Variant report

Variant	nsv1046253
Chromosome Location	chr15:31364402-31412706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:454)
CpG islands
(count:976)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:454 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31384908-31385320	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:31381129-31381842	HepG2	liver:	n/a	n/a
3	ATF1	chr15:31371191-31371230	K562	blood:	n/a	n/a
4	ATF1	chr15:31376612-31376664	K562	blood:	n/a	n/a
5	BACH1	chr15:31373087-31373180	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr15:31396399-31396673	GM12878	blood:	n/a	n/a
7	BCL3	chr15:31384773-31385276	A549	lung:	n/a	n/a
8	BCL3	chr15:31369836-31370207	GM12878	blood:	n/a	n/a
9	BHLHE40	chr15:31384869-31385246	HepG2	liver:	n/a	n/a
10	BHLHE40	chr15:31381061-31382012	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:31381201-31381538	K562	blood:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
12	CEBPB	chr15:31381102-31381941	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
13	CEBPB	chr15:31381210-31381539	IMR90	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
14	CEBPB	chr15:31409068-31409078	HepG2	liver:	n/a	n/a
15	CEBPB	chr15:31381279-31381497	H1-hESC	embryonic stem cell:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
16	CEBPB	chr15:31381146-31381608	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
17	CEBPB	chr15:31381253-31381467	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
18	CEBPB	chr15:31381210-31381544	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
19	CEBPB	chr15:31371688-31372101	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:31381101-31381576	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
21	CEBPB	chr15:31380951-31381935	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
22	CEBPD	chr15:31381206-31381450	HepG2	liver:	n/a	n/a
23	CEBPD	chr15:31380900-31381232	HepG2	liver:	n/a	n/a
24	CHD2	chr15:31384828-31385165	HepG2	liver:	n/a	n/a
25	CHD2	chr15:31381045-31381371	HepG2	liver:	n/a	n/a
26	CHD2	chr15:31390949-31391119	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr15:31391094-31391108	HepG2	liver:	n/a	n/a
28	CHD2	chr15:31384391-31384410	HepG2	liver:	n/a	n/a
29	CHD2	chr15:31381613-31381922	HepG2	liver:	n/a	n/a
30	CTCF	chr15:31390900-31391050	GM06990	blood:	n/a	n/a
31	CTCF	chr15:31391620-31391770	GM12878	blood:	n/a	n/a
32	CTCF	chr15:31391580-31391730	HMEC	breast:	n/a	n/a
33	CTCF	chr15:31391620-31391770	AG04449	skin:	n/a	n/a
34	CTCF	chr15:31396356-31396383	GM19240	blood:	n/a	n/a
35	CTCF	chr15:31391800-31391950	A549	lung:	n/a	n/a
36	CTCF	chr15:31373040-31373190	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr15:31391660-31391810	GM12871	blood:	n/a	n/a
38	CTCF	chr15:31391560-31391710	HMF	breast:	n/a	n/a
39	CTCF	chr15:31391655-31391773	LNCaP	prostate:	n/a	n/a
40	CTCF	chr15:31391560-31391710	AG09309	skin:	n/a	n/a
41	CTCF	chr15:31396240-31396510	K562	blood:	n/a	n/a
42	CTCF	chr15:31391540-31391690	HCT-116	colon:	n/a	n/a
43	CTCF	chr15:31391538-31391830	K562	blood:	n/a	n/a
44	CTCF	chr15:31391440-31391590	GM06990	blood:	n/a	n/a
45	CTCF	chr15:31391680-31391830	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr15:31396313-31396427	GM12892	blood:	n/a	n/a
47	CTCF	chr15:31381160-31381199	GM10248	blood:	n/a	n/a
48	CTCF	chr15:31405140-31405290	GM12867	blood:	n/a	n/a
