Variant report

Variant	nsv974708
Chromosome Location	chr15:30294538-30346889
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	chr15:30318705-30318959	K562	blood:	n/a	n/a
2	BRCA1	chr15:30333944-30334068	GM12878	blood:	n/a	n/a
3	BRCA1	chr15:30299806-30299977	GM12878	blood:	n/a	n/a
4	CEBPB	chr15:30320812-30320869	A549	lung:	n/a	n/a
5	CEBPB	chr15:30306024-30306117	A549	lung:	n/a	n/a
6	CEBPB	chr15:30331155-30331602	Hela-S3	cervix:	n/a	chr15:30331295-30331307
7	CEBPB	chr15:30343011-30343208	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:30324857-30325057	HepG2	liver:	n/a	chr15:30324984-30324995
9	CHD1	chr15:30320265-30320466	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr15:30335445-30335601	GM12878	blood:	n/a	n/a
11	CHD1	chr15:30330953-30331153	GM12878	blood:	n/a	n/a
12	CHD2	chr15:30331324-30331787	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr15:30322680-30322830	AG04449	skin:	n/a	n/a
14	CTCF	chr15:30335540-30335690	HPF	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
15	CTCF	chr15:30322664-30322852	K562	blood:	n/a	n/a
16	CTCF	chr15:30338100-30338250	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr15:30335560-30335710	AoAF	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
18	CTCF	chr15:30322720-30322870	HCT-116	colon:	n/a	n/a
19	CTCF	chr15:30322700-30322850	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr15:30335540-30335690	HCM	heart:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
21	CTCF	chr15:30322682-30322815	LNCaP	prostate:	n/a	n/a
22	CTCF	chr15:30338000-30338150	RPTEC	kidney:	n/a	n/a
23	CTCF	chr15:30322660-30322810	HepG2	liver:	n/a	n/a
24	CTCF	chr15:30335500-30335650	HRPEpiC	eye:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
25	CTCF	chr15:30322724-30322821	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr15:30322663-30322810	NHEK	skin:	n/a	n/a
27	CTCF	chr15:30335560-30335710	AG04450	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
28	CTCF	chr15:30322640-30322790	NHEK	skin:	n/a	n/a
29	CTCF	chr15:30335520-30335670	HUVEC	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
30	CTCF	chr15:30335540-30335690	HCPEpiC	choroid plexus:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
31	CTCF	chr15:30335401-30335864	MCF-7	breast:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
32	CTCF	chr15:30322660-30322810	HMEC	breast:	n/a	n/a
33	CTCF	chr15:30335509-30335719	Hela-S3	cervix:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
34	CTCF	chr15:30322639-30322880	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr15:30322680-30322830	Caco-2	colon:	n/a	n/a
36	CTCF	chr15:30322720-30322870	AG09319	gingival:	n/a	n/a
37	CTCF	chr15:30335526-30335733	LNCaP	prostate:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
38	CTCF	chr15:30335500-30335650	NHDF-neo	bronchial:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
39	CTCF	chr15:30335532-30335761	Lung_OC	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
40	CTCF	chr15:30322760-30322910	K562	blood:	n/a	n/a
41	CTCF	chr15:30322660-30322810	HCT-116	colon:	n/a	n/a
42	CTCF	chr15:30335440-30335590	HMEC	breast:	n/a	n/a
43	CTCF	chr15:30337014-30337058	Fibrobl	skin:	n/a	n/a
44	CTCF	chr15:30337041-30337055	MCF-7	breast:	n/a	n/a
45	CTCF	chr15:30335560-30335710	HBMEC	blood vessel:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
46	CTCF	chr15:30322660-30322810	AG09309	skin:	n/a	n/a
47	CTCF	chr15:30338071-30338223	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:30335280-30335430	AG04450	lung:	n/a	n/a
49	CTCF	chr15:30335520-30335670	WI-38	lung:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335598-30335619 chr15:30335608-30335616
50	CTCF	chr15:30335600-30335750	SAEC	small airway:	n/a	chr15:30335604-30335620 chr15:30335603-30335621 chr15:30335608-30335616

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30337875-30337925	LNCaP	prostate:	n/a
2	chr15:30336940-30336990	Caco-2	colon:	n/a
3	chr15:30337875-30337925	LNCaP	prostate:	n/a
4	chr15:30336940-30336990	Caco-2	colon:	n/a
5	chr15:30334898-30334948	AG09319	gingival:	n/a
6	chr15:30336678-30336728	LNCaP	prostate:	n/a
7	chr15:30337366-30337416	BJ	skin:	n/a
8	chr15:30336678-30336728	RPTEC	kidney:	n/a
9	chr15:30336678-30336728	GM12892	blood:	n/a
10	chr15:30337366-30337416	PANC-1	pancreas:	n/a
11	chr15:30336940-30336990	HL-60	blood:	n/a
12	chr15:30336915-30336965	ProgFib	skin:	n/a
13	chr15:30336940-30336990	K562	blood:	n/a
14	chr15:30333911-30333961	Caco-2	colon:	n/a
15	chr15:30336678-30336728	Caco-2	colon:	n/a
16	chr15:30337875-30337925	NH-A	brain:	n/a
17	chr15:30336678-30336728	HMEC	breast:	n/a
18	chr15:30336940-30336990	HPAEpiC	pulmonary alveolar:	n/a
19	chr15:30336678-30336728	HCF	heart:	n/a
20	chr15:30336915-30336965	H1-hESC	embryonic stem cell:	embryo
21	chr15:30336678-30336728	GM19239	blood:	n/a
22	chr15:30333911-30333961	PrEC	prostate:	n/a
23	chr15:30333911-30333961	HMEC	breast:	n/a
24	chr15:30334898-30334948	IMR90	lung:	fetal
25	chr15:30337018-30337068	HPAEpiC	pulmonary alveolar:	n/a
26	chr15:30337875-30337925	HepG2	liver:	n/a
27	chr15:30337366-30337416	HepG2	liver:	n/a
28	chr15:30337018-30337068	Jurkat	blood:	n/a
29	chr15:30337875-30337925	HEK293	kidney:	embryo
