Variant report

Variant	nsv832950
Chromosome Location	chr15:30954625-31146464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1511)
CpG islands
(count:976)
Chromatin interactive
region (count:5)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1511 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31058643-31058927	HepG2	liver:	n/a	n/a
2	ATF1	chr15:31120556-31120738	K562	blood:	n/a	n/a
3	BACH1	chr15:31122441-31122516	K562	blood:	n/a	n/a
4	BACH1	chr15:31056549-31056561	K562	blood:	n/a	n/a
5	BATF	chr15:30988651-30989902	GM12878	blood:	n/a	n/a
6	BATF	chr15:30988887-30989837	GM12878	blood:	n/a	n/a
7	BATF	chr15:31138350-31138513	GM12878	blood:	n/a	n/a
8	BATF	chr15:31078925-31079140	GM12878	blood:	n/a	n/a
9	BATF	chr15:31001037-31001298	GM12878	blood:	n/a	chr15:31001194-31001205
10	BATF	chr15:31047306-31047532	GM12878	blood:	n/a	n/a
11	BATF	chr15:31137167-31137339	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:30989215-30989908	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:31135323-31135559	GM12878	blood:	n/a	chr15:31135479-31135488 chr15:31135476-31135485
14	BCL11A	chr15:30988850-30989149	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:30988813-30989894	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:30988374-30988675	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:31138421-31138582	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:31135355-31135662	GM12878	blood:	n/a	chr15:31135479-31135488 chr15:31135476-31135485
19	BCL11A	chr15:31047283-31047543	GM12878	blood:	n/a	n/a
20	BHLHE40	chr15:31135331-31135708	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:30959588-30959606	K562	blood:	n/a	n/a
22	BHLHE40	chr15:30968872-30968884	K562	blood:	n/a	n/a
23	BHLHE40	chr15:30989526-30989883	GM12878	blood:	n/a	n/a
24	CEBPB	chr15:31058561-31059006	Hela-S3	cervix:	n/a	chr15:31058745-31058756
25	CEBPB	chr15:31139273-31139346	HepG2	liver:	n/a	n/a
26	CEBPB	chr15:31058558-31059008	IMR90	lung:	n/a	chr15:31058745-31058756
27	CEBPB	chr15:31058568-31058944	HepG2	liver:	n/a	chr15:31058745-31058756
28	CEBPB	chr15:31116931-31117112	K562	blood:	n/a	n/a
29	CEBPB	chr15:30967352-30967663	HepG2	liver:	n/a	chr15:30967474-30967485
30	CEBPB	chr15:31058570-31058941	A549	lung:	n/a	chr15:31058745-31058756
31	CEBPB	chr15:31084274-31084474	HepG2	liver:	n/a	n/a
32	CEBPB	chr15:31058652-31058827	HepG2	liver:	n/a	chr15:31058745-31058756
33	CEBPB	chr15:30958152-30958542	K562	blood:	n/a	n/a
34	CEBPB	chr15:31058645-31058938	HepG2	liver:	n/a	chr15:31058745-31058756
35	CEBPB	chr15:31058573-31058941	H1-hESC	embryonic stem cell:	n/a	chr15:31058745-31058756
36	CEBPB	chr15:30983782-30984067	IMR90	lung:	n/a	n/a
37	CEBPB	chr15:31138543-31138576	A549	lung:	n/a	n/a
38	CEBPB	chr15:31137627-31139644	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr15:30965736-30965777	A549	lung:	n/a	n/a
40	CEBPB	chr15:31137292-31138131	A549	lung:	n/a	n/a
41	CEBPB	chr15:30983881-30984093	HepG2	liver:	n/a	n/a
42	CEBPB	chr15:31120537-31120733	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr15:30958228-30958528	HepG2	liver:	n/a	n/a
44	CEBPB	chr15:30964859-30965084	K562	blood:	n/a	n/a
45	CEBPB	chr15:31058670-31058834	K562	blood:	n/a	chr15:31058745-31058756
46	CEBPB	chr15:31137895-31137956	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr15:31138908-31139622	A549	lung:	n/a	n/a
