Variant report

Variant	nsv934254
Chromosome Location	chr2:51152718-51314430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:51259057-51259636	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr2:51259020-51259511	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:51155966-51156146	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:51246247-51246255	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:51240144-51240458	H1-hESC	embryonic stem cell:	n/a	n/a
6	BRCA1	chr2:51259605-51259656	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr2:51179768-51180665	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr2:51214813-51214934	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr2:51185262-51185455	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr2:51240017-51240569	HCT-116	colon:	n/a	n/a
11	CEBPB	chr2:51229679-51229969	HepG2	liver:	n/a	chr2:51229820-51229831
12	CEBPB	chr2:51180127-51180593	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
13	CEBPB	chr2:51172595-51172790	HepG2	liver:	n/a	chr2:51172679-51172690
14	CEBPB	chr2:51180120-51180462	HepG2	liver:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
15	CEBPB	chr2:51185023-51185436	MCF-7	breast:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
16	CEBPB	chr2:51185053-51185350	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
17	CEBPB	chr2:51185035-51185357	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
18	CEBPB	chr2:51179763-51180618	IMR90	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
19	CEBPB	chr2:51255989-51256366	IMR90	lung:	n/a	chr2:51256172-51256183
20	CEBPB	chr2:51255980-51256366	H1-hESC	embryonic stem cell:	n/a	chr2:51256172-51256183
21	CEBPB	chr2:51185072-51185406	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
22	CEBPB	chr2:51163520-51163763	A549	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163616-51163627
23	CEBPB	chr2:51255896-51256399	A549	lung:	n/a	chr2:51256172-51256183
24	CEBPB	chr2:51229696-51229991	IMR90	lung:	n/a	chr2:51229820-51229831
25	CEBPB	chr2:51256005-51256373	Hela-S3	cervix:	n/a	chr2:51256172-51256183
26	CEBPB	chr2:51255984-51256364	HepG2	liver:	n/a	chr2:51256172-51256183
27	CEBPB	chr2:51196168-51196459	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:51163327-51163752	IMR90	lung:	n/a	chr2:51163617-51163628 chr2:51163618-51163627 chr2:51163616-51163629 chr2:51163420-51163433 chr2:51163616-51163627
29	CEBPB	chr2:51255964-51256336	MCF-7	breast:	n/a	chr2:51256172-51256183
30	CEBPB	chr2:51282778-51283040	IMR90	lung:	n/a	chr2:51282886-51282897
31	CEBPB	chr2:51184010-51184263	HepG2	liver:	n/a	chr2:51184131-51184142
32	CEBPB	chr2:51185063-51185361	K562	blood:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
33	CEBPB	chr2:51240147-51240542	MCF-7	breast:	n/a	n/a
34	CEBPB	chr2:51178589-51178949	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr2:51196305-51196335	K562	blood:	n/a	n/a
36	CEBPB	chr2:51180217-51180418	K562	blood:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
37	CEBPB	chr2:51185039-51185390	A549	lung:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
38	CEBPB	chr2:51236313-51236416	A549	lung:	n/a	n/a
39	CEBPB	chr2:51229690-51229927	A549	lung:	n/a	chr2:51229820-51229831
40	CEBPB	chr2:51256083-51256253	HepG2	liver:	n/a	chr2:51256172-51256183
41	CEBPB	chr2:51196131-51196377	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr2:51185052-51185376	ECC-1	luminal epithelium:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
43	CEBPB	chr2:51185019-51185391	H1-hESC	embryonic stem cell:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
44	CEBPB	chr2:51185020-51185401	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185296-51185308 chr2:51185201-51185210 chr2:51185201-51185210
45	CEBPB	chr2:51180081-51180588	ECC-1	luminal epithelium:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
46	CEBPB	chr2:51185077-51185269	HepG2	liver:	n/a	chr2:51185199-51185212 chr2:51185201-51185210 chr2:51185199-51185210 chr2:51185201-51185210 chr2:51185201-51185210 chr2:51185201-51185210
47	CEBPB	chr2:51272237-51272566	HepG2	liver:	n/a	chr2:51272397-51272408 chr2:51272396-51272409
48	CEBPB	chr2:51180165-51180469	A549	lung:	n/a	chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180278-51180287 chr2:51180276-51180287 chr2:51180278-51180287
49	CEBPB	chr2:51282756-51283052	HepG2	liver:	n/a	chr2:51282886-51282897
50	CEBPB	chr2:51255998-51256347	A549	lung:	n/a	chr2:51256172-51256183

