Variant report

Variant	nsv984196
Chromosome Location	chr15:30263786-30291037
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:214)
CpG islands
(count:123)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:30267724-30267889	K562	blood:	n/a	n/a
2	CEBPB	chr15:30277304-30277626	A549	lung:	n/a	n/a
3	CEBPB	chr15:30277206-30277968	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr15:30283234-30283651	Hela-S3	cervix:	n/a	chr15:30283507-30283518
5	CEBPB	chr15:30269272-30269808	A549	lung:	n/a	n/a
6	CEBPB	chr15:30285552-30285793	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr15:30271059-30271395	A549	lung:	n/a	n/a
8	CEBPB	chr15:30270924-30271477	A549	lung:	n/a	n/a
9	CEBPB	chr15:30271166-30271384	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr15:30269521-30269769	HepG2	liver:	n/a	n/a
11	CEBPB	chr15:30271169-30271369	HepG2	liver:	n/a	n/a
12	CEBPB	chr15:30271072-30271371	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr15:30271059-30271401	IMR90	lung:	n/a	n/a
14	CEBPB	chr15:30285632-30285705	K562	blood:	n/a	n/a
15	CHD1	chr15:30271019-30271558	IMR90	lung:	n/a	n/a
16	CTCF	chr15:30277601-30277790	ProgFib	skin:	n/a	n/a
17	CTCF	chr15:30277520-30277670	MCF-7	breast:	n/a	n/a
18	CTCF	chr15:30277815-30277816	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr15:30277567-30277790	Gliobla	brain:	n/a	n/a
20	CTCF	chr15:30277600-30277750	GM12874	blood:	n/a	n/a
21	CTCF	chr15:30277604-30277761	MCF-7	breast:	n/a	n/a
22	CTCF	chr15:30277600-30277750	HEK293	kidney:	n/a	n/a
23	CTCF	chr15:30277865-30277875	A549	lung:	n/a	n/a
24	CTCF	chr15:30277640-30277790	HRE	kidney:	n/a	n/a
25	CTCF	chr15:30277469-30277827	K562	blood:	n/a	n/a
26	CTCF	chr15:30277452-30277885	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr15:30277475-30277791	A549	lung:	n/a	n/a
28	CTCF	chr15:30277520-30277670	NHEK	skin:	n/a	n/a
29	CTCF	chr15:30277540-30277690	BE2_C	brain:	n/a	n/a
30	CTCF	chr15:30277560-30277710	HCM	heart:	n/a	n/a
31	CTCF	chr15:30277560-30277710	AG04450	lung:	n/a	n/a
32	CTCF	chr15:30277575-30277700	GM10266	blood:	n/a	n/a
33	CTCF	chr15:30277780-30277930	GM12870	blood:	n/a	n/a
34	CTCF	chr15:30277600-30277750	HVMF	connective:	n/a	n/a
35	CTCF	chr15:30277640-30277790	GM12873	blood:	n/a	n/a
36	CTCF	chr15:30277658-30277695	GM12891	blood:	n/a	n/a
37	CTCF	chr15:30277560-30277710	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr15:30277566-30277800	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr15:30277600-30277750	GM12871	blood:	n/a	n/a
40	CTCF	chr15:30270988-30271002	Lung_OC	lung:	n/a	n/a
41	CTCF	chr15:30277828-30277887	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr15:30277520-30277670	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr15:30277420-30277570	GM12864	blood:	n/a	n/a
44	CTCF	chr15:30277580-30277730	GM12869	blood:	n/a	n/a
45	CTCF	chr15:30277520-30277670	GM12870	blood:	n/a	n/a
46	CTCF	chr15:30277620-30277770	A549	lung:	n/a	n/a
47	CTCF	chr15:30277584-30277823	A549	lung:	n/a	n/a
48	CTCF	chr15:30277580-30277730	HMF	breast:	n/a	n/a
49	CTCF	chr15:30277560-30277710	NHEK	skin:	n/a	n/a
50	CTCF	chr15:30277580-30277730	AG04449	skin:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30264290-30264340	Jurkat	blood:	n/a
2	chr15:30264290-30264340	Jurkat	blood:	n/a
3	chr15:30264290-30264340	GM12891	blood:	n/a
4	chr15:30264290-30264340	NHBE	bronchial:	n/a
5	chr15:30277796-30277846	NHBE	bronchial:	n/a
6	chr15:30264290-30264340	HRCEpiC	kidney:	n/a
7	chr15:30264290-30264340	A549	lung:	n/a
8	chr15:30277796-30277846	HIPEpiC	eye:	n/a
9	chr15:30277796-30277846	GM12891	blood:	n/a
10	chr15:30277796-30277846	SK-N-SH	brain:	n/a
11	chr15:30277796-30277846	ProgFib	skin:	n/a
12	chr15:30277796-30277846	NH-A	brain:	n/a
13	chr15:30264290-30264340	PrEC	prostate:	n/a
14	chr15:30264290-30264340	HCPEpiC	choroid plexus:	n/a
15	chr15:30277796-30277846	AG09319	gingival:	n/a
16	chr15:30264290-30264340	NH-A	brain:	n/a
17	chr15:30264290-30264340	SK-N-SH	brain:	n/a
18	chr15:30277796-30277846	AG04449	skin:	fetal
19	chr15:30277796-30277846	LNCaP	prostate:	n/a
20	chr15:30264290-30264340	ProgFib	skin:	n/a
21	chr15:30264290-30264340	AG10803	skin:	n/a
22	chr15:30264290-30264340	Hela-S3	cervix:	n/a
23	chr15:30277796-30277846	HMEC	breast:	n/a
24	chr15:30277796-30277846	BE2_C	brain:	n/a
25	chr15:30277796-30277846	MCF10A-Er-Src	breast:	n/a
26	chr15:30277796-30277846	SK-N-SH_RA	brain:	n/a
27	chr15:30264290-30264340	K562	blood:	n/a
28	chr15:30277796-30277846	GM12878	blood:	n/a
29	chr15:30277796-30277846	PFSK-1	brain:	n/a
30	chr15:30264290-30264340	HL-60	blood:	n/a
31	chr15:30277796-30277846	SK-N-MC	brain:	n/a
