Variant report

Variant	nsv1039621
Chromosome Location	chr15:30948624-31110531
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1470)
CpG islands
(count:611)
Chromatin interactive
region (count:4)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

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	BACH1	chr15:31056549-31056561	K562	blood:	n/a	n/a
3	BATF	chr15:31047306-31047532	GM12878	blood:	n/a	n/a
4	BATF	chr15:31001037-31001298	GM12878	blood:	n/a	chr15:31001194-31001205
5	BATF	chr15:30988887-30989837	GM12878	blood:	n/a	n/a
6	BATF	chr15:30988651-30989902	GM12878	blood:	n/a	n/a
7	BATF	chr15:31078925-31079140	GM12878	blood:	n/a	n/a
8	BCL11A	chr15:30988813-30989894	GM12878	blood:	n/a	n/a
9	BCL11A	chr15:30989215-30989908	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:31047283-31047543	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:30988850-30989149	GM12878	blood:	n/a	n/a
12	BCL11A	chr15:30988374-30988675	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:30989526-30989883	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:30968872-30968884	K562	blood:	n/a	n/a
15	BHLHE40	chr15:30959588-30959606	K562	blood:	n/a	n/a
16	CEBPB	chr15:30967306-30967676	IMR90	lung:	n/a	chr15:30967474-30967485
17	CEBPB	chr15:31058645-31058938	HepG2	liver:	n/a	chr15:31058745-31058756
18	CEBPB	chr15:30958228-30958528	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:31105872-31106046	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:30989170-30989954	GM12878	blood:	n/a	n/a
21	CEBPB	chr15:31058652-31058827	HepG2	liver:	n/a	chr15:31058745-31058756
22	CEBPB	chr15:31058573-31058941	H1-hESC	embryonic stem cell:	n/a	chr15:31058745-31058756
23	CEBPB	chr15:30983742-30983960	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr15:30953404-30953637	K562	blood:	n/a	chr15:30953517-30953528
25	CEBPB	chr15:30967310-30967751	A549	lung:	n/a	chr15:30967474-30967485
26	CEBPB	chr15:30967400-30967648	A549	lung:	n/a	chr15:30967474-30967485
27	CEBPB	chr15:31058561-31059006	Hela-S3	cervix:	n/a	chr15:31058745-31058756
28	CEBPB	chr15:30967352-30967663	HepG2	liver:	n/a	chr15:30967474-30967485
29	CEBPB	chr15:31035071-31035332	IMR90	lung:	n/a	n/a
30	CEBPB	chr15:31058558-31059008	IMR90	lung:	n/a	chr15:31058745-31058756
31	CEBPB	chr15:30983872-30983981	K562	blood:	n/a	n/a
32	CEBPB	chr15:30983881-30984093	HepG2	liver:	n/a	n/a
33	CEBPB	chr15:31058670-31058834	K562	blood:	n/a	chr15:31058745-31058756
34	CEBPB	chr15:30983791-30984131	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr15:30953401-30953667	IMR90	lung:	n/a	chr15:30953517-30953528
36	CEBPB	chr15:30965736-30965777	A549	lung:	n/a	n/a
37	CEBPB	chr15:30967261-30967669	K562	blood:	n/a	chr15:30967474-30967485
38	CEBPB	chr15:30964859-30965084	K562	blood:	n/a	n/a
39	CEBPB	chr15:30958152-30958542	K562	blood:	n/a	n/a
40	CEBPB	chr15:30983782-30984067	IMR90	lung:	n/a	n/a
41	CEBPB	chr15:30958201-30958546	IMR90	lung:	n/a	n/a
42	CEBPB	chr15:31084274-31084474	HepG2	liver:	n/a	n/a
43	CEBPB	chr15:30953382-30953692	K562	blood:	n/a	chr15:30953517-30953528
44	CEBPB	chr15:30953435-30953668	A549	lung:	n/a	chr15:30953517-30953528
45	CEBPB	chr15:30967341-30967670	A549	lung:	n/a	chr15:30967474-30967485
46	CEBPB	chr15:30983768-30983986	A549	lung:	n/a	n/a
47	CEBPB	chr15:31058570-31058941	A549	lung:	n/a	chr15:31058745-31058756
48	CEBPB	chr15:30967357-30967622	Hela-S3	cervix:	n/a	chr15:30967474-30967485
49	CEBPB	chr15:31058568-31058944	HepG2	liver:	n/a	chr15:31058745-31058756
50	CEBPB	chr15:31058594-31058887	HepG2	liver:	n/a	chr15:31058745-31058756

