Variant report

Variant	nsv481960
Chromosome Location	chr6:163016189-163240987
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	chr6:163148702-163148902	K562	blood:	n/a	n/a
2	ARID3A	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:163148619-163149118	HepG2	liver:	n/a	n/a
4	ATF1	chr6:163148753-163149159	K562	blood:	n/a	n/a
5	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
6	ATF1	chr6:163183429-163183540	K562	blood:	n/a	n/a
7	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
8	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
9	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
10	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
11	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
12	ATF3	chr6:163148498-163149119	HepG2	liver:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
13	ATF3	chr6:163148738-163149179	K562	blood:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
14	ATF3	chr6:163148789-163149068	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
15	ATF3	chr6:163148710-163149085	K562	blood:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
16	ATF3	chr6:163148729-163149180	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968 chr6:163148970-163148979 chr6:163148959-163148967 chr6:163148957-163148970 chr6:163148955-163148970 chr6:163148957-163148968 chr6:163148959-163148970 chr6:163148958-163148978 chr6:163148956-163148969 chr6:163148848-163148857 chr6:163148959-163148969
17	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
18	BACH1	chr6:163209996-163210055	K562	blood:	n/a	n/a
19	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
21	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
22	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
23	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
24	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:163148554-163149138	HepG2	liver:	n/a	chr6:163148747-163148763
26	BHLHE40	chr6:163148697-163149088	GM12878	blood:	n/a	chr6:163148747-163148763
27	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
28	BHLHE40	chr6:163148582-163149115	K562	blood:	n/a	chr6:163148747-163148763
29	BRCA1	chr6:163148841-163149053	HepG2	liver:	n/a	n/a
30	BRCA1	chr6:163148845-163149085	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr6:163148516-163149230	K562	blood:	n/a	n/a
32	CCNT2	chr6:163148390-163149101	K562	blood:	n/a	chr6:163148913-163148922 chr6:163148970-163148979 chr6:163149075-163149084
33	CEBPB	chr6:163206813-163207236	A549	lung:	n/a	n/a
34	CEBPB	chr6:163185436-163185658	HepG2	liver:	n/a	chr6:163185502-163185513 chr6:163185502-163185515 chr6:163185504-163185515 chr6:163185525-163185536
35	CEBPB	chr6:163036076-163036363	H1-hESC	embryonic stem cell:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
36	CEBPB	chr6:163148686-163149168	A549	lung:	n/a	n/a
37	CEBPB	chr6:163206896-163207154	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr6:163218870-163218983	HepG2	liver:	n/a	n/a
39	CEBPB	chr6:163063853-163064152	HepG2	liver:	n/a	chr6:163063991-163064002
40	CEBPB	chr6:163042256-163042790	HCT-116	colon:	n/a	n/a
41	CEBPB	chr6:163036070-163036411	IMR90	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
42	CEBPB	chr6:163206936-163207086	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:163148779-163149062	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:163148769-163149119	MCF-7	breast:	n/a	n/a
45	CEBPB	chr6:163095583-163095738	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
46	CEBPB	chr6:163206824-163207160	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr6:163102596-163102728	HepG2	liver:	n/a	n/a
48	CEBPB	chr6:163196390-163196524	A549	lung:	n/a	chr6:163196436-163196445 chr6:163196436-163196445 chr6:163196434-163196447 chr6:163196436-163196445
49	CEBPB	chr6:163067647-163067800	HepG2	liver:	n/a	chr6:163067696-163067707
50	CEBPB	chr6:163036084-163036403	A549	lung:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163148022-163148072	Hepatocyte	liver:	n/a
2	chr6:163200038-163200088	GM12891	blood:	n/a
3	chr6:163024624-163024674	AoSMC	blood vessel:	n/a
4	chr6:163148903-163148953	A549	lung:	n/a
5	chr6:163148022-163148072	Hepatocyte	liver:	n/a
6	chr6:163200038-163200088	GM12891	blood:	n/a
7	chr6:163024624-163024674	AoSMC	blood vessel:	n/a
8	chr6:163148903-163148953	A549	lung:	n/a
9	chr6:163024624-163024674	MCF-7	breast:	n/a
10	chr6:163146217-163146267	Hepatocyte	liver:	n/a
11	chr6:163148853-163148903	T-47D	breast:	n/a
12	chr6:163148853-163148903	IMR90	lung:	fetal
13	chr6:163199983-163200033	HCF	heart:	n/a
14	chr6:163148903-163148953	SK-N-SH_RA	brain:	n/a
15	chr6:163147737-163147787	BE2_C	brain:	n/a
16	chr6:163148018-163148068	AG09319	gingival:	n/a
17	chr6:163148777-163148827	HUVEC	blood vessel:	n/a
18	chr6:163147733-163147783	AG04450	lung:	fetal
19	chr6:163148022-163148072	HRE	kidney:	n/a
20	chr6:163146217-163146267	ovcar-3	ovarian:	n/a
21	chr6:163147737-163147787	K562	blood:	n/a
22	chr6:163148718-163148768	HAEpiC	amniotic membrane:	n/a
23	chr6:163148853-163148903	HNPCEpiC	eye:	n/a
24	chr6:163024624-163024674	AG10803	skin:	n/a
25	chr6:163147733-163147783	T-47D	breast:	n/a
26	chr6:163149453-163149503	A549	lung:	n/a
27	chr6:163147737-163147787	NHDF-neo	bronchial:	n/a
28	chr6:163146217-163146267	U87	brain:	n/a
29	chr6:163148853-163148903	GM19239	blood:	n/a
30	chr6:163200038-163200088	HCPEpiC	choroid plexus:	n/a
31	chr6:163149167-163149217	Hela-S3	cervix:	n/a
32	chr6:163149320-163149370	NH-A	brain:	n/a
33	chr6:163148718-163148768	AG04450	lung:	fetal
34	chr6:163148903-163148953	BJ	skin:	n/a
35	chr6:163135177-163135227	HCM	heart:	n/a
36	chr6:163148290-163148340	PFSK-1	brain:	n/a