32	chr15:30264290-30264340	AG09309	skin:	n/a
33	chr15:30277796-30277846	ovcar-3	ovarian:	n/a
34	chr15:30264290-30264340	CMK	blood:	n/a
35	chr15:30264290-30264340	RPTEC	kidney:	n/a
36	chr15:30277796-30277846	MCF-7	breast:	n/a
37	chr15:30277796-30277846	HEK293	kidney:	embryo
38	chr15:30277796-30277846	K562	blood:	n/a
39	chr15:30277796-30277846	HL-60	blood:	n/a
40	chr15:30277796-30277846	RPTEC	kidney:	n/a
41	chr15:30264290-30264340	MCF-7	breast:	n/a
42	chr15:30264290-30264340	U87	brain:	n/a
43	chr15:30264290-30264340	HAEpiC	amniotic membrane:	n/a
44	chr15:30264290-30264340	HepG2	liver:	n/a
45	chr15:30264290-30264340	HEEpiC	esophagus:	n/a
46	chr15:30264290-30264340	NHDF-neo	bronchial:	n/a
47	chr15:30277796-30277846	HAEpiC	amniotic membrane:	n/a
48	chr15:30277796-30277846	SAEC	small airway:	n/a
49	chr15:30277796-30277846	PrEC	prostate:	n/a
50	chr15:30277796-30277846	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
TJP1	TF binding region
TJP1	CpG island

Extended variants
information (count: 998 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:998 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138771714	chr15:30263807-30263808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538867198	chr15:30263825-30263826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552689624	chr15:30263876-30263877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141816796	chr15:30263903-30263904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534678182	chr15:30263961-30263962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs578066173	chr15:30263973-30263974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1568633	chr15:30263992-30263993	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs373966553	chr15:30264045-30264046	Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574534349	chr15:30264054-30264055	Bivalent/Poised TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537036843	chr15:30264092-30264093	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs117029312	chr15:30264181-30264182	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs545765617	chr15:30264238-30264239	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs56031155	chr15:30264290-30264291	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs61487242	chr15:30264307-30264308	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs188517761	chr15:30264309-30264310	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs572936215	chr15:30264322-30264323	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs7181195	chr15:30264344-30264345	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs561042223	chr15:30264348-30264349	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7163646	chr15:30264363-30264364	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs150306253	chr15:30264399-30264400	Bivalent/Poised TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs563640640	chr15:30264436-30264437	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs532809314	chr15:30264525-30264526	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs540760036	chr15:30264539-30264540	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs552509092	chr15:30264540-30264541	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs193123451	chr15:30264559-30264560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534906341	chr15:30264583-30264584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34556838	chr15:30264600-30264601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548346621	chr15:30264607-30264608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568123659	chr15:30264640-30264641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537047406	chr15:30264659-30264660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556969678	chr15:30264719-30264720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184535792	chr15:30264743-30264744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539755648	chr15:30264754-30264755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552970357	chr15:30264812-30264813	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs369648791	chr15:30264835-30264836	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs573040369	chr15:30264873-30264874	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs541613164	chr15:30264885-30264886	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs6492896	chr15:30264991-30264992	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs529470539	chr15:30265035-30265036	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs532869193	