Variant report

Variant	nsv876616
Chromosome Location	chr3:21946847-22310622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1366)
CpG islands
(count:183)
Chromatin interactive
region (count:40)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:22162549-22162915	HepG2	liver:	n/a	n/a
2	ATF1	chr3:22262669-22262674	K562	blood:	n/a	n/a
3	BACH1	chr3:22278430-22278679	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:22164128-22164369	GM12878	blood:	n/a	chr3:22164265-22164276
5	BATF	chr3:22278454-22278659	GM12878	blood:	n/a	chr3:22278545-22278556
6	BATF	chr3:22164137-22164374	GM12878	blood:	n/a	chr3:22164265-22164276
7	BATF	chr3:22278419-22278711	GM12878	blood:	n/a	chr3:22278545-22278556
8	BCL3	chr3:22272575-22272895	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:22164062-22164443	GM12878	blood:	n/a	n/a
10	BHLHE40	chr3:22159971-22159994	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:22159425-22159426	K562	blood:	n/a	n/a
12	BHLHE40	chr3:22130865-22131163	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:22261633-22261739	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:22147560-22148537	Hela-S3	cervix:	n/a	n/a
15	CCNT2	chr3:22258598-22258798	K562	blood:	n/a	n/a
16	CCNT2	chr3:21953424-21953558	K562	blood:	n/a	n/a
17	CEBPB	chr3:22298770-22299053	A549	lung:	n/a	chr3:22298928-22298939
18	CEBPB	chr3:22150505-22150716	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr3:22304552-22304930	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:22159289-22159588	K562	blood:	n/a	n/a
21	CEBPB	chr3:22147569-22148482	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:22137588-22137831	A549	lung:	n/a	chr3:22137755-22137766
23	CEBPB	chr3:22053597-22053883	A549	lung:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
24	CEBPB	chr3:22280697-22280842	A549	lung:	n/a	n/a
25	CEBPB	chr3:22298793-22299012	K562	blood:	n/a	chr3:22298928-22298939
26	CEBPB	chr3:22273498-22273797	A549	lung:	n/a	chr3:22273665-22273676
27	CEBPB	chr3:22298761-22299071	HepG2	liver:	n/a	chr3:22298928-22298939
28	CEBPB	chr3:22048734-22049247	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:22048834-22049295	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr3:22237586-22237702	A549	lung:	n/a	n/a
31	CEBPB	chr3:22200917-22201096	HepG2	liver:	n/a	chr3:22201008-22201021
32	CEBPB	chr3:22038225-22038503	IMR90	lung:	n/a	chr3:22038377-22038388
33	CEBPB	chr3:22053532-22054406	Hela-S3	cervix:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
34	CEBPB	chr3:22200899-22201125	HepG2	liver:	n/a	chr3:22201008-22201021
35	CEBPB	chr3:22273512-22273819	IMR90	lung:	n/a	chr3:22273665-22273676
36	CEBPB	chr3:21961843-21962449	IMR90	lung:	n/a	n/a
37	CEBPB	chr3:22298748-22299077	IMR90	lung:	n/a	chr3:22298928-22298939
38	CEBPB	chr3:22137582-22137905	IMR90	lung:	n/a	chr3:22137755-22137766
39	CEBPB	chr3:21955978-21956313	Hela-S3	cervix:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
40	CEBPB	chr3:22038218-22038531	HepG2	liver:	n/a	chr3:22038377-22038388
41	CEBPB	chr3:22200829-22201208	HepG2	liver:	n/a	chr3:22201008-22201021
42	CEBPB	chr3:22147693-22148379	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:22048817-22049249	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:21955973-21956275	HepG2	liver:	n/a	chr3:21956123-21956136 chr3:21956123-21956134
45	CEBPB	chr3:22273501-22273834	HepG2	liver:	n/a	chr3:22273665-22273676
46	CEBPB	chr3:22148135-22148381	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:22053600-22053821	HepG2	liver:	n/a	chr3:22053728-22053739 chr3:22053726-22053739 chr3:22053726-22053737
48	CEBPB	chr3:22227764-22227995	A549	lung:	n/a	n/a
49	CEBPB	chr3:22162691-22163152	HepG2	liver:	n/a	chr3:22163128-22163139
50	CEBPB	chr3:21955980-21956311	IMR90	lung:	n/a	chr3:21956123-21956136 chr3:21956123-21956134

