Variant report

Variant	nsv456744
Chromosome Location	chr15:30936285-31123235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1713)
CpG islands
(count:979)
Chromatin interactive
region (count:5)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1713 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

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	ATF1	chr15:31120556-31120738	K562	blood:	n/a	n/a
5	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
6	BACH1	chr15:31122441-31122516	K562	blood:	n/a	n/a
7	BACH1	chr15:31056549-31056561	K562	blood:	n/a	n/a
8	BATF	chr15:31078925-31079140	GM12878	blood:	n/a	n/a
9	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
10	BATF	chr15:30988651-30989902	GM12878	blood:	n/a	n/a
11	BATF	chr15:31047306-31047532	GM12878	blood:	n/a	n/a
12	BATF	chr15:31001037-31001298	GM12878	blood:	n/a	chr15:31001194-31001205
13	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
14	BATF	chr15:30988887-30989837	GM12878	blood:	n/a	n/a
15	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
16	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:30989215-30989908	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:31047283-31047543	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:30942112-30942840	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:30988813-30989894	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:30988850-30989149	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:30988374-30988675	GM12878	blood:	n/a	n/a
23	BCLAF1	chr15:30942082-30942772	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:30968872-30968884	K562	blood:	n/a	n/a
25	BHLHE40	chr15:30941983-30942693	GM12878	blood:	n/a	n/a
26	BHLHE40	chr15:30989526-30989883	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:30959588-30959606	K562	blood:	n/a	n/a
28	CEBPB	chr15:30983872-30983981	K562	blood:	n/a	n/a
29	CEBPB	chr15:30967357-30967622	Hela-S3	cervix:	n/a	chr15:30967474-30967485
30	CEBPB	chr15:31058594-31058887	HepG2	liver:	n/a	chr15:31058745-31058756
31	CEBPB	chr15:31120537-31120733	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:31058561-31059006	Hela-S3	cervix:	n/a	chr15:31058745-31058756
33	CEBPB	chr15:30958228-30958528	HepG2	liver:	n/a	n/a
34	CEBPB	chr15:31058558-31059008	IMR90	lung:	n/a	chr15:31058745-31058756
35	CEBPB	chr15:31058652-31058827	HepG2	liver:	n/a	chr15:31058745-31058756
36	CEBPB	chr15:31058570-31058941	A549	lung:	n/a	chr15:31058745-31058756
37	CEBPB	chr15:31105872-31106046	IMR90	lung:	n/a	n/a
38	CEBPB	chr15:30989170-30989954	GM12878	blood:	n/a	n/a
39	CEBPB	chr15:30967352-30967663	HepG2	liver:	n/a	chr15:30967474-30967485
40	CEBPB	chr15:30953401-30953667	IMR90	lung:	n/a	chr15:30953517-30953528
41	CEBPB	chr15:30983782-30984067	IMR90	lung:	n/a	n/a
42	CEBPB	chr15:30958201-30958546	IMR90	lung:	n/a	n/a
43	CEBPB	chr15:30953404-30953637	K562	blood:	n/a	chr15:30953517-30953528
44	CEBPB	chr15:30953382-30953692	K562	blood:	n/a	chr15:30953517-30953528
45	CEBPB	chr15:30936260-30936445	IMR90	lung:	n/a	n/a
46	CEBPB	chr15:30942518-30943053	IMR90	lung:	n/a	n/a
47	CEBPB	chr15:30967400-30967648	A549	lung:	n/a	chr15:30967474-30967485
48	CEBPB	chr15:31035071-31035332	IMR90	lung:	n/a	n/a
49	CEBPB	chr15:31058568-31058944	HepG2	liver:	n/a	chr15:31058745-31058756
50	CEBPB	chr15:30953435-30953668	A549	lung:	n/a	chr15:30953517-30953528

