Variant report

Variant	nsv568754
Chromosome Location	chr15:30927210-31094479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1625)
CpG islands
(count:611)
Chromatin interactive
region (count:4)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1625 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

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	ARID3A	chr15:30941065-30941323	HepG2	liver:	n/a	chr15:30941184-30941200 chr15:30941198-30941214
3	ATF1	chr15:30942408-30942747	K562	blood:	n/a	n/a
4	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
5	BACH1	chr15:31056549-31056561	K562	blood:	n/a	n/a
6	BATF	chr15:30988887-30989837	GM12878	blood:	n/a	n/a
7	BATF	chr15:31001037-31001298	GM12878	blood:	n/a	chr15:31001194-31001205
8	BATF	chr15:31078925-31079140	GM12878	blood:	n/a	n/a
9	BATF	chr15:31047306-31047532	GM12878	blood:	n/a	n/a
10	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
11	BATF	chr15:30988651-30989902	GM12878	blood:	n/a	n/a
12	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
13	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
14	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:30988850-30989149	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:30988813-30989894	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:30942112-30942840	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:30988374-30988675	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:31047283-31047543	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:30989215-30989908	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:30942082-30942772	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:30941983-30942693	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:30989526-30989883	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:30959588-30959606	K562	blood:	n/a	n/a
25	BHLHE40	chr15:30968872-30968884	K562	blood:	n/a	n/a
26	CEBPB	chr15:31035071-31035332	IMR90	lung:	n/a	n/a
27	CEBPB	chr15:30967357-30967622	Hela-S3	cervix:	n/a	chr15:30967474-30967485
28	CEBPB	chr15:30958152-30958542	K562	blood:	n/a	n/a
29	CEBPB	chr15:30983782-30984067	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:31058561-31059006	Hela-S3	cervix:	n/a	chr15:31058745-31058756
31	CEBPB	chr15:30967352-30967663	HepG2	liver:	n/a	chr15:30967474-30967485
32	CEBPB	chr15:30967261-30967669	K562	blood:	n/a	chr15:30967474-30967485
33	CEBPB	chr15:30967341-30967670	A549	lung:	n/a	chr15:30967474-30967485
34	CEBPB	chr15:31058670-31058834	K562	blood:	n/a	chr15:31058745-31058756
35	CEBPB	chr15:30964859-30965084	K562	blood:	n/a	n/a
36	CEBPB	chr15:30983872-30983981	K562	blood:	n/a	n/a
37	CEBPB	chr15:30983768-30983986	A549	lung:	n/a	n/a
38	CEBPB	chr15:30967306-30967676	IMR90	lung:	n/a	chr15:30967474-30967485
39	CEBPB	chr15:30967310-30967751	A549	lung:	n/a	chr15:30967474-30967485
40	CEBPB	chr15:30958201-30958546	IMR90	lung:	n/a	n/a
41	CEBPB	chr15:30989170-30989954	GM12878	blood:	n/a	n/a
42	CEBPB	chr15:30983791-30984131	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr15:30953404-30953637	K562	blood:	n/a	chr15:30953517-30953528
44	CEBPB	chr15:31058568-31058944	HepG2	liver:	n/a	chr15:31058745-31058756
45	CEBPB	chr15:30967400-30967648	A549	lung:	n/a	chr15:30967474-30967485
46	CEBPB	chr15:30965736-30965777	A549	lung:	n/a	n/a
47	CEBPB	chr15:30953382-30953692	K562	blood:	n/a	chr15:30953517-30953528
48	CEBPB	chr15:31058652-31058827	HepG2	liver:	n/a	chr15:31058745-31058756