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31090995-31091045	ProgFib	skin:	n/a
2	chr15:31090995-31091045	ProgFib	skin:	n/a
3	chr15:31093049-31093099	NHDF-neo	bronchial:	n/a
4	chr15:31092120-31092170	AG04449	skin:	fetal
5	chr15:31090995-31091045	SAEC	small airway:	n/a
6	chr15:31086755-31086805	HCT-116	colon:	n/a
7	chr15:31108938-31108988	HRPEpiC	eye:	n/a
8	chr15:31108938-31108988	HepG2	liver:	n/a
9	chr15:31093811-31093861	PrEC	prostate:	n/a
10	chr15:31092120-31092170	HCPEpiC	choroid plexus:	n/a
11	chr15:31088666-31088716	LNCaP	prostate:	n/a
12	chr15:31093049-31093099	MCF10A-Er-Src	breast:	n/a
13	chr15:31090995-31091045	SK-N-MC	brain:	n/a
14	chr15:31066090-31066140	Hela-S3	cervix:	n/a
15	chr15:31093040-31093090	Caco-2	colon:	n/a
16	chr15:31088666-31088716	GM06990	blood:	n/a
17	chr15:31093040-31093090	PANC-1	pancreas:	n/a
18	chr15:31066090-31066140	HRCEpiC	kidney:	n/a
19	chr15:31093049-31093099	IMR90	lung:	fetal
20	chr15:31108938-31108988	HIPEpiC	eye:	n/a
21	chr15:31093811-31093861	NB4	blood:	n/a
22	chr15:31092120-31092170	HRPEpiC	eye:	n/a
23	chr15:31093811-31093861	MCF-7	breast:	n/a
24	chr15:31108938-31108988	SKMC	muscle:	n/a
25	chr15:31066090-31066140	SK-N-MC	brain:	n/a
26	chr15:31086755-31086805	H1-hESC	embryonic stem cell:	embryo
27	chr15:31093049-31093099	BE2_C	brain:	n/a
28	chr15:31088666-31088716	HCPEpiC	choroid plexus:	n/a
29	chr15:31093811-31093861	SK-N-SH_RA	brain:	n/a
30	chr15:31108938-31108988	BE2_C	brain:	n/a
31	chr15:31092120-31092170	NB4	blood:	n/a
32	chr15:31108938-31108988	NHBE	bronchial:	n/a
33	chr15:31092120-31092170	RPTEC	kidney:	n/a
34	chr15:31092120-31092170	Hela-S3	cervix:	n/a
35	chr15:31093040-31093090	AG09319	gingival:	n/a
36	chr15:31093811-31093861	HMEC	breast:	n/a
37	chr15:31090995-31091045	ovcar-3	ovarian:	n/a
38	chr15:31093811-31093861	ECC-1	luminal epithelium:	n/a
39	chr15:31090995-31091045	HUVEC	blood vessel:	n/a
40	chr15:31088666-31088716	HCF	heart:	n/a
41	chr15:31090995-31091045	HCT-116	colon:	n/a
42	chr15:31086755-31086805	SAEC	small airway:	n/a
43	chr15:31090636-31090686	Hela-S3	cervix:	n/a
44	chr15:31108938-31108988	GM12891	blood:	n/a
45	chr15:31108938-31108988	MCF-7	breast:	n/a
46	chr15:31090636-31090686	T-47D	breast:	n/a
47	chr15:31088666-31088716	HEEpiC	esophagus:	n/a
48	chr15:31093040-31093090	GM06990	blood:	n/a
49	chr15:31066090-31066140	AoSMC	blood vessel:	n/a
50	chr15:31093040-31093090	LNCaP	prostate:	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-chr15:30969306..30971745,2	K562	blood:
3	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
4	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:

(count:10 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
HERC2P10	TF binding region
GOLGA8UP	TF binding region
ARHGAP11B	TF binding region
ENSG00000206846	TF binding region
ENSG00000221379	TF binding region
RN7SL82P	TF binding region
HERC2P10	CpG island
GOLGA8UP	CpG island
ARHGAP11B	CpG island
ENSG00000206846	CpG island
ENSG00000221379	CpG island
RN7SL82P	CpG island