49	CTCF	chr15:31391480-31391630	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr15:31396334-31396393	Hela-S3	cervix:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31383719-31383769	HMEC	breast:	n/a
2	chr15:31372889-31372939	GM12878	blood:	n/a
3	chr15:31372742-31372792	HRCEpiC	kidney:	n/a
4	chr15:31393845-31393895	Jurkat	blood:	n/a
5	chr15:31372889-31372939	AG09319	gingival:	n/a
6	chr15:31372997-31373047	HEEpiC	esophagus:	n/a
7	chr15:31394188-31394238	HNPCEpiC	eye:	n/a
8	chr15:31370762-31370812	Jurkat	blood:	n/a
9	chr15:31381015-31381065	U87	brain:	n/a
10	chr15:31383719-31383769	NT2-D1	testis:	n/a
11	chr15:31395221-31395271	HEEpiC	esophagus:	n/a
12	chr15:31372889-31372939	GM19239	blood:	n/a
13	chr15:31393845-31393895	Hepatocyte	liver:	n/a
14	chr15:31370762-31370812	K562	blood:	n/a
15	chr15:31383719-31383769	HCPEpiC	choroid plexus:	n/a
16	chr15:31380908-31380958	T-47D	breast:	n/a
17	chr15:31381816-31381866	AG04450	lung:	fetal
18	chr15:31394021-31394071	HIPEpiC	eye:	n/a
19	chr15:31380908-31380958	Hela-S3	cervix:	n/a
20	chr15:31383719-31383769	HIPEpiC	eye:	n/a
21	chr15:31370762-31370812	ECC-1	luminal epithelium:	n/a
22	chr15:31381816-31381866	GM12878	blood:	n/a
23	chr15:31372889-31372939	ovcar-3	ovarian:	n/a
24	chr15:31395221-31395271	AG09309	skin:	n/a
25	chr15:31394021-31394071	HCPEpiC	choroid plexus:	n/a
26	chr15:31370762-31370812	AoSMC	blood vessel:	n/a
27	chr15:31395221-31395271	HEK293	kidney:	embryo
28	chr15:31381816-31381866	ECC-1	luminal epithelium:	n/a
29	chr15:31372742-31372792	HEEpiC	esophagus:	n/a
30	chr15:31383719-31383769	NH-A	brain:	n/a
31	chr15:31372742-31372792	Hepatocyte	liver:	n/a
32	chr15:31370762-31370812	ProgFib	skin:	n/a
33	chr15:31372997-31373047	GM12878	blood:	n/a
34	chr15:31372742-31372792	CMK	blood:	n/a
35	chr15:31379377-31379427	LNCaP	prostate:	n/a
36	chr15:31380908-31380958	HRCEpiC	kidney:	n/a
37	chr15:31394188-31394238	HAEpiC	amniotic membrane:	n/a
38	chr15:31391491-31391541	AG10803	skin:	n/a
39	chr15:31380908-31380958	HMEC	breast:	n/a
40	chr15:31370762-31370812	HRCEpiC	kidney:	n/a
41	chr15:31394188-31394238	H1-hESC	embryonic stem cell:	embryo
42	chr15:31394285-31394335	HRE	kidney:	n/a
43	chr15:31373178-31373228	Hepatocyte	liver:	n/a
44	chr15:31395221-31395271	AG04449	skin:	fetal
45	chr15:31395221-31395271	HCT-116	colon:	n/a
46	chr15:31383719-31383769	HRE	kidney:	n/a
47	chr15:31394285-31394335	Jurkat	blood:	n/a
48	chr15:31395221-31395271	NB4	blood:	n/a
49	chr15:31372997-31373047	HUVEC	blood vessel:	n/a
50	chr15:31372997-31373047	MCF-7	breast:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:31197730..31198708-chr15:31390791..31392081,3	MCF-7	breast:
2	chr15:31282551..31285125-chr15:31384026..31386861,2	MCF-7	breast:
3	chr15:31197732..31198235-chr15:31391287..31392163,2	MCF-7	breast:
4	chr15:31283182..31285507-chr15:31372643..31376293,4	MCF-7	breast:
5	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
6	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
7	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
8	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
9	chr15:31196058..31198354-chr15:31402829..31405030,2	MCF-7	breast:
10	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
11	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTMR10-1	chr15:31383179-31383431	l_1124_chr15:31383178-31385928_brain
2	lnc-MTMR10-1	chr15:31385825-31385928	l_1124_chr15:31383178-31385928_brain

