Variant report

Variant	nsv1025817
Chromosome Location	chr6:114715204-115006108
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:693)
CpG islands
(count:428)
Chromatin interactive
region (count:20)
LncRNA
region (count:53)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:114719700-114720055	HepG2	liver:	n/a	n/a
2	ATF2	chr6:114740396-114740716	GM12878	blood:	n/a	n/a
3	ATF2	chr6:114725720-114726354	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr6:114742313-114742815	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:114742286-114742964	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:114740228-114740801	GM12878	blood:	n/a	n/a
7	BATF	chr6:114740282-114740635	GM12878	blood:	n/a	chr6:114740550-114740558
8	BATF	chr6:114740453-114740646	GM12878	blood:	n/a	chr6:114740550-114740558
9	BCL11A	chr6:114740341-114740587	GM12878	blood:	n/a	chr6:114740537-114740546
10	BCL11A	chr6:114740306-114740650	GM12878	blood:	n/a	chr6:114740537-114740546
11	BCL3	chr6:114740370-114740686	GM12878	blood:	n/a	chr6:114740537-114740546
12	BHLHE40	chr6:114740465-114740913	GM12878	blood:	n/a	n/a
13	BRCA1	chr6:114740396-114740411	GM12878	blood:	n/a	n/a
14	CCNT2	chr6:114898449-114898632	K562	blood:	n/a	n/a
15	CEBPB	chr6:114962211-114962416	A549	lung:	n/a	chr6:114962343-114962354 chr6:114962291-114962302 chr6:114962293-114962304 chr6:114962293-114962302
16	CEBPB	chr6:114842556-114842855	H1-hESC	embryonic stem cell:	n/a	chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842699-114842710 chr6:114842701-114842710 chr6:114842701-114842712 chr6:114842699-114842712
17	CEBPB	chr6:114740451-114740890	Hela-S3	cervix:	n/a	chr6:114740826-114740835 chr6:114740824-114740837 chr6:114740824-114740837 chr6:114740826-114740837
18	CEBPB	chr6:114919355-114919671	IMR90	lung:	n/a	n/a
19	CEBPB	chr6:114891254-114891267	K562	blood:	n/a	n/a
20	CEBPB	chr6:114919375-114919574	A549	lung:	n/a	n/a
21	CEBPB	chr6:114859942-114860242	IMR90	lung:	n/a	chr6:114860094-114860105
22	CEBPB	chr6:114845411-114845552	HepG2	liver:	n/a	chr6:114845457-114845468 chr6:114845455-114845468 chr6:114845455-114845466
23	CEBPB	chr6:114842591-114842887	IMR90	lung:	n/a	chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842699-114842710 chr6:114842701-114842710 chr6:114842701-114842712 chr6:114842699-114842712
24	CEBPB	chr6:114859957-114860243	HepG2	liver:	n/a	chr6:114860094-114860105
25	CEBPB	chr6:114919372-114919590	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:114942471-114942729	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:114891104-114891223	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr6:114842516-114842808	MCF-7	breast:	n/a	chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842699-114842710 chr6:114842701-114842710 chr6:114842701-114842712 chr6:114842699-114842712
29	CEBPB	chr6:114865141-114865517	MCF-7	breast:	n/a	chr6:114865365-114865378
30	CEBPB	chr6:114808463-114808511	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr6:114859965-114860164	A549	lung:	n/a	chr6:114860094-114860105
32	CEBPB	chr6:114962150-114962476	HepG2	liver:	n/a	chr6:114962343-114962354 chr6:114962291-114962302 chr6:114962293-114962304 chr6:114962293-114962302
33	CEBPB	chr6:114740419-114740988	HepG2	liver:	n/a	chr6:114740826-114740835 chr6:114740824-114740837 chr6:114740824-114740837 chr6:114740826-114740837
34	CEBPB	chr6:114842561-114842765	HepG2	liver:	n/a	chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842699-114842710 chr6:114842701-114842710 chr6:114842701-114842712 chr6:114842699-114842712
35	CEBPB	chr6:114865222-114865502	HepG2	liver:	n/a	chr6:114865365-114865378
36	CEBPB	chr6:114719661-114720027	HepG2	liver:	n/a	chr6:114719840-114719851
37	CEBPB	chr6:114893165-114893409	HepG2	liver:	n/a	chr6:114893274-114893287 chr6:114893274-114893285
38	CEBPB	chr6:114942554-114942706	K562	blood:	n/a	n/a
39	CEBPB	chr6:114719688-114719966	H1-hESC	embryonic stem cell:	n/a	chr6:114719840-114719851
40	CEBPB	chr6:114719715-114719925	HepG2	liver:	n/a	chr6:114719840-114719851
41	CEBPB	chr6:114842530-114842885	HepG2	liver:	n/a	chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842701-114842710 chr6:114842699-114842710 chr6:114842701-114842710 chr6:114842701-114842712 chr6:114842699-114842712
