Variant report

Variant	nsv969456
Chromosome Location	chr6:150263659-150269861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTBP2	chr6:150262374-150263823	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr6:150263620-150263770	BJ	skin:	n/a	n/a
3	CTCF	chr6:150263680-150263830	WI-38	lung:	n/a	n/a
4	CTCF	chr6:150263687-150263805	Gliobla	brain:	n/a	n/a
5	CTCF	chr6:150263560-150263710	HMEC	breast:	n/a	n/a
6	CTCF	chr6:150263729-150263754	MCF-7	breast:	n/a	n/a
7	CTCF	chr6:150263620-150263770	HBMEC	blood vessel:	n/a	n/a
8	CTCF	chr6:150263600-150263750	NHEK	skin:	n/a	n/a
9	CTCF	chr6:150263620-150263770	HCFaa	heart:	n/a	n/a
10	CTCF	chr6:150263600-150263750	HA-sp	spinal cord:	n/a	n/a
11	CTCF	chr6:150263600-150263750	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr6:150263667-150263813	Fibrobl	skin:	n/a	n/a
13	CTCF	chr6:150263680-150263830	AG10803	skin:	n/a	n/a
14	CTCF	chr6:150263680-150263830	SAEC	small airway:	n/a	n/a
15	CTCF	chr6:150263500-150263750	HRE	kidney:	n/a	n/a
16	CTCF	chr6:150268200-150268350	NHEK	skin:	n/a	chr6:150268214-150268227
17	CTCF	chr6:150263600-150263750	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr6:150263600-150263750	AG04450	lung:	n/a	n/a
19	CTCF	chr6:150263600-150263750	HBMEC	blood vessel:	n/a	n/a
20	CTCF	chr6:150263600-150263750	HEK293	kidney:	n/a	n/a
21	CTCF	chr6:150263600-150263750	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr6:150263698-150263769	HUVEC	blood vessel:	n/a	n/a
23	CTCF	chr6:150263718-150263768	GM19238	blood:	n/a	n/a
24	CTCF	chr6:150263723-150263761	ProgFib	skin:	n/a	n/a
25	CTCF	chr6:150263680-150263830	AG04449	skin:	n/a	n/a
26	CTCF	chr6:150263660-150263810	HPAF	blood vessel:	n/a	n/a
27	CTCF	chr6:150263600-150263750	AG04449	skin:	n/a	n/a
28	CTCF	chr6:150263702-150263815	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:150263739-150263757	GM12878	blood:	n/a	n/a
30	CTCF	chr6:150263580-150263730	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr6:150263600-150263750	BJ	skin:	n/a	n/a
32	CTCF	chr6:150263686-150263804	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:150263672-150263780	NHEK	skin:	n/a	n/a
34	CTCF	chr6:150263620-150263770	HAc	cerebellar:	n/a	n/a
35	CTCF	chr6:150263660-150263810	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr6:150268200-150268350	HEK293	kidney:	n/a	chr6:150268214-150268227
37	EBF1	chr6:150266439-150266694	GM12878	blood:	n/a	n/a
38	EBF1	chr6:150266440-150266727	GM12878	blood:	n/a	n/a
39	GABPA	chr6:150262610-150263770	MCF-7	breast:	n/a	n/a
40	MAX	chr6:150264524-150264741	K562	blood:	n/a	n/a
41	MYC	chr6:150268271-150268402	GM12878	blood:	n/a	n/a
42	MYC	chr6:150268690-150268787	HepG2	liver:	n/a	n/a
43	MYC	chr6:150266553-150266636	HUVEC	blood vessel:	n/a	n/a
44	POLR2A	chr6:150266057-150266095	MCF-7	breast:	n/a	n/a
45	REST	chr6:150262686-150263706	H1-neurons	neurons:	n/a	n/a
46	SUZ12	chr6:150262966-150263983	H1-hESC	embryonic stem cell:	n/a	n/a
47	USF1	chr6:150266043-150266248	HepG2	liver:	n/a	chr6:150266167-150266178
48	ZBTB7A	chr6:150262908-150263813	ECC-1	luminal epithelium:	n/a	chr6:150263746-150263755
49	ZBTB7A	chr6:150262925-150263665	ECC-1	luminal epithelium:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150266173-150266223	AoSMC	blood vessel:	n/a
2	chr6:150263722-150263772	HCT-116	colon:	n/a
3	chr6:150263722-150263772	Hela-S3	cervix:	n/a
4	chr6:150266173-150266223	HAEpiC	amniotic membrane:	n/a
5	chr6:150266173-150266223	RPTEC	kidney:	n/a
6	chr6:150263722-150263772	SKMC	muscle:	n/a
7	chr6:150269220-150269270	NH-A	brain:	n/a
8	chr6:150263722-150263772	NH-A	brain:	n/a
9	chr6:150266173-150266223	HCM	heart:	n/a
10	chr6:150269220-150269270	CMK	blood:	n/a
11	chr6:150269220-150269270	SKMC	muscle:	n/a
12	chr6:150263722-150263772	AG04450	lung:	fetal
13	chr6:150269220-150269270	U87	brain:	n/a
14	chr6:150269220-150269270	ProgFib	skin:	n/a
15	chr6:150269220-150269270	HepG2	liver:	n/a
16	chr6:150263722-150263772	CMK	blood:	n/a
17	chr6:150266173-150266223	AG04449	skin:	fetal
18	chr6:150263722-150263772	ovcar-3	ovarian:	n/a
19	chr6:150263722-150263772	SAEC	small airway:	n/a
20	chr6:150266173-150266223	IMR90	lung:	fetal
21	chr6:150263722-150263772	Caco-2	colon:	n/a
22	chr6:150263722-150263772	NHDF-neo	bronchial:	n/a
23	chr6:150269220-150269270	HCPEpiC	choroid plexus:	n/a
24	chr6:150266173-150266223	GM12878	blood:	n/a
25	chr6:150263722-150263772	GM12891	blood:	n/a
26	chr6:150266173-150266223	NHBE	bronchial:	n/a
27	chr6:150269220-150269270	Caco-2	colon:	n/a
28	chr6:150269220-150269270	HCF	heart:	n/a
29	chr6:150266173-150266223	HL-60	blood:	n/a
30	chr6:150266173-150266223	MCF10A-Er-Src	breast:	n/a
31	chr6:150263722-150263772	HNPCEpiC	eye:	n/a
32	chr6:150269220-150269270	T-47D	breast:	n/a
