Variant report

Variant	nsv886890
Chromosome Location	chr6:162871195-163248589
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	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:163148702-163148902	K562	blood:	n/a	n/a
3	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:163148619-163149118	HepG2	liver:	n/a	n/a
5	ATF1	chr6:163183429-163183540	K562	blood:	n/a	n/a
6	ATF1	chr6:163148753-163149159	K562	blood:	n/a	n/a
7	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
8	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
9	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
10	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
11	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
12	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
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	chr6:163148729-163149180	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
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	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
18	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
19	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:163209996-163210055	K562	blood:	n/a	n/a
21	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
22	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
23	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
24	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
25	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
26	BHLHE40	chr6:163148697-163149088	GM12878	blood:	n/a	chr6:163148747-163148763
27	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
28	BHLHE40	chr6:163148582-163149115	K562	blood:	n/a	chr6:163148747-163148763
29	BHLHE40	chr6:163148554-163149138	HepG2	liver:	n/a	chr6:163148747-163148763
30	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
32	BRCA1	chr6:163148845-163149085	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr6:163148841-163149053	HepG2	liver:	n/a	n/a
34	BRCA1	chr6:162871740-162871751	H1-hESC	embryonic stem cell:	n/a	n/a
35	CBX3	chr6:163148516-163149230	K562	blood:	n/a	n/a
36	CCNT2	chr6:163001825-163002025	K562	blood:	n/a	n/a
37	CCNT2	chr6:163148390-163149101	K562	blood:	n/a	chr6:163148913-163148922 chr6:163148970-163148979 chr6:163149075-163149084
38	CEBPB	chr6:163192040-163192363	HepG2	liver:	n/a	chr6:163192194-163192205
39	CEBPB	chr6:163102596-163102728	HepG2	liver:	n/a	n/a
40	CEBPB	chr6:162876192-162876578	MCF-7	breast:	n/a	n/a
41	CEBPB	chr6:163063873-163064127	IMR90	lung:	n/a	chr6:163063991-163064002
42	CEBPB	chr6:163036133-163036384	Hela-S3	cervix:	n/a	chr6:163036237-163036246 chr6:163036237-163036246 chr6:163036235-163036248 chr6:163036235-163036248 chr6:163036237-163036246 chr6:163036236-163036247
43	CEBPB	chr6:162910422-162910805	HepG2	liver:	n/a	n/a
44	CEBPB	chr6:163042252-163042579	MCF-7	breast:	n/a	n/a
45	CEBPB	chr6:163122194-163122394	HepG2	liver:	n/a	chr6:163122352-163122363
46	CEBPB	chr6:162910493-162910789	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:163206905-163207198	IMR90	lung:	n/a	n/a
48	CEBPB	chr6:163206848-163207222	HepG2	liver:	n/a	n/a
49	CEBPB	chr6:163206891-163207206	A549	lung:	n/a	n/a
50	CEBPB	chr6:163218870-163218983	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163148018-163148068	HNPCEpiC	eye:	n/a
2	chr6:163148018-163148068	HNPCEpiC	eye:	n/a
3	chr6:163147733-163147783	K562	blood:	n/a
4	chr6:163148718-163148768	IMR90	lung:	fetal
5	chr6:163148290-163148340	ECC-1	luminal epithelium:	n/a
6	chr6:163148022-163148072	NH-A	brain:	n/a
7	chr6:163110854-163110904	HUVEC	blood vessel:	n/a
8	chr6:163148018-163148068	SKMC	muscle:	n/a
9	chr6:163135177-163135227	H1-hESC	embryonic stem cell:	embryo
10	chr6:163148718-163148768	MCF-7	breast:	n/a
11	chr6:163148290-163148340	SKMC	muscle:	n/a
12	chr6:163148018-163148068	T-47D	breast:	n/a
13	chr6:163149169-163149219	Jurkat	blood:	n/a
14	chr6:163149169-163149219	BJ	skin:	n/a
15	chr6:163148501-163148551	AG09309	skin:	n/a
16	chr6:163148290-163148340	AG10803	skin:	n/a
17	chr6:163110854-163110904	A549	lung:	n/a
18	chr6:163149674-163149724	AG09319	gingival:	n/a
19	chr6:163147999-163148049	U87	brain:	n/a
20	chr6:163147733-163147783	SK-N-MC	brain:	n/a
21	chr6:163149453-163149503	AG04450	lung:	fetal
22	chr6:163148501-163148551	HIPEpiC	eye:	n/a
23	chr6:163149167-163149217	GM12878	blood:	n/a
24	chr6:163148777-163148827	HRCEpiC	kidney:	n/a
25	chr6:163149167-163149217	Jurkat	blood:	n/a
26	chr6:163149674-163149724	MCF-7	breast:	n/a
27	chr6:163200038-163200088	BE2_C	brain:	n/a
28	chr6:163148718-163148768	HRPEpiC	eye:	n/a
29	chr6:163147733-163147783	AG04450	lung:	fetal
30	chr6:163024624-163024674	HIPEpiC	eye:	n/a
31	chr6:163148290-163148340	NHBE	bronchial:	n/a
32	chr6:163148777-163148827	BE2_C	brain:	n/a
33	chr6:163149453-163149503	AG09319	gingival:	n/a
34	chr6:163149320-163149370	ovcar-3	ovarian:	n/a
35	chr6:163200038-163200088	SKMC	muscle:	n/a
36	chr6:163149674-163149724	HPAEpiC	pulmonary alveolar:	n/a
37	chr6:163147999-163148049	GM06990	blood:	n/a
38	chr6:163148853-163148903	HCF	heart:	n/a
39	chr6:163199983-163200033	SK-N-MC	brain:	n/a
40	chr6:163149320-163149370	NHBE	bronchial:	n/a
41	chr6:163149167-163149217	HRPEpiC	eye:	n/a
42	chr6:163149453-163149503	ECC-1	luminal epithelium:	n/a
43	chr6:163149320-163149370	SKMC	muscle:	n/a
44	chr6:163147733-163147783	HCT-116	colon:	n/a
