Variant report

Variant	nsv974549
Chromosome Location	chr15:31183683-31193060
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	BACH1	chr15:31186635-31187019	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr15:31186759-31186945	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr15:31186710-31186932	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr15:31186676-31186970	K562	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
5	CTCF	chr15:31186820-31186970	GM12878	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
6	CTCF	chr15:31186780-31186930	GM12873	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
7	CTCF	chr15:31186752-31186961	HepG2	liver:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
8	CTCF	chr15:31186820-31186970	GM12875	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
9	CTCF	chr15:31186780-31186930	WERI-Rb-1	eye:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
10	CTCF	chr15:31188568-31188626	MCF-7	breast:	n/a	n/a
11	CTCF	chr15:31186704-31186968	T-47D	breast:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
12	CTCF	chr15:31186717-31186908	A549	lung:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
13	CTCF	chr15:31186741-31186966	Kidney_OC	kidney:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
14	CTCF	chr15:31186656-31187040	GM12878	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
15	CTCF	chr15:31186780-31186930	HBMEC	blood vessel:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
16	CTCF	chr15:31186737-31186985	MCF-7	breast:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
17	CTCF	chr15:31190660-31190810	HMF	breast:	n/a	n/a
18	CTCF	chr15:31186808-31186906	H1-hESC	embryonic stem cell:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
19	CTCF	chr15:31186780-31186930	HRE	kidney:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
20	CTCF	chr15:31186820-31186970	GM12864	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
21	CTCF	chr15:31188480-31188630	GM12873	blood:	n/a	n/a
22	CTCF	chr15:31186677-31186940	K562	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
23	CTCF	chr15:31186780-31186930	GM12865	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
24	CTCF	chr15:31186747-31186969	Fibrobl	skin:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
25	CTCF	chr15:31186820-31186970	HEEpiC	esophagus:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
26	CTCF	chr15:31186720-31186870	HRPEpiC	eye:	n/a	chr15:31186859-31186867
27	CTCF	chr15:31186900-31187050	GM06990	blood:	n/a	n/a
28	CTCF	chr15:31186800-31186950	Hela-S3	cervix:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
29	CTCF	chr15:31186800-31186950	HEK293	kidney:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
30	CTCF	chr15:31186806-31186896	Medullo	brain:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
31	CTCF	chr15:31186780-31186930	GM12867	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
32	CTCF	chr15:31186820-31186970	HepG2	liver:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
33	CTCF	chr15:31186598-31187066	HCT-116	colon:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
34	CTCF	chr15:31186820-31186970	WERI-Rb-1	eye:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
35	CTCF	chr15:31186738-31186991	GM12878	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
36	CTCF	chr15:31186600-31186750	GM12870	blood:	n/a	n/a
37	CTCF	chr15:31186716-31186998	GM12892	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
38	CTCF	chr15:31186828-31186845	IMR90	lung:	n/a	n/a
39	CTCF	chr15:31186756-31186956	ProgFib	skin:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
40	CTCF	chr15:31186840-31186990	HEK293	kidney:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