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:51228125-51228175	MCF10A-Er-Src	breast:	n/a
2	chr2:51259807-51259857	MCF-7	breast:	n/a
3	chr2:51255324-51255374	SAEC	small airway:	n/a
4	chr2:51228125-51228175	MCF10A-Er-Src	breast:	n/a
5	chr2:51259807-51259857	MCF-7	breast:	n/a
6	chr2:51255324-51255374	SAEC	small airway:	n/a
7	chr2:51254021-51254071	AG09319	gingival:	n/a
8	chr2:51254102-51254152	ProgFib	skin:	n/a
9	chr2:51259697-51259747	AG09309	skin:	n/a
10	chr2:51254823-51254873	MCF10A-Er-Src	breast:	n/a
11	chr2:51259493-51259543	GM12892	blood:	n/a
12	chr2:51255324-51255374	AG09319	gingival:	n/a
13	chr2:51254981-51255031	HCF	heart:	n/a
14	chr2:51255324-51255374	GM19239	blood:	n/a
15	chr2:51231649-51231699	HMEC	breast:	n/a
16	chr2:51255627-51255677	CMK	blood:	n/a
17	chr2:51240310-51240360	AG09309	skin:	n/a
18	chr2:51259703-51259753	HL-60	blood:	n/a
19	chr2:51255627-51255677	HUVEC	blood vessel:	n/a
20	chr2:51259493-51259543	K562	blood:	n/a
21	chr2:51240310-51240360	RPTEC	kidney:	n/a
22	chr2:51259493-51259543	ECC-1	luminal epithelium:	n/a
23	chr2:51259786-51259836	GM12891	blood:	n/a
24	chr2:51254102-51254152	Caco-2	colon:	n/a
25	chr2:51255306-51255356	HRCEpiC	kidney:	n/a
26	chr2:51254132-51254182	HRPEpiC	eye:	n/a
27	chr2:51218880-51218930	NT2-D1	testis:	n/a
28	chr2:51254102-51254152	GM12891	blood:	n/a
29	chr2:51254132-51254182	HCPEpiC	choroid plexus:	n/a
30	chr2:51254823-51254873	GM12878	blood:	n/a
31	chr2:51240310-51240360	AG04450	lung:	fetal
32	chr2:51228125-51228175	HMEC	breast:	n/a
33	chr2:51255324-51255374	HMEC	breast:	n/a
34	chr2:51231649-51231699	BJ	skin:	n/a
35	chr2:51228125-51228175	HRE	kidney:	n/a
36	chr2:51259552-51259602	GM19239	blood:	n/a
37	chr2:51228125-51228175	NHDF-neo	bronchial:	n/a
38	chr2:51252301-51252351	RPTEC	kidney:	n/a
39	chr2:51259697-51259747	Caco-2	colon:	n/a
40	chr2:51218880-51218930	HL-60	blood:	n/a
41	chr2:51254170-51254220	PFSK-1	brain:	n/a
42	chr2:51259697-51259747	HNPCEpiC	eye:	n/a
43	chr2:51255627-51255677	AG09309	skin:	n/a
44	chr2:51259493-51259543	PANC-1	pancreas:	n/a
45	chr2:51254132-51254182	NT2-D1	testis:	n/a
46	chr2:51254981-51255031	Hepatocyte	liver:	n/a
47	chr2:51255324-51255374	IMR90	lung:	fetal
48	chr2:51255324-51255374	SK-N-MC	brain:	n/a
49	chr2:51259493-51259543	ProgFib	skin:	n/a
50	chr2:51259807-51259857	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
2	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
3	chr2:51260931..51263493-chr2:51269854..51271859,2	MCF-7	breast:
4	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:
5	chr2:51281367..51284227-chr2:51284549..51287538,2	K562	blood:
6	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
7	chr2:51313706..51316467-chr2:51317325..51319738,2	K562	blood:
8	chr2:51288072..51290967-chr2:232569534..232571521,2	MCF-7	breast:
9	chr2:51171851..51174700-chr2:51189688..51191274,2	MCF-7	breast:
10	chr2:51152622..51154221-chr2:51156441..51158727,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRXN1-3	chr2:51294575-51294743	l_1833_chr2:51283578-51306188_testes
2	lnc-CHAC2-4	chr2:51259739-51260154	ENSG00000231918.1
3	lnc-NRXN1-3	chr2:51302313-51302437	l_1833_chr2:51283578-51306188_testes
4	lnc-NRXN1-3	chr2:51306149-51306209	l_1833_chr2:51283578-51306188_testes
5	lnc-NRXN1-3	chr2:51283633-51283791	NONHSAT070652
6	lnc-NRXN1-3	chr2:51302314-51302406	NONHSAT070652
7	lnc-NRXN1-3	chr2:51283579-51283793	l_1833_chr2:51283578-51306188_testes
8	lnc-NRXN1-3	chr2:51282723-51282956	NONHSAT070652
9	lnc-CHAC2-4	chr2:51279495-51279592	ENSG00000231918.1

Variant related genes	Relation type
ENSG00000231918	TF binding region
NRXN1	TF binding region
ENSG00000216011	TF binding region
ENSG00000272385	TF binding region
ENSG00000231918	CpG island
NRXN1	CpG island
ENSG00000216011	CpG island
ENSG00000272385	CpG island

