Variant report

Variant	nsv1040388
Chromosome Location	chr15:30920612-31084331
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1309)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1309 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

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	chr15:31047306-31047532	GM12878	blood:	n/a	n/a
7	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
8	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
9	BATF	chr15:31078925-31079140	GM12878	blood:	n/a	n/a
10	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
11	BATF	chr15:31001037-31001298	GM12878	blood:	n/a	chr15:31001194-31001205
12	BATF	chr15:30988651-30989902	GM12878	blood:	n/a	n/a
13	BATF	chr15:30988887-30989837	GM12878	blood:	n/a	n/a
14	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
15	BCL11A	chr15:30942112-30942840	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:30988850-30989149	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:30988374-30988675	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:31047283-31047543	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:30988813-30989894	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	chr15:30989526-30989883	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:30959588-30959606	K562	blood:	n/a	n/a
24	BHLHE40	chr15:30941983-30942693	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:30968872-30968884	K562	blood:	n/a	n/a
26	CEBPB	chr15:30936260-30936445	IMR90	lung:	n/a	n/a
27	CEBPB	chr15:30958201-30958546	IMR90	lung:	n/a	n/a
28	CEBPB	chr15:30965736-30965777	A549	lung:	n/a	n/a
29	CEBPB	chr15:30964859-30965084	K562	blood:	n/a	n/a
30	CEBPB	chr15:30967400-30967648	A549	lung:	n/a	chr15:30967474-30967485
31	CEBPB	chr15:30983881-30984093	HepG2	liver:	n/a	n/a
32	CEBPB	chr15:30983768-30983986	A549	lung:	n/a	n/a
33	CEBPB	chr15:31058561-31059006	Hela-S3	cervix:	n/a	chr15:31058745-31058756
34	CEBPB	chr15:30967310-30967751	A549	lung:	n/a	chr15:30967474-30967485
35	CEBPB	chr15:31058652-31058827	HepG2	liver:	n/a	chr15:31058745-31058756
36	CEBPB	chr15:31058594-31058887	HepG2	liver:	n/a	chr15:31058745-31058756
37	CEBPB	chr15:31058645-31058938	HepG2	liver:	n/a	chr15:31058745-31058756
38	CEBPB	chr15:30967306-30967676	IMR90	lung:	n/a	chr15:30967474-30967485
39	CEBPB	chr15:31058573-31058941	H1-hESC	embryonic stem cell:	n/a	chr15:31058745-31058756
40	CEBPB	chr15:30983791-30984131	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:30942518-30943053	IMR90	lung:	n/a	n/a
42	CEBPB	chr15:31058558-31059008	IMR90	lung:	n/a	chr15:31058745-31058756
43	CEBPB	chr15:30983782-30984067	IMR90	lung:	n/a	n/a
44	CEBPB	chr15:31058570-31058941	A549	lung:	n/a	chr15:31058745-31058756
45	CEBPB	chr15:30953404-30953637	K562	blood:	n/a	chr15:30953517-30953528
46	CEBPB	chr15:30967357-30967622	Hela-S3	cervix:	n/a	chr15:30967474-30967485
47	CEBPB	chr15:30989170-30989954	GM12878	blood:	n/a	n/a
48	CEBPB	chr15:31058568-31058944	HepG2	liver:	n/a	chr15:31058745-31058756
49	CEBPB	chr15:30953401-30953667	IMR90	lung:	n/a	chr15:30953517-30953528
50	CEBPB	chr15:30967261-30967669	K562	blood:	n/a	chr15:30967474-30967485