chr15:30265051-30265052	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs549328476	chr15:30265083-30265084	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs574543763	chr15:30265107-30265108	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs377252651	chr15:30265108-30265109	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs543432117	chr15:30265181-30265182	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs563663028	chr15:30265202-30265203	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs188202898	chr15:30265208-30265209	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs8025920	chr15:30265210-30265211	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559789609	chr15:30265261-30265262	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs149496123	chr15:30265305-30265306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs8024444	chr15:30265350-30265351	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30263200-30270200	Weak transcription	Brain Substantia Nigra	brain
2	chr15:30264000-30264400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
3	chr15:30264000-30264400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr15:30264000-30264400	Enhancers	NHEK	skin
5	chr15:30269400-30270600	Enhancers	Brain Hippocampus Middle	brain
6	chr15:30269400-30270600	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr15:30269600-30271000	Enhancers	Brain Cingulate Gyrus	brain
8	chr15:30270200-30270800	Enhancers	Brain Anterior Caudate	brain
9	chr15:30270200-30271200	Enhancers	Brain Substantia Nigra	brain
10	chr15:30270400-30270800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr15:30270400-30271000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr15:30270400-30271400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr15:30270400-30271400	Enhancers	Brain Angular Gyrus	brain
14	chr15:30270600-30271000	Flanking Active TSS	Brain Hippocampus Middle	brain
15	chr15:30270600-30271200	Active TSS	Brain Inferior Temporal Lobe	brain
16	chr15:30270600-30271200	Enhancers	A549	lung
17	chr15:30270800-30271000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr15:30270800-30271000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr15:30270800-30271000	Flanking Active TSS	Brain Anterior Caudate	brain
20	chr15:30270800-30271000	Flanking Active TSS	Osteobl	bone
21	chr15:30270800-30271200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr15:30270800-30271400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr15:30271000-30271200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr15:30271000-30271200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:30271000-30271400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:30271000-30271400	Enhancers	Brain Anterior Caudate	brain
27	chr15:30271000-30271400	Enhancers	Colon Smooth Muscle	Colon
28	chr15:30271000-30271400	Enhancers	Osteobl	bone
29	chr15:30271000-30271600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr15:30271000-30271600	Enhancers	Brain Hippocampus Middle	brain
31	chr15:30271000-30277600	Weak transcription	Brain Cingulate Gyrus	brain
32	chr15:30271200-30271400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr15:30271200-30277400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr15:30271200-30277600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:30271400-30271800	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr15:30271400-30272800	Weak transcription	Brain Angular Gyrus	brain
37	chr15:30271400-30275200	Weak transcription	Brain Anterior Caudate	brain
38	chr15:30271400-30277600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr15:30271600-30272200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr15:30271600-30277800	Weak transcription	Brain Hippocampus Middle	brain
41	chr15:30271800-30277400	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr15:30275000-30275400	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr15:30275200-30275400	Enhancers	Brain Anterior Caudate	brain
44	chr15:30275400-30275600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr15:30275400-30277000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr15:30275400-30277400	Weak transcription	Brain Anterior Caudate	brain
47	chr15:30275600-30277200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr15:30275800-30277600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr15:30276400-30277400	Weak transcription	Brain Angular Gyrus	brain
50	chr15:30277000-30277200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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