Variant report

Variant	nsv428501
Chromosome Location	chr7:15666307-15817662
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	BACH1	chr7:15727089-15727614	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:15725890-15726236	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr7:15691392-15691632	GM12878	blood:	n/a	chr7:15691541-15691550
4	BHLHE40	chr7:15691406-15691662	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:15698323-15698507	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:15677006-15677205	GM12878	blood:	n/a	n/a
7	CCNT2	chr7:15718332-15718546	K562	blood:	n/a	n/a
8	CEBPB	chr7:15725843-15726020	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:15812426-15812630	HepG2	liver:	n/a	chr7:15812544-15812555
10	CEBPB	chr7:15815945-15816122	HepG2	liver:	n/a	chr7:15816020-15816033 chr7:15816021-15816032 chr7:15816020-15816033 chr7:15816020-15816033
11	CEBPB	chr7:15709075-15709428	IMR90	lung:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
12	CEBPB	chr7:15686958-15687201	HepG2	liver:	n/a	chr7:15687077-15687088
13	CEBPB	chr7:15671142-15671414	HepG2	liver:	n/a	chr7:15671295-15671306 chr7:15671283-15671294
14	CEBPB	chr7:15709096-15709399	A549	lung:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
15	CEBPB	chr7:15724934-15725159	Hela-S3	cervix:	n/a	chr7:15725044-15725053 chr7:15725043-15725054 chr7:15725044-15725053 chr7:15725044-15725053 chr7:15725042-15725055 chr7:15725044-15725053 chr7:15725042-15725053
16	CEBPB	chr7:15678031-15678341	Hela-S3	cervix:	n/a	chr7:15678174-15678185
17	CEBPB	chr7:15752534-15752611	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:15710902-15711209	HepG2	liver:	n/a	chr7:15711028-15711039 chr7:15711082-15711093 chr7:15711027-15711040
19	CEBPB	chr7:15724858-15725241	IMR90	lung:	n/a	chr7:15725044-15725053 chr7:15725043-15725054 chr7:15725044-15725053 chr7:15725044-15725053 chr7:15725042-15725055 chr7:15725044-15725053 chr7:15725042-15725053
20	CEBPB	chr7:15709074-15709419	MCF-7	breast:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
21	CEBPB	chr7:15678069-15678328	A549	lung:	n/a	chr7:15678174-15678185
22	CEBPB	chr7:15724582-15725371	H1-hESC	embryonic stem cell:	n/a	chr7:15725044-15725053 chr7:15725043-15725054 chr7:15725044-15725053 chr7:15725044-15725053 chr7:15725042-15725055 chr7:15725044-15725053 chr7:15725042-15725053
23	CEBPB	chr7:15709051-15709434	H1-hESC	embryonic stem cell:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
24	CEBPB	chr7:15678001-15678343	HepG2	liver:	n/a	chr7:15678174-15678185
25	CEBPB	chr7:15736390-15736571	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:15709038-15709412	A549	lung:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
27	CEBPB	chr7:15710922-15711201	IMR90	lung:	n/a	chr7:15711028-15711039 chr7:15711082-15711093 chr7:15711027-15711040
28	CEBPB	chr7:15701369-15701625	A549	lung:	n/a	chr7:15701544-15701555 chr7:15701518-15701529 chr7:15701544-15701557 chr7:15701544-15701557 chr7:15701518-15701527 chr7:15701545-15701556 chr7:15701516-15701527 chr7:15701516-15701529
29	CEBPB	chr7:15709079-15709423	A549	lung:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
30	CEBPB	chr7:15724896-15725214	K562	blood:	n/a	chr7:15725044-15725053 chr7:15725043-15725054 chr7:15725044-15725053 chr7:15725044-15725053 chr7:15725042-15725055 chr7:15725044-15725053 chr7:15725042-15725053
31	CEBPB	chr7:15678011-15678347	IMR90	lung:	n/a	chr7:15678174-15678185
32	CEBPB	chr7:15709099-15709410	K562	blood:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
33	CEBPB	chr7:15709058-15709434	HepG2	liver:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