42	CEBPB	chr6:114933521-114933726	HepG2	liver:	n/a	chr6:114933573-114933584
43	CHD1	chr6:114753670-114753678	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr6:114746849-114747456	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr6:114741717-114742852	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr6:114753659-114753690	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr6:114751679-114751945	H1-hESC	embryonic stem cell:	n/a	n/a
48	CREB1	chr6:114740402-114740739	GM12878	blood:	n/a	n/a
49	CREB1	chr6:114740278-114740842	GM12878	blood:	n/a	n/a
50	CTCF	chr6:114945498-114945615	Medullo	brain:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:114891274-114891324	GM12892	blood:	n/a
2	chr6:114891274-114891324	GM12892	blood:	n/a
3	chr6:114815726-114815776	NT2-D1	testis:	n/a
4	chr6:114751873-114751923	K562	blood:	n/a
5	chr6:114815726-114815776	HCT-116	colon:	n/a
6	chr6:114844832-114844882	Caco-2	colon:	n/a
7	chr6:114741679-114741729	ovcar-3	ovarian:	n/a
8	chr6:114815726-114815776	MCF10A-Er-Src	breast:	n/a
9	chr6:114815726-114815776	SK-N-SH	brain:	n/a
10	chr6:114891274-114891324	HMEC	breast:	n/a
11	chr6:114751873-114751923	HCM	heart:	n/a
12	chr6:114891274-114891324	SK-N-SH_RA	brain:	n/a
13	chr6:114844832-114844882	HCT-116	colon:	n/a
14	chr6:114815726-114815776	AG04449	skin:	fetal
15	chr6:114725242-114725292	K562	blood:	n/a
16	chr6:114844832-114844882	HUVEC	blood vessel:	n/a
17	chr6:114898257-114898307	AoSMC	blood vessel:	n/a
18	chr6:114725242-114725292	HCPEpiC	choroid plexus:	n/a
19	chr6:114725242-114725292	HMEC	breast:	n/a
20	chr6:114844832-114844882	CMK	blood:	n/a
21	chr6:114725242-114725292	GM06990	blood:	n/a
22	chr6:114898257-114898307	HIPEpiC	eye:	n/a
23	chr6:114815726-114815776	HRCEpiC	kidney:	n/a
24	chr6:114751873-114751923	HRCEpiC	kidney:	n/a
25	chr6:114844832-114844882	GM12878	blood:	n/a
26	chr6:114751873-114751923	GM06990	blood:	n/a
27	chr6:114741679-114741729	HCM	heart:	n/a
28	chr6:114725242-114725292	HepG2	liver:	n/a
29	chr6:114751873-114751923	MCF-7	breast:	n/a
30	chr6:114844832-114844882	LNCaP	prostate:	n/a
31	chr6:114898257-114898307	HepG2	liver:	n/a
32	chr6:114725242-114725292	NHBE	bronchial:	n/a
33	chr6:114844832-114844882	HEEpiC	esophagus:	n/a
34	chr6:114844832-114844882	IMR90	lung:	fetal
35	chr6:114815726-114815776	HMEC	breast:	n/a
36	chr6:114751873-114751923	NH-A	brain:	n/a
37	chr6:114891274-114891324	AG04450	lung:	fetal
38	chr6:114751873-114751923	HCPEpiC	choroid plexus:	n/a
39	chr6:114725242-114725292	AG04449	skin:	fetal
40	chr6:114725242-114725292	HEK293	kidney:	embryo
41	chr6:114741679-114741729	PANC-1	pancreas:	n/a
42	chr6:114844832-114844882	H1-hESC	embryonic stem cell:	embryo
43	chr6:114898257-114898307	T-47D	breast:	n/a
44	chr6:114725242-114725292	HRE	kidney:	n/a
45	chr6:114751873-114751923	HEEpiC	esophagus:	n/a
46	chr6:114898257-114898307	ECC-1	luminal epithelium:	n/a
47	chr6:114898257-114898307	NT2-D1	testis:	n/a
48	chr6:114844832-114844882	U87	brain:	n/a
49	chr6:114844832-114844882	MCF-7	breast:	n/a
50	chr6:114725242-114725292	Hela-S3	cervix:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:114716541..114719212-chr6:114721790..114724337,2	MCF-7	breast:
2	chr6:114942645..114945445-chr6:114947272..114949668,2	K562	blood:
3	chr6:114937519..114939920-chr6:114943171..114945017,2	MCF-7	breast:
4	chr6:114810855..114812867-chr6:114817060..114819585,2	K562	blood:
5	chr6:114986516..114988404-chr6:115008661..115011647,2	K562	blood:
6	chr6:114810855..114812867-chr6:114817060..114819585,2	K562	blood:
7	chr6:114886429..114888208-chr6:114888980..114890992,2	MCF-7	breast:
8	chr6:114942645..114945445-chr6:114947272..114949668,2	K562	blood:
9	chr6:114989226..114991052-chr6:114995557..114998159,2	K562	blood:
10	chr6:114716541..114719212-chr6:114721790..114724337,2	MCF-7	breast:
11	chr6:114663101..114665339-chr6:114863866..114866852,2	MCF-7	breast:
12	chr6:114919212..114921990-chr6:114922812..114925771,2	K562	blood:
13	chr6:114662992..114664998-chr6:114748035..114750370,2	MCF-7	breast:
14	chr6:114663311..114665223-chr6:114841151..114843643,2	MCF-7	breast:
15	chr6:114886429..114888208-chr6:114888980..114890992,2	MCF-7	breast:
16	chr6:114919212..114921990-chr6:114922812..114925771,2	K562	blood:
17	chr6:114937519..114939920-chr6:114943171..114945017,2	MCF-7	breast:
18	chr6:114983151..114986089-chr6:114986914..114989213,2	K562	blood:
19	chr6:114983151..114986089-chr6:114986914..114989213,2	K562	blood:
20	chr6:114989226..114991052-chr6:114995557..114998159,2	K562	blood:

(count:53 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MARCKS-5	chr6:114792579-114792869	ENSG00000228624
2	lnc-MARCKS-5	chr6:114736766-114736776	XLOC_005441
3	lnc-MARCKS-5	chr6:114727807-114727832	ENSG00000228624
4	lnc-HS3ST5-2	chr6:114856880-114857039	XLOC_005813
5	lnc-HS3ST5-8	chr6:114905207-114905363	NONHSAT114622
6	lnc-MARCKS-5	chr6:114770080-114770195	NONHSAT114614
7	lnc-HS3ST5-1	chr6:114809752-114809916	XLOC_005812
8	lnc-MARCKS-5	chr6:114789659-114789775	ENSG00000228624
9	lnc-HS3ST5-2	chr6:114844608-114844856	XLOC_005813
10	lnc-HS3ST5-2	chr6:114866407-114866483	NONHSAT114618
11	lnc-HS3ST5-8	chr6:114916445-114916538	NONHSAT114622
12	lnc-MARCKS-5	chr6:114770124-114770195	ENSG00000228624
13	lnc-MARCKS-5	chr6:114789659-114789738	ENSG00000228624
14	lnc-HS3ST5-9	chr6:114951429-114951549	l_3243_chr6:114951300-114973176_testes
15	lnc-MARCKS-5	chr6:114777021-114777853	NONHSAT114614
16	lnc-HS3ST5-2	chr6:114864957-114865085	NONHSAT114617
17	lnc-HS3ST5-2	chr6:114864956-114865085	NONHSAT114618
18	lnc-HS3ST5-2	chr6:114864957-114865085	XLOC_005813
19	lnc-MARCKS-5	chr6:114790310-114790463	ENSG00000228624
20	lnc-HS3ST5-2	chr6:114866408-114866452	NONHSAT114617
21	lnc-HS3ST5-1	chr6:114809752-114809845	XLOC_005812
22	lnc-HS3ST5-2	chr6:114866408-114866483	XLOC_005813
23	lnc-HS3ST5-1	chr6:114802589-114803209	XLOC_005812
24	lnc-HS3ST5-8	chr6:114909282-114909902	NONHSAT114623
25	lnc-HS3ST5-9	chr6:114963573-114963732	NONHSAT114624
26	lnc-MARCKS-5	chr6:114777021-114777802	XLOC_005441
27	lnc-MARCKS-5	chr6:114777021-114777798	ENSG00000228624
28	lnc-HS3ST5-2	chr6:114844615-114844856	XLOC_005813
29	lnc-MARCKS-5	chr6:114770131-114770195	XLOC_005441
30	lnc-MARCKS-5	chr6:114770131-114770195	ENSG00000228624
31	lnc-MARCKS-19	chr6:114834500-114840824	l_3241_chr6:114823058-114843229_76bGuttman_hES
32	lnc-MARCKS-5	chr6:114746776-114746836	ENSG00000228624
33	lnc-MARCKS-19	chr6:114823059-114823138	l_3241_chr6:114823058-114843229_76bGuttman_hES
34	lnc-HS3ST5-7	chr6:114776942-114777358	NONHSAT114610
35	lnc-MARCKS-5	chr6:114770131-114770195	ENSG00000228624
36	lnc-HS3ST5-9	chr6:114971650-114971778	l_3243_chr6:114951300-114973176_testes
37	lnc-HS3ST5-7	chr6:114744178-114745122	NONHSAT114610
38	lnc-HS3ST5-7	chr6:114730053-114731474	NONHSAT114610
39	lnc-MARCKS-5	chr6:114775079-114775243	XLOC_005441
40	lnc-HS3ST5-2	chr6:114844607-114844856	NONHSAT114618
41	lnc-HS3ST5-2	chr6:114866408-114866452	NONHSAT114621
42	lnc-HS3ST5-9	chr6:114951301-114951426	l_3243_chr6:114951300-114973176_testes
43	lnc-HS3ST5-8	chr6:114916445-114916609	NONHSAT114623
44	lnc-HS3ST5-2	chr6:114856880-114857230	NONHSAT114621
45	lnc-HS3ST5-1	chr6:114798514-114798670	XLOC_005812
46	lnc-HS3ST5-9	chr6:114973101-114973176	l_3243_chr6:114951300-114973176_testes
47	lnc-HS3ST5-2	chr6:114809761-114809913	NONHSAT114617
48	lnc-MARCKS-19	chr6:114840834-114843229	l_3241_chr6:114823058-114843229_76bGuttman_hES
49	lnc-MARCKS-5	chr6:114759133-114759230	ENSG00000228624
50	lnc-HS3ST5-9	chr6:114951308-114951549	NONHSAT114624

No data

Variant related genes	Relation type
ENSG00000228624	TF binding region
ENSG00000232395	TF binding region
ENSG00000226079	TF binding region
ENSG00000228624	CpG island
ENSG00000232395	CpG island
ENSG00000226079	CpG island
ENSG00000249853	chromatin interactions
NTRK3	miRNA target sites
HN1L	miRNA target sites
ZNF638	miRNA target sites
YARS2	miRNA target sites
THBS1	miRNA target sites
TMEM41A	miRNA target sites
AHNAK2	miRNA target sites
MXI1	miRNA target sites
CHRAC1	miRNA target sites
UBE2D3	miRNA target sites
HMGN2	miRNA target sites
TP53	miRNA target sites
TLK1	miRNA target sites

Extended variants
