	chr6:87788840-87788990	NB4	blood:	n/a	chr6:87788918-87788931
34	CTCF	chr6:87788820-87788970	HFF-Myc	foreskin:	n/a	chr6:87788918-87788931
35	CTCF	chr6:87788762-87789140	A549	lung:	n/a	chr6:87788918-87788931
36	CTCF	chr6:87781566-87781620	GM19240	blood:	n/a	n/a
37	CTCF	chr6:87788840-87788990	HEEpiC	esophagus:	n/a	chr6:87788918-87788931
38	CTCF	chr6:87788820-87788970	AG04449	skin:	n/a	chr6:87788918-87788931
39	CTCF	chr6:87788860-87789010	HRE	kidney:	n/a	chr6:87788918-87788931
40	CTCF	chr6:87788820-87788970	GM12866	blood:	n/a	chr6:87788918-87788931
41	CTCF	chr6:87788840-87788990	HCM	heart:	n/a	chr6:87788918-87788931
42	CTCF	chr6:87788880-87789030	NHLF	lung:	n/a	chr6:87788918-87788931
43	CTCF	chr6:87788800-87788950	NHDF-neo	bronchial:	n/a	chr6:87788918-87788931
44	CTCF	chr6:87788840-87788990	SAEC	small airway:	n/a	chr6:87788918-87788931
45	CTCF	chr6:87788797-87789044	HepG2	liver:	n/a	chr6:87788918-87788931
46	CTCF	chr6:87788860-87789010	HFF-Myc	foreskin:	n/a	chr6:87788918-87788931
47	CTCF	chr6:87788820-87788970	NHEK	skin:	n/a	chr6:87788918-87788931
48	CTCF	chr6:87788759-87789088	GM19238	blood:	n/a	chr6:87788918-87788931
49	CTCF	chr6:87788763-87789077	MCF-7	breast:	n/a	chr6:87788918-87788931
50	CTCF	chr6:87788840-87788990	GM12864	blood:	n/a	chr6:87788918-87788931

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:87802626-87802676	MCF-7	breast:	n/a
2	chr6:87802626-87802676	AoSMC	blood vessel:	n/a
3	chr6:87802626-87802676	HCM	heart:	n/a
4	chr6:87802626-87802676	HMEC	breast:	n/a
5	chr6:87802626-87802676	ECC-1	luminal epithelium:	n/a
6	chr6:87802626-87802676	Caco-2	colon:	n/a
7	chr6:87802626-87802676	HNPCEpiC	eye:	n/a
8	chr6:87802626-87802676	GM12892	blood:	n/a
9	chr6:87802626-87802676	HRCEpiC	kidney:	n/a
10	chr6:87802626-87802676	HEK293	kidney:	embryo
11	chr6:87802626-87802676	PFSK-1	brain:	n/a
12	chr6:87802626-87802676	HCT-116	colon:	n/a
13	chr6:87802626-87802676	HCPEpiC	choroid plexus:	n/a
14	chr6:87802626-87802676	IMR90	lung:	fetal
15	chr6:87802626-87802676	NB4	blood:	n/a
16	chr6:87802626-87802676	SK-N-SH	brain:	n/a
17	chr6:87802626-87802676	Jurkat	blood:	n/a
18	chr6:87802626-87802676	HAEpiC	amniotic membrane:	n/a
19	chr6:87802626-87802676	BJ	skin:	n/a
20	chr6:87802626-87802676	GM12891	blood:	n/a
21	chr6:87802626-87802676	HCF	heart:	n/a
22	chr6:87802626-87802676	NH-A	brain:	n/a
23	chr6:87802626-87802676	CMK	blood:	n/a
24	chr6:87802626-87802676	Hela-S3	cervix:	n/a
25	chr6:87802626-87802676	U87	brain:	n/a
26	chr6:87802626-87802676	HUVEC	blood vessel:	n/a
27	chr6:87802626-87802676	MCF10A-Er-Src	breast:	n/a
28	chr6:87802626-87802676	NHDF-neo	bronchial:	n/a
29	chr6:87802626-87802676	K562	blood:	n/a
30	chr6:87802626-87802676	PANC-1	pancreas:	n/a
31	chr6:87802626-87802676	LNCaP	prostate:	n/a
32	chr6:87802626-87802676	RPTEC	kidney:	n/a
33	chr6:87802626-87802676	H1-hESC	embryonic stem cell:	embryo
34	chr6:87802626-87802676	SK-N-SH_RA	brain:	n/a
35	chr6:87802626-87802676	SKMC	muscle:	n/a
36	chr6:87802626-87802676	SK-N-MC	brain:	n/a
37	chr6:87802626-87802676	Hepatocyte	liver:	n/a
38	chr6:87802626-87802676	ProgFib	skin:	n/a
39	chr6:87802626-87802676	HRPEpiC	eye:	n/a
40	chr6:87802626-87802676	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:87802626-87802676	AG09319	gingival:	n/a
42	chr6:87802626-87802676	AG10803	skin:	n/a
43	chr6:87802626-87802676	HepG2	liver:	n/a
44	chr6:87802626-87802676	A549	lung:	n/a
45	chr6:87802626-87802676	NT2-D1	testis:	n/a
46	chr6:87802626-87802676	AG04449	skin:	fetal
47	chr6:87802626-87802676	T-47D	breast:	n/a
48	chr6:87802626-87802676	HRE	kidney:	n/a
49	chr6:87802626-87802676	HL-60	blood:	n/a
50	chr6:87802626-87802676	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:87789226..87790732-chr6:87794986..87797378,2	MCF-7	breast:
2	chr6:87793956..87798150-chr6:87800009..87803465,4	K562	blood:
3	chr6:87789226..87790732-chr6:87794986..87797378,2	MCF-7	breast:
4	chr6:87793956..87798150-chr6:87800009..87803465,4	K562	blood:
5	chr6:87786543..87788379-chr6:87789393..87791059,2	MCF-7	breast:
6	chr6:87786543..87788379-chr6:87789393..87791059,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HTR1E-2	chr6:87792951-87793254	NONHSAT113894
