Variant report

Variant	nsv903837
Chromosome Location	chr15:31362654-31418766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:976)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 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	chr15:31376612-31376664	K562	blood:	n/a	n/a
4	ATF1	chr15:31371191-31371230	K562	blood:	n/a	n/a
5	BACH1	chr15:31373087-31373180	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr15:31369836-31370207	GM12878	blood:	n/a	n/a
7	BCL3	chr15:31396399-31396673	GM12878	blood:	n/a	n/a
8	BCL3	chr15:31384773-31385276	A549	lung:	n/a	n/a
9	BHLHE40	chr15:31417481-31417552	HepG2	liver:	n/a	n/a
10	BHLHE40	chr15:31381061-31382012	HepG2	liver:	n/a	n/a
11	BHLHE40	chr15:31384869-31385246	HepG2	liver:	n/a	n/a
12	CEBPB	chr15:31381146-31381608	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
13	CEBPB	chr15:31409068-31409078	HepG2	liver:	n/a	n/a
14	CEBPB	chr15:31380951-31381935	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
15	CEBPB	chr15:31381210-31381544	A549	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
16	CEBPB	chr15:31381102-31381941	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
17	CEBPB	chr15:31381279-31381497	H1-hESC	embryonic stem cell:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
18	CEBPB	chr15:31381253-31381467	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
19	CEBPB	chr15:31381101-31381576	HepG2	liver:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
20	CEBPB	chr15:31381201-31381538	K562	blood:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
21	CEBPB	chr15:31371688-31372101	IMR90	lung:	n/a	n/a
22	CEBPB	chr15:31381210-31381539	IMR90	lung:	n/a	chr15:31381378-31381387 chr15:31381377-31381388 chr15:31381376-31381387
23	CEBPD	chr15:31381206-31381450	HepG2	liver:	n/a	n/a
24	CEBPD	chr15:31380900-31381232	HepG2	liver:	n/a	n/a
25	CHD2	chr15:31390949-31391119	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr15:31381613-31381922	HepG2	liver:	n/a	n/a
27	CHD2	chr15:31384828-31385165	HepG2	liver:	n/a	n/a
28	CHD2	chr15:31391094-31391108	HepG2	liver:	n/a	n/a
29	CHD2	chr15:31384391-31384410	HepG2	liver:	n/a	n/a
30	CHD2	chr15:31381045-31381371	HepG2	liver:	n/a	n/a
31	CTCF	chr15:31391660-31391810	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr15:31391478-31391909	HCT-116	colon:	n/a	n/a
33	CTCF	chr15:31391680-31391830	NHDF-neo	bronchial:	n/a	n/a
34	CTCF	chr15:31391655-31391704	Lung_OC	lung:	n/a	n/a
35	CTCF	chr15:31391640-31391790	NHEK	skin:	n/a	n/a
36	CTCF	chr15:31391620-31391770	GM12878	blood:	n/a	n/a
37	CTCF	chr15:31391540-31391690	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr15:31373994-31374013	MCF-7	breast:	n/a	n/a
39	CTCF	chr15:31391800-31391950	A549	lung:	n/a	n/a
40	CTCF	chr15:31396313-31396427	GM12892	blood:	n/a	n/a
41	CTCF	chr15:31375940-31376090	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr15:31391540-31391690	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr15:31396323-31396425	GM19239	blood:	n/a	n/a
44	CTCF	chr15:31390900-31391050	GM06990	blood:	n/a	n/a
45	CTCF	chr15:31391620-31391770	AG09319	gingival:	n/a	n/a
46	CTCF	chr15:31402713-31402750	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr15:31391618-31391772	GM12878	blood:	n/a	n/a
48	CTCF	chr15:31391695-31391714	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr15:31391540-31391690	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr15:31372940-31373090	HBMEC	blood vessel:	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	chr15:31380908-31380958	MCF10A-Er-Src	breast:	n/a
2	chr15:31372742-31372792	HCPEpiC	choroid plexus:	n/a
3	chr15:31379377-31379427	HMEC	breast:	n/a
4	chr15:31393845-31393895	NHDF-neo	bronchial:	n/a
5	chr15:31372889-31372939	Jurkat	blood:	n/a
6	chr15:31373178-31373228	HCM	heart:	n/a
7	chr15:31372742-31372792	RPTEC	kidney:	n/a
8	chr15:31379377-31379427	NH-A	brain:	n/a
9	chr15:31391491-31391541	AG09319	gingival:	n/a
10	chr15:31380908-31380958	MCF-7	breast:	n/a
11	chr15:31373178-31373228	K562	blood:	n/a
12	chr15:31383719-31383769	NB4	blood:	n/a
13	chr15:31394285-31394335	HL-60	blood:	n/a
14	chr15:31372889-31372939	U87	brain:	n/a
15	chr15:31379377-31379427	NHBE	bronchial:	n/a
16	chr15:31383719-31383769	Hepatocyte	liver:	n/a
17	chr15:31393845-31393895	AG09319	gingival:	n/a
18	chr15:31379377-31379427	AG04450	lung:	fetal
19	chr15:31373178-31373228	HEEpiC	esophagus:	n/a
20	chr15:31383719-31383769	LNCaP	prostate:	n/a
21	chr15:31391491-31391541	BE2_C	brain:	n/a
22	chr15:31372742-31372792	PrEC	prostate:	n/a
23	chr15:31372742-31372792	SKMC	muscle:	n/a
24	chr15:31383719-31383769	HCF	heart:	n/a
25	chr15:31372997-31373047	Jurkat	blood:	n/a
26	chr15:31370762-31370812	HRE	kidney:	n/a
27	chr15:31381816-31381866	AG10803	skin:	n/a
28	chr15:31380908-31380958	IMR90	lung:	fetal
29	chr15:31383719-31383769	Hela-S3	cervix:	n/a
30	chr15:31381816-31381866	HCPEpiC	choroid plexus:	n/a
31	chr15:31393845-31393895	RPTEC	kidney:	n/a