34	CEBPB	chr7:15724875-15725240	HepG2	liver:	n/a	chr7:15725044-15725053 chr7:15725043-15725054 chr7:15725044-15725053 chr7:15725044-15725053 chr7:15725042-15725055 chr7:15725044-15725053 chr7:15725042-15725053
35	CEBPB	chr7:15775330-15775639	HepG2	liver:	n/a	chr7:15775488-15775499
36	CEBPB	chr7:15672042-15672219	A549	lung:	n/a	n/a
37	CEBPB	chr7:15678055-15678267	K562	blood:	n/a	chr7:15678174-15678185
38	CEBPB	chr7:15701375-15701701	HepG2	liver:	n/a	chr7:15701544-15701555 chr7:15701518-15701529 chr7:15701544-15701557 chr7:15701544-15701557 chr7:15701518-15701527 chr7:15701545-15701556 chr7:15701516-15701527 chr7:15701516-15701529
39	CEBPB	chr7:15724880-15725230	A549	lung:	n/a	chr7:15725044-15725053 chr7:15725043-15725054 chr7:15725044-15725053 chr7:15725044-15725053 chr7:15725042-15725055 chr7:15725044-15725053 chr7:15725042-15725053
40	CEBPB	chr7:15671219-15671337	A549	lung:	n/a	chr7:15671295-15671306 chr7:15671283-15671294
41	CEBPB	chr7:15709089-15709416	MCF-7	breast:	n/a	chr7:15709242-15709251 chr7:15709239-15709256 chr7:15709242-15709251 chr7:15709240-15709253 chr7:15709242-15709251 chr7:15709240-15709251
42	CHD1	chr7:15725267-15725482	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr7:15725165-15727652	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr7:15760660-15760810	GM12867	blood:	n/a	chr7:15760701-15760717
45	CTCF	chr7:15682640-15682790	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr7:15760620-15760770	HL-60	blood:	n/a	chr7:15760701-15760717
47	CTCF	chr7:15727360-15727510	HRE	kidney:	n/a	n/a
48	CTCF	chr7:15760620-15760770	HEEpiC	esophagus:	n/a	chr7:15760701-15760717
49	CTCF	chr7:15760540-15760782	A549	lung:	n/a	chr7:15760701-15760717
50	CTCF	chr7:15760595-15760832	T-47D	breast:	n/a	chr7:15760701-15760717

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:15726411-15726461	HCPEpiC	choroid plexus:	n/a
2	chr7:15725196-15725246	BJ	skin:	n/a
3	chr7:15727525-15727575	AG04450	lung:	fetal
4	chr7:15727525-15727575	SAEC	small airway:	n/a
5	chr7:15726166-15726216	HUVEC	blood vessel:	n/a
6	chr7:15726411-15726461	HCPEpiC	choroid plexus:	n/a
7	chr7:15725196-15725246	BJ	skin:	n/a
8	chr7:15727525-15727575	AG04450	lung:	fetal
9	chr7:15727525-15727575	SAEC	small airway:	n/a
10	chr7:15726166-15726216	HUVEC	blood vessel:	n/a
11	chr7:15726166-15726216	HRE	kidney:	n/a
12	chr7:15727127-15727177	HCF	heart:	n/a
13	chr7:15727127-15727177	T-47D	breast:	n/a
14	chr7:15726411-15726461	ProgFib	skin:	n/a
15	chr7:15726064-15726114	PANC-1	pancreas:	n/a
16	chr7:15726411-15726461	AG09319	gingival:	n/a
17	chr7:15725086-15725136	NH-A	brain:	n/a
18	chr7:15726466-15726516	NT2-D1	testis:	n/a
19	chr7:15727127-15727177	A549	lung:	n/a
20	chr7:15725086-15725136	ProgFib	skin:	n/a
21	chr7:15726166-15726216	GM12892	blood:	n/a
22	chr7:15726821-15726871	PFSK-1	brain:	n/a
23	chr7:15726166-15726216	RPTEC	kidney:	n/a
24	chr7:15726411-15726461	NHBE	bronchial:	n/a
25	chr7:15727525-15727575	GM06990	blood:	n/a
26	chr7:15727598-15727648	HCT-116	colon:	n/a
27	chr7:15764568-15764618	LNCaP	prostate:	n/a
28	chr7:15725196-15725246	HAEpiC	amniotic membrane:	n/a
29	chr7:15727598-15727648	AG09319	gingival:	n/a
30	chr7:15727127-15727177	AG04450	lung:	fetal
31	chr7:15726821-15726871	Hela-S3	cervix:	n/a
32	chr7:15727441-15727491	NH-A	brain:	n/a
33	chr7:15726821-15726871	HL-60	blood:	n/a
34	chr7:15726166-15726216	GM19239	blood:	n/a
35	chr7:15727525-15727575	IMR90	lung:	fetal
36	chr7:15726466-15726516	GM12891	blood:	n/a
37	chr7:15726649-15726699	HIPEpiC	eye:	n/a
38	chr7:15726064-15726114	T-47D	breast:	n/a
39	chr7:15725086-15725136	BJ	skin:	n/a
40	chr7:15725086-15725136	HRPEpiC	eye:	n/a
41	chr7:15727525-15727575	LNCaP	prostate:	n/a
42	chr7:15727598-15727648	PFSK-1	brain:	n/a
43	chr7:15764568-15764618	NHDF-neo	bronchial:	n/a
