Variant report

Variant	esv2764028
Chromosome Location	chr7:78874740-79112630
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2187)
CpG islands
(count:2324)
Chromatin interactive
region (count:24)
LncRNA
region (count:58)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2187 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:78901378-78901750	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:79091709-79092003	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:79080953-79082067	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:78901558-78901758	K562	blood:	n/a	n/a
5	ARID3A	chr7:79049809-79050297	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:78922900-78923304	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:78937579-78937886	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:79083406-79083410	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:79064193-79064646	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:79090760-79091411	HepG2	liver:	n/a	n/a
11	ATF3	chr7:78922855-78923475	A549	lung:	n/a	n/a
12	ATF3	chr7:79081552-79081741	HepG2	liver:	n/a	n/a
13	ATF3	chr7:79049698-79050229	A549	lung:	n/a	n/a
14	ATF3	chr7:79081448-79081794	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr7:78922705-78923470	A549	lung:	n/a	n/a
16	ATF3	chr7:79081477-79081784	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr7:78910752-78911100	K562	blood:	n/a	n/a
18	BACH1	chr7:79081632-79081831	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:78910738-78911098	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:79083014-79083901	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr7:79049614-79050242	A549	lung:	n/a	n/a
22	BCL3	chr7:78922698-78923411	A549	lung:	n/a	n/a
23	BCL3	chr7:79090906-79091522	A549	lung:	n/a	n/a
24	BCL3	chr7:78976025-78976341	GM12878	blood:	n/a	n/a
25	BCL3	chr7:78972497-78972744	GM12878	blood:	n/a	n/a
26	BCL3	chr7:78912151-78913001	A549	lung:	n/a	n/a
27	BCL3	chr7:79081311-79081823	A549	lung:	n/a	n/a
28	BCL3	chr7:78922608-78923439	A549	lung:	n/a	n/a
29	BHLHE40	chr7:79081336-79082559	HepG2	liver:	n/a	chr7:79081666-79081675 chr7:79081664-79081677 chr7:79081667-79081676 chr7:79081666-79081675
30	BHLHE40	chr7:78923013-78923297	HepG2	liver:	n/a	n/a
31	BHLHE40	chr7:79081521-79081847	HepG2	liver:	n/a	chr7:79081666-79081675 chr7:79081664-79081677 chr7:79081667-79081676 chr7:79081666-79081675
32	BHLHE40	chr7:79081520-79081884	A549	lung:	n/a	chr7:79081666-79081675 chr7:79081664-79081677 chr7:79081667-79081676 chr7:79081666-79081675
33	BHLHE40	chr7:79082914-79083646	HepG2	liver:	n/a	n/a
34	BHLHE40	chr7:79081417-79081819	HepG2	liver:	n/a	chr7:79081666-79081675 chr7:79081664-79081677 chr7:79081667-79081676 chr7:79081666-79081675
35	BRCA1	chr7:79082346-79082437	HepG2	liver:	n/a	n/a
36	BRCA1	chr7:79083157-79083585	HepG2	liver:	n/a	n/a
37	BRCA1	chr7:78927627-78927704	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr7:79081896-79081993	HepG2	liver:	n/a	n/a
39	BRCA1	chr7:79081154-79081543	HepG2	liver:	n/a	n/a
40	BRCA1	chr7:79083435-79083594	H1-hESC	embryonic stem cell:	n/a	n/a
41	CCNT2	chr7:79109715-79109825	K562	blood:	n/a	n/a
42	CCNT2	chr7:78877079-78877222	K562	blood:	n/a	n/a
43	CEBPB	chr7:79091024-79091356	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr7:79027775-79028070	A549	lung:	n/a	chr7:79028020-79028031
45	CEBPB	chr7:79049501-79050238	IMR90	lung:	n/a	chr7:79050027-79050038
46	CEBPB	chr7:78911393-78911718	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr7:78911355-78911778	MCF-7	breast:	n/a	n/a
48	CEBPB	chr7:78922915-78923422	A549	lung:	n/a	n/a
49	CEBPB	chr7:78911346-78911747	IMR90	lung:	n/a	n/a
50	CEBPB	chr7:79089670-79089963	HepG2	liver:	n/a	n/a

(count:2324 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:79084048-79084098	HepG2	liver:	n/a
2	chr7:79083753-79083803	HAEpiC	amniotic membrane:	n/a
3	chr7:79080535-79080585	HepG2	liver:	n/a
4	chr7:79083445-79083495	AG10803	skin:	n/a
5	chr7:79050007-79050057	NH-A	brain:	n/a
6	chr7:79084196-79084246	Hela-S3	cervix:	n/a
7	chr7:79084048-79084098	HepG2	liver:	n/a
8	chr7:79083753-79083803	HAEpiC	amniotic membrane:	n/a
9	chr7:79080535-79080585	HepG2	liver:	n/a
10	chr7:79083445-79083495	AG10803	skin:	n/a
11	chr7:79050007-79050057	NH-A	brain:	n/a
12	chr7:79084196-79084246	Hela-S3	cervix:	n/a
13	chr7:79084038-79084088	Jurkat	blood:	n/a
14	chr7:79081807-79081857	HIPEpiC	eye:	n/a
15	chr7:79083753-79083803	HCF	heart:	n/a
16	chr7:79082393-79082443	SK-N-SH_RA	brain:	n/a
17	chr7:79082038-79082088	BE2_C	brain:	n/a
18	chr7:79084166-79084216	AG04450	lung:	fetal
19	chr7:79083944-79083994	A549	lung:	n/a
20	chr7:79082647-79082697	HNPCEpiC	eye:	n/a