2	lnc-HTR1E-1	chr6:87784151-87784384	NONHSAT113893

Variant related genes	Relation type
RN7SKP209	TF binding region
ENSG00000217776	TF binding region
RN7SKP209	CpG island
ENSG00000217776	CpG island

Extended variants
information (count: 837 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:837 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534828106	chr6:87781053-87781054	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs35976211	chr6:87781058-87781059	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs546901275	chr6:87781077-87781078	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs533000727	chr6:87781120-87781121	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs568309783	chr6:87781141-87781142	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs182376134	chr6:87781143-87781144	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs71572742	chr6:87781172-87781173	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs554625192	chr6:87781184-87781185	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs78596773	chr6:87781261-87781262	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs537118553	chr6:87781273-87781274	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs558640767	chr6:87781325-87781326	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs554070969	chr6:87781348-87781349	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs78688461	chr6:87781373-87781374	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs186659851	chr6:87781394-87781395	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs192257652	chr6:87781458-87781459	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs571203959	chr6:87781463-87781464	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs372456968	chr6:87781465-87781466	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs367914658	chr6:87781506-87781507	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs575073712	chr6:87781573-87781574	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs542521135	chr6:87781602-87781603	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs540799339	chr6:87781617-87781618	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs530543690	chr6:87781697-87781698	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs149121352	chr6:87781704-87781705	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs111685701	chr6:87781711-87781712	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs564204683	chr6:87781724-87781725	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs528274160	chr6:87781759-87781760	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs74415208	chr6:87781783-87781784	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs568254483	chr6:87781799-87781800	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs530695692	chr6:87781804-87781805	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs535341433	chr6:87781805-87781806	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs540144553	chr6:87781836-87781837	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs146132675	chr6:87781843-87781844	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs79690013	chr6:87781863-87781864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs62439468	chr6:87781889-87781890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115390831	chr6:87781919-87781920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558602243	chr6:87781967-87781968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138877504	chr6:87781974-87781975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534882097	chr6:87781995-87781996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141340201	chr6:87782007-87782008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76150646	chr6:87782016-87782017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs115985460	chr6:87782041-87782042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs146973468	chr6:87782047-87782048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs575333704	chr6:87782067-87782068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148012333	