Variant report

Variant	nsv1030546
Chromosome Location	chr6:162748287-163475085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2867)
CpG islands
(count:2506)
Chromatin interactive
region (count:69)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2867 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:162910482-162910786	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:162857639-162857816	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:163102512-163102850	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:163148619-163149118	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:163304083-163304357	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:162794306-162794665	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:163148702-163148902	K562	blood:	n/a	n/a
8	ATF1	chr6:162812215-162812339	K562	blood:	n/a	n/a
9	ATF1	chr6:162812647-162812847	K562	blood:	n/a	n/a
10	ATF1	chr6:162782228-162782581	K562	blood:	n/a	n/a
11	ATF1	chr6:163148753-163149159	K562	blood:	n/a	n/a
12	ATF1	chr6:162784797-162785113	K562	blood:	n/a	n/a
13	ATF1	chr6:163037119-163037243	K562	blood:	n/a	n/a
14	ATF1	chr6:163183429-163183540	K562	blood:	n/a	n/a
15	ATF2	chr6:163148704-163149149	GM12878	blood:	n/a	chr6:163148957-163148968
16	ATF2	chr6:163042363-163042635	GM12878	blood:	n/a	n/a
17	ATF2	chr6:163422341-163422769	GM12878	blood:	n/a	n/a
18	ATF2	chr6:163148726-163149178	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
19	ATF2	chr6:163148705-163149166	GM12878	blood:	n/a	chr6:163148957-163148968
20	ATF2	chr6:163148711-163149191	H1-hESC	embryonic stem cell:	n/a	chr6:163148957-163148968
21	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
22	ATF3	chr6:163303885-163304152	H1-hESC	embryonic stem cell:	n/a	n/a
23	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
24	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
25	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
26	ATF3	chr6:163303817-163304198	H1-hESC	embryonic stem cell:	n/a	n/a
27	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
28	ATF3	chr6:163042298-163042684	HCT-116	colon:	n/a	n/a
29	ATF3	chr6:162784742-162785052	K562	blood:	n/a	n/a
30	BACH1	chr6:163148603-163148838	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:163149073-163149266	K562	blood:	n/a	n/a
32	BACH1	chr6:163209996-163210055	K562	blood:	n/a	n/a
33	BACH1	chr6:162975725-162976098	K562	blood:	n/a	n/a
34	BACH1	chr6:163277893-163278240	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr6:163422337-163422713	GM12878	blood:	n/a	chr6:163422593-163422603
36	BATF	chr6:163042347-163042655	GM12878	blood:	n/a	chr6:163042519-163042530
37	BATF	chr6:163042398-163042636	GM12878	blood:	n/a	chr6:163042519-163042530
38	BATF	chr6:163422365-163422747	GM12878	blood:	n/a	chr6:163422593-163422603
39	BCL11A	chr6:163422413-163422668	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:163422425-163422741	GM12878	blood:	n/a	n/a
41	BCL3	chr6:163295660-163296500	GM12878	blood:	n/a	n/a
42	BCL3	chr6:163295916-163296614	GM12878	blood:	n/a	n/a
43	BCLAF1	chr6:163148707-163149054	GM12878	blood:	n/a	chr6:163148747-163148760
44	BHLHE40	chr6:162899266-162899534	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:163148582-163149115	K562	blood:	n/a	chr6:163148747-163148763
46	BHLHE40	chr6:163102590-163102846	HepG2	liver:	n/a	n/a
47	BHLHE40	chr6:163148554-163149138	HepG2	liver:	n/a	chr6:163148747-163148763
48	BHLHE40	chr6:163042376-163042676	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:163304111-163304430	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:163148697-163149088	GM12878	blood:	n/a	chr6:163148747-163148763