21	chr7:79081455-79081505	HEK293	kidney:	embryo
22	chr7:79081666-79081716	BJ	skin:	n/a
23	chr7:79083408-79083458	MCF10A-Er-Src	breast:	n/a
24	chr7:79082291-79082341	HRCEpiC	kidney:	n/a
25	chr7:79080588-79080638	GM12891	blood:	n/a
26	chr7:79050007-79050057	IMR90	lung:	fetal
27	chr7:78947094-78947144	HCM	heart:	n/a
28	chr7:79082393-79082443	AG04450	lung:	fetal
29	chr7:79083408-79083458	HCT-116	colon:	n/a
30	chr7:79081791-79081841	SK-N-SH_RA	brain:	n/a
31	chr7:79083507-79083557	NHDF-neo	bronchial:	n/a
32	chr7:79083408-79083458	HUVEC	blood vessel:	n/a
33	chr7:79083635-79083685	ovcar-3	ovarian:	n/a
34	chr7:79084038-79084088	ovcar-3	ovarian:	n/a
35	chr7:79083408-79083458	NB4	blood:	n/a
36	chr7:79082186-79082236	A549	lung:	n/a
37	chr7:79083056-79083106	PANC-1	pancreas:	n/a
38	chr7:78948064-78948114	AG04450	lung:	fetal
39	chr7:79084048-79084098	PANC-1	pancreas:	n/a
40	chr7:79082647-79082697	HRCEpiC	kidney:	n/a
41	chr7:78948064-78948114	HL-60	blood:	n/a
42	chr7:79084127-79084177	GM19239	blood:	n/a
43	chr7:79080588-79080638	Hela-S3	cervix:	n/a
44	chr7:78947094-78947144	AG09309	skin:	n/a
45	chr7:79083507-79083557	GM19239	blood:	n/a
46	chr7:79082531-79082581	GM12892	blood:	n/a
47	chr7:79082647-79082697	NHDF-neo	bronchial:	n/a
48	chr7:79083635-79083685	AG04449	skin:	fetal
49	chr7:79084011-79084061	HNPCEpiC	eye:	n/a
50	chr7:79084048-79084098	HUVEC	blood vessel:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:79011096..79013975-chr7:79014209..79017133,2	MCF-7	breast:
2	chr7:78977361..78978896-chr7:79043903..79046403,2	K562	blood:
3	chr7:78936738..78938800-chr7:78940617..78942122,2	MCF-7	breast:
4	chr7:79017286..79019685-chr7:79023052..79025297,2	MCF-7	breast:
5	chr17:34140775..34141275-chr7:78979249..78979789,2	NB4	blood:
6	chr7:78949110..78950996-chr7:78951230..78952758,2	MCF-7	breast:
7	chr7:79095989..79098582-chr7:79174957..79177392,2	K562	blood:
8	chr7:78927198..78927954-chr7:79647855..79648713,2	MCF-7	breast:
9	chr7:78901152..78901823-chr7:79676996..79677853,2	MCF-7	breast:
10	chr7:78927254..78927762-chr7:79370740..79371579,2	MCF-7	breast:
11	chr7:79011096..79013975-chr7:79014209..79017133,2	MCF-7	breast:
12	chr7:78926978..78927922-chr7:79676854..79677685,3	MCF-7	breast:
13	chr7:78900547..78903338-chr7:78905670..78907338,2	MCF-7	breast:
14	chr7:78936738..78938800-chr7:78940617..78942122,2	MCF-7	breast:
15	chr7:78949110..78950996-chr7:78951230..78952758,2	MCF-7	breast:
16	chr7:79017286..79019685-chr7:79023052..79025297,2	MCF-7	breast:
17	chr7:79053495..79057290-chr7:79076509..79078816,3	MCF-7	breast:
18	chr7:79053495..79057290-chr7:79076509..79078816,3	MCF-7	breast:
19	chr7:79036736..79038245-chr7:79041747..79043274,2	K562	blood:
20	chr7:79036736..79038245-chr7:79041747..79043274,2	K562	blood:
21	chr7:78901096..78902018-chr7:79648257..79649001,2	MCF-7	breast:
22	chr7:78977361..78978896-chr7:79043903..79046403,2	K562	blood:
23	chr7:78900547..78903338-chr7:78905670..78907338,2	MCF-7	breast:
24	chr14:28170954..28172471-chr7:78954883..78956578,2	MCF-7	breast:

(count:58 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-2	chr7:79088163-79088315	ENSG00000234456.2
2	lnc-GNAI1-2	chr7:79082427-79082507	ENSG00000234456.2
3	lnc-GNAI1-2	chr7:79088021-79088315	ENSG00000234456.2
4	lnc-GNAI1-2	chr7:79088852-79096786	ENSG00000234456.3
5	lnc-GNAI1-2	chr7:79088163-79088256	ENSG00000234456.2
6	lnc-GNAI1-2	chr7:79100099-79100516	ENSG00000234456.2
7	lnc-GNAI1-2	chr7:79091029-79091950	NONHSAT121718
8	lnc-GNAI1-2	chr7:79085429-79085496	NONHSAT121719
9	lnc-GNAI1-2	chr7:79088852-79089155	ENSG00000234456.2
10	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121723
11	lnc-GNAI1-2	chr7:79088852-79093061	ENSG00000234456.2
12	lnc-MAGI2-1	chr7:79092173-79093984	XLOC_006507
13	lnc-GNAI1-2	chr7:79100099-79100512	ENSG00000234456.2
14	lnc-GNAI1-2	chr7:79099743-79099995	ENSG00000234456.2
15	lnc-GNAI1-2	chr7:79084202-79084325	NONHSAT121718
16	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121719
17	lnc-GNAI1-2	chr7:79082225-79082507	NONHSAT121703
18	lnc-GNAI1-2	chr7:79100099-79100431	NONHSAT121719
19	lnc-GNAI1-2	chr7:79100099-79100515	NONHSAT121718
20	lnc-GNAI1-2	chr7:79100099-79100185	NONHSAT121703
21	lnc-GNAI1-2	chr7:79098343-79098762	NONHSAT121725
22	lnc-GNAI1-7	chr7:78926788-78930237	ucscGeneNc_uc010lea_1
23	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121718
24	lnc-GNAI1-2	chr7:79082474-79082507	ENSG00000234456.2
25	lnc-GNAI1-2	chr7:79088163-79088315	ENSG00000234456.2
26	lnc-GNAI1-2	chr7:79088163-79088315	ENSG00000234456.2
27	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121703
28	lnc-GNAI1-2	chr7:79100099-79100170	NONHSAT121723