Extended variants
information (count: 5560 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5560 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536352170	chr2:51152728-51152729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554654601	chr2:51152789-51152790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188520719	chr2:51152798-51152799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538449845	chr2:51152810-51152811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192245745	chr2:51152831-51152832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577895854	chr2:51152832-51152833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202037888	chr2:51152842-51152843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149195256	chr2:51152843-51152844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553746980	chr2:51152845-51152846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143358779	chr2:51152867-51152868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542714017	chr2:51152896-51152897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs184263657	chr2:51152905-51152906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531374937	chr2:51152931-51152932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370495312	chr2:51152959-51152960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564970229	chr2:51152973-51152974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532440620	chr2:51152989-51152990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371281916	chr2:51153010-51153011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs200674979	chr2:51153029-51153030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375866317	chr2:51153057-51153058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs202041551	chr2:51153060-51153061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs199971936	chr2:51153061-51153062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs151293975	chr2:51153062-51153063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141903943	chr2:51153084-51153085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569755194	chr2:51153112-51153113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372277834	chr2:51153127-51153128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200626622	chr2:51153128-51153129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112297733	chr2:51153131-51153132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189877713	chr2:51153154-51153155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182455545	chr2:51153157-51153158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538898544	chr2:51153203-51153204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554051361	chr2:51153204-51153205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs375283196	chr2:51153210-51153211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs147111699	chr2:51153211-51153212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561782973	chr2:51153225-51153226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536674170	chr2:51153270-51153271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75071398	chr2:51153279-51153280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554691829	chr2:51153313-51153314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs187018233	chr2:51153359-51153360	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs543596568	chr2:51153376-51153377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs59833064	chr2:51153430-51153431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550421383	chr2:51153449-51153450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577117108	chr2:51153459-51153460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541288546	chr2:51153562-51153563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539083278	chr2:51153588-51153589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570417465	chr2:51153595-51153596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189464283	chr2:51153617-51153618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368319970	chr2:51153627-51153628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs559701340	chr2:51153645-51153646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62142986	chr2:51153674-51153675	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546692019	chr2:51153677-51153678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Basal cell lymphoma	21115979	CNVD
Cognitive impairment	21505072	CNVD
Schizophrenia	22885689	CNVD
Autism	20964600	CNVD
Schizophrenia	19521646	CNVD
Attention deficit hyperactivity disorder	22214315	CNVD
Chronic motor tic disorder	22214315	CNVD
Schizophrenia	22214315	CNVD
Mental retardation	19896112	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	17989066	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:936 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51150200-51155200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr2:51150400-51154800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:51150400-51155000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:51150400-51155400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:51150400-51156800	Weak transcription	Brain Anterior Caudate	brain
6	chr2:51151800-51155000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr2:51151800-51155800	Weak transcription	Brain Germinal Matrix	brain
8	chr2:51151800-51156600	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr2:51153000-51153400	Enhancers	Brain Substantia Nigra	brain
10	chr2:51153400-51156600	Weak transcription	Brain Substantia Nigra	brain
11	chr2:51154800-51155200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:51155000-51155200	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr2:51155000-51155400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr2:51155200-51155600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr2:51155200-51155600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr2:51155400-51155600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:51155400-51156000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr2:51155600-51156000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr2:51155600-51156600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr2:51155600-51158400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:51155800-51156000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:51155800-51156800	Enhancers	Fetal Brain Female	brain
23	chr2:51155800-51157400	Enhancers	Brain Germinal Matrix	brain
24	chr2:51156000-51156600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr2:51156000-51156600	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr2:51156200-51159600	Weak transcription	NHDF-Ad	bronchial
27	chr2:51156400-51156600	Enhancers	Brain Hippocampus Middle	brain
28	chr2:51156600-51156800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr2:51156600-51157000	Flanking Active TSS	Brain Hippocampus Middle	brain
30	chr2:51156600-51157000	Active TSS	Brain Substantia Nigra	brain
31	chr2:51156600-51157000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr2:51156600-51157200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:51156800-51157000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr2:51156800-51157200	Active TSS	Brain Anterior Caudate	brain
35	chr2:51156800-51159400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:51157000-51157200	Enhancers	Brain Hippocampus Middle	brain
37	chr2:51157000-51157800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr2:51157200-51157400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr2:51157200-51159600	Weak transcription	Brain Anterior Caudate	brain
40	chr2:51157400-51158200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:51157800-51158200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr2:51158000-51158200	Enhancers	Fetal Brain Male	brain
43	chr2:51158000-51158200	Active TSS	Pancreas	Pancrea
44	chr2:51158200-51161600	Weak transcription	Pancreas	Pancrea
45	chr2:51158200-51163200	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr2:51158200-51171000	Weak transcription	Fetal Brain Male	brain
47	chr2:51159400-51159600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
48	chr2:51159600-51159800	Enhancers	Brain Anterior Caudate	brain
49	chr2:51159600-51159800	Active TSS	NHDF-Ad	bronchial
50	chr2:51161600-51161800	Enhancers	Pancreas	Pancrea

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