30	chr15:30337018-30337068	Caco-2	colon:	n/a
31	chr15:30336915-30336965	ovcar-3	ovarian:	n/a
32	chr15:30334898-30334948	HRE	kidney:	n/a
33	chr15:30337366-30337416	T-47D	breast:	n/a
34	chr15:30337018-30337068	PrEC	prostate:	n/a
35	chr15:30339875-30339925	PrEC	prostate:	n/a
36	chr15:30336915-30336965	HPAEpiC	pulmonary alveolar:	n/a
37	chr15:30337018-30337068	K562	blood:	n/a
38	chr15:30337366-30337416	K562	blood:	n/a
39	chr15:30333911-30333961	NHDF-neo	bronchial:	n/a
40	chr15:30334898-30334948	AG04450	lung:	fetal
41	chr15:30336940-30336990	SK-N-SH	brain:	n/a
42	chr15:30334898-30334948	HRCEpiC	kidney:	n/a
43	chr15:30336678-30336728	GM06990	blood:	n/a
44	chr15:30337018-30337068	AoSMC	blood vessel:	n/a
45	chr15:30339875-30339925	HEK293	kidney:	embryo
46	chr15:30336915-30336965	A549	lung:	n/a
47	chr15:30334898-30334948	HEEpiC	esophagus:	n/a
48	chr15:30337366-30337416	AG04450	lung:	fetal
49	chr15:30337875-30337925	PFSK-1	brain:	n/a
50	chr15:30336915-30336965	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr15:30234442..30235027-chr15:30335180..30335724,2	MCF-7	breast:
2	chr15:29960081..29960738-chr15:30322588..30323155,2	MCF-7	breast:
3	chr15:30232675..30233456-chr15:30322159..30323009,2	MCF-7	breast:
4	chr15:30234111..30234981-chr15:30322295..30322806,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TJP1-1	chr15:30297646-30297992	ENSG00000259647.1
2	lnc-TJP1-1	chr15:30337914-30338051	ENSG00000259647.1

Variant related genes	Relation type
ENSG00000259647	TF binding region
ENSG00000259749	TF binding region
ENSG00000260174	TF binding region
ENSG00000259647	CpG island
ENSG00000259749	CpG island
ENSG00000260174	CpG island

Extended variants
information (count: 1458 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557560440	chr15:30294538-30294539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76177214	chr15:30294552-30294553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539527998	chr15:30294636-30294637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552745810	chr15:30294654-30294655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556242535	chr15:30294688-30294689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549131042	chr15:30294714-30294715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541388095	chr15:30294747-30294748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554924049	chr15:30294776-30294777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565908253	chr15:30294790-30294791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575187418	chr15:30294824-30294825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544173610	chr15:30294883-30294884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369307063	chr15:30294905-30294906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117001585	chr15:30294920-30294921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546285319	chr15:30294923-30294924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559860127	chr15:30294932-30294933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528512699	chr15:30295009-30295010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548638215	chr15:30295048-30295049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191984608	chr15:30295050-30295051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531272156	chr15:30295059-30295060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550950993	chr15:30295091-30295092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375339131	chr15:30295095-30295096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376673408	chr15:30295102-30295103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs571028093	chr15:30295110-30295111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539617825	chr15:30295117-30295118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553045207	chr15:30295144-30295145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11630205	chr15:30295152-30295153	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs535154901	chr15:30295154-30295155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551943752	chr15:30295155-30295156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374519983	chr15:30295157-30295158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182827049	chr15:30295159-30295160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs544507023	chr15:30295168-30295169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557723398	chr15:30295170-30295171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571663830	chr15:30295199-30295200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540020546	chr15:30295205-30295206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs527686483	chr15:30295207-30295208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528625994	chr15:30295209-30295210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187246522	chr15:30295210-30295211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543000699	chr15:30295219-30295220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28378102	chr15:30295220-30295221	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs551278506	