44	chr7:15725322-15725372	HEK293	kidney:	embryo
45	chr7:15725652-15725702	ECC-1	luminal epithelium:	n/a
46	chr7:15725086-15725136	MCF10A-Er-Src	breast:	n/a
47	chr7:15725196-15725246	U87	brain:	n/a
48	chr7:15726411-15726461	GM06990	blood:	n/a
49	chr7:15726479-15726529	HNPCEpiC	eye:	n/a
50	chr7:15726466-15726516	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:14757083..14757697-chr7:15760291..15761216,2	MCF-7	breast:
2	chr7:15364860..15366538-chr7:15760053..15761291,7	MCF-7	breast:
3	chr7:15757039..15758672-chr7:15760864..15763704,2	K562	blood:
4	chr7:15365412..15365978-chr7:15759570..15760468,2	MCF-7	breast:
5	chr7:15365379..15366315-chr7:15760483..15761223,4	MCF-7	breast:
6	chr7:15344411..15345401-chr7:15760276..15761708,4	MCF-7	breast:
7	chr1:206717972..206718558-chr7:15736544..15737378,2	MCF-7	breast:
8	chr7:15758705..15760238-chr7:15762223..15764953,2	K562	blood:
9	chr7:15760297..15761259-chr7:15928859..15929813,2	MCF-7	breast:
10	chr7:15543347..15544306-chr7:15760242..15761135,3	MCF-7	breast:
11	chr7:15744130..15746102-chr7:15747720..15750645,2	K562	blood:
12	chr7:15702914..15705810-chr7:15749778..15751853,2	K562	blood:
13	chr7:15758705..15760238-chr7:15762223..15764953,2	K562	blood:
14	chr7:15744130..15746102-chr7:15747720..15750645,2	K562	blood:
15	chr7:15702914..15705810-chr7:15749778..15751853,2	K562	blood:
16	chr7:15760649..15761697-chr7:16110615..16111343,3	MCF-7	breast:
17	chr7:15344361..15344992-chr7:15760353..15761140,2	MCF-7	breast:
18	chr7:15798256..15800114-chr7:15802813..15804689,2	K562	blood:
19	chr7:15798256..15800114-chr7:15802813..15804689,2	K562	blood:
20	chr7:15757039..15758672-chr7:15760864..15763704,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC006035.2-3	chr7:15717088-15717272	ENSG00000237070
2	lnc-AC006035.2-3	chr7:15718539-15721605	ENSG00000237070
3	lnc-AC006035.2-2	chr7:15728053-15728077	XLOC_005991
4	lnc-MEOX2-3	chr7:15741060-15741377	NONHSAT119286
5	lnc-AGMO-1	chr7:15695225-15695379	NONHSAT119279
6	lnc-MEOX2-3	chr7:15741057-15741377	NONHSAT119285
7	lnc-AC006035.2-2	chr7:15728003-15728077	NR_110094
8	lnc-AC006035.2-2	chr7:15734495-15736517	NR_110094
9	lnc-AC006035.2-2	chr7:15734495-15735116	XLOC_005991
10	lnc-AC006035.2-2	chr7:15735961-15736507	XLOC_005991
11	lnc-AC006035.2-2	chr7:15728003-15728077	XLOC_005991
12	lnc-AC006035.2-7	chr7:15694528-15694602	NONHSAT119278
13	lnc-AC006035.2-3	chr7:15707572-15707921	ENSG00000237070
14	lnc-AC006035.2-7	chr7:15701004-15703032	l_3365_chr7:15694555-15702238_placenta
15	lnc-AC006035.2-7	chr7:15701020-15701641	NONHSAT119278
16	lnc-AC006035.2-2	chr7:15734495-15735098	XLOC_005991
17	lnc-AC006035.2-2	chr7:15734578-15735098	XLOC_005991
18	lnc-AGMO-1	chr7:15696848-15697004	NONHSAT119279
19	lnc-AC006035.2-3	chr7:15715645-15715785	ENSG00000237070
20	lnc-AC006035.2-2	chr7:15728026-15728077	XLOC_005991
21	lnc-AC006035.2-2	chr7:15735961-15736507	XLOC_005991
22	lnc-AC006035.2-7	chr7:15694556-15694602	l_3365_chr7:15694555-15702238_placenta

Variant related genes	Relation type
MEOX2	TF binding region
ENSG00000237070	TF binding region
RPL36AP26	TF binding region
ENSG00000225974	TF binding region
ENSG00000229108	TF binding region
MEOX2	CpG island
ENSG00000237070	CpG island
RPL36AP26	CpG island
ENSG00000225974	CpG island
ENSG00000229108	CpG island
HMGA2	miRNA target sites
C9orf40	miRNA target sites

Extended variants