48	CEBPB	chr15:30983742-30983960	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr15:30983872-30983981	K562	blood:	n/a	n/a
50	CEBPB	chr15:31035071-31035332	IMR90	lung:	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	chr15:31122726-31122776	RPTEC	kidney:	n/a
2	chr15:31093811-31093861	HRCEpiC	kidney:	n/a
3	chr15:31122537-31122587	AoSMC	blood vessel:	n/a
4	chr15:31090636-31090686	MCF-7	breast:	n/a
5	chr15:31108938-31108988	HEK293	kidney:	embryo
6	chr15:31115862-31115912	BE2_C	brain:	n/a
7	chr15:31093811-31093861	GM12878	blood:	n/a
8	chr15:31108938-31108988	SKMC	muscle:	n/a
9	chr15:31122726-31122776	HIPEpiC	eye:	n/a
10	chr15:31066090-31066140	HMEC	breast:	n/a
11	chr15:31092120-31092170	H1-hESC	embryonic stem cell:	embryo
12	chr15:31122726-31122776	NT2-D1	testis:	n/a
13	chr15:31066090-31066140	HAEpiC	amniotic membrane:	n/a
14	chr15:31086755-31086805	H1-hESC	embryonic stem cell:	embryo
15	chr15:31093049-31093099	ovcar-3	ovarian:	n/a
16	chr15:31090995-31091045	HIPEpiC	eye:	n/a
17	chr15:31093049-31093099	AoSMC	blood vessel:	n/a
18	chr15:31093811-31093861	HCPEpiC	choroid plexus:	n/a
19	chr15:31088666-31088716	H1-hESC	embryonic stem cell:	embryo
20	chr15:31122726-31122776	LNCaP	prostate:	n/a
21	chr15:31093040-31093090	BJ	skin:	n/a
22	chr15:31122537-31122587	GM06990	blood:	n/a
23	chr15:31090995-31091045	NHBE	bronchial:	n/a
24	chr15:31093040-31093090	Jurkat	blood:	n/a
25	chr15:31093049-31093099	H1-hESC	embryonic stem cell:	embryo
26	chr15:31093811-31093861	BJ	skin:	n/a
27	chr15:31115839-31115889	AG04450	lung:	fetal
28	chr15:31066090-31066140	ProgFib	skin:	n/a
29	chr15:31092120-31092170	HL-60	blood:	n/a
30	chr15:31093049-31093099	ProgFib	skin:	n/a
31	chr15:31122537-31122587	RPTEC	kidney:	n/a
32	chr15:31122726-31122776	HCPEpiC	choroid plexus:	n/a
33	chr15:31090636-31090686	HNPCEpiC	eye:	n/a
34	chr15:31088666-31088716	GM06990	blood:	n/a
35	chr15:31115862-31115912	Jurkat	blood:	n/a
36	chr15:31108938-31108988	NH-A	brain:	n/a
37	chr15:31090636-31090686	GM12891	blood:	n/a
38	chr15:31090995-31091045	HCPEpiC	choroid plexus:	n/a
39	chr15:31093811-31093861	LNCaP	prostate:	n/a
40	chr15:31115862-31115912	HEEpiC	esophagus:	n/a
41	chr15:31093811-31093861	RPTEC	kidney:	n/a
42	chr15:31122751-31122801	SK-N-SH	brain:	n/a
43	chr15:31093040-31093090	CMK	blood:	n/a
44	chr15:31115839-31115889	A549	lung:	n/a
45	chr15:31086755-31086805	Hepatocyte	liver:	n/a
46	chr15:31093040-31093090	NH-A	brain:	n/a
47	chr15:31088666-31088716	Hela-S3	cervix:	n/a
48	chr15:31122537-31122587	U87	brain:	n/a
49	chr15:31093049-31093099	NH-A	brain:	n/a
50	chr15:31122751-31122801	SK-N-SH_RA	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
2	chr15:31120296..31121046-chr17:8075920..8076839,2	HCT-116	colon:
3	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
4	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
5	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP11B-1	chr15:31061535-31065196	NONHSAT041388
2	lnc-ARHGAP11B-5	chr15:31092352-31092630	NONHSAT041399
3	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041382
4	lnc-ARHGAP11B-1	chr15:31060916-31061371	NONHSAT041387
5	lnc-ARHGAP11B-1	chr15:31042605-31042759	NONHSAT041384
6	lnc-ARHGAP11B-1	chr15:31015549-31015698	NONHSAT041382
7	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041384
8	lnc-ARHGAP11B-3	chr15:31074599-31075123	NONHSAT041397
9	lnc-ARHGAP11B-1	chr15:31060061-31065209	NONHSAT041384