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31088666-31088716	GM12892	blood:	n/a
2	chr15:31115862-31115912	SAEC	small airway:	n/a
3	chr15:31122751-31122801	HCF	heart:	n/a
4	chr15:31088666-31088716	GM12892	blood:	n/a
5	chr15:31115862-31115912	SAEC	small airway:	n/a
6	chr15:31122751-31122801	HCF	heart:	n/a
7	chr15:31066090-31066140	HRCEpiC	kidney:	n/a
8	chr15:31093040-31093090	AG04449	skin:	fetal
9	chr15:31090995-31091045	RPTEC	kidney:	n/a
10	chr15:31092120-31092170	HRCEpiC	kidney:	n/a
11	chr15:31108938-31108988	AoSMC	blood vessel:	n/a
12	chr15:31090636-31090686	Caco-2	colon:	n/a
13	chr15:31092120-31092170	HL-60	blood:	n/a
14	chr15:31115839-31115889	H1-hESC	embryonic stem cell:	embryo
15	chr15:31122726-31122776	NHBE	bronchial:	n/a
16	chr15:31090636-31090686	BJ	skin:	n/a
17	chr15:31122537-31122587	U87	brain:	n/a
18	chr15:31093049-31093099	Hela-S3	cervix:	n/a
19	chr15:31088666-31088716	MCF-7	breast:	n/a
20	chr15:31092120-31092170	HCF	heart:	n/a
21	chr15:31093040-31093090	Caco-2	colon:	n/a
22	chr15:31086755-31086805	NHBE	bronchial:	n/a
23	chr15:31115839-31115889	NB4	blood:	n/a
24	chr15:31066090-31066140	HRE	kidney:	n/a
25	chr15:31090995-31091045	T-47D	breast:	n/a
26	chr15:31108938-31108988	Caco-2	colon:	n/a
27	chr15:31122537-31122587	HCF	heart:	n/a
28	chr15:31093049-31093099	HCM	heart:	n/a
29	chr15:31115862-31115912	HCM	heart:	n/a
30	chr15:31122751-31122801	ovcar-3	ovarian:	n/a
31	chr15:31066090-31066140	HepG2	liver:	n/a
32	chr15:31115862-31115912	HEEpiC	esophagus:	n/a
33	chr15:31122726-31122776	AoSMC	blood vessel:	n/a
34	chr15:31115871-31115921	RPTEC	kidney:	n/a
35	chr15:31122537-31122587	ProgFib	skin:	n/a
36	chr15:31122537-31122587	GM12892	blood:	n/a
37	chr15:31115839-31115889	Caco-2	colon:	n/a
38	chr15:31122751-31122801	GM12892	blood:	n/a
39	chr15:31086755-31086805	Caco-2	colon:	n/a
40	chr15:31088666-31088716	A549	lung:	n/a
41	chr15:31066090-31066140	U87	brain:	n/a
42	chr15:31090636-31090686	HRCEpiC	kidney:	n/a
43	chr15:31122537-31122587	Caco-2	colon:	n/a
44	chr15:31066090-31066140	AG04449	skin:	fetal
45	chr15:31122537-31122587	HAEpiC	amniotic membrane:	n/a
46	chr15:31093049-31093099	K562	blood:	n/a
47	chr15:31122537-31122587	AoSMC	blood vessel:	n/a
48	chr15:31066090-31066140	SK-N-SH_RA	brain:	n/a
49	chr15:31066090-31066140	HMEC	breast:	n/a
50	chr15:31122751-31122801	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr15:31120296..31121046-chr17:8075920..8076839,2	HCT-116	colon:
2	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
3	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
4	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
5	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-1	chr15:30939871-30939917	NONHSAT041382
2	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041382
3	lnc-GOLGA8H-2	chr15:30941000-30941732	ENSG00000269974.1
4	lnc-ARHGAP11B-3	chr15:31074599-31075123	NONHSAT041397
5	lnc-ARHGAP11B-1	chr15:31015549-31015698	NONHSAT041382
6	lnc-ARHGAP11B-5	chr15:31092352-31092630	NONHSAT041399
7	lnc-ARHGAP11B-1	chr15:31008423-31008545	NONHSAT041384
8	lnc-ARHGAP11B-1	chr15:30950920-30951047	NONHSAT041384
9	lnc-ARHGAP11B-1	chr15:31042605-31042759	NONHSAT041384
10	lnc-ARHGAP11B-1	chr15:31061535-31065196	NONHSAT041388
11	lnc-ARHGAP11B-1	chr15:31060916-31061371	NONHSAT041387
12	lnc-ARHGAP11B-1	chr15:31060061-31065209	NONHSAT041384
13	lnc-ARHGAP11B-1	chr15:30938335-30938498	NONHSAT041382

No data

Variant related genes	Relation type
HERC2P10	TF binding region
GOLGA8UP	TF binding region
ARHGAP11B	TF binding region
ENSG00000269974	TF binding region
ENSG00000206846	TF binding region
ENSG00000221379	TF binding region
RN7SL82P	TF binding region
HERC2P10	CpG island
GOLGA8UP	CpG island
ARHGAP11B	CpG island
ENSG00000269974	CpG island
ENSG00000206846	CpG island
ENSG00000221379	CpG island
RN7SL82P	CpG island