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:22192127-22192177	BE2_C	brain:	n/a
2	chr3:22192127-22192177	SKMC	muscle:	n/a
3	chr3:22192127-22192177	HMEC	breast:	n/a
4	chr3:22192127-22192177	HEK293	kidney:	embryo
5	chr3:22030381-22030431	HEEpiC	esophagus:	n/a
6	chr3:22192127-22192177	GM12878	blood:	n/a
7	chr3:22192127-22192177	PANC-1	pancreas:	n/a
8	chr3:22030381-22030431	HepG2	liver:	n/a
9	chr3:22192127-22192177	Jurkat	blood:	n/a
10	chr3:22030381-22030431	CMK	blood:	n/a
11	chr3:21960904-21960954	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:21960904-21960954	SK-N-SH_RA	brain:	n/a
13	chr3:22030381-22030431	SK-N-SH	brain:	n/a
14	chr3:22030381-22030431	T-47D	breast:	n/a
15	chr3:21960904-21960954	MCF-7	breast:	n/a
16	chr3:22030381-22030431	BJ	skin:	n/a
17	chr3:21960904-21960954	AG04450	lung:	fetal
18	chr3:21960904-21960954	SKMC	muscle:	n/a
19	chr3:21960904-21960954	NH-A	brain:	n/a
20	chr3:22030381-22030431	AG10803	skin:	n/a
21	chr3:21960904-21960954	Jurkat	blood:	n/a
22	chr3:22192127-22192177	Hepatocyte	liver:	n/a
23	chr3:21960904-21960954	HRCEpiC	kidney:	n/a
24	chr3:21960904-21960954	HIPEpiC	eye:	n/a
25	chr3:21960904-21960954	BJ	skin:	n/a
26	chr3:22030381-22030431	U87	brain:	n/a
27	chr3:21960904-21960954	BE2_C	brain:	n/a
28	chr3:22030381-22030431	GM12878	blood:	n/a
29	chr3:22192127-22192177	RPTEC	kidney:	n/a
30	chr3:22192127-22192177	NHBE	bronchial:	n/a
31	chr3:22030381-22030431	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:22030381-22030431	AG04449	skin:	fetal
33	chr3:22030381-22030431	HIPEpiC	eye:	n/a
34	chr3:22030381-22030431	H1-hESC	embryonic stem cell:	embryo
35	chr3:21960904-21960954	HCF	heart:	n/a
36	chr3:21960904-21960954	GM06990	blood:	n/a
37	chr3:22192127-22192177	HRPEpiC	eye:	n/a
38	chr3:22030381-22030431	NHDF-neo	bronchial:	n/a
39	chr3:22030381-22030431	PANC-1	pancreas:	n/a
40	chr3:22192127-22192177	HRE	kidney:	n/a
41	chr3:21960904-21960954	HepG2	liver:	n/a
42	chr3:21960904-21960954	SK-N-MC	brain:	n/a
43	chr3:22030381-22030431	HCF	heart:	n/a
44	chr3:21960904-21960954	NT2-D1	testis:	n/a
45	chr3:22192127-22192177	H1-hESC	embryonic stem cell:	embryo
46	chr3:22030381-22030431	GM19239	blood:	n/a
47	chr3:21960904-21960954	GM12892	blood:	n/a
48	chr3:22030381-22030431	NH-A	brain:	n/a
49	chr3:22192127-22192177	AG04450	lung:	fetal
50	chr3:21960904-21960954	MCF10A-Er-Src	breast:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:22130650..22131348-chr3:22159010..22159875,2	MCF-7	breast:
2	chr3:22202679..22204689-chr3:22233994..22235730,2	K562	blood:
3	chr3:22115704..22118143-chr3:22137096..22138813,2	MCF-7	breast:
4	chr3:22282412..22284259-chr3:22284738..22287975,3	MCF-7	breast:
5	chr3:21948578..21950299-chr3:21951052..21953875,2	MCF-7	breast:
6	chr3:22202679..22204689-chr3:22233994..22235730,2	K562	blood:
7	chr3:22056493..22058211-chr3:22060114..22061974,2	K562	blood:
8	chr3:21954020..21955585-chr3:21957563..21959846,2	MCF-7	breast:
9	chr3:22269821..22272755-chr3:22274788..22276504,2	MCF-7	breast:
10	chr3:22130685..22131408-chr3:22159081..22159858,3	MCF-7	breast:
11	chr3:21948578..21950299-chr3:21951052..21953875,2	MCF-7	breast:
12	chr3:22042480..22044020-chr3:22057123..22059814,2	K562	blood:
13	chr3:22130623..22131453-chr3:22928892..22930144,3	K562	blood:
14	chr3:22217113..22218017-chr3:22727091..22727719,2	MCF-7	breast:
15	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
16	chr3:22218049..22218903-chr9:120895826..120896702,2	MCF-7	breast:
17	chr3:22051906..22054873-chr3:22056499..22059265,2	K562	blood:
18	chr3:22090916..22093719-chr3:22096309..22098471,5	MCF-7	breast:
19	chr3:22115704..22118143-chr3:22137096..22138813,2	MCF-7	breast:
20	chr3:22195364..22197977-chr3:22208185..22210526,2	K562	blood:
21	chr3:22056493..22058211-chr3:22060114..22061974,2	K562	blood:
22	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
23	chr3:22130685..22131408-chr3:22159081..22159858,3	MCF-7	breast:
24	chr3:22060147..22061903-chr3:22064159..22066026,2	K562	blood:
25	chr3:21942258..21944994-chr3:21945829..21948153,2	K562	blood:
26	chr3:21946123..21950317-chr3:21950645..21954305,3	K562	blood:
27	chr3:22127371..22129495-chr3:22135710..22137615,2	K562	blood:
28	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
29	chr3:22130650..22131348-chr3:22159010..22159875,2	MCF-7	breast:
30	chr3:22282412..22284259-chr3:22284738..22287975,3	MCF-7	breast:
31	chr3:22051906..22054873-chr3:22056499..22059265,2	K562	blood:
32	chr3:21946123..21950317-chr3:21950645..21954305,3	K562	blood:
33	chr3:22042480..22044020-chr3:22057123..22059814,2	K562	blood:
34	chr11:126141332..126144254-chr3:22001697..22003217,2	K562	blood:
35	chr3:21939959..21942443-chr3:21956783..21959351,2	K562	blood:
36	chr3:22090916..22093719-chr3:22096309..22098471,5	MCF-7	breast:
37	chr3:22127371..22129495-chr3:22135710..22137615,2	K562	blood:
38	chr3:22269821..22272755-chr3:22274788..22276504,2	MCF-7	breast:
39	chr3:22060147..22061903-chr3:22064159..22066026,2	K562	blood:
40	chr3:21954020..21955585-chr3:21957563..21959846,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SGOL1-3	chr3:22175811-22175883	NONHSAT088653
2	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351
3	lnc-UBE2E2-7	chr3:21982020-21982219	l_2330_chr3:21975326-21982219_testes
4	lnc-UBE2E2-2	chr3:22019707-22019783	ENSG00000223351
5	lnc-UBE2E2-2	chr3:21998631-21998684	ENSG00000223351
6	lnc-UBE2E2-2	chr3:22002908-22003032	ENSG00000223351
7	lnc-SGOL1-3	chr3:22210309-22210443	NONHSAT088650
8	lnc-UBE2E2-2	chr3:22000324-22000415	ENSG00000223351
9	lnc-UBE2E2-2	chr3:21998628-21998684	ENSG00000223351
10	lnc-SGOL1-3	chr3:22210309-22210508	NONHSAT088653
11	lnc-SGOL1-3	chr3:22175074-22175484	NONHSAT088653
12	lnc-UBE2E2-2	chr3:21984058-21984156	ENSG00000223351
13	lnc-UBE2E2-7	chr3:21975327-21975419	l_2330_chr3:21975326-21982219_testes
14	lnc-UBE2E2-2	chr3:22021123-22021320	ENSG00000223351

