Variant report

Variant	nsv970175
Chromosome Location	chr6:150286661-150300237
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:69)
CpG islands
(count:244)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:69 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:150296076-150296311	K562	blood:	n/a	n/a
2	BACH1	chr6:150284433-150286779	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:150289655-150289983	GM12878	blood:	n/a	n/a
4	BATF	chr6:150289623-150289977	GM12878	blood:	n/a	n/a
5	BATF	chr6:150298528-150298786	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:150289639-150290006	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:150289721-150289956	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:150295579-150295714	K562	blood:	n/a	n/a
9	BHLHE40	chr6:150295574-150295710	GM12878	blood:	n/a	n/a
10	CEBPB	chr6:150296087-150296285	K562	blood:	n/a	n/a
11	CTBP2	chr6:150286470-150287104	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr6:150287230-150287309	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr6:150296100-150296250	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr6:150296100-150296250	GM12865	blood:	n/a	n/a
15	CTCF	chr6:150296161-150296302	K562	blood:	n/a	n/a
16	CTCF	chr6:150296080-150296230	HEK293	kidney:	n/a	n/a
17	CTCF	chr6:150289475-150289519	GM19239	blood:	n/a	n/a
18	CTCF	chr6:150289845-150289906	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr6:150296060-150296210	HL-60	blood:	n/a	n/a
20	CTCF	chr6:150296217-150296283	GM12878	blood:	n/a	n/a
21	CTCF	chr6:150296069-150296330	K562	blood:	n/a	n/a
22	CTCF	chr6:150290075-150290112	GM10248	blood:	n/a	n/a
23	CTCF	chr6:150295702-150295744	GM10248	blood:	n/a	n/a
24	CTCF	chr6:150296160-150296310	NB4	blood:	n/a	n/a
25	CTCF	chr6:150296140-150296290	K562	blood:	n/a	n/a
26	CTCF	chr6:150296180-150296330	GM12874	blood:	n/a	n/a
27	CTCF	chr6:150286580-150286730	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr6:150296120-150296270	GM12872	blood:	n/a	n/a
29	CTCF	chr6:150287224-150287228	Kidney_OC	kidney:	n/a	n/a
30	EBF1	chr6:150295573-150295844	GM12878	blood:	n/a	n/a
31	ELF1	chr6:150296034-150296256	K562	blood:	n/a	n/a
32	HCFC1	chr6:150296057-150296224	K562	blood:	n/a	n/a
33	IRF4	chr6:150289595-150290005	GM12878	blood:	n/a	n/a
34	IRF4	chr6:150289623-150290086	GM12878	blood:	n/a	n/a
35	JUN	chr6:150286760-150286774	H1-hESC	embryonic stem cell:	n/a	n/a
36	JUND	chr6:150296135-150296201	K562	blood:	n/a	n/a
37	MAX	chr6:150296009-150296280	NB4	blood:	n/a	chr6:150296199-150296208
38	NFIC	chr6:150289719-150290105	GM12878	blood:	n/a	n/a
39	NR2F2	chr6:150299771-150300112	MCF-7	breast:	n/a	n/a
40	PAX5	chr6:150289550-150290061	GM12878	blood:	n/a	n/a
41	PBX3	chr6:150295636-150295771	GM12878	blood:	n/a	n/a
42	POLR2A	chr6:150294959-150295375	K562	blood:	n/a	n/a
43	POLR2A	chr6:150295564-150295766	HCT-116	colon:	n/a	n/a
44	POLR2A	chr6:150286774-150286780	K562	blood:	n/a	n/a
45	POLR2A	chr6:150298226-150298239	MCF-7	breast:	n/a	n/a
46	POLR2A	chr6:150295767-150295816	A549	lung:	n/a	n/a
47	POLR2A	chr6:150287056-150287264	K562	blood:	n/a	n/a
48	POLR2A	chr6:150294255-150294286	GM12878	blood:	n/a	n/a
49	POLR2A	chr6:150286841-150287021	K562	blood:	n/a	n/a
50	POLR2A	chr6:150294353-150294618	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:150286646-150286696	IMR90	lung:	fetal