49	CEBPB	chr15:31058570-31058941	A549	lung:	n/a	chr15:31058745-31058756
50	CEBPB	chr15:30983881-30984093	HepG2	liver:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31086755-31086805	AG09309	skin:	n/a
2	chr15:31086755-31086805	AG09309	skin:	n/a
3	chr15:31090636-31090686	AG09309	skin:	n/a
4	chr15:31093049-31093099	GM12891	blood:	n/a
5	chr15:31093811-31093861	Jurkat	blood:	n/a
6	chr15:31092120-31092170	BE2_C	brain:	n/a
7	chr15:31086755-31086805	HEK293	kidney:	embryo
8	chr15:31093049-31093099	HNPCEpiC	eye:	n/a
9	chr15:31093811-31093861	HCM	heart:	n/a
10	chr15:31090995-31091045	SK-N-SH_RA	brain:	n/a
11	chr15:31086755-31086805	Caco-2	colon:	n/a
12	chr15:31066090-31066140	T-47D	breast:	n/a
13	chr15:31090995-31091045	NHDF-neo	bronchial:	n/a
14	chr15:31093049-31093099	T-47D	breast:	n/a
15	chr15:31090995-31091045	MCF-7	breast:	n/a
16	chr15:31090995-31091045	HRPEpiC	eye:	n/a
17	chr15:31090636-31090686	SAEC	small airway:	n/a
18	chr15:31090995-31091045	HMEC	breast:	n/a
19	chr15:31086755-31086805	ECC-1	luminal epithelium:	n/a
20	chr15:31066090-31066140	HL-60	blood:	n/a
21	chr15:31090636-31090686	MCF10A-Er-Src	breast:	n/a
22	chr15:31093040-31093090	HCM	heart:	n/a
23	chr15:31088666-31088716	GM12878	blood:	n/a
24	chr15:31086755-31086805	U87	brain:	n/a
25	chr15:31090995-31091045	SK-N-SH	brain:	n/a
26	chr15:31066090-31066140	ECC-1	luminal epithelium:	n/a
27	chr15:31093811-31093861	PrEC	prostate:	n/a
28	chr15:31093811-31093861	H1-hESC	embryonic stem cell:	embryo
29	chr15:31088666-31088716	NHDF-neo	bronchial:	n/a
30	chr15:31090636-31090686	HPAEpiC	pulmonary alveolar:	n/a
31	chr15:31092120-31092170	HIPEpiC	eye:	n/a
32	chr15:31088666-31088716	AG09319	gingival:	n/a
33	chr15:31088666-31088716	RPTEC	kidney:	n/a
34	chr15:30930499-30930549	HEK293	kidney:	embryo
35	chr15:31090636-31090686	NT2-D1	testis:	n/a
36	chr15:31088666-31088716	CMK	blood:	n/a
37	chr15:31088666-31088716	HRE	kidney:	n/a
38	chr15:31066090-31066140	HAEpiC	amniotic membrane:	n/a
39	chr15:31066090-31066140	Hepatocyte	liver:	n/a
40	chr15:31088666-31088716	SKMC	muscle:	n/a
41	chr15:31088666-31088716	SAEC	small airway:	n/a
42	chr15:31088666-31088716	HMEC	breast:	n/a
43	chr15:31066090-31066140	CMK	blood:	n/a
44	chr15:31093040-31093090	AG09319	gingival:	n/a
45	chr15:30930499-30930549	CMK	blood:	n/a
46	chr15:31093049-31093099	SK-N-SH	brain:	n/a
47	chr15:30930499-30930549	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:31066090-31066140	GM06990	blood:	n/a
49	chr15:31086755-31086805	BJ	skin:	n/a
50	chr15:31066090-31066140	NT2-D1	testis:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
2	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
3	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
4	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP11B-5	chr15:31092352-31092630	NONHSAT041399
2	lnc-ARHGAP11B-1	chr15:31042605-31042759	NONHSAT041384
3	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041382
4	lnc-ARHGAP11B-1	chr15:31061535-31065196	NONHSAT041388
5	lnc-GOLGA8H-2	chr15:30941000-30941732	ENSG00000269974.1
6	lnc-ARHGAP11B-1	chr15:31060061-31065209	NONHSAT041384
7	lnc-ARHGAP11B-1	chr15:31060916-31061371	NONHSAT041387
8	lnc-ARHGAP11B-1	chr15:31015549-31015698	NONHSAT041382
9	lnc-ARHGAP11B-1	chr15:30950920-30951047	NONHSAT041384
10	lnc-ARHGAP11B-3	chr15:31074599-31075123	NONHSAT041397
11	lnc-ARHGAP11B-1	chr15:30938335-30938498	NONHSAT041382
12	lnc-ARHGAP11B-1	chr15:30939871-30939917	NONHSAT041382
13	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041384