32	chr15:31394188-31394238	Hela-S3	cervix:	n/a
33	chr15:31394188-31394238	SKMC	muscle:	n/a
34	chr15:31370762-31370812	SK-N-SH	brain:	n/a
35	chr15:31395221-31395271	IMR90	lung:	fetal
36	chr15:31394188-31394238	IMR90	lung:	fetal
37	chr15:31372889-31372939	Caco-2	colon:	n/a
38	chr15:31370762-31370812	SAEC	small airway:	n/a
39	chr15:31391491-31391541	Hela-S3	cervix:	n/a
40	chr15:31394021-31394071	GM19239	blood:	n/a
41	chr15:31394021-31394071	AoSMC	blood vessel:	n/a
42	chr15:31372742-31372792	NHDF-neo	bronchial:	n/a
43	chr15:31393845-31393895	HEK293	kidney:	embryo
44	chr15:31394188-31394238	U87	brain:	n/a
45	chr15:31393845-31393895	GM12892	blood:	n/a
46	chr15:31380908-31380958	AG09309	skin:	n/a
47	chr15:31394285-31394335	GM12878	blood:	n/a
48	chr15:31372889-31372939	HL-60	blood:	n/a
49	chr15:31372997-31373047	CMK	blood:	n/a
50	chr15:31381015-31381065	AG09319	gingival:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:31197732..31198235-chr15:31391287..31392163,2	MCF-7	breast:
2	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
3	chr15:31372825..31374445-chr15:31376180..31377708,2	K562	blood:
4	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
5	chr15:31197730..31198708-chr15:31390791..31392081,3	MCF-7	breast:
6	chr15:31282551..31285125-chr15:31384026..31386861,2	MCF-7	breast:
7	chr15:31376554..31379301-chr15:31382366..31384596,2	MCF-7	breast:
8	chr15:31382233..31384961-chr15:31390192..31392345,2	K562	blood:
9	chr15:31196058..31198354-chr15:31402829..31405030,2	MCF-7	breast:
10	chr15:31283182..31285507-chr15:31372643..31376293,4	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
ENSG00000198690	chromatin interactions
ENSG00000166912	chromatin interactions

Extended variants
information (count: 1870 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:1870 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17815804	chr15:31362654-31362655	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557552524	chr15:31362684-31362685	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577532722	chr15:31362692-31362693	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546453069	chr15:31362741-31362742	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559828448	chr15:31362810-31362811	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573183068	chr15:31362834-31362835	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541907736	chr15:31362854-31362855	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541133400	chr15:31363000-31363001	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183920428	chr15:31363001-31363002	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577033175	chr15:31363026-31363027	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530875379	chr15:31363037-31363038	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189091499	chr15:31363111-31363112	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs147194913	chr15:31363121-31363122	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs532989682	chr15:31363122-31363123	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs181546011	chr15:31363166-31363167	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs535743861	chr15:31363187-31363188	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs372391625	chr15:31363196-31363197	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs568886866	chr15:31363243-31363244	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs184170374	chr15:31363250-31363251	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs368229669	chr15:31363259-31363260	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs557912341	chr15:31363310-31363311	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs577495839	chr15:31363471-31363472	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs72712237	chr15:31363537-31363538	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548385041	chr15:31363576-31363577	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11638753	chr15:31363605-31363606	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs566900033	chr15:31363623-31363624	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534201702	chr15:31363624-31363625	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150752129	chr15:31363629-31363630	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542521168	chr15:31363639-31363640	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561714878	chr15:31363661-31363662	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11633683	chr15:31363692-31363693	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs56070969	chr15:31363724-31363725	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534698719	chr15:31363736-31363737	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs544278766	chr15:31363761-31363762	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374988301	chr15:31363791-31363792	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375747299	