No data

Variant related genes	Relation type
TRPM1	TF binding region
TRPM1	CpG island
ENSG00000166912	chromatin interactions
ENSG00000198690	chromatin interactions

Extended variants
information (count: 1777 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73374037	chr15:31364406-31364407	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12898941	chr15:31364474-31364475	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs80046858	chr15:31364488-31364489	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544241438	chr15:31364571-31364572	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557732701	chr15:31364618-31364619	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78761205	chr15:31364648-31364649	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540735274	chr15:31364649-31364650	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs28878478	chr15:31364658-31364659	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs146622877	chr15:31364678-31364679	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140187578	chr15:31364705-31364706	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs8023430	chr15:31364766-31364767	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531328873	chr15:31364777-31364778	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs551351074	chr15:31364832-31364833	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571233868	chr15:31364861-31364862	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71399740	chr15:31364871-31364872	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs143945882	chr15:31364880-31364881	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568506160	chr15:31364888-31364889	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190959689	chr15:31364940-31364941	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs532884140	chr15:31364944-31364945	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559518076	chr15:31364947-31364948	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374227830	chr15:31365022-31365023	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181388511	chr15:31365025-31365026	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs60993672	chr15:31365044-31365045	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185675996	chr15:31365045-31365046	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148091269	chr15:31365075-31365076	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569258145	chr15:31365086-31365087	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145811948	chr15:31365104-31365105	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74892189	chr15:31365121-31365122	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148988398	chr15:31365191-31365192	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs190826929	chr15:31365192-31365193	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs57712238	chr15:31365236-31365237	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563475612	chr15:31365237-31365238	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540350044	chr15:31365242-31365243	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs554272607	chr15:31365286-31365287	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573742786	chr15:31365296-31365297	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183053437	chr15:31365444-31365445	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562677364	chr15:31365460-31365461	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188501369	chr15:31365472-31365473	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545339812	chr15:31365473-31365474	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111582285	chr15:31365515-31365516	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547161705	chr15:31365529-31365530	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs374867807	chr15:31365559-31365560	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79379776	chr15:31365568-31365569	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192017193	chr15:31365589-31365590	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs151067579	chr15:31365604-31365605	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369993387	chr15:31365630-31365631	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569122458	chr15:31365738-31365739	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs8029784	chr15:31365766-31365767	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528511845	chr15:31365777-31365778	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs56278662	chr15:31365789-31365790	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:156)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31353400-31365200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:31355600-31367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:31363600-31366200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr15:31363600-31372600	Weak transcription	Spleen	Spleen
5	chr15:31363800-31365400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:31365000-31369800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr15:31365400-31365600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr15:31365600-31368200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:31366200-31367800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr15:31367400-31369600	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr15:31367400-31371400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr15:31367400-31371400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr15:31367400-31372600	Enhancers	H1 Cell Line	embryonic stem cell
14	chr15:31367600-31368400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr15:31367600-31370000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr15:31367600-31371600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr15:31367800-31368400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:31367800-31371000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr15:31367800-31371000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr15:31367800-31375600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:31368000-31368400	Enhancers	Fetal Brain Female	brain
22	chr15:31368000-31374600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:31368200-31368400	Enhancers	H9 Cell Line	embryonic stem cell
24	chr15:31368200-31368400	Enhancers	Fetal Brain Male	brain
25	chr15:31368200-31368400	Enhancers	Lung	lung
26	chr15:31368200-31369400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr15:31368400-31369400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr15:31368400-31369400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr15:31368400-31369400	Weak transcription	Fetal Brain Male	brain
30	chr15:31368400-31369600	Weak transcription	Fetal Brain Female	brain
31	chr15:31368400-31369800	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr15:31368400-31369800	Weak transcription	Lung	lung
33	chr15:31368400-31371000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr15:31369200-31370400	Enhancers	GM12878-XiMat	blood
35	chr15:31369400-31369600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr15:31369400-31369600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr15:31369400-31370000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr15:31369400-31370200	Enhancers	Primary B cells from peripheral blood	blood
39	chr15:31369400-31370200	Enhancers	Gastric	stomach
40	chr15:31369400-31370200	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr15:31369400-31371000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr15:31369400-31372200	Enhancers	Fetal Brain Male	brain
43	chr15:31369400-31373000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr15:31369600-31369800	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr15:31369600-31370200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
46	chr15:31369600-31370200	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr15:31369600-31370400	Enhancers	Stomach Mucosa	stomach
48	chr15:31369600-31370600	Enhancers	Fetal Intestine Large	intestine
49	chr15:31369600-31371800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:31369600-31373000	Enhancers	Placenta	Placenta

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