33	chr6:150266173-150266223	HNPCEpiC	eye:	n/a
34	chr6:150266173-150266223	NHDF-neo	bronchial:	n/a
35	chr6:150266173-150266223	NH-A	brain:	n/a
36	chr6:150263722-150263772	GM12892	blood:	n/a
37	chr6:150263722-150263772	U87	brain:	n/a
38	chr6:150269220-150269270	HRCEpiC	kidney:	n/a
39	chr6:150266173-150266223	T-47D	breast:	n/a
40	chr6:150263722-150263772	HUVEC	blood vessel:	n/a
41	chr6:150263722-150263772	HEEpiC	esophagus:	n/a
42	chr6:150266173-150266223	AG09309	skin:	n/a
43	chr6:150269220-150269270	MCF10A-Er-Src	breast:	n/a
44	chr6:150263722-150263772	AoSMC	blood vessel:	n/a
45	chr6:150263722-150263772	PrEC	prostate:	n/a
46	chr6:150269220-150269270	HEEpiC	esophagus:	n/a
47	chr6:150266173-150266223	GM19239	blood:	n/a
48	chr6:150263722-150263772	AG09309	skin:	n/a
49	chr6:150266173-150266223	PANC-1	pancreas:	n/a
50	chr6:150269220-150269270	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:150263150..150264777-chr6:150325600..150328449,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000215094	TF binding region
ENSG00000215094	CpG island
ENSG00000218358	chromatin interactions

Extended variants
information (count: 382 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572558542	chr6:150263720-150263721	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568258048	chr6:150263729-150263730	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541479654	chr6:150263741-150263742	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537034606	chr6:150263750-150263751	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs370126198	chr6:150263755-150263756	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs570778930	chr6:150263771-150263772	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539758354	chr6:150263773-150263774	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs11381985	chr6:150263786-150263787	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs397887957	chr6:150263789-150263790	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs56985227	chr6:150263798-150263799	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573359177	chr6:150263815-150263816	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs113029965	chr6:150263820-150263821	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555160013	chr6:150263837-150263838	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575445653	chr6:150263873-150263874	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34666679	chr6:150263936-150263937	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs544200424	chr6:150263959-150263960	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564086829	chr6:150263961-150263962	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542914116	chr6:150263962-150263963	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7748709	chr6:150263996-150263997	Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184847473	chr6:150264005-150264006	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs368437980	chr6:150264018-150264019	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375570158	chr6:150264032-150264033	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7748726	chr6:150264033-150264034	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542844392	chr6:150264070-150264071	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561827653	chr6:150264115-150264116	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530931331	chr6:150264116-150264117	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548482970	chr6:150264119-150264120	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs60248818	chr6:150264134-150264135	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs148021014	chr6:150264140-150264141	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141692740	chr6:150264142-150264143	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs28431039	chr6:150264147-150264148	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567194415	chr6:150264155-150264156	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181307692	chr6:150264164-150264165	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs73782157	chr6:150264188-150264189	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs568939999	chr6:150264198-150264199	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs375244060	chr6:150264233-150264234	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557740674	chr6:150264243-150264244	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs184403861	chr6:150264244-150264245	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs372951896	chr6:150264249-150264250	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs141014319	chr6:150264271-150264272	