Variant report

Variant	nsv996300
Chromosome Location	chr7:146236230-146663300
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	ARID3A	chr7:146264700-146264703	K562	blood:	n/a	n/a
2	ATF1	chr7:146554072-146554083	K562	blood:	n/a	n/a
3	ATF1	chr7:146424454-146424457	K562	blood:	n/a	n/a
4	ATF2	chr7:146488664-146489290	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr7:146488761-146489246	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:146255445-146255494	K562	blood:	n/a	n/a
7	BACH1	chr7:146334822-146334825	K562	blood:	n/a	n/a
8	BACH1	chr7:146469204-146469208	K562	blood:	n/a	n/a
9	BACH1	chr7:146427038-146427199	K562	blood:	n/a	n/a
10	BACH1	chr7:146388134-146388413	H1-hESC	embryonic stem cell:	n/a	chr7:146388281-146388295
11	BATF	chr7:146241905-146242175	GM12878	blood:	n/a	chr7:146242043-146242051 chr7:146242071-146242082
12	BCL11A	chr7:146488748-146488970	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr7:146488707-146489095	H1-hESC	embryonic stem cell:	n/a	n/a
14	CBX3	chr7:146437201-146437466	K562	blood:	n/a	n/a
15	CCNT2	chr7:146463543-146463700	K562	blood:	n/a	n/a
16	CCNT2	chr7:146377787-146377817	K562	blood:	n/a	n/a
17	CCNT2	chr7:146578068-146578178	K562	blood:	n/a	n/a
18	CEBPB	chr7:146471161-146471490	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:146631955-146632230	A549	lung:	n/a	n/a
20	CEBPB	chr7:146571852-146572197	IMR90	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
21	CEBPB	chr7:146472354-146472570	HepG2	liver:	n/a	chr7:146472465-146472476
22	CEBPB	chr7:146502234-146502442	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr7:146582398-146582629	ECC-1	luminal epithelium:	n/a	chr7:146582542-146582553
24	CEBPB	chr7:146532369-146532435	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr7:146258765-146259071	HepG2	liver:	n/a	chr7:146258937-146258948
26	CEBPB	chr7:146345513-146345713	K562	blood:	n/a	chr7:146345579-146345592 chr7:146345579-146345590
27	CEBPB	chr7:146631945-146632234	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:146653225-146653552	A549	lung:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
29	CEBPB	chr7:146658691-146659162	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr7:146471196-146471467	IMR90	lung:	n/a	n/a
31	CEBPB	chr7:146650551-146650805	IMR90	lung:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
32	CEBPB	chr7:146472308-146472591	IMR90	lung:	n/a	chr7:146472465-146472476
33	CEBPB	chr7:146653286-146653563	HepG2	liver:	n/a	chr7:146653389-146653398 chr7:146653389-146653398 chr7:146653387-146653400 chr7:146653389-146653398
34	CEBPB	chr7:146248978-146249070	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:146550344-146550639	HepG2	liver:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
36	CEBPB	chr7:146397006-146397177	A549	lung:	n/a	n/a
37	CEBPB	chr7:146547720-146547928	HepG2	liver:	n/a	chr7:146547770-146547781
38	CEBPB	chr7:146258784-146259074	IMR90	lung:	n/a	chr7:146258937-146258948
39	CEBPB	chr7:146461096-146461208	HepG2	liver:	n/a	chr7:146461132-146461143
40	CEBPB	chr7:146650625-146650798	K562	blood:	n/a	chr7:146650646-146650655 chr7:146650646-146650655
41	CEBPB	chr7:146573237-146573380	HepG2	liver:	n/a	chr7:146573302-146573313
42	CEBPB	chr7:146550317-146550587	A549	lung:	n/a	chr7:146550457-146550468 chr7:146550456-146550467
43	CEBPB	chr7:146571827-146572187	K562	blood:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
44	CEBPB	chr7:146571860-146572193	HepG2	liver:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
45	CEBPB	chr7:146487554-146487672	K562	blood:	n/a	n/a
46	CEBPB	chr7:146471198-146471404	A549	lung:	n/a	n/a
47	CEBPB	chr7:146571842-146572194	H1-hESC	embryonic stem cell:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
48	CEBPB	chr7:146571872-146572192	A549	lung:	n/a	chr7:146572003-146572012 chr7:146572001-146572014 chr7:146572002-146572013 chr7:146572003-146572012 chr7:146572003-146572012 chr7:146572003-146572012
49	CEBPB	chr7:146367649-146367955	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr7:146547738-146547759	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:146603166-146603216	PFSK-1	brain:	n/a
2	chr7:146603166-146603216	PFSK-1	brain:	n/a
3	chr7:146572638-146572688	GM19239	blood:	n/a
4	chr7:146484504-146484554	H1-hESC	embryonic stem cell:	embryo
5	chr7:146489513-146489563	GM19239	blood:	n/a
6	chr7:146635353-146635403	HEEpiC	esophagus:	n/a
7	chr7:146484504-146484554	GM12891	blood:	n/a