Extended variants
information (count: 5657 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:5657 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114735840	chr15:30948625-30948626	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs142938739	chr15:30948673-30948674	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs112694866	chr15:30948699-30948700	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs535149865	chr15:30948758-30948759	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs555085302	chr15:30948788-30948789	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139018801	chr15:30948795-30948796	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs543835044	chr15:30948802-30948803	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs149420735	chr15:30948817-30948818	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs185179319	chr15:30948822-30948823	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs577485426	chr15:30948904-30948905	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs546449015	chr15:30948905-30948906	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs559725339	chr15:30948994-30948995	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs528648903	chr15:30948995-30948996	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs541568461	chr15:30949011-30949012	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs368851407	chr15:30949040-30949041	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs562897362	chr15:30949059-30949060	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs376044498	chr15:30949060-30949061	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs34961090	chr15:30949098-30949099	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs578253407	chr15:30949145-30949146	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs545686922	chr15:30949150-30949151	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs560741937	chr15:30949176-30949177	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs528129774	chr15:30949182-30949183	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs530477927	chr15:30949187-30949188	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs546272536	chr15:30949201-30949202	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs550312382	chr15:30949215-30949216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570391492	chr15:30949302-30949303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533095151	chr15:30949306-30949307	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546848699	chr15:30949344-30949345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566707438	chr15:30949352-30949353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189696594	chr15:30949353-30949354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555146896	chr15:30949354-30949355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148500815	chr15:30949371-30949372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12898548	chr15:30949394-30949395	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs62014601	chr15:30949425-30949426	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs186366803	chr15:30949467-30949468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4779757	chr15:30949481-30949482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs368498947	chr15:30949487-30949488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546213706	chr15:30949503-30949504	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs553243911	chr15:30949504-30949505	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs139705288	chr15:30949531-30949532	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs559393228	chr15:30949543-30949544	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs542024773	chr15:30949545-30949546	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs561903707	chr15:30949547-30949548	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs191312159	chr15:30949551-30949552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145231105	chr15:30949561-30949562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147602412	chr15:30949587-30949588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533079859	chr15:30949598-30949599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551291164	chr15:30949612-30949613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183499954	chr15:30949617-30949618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566769110	chr15:30949620-30949621	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:999 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

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	chr15:30920800-30950400	Weak transcription	NHEK	skin
11	chr15:30921200-30982400	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr15:30922400-30952400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr15:30924600-30961800	Weak transcription	Fetal Stomach	stomach
14	chr15:30931800-30952400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr15:30934000-30951400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr15:30936000-30952600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:30937000-30971200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr15:30938000-30961600	Weak transcription	Small Intestine	intestine
19	chr15:30938800-30957800	Weak transcription	Hela-S3	cervix
20	chr15:30938800-30969200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr15:30938800-30974000	Weak transcription	Primary B cells from cord blood	blood
22	chr15:30939400-30954200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr15:30939600-30969600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr15:30940800-30959400	Weak transcription	Fetal Muscle Leg	muscle
25	chr15:30941000-30950800	Weak transcription	HSMM	muscle
26	chr15:30941000-30962400	Weak transcription	NHDF-Ad	bronchial
27	chr15:30941000-30988600	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr15:30941200-30958000	Weak transcription	Primary hematopoietic stem cells	blood
29	chr15:30941400-30950800	Weak transcription	Thymus	Thymus
30	chr15:30942400-30950600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr15:30942600-30950600	Weak transcription	Fetal Thymus	thymus
32	chr15:30942600-30952000	Weak transcription	HMEC	breast
33	chr15:30942600-30962200	Weak transcription	NHLF	lung
34	chr15:30942800-30950400	Weak transcription	HepG2	liver
35	chr15:30942800-30973600	Weak transcription	Primary T cells from cord blood	blood
36	chr15:30943000-30950600	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr15:30943000-30958800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr15:30943200-30949400	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr15:30943200-30950400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr15:30943200-30950400	Weak transcription	A549	lung
41	chr15:30943600-30950800	Weak transcription	K562	blood
42	chr15:30943800-30958000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr15:30945800-30951200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr15:30945800-30953800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr15:30945800-30964400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr15:30946000-30949000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr15:30946400-30949400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr15:30946400-30949400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:30946400-30954000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr15:30946400-30956000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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