chr15:31363802-31363803	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs143676287	chr15:31363810-31363811	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369777289	chr15:31363813-31363814	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564276620	chr15:31363854-31363855	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs577327433	chr15:31363870-31363871	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533142577	chr15:31363901-31363902	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs546430102	chr15:31363905-31363906	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11633780	chr15:31363906-31363907	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs568191132	chr15:31363938-31363939	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529140990	chr15:31363940-31363941	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs386782636	chr15:31363963-31363964	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182238922	chr15:31363964-31363965	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs144001881	chr15:31363996-31363997	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs202096702	chr15:31364024-31364025	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34330757	chr15:31364026-31364027	Weak transcription Strong 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:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31353200-31363400	Weak transcription	Right Atrium	heart
2	chr15:31353400-31365200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:31354400-31363200	Weak transcription	Left Ventricle	heart
4	chr15:31355600-31367800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:31359600-31363400	Enhancers	Ovary	ovary
6	chr15:31360000-31363600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr15:31360000-31363600	Enhancers	Adipose Nuclei	Adipose
8	chr15:31360400-31362800	Enhancers	Liver	Liver
9	chr15:31362000-31363200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr15:31362000-31363400	Weak transcription	Gastric	stomach
11	chr15:31362000-31363600	Enhancers	Spleen	Spleen
12	chr15:31363200-31363800	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr15:31363400-31363600	Enhancers	Left Ventricle	heart
14	chr15:31363400-31363600	Enhancers	Right Atrium	heart
15	chr15:31363600-31366200	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:31363600-31372600	Weak transcription	Spleen	Spleen
17	chr15:31363800-31365400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr15:31365000-31369800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr15:31365400-31365600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:31365600-31368200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:31366200-31367800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr15:31367400-31369600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr15:31367400-31371400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr15:31367400-31371400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr15:31367400-31372600	Enhancers	H1 Cell Line	embryonic stem cell
26	chr15:31367600-31368400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr15:31367600-31370000	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr15:31367600-31371600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr15:31367800-31368400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr15:31367800-31371000	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr15:31367800-31371000	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr15:31367800-31375600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr15:31368000-31368400	Enhancers	Fetal Brain Female	brain
34	chr15:31368000-31374600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr15:31368200-31368400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr15:31368200-31368400	Enhancers	Fetal Brain Male	brain
37	chr15:31368200-31368400	Enhancers	Lung	lung
38	chr15:31368200-31369400	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr15:31368400-31369400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr15:31368400-31369400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr15:31368400-31369400	Weak transcription	Fetal Brain Male	brain
42	chr15:31368400-31369600	Weak transcription	Fetal Brain Female	brain
43	chr15:31368400-31369800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr15:31368400-31369800	Weak transcription	Lung	lung
45	chr15:31368400-31371000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr15:31369200-31370400	Enhancers	GM12878-XiMat	blood
47	chr15:31369400-31369600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:31369400-31369600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr15:31369400-31370000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:31369400-31370200	Enhancers	Primary B cells from peripheral blood	blood

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