41	CTCF	chr15:31186597-31187143	SK-N-SH	brain:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
42	CTCF	chr15:31186700-31186850	GM12873	blood:	n/a	n/a
43	CTCF	chr15:31186745-31186966	GM13977	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
44	CTCF	chr15:31186763-31186951	HUVEC	blood vessel:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
45	CTCF	chr15:31186820-31186970	HMEC	breast:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
46	CTCF	chr15:31186800-31186950	GM12865	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
47	CTCF	chr15:31186748-31186990	LNCaP	prostate:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
48	CTCF	chr15:31186800-31186950	GM12870	blood:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
49	CTCF	chr15:31186780-31186930	Caco-2	colon:	n/a	chr15:31186856-31186874 chr15:31186858-31186879 chr15:31186859-31186867
50	CTCF	chr15:31186900-31187050	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31192891-31192941	AG04449	skin:	fetal
2	chr15:31192891-31192941	HPAEpiC	pulmonary alveolar:	n/a
3	chr15:31192891-31192941	ProgFib	skin:	n/a
4	chr15:31192891-31192941	CMK	blood:	n/a
5	chr15:31192891-31192941	NB4	blood:	n/a
6	chr15:31192891-31192941	BJ	skin:	n/a
7	chr15:31192891-31192941	HRCEpiC	kidney:	n/a
8	chr15:31192891-31192941	BE2_C	brain:	n/a
9	chr15:31192891-31192941	NH-A	brain:	n/a
10	chr15:31192891-31192941	AG10803	skin:	n/a
11	chr15:31192891-31192941	MCF-7	breast:	n/a
12	chr15:31192891-31192941	HepG2	liver:	n/a
13	chr15:31192891-31192941	Hela-S3	cervix:	n/a
14	chr15:31192891-31192941	Jurkat	blood:	n/a
15	chr15:31192891-31192941	SK-N-SH_RA	brain:	n/a
16	chr15:31192891-31192941	ECC-1	luminal epithelium:	n/a
17	chr15:31192891-31192941	MCF10A-Er-Src	breast:	n/a
18	chr15:31192891-31192941	PFSK-1	brain:	n/a
19	chr15:31192891-31192941	GM19239	blood:	n/a
20	chr15:31192891-31192941	SAEC	small airway:	n/a
21	chr15:31192891-31192941	HRPEpiC	eye:	n/a
22	chr15:31192891-31192941	ovcar-3	ovarian:	n/a
23	chr15:31192891-31192941	AG09309	skin:	n/a
24	chr15:31192891-31192941	HAEpiC	amniotic membrane:	n/a
25	chr15:31192891-31192941	SK-N-MC	brain:	n/a
26	chr15:31192891-31192941	HEK293	kidney:	embryo
27	chr15:31192891-31192941	PANC-1	pancreas:	n/a
28	chr15:31192891-31192941	SKMC	muscle:	n/a
29	chr15:31192891-31192941	GM12878	blood:	n/a
30	chr15:31192891-31192941	GM12891	blood:	n/a
31	chr15:31192891-31192941	HNPCEpiC	eye:	n/a
32	chr15:31192891-31192941	HCM	heart:	n/a
33	chr15:31192891-31192941	A549	lung:	n/a
34	chr15:31192891-31192941	HEEpiC	esophagus:	n/a
35	chr15:31192891-31192941	Caco-2	colon:	n/a
36	chr15:31192891-31192941	NHDF-neo	bronchial:	n/a
37	chr15:31192891-31192941	U87	brain:	n/a
38	chr15:31192891-31192941	Hepatocyte	liver:	n/a
39	chr15:31192891-31192941	HUVEC	blood vessel:	n/a
40	chr15:31192891-31192941	RPTEC	kidney:	n/a
41	chr15:31192891-31192941	HL-60	blood:	n/a
42	chr15:31192891-31192941	H1-hESC	embryonic stem cell:	embryo
43	chr15:31192891-31192941	AoSMC	blood vessel:	n/a
44	chr15:31192891-31192941	NT2-D1	testis:	n/a
45	chr15:31192891-31192941	GM06990	blood:	n/a
46	chr15:31192891-31192941	HCPEpiC	choroid plexus:	n/a
47	chr15:31192891-31192941	NHBE	bronchial:	n/a
48	chr15:31192891-31192941	LNCaP	prostate:	n/a
49	chr15:31192891-31192941	HIPEpiC	eye:	n/a
50	chr15:31192891-31192941	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31179092..31180650-chr15:31183037..31185213,2	K562	blood:
2	chr15:31186419..31186925-chr15:31421231..31422125,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAN1-3	chr15:31192343-31193819	NONHSAT041414
2	lnc-FAN1-4	chr15:31184228-31185545	NONHSAT041412
3	lnc-FAN1-3	chr15:31191683-31191839	NONHSAT041413
4	lnc-FAN1-3	chr15:31192358-31192530	NONHSAT041413
5	lnc-FAN1-5	chr15:31182115-31183958	NONHSAT041411