29	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121717
30	lnc-GNAI1-2	chr7:79088021-79088315	ENSG00000234456.3
31	lnc-GNAI1-6	chr7:78982726-78983708	NONHSAT121700
32	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121717
33	lnc-GNAI1-2	chr7:79099910-79099995	NONHSAT121725
34	lnc-GNAI1-2	chr7:79100099-79100447	NONHSAT121717
35	lnc-GNAI1-2	chr7:79084149-79084323	ENSG00000234456.2
36	lnc-GNAI1-2	chr7:79100099-79100452	NONHSAT121725
37	lnc-GNAI1-2	chr7:79099907-79099997	NONHSAT121718
38	lnc-GNAI1-2	chr7:79088852-79090496	NONHSAT121718
39	lnc-MAGI2-1	chr7:79093975-79096779	ENSG00000249657
40	lnc-GNAI1-2	chr7:79088120-79088315	NONHSAT121723
41	lnc-GNAI1-2	chr7:79083830-79084323	NONHSAT121717
42	lnc-MAGI2-1	chr7:79085481-79085594	ENSG00000249657
43	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121716
44	lnc-GNAI1-2	chr7:79088852-79089916	NONHSAT121716
45	lnc-GNAI1-2	chr7:79088163-79088315	NONHSAT121719
46	lnc-GNAI1-2	chr7:79100099-79100524	ENSG00000234456.2
47	lnc-GNAI1-7	chr7:78926099-78926251	ucscGeneNc_uc010lea_1
48	lnc-GNAI1-2	chr7:79099910-79099995	ENSG00000234456.2
49	lnc-GNAI1-7	chr7:78922138-78922259	ucscGeneNc_uc010lea_1
50	lnc-GNAI1-2	chr7:79083649-79084323	NONHSAT121716

No data

Variant related genes	Relation type
MAGI2-AS3	TF binding region
RNU6-530P	TF binding region
MAGI2	TF binding region
ENSG00000222024	TF binding region
MAGI2-AS3	CpG island
RNU6-530P	CpG island
MAGI2	CpG island
ENSG00000222024	CpG island
USP38	miRNA target sites
B4GALT1	miRNA target sites
TNRC6A	miRNA target sites

Extended variants
information (count: 8500 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:8500 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138983784	chr7:78874746-78874747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs552364452	chr7:78874752-78874753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565845033	chr7:78874765-78874766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1609277	chr7:78874777-78874778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs548184838	chr7:78874794-78874795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568088234	chr7:78874820-78874821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112925460	chr7:78874865-78874866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556659887	chr7:78874873-78874874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542713717	chr7:78874893-78874894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561897355	chr7:78874930-78874931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141620050	chr7:78874979-78874980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs539654904	chr7:78875018-78875019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188756800	chr7:78875028-78875029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573357161	chr7:78875050-78875051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193293296	chr7:78875070-78875071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555766240	chr7:78875107-78875108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184257919	chr7:78875145-78875146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144510062	chr7:78875161-78875162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62460857	chr7:78875164-78875165	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs148434306	chr7:78875168-78875169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs578113849	chr7:78875184-78875185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113039173	chr7:78875200-78875201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114631992	chr7:78875203-78875204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112761119	chr7:78875205-78875206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548492958	chr7:78875220-78875221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561805825	chr7:78875239-78875240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs71555036	chr7:78875287-78875288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111782248	chr7:78875292-78875293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77469563	chr7:78875339-78875340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550121109	chr7:78875365-78875366	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs570218527	chr7:78875367-78875368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543706381	chr7:78886802-78886803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563742849	chr7:78886862-78886863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546418902	chr7:78886869-78886870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs193143901	