Extended variants
information (count: 6716 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:6716 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2046362	chr15:30936285-30936286	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567741917	chr15:30936329-30936330	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs550143945	chr15:30936340-30936341	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs553853163	chr15:30936404-30936405	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs577482554	chr15:30936410-30936411	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs571814989	chr15:30936425-30936426	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs138123748	chr15:30936452-30936453	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs539346752	chr15:30936457-30936458	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs552866748	chr15:30936465-30936466	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs115570031	chr15:30936471-30936472	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs184463392	chr15:30936480-30936481	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs554410320	chr15:30936503-30936504	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs556801705	chr15:30936529-30936530	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs576759824	chr15:30936530-30936531	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs188846209	chr15:30936583-30936584	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs536701367	chr15:30936659-30936660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374128252	chr15:30936679-30936680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182023722	chr15:30936699-30936700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs542889132	chr15:30936714-30936715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34265513	chr15:30936726-30936727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377080120	chr15:30936731-30936732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186211087	chr15:30936732-30936733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545715124	chr15:30936745-30936746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559199584	chr15:30936755-30936756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542434199	chr15:30936798-30936799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs190211934	chr15:30936836-30936837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs541996906	chr15:30936862-30936863	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs2648148	chr15:30936875-30936876	Weak transcription Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs150511562	chr15:30936894-30936895	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs549962935	chr15:30936922-30936923	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs201768458	chr15:30936928-30936929	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs368150208	chr15:30936939-30936940	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs138514498	chr15:30936940-30936941	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs67309432	chr15:30936941-30936942	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs112174166	chr15:30936943-30936944	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs180909755	chr15:30936978-30936979	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs532531002	chr15:30936991-30936992	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs2648149	chr15:30936998-30936999	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs149279380	chr15:30937009-30937010	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs185839682	chr15:30937083-30937084	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs112294270	chr15:30937124-30937125	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs369936401	chr15:30937175-30937176	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs568522105	chr15:30937182-30937183	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs372470711	chr15:30937218-30937219	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs537164933	chr15:30937225-30937226	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs556612221	chr15:30937353-30937354	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62014564	chr15:30937399-30937400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532444495	chr15:30937432-30937433	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570140685	chr15:30937467-30937468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539031656	chr15:30937481-30937482	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:1384 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30919200-30942400	Weak transcription	Primary T cells from cord blood	blood
2	chr15:30919200-30966400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:30919400-30938400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr15:30919400-30959800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr15:30919400-30969800	Weak transcription	Fetal Lung	lung
6	chr15:30919400-30972800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:30919600-30939200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr15:30919600-30948200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr15:30919600-30964000	Weak transcription	Fetal Intestine Large	intestine
10	chr15:30919600-31023200	Weak transcription	Fetal Intestine Small	intestine
11	chr15:30919800-30940400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr15:30919800-30942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:30919800-30961800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr15:30920000-30938000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr15:30920000-30938800	Weak transcription	Thymus	Thymus
16	chr15:30920000-30939200	Weak transcription	Fetal Muscle Leg	muscle
17	chr15:30920000-30939800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr15:30920000-30940600	Weak transcription	Primary hematopoietic stem cells	blood
19	chr15:30920000-30955400	Weak transcription	NH-A	brain
20	chr15:30920000-31028200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:30920800-30940400	Weak transcription	HSMM	muscle
22	chr15:30920800-30950400	Weak transcription	NHEK	skin
23	chr15:30921200-30938000	Weak transcription	NHDF-Ad	bronchial
24	chr15:30921200-30982400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr15:30922200-30938600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr15:30922200-30940400	Weak transcription	HUVEC	blood vessel
27	chr15:30922400-30938000	Weak transcription	HepG2	liver
28	chr15:30922400-30952400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr15:30924600-30961800	Weak transcription	Fetal Stomach	stomach
30	chr15:30928000-30945800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:30928600-30938200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr15:30929400-30942200	Weak transcription	Primary T helper cells fromperipheralblood	blood
33	chr15:30930200-30938000	Weak transcription	Osteobl	bone
34	chr15:30931800-30952400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr15:30932200-30942200	Weak transcription	NHLF	lung
36	chr15:30933000-30936400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr15:30933000-30941200	Strong transcription	Monocytes-CD14+_RO01746	blood
38	chr15:30933000-30943200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:30933000-30944600	Strong transcription	Dnd41	blood
40	chr15:30933400-30936400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
41	chr15:30933400-30943800	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr15:30933600-30943800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr15:30933800-30936600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:30934000-30936400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
45	chr15:30934000-30936600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr15:30934000-30936600	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr15:30934000-30939400	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr15:30934000-30951400	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr15:30935000-30936400	Strong transcription	Hela-S3	cervix
50	chr15:30935000-30936600	Strong transcription	Fetal Thymus	thymus

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