37	chr6:163149169-163149219	HUVEC	blood vessel:	n/a
38	chr6:163149320-163149370	HCF	heart:	n/a
39	chr6:163148718-163148768	ProgFib	skin:	n/a
40	chr6:163147733-163147783	H1-hESC	embryonic stem cell:	embryo
41	chr6:163147999-163148049	HUVEC	blood vessel:	n/a
42	chr6:163146217-163146267	HCM	heart:	n/a
43	chr6:163147737-163147787	ProgFib	skin:	n/a
44	chr6:163148853-163148903	HEK293	kidney:	embryo
45	chr6:163148762-163148812	PFSK-1	brain:	n/a
46	chr6:163149453-163149503	LNCaP	prostate:	n/a
47	chr6:163148501-163148551	IMR90	lung:	fetal
48	chr6:163148762-163148812	BE2_C	brain:	n/a
49	chr6:163148022-163148072	GM06990	blood:	n/a
50	chr6:163024624-163024674	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
2	chr6:163132663..163134210-chr6:163147086..163148664,2	K562	blood:
3	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
4	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
5	chr6:163139294..163141851-chr6:163147296..163150092,3	MCF-7	breast:
6	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
7	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
8	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
9	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
10	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
11	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:
12	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
13	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
14	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
15	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
16	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
17	chr6:163136674..163141943-chr6:163143603..163148822,6	K562	blood:
18	chr6:163146966..163150271-chr6:163157232..163160053,3	K562	blood:
19	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
20	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
21	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
22	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:
23	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
24	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
25	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
26	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
27	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
28	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
29	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
30	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:

Variant related genes	Relation type
PACRG	TF binding region
PARK2	TF binding region
PACRG	CpG island
PARK2	CpG island
ENSG00000112530	chromatin interactions
ENSG00000185345	chromatin interactions

Extended variants
information (count: 6099 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:6099 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190720073	chr6:163016190-163016191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs181963651	chr6:163016193-163016194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs560863710	chr6:163016207-163016208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574263291	chr6:163016266-163016267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185207838	chr6:163016373-163016374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573314742	chr6:163016374-163016375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528574600	chr6:163016448-163016449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551633436	chr6:163016451-163016452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189627658	chr6:163016499-163016500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565263139	chr6:163016514-163016515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530964740	chr6:163016536-163016537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs182681409	chr6:163016542-163016543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567983494	chr6:163016545-163016546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs13208136	chr6:163016557-163016558	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs185510652	chr6:163016563-163016564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566993870	chr6:163016565-163016566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375958231	chr6:163016580-163016581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538704502	chr6:163016623-163016624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558402070	chr6:163016643-163016644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75623476	chr6:163016665-163016666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537468709	chr6:163016670-163016671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554394615	chr6:163016777-163016778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190999181	chr6:163016838-163016839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565235688	chr6:163016884-163016885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540174020	chr6:163016933-163016934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183762123	chr6:163016962-163016963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533602684	chr6:163016992-163016993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74758684	chr6:163016998-163016999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560936810	chr6:163017042-163017043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565253112	chr6:163017049-163017050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116266238	chr6:163017058-163017059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs36004212	chr6:163017098-163017099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544622056	