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs564672201	chr6:150264280-150264281	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs573909809	chr6:150264303-150264304	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542427395	chr6:150264324-150264325	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145815080	chr6:150264346-150264347	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530871578	chr6:150264360-150264361	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544301270	chr6:150264392-150264393	Weak transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs527375850	chr6:150264413-150264414	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189161727	chr6:150264418-150264419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs116264270	chr6:150264420-150264421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547005549	chr6:150264444-150264445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150261400-150264000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr6:150262400-150263800	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:150262400-150263800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
4	chr6:150262400-150263800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:150262400-150263800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
6	chr6:150262400-150263800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:150262400-150263800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:150262400-150263800	Active TSS	Brain Angular Gyrus	brain
9	chr6:150262400-150263800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
10	chr6:150262400-150263800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
11	chr6:150262400-150263800	Active TSS	HSMMtube	muscle
12	chr6:150262400-150264000	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:150262400-150264000	Bivalent/Poised TSS	Fetal Brain Female	brain
14	chr6:150262400-150264000	Active TSS	NHLF	lung
15	chr6:150262600-150263800	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:150262600-150263800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
17	chr6:150262600-150263800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
18	chr6:150262600-150263800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
19	chr6:150262600-150263800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr6:150262600-150263800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
21	chr6:150262600-150263800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
22	chr6:150262600-150263800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:150262600-150263800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr6:150262600-150263800	Active TSS	Breast Myoepithelial Primary Cells	Breast
25	chr6:150262600-150263800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:150262600-150263800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
27	chr6:150262600-150263800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
28	chr6:150262600-150263800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
29	chr6:150262600-150263800	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
30	chr6:150262600-150263800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
31	chr6:150262600-150263800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
32	chr6:150262600-150263800	Flanking Bivalent TSS/Enh	Placenta	Placenta
33	chr6:150262600-150263800	Active TSS	A549	lung
34	chr6:150262600-150263800	Active TSS	Osteobl	bone
35	chr6:150262600-150264000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr6:150262600-150264000	Active TSS	Muscle Satellite Cultured Cells	--
37	chr6:150262800-150263800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:150262800-150263800	Active TSS	K562	blood
39	chr6:150262800-150264000	Active TSS	NH-A	brain
40	chr6:150262800-150264000	Active TSS	NHDF-Ad	bronchial
41	chr6:150263000-150263800	Active TSS	Primary T cells from cord blood	blood
42	chr6:150263200-150263800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:150263200-150263800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
44	chr6:150263200-150263800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr6:150263200-150263800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr6:150263200-150263800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr6:150263200-150263800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:150263200-150263800	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
49	chr6:150263200-150263800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
50	chr6:150263200-150264000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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