45	chr6:163148762-163148812	GM12878	blood:	n/a
46	chr6:162964378-162964428	T-47D	breast:	n/a
47	chr6:163147737-163147787	SK-N-SH	brain:	n/a
48	chr6:163147999-163148049	AG09309	skin:	n/a
49	chr6:163149453-163149503	SK-N-SH	brain:	n/a
50	chr6:163148501-163148551	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:163146966..163150271-chr6:163157232..163160053,3	K562	blood:
2	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:
3	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
4	chr6:163136674..163141943-chr6:163143603..163148822,6	K562	blood:
5	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
6	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
7	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:
8	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
9	chr6:163138973..163143825-chr6:163144102..163148168,6	K562	blood:
10	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
11	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
12	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
13	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
14	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
15	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
16	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
17	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
18	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
19	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
20	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
21	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
22	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
23	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
24	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
25	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
26	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
27	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
28	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
29	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
30	chr6:163132663..163134210-chr6:163147086..163148664,2	K562	blood:
31	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
32	chr6:163139294..163141851-chr6:163147296..163150092,3	MCF-7	breast:
33	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
34	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
35	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
36	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:

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: 12525 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:12525 , 50 per page) page: 1 2 3 4 5 6 7 ... 251

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10945835	chr6:162871195-162871196	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs186228437	chr6:162871196-162871197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554231478	chr6:162871198-162871199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577228600	chr6:162871260-162871261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs6914057	chr6:162871262-162871263	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs79319598	chr6:162871268-162871269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576822288	chr6:162871277-162871278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542522268	chr6:162871291-162871292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373870575	chr6:162871297-162871298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377576443	chr6:162871298-162871299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12194250	chr6:162871303-162871304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79126124	chr6:162871311-162871312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144528169	chr6:162871317-162871318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs111919445	chr6:162871327-162871328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564217366	chr6:162871339-162871340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532840114	chr6:162871344-162871345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549581643	chr6:162871345-162871346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376584730	chr6:162871348-162871349	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189906262	chr6:162871349-162871350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548865995	chr6:162871360-162871361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9365437	chr6:162871361-162871362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62430723	chr6:162871367-162871368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547429667	chr6:162871379-162871380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113145210	chr6:162871382-162871383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111315139	chr6:162871388-162871389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539513059	chr6:162871396-162871397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs71544933	chr6:162871402-162871403	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556828355	chr6:162871407-162871408	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201023311	chr6:162871411-162871412	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375003698	chr6:162871413-162871414	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576686214	