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30930499-30930549	AoSMC	blood vessel:	n/a
2	chr15:30930499-30930549	ovcar-3	ovarian:	n/a
3	chr15:31066090-31066140	AG09309	skin:	n/a
4	chr15:31066090-31066140	SK-N-SH_RA	brain:	n/a
5	chr15:31066090-31066140	IMR90	lung:	fetal
6	chr15:31066090-31066140	GM12891	blood:	n/a
7	chr15:30920627-30920677	AG09319	gingival:	n/a
8	chr15:30930499-30930549	HEK293	kidney:	embryo
9	chr15:31066090-31066140	SK-N-SH	brain:	n/a
10	chr15:30920627-30920677	NB4	blood:	n/a
11	chr15:30930499-30930549	HAEpiC	amniotic membrane:	n/a
12	chr15:31066090-31066140	A549	lung:	n/a
13	chr15:30920627-30920677	SKMC	muscle:	n/a
14	chr15:30920627-30920677	RPTEC	kidney:	n/a
15	chr15:30920627-30920677	PrEC	prostate:	n/a
16	chr15:30920627-30920677	HEK293	kidney:	embryo
17	chr15:30930499-30930549	H1-hESC	embryonic stem cell:	embryo
18	chr15:30920627-30920677	SAEC	small airway:	n/a
19	chr15:30930499-30930549	HUVEC	blood vessel:	n/a
20	chr15:31066090-31066140	HPAEpiC	pulmonary alveolar:	n/a
21	chr15:31066090-31066140	MCF-7	breast:	n/a
22	chr15:30920627-30920677	PANC-1	pancreas:	n/a
23	chr15:30920627-30920677	MCF-7	breast:	n/a
24	chr15:30920627-30920677	AG04450	lung:	fetal
25	chr15:30930499-30930549	AG09309	skin:	n/a
26	chr15:30920627-30920677	NH-A	brain:	n/a
27	chr15:31066090-31066140	T-47D	breast:	n/a
28	chr15:30930499-30930549	HCT-116	colon:	n/a
29	chr15:31066090-31066140	GM12878	blood:	n/a
30	chr15:30920627-30920677	U87	brain:	n/a
31	chr15:30920627-30920677	BJ	skin:	n/a
32	chr15:30920627-30920677	LNCaP	prostate:	n/a
33	chr15:30930499-30930549	MCF10A-Er-Src	breast:	n/a
34	chr15:30920627-30920677	Hela-S3	cervix:	n/a
35	chr15:30920627-30920677	GM12891	blood:	n/a
36	chr15:30930499-30930549	ProgFib	skin:	n/a
37	chr15:31066090-31066140	PANC-1	pancreas:	n/a
38	chr15:30930499-30930549	Caco-2	colon:	n/a
39	chr15:31066090-31066140	SAEC	small airway:	n/a
40	chr15:30930499-30930549	HRCEpiC	kidney:	n/a
41	chr15:30920627-30920677	K562	blood:	n/a
42	chr15:30930499-30930549	HMEC	breast:	n/a
43	chr15:31066090-31066140	PrEC	prostate:	n/a
44	chr15:30920627-30920677	ProgFib	skin:	n/a
45	chr15:30930499-30930549	NB4	blood:	n/a
46	chr15:30930499-30930549	PrEC	prostate:	n/a
47	chr15:30920627-30920677	GM19239	blood:	n/a
48	chr15:30930499-30930549	U87	brain:	n/a
49	chr15:30930499-30930549	NH-A	brain:	n/a
50	chr15:30930499-30930549	HL-60	blood:	n/a

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

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

(count:12 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
GOLGA8UP	TF binding region
ARHGAP11B	TF binding region
ENSG00000247728	TF binding region
ENSG00000252602	TF binding region
ENSG00000269974	TF binding region
ENSG00000206846	TF binding region
GOLGA8UP	CpG island
ARHGAP11B	CpG island
ENSG00000247728	CpG island
ENSG00000252602	CpG island
ENSG00000269974	CpG island
ENSG00000206846	CpG island