chr15:30295222-30295223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542989943	chr15:30295226-30295227	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555201369	chr15:30295231-30295232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142353904	chr15:30295242-30295243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28569238	chr15:30295244-30295245	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs370980543	chr15:30295251-30295252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367710783	chr15:30295260-30295261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561335004	chr15:30295261-30295262	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568518423	chr15:30295282-30295283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs537418534	chr15:30295286-30295287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371540509	chr15:30295288-30295289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:152)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
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
Schizophrenia	19197363	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
idiopathic generalized epilepsy	19843651	CNVD
Autism	20531469	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Mental retardation	17124404	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	19843651	CNVD
Schizophrenia	19843651	CNVD
Schizophrenia	23813976	CNVD
Cognitive impairment	21505072	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495309	CNVD
Schizophrenia	20388499	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30292600-30298000	Enhancers	Brain Substantia Nigra	brain
2	chr15:30293000-30295800	Enhancers	Brain Hippocampus Middle	brain
3	chr15:30293400-30294800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr15:30293600-30294600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
5	chr15:30293600-30294800	Enhancers	Brain Cingulate Gyrus	brain
6	chr15:30293600-30295000	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr15:30293800-30294800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr15:30293800-30294800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:30294200-30294600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:30294200-30294800	Enhancers	Brain Angular Gyrus	brain
11	chr15:30294400-30294800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr15:30294400-30294800	Enhancers	Brain Anterior Caudate	brain
13	chr15:30294800-30295200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr15:30294800-30296000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr15:30294800-30296800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:30294800-30297000	Weak transcription	Brain Anterior Caudate	brain
17	chr15:30294800-30297000	Weak transcription	Brain Cingulate Gyrus	brain
18	chr15:30295000-30297000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr15:30295200-30295600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr15:30295800-30297000	Weak transcription	Brain Hippocampus Middle	brain
21	chr15:30296000-30296200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr15:30296200-30296600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:30296600-30297200	Enhancers	Fetal Lung	lung
24	chr15:30296600-30298000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr15:30296800-30298000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:30297000-30298000	Enhancers	Brain Anterior Caudate	brain
27	chr15:30297000-30298000	Enhancers	Brain Cingulate Gyrus	brain
28	chr15:30297000-30298000	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr15:30297000-30298400	Enhancers	Brain Hippocampus Middle	brain
30	chr15:30298000-30299200	Weak transcription	Brain Substantia Nigra	brain
31	chr15:30298000-30300600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr15:30298400-30299400	Weak transcription	Brain Hippocampus Middle	brain
33	chr15:30299200-30299400	Enhancers	Brain Substantia Nigra	brain
34	chr15:30299400-30299600	Enhancers	Brain Hippocampus Middle	brain
35	chr15:30300000-30300400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr15:30300400-30300800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr15:30300400-30301000	Enhancers	HSMM	muscle
38	chr15:30300800-30301400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
39	chr15:30306600-30307200	Enhancers	Brain Hippocampus Middle	brain
40	chr15:30315800-30316600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr15:30315800-30316800	Enhancers	Brain Angular Gyrus	brain
42	chr15:30315800-30316800	Enhancers	Brain Anterior Caudate	brain
43	chr15:30315800-30316800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr15:30315800-30316800	Enhancers	Brain Substantia Nigra	brain
45	chr15:30316000-30316400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:30316000-30316800	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr15:30316200-30316600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr15:30316200-30316600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr15:30316200-30316600	Enhancers	Brain Cingulate Gyrus	brain
50	chr15:30316200-30316800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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