(count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:163289702-163289752	GM12892	blood:	n/a
2	chr6:163148718-163148768	HCF	heart:	n/a
3	chr6:163149453-163149503	HCT-116	colon:	n/a
4	chr6:163148777-163148827	T-47D	breast:	n/a
5	chr6:163148762-163148812	MCF10A-Er-Src	breast:	n/a
6	chr6:163289702-163289752	GM12892	blood:	n/a
7	chr6:163148718-163148768	HCF	heart:	n/a
8	chr6:163149453-163149503	HCT-116	colon:	n/a
9	chr6:163148777-163148827	T-47D	breast:	n/a
10	chr6:163148762-163148812	MCF10A-Er-Src	breast:	n/a
11	chr6:163321305-163321355	HIPEpiC	eye:	n/a
12	chr6:163149167-163149217	NHBE	bronchial:	n/a
13	chr6:162831837-162831887	GM19239	blood:	n/a
14	chr6:163275980-163276030	CMK	blood:	n/a
15	chr6:163362155-163362205	HRPEpiC	eye:	n/a
16	chr6:163275980-163276030	RPTEC	kidney:	n/a
17	chr6:163149453-163149503	BE2_C	brain:	n/a
18	chr6:163321157-163321207	SKMC	muscle:	n/a
19	chr6:163273217-163273267	HAEpiC	amniotic membrane:	n/a
20	chr6:163147737-163147787	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:163149453-163149503	Hepatocyte	liver:	n/a
22	chr6:163275952-163276002	BJ	skin:	n/a
23	chr6:163024624-163024674	GM12892	blood:	n/a
24	chr6:163199983-163200033	NHBE	bronchial:	n/a
25	chr6:163149169-163149219	HMEC	breast:	n/a
26	chr6:163148022-163148072	NHBE	bronchial:	n/a
27	chr6:163148777-163148827	GM06990	blood:	n/a
28	chr6:163147999-163148049	SK-N-SH_RA	brain:	n/a
29	chr6:163321435-163321485	HCM	heart:	n/a
30	chr6:163321157-163321207	HAEpiC	amniotic membrane:	n/a
31	chr6:163149167-163149217	HL-60	blood:	n/a
32	chr6:162831837-162831887	NT2-D1	testis:	n/a
33	chr6:163321157-163321207	A549	lung:	n/a
34	chr6:163200038-163200088	GM12878	blood:	n/a
35	chr6:163149674-163149724	HCM	heart:	n/a
36	chr6:163148022-163148072	GM12891	blood:	n/a
37	chr6:163148853-163148903	PANC-1	pancreas:	n/a
38	chr6:162831837-162831887	U87	brain:	n/a
39	chr6:163321305-163321355	CMK	blood:	n/a
40	chr6:163276038-163276088	BJ	skin:	n/a
41	chr6:163199983-163200033	HIPEpiC	eye:	n/a
42	chr6:163321435-163321485	HCT-116	colon:	n/a
43	chr6:163148762-163148812	NHDF-neo	bronchial:	n/a
44	chr6:163146217-163146267	GM19239	blood:	n/a
45	chr6:163148290-163148340	GM19239	blood:	n/a
46	chr6:163147733-163147783	SK-N-MC	brain:	n/a
47	chr6:163110854-163110904	ECC-1	luminal epithelium:	n/a
48	chr6:163362155-163362205	NHBE	bronchial:	n/a
49	chr6:162865258-162865308	PANC-1	pancreas:	n/a
50	chr6:163276038-163276088	AG09309	skin:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
2	chr6:163258403..163260425-chr6:163266356..163268701,2	K562	blood:
3	chr6:163103043..163104996-chr6:163109382..163111025,2	K562	blood:
4	chr6:163130642..163133409-chr6:163136938..163139480,2	K562	blood:
5	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
6	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
7	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
8	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
9	chr6:163080104..163081787-chr6:163082227..163083951,2	K562	blood:
10	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
11	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
12	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
13	chr6:163320477..163321997-chr6:163470936..163472773,2	K562	blood:
14	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
15	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
16	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
17	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
18	chr6:163146966..163150271-chr6:163157232..163160053,3	K562	blood:
19	chr6:163238180..163239692-chr6:163244197..163245718,2	K562	blood:
20	chr6:163312379..163314050-chr6:163315693..163317902,2	K562	blood:
21	chr6:163100762..163102270-chr6:163108804..163111519,2	K562	blood:
22	chr6:162863367..162864320-chr6:163157771..163158572,4	MCF-7	breast:
23	chr6:163458107..163459739-chr6:163463183..163466142,2	K562	blood:
24	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
25	chr6:163135428..163138047-chr6:163139216..163143407,3	K562	blood:
26	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:
27	chr6:162902802..162905070-chr6:162905406..162907332,2	K562	blood:
28	chr6:163131701..163133797-chr6:163141922..163143768,2	K562	blood:
29	chr6:162960178..162962006-chr6:162962880..162965078,2	K562	blood:
30	chr6:163316641..163319996-chr6:163320032..163324686,4	K562	blood:
31	chr4:72393798..72394589-chr6:163273105..163273631,2	MCF-7	breast:
32	chr6:163467143..163469243-chr6:163471356..163474324,2	K562	blood:
33	chr6:163117200..163118947-chr6:163123211..163125034,2	K562	blood:
34	chr6:163111769..163114753-chr6:163116374..163118174,2	K562	blood:
35	chr6:163132663..163134210-chr6:163147086..163148664,2	K562	blood:
36	chr6:162863816..162864618-chr6:163271757..163272511,2	MCF-7	breast:
37	chr6:163138657..163141393-chr6:163146602..163148183,2	MCF-7	breast:
38	chr6:163429068..163430008-chrX:51497389..51498171,2	MCF-7	breast:
39	chr6:163426091..163427659-chr6:163429418..163431049,2	K562	blood:
40	chr6:162799485..162803733-chr6:162804296..162807777,5	K562	blood:
41	chr6:163077595..163080176-chr6:163085064..163087575,2	K562	blood:
42	chr6:162820265..162823089-chr6:162827852..162829559,2	K562	blood:
43	chr6:162763017..162765353-chr6:162767098..162769301,2	K562	blood:
44	chr6:163204105..163206331-chr6:163210537..163212839,2	K562	blood:
45	chr12:104252627..104253426-chr6:163440642..163441162,2	MCF-7	breast:
46	chr6:162671180..162673472-chr6:162808694..162811227,2	K562	blood:
47	chr6:162768506..162770213-chr6:162786241..162788330,2	K562	blood:
48	chr6:163142325..163145868-chr6:163146633..163149200,3	K562	blood:
49	chr6:163002877..163005708-chr6:163021910..163024946,3	K562	blood:
50	chr6:163332495..163335026-chr6:163337698..163339412,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
2	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
3	lnc-AL078585.1-1	chr6:163472292-163473064	ENSG00000225437.1
4	lnc-AL078585.1-1	chr6:163463589-163463729	ENSG00000225437.1
5	lnc-AL078585.1-1	chr6:163464012-163464201	ENSG00000225437.1
6	lnc-AL078585.1-13	chr6:163384002-163384191	ucscGeneNc_uc003qud_1
7	lnc-AL078585.1-14	chr6:163378290-163378580	NONHSAT115947
8	lnc-AL078585.1-1	chr6:163471578-163473064	NONHSAT115951
9	lnc-AL078585.1-1	chr6:163467647-163467715	NONHSAT115951
10	lnc-AL078585.1-1	chr6:163467616-163467715	ENSG00000225437.1
11	lnc-AL078585.1-1	chr6:163464011-163464201	ENSG00000225437.1
12	lnc-AL078585.1-1	chr6:163467616-163467717	ENSG00000225437.1
13	lnc-AL078585.1-13	chr6:163387606-163387705	ucscGeneNc_uc003qud_1
14	lnc-AL078585.1-1	chr6:163472292-163472446	ENSG00000225437.1
15	lnc-AL078585.1-13	chr6:163392282-163393054	ucscGeneNc_uc003qud_1
16	lnc-AL078585.1-1	chr6:163474957-163475173	NONHSAT115951
17	lnc-QKI-10	chr6:163307016-163311030	NONHSAT115946
18	lnc-AL078585.1-1	chr6:163465681-163465778	ENSG00000225437.1
19	lnc-AL078585.1-1	chr6:163474957-163475193	ENSG00000225437.1
20	lnc-AL078585.1-13	chr6:163394947-163395183	ucscGeneNc_uc003qud_1
21	lnc-AL078585.1-1	chr6:163464086-163464201	ENSG00000225437.1