chr6:87782119-87782120	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs183390912	chr6:87782137-87782138	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs545842204	chr6:87782160-87782161	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs543827685	chr6:87782192-87782193	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs528152537	chr6:87782231-87782232	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs141669519	chr6:87782258-87782259	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs377199001	chr6:87782328-87782329	Weak transcription Enhancers	TF binding 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
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:87769000-87784000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:87779800-87781600	Enhancers	Duodenum Mucosa	Duodenum
3	chr6:87779800-87781600	Enhancers	Fetal Intestine Large	intestine
4	chr6:87779800-87785200	Enhancers	Fetal Intestine Small	intestine
5	chr6:87780400-87784000	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:87780600-87783600	Weak transcription	Stomach Mucosa	stomach
7	chr6:87780600-87784000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr6:87781000-87781600	Bivalent Enhancer	Small Intestine	intestine
9	chr6:87781000-87783800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:87781600-87782400	Weak transcription	Duodenum Mucosa	Duodenum
11	chr6:87781600-87782800	Weak transcription	Fetal Intestine Large	intestine
12	chr6:87782400-87784400	Enhancers	Duodenum Mucosa	Duodenum
13	chr6:87782800-87785200	Enhancers	Fetal Intestine Large	intestine
14	chr6:87783400-87784200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr6:87783600-87784400	Enhancers	Stomach Mucosa	stomach
16	chr6:87783800-87784400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr6:87784000-87784200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr6:87784000-87784400	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr6:87784000-87784400	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr6:87784000-87784400	Enhancers	Small Intestine	intestine
21	chr6:87784000-87784400	Enhancers	HepG2	liver
22	chr6:87784000-87785200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr6:87784000-87785200	Enhancers	Adipose Nuclei	Adipose
24	chr6:87784000-87785400	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr6:87784200-87784400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:87784400-87786400	Weak transcription	Stomach Mucosa	stomach
27	chr6:87784600-87785400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr6:87785200-87786600	Weak transcription	Fetal Intestine Small	intestine
29	chr6:87785200-87789000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:87786400-87786800	Enhancers	Stomach Mucosa	stomach
31	chr6:87786600-87786800	Enhancers	Fetal Intestine Small	intestine
32	chr6:87788600-87789200	Enhancers	Brain Substantia Nigra	brain
33	chr6:87788800-87789000	Enhancers	GM12878-XiMat	blood
34	chr6:87788800-87789400	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr6:87789000-87789200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr6:87789000-87789200	Enhancers	Spleen	Spleen
37	chr6:87789000-87790600	Weak transcription	GM12878-XiMat	blood
38	chr6:87790600-87793200	Enhancers	GM12878-XiMat	blood
39	chr6:87791600-87793200	Enhancers	Primary B cells from peripheral blood	blood
40	chr6:87792200-87794000	Weak transcription	Placenta	Placenta
41	chr6:87792800-87793000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:87793000-87798200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:87793200-87797600	Weak transcription	GM12878-XiMat	blood
44	chr6:87794000-87799800	Strong transcription	Placenta	Placenta
45	chr6:87797600-87798200	Enhancers	GM12878-XiMat	blood
46	chr6:87799800-87801400	Weak transcription	Placenta	Placenta
47	chr6:87801400-87804800	Active TSS	Placenta	Placenta
48	chr6:87801400-87805000	Active TSS	Hela-S3	cervix
49	chr6:87803000-87803800	Enhancers	HMEC	breast
50	chr6:87803000-87804000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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