chr7:78886873-78886874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546308006	chr7:78886907-78886908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559552825	chr7:78886973-78886974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527489061	chr7:78886995-78886996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547567279	chr7:78887002-78887003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561059234	chr7:78887070-78887071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113037678	chr7:78887106-78887107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530054279	chr7:78887142-78887143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147356702	chr7:78887152-78887153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373881094	chr7:78887154-78887155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs184417645	chr7:78887171-78887172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs189294505	chr7:78887190-78887191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180934515	chr7:78887195-78887196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565599386	chr7:78887227-78887228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534894405	chr7:78887233-78887234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs554791344	chr7:78887271-78887272	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1760 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78871200-78875000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:78871400-78875400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:78873400-78874800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr7:78875000-78875400	Enhancers	Liver	Liver
5	chr7:78886800-78887400	Enhancers	Brain Cingulate Gyrus	brain
6	chr7:78886800-78887400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr7:78886800-78888400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:78887400-78887800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr7:78887800-78888400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr7:78888400-78898000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr7:78894000-78894200	Enhancers	Aorta	Aorta
12	chr7:78894000-78894400	Enhancers	Psoas Muscle	Psoas
13	chr7:78894200-78896600	Weak transcription	Aorta	Aorta
14	chr7:78894400-78894600	Enhancers	NHLF	lung
15	chr7:78894600-78898400	Weak transcription	NHLF	lung
16	chr7:78896200-78896400	Enhancers	Brain Substantia Nigra	brain
17	chr7:78896400-78897400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:78896600-78896800	Enhancers	Aorta	Aorta
19	chr7:78896600-78896800	Enhancers	Ovary	ovary
20	chr7:78896600-78897800	Weak transcription	Brain Substantia Nigra	brain
21	chr7:78896800-78898400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr7:78896800-78899200	Weak transcription	Ovary	ovary
23	chr7:78896800-78911600	Weak transcription	Aorta	Aorta
24	chr7:78897400-78897800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr7:78897800-78898200	Enhancers	Brain Substantia Nigra	brain
26	chr7:78897800-78898400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr7:78898000-78898400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr7:78898000-78898400	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr7:78898000-78898400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr7:78898000-78898400	Enhancers	Fetal Lung	lung
31	chr7:78898400-78898600	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr7:78898400-78898600	Enhancers	NHLF	lung
33	chr7:78898400-78899400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr7:78898600-78899200	Weak transcription	NHLF	lung
35	chr7:78899000-78899600	Enhancers	Stomach Mucosa	stomach
36	chr7:78899200-78899400	Enhancers	NHLF	lung
37	chr7:78899200-78899600	Enhancers	Ovary	ovary
38	chr7:78899400-78899600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr7:78899400-78909600	Weak transcription	NHLF	lung
40	chr7:78899600-78900600	Weak transcription	Ovary	ovary
41	chr7:78900400-78900800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:78900600-78900800	Enhancers	Ovary	ovary
43	chr7:78900800-78903600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr7:78901800-78902400	Enhancers	Osteobl	bone
45	chr7:78902000-78902800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:78902200-78902800	Enhancers	HUVEC	blood vessel
47	chr7:78902400-78902600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr7:78902400-78910200	Weak transcription	Osteobl	bone
49	chr7:78902600-78911600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr7:78903200-78903600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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