2	chr6:150289488-150289538	HEEpiC	esophagus:	n/a
3	chr6:150289488-150289538	GM12891	blood:	n/a
4	chr6:150286646-150286696	HepG2	liver:	n/a
5	chr6:150286838-150286888	NB4	blood:	n/a
6	chr6:150286838-150286888	NHBE	bronchial:	n/a
7	chr6:150286838-150286888	Jurkat	blood:	n/a
8	chr6:150293190-150293240	PANC-1	pancreas:	n/a
9	chr6:150286646-150286696	PFSK-1	brain:	n/a
10	chr6:150286646-150286696	GM12892	blood:	n/a
11	chr6:150286838-150286888	PANC-1	pancreas:	n/a
12	chr6:150286838-150286888	GM12891	blood:	n/a
13	chr6:150286646-150286696	GM12891	blood:	n/a
14	chr6:150286646-150286696	AG09319	gingival:	n/a
15	chr6:150293190-150293240	SK-N-SH	brain:	n/a
16	chr6:150286838-150286888	IMR90	lung:	fetal
17	chr6:150293190-150293240	GM12892	blood:	n/a
18	chr6:150286838-150286888	RPTEC	kidney:	n/a
19	chr6:150289488-150289538	HCT-116	colon:	n/a
20	chr6:150293190-150293240	Jurkat	blood:	n/a
21	chr6:150293190-150293240	MCF-7	breast:	n/a
22	chr6:150286838-150286888	GM12892	blood:	n/a
23	chr6:150286646-150286696	U87	brain:	n/a
24	chr6:150293190-150293240	ECC-1	luminal epithelium:	n/a
25	chr6:150293190-150293240	SK-N-SH_RA	brain:	n/a
26	chr6:150286838-150286888	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:150286646-150286696	SK-N-SH	brain:	n/a
28	chr6:150289488-150289538	HCPEpiC	choroid plexus:	n/a
29	chr6:150289488-150289538	BJ	skin:	n/a
30	chr6:150289488-150289538	HRE	kidney:	n/a
31	chr6:150286838-150286888	HRCEpiC	kidney:	n/a
32	chr6:150293190-150293240	Caco-2	colon:	n/a
33	chr6:150286646-150286696	HPAEpiC	pulmonary alveolar:	n/a
34	chr6:150286838-150286888	T-47D	breast:	n/a
35	chr6:150286838-150286888	SK-N-SH	brain:	n/a
36	chr6:150286646-150286696	NHDF-neo	bronchial:	n/a
37	chr6:150286646-150286696	T-47D	breast:	n/a
38	chr6:150289488-150289538	HIPEpiC	eye:	n/a
39	chr6:150293190-150293240	AG04449	skin:	fetal
40	chr6:150286838-150286888	HUVEC	blood vessel:	n/a
41	chr6:150286646-150286696	Jurkat	blood:	n/a
42	chr6:150289488-150289538	GM12892	blood:	n/a
43	chr6:150286646-150286696	HCF	heart:	n/a
44	chr6:150293190-150293240	HAEpiC	amniotic membrane:	n/a
45	chr6:150286646-150286696	LNCaP	prostate:	n/a
46	chr6:150289488-150289538	HMEC	breast:	n/a
47	chr6:150286838-150286888	A549	lung:	n/a
48	chr6:150293190-150293240	HRCEpiC	kidney:	n/a
49	chr6:150286838-150286888	PrEC	prostate:	n/a
50	chr6:150289488-150289538	RPTEC	kidney:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:150284327..150286937-chr6:150287191..150290217,6	K562	blood:
2	chr6:150286573..150288463-chr6:150317408..150319689,2	K562	blood:
3	chr6:150281848..150284809-chr6:150294278..150296186,2	MCF-7	breast:
4	chr6:150287137..150289834-chr6:150291906..150294473,3	K562	blood:
5	chr6:150286967..150289038-chr6:150325599..150328579,2	K562	blood:
6	chr6:150287137..150289834-chr6:150291906..150294473,3	K562	blood:
7	chr6:150295506..150297191-chr6:150310699..150313123,2	K562	blood:
8	chr6:150294863..150297113-chr6:150298287..150300861,2	K562	blood:
9	chr6:150285227..150287207-chr6:150324215..150327395,3	MCF-7	breast:
10	chr6:150290771..150293444-chr6:150298417..150300274,2	K562	blood:
11	chr6:150288130..150291946-chr6:150324543..150327440,3	MCF-7	breast:
12	chr6:150299443..150301992-chr6:150305424..150307057,2	MCF-7	breast:
13	chr6:150284181..150286252-chr6:150288131..150290781,3	MCF-7	breast:

No data

Variant related genes	Relation type
BTF3P10	TF binding region
ENSG00000219298	TF binding region
BTF3P10	CpG island
ENSG00000219298	CpG island
ENSG00000111981	chromatin interactions
ENSG00000219298	chromatin interactions
ENSG00000231120	chromatin interactions
ENSG00000218358	chromatin interactions

Extended variants
information (count: 637 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:637 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569194901	chr6:150286689-150286690	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs538525718	chr6:150286713-150286714	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552490360	chr6:150286735-150286736	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs566209261	chr6:150286749-150286750	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551812161	chr6:150286768-150286769	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs6911137	chr6:150286878-150286879	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373706045	chr6:150286883-150286884	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs528577589	chr6:150286933-150286934	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs534147339	chr6:150286934-150286935	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553407116	chr6:150286935-150286936	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573413217	chr6:150286938-150286939	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs185123550	chr6:150286940-150286941	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145110046	chr6:150286989-150286990	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs386706976	chr6:150287025-150287026	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs56855094	chr6:150287026-150287027	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs117826245	chr6:150287060-150287061	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201796026	chr6:150287065-150287066	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572240457	chr6:150287085-150287086	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs568376538	chr6:150287094-150287095	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138938297	chr6:150287095-150287096	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200780769	chr6:150287106-150287107	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9478311	chr6:150287135-150287136	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs367863620	chr6:150287151-150287152	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs56363137	chr6:150287154-150287155	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190053089	chr6:150287168-150287169	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs370060827	chr6:150287194-150287195	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs569598946	chr6:150287196-150287197	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs552024755	chr6:150287201-150287202	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs149381374	chr6:150287208-150287209	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs55908620	chr6:150287243-150287244	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148094617	chr6:150287289-150287290	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs567568561	chr6:150287298-150287299	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs71665652	chr6:150287318-150287319	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs535920646	chr6:150287379-150287380	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs56293488	chr6:150287489-150287490	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs193225777	chr6:150287510-150287511	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538276278	chr6:150287516-150287517	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs558767912	chr6:150287531-150287532	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs572379400	chr6:150287582-150287583	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs141838450	chr6:150287594-150287595	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs58431567	chr6:150287601-150287602	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116003865	chr6:150287646-150287647	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543089861	chr6:150287673-150287674	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs540786490	chr6:150287674-150287675	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs562855178	chr6:150287695-150287696	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs116280008	chr6:150287711-150287712	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs545083363	chr6:150287717-150287718	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs56068098	chr6:150287724-150287725	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs564981153	chr6:150287757-150287758	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs527978823	chr6:150287776-150287777	Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 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:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150284200-150286800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
2	chr6:150284200-150286800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
3	chr6:150284200-150286800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:150284200-150287000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
5	chr6:150284400-150286800	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr6:150284400-150286800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
7	chr6:150284400-150286800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
8	chr6:150284400-150286800	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
9	chr6:150284600-150286800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:150284600-150286800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
11	chr6:150284600-150286800	Active TSS	HSMMtube	muscle
12	chr6:150284800-150286800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr6:150284800-150286800	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
14	chr6:150285000-150286800	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:150285000-150286800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:150285000-150286800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
17	chr6:150285000-150286800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
18	chr6:150285200-150286800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:150285200-150286800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
20	chr6:150285200-150286800	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
21	chr6:150285200-150286800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
22	chr6:150285200-150286800	Flanking Bivalent TSS/Enh	Rectal Smooth Muscle	rectum
23	chr6:150285200-150286800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
24	chr6:150285200-150286800	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr6:150285200-150287000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr6:150285400-150286800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
27	chr6:150285400-150286800	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
28	chr6:150285400-150286800	Bivalent Enhancer	Fetal Intestine Large	intestine
29	chr6:150285400-150286800	Bivalent Enhancer	Fetal Intestine Small	intestine
30	chr6:150285600-150286800	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:150285800-150286800	Bivalent Enhancer	Fetal Brain Male	brain
32	chr6:150285800-150286800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
33	chr6:150285800-150287000	Bivalent/Poised TSS	Osteobl	bone
34	chr6:150286000-150286800	Bivalent/Poised TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr6:150286000-150286800	Enhancers	Pancreas	Pancrea
36	chr6:150286200-150286800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
37	chr6:150286200-150286800	Bivalent Enhancer	Fetal Lung	lung
38	chr6:150286200-150286800	Active TSS	Right Atrium	heart
39	chr6:150286200-150286800	Active TSS	HSMM	muscle
40	chr6:150286200-150286800	Flanking Bivalent TSS/Enh	NHEK	skin
41	chr6:150286200-150287000	Bivalent Enhancer	Esophagus	oesophagus
42	chr6:150286200-150287000	Enhancers	Gastric	stomach
43	chr6:150286400-150286800	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:150286400-150286800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
45	chr6:150286400-150286800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
46	chr6:150286400-150286800	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
47	chr6:150286400-150286800	Bivalent Enhancer	Brain Angular Gyrus	brain
48	chr6:150286400-150286800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
49	chr6:150286400-150286800	Bivalent Enhancer	Fetal Stomach	stomach
50	chr6:150286400-150286800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum

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