Variant related genes	Relation type
ENSG00000261628	TF binding region
FAN1	TF binding region
ENSG00000261628	CpG island
FAN1	CpG island

Extended variants
information (count: 353 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:353 , 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	rs553464385	chr15:31183706-31183707	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
2	rs7174744	chr15:31183747-31183748	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs536050070	chr15:31183794-31183795	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs151253349	chr15:31183853-31183854	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs191414616	chr15:31183854-31183855	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs530597919	chr15:31183896-31183897	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs544599961	chr15:31183911-31183912	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs368453226	chr15:31183943-31183944	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs146255222	chr15:31183948-31183949	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs11324352	chr15:31183949-31183950	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs375000282	chr15:31183952-31183953	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs552321832	chr15:31184040-31184041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs578083053	chr15:31184057-31184058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564242841	chr15:31184092-31184093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs540691946	chr15:31184093-31184094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs560571639	chr15:31184097-31184098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11070647	chr15:31184105-31184106	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
18	rs144525059	chr15:31184137-31184138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188722834	chr15:31184138-31184139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547022316	chr15:31184140-31184141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147812562	chr15:31184161-31184162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564503810	chr15:31184193-31184194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568464323	chr15:31184199-31184200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10467918	chr15:31184238-31184239	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs547040265	chr15:31184241-31184242	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs550773168	chr15:31184244-31184245	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs35678281	chr15:31184282-31184283	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs567401553	chr15:31184290-31184291	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs535661548	chr15:31184387-31184388	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs375998809	chr15:31184430-31184431	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs541597668	chr15:31184441-31184442	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs561802033	chr15:31184455-31184456	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs141333863	chr15:31184469-31184470	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs569427444	chr15:31184485-31184486	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs538507012	chr15:31184542-31184543	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs181279446	chr15:31184621-31184622	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs569304347	chr15:31184658-31184659	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs540344481	chr15:31184726-31184727	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs184709980	chr15:31184754-31184755	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs539657542	chr15:31184771-31184772	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs534232571	chr15:31184772-31184773	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs1880500	chr15:31184786-31184787	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs1852035	chr15:31184803-31184804	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555235943	chr15:31184845-31184846	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs542437868	chr15:31184856-31184857	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs62000215	chr15:31184858-31184859	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs4779792	chr15:31184874-31184875	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs574079984	chr15:31184998-31184999	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs144940038	chr15:31185068-31185069	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs149067167	chr15:31185093-31185094	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

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
Intellectual disability	21811512	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31132800-31195600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:31175600-31186200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:31179600-31192800	Weak transcription	Dnd41	blood
4	chr15:31181600-31186800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:31181600-31186800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr15:31181800-31186200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr15:31181800-31186400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr15:31182000-31186800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:31182600-31186600	Weak transcription	NH-A	brain
10	chr15:31184800-31185200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr15:31185800-31186000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:31186000-31186400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr15:31186000-31186600	Active TSS	Hela-S3	cervix
14	chr15:31186000-31186800	Enhancers	NHEK	skin
15	chr15:31186000-31187000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr15:31186000-31187400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr15:31186000-31188000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr15:31186200-31186400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr15:31186200-31186400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr15:31186200-31186800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:31186200-31187000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr15:31186200-31187000	Enhancers	HUVEC	blood vessel
23	chr15:31186200-31187400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr15:31186200-31188000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr15:31186400-31186800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr15:31186400-31186800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr15:31186400-31187600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr15:31186400-31188000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr15:31186600-31186800	Flanking Active TSS	Hela-S3	cervix
30	chr15:31186600-31187000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr15:31186600-31187000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr15:31186600-31187000	Enhancers	NH-A	brain
33	chr15:31186600-31187200	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr15:31186600-31187400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr15:31186600-31187400	Enhancers	Brain Hippocampus Middle	brain
36	chr15:31186800-31187000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr15:31186800-31187000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr15:31186800-31187000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr15:31186800-31187200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr15:31186800-31187400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr15:31186800-31187400	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr15:31186800-31187400	Enhancers	Brain Cingulate Gyrus	brain
43	chr15:31186800-31187600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr15:31186800-31187800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr15:31186800-31188400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr15:31187000-31187400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr15:31187000-31187400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr15:31187000-31187400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr15:31187000-31187400	Enhancers	Fetal Kidney	kidney
50	chr15:31187000-31195400	Weak transcription	NH-A	brain

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