Variant report

Variant	nsv481693
Chromosome Location	chr6:162935354-163162438
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	chr6:163148619-163149118	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:163148702-163148902	K562	blood:	n/a	n/a
4	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
5	ATF1	chr6:163148753-163149159	K562	blood:	n/a	n/a
6	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
7	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
8	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
9	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
10	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
11	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
12	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
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	chr6:163148498-163149119	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
16	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
17	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
19	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
20	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
21	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
22	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
23	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:163148582-163149115	K562	blood:	n/a	chr6:163148747-163148763
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	BRCA1	chr6:163148841-163149053	HepG2	liver:	n/a	n/a
29	BRCA1	chr6:163148845-163149085	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr6:163148516-163149230	K562	blood:	n/a	n/a
31	CCNT2	chr6:163001825-163002025	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	chr6:163148686-163149168	A549	lung:	n/a	n/a
34	CEBPB	chr6:163095583-163095738	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
35	CEBPB	chr6:163095503-163095821	HepG2	liver:	n/a	chr6:163095668-163095677 chr6:163095667-163095678
36	CEBPB	chr6:163148771-163149153	HepG2	liver:	n/a	n/a
37	CEBPB	chr6:163063853-163064152	HepG2	liver:	n/a	chr6:163063991-163064002
38	CEBPB	chr6:163148788-163149168	A549	lung:	n/a	n/a
39	CEBPB	chr6:163122194-163122394	HepG2	liver:	n/a	chr6:163122352-163122363
40	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
41	CEBPB	chr6:163146789-163146918	HepG2	liver:	n/a	chr6:163146839-163146850 chr6:163146838-163146849 chr6:163146838-163146849
42	CEBPB	chr6:163148643-163149149	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:163036055-163036678	HepG2	liver:	n/a	chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036237-163036246 chr6:163036118-163036129 chr6:163036235-163036248 chr6:163036565-163036582 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036116-163036129 chr6:163036236-163036247
44	CEBPB	chr6:162943679-162943865	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:163063888-163064088	H1-hESC	embryonic stem cell:	n/a	chr6:163063991-163064002
46	CEBPB	chr6:163148769-163149119	MCF-7	breast:	n/a	n/a
47	CEBPB	chr6:163148713-163149149	IMR90	lung:	n/a	n/a
48	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
49	CEBPB	chr6:163148738-163149145	K562	blood:	n/a	n/a
50	CEBPB	chr6:163148750-163149181	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163148853-163148903	AG09319	gingival:	n/a
2	chr6:163135177-163135227	HIPEpiC	eye:	n/a
3	chr6:163148853-163148903	AG09319	gingival:	n/a
4	chr6:163135177-163135227	HIPEpiC	eye:	n/a
5	chr6:163148903-163148953	AoSMC	blood vessel:	n/a
6	chr6:163147999-163148049	HEEpiC	esophagus:	n/a
7	chr6:163149167-163149217	HRCEpiC	kidney:	n/a
8	chr6:163110854-163110904	SKMC	muscle:	n/a
9	chr6:163148903-163148953	ovcar-3	ovarian:	n/a
10	chr6:163147999-163148049	AoSMC	blood vessel:	n/a
11	chr6:163148022-163148072	SKMC	muscle:	n/a
12	chr6:163148903-163148953	CMK	blood:	n/a
13	chr6:163148903-163148953	HCM	heart:	n/a
14	chr6:163149674-163149724	NB4	blood:	n/a
15	chr6:163146217-163146267	HepG2	liver:	n/a
16	chr6:163148018-163148068	SK-N-SH	brain:	n/a
17	chr6:163148777-163148827	AoSMC	blood vessel:	n/a
18	chr6:163148501-163148551	Hepatocyte	liver:	n/a
19	chr6:163148018-163148068	ECC-1	luminal epithelium:	n/a
20	chr6:163110854-163110904	HEEpiC	esophagus:	n/a
21	chr6:163024624-163024674	SK-N-SH_RA	brain:	n/a
22	chr6:162964378-162964428	NH-A	brain:	n/a
23	chr6:163148777-163148827	NT2-D1	testis:	n/a
24	chr6:163147999-163148049	BJ	skin:	n/a
25	chr6:163146217-163146267	NT2-D1	testis:	n/a
26	chr6:163148290-163148340	SKMC	muscle:	n/a
27	chr6:163148777-163148827	NB4	blood:	n/a
28	chr6:163148762-163148812	NB4	blood:	n/a
29	chr6:163110854-163110904	AG04449	skin:	fetal
30	chr6:163135177-163135227	LNCaP	prostate:	n/a
31	chr6:163148501-163148551	HAEpiC	amniotic membrane:	n/a
32	chr6:163149167-163149217	HCF	heart:	n/a
33	chr6:163148762-163148812	HNPCEpiC	eye:	n/a
34	chr6:163147737-163147787	Jurkat	blood:	n/a
35	chr6:163148022-163148072	H1-hESC	embryonic stem cell:	embryo
36	chr6:163148290-163148340	GM12892	blood:	n/a
37	chr6:163148018-163148068	Jurkat	blood:	n/a
38	chr6:163148022-163148072	HepG2	liver:	n/a
39	chr6:163148853-163148903	Hepatocyte	liver:	n/a
40	chr6:163149320-163149370	HIPEpiC	eye:	n/a
41	chr6:163149674-163149724	AG10803	skin:	n/a
42	chr6:163148290-163148340	NHBE	bronchial:	n/a
43	chr6:163110854-163110904	Jurkat	blood:	n/a
44	chr6:163149453-163149503	HCM	heart:	n/a
45	chr6:163149453-163149503	AG04450	lung:	fetal
46	chr6:163110854-163110904	NT2-D1	testis:	n/a
47	chr6:163135177-163135227	HRCEpiC	kidney:	n/a
48	chr6:163149674-163149724	AoSMC	blood vessel:	n/a
49	chr6:163148853-163148903	HRPEpiC	eye:	n/a
50	chr6:162964378-162964428	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
2	chr6:163136674..163141943-chr6:163143603..163148822,6	K562	blood:
3	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
4	chr6:163146966..163150271-chr6:163157232..163160053,3	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	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:
9	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
10	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
11	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
12	chr6:163132663..163134210-chr6:163147086..163148664,2	K562	blood:
13	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
14	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
15	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
16	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
17	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
18	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
19	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
20	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
21	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
22	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
23	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
24	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
25	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
26	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
27	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
28	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
29	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
30	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:

Variant related genes	Relation type
KRT8P44	TF binding region
PACRG	TF binding region
PARK2	TF binding region
KRT8P44	CpG island
PACRG	CpG island
PARK2	CpG island
ENSG00000185345	chromatin interactions
ENSG00000112530	chromatin interactions

Extended variants
information (count: 8809 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:8809 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78735976	chr6:162937001-162937002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79618438	chr6:162937008-162937009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558158368	chr6:162937060-162937061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553916368	chr6:162937068-162937069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374462827	chr6:162937070-162937071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370602324	chr6:162937076-162937077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189640110	chr6:162937087-162937088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574425585	chr6:162937093-162937094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs9356031	chr6:162937115-162937116	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs182708863	chr6:162937132-162937133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186974711	chr6:162937133-162937134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73037930	chr6:162937146-162937147	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs77884815	chr6:162937167-162937168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs202216736	chr6:162937180-162937181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs73037932	chr6:162937264-162937265	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs191517087	chr6:162937281-162937282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544764199	chr6:162937333-162937334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35701794	chr6:162941216-162941217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563746848	chr6:162941239-162941240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs67303732	chr6:162941245-162941246	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs571073494	chr6:162941332-162941333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549315365	chr6:162941374-162941375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538127894	chr6:162941410-162941411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs67511878	chr6:162941422-162941423	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs535092998	chr6:162941424-162941425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552031722	chr6:162941487-162941488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571853261	chr6:162941499-162941500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113105296	chr6:162941506-162941507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189007477	chr6:162941545-162941546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557368627	chr6:162941612-162941613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11962498	chr6:162941618-162941619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs148587037	chr6:162941621-162941622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552899852	chr6:162941645-162941646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572628071	chr6:162941724-162941725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544684270	chr6:162941764-162941765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2022998	chr6:162941823-162941824	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs575087744	chr6:162941830-162941831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529792174	chr6:162941831-162941832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373413741	chr6:162941832-162941833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544344840	chr6:162941857-162941858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572808973	chr6:162941863-162941864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561034426	chr6:162941884-162941885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73591829	chr6:162941890-162941891	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549128701	chr6:162941894-162941895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs78535625	chr6:162941912-162941913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528631845	chr6:162941944-162941945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558467245	chr6:162942000-162942001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551894749	chr6:162942018-162942019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201807418	chr6:162942044-162942045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113211590	chr6:162942070-162942071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162937000-162937400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:162941200-162989400	Weak transcription	Aorta	Aorta
3	chr6:162943600-162944000	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr6:162944000-162944200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:162944000-162947800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:162944200-162945200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr6:162945200-162946200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr6:162946000-162946600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:162946000-162946600	Enhancers	Fetal Muscle Trunk	muscle
10	chr6:162946000-162946600	Enhancers	Fetal Muscle Leg	muscle
11	chr6:162946200-162946400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:162946200-162946400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:162946200-162946600	Enhancers	Ovary	ovary
14	chr6:162946200-162947000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr6:162946400-162946600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:162946400-162946600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:162946600-162948000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:162946600-162953400	Weak transcription	Fetal Muscle Leg	muscle
19	chr6:162946800-162947800	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr6:162947400-162948000	Enhancers	Duodenum Mucosa	Duodenum
21	chr6:162947800-162948400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:162947800-162948400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:162947800-162948400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:162947800-162948400	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr6:162947800-162948600	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:162947800-162949000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr6:162947800-162949000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr6:162947800-162949000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr6:162947800-162949200	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr6:162948000-162948200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr6:162948000-162948400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr6:162948000-162948400	Flanking Active TSS	Duodenum Mucosa	Duodenum
33	chr6:162948000-162949000	Enhancers	Liver	Liver
34	chr6:162948000-162949800	Enhancers	Fetal Intestine Large	intestine
35	chr6:162948200-162948400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:162948200-162948800	Enhancers	Fetal Kidney	kidney
37	chr6:162948400-162949800	Enhancers	Duodenum Mucosa	Duodenum
38	chr6:162948400-162953200	Weak transcription	Sigmoid Colon	Sigmoid Colon
39	chr6:162948600-162949800	Enhancers	Fetal Intestine Small	intestine
40	chr6:162949000-162949400	Weak transcription	Liver	Liver
41	chr6:162949200-162949600	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr6:162949400-162950000	Enhancers	Liver	Liver
43	chr6:162949600-162949800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr6:162949800-162952600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr6:162949800-162953600	Weak transcription	Duodenum Mucosa	Duodenum
46	chr6:162952600-162952800	Enhancers	Rectal Mucosa Donor 31	rectum
47	chr6:162952600-162954600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:162952800-162953200	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr6:162953000-162955600	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr6:162953200-162954200	Enhancers	Colon Smooth Muscle	Colon

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