No data

Variant related genes	Relation type
KRT8P44	TF binding region
ENSG00000225437	TF binding region
PACRG	TF binding region
ENSG00000217557	TF binding region
PARK2	TF binding region
KRT8P44	CpG island
ENSG00000225437	CpG island
PACRG	CpG island
ENSG00000217557	CpG island
PARK2	CpG island
ENSG00000112530	chromatin interactions
ENSG00000225437	chromatin interactions
ENSG00000270419	chromatin interactions
ENSG00000185345	chromatin interactions
ENSG00000112531	chromatin interactions

Extended variants
information (count: 23045 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:23045 , 50 per page) page: 1 2 3 4 5 6 7 ... 461

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185570568	chr6:162748309-162748310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs143108489	chr6:162748377-162748378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561208310	chr6:162748385-162748386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112168971	chr6:162748392-162748393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115854366	chr6:162748397-162748398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190476326	chr6:162748404-162748405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558804756	chr6:162748448-162748449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs114323888	chr6:162748501-162748502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs538908702	chr6:162748521-162748522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558481979	chr6:162748541-162748542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568486687	chr6:162748549-162748550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9458524	chr6:162748555-162748556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs181036290	chr6:162748559-162748560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112274139	chr6:162748595-162748596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113796909	chr6:162748607-162748608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62430692	chr6:162748613-162748614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138726217	chr6:162748629-162748630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372092499	chr6:162748630-162748631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184374952	chr6:162748639-162748640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs62430693	chr6:162748649-162748650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs62430694	chr6:162748661-162748662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs62430695	chr6:162748667-162748668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs67927985	chr6:162748678-162748679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577082195	chr6:162748728-162748729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546090943	chr6:162748792-162748793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562749018	chr6:162748805-162748806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148525328	chr6:162748846-162748847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544606019	chr6:162748850-162748851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73600117	chr6:162748863-162748864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530089821	chr6:162748908-162748909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547184751	chr6:162748918-162748919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574879353	chr6:162748927-162748928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113475865	chr6:162748948-162748949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532690055	chr6:162748952-162748953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79473416	chr6:162748976-162748977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75642238	chr6:162748977-162748978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6905464	chr6:162748993-162748994	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371947217	chr6:162749023-162749024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547873854	chr6:162749038-162749039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568151136	chr6:162749040-162749041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375086126	chr6:162749051-162749052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs71567639	chr6:162749055-162749056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74724292	chr6:162749067-162749068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181246655	chr6:162749075-162749076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185349071	chr6:162749093-162749094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577137924	chr6:162749132-162749133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539626660	chr6:162749133-162749134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188940993	chr6:162749155-162749156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375850136	chr6:162749162-162749163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs386409190	chr6:162749165-162749166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Schizophrenia	20967226	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
Autism	22495309	CNVD
Glioblastoma multiforme	21138945	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	19805367	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:2882 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:162728000-162765600	Weak transcription	Pancreas	Pancrea
2	chr6:162747400-162749800	Weak transcription	Ovary	ovary
3	chr6:162749600-162753000	Weak transcription	Aorta	Aorta
4	chr6:162749800-162750000	Strong transcription	Ovary	ovary
5	chr6:162750000-162753800	Weak transcription	Ovary	ovary
6	chr6:162753200-162753600	Enhancers	Adipose Nuclei	Adipose
7	chr6:162753600-162761000	Weak transcription	Adipose Nuclei	Adipose
8	chr6:162755000-162766200	Weak transcription	Ovary	ovary
9	chr6:162757800-162758000	Enhancers	Gastric	stomach
10	chr6:162757800-162758800	Enhancers	Fetal Heart	heart
11	chr6:162758600-162758800	Enhancers	Gastric	stomach
12	chr6:162761400-162761600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:162761600-162766000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:162762600-162763000	Weak transcription	Adipose Nuclei	Adipose
15	chr6:162763400-162763800	Enhancers	Fetal Lung	lung
16	chr6:162763600-162764200	Enhancers	Stomach Mucosa	stomach
17	chr6:162763800-162765200	Weak transcription	Fetal Lung	lung
18	chr6:162764000-162764600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:162764400-162764800	Enhancers	Brain Cingulate Gyrus	brain
20	chr6:162764400-162765400	Active TSS	Adipose Nuclei	Adipose
21	chr6:162764400-162766200	Enhancers	Fetal Muscle Leg	muscle
22	chr6:162764400-162766400	Enhancers	NHDF-Ad	bronchial
23	chr6:162764400-162766800	Enhancers	Brain Hippocampus Middle	brain
24	chr6:162764400-162767200	Enhancers	HMEC	breast
25	chr6:162764400-162767400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:162764400-162767600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr6:162764600-162765400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:162764600-162766400	Enhancers	Fetal Brain Male	brain
29	chr6:162764600-162767000	Enhancers	Fetal Heart	heart
30	chr6:162764800-162765400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr6:162764800-162766200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr6:162765000-162765400	Enhancers	HSMM	muscle
33	chr6:162765000-162765600	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr6:162765000-162765800	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr6:162765000-162766200	Enhancers	Brain Substantia Nigra	brain
36	chr6:162765000-162766400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:162765000-162766400	Enhancers	Brain Angular Gyrus	brain
38	chr6:162765000-162766400	Enhancers	Right Atrium	heart
39	chr6:162765000-162766800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr6:162765000-162767200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:162765000-162767200	Enhancers	NHEK	skin
42	chr6:162765200-162765600	Enhancers	Fetal Lung	lung
43	chr6:162765200-162766200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:162765200-162767000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr6:162765400-162765800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr6:162765400-162765800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr6:162765400-162765800	Enhancers	Adipose Nuclei	Adipose
48	chr6:162765400-162765800	Enhancers	Fetal Brain Female	brain
49	chr6:162765400-162765800	Enhancers	Fetal Muscle Trunk	muscle
50	chr6:162765400-162765800	Weak transcription	HSMM	muscle

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