Extended variants
information (count: 6270 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:6270 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558668668	chr15:30920628-30920629	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
2	rs574728609	chr15:30920677-30920678	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
3	rs535007250	chr15:30920686-30920687	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs555271380	chr15:30920714-30920715	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs575100972	chr15:30920718-30920719	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs80068880	chr15:30920743-30920744	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs373846023	chr15:30920830-30920831	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs142722356	chr15:30920868-30920869	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs372584236	chr15:30920882-30920883	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs28733411	chr15:30920919-30920920	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs545824841	chr15:30921004-30921005	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs559097677	chr15:30921048-30921049	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs139834801	chr15:30921082-30921083	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs541744655	chr15:30921117-30921118	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs561617452	chr15:30921133-30921134	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs192078682	chr15:30921134-30921135	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs566433165	chr15:30921135-30921136	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs550341673	chr15:30921137-30921138	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs570181025	chr15:30921158-30921159	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs532506866	chr15:30921239-30921240	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs183974206	chr15:30921267-30921268	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs565958718	chr15:30921270-30921271	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs534979202	chr15:30921274-30921275	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs533797270	chr15:30921299-30921300	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs187774071	chr15:30921301-30921302	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568748176	chr15:30921309-30921310	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs543910478	chr15:30921337-30921338	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs537686657	chr15:30921361-30921362	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs189678810	chr15:30921370-30921371	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs376887552	chr15:30921371-30921372	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs577327932	chr15:30921435-30921436	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555358201	chr15:30921455-30921456	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182080290	chr15:30921467-30921468	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553004362	chr15:30921492-30921493	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572767349	chr15:30921494-30921495	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541412463	chr15:30921512-30921513	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187034948	chr15:30921513-30921514	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191573385	chr15:30921528-30921529	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs530713338	chr15:30921529-30921530	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs35981302	chr15:30921569-30921570	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs544059444	chr15:30921574-30921575	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs71397301	chr15:30921629-30921630	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs201797142	chr15:30921639-30921640	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200360197	chr15:30921654-30921655	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537830723	chr15:30921680-30921681	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556654477	chr15:30921687-30921688	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs528523220	chr15:30921705-30921706	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548597440	chr15:30921712-30921713	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112354993	chr15:30921746-30921747	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568809588	chr15:30921751-30921752	Weak transcription Active TSS Enhancers	TF binding region	2 gene(s)	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:1326 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30916000-30921200	Active TSS	K562	blood
2	chr15:30916000-30922400	Active TSS	GM12878-XiMat	blood
3	chr15:30916200-30921000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr15:30916600-30920800	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr15:30916600-30921200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr15:30916600-30921200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr15:30917600-30920800	Active TSS	HSMM	muscle
8	chr15:30918800-30931200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr15:30919200-30931000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:30919200-30935400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr15:30919200-30942400	Weak transcription	Primary T cells from cord blood	blood
12	chr15:30919200-30966400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr15:30919400-30924600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr15:30919400-30938400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr15:30919400-30959800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr15:30919400-30969800	Weak transcription	Fetal Lung	lung
17	chr15:30919400-30972800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr15:30919600-30924200	Weak transcription	Fetal Stomach	stomach
19	chr15:30919600-30928800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr15:30919600-30928800	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr15:30919600-30935200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr15:30919600-30935400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr15:30919600-30939200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr15:30919600-30948200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr15:30919600-30964000	Weak transcription	Fetal Intestine Large	intestine
26	chr15:30919600-31023200	Weak transcription	Fetal Intestine Small	intestine
27	chr15:30919800-30922000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr15:30919800-30933000	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr15:30919800-30940400	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr15:30919800-30942200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr15:30919800-30961800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr15:30920000-30920800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr15:30920000-30920800	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr15:30920000-30921000	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr15:30920000-30921000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr15:30920000-30921000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr15:30920000-30921400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr15:30920000-30922400	Weak transcription	Fetal Heart	heart
39	chr15:30920000-30923600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr15:30920000-30923600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:30920000-30926600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr15:30920000-30927200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:30920000-30928800	Weak transcription	Osteobl	bone
44	chr15:30920000-30938000	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr15:30920000-30938800	Weak transcription	Thymus	Thymus
46	chr15:30920000-30939200	Weak transcription	Fetal Muscle Leg	muscle
47	chr15:30920000-30939800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr15:30920000-30940600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr15:30920000-30955400	Weak transcription	NH-A	brain
50	chr15:30920000-31028200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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