8	chr7:146635353-146635403	PANC-1	pancreas:	n/a
9	chr7:146603166-146603216	U87	brain:	n/a
10	chr7:146321053-146321103	HL-60	blood:	n/a
11	chr7:146351256-146351306	HNPCEpiC	eye:	n/a
12	chr7:146321053-146321103	HUVEC	blood vessel:	n/a
13	chr7:146321053-146321103	HEEpiC	esophagus:	n/a
14	chr7:146572638-146572688	HEEpiC	esophagus:	n/a
15	chr7:146489513-146489563	HMEC	breast:	n/a
16	chr7:146489513-146489563	BE2_C	brain:	n/a
17	chr7:146489513-146489563	SAEC	small airway:	n/a
18	chr7:146484518-146484568	AG10803	skin:	n/a
19	chr7:146484609-146484659	HL-60	blood:	n/a
20	chr7:146484518-146484568	HEEpiC	esophagus:	n/a
21	chr7:146484518-146484568	BE2_C	brain:	n/a
22	chr7:146635353-146635403	HRCEpiC	kidney:	n/a
23	chr7:146603166-146603216	HCT-116	colon:	n/a
24	chr7:146321053-146321103	NH-A	brain:	n/a
25	chr7:146484609-146484659	HIPEpiC	eye:	n/a
26	chr7:146484609-146484659	NHBE	bronchial:	n/a
27	chr7:146351256-146351306	HCF	heart:	n/a
28	chr7:146635353-146635403	GM06990	blood:	n/a
29	chr7:146489513-146489563	HIPEpiC	eye:	n/a
30	chr7:146321053-146321103	AoSMC	blood vessel:	n/a
31	chr7:146572638-146572688	AG09309	skin:	n/a
32	chr7:146489513-146489563	PFSK-1	brain:	n/a
33	chr7:146351256-146351306	SK-N-SH	brain:	n/a
34	chr7:146489513-146489563	GM12892	blood:	n/a
35	chr7:146484518-146484568	U87	brain:	n/a
36	chr7:146489513-146489563	NB4	blood:	n/a
37	chr7:146484504-146484554	PrEC	prostate:	n/a
38	chr7:146484609-146484659	ECC-1	luminal epithelium:	n/a
39	chr7:146351256-146351306	IMR90	lung:	fetal
40	chr7:146572638-146572688	AG04450	lung:	fetal
41	chr7:146635353-146635403	H1-hESC	embryonic stem cell:	embryo
42	chr7:146351256-146351306	HCT-116	colon:	n/a
43	chr7:146332766-146332816	AG10803	skin:	n/a
44	chr7:146484518-146484568	K562	blood:	n/a
45	chr7:146484609-146484659	GM12891	blood:	n/a
46	chr7:146635353-146635403	HNPCEpiC	eye:	n/a
47	chr7:146603166-146603216	NHBE	bronchial:	n/a
48	chr7:146489513-146489563	AG04450	lung:	fetal
49	chr7:146332766-146332816	SK-N-SH_RA	brain:	n/a
50	chr7:146635353-146635403	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
2	chr7:146392626..146394325-chr7:146397698..146400118,2	K562	blood:
3	chr7:146500988..146503359-chr7:146527735..146530660,2	K562	blood:
4	chr7:146500988..146503359-chr7:146527735..146530660,2	K562	blood:
5	chr7:146299400..146301210-chr7:146301475..146303018,2	MCF-7	breast:
6	chr7:146392626..146394325-chr7:146397698..146400118,2	K562	blood:
7	chr7:146433750..146434499-chr7:147781098..147781819,2	MCF-7	breast:
8	chr7:146235172..146238852-chr7:146239684..146242381,3	K562	blood:
9	chr16:283786..286287-chr7:146321086..146324044,2	MCF-7	breast:
10	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
11	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
12	chr7:146433613..146434480-chr7:146942002..146942841,3	MCF-7	breast:
13	chr7:146299400..146301210-chr7:146301475..146303018,2	MCF-7	breast:
14	chr7:146259240..146261148-chr7:146262758..146264665,2	K562	blood:
15	chr16:70557427..70557946-chr7:146244932..146245452,2	Hela-S3	cervix:
16	chr7:146250194..146253829-chr7:146254649..146256608,3	K562	blood:
17	chr7:146657758..146660161-chr7:146662601..146665251,2	K562	blood:
18	chr7:146465957..146468048-chr7:146468672..146471163,2	K562	blood:
19	chr7:146486735..146488259-chr7:146492496..146494438,2	K562	blood:
20	chr7:146498401..146500562-chr7:146505202..146506866,2	K562	blood:
21	chr7:146537182..146538796-chr7:146543002..146544884,2	K562	blood:
22	chr4:31335976..31336496-chr7:146308823..146309343,2	MCF-7	breast:
23	chr7:144849072..144851097-chr7:146354909..146357646,2	K562	blood:
24	chr7:146486735..146488259-chr7:146492496..146494438,2	K562	blood:
25	chr7:146235172..146238852-chr7:146239684..146242381,3	K562	blood:
26	chr7:146233829..146237981-chr7:146239048..146242381,3	K562	blood:
27	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
28	chr7:146250194..146253829-chr7:146254649..146256608,3	K562	blood:
29	chr7:146465957..146468048-chr7:146468672..146471163,2	K562	blood:
30	chr7:146479043..146481876-chr7:146483638..146485825,2	K562	blood:
31	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:
32	chr11:86510283..86512929-chr7:146532947..146535829,2	MCF-7	breast:
33	chr7:146233829..146237981-chr7:146239048..146242381,3	K562	blood:
34	chr7:146253504..146256343-chr7:146261873..146263479,2	K562	blood:
35	chr7:146371392..146373633-chr7:146379567..146381650,2	MCF-7	breast:
36	chr7:146531380..146533231-chr7:146533268..146535989,2	K562	blood:
37	chr7:146371392..146373633-chr7:146379567..146381650,2	MCF-7	breast:
38	chr7:146259240..146261148-chr7:146262758..146264665,2	K562	blood:
39	chr7:146253504..146256343-chr7:146261873..146263479,2	K562	blood:
40	chr7:146498401..146500562-chr7:146505202..146506866,2	K562	blood:
41	chr7:146479043..146481876-chr7:146483638..146485825,2	K562	blood:
42	chr7:146570862..146573024-chr7:146579800..146582486,2	K562	blood:
43	chr7:146651547..146653225-chr7:146656495..146658548,2	K562	blood:

Variant related genes	Relation type
ENSG00000221766	TF binding region
ENSG00000221766	CpG island
ENSG00000167930	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000150687	chromatin interactions

Extended variants
information (count: 6677 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:6677 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559863246	chr7:146236269-146236270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373398502	chr7:146236270-146236271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528682469	chr7:146236335-146236336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112221241	chr7:146236344-146236345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7458453	chr7:146236383-146236384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71530744	chr7:146236395-146236396	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs182710851	chr7:146236546-146236547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563397543	chr7:146236551-146236552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549703753	chr7:146236571-146236572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145574679	chr7:146236592-146236593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549908484	chr7:146236617-146236618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116630957	chr7:146236618-146236619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548830637	chr7:146236627-146236628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372250803	chr7:146236629-146236630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs5888211	chr7:146236630-146236631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs565811718	chr7:146236672-146236673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs207468742	chr7:146236676-146236677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188967935	chr7:146236692-146236693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs138085523	chr7:146236697-146236698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571561182	chr7:146236699-146236700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs112880018	chr7:146236737-146236738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551883228	chr7:146236780-146236781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77989755	chr7:146236781-146236782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573966170	chr7:146236802-146236803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536722329	chr7:146236813-146236814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73164078	chr7:146236869-146236870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs1526164	chr7:146236872-146236873	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs545193703	chr7:146236883-146236884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565142344	chr7:146236893-146236894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs5004611	chr7:146236901-146236902	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs376375029	chr7:146236975-146236976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73741740	chr7:146236987-146236988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534501448	chr7:146236991-146236992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563268890	chr7:146237081-146237082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2693407	chr7:146237084-146237085	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs116229662	chr7:146237092-146237093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559478852	chr7:146237115-146237116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551194852	chr7:146237129-146237130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551552696	chr7:146237161-146237162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571475305	chr7:146237173-146237174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537315916	chr7:146237229-146237230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550622772	