chr6:162871414-162871415	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113359178	chr6:162871417-162871418	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556565201	chr6:162871418-162871419	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143258121	chr6:162871430-162871431	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369971670	chr6:162871436-162871437	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376580692	chr6:162871437-162871438	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117765565	chr6:162871441-162871442	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9365438	chr6:162871447-162871448	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9356023	chr6:162871448-162871449	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554289061	chr6:162871484-162871485	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75280422	chr6:162871486-162871487	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563190750	chr6:162871541-162871542	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73606343	chr6:162871571-162871572	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs540156610	chr6:162871587-162871588	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548730423	chr6:162871602-162871603	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182139080	chr6:162871610-162871611	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201948456	chr6:162871611-162871612	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73783585	chr6:162871615-162871616	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs372380009	chr6:162871626-162871627	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs151246903	chr6:162871638-162871639	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1593 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162861800-162872600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr6:162863800-162877400	Weak transcription	Aorta	Aorta
3	chr6:162864000-162871400	Weak transcription	Ovary	ovary
4	chr6:162865000-162871200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr6:162871000-162871200	Enhancers	Left Ventricle	heart
6	chr6:162871200-162871400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr6:162871200-162871800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr6:162871200-162871800	Enhancers	HepG2	liver
9	chr6:162871400-162871600	Enhancers	Ovary	ovary
10	chr6:162871400-162871800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
11	chr6:162871400-162871800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:162871400-162872000	Enhancers	Liver	Liver
13	chr6:162882600-162895600	Weak transcription	Right Atrium	heart
14	chr6:162884400-162884800	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr6:162884400-162885000	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr6:162884600-162884800	Enhancers	Psoas Muscle	Psoas
17	chr6:162884800-162886000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr6:162884800-162888800	Weak transcription	Psoas Muscle	Psoas
19	chr6:162885000-162886000	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr6:162885800-162886800	Enhancers	Fetal Heart	heart
21	chr6:162886000-162886200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
22	chr6:162886000-162886400	Active TSS	Skeletal Muscle Male	skeletal muscle
23	chr6:162886200-162886400	Active TSS	Skeletal Muscle Female	skeletal muscle
24	chr6:162886400-162887200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr6:162886400-162887400	Enhancers	Skeletal Muscle Male	skeletal muscle
26	chr6:162886800-162887200	Weak transcription	Fetal Heart	heart
27	chr6:162887200-162887400	Enhancers	Fetal Heart	heart
28	chr6:162887200-162887600	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr6:162887400-162888400	Weak transcription	Fetal Heart	heart
30	chr6:162887400-162888800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr6:162887600-162888800	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr6:162888400-162890800	Enhancers	Fetal Heart	heart
33	chr6:162888600-162889800	Enhancers	Fetal Muscle Leg	muscle
34	chr6:162888600-162890600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:162888800-162889000	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr6:162888800-162889200	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr6:162888800-162889200	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr6:162888800-162889600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:162888800-162889600	Enhancers	Brain Germinal Matrix	brain
40	chr6:162888800-162889800	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr6:162888800-162889800	Enhancers	Fetal Brain Female	brain
42	chr6:162888800-162890000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr6:162888800-162890400	Enhancers	NHEK	skin
44	chr6:162888800-162890600	Enhancers	Psoas Muscle	Psoas
45	chr6:162889000-162889400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr6:162889000-162889600	Enhancers	NH-A	brain
47	chr6:162889000-162889800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr6:162889000-162889800	Enhancers	Brain Cingulate Gyrus	brain
49	chr6:162889200-162889400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
50	chr6:162889200-162889600	Enhancers	Brain Anterior Caudate	brain

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