No data

Variant related genes	Relation type
ZNF385D-AS2	TF binding region
ZNF385D	TF binding region
ZNF385D-AS2	CpG island
ZNF385D	CpG island
ENSG00000110074	chromatin interactions
ENSG00000151789	chromatin interactions

Extended variants
information (count: 10899 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:10899 , 50 per page) page: 1 2 3 4 5 6 7 ... 218

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77043907	chr3:21947004-21947005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs560691804	chr3:21947005-21947006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143355104	chr3:21947011-21947012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192372240	chr3:21947013-21947014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184269330	chr3:21947022-21947023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189677467	chr3:21947043-21947044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181066395	chr3:21947068-21947069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111483424	chr3:21947093-21947094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185398219	chr3:21947101-21947102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs386355793	chr3:21947182-21947183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4044583	chr3:21947185-21947186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs397843057	chr3:21947197-21947198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs10595043	chr3:21947200-21947201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548399835	chr3:21947239-21947240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541882926	chr3:21947285-21947286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563253528	chr3:21947309-21947310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530491989	chr3:21947317-21947318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546195820	chr3:21947320-21947321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563562536	chr3:21947327-21947328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564761382	chr3:21947353-21947354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528682021	chr3:21947399-21947400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550084152	chr3:21947404-21947405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370464460	chr3:21947410-21947411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1479972	chr3:21947446-21947447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531347022	chr3:21947457-21947458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs259505	chr3:21947463-21947464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs568025820	chr3:21947497-21947498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529325747	chr3:21947504-21947505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs116285481	chr3:21947539-21947540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201742749	chr3:21947548-21947549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs568924839	chr3:21947563-21947564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs151185891	chr3:21947565-21947566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs139151399	chr3:21947567-21947568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570718226	chr3:21947589-21947590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528515744	chr3:21947617-21947618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73129340	chr3:21947665-21947666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs574615677	chr3:21947746-21947747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs17010054	chr3:21947772-21947773	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs78417373	chr3:21947783-21947784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189035954	chr3:21947809-21947810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs545736935	chr3:21947810-21947811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564673852	chr3:21947847-21947848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568517855	chr3:21947905-21947906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573467098	chr3:21947949-21947950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs202153911	chr3:21947951-21947952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs540498390	chr3:21947966-21947967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561965649	chr3:21947973-21947974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553868600	chr3:21947987-21947988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76168899	chr3:21948014-21948015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs367774327	chr3:21948025-21948026	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:437 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21947000-21947200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr3:21947200-21948000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr3:21948000-21948400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr3:21948400-21950000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr3:21950000-21950800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr3:21950600-21951400	Enhancers	Fetal Lung	lung
7	chr3:21951400-21953800	Weak transcription	Fetal Lung	lung
8	chr3:21953800-21955400	Enhancers	Colon Smooth Muscle	Colon
9	chr3:21953800-21956800	Enhancers	Fetal Lung	lung
10	chr3:21954000-21954200	Enhancers	Placenta Amnion	Placenta Amnion
11	chr3:21954000-21954800	Enhancers	Duodenum Smooth Muscle	Duodenum
12	chr3:21954000-21955400	Enhancers	NH-A	brain
13	chr3:21954000-21955600	Enhancers	Fetal Muscle Leg	muscle
14	chr3:21954000-21955600	Enhancers	NHLF	lung
15	chr3:21954000-21955800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr3:21954000-21956600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr3:21954000-21956600	Enhancers	NHDF-Ad	bronchial
18	chr3:21954200-21955600	Enhancers	Fetal Stomach	stomach
19	chr3:21954400-21960800	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr3:21954600-21955800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr3:21954600-21956200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr3:21954600-21956400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr3:21954800-21957000	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr3:21955400-21956400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:21955400-21960600	Weak transcription	NH-A	brain
26	chr3:21955600-21960600	Weak transcription	Fetal Stomach	stomach
27	chr3:21955600-21960800	Weak transcription	NHLF	lung
28	chr3:21955800-21961200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr3:21956200-21960600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:21956400-21960800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:21956400-21960800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr3:21956600-21960400	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr3:21956600-21960400	Weak transcription	NHDF-Ad	bronchial
34	chr3:21956800-21957400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr3:21956800-21957400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr3:21956800-21957400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr3:21956800-21960400	Weak transcription	Fetal Lung	lung
38	chr3:21957000-21957400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:21957000-21960400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr3:21957400-21960600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr3:21957400-21960800	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr3:21957400-21960800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr3:21957400-21961000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr3:21960400-21961000	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr3:21960400-21961800	Enhancers	Fetal Lung	lung
46	chr3:21960400-21962400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr3:21960400-21963000	Enhancers	NHDF-Ad	bronchial
48	chr3:21960600-21961200	Enhancers	Brain Germinal Matrix	brain
49	chr3:21960600-21961400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:21960600-21961800	Enhancers	HUES48 Cell Line	embryonic stem cell

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