chr7:146237335-146237336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193150794	chr7:146237361-146237362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536242060	chr7:146237373-146237374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1997126	chr7:146237437-146237438	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs530879176	chr7:146237451-146237452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116723694	chr7:146237456-146237457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538758401	chr7:146237460-146237461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200118780	chr7:146237548-146237549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558166151	chr7:146237600-146237601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Autism	20964600	CNVD
Epilepsy	17646849	CNVD
Mental retardation	19896112	CNVD
Epilepsy	20502679	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Medulloblastoma	21163964	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:146231400-146242000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:146235600-146236600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:146236200-146237800	Enhancers	Fetal Kidney	kidney
4	chr7:146236600-146237000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:146238800-146239400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:146239000-146239400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr7:146239200-146239400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr7:146260000-146260400	Enhancers	Fetal Kidney	kidney
9	chr7:146260200-146260800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr7:146262800-146263200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr7:146262800-146263200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr7:146262800-146263200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr7:146262800-146263200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:146262800-146263400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr7:146262800-146263400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr7:146263000-146263400	Enhancers	Ovary	ovary
17	chr7:146279000-146279600	Enhancers	Fetal Kidney	kidney
18	chr7:146289000-146290200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:146304600-146305000	Enhancers	Stomach Mucosa	stomach
20	chr7:146316600-146317400	Enhancers	Fetal Brain Female	brain
21	chr7:146321800-146323000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr7:146326000-146326400	Enhancers	Fetal Lung	lung
23	chr7:146330200-146331600	Enhancers	Fetal Brain Male	brain
24	chr7:146330400-146331200	Enhancers	Fetal Brain Female	brain
25	chr7:146331200-146334200	Enhancers	Brain Germinal Matrix	brain
26	chr7:146331600-146333200	Weak transcription	Fetal Brain Male	brain
27	chr7:146332000-146333200	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr7:146332200-146333200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr7:146332200-146333400	Enhancers	Fetal Thymus	thymus
30	chr7:146332400-146332800	Enhancers	H1 Cell Line	embryonic stem cell
31	chr7:146332400-146333000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:146332400-146333000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:146332400-146333200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr7:146332400-146333200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr7:146332400-146333200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr7:146332400-146333200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:146332600-146333200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr7:146332600-146333400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr7:146332800-146333200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr7:146333000-146333400	Enhancers	Thymus	Thymus
41	chr7:146333000-146333800	Enhancers	Fetal Kidney	kidney
42	chr7:146333200-146334000	Enhancers	Fetal Brain Male	brain
43	chr7:146333200-146334000	Enhancers	Fetal Stomach	stomach
44	chr7:146333200-146334800	Enhancers	Fetal Lung	lung
45	chr7:146333400-146338200	Weak transcription	Fetal Thymus	thymus
46	chr7:146338200-146338800	Enhancers	Fetal Thymus	thymus
47	chr7:146338800-146342200	Weak transcription	Fetal Thymus	thymus
48	chr7:146342200-146343200	Enhancers	Fetal Thymus	thymus
49	chr7:146342400-146342600	Enhancers	Pancreas	Pancrea
50	chr7:146342400-146342600	Enhancers	Thymus	Thymus

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