No data

Variant related genes	Relation type
HERC2P10	TF binding region
GOLGA8UP	TF binding region
ENSG00000206846	TF binding region
ENSG00000221379	TF binding region
RN7SL82P	TF binding region
HERC2P10	CpG island
GOLGA8UP	CpG island
ENSG00000206846	CpG island
ENSG00000221379	CpG island
RN7SL82P	CpG island

Extended variants
information (count: 6980 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:6980 , 50 per page) page: 1 2 3 4 5 6 7 ... 140

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564646901	chr15:30954758-30954759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12903027	chr15:30954789-30954790	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs35749385	chr15:30954793-30954794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78969004	chr15:30954812-30954813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569332570	chr15:30954813-30954814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76628053	chr15:30954816-30954817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76598855	chr15:30954817-30954818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34639701	chr15:30954818-30954819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs10152321	chr15:30954833-30954834	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs145946909	chr15:30954856-30954857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs184473076	chr15:30954862-30954863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537312712	chr15:30954869-30954870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs540242082	chr15:30954891-30954892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs189449556	chr15:30954893-30954894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573899712	chr15:30954894-30954895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551569749	chr15:30954895-30954896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577245769	chr15:30954916-30954917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538228683	chr15:30954933-30954934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115266548	chr15:30954944-30954945	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181441624	chr15:30954965-30954966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544344197	chr15:30955011-30955012	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs11630425	chr15:30955055-30955056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4465573	chr15:30955149-30955150	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs533215737	chr15:30955158-30955159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370522795	chr15:30955178-30955179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566503555	chr15:30955183-30955184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs5811606	chr15:30955188-30955189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529622187	chr15:30955267-30955268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35807533	chr15:30955294-30955295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549398309	chr15:30955300-30955301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569475914	chr15:30955303-30955304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201856570	chr15:30955309-30955310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35066139	chr15:30955349-30955350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35313885	chr15:30955395-30955396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185747829	chr15:30955418-30955419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558337316	chr15:30955428-30955429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370173697	chr15:30955495-30955496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs571381108	chr15:30955523-30955524	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76846065	chr15:30955524-30955525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553830060	chr15:30955549-30955550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145317931	chr15:30955584-30955585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372354276	chr15:30955585-30955586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542946739	chr15:30955618-30955619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370874965	chr15:30955661-30955662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181660202	chr15:30955703-30955704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs143305752	chr15:30955736-30955737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544810668	chr15:30955770-30955771	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564707031	chr15:30955813-30955814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577739198	chr15:30955827-30955828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540310320	chr15:30955838-30955839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

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
Glioma	20126413	CNVD

Chromatin state (count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30919200-30966400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:30919400-30959800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr15:30919400-30969800	Weak transcription	Fetal Lung	lung
4	chr15:30919400-30972800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr15:30919600-30964000	Weak transcription	Fetal Intestine Large	intestine
6	chr15:30919600-31023200	Weak transcription	Fetal Intestine Small	intestine
7	chr15:30919800-30961800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr15:30920000-30955400	Weak transcription	NH-A	brain
9	chr15:30920000-31028200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr15:30921200-30982400	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr15:30924600-30961800	Weak transcription	Fetal Stomach	stomach
12	chr15:30937000-30971200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr15:30938000-30961600	Weak transcription	Small Intestine	intestine
14	chr15:30938800-30957800	Weak transcription	Hela-S3	cervix
15	chr15:30938800-30969200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:30938800-30974000	Weak transcription	Primary B cells from cord blood	blood
17	chr15:30939600-30969600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr15:30940800-30959400	Weak transcription	Fetal Muscle Leg	muscle
19	chr15:30941000-30962400	Weak transcription	NHDF-Ad	bronchial
20	chr15:30941000-30988600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr15:30941200-30958000	Weak transcription	Primary hematopoietic stem cells	blood
22	chr15:30942600-30962200	Weak transcription	NHLF	lung
23	chr15:30942800-30973600	Weak transcription	Primary T cells from cord blood	blood
24	chr15:30943000-30958800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr15:30943800-30958000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr15:30945800-30964400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr15:30946400-30956000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:30946400-30957800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr15:30946400-30958600	Weak transcription	Osteobl	bone
30	chr15:30946400-30959600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr15:30946400-30960000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr15:30946400-30961000	Weak transcription	Fetal Heart	heart
33	chr15:30946400-30962400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:30946400-30965000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr15:30948600-30962400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:30948800-30976200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr15:30950000-30964400	Strong transcription	Dnd41	blood
38	chr15:30950600-30956400	Strong transcription	Fetal Thymus	thymus
39	chr15:30950800-30958000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:30951000-30962400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:30951000-30977000	Weak transcription	HepG2	liver
42	chr15:30951200-30955400	Weak transcription	HSMM	muscle
43	chr15:30951200-30955600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr15:30951200-30955800	Weak transcription	K562	blood
45	chr15:30951200-30958800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:30951200-30959400	Weak transcription	Thymus	Thymus
47	chr15:30951200-30960000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr15:30951200-30961000	Weak transcription	HUVEC	blood vessel
49	chr15:30951200-30961400	Weak transcription	NHEK	skin
50	chr15:30951200-30962200	Weak transcription	H1 Cell Line	embryonic stem cell

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