No data

Variant related genes	Relation type
GOLGA8UP	TF binding region
ARHGAP11B	TF binding region
ENSG00000269974	TF binding region
ENSG00000206846	TF binding region
ENSG00000221379	TF binding region
RN7SL82P	TF binding region
ENSG00000252602	TF binding region
GOLGA8UP	CpG island
ARHGAP11B	CpG island
ENSG00000269974	CpG island
ENSG00000206846	CpG island
ENSG00000221379	CpG island
RN7SL82P	CpG island
ENSG00000252602	CpG island

Extended variants
information (count: 6348 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:6348 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8038419	chr15:30927210-30927211	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553820862	chr15:30927215-30927216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs376305602	chr15:30927238-30927239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370436634	chr15:30927246-30927247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374071695	chr15:30927268-30927269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556844439	chr15:30927300-30927301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs14618	chr15:30927334-30927335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576661518	chr15:30927351-30927352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143787832	chr15:30927362-30927363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545624544	chr15:30927367-30927368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs367647653	chr15:30927376-30927377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs565349273	chr15:30927379-30927380	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs14619	chr15:30927380-30927381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371324595	chr15:30927401-30927402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150590279	chr15:30927415-30927416	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373402272	chr15:30927416-30927417	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374363097	chr15:30927426-30927427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368543744	chr15:30927428-30927429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372915298	chr15:30927436-30927437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572627526	chr15:30927470-30927471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541151559	chr15:30927517-30927518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560934228	chr15:30927568-30927569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529739004	chr15:30927595-30927596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs549506180	chr15:30927599-30927600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs56230817	chr15:30927631-30927632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs532312919	chr15:30927641-30927642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377077753	chr15:30927643-30927644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368349923	chr15:30927670-30927671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs565559996	chr15:30927674-30927675	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113953826	chr15:30927684-30927685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372005915	chr15:30927781-30927782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376751790	chr15:30927785-30927786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369518739	chr15:30927798-30927799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146907163	chr15:30927812-30927813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528237415	chr15:30927841-30927842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs199799461	chr15:30927851-30927852	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62014561	chr15:30927867-30927868	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs369865570	chr15:30927871-30927872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539382545	chr15:30927901-30927902	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536295310	chr15:30927979-30927980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556274799	chr15:30927986-30927987	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62014562	chr15:30928055-30928056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538969427	chr15:30928119-30928120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559178592	chr15:30928162-30928163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572697847	chr15:30928227-30928228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs543220683	chr15:30928239-30928240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541614343	chr15:30928264-30928265	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554749699	chr15:30928452-30928453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574572556	chr15:30928469-30928470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543463558	chr15:30928520-30928521	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:1268 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30918800-30931200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr15:30919200-30931000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:30919200-30935400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:30919200-30942400	Weak transcription	Primary T cells from cord blood	blood
5	chr15:30919200-30966400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr15:30919400-30938400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr15:30919400-30959800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr15:30919400-30969800	Weak transcription	Fetal Lung	lung
9	chr15:30919400-30972800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr15:30919600-30928800	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr15:30919600-30928800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr15:30919600-30935200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr15:30919600-30935400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr15:30919600-30939200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:30919600-30948200	Weak transcription	Duodenum Mucosa	Duodenum
16	chr15:30919600-30964000	Weak transcription	Fetal Intestine Large	intestine
17	chr15:30919600-31023200	Weak transcription	Fetal Intestine Small	intestine
18	chr15:30919800-30933000	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr15:30919800-30940400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr15:30919800-30942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr15:30919800-30961800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr15:30920000-30928800	Weak transcription	Osteobl	bone
23	chr15:30920000-30938000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr15:30920000-30938800	Weak transcription	Thymus	Thymus
25	chr15:30920000-30939200	Weak transcription	Fetal Muscle Leg	muscle
26	chr15:30920000-30939800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr15:30920000-30940600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr15:30920000-30955400	Weak transcription	NH-A	brain
29	chr15:30920000-31028200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr15:30920200-30929400	Weak transcription	Fetal Thymus	thymus
31	chr15:30920800-30928800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr15:30920800-30933800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr15:30920800-30940400	Weak transcription	HSMM	muscle
34	chr15:30920800-30950400	Weak transcription	NHEK	skin
35	chr15:30921000-30936000	Weak transcription	HMEC	breast
36	chr15:30921200-30936000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:30921200-30938000	Weak transcription	NHDF-Ad	bronchial
38	chr15:30921200-30982400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr15:30921400-30933800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr15:30922200-30938600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr15:30922200-30940400	Weak transcription	HUVEC	blood vessel
42	chr15:30922400-30933800	Weak transcription	GM12878-XiMat	blood
43	chr15:30922400-30935200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr15:30922400-30935200	Weak transcription	K562	blood
45	chr15:30922400-30938000	Weak transcription	HepG2	liver
46	chr15:30922400-30952400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr15:30922600-30931400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:30922600-30936200	Weak transcription	Fetal Heart	heart
49	chr15:30923400-30931400	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr15:30923600-30929000	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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