information (count: 5706 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:5706 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144093914	chr7:15666330-15666331	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540917999	chr7:15666343-15666344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181631911	chr7:15666358-15666359	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563641807	chr7:15666407-15666408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574755420	chr7:15666413-15666414	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375199918	chr7:15666450-15666451	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112262227	chr7:15666458-15666459	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569517497	chr7:15666511-15666512	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371557289	chr7:15666516-15666517	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370166690	chr7:15666547-15666548	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541993792	chr7:15666581-15666582	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563767319	chr7:15666601-15666602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531030875	chr7:15666602-15666603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560701668	chr7:15666624-15666625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146520307	chr7:15666640-15666641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs564779153	chr7:15666643-15666644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs202182874	chr7:15666644-15666645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547309136	chr7:15666655-15666656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565566970	chr7:15666685-15666686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113051023	chr7:15666687-15666688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544600165	chr7:15666688-15666689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529659583	chr7:15666696-15666697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548002691	chr7:15666697-15666698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569686467	chr7:15666698-15666699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113309389	chr7:15666749-15666750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs113782262	chr7:15666750-15666751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113001727	chr7:15666751-15666752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs570313531	chr7:15666778-15666779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141068618	chr7:15666779-15666780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552834542	chr7:15666804-15666805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574754777	chr7:15666807-15666808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560428266	chr7:15666818-15666819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542176643	chr7:15666828-15666829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs58533838	chr7:15666868-15666869	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs575650605	chr7:15666884-15666885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546309288	chr7:15666894-15666895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531999847	chr7:15666904-15666905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564715808	chr7:15666921-15666922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528673575	chr7:15666954-15666955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540961199	chr7:15666986-15666987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562379173	chr7:15667007-15667008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529660830	chr7:15667009-15667010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548127892	chr7:15667015-15667016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552118968	chr7:15667020-15667021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17168920	chr7:15667079-15667080	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs186023902	chr7:15667126-15667127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551835742	chr7:15667129-15667130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149777966	chr7:15667137-15667138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17168922	chr7:15667147-15667148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552869667	chr7:15667156-15667157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15645400-15668200	Weak transcription	Right Ventricle	heart