information (count: 6674 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:6674 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569029266	chr6:114715209-114715210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs564754282	chr6:114715215-114715216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs550675474	chr6:114715305-114715306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568971641	chr6:114715306-114715307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539452468	chr6:114715362-114715363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs35450008	chr6:114715394-114715395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532432046	chr6:114715430-114715431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12202564	chr6:114715463-114715464	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12196343	chr6:114715495-114715496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs534954264	chr6:114715609-114715610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145979223	chr6:114715668-114715669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73546503	chr6:114715675-114715676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372471263	chr6:114715685-114715686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12197768	chr6:114715705-114715706	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs73769408	chr6:114715735-114715736	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs370635587	chr6:114715829-114715830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570148215	chr6:114715874-114715875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563374161	chr6:114715886-114715887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537184680	chr6:114715975-114715976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190128636	chr6:114715995-114715996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142072637	chr6:114716003-114716004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558029046	chr6:114716007-114716008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564102907	chr6:114716088-114716089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182592209	chr6:114716103-114716104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186930232	chr6:114716104-114716105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375831890	chr6:114716132-114716133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73769409	chr6:114716199-114716200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190747807	chr6:114716200-114716201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184239039	chr6:114716282-114716283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs36058420	chr6:114716337-114716338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558892262	chr6:114716346-114716347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569106419	chr6:114716367-114716368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188591627	chr6:114716375-114716376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551446523	chr6:114716397-114716398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193166974	chr6:114716403-114716404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540746103	chr6:114716423-114716424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553249490	chr6:114716446-114716447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370626628	chr6:114716478-114716479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4090284	chr6:114716486-114716487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184227679	chr6:114716516-114716517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs139204538	chr6:114716525-114716526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367688644	chr6:114716553-114716554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534980062	chr6:114716560-114716561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537899700	chr6:114716570-114716571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34144978	chr6:114716591-114716592	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557539939	chr6:114716603-114716604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35324648	chr6:114716622-114716623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115471020	