chr6:163017131-163017132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561525969	chr6:163017140-163017141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13212900	chr6:163017170-163017171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562910962	chr6:163017241-163017242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59962412	chr6:163017299-163017300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567037888	chr6:163017340-163017341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532611201	chr6:163017378-163017379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530550613	chr6:163017402-163017403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144604099	chr6:163017454-163017455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566770687	chr6:163017547-163017548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369628410	chr6:163017565-163017566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529972725	chr6:163017579-163017580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374167088	chr6:163017580-163017581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188248800	chr6:163017658-163017659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367722008	chr6:163017814-163017815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs193289372	chr6:163017820-163017821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs533817251	chr6:163017840-163017841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553818276	chr6:163017841-163017842	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Breast cancer	16397240	CNVD
Atherosclerosis	21956041	CNVD
Maculopathy	20981449	CNVD
Retinoblastoma	22278416	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Uveal melanoma	20484589	CNVD
Glioblastoma multiforme	19435819	CNVD
Astrocytoma	16205629	CNVD
Parkinson disease	17160897	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20838587	CNVD
Early-onset parkinson disease	21993715	CNVD
Glioblastoma	18772890	CNVD
Pancreatic cancer	20981101	CNVD
Autism	21360662	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Parkinson disease	0	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163014400-163017800	Weak transcription	Fetal Heart	heart
2	chr6:163014800-163017800	Weak transcription	Left Ventricle	heart
3	chr6:163017600-163018200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:163017800-163018000	Enhancers	Left Ventricle	heart
5	chr6:163017800-163018000	Enhancers	Pancreas	Pancrea
6	chr6:163017800-163018000	Enhancers	Right Atrium	heart
7	chr6:163018000-163019600	Weak transcription	Left Ventricle	heart
8	chr6:163018000-163022000	Weak transcription	Right Atrium	heart
9	chr6:163018000-163036400	Weak transcription	Pancreas	Pancrea
10	chr6:163018400-163019800	Enhancers	Fetal Brain Male	brain
11	chr6:163019600-163020400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:163019600-163020800	Enhancers	Left Ventricle	heart
13	chr6:163019800-163020400	Weak transcription	Fetal Brain Male	brain
14	chr6:163020000-163020400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:163020000-163020400	Enhancers	Adipose Nuclei	Adipose
16	chr6:163020400-163020600	Enhancers	Fetal Brain Male	brain
17	chr6:163020600-163024400	Weak transcription	Fetal Brain Male	brain
18	chr6:163020800-163024400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:163020800-163024800	Weak transcription	Left Ventricle	heart
20	chr6:163023200-163023400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr6:163023600-163024400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr6:163023800-163024000	Enhancers	Brain Anterior Caudate	brain
23	chr6:163023800-163024600	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr6:163024000-163027400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:163024200-163025600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr6:163024200-163025800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:163024200-163026000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:163024400-163024600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr6:163024400-163025000	Enhancers	Fetal Brain Male	brain
30	chr6:163024400-163025200	Enhancers	H9 Cell Line	embryonic stem cell
31	chr6:163024400-163025200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr6:163024400-163025200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr6:163024400-163025200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr6:163024400-163025400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:163024400-163025600	Enhancers	Fetal Brain Female	brain
36	chr6:163024400-163027400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:163024600-163025000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr6:163024600-163025200	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr6:163024600-163025400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr6:163024600-163025400	Enhancers	Fetal Heart	heart
41	chr6:163024800-163025200	Enhancers	Left Ventricle	heart
42	chr6:163025000-163025400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:163025000-163025400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr6:163025200-163025400	Enhancers	Psoas Muscle	Psoas
45	chr6:163025200-163025600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:163025200-163029800	Weak transcription	Left Ventricle	heart
47	chr6:163025400-163043400	Weak transcription	Psoas Muscle	Psoas
48	chr6:163026400-163031200	Weak transcription	Aorta	Aorta
49	chr6:163027200-163036400	Weak transcription	Ovary	ovary
50	chr6:163027400-163036000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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