2	chr7:15647800-15668000	Weak transcription	Fetal Stomach	stomach
3	chr7:15652000-15683400	Weak transcription	Adipose Nuclei	Adipose
4	chr7:15657400-15673000	Weak transcription	Psoas Muscle	Psoas
5	chr7:15660800-15668200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:15661400-15668000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:15663400-15666400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:15663800-15666600	Strong transcription	Fetal Muscle Trunk	muscle
9	chr7:15664000-15666600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:15664000-15666800	Enhancers	NHDF-Ad	bronchial
11	chr7:15664200-15668000	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr7:15664400-15666800	Enhancers	Osteobl	bone
13	chr7:15664400-15668000	Weak transcription	Fetal Muscle Leg	muscle
14	chr7:15664400-15668000	Weak transcription	Left Ventricle	heart
15	chr7:15664800-15666800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr7:15665000-15668200	Weak transcription	NHLF	lung
17	chr7:15665200-15666800	Enhancers	HUVEC	blood vessel
18	chr7:15665400-15668000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr7:15666000-15666400	Strong transcription	Fetal Lung	lung
20	chr7:15666400-15668200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr7:15666600-15668000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr7:15666600-15682600	Weak transcription	Fetal Muscle Trunk	muscle
23	chr7:15666800-15667000	Weak transcription	HUVEC	blood vessel
24	chr7:15666800-15667800	Weak transcription	NHDF-Ad	bronchial
25	chr7:15666800-15667800	Weak transcription	Osteobl	bone
26	chr7:15666800-15668200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr7:15667200-15668000	Bivalent Enhancer	Fetal Lung	lung
28	chr7:15667800-15669600	Enhancers	Osteobl	bone
29	chr7:15667800-15670000	Enhancers	NHDF-Ad	bronchial
30	chr7:15668000-15668400	Flanking Bivalent TSS/Enh	Fetal Lung	lung
31	chr7:15668000-15668400	Enhancers	Left Ventricle	heart
32	chr7:15668000-15668400	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr7:15668000-15668600	Enhancers	Fetal Muscle Leg	muscle
34	chr7:15668000-15669200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:15668000-15669200	Enhancers	Fetal Stomach	stomach
36	chr7:15668000-15669400	Enhancers	Muscle Satellite Cultured Cells	--
37	chr7:15668000-15670600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:15668200-15668400	Enhancers	Right Ventricle	heart
39	chr7:15668200-15668600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr7:15668200-15668800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr7:15668200-15668800	Enhancers	NHLF	lung
42	chr7:15668200-15669200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr7:15668200-15669200	Enhancers	NH-A	brain
44	chr7:15668200-15669600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr7:15668400-15668800	Bivalent Enhancer	Fetal Lung	lung
46	chr7:15668400-15669200	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr7:15668400-15677000	Weak transcription	Left Ventricle	heart
48	chr7:15668600-15676200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:15668800-15669800	Weak transcription	NHLF	lung
50	chr7:15669200-15669600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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