chr6:114716641-114716642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539804130	chr6:114716655-114716656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187097544	chr6:114716696-114716697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Salivary gland tumor	18059337	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Acute myeloid leukemia	19651600	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114701600-114719400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:114711600-114719600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr6:114711800-114715600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:114711800-114725000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr6:114712200-114719400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr6:114713400-114721200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr6:114715600-114715800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:114719200-114721800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:114719400-114719600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr6:114719400-114720000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:114719400-114720000	Enhancers	H9 Cell Line	embryonic stem cell
12	chr6:114719400-114720400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:114719400-114720400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:114719400-114720400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:114719400-114720400	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:114719400-114720400	Enhancers	HepG2	liver
17	chr6:114719600-114720400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr6:114719600-114720800	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr6:114720000-114723000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr6:114720000-114740200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr6:114720200-114720400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr6:114720400-114724600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr6:114720400-114725000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr6:114720400-114725200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr6:114720400-114725200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr6:114720400-114725200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr6:114720800-114721200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr6:114721200-114721400	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr6:114721200-114721600	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr6:114721400-114724400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr6:114721600-114724600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr6:114721800-114724000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr6:114723000-114723400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:114723000-114723400	Active TSS	Brain Substantia Nigra	brain
35	chr6:114724000-114726800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr6:114724400-114724600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr6:114724600-114725200	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr6:114724600-114726200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr6:114724600-114726600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr6:114725000-114726400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr6:114725000-114726400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr6:114725200-114725400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:114725200-114726400	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr6:114725200-114726400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:114725200-114727000	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr6:114725400-114725800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr6:114725800-114726000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr6:114725800-114726600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:114726000-114731000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:114726200-114731400	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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