Variant report

Variant	nsv522743
Chromosome Location	chr7:104411273-104486707
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:427)
Chromatin interactive
region (count:36)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:104482307-104482460	K562	blood:	n/a	n/a
2	ATF1	chr7:104482256-104482566	K562	blood:	n/a	n/a
3	ATF2	chr7:104412705-104413324	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr7:104412806-104413332	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr7:104412765-104413374	H1-hESC	embryonic stem cell:	n/a	chr7:104413256-104413270
6	BACH1	chr7:104448236-104448258	K562	blood:	n/a	n/a
7	BCL11A	chr7:104412851-104413116	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr7:104412839-104413127	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr7:104433576-104433893	A549	lung:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
10	CEBPB	chr7:104483828-104484013	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:104479052-104479240	K562	blood:	n/a	n/a
12	CEBPB	chr7:104483818-104484022	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr7:104433614-104433830	A549	lung:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
14	CEBPB	chr7:104433473-104433846	MCF-7	breast:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
15	CEBPB	chr7:104433532-104433845	IMR90	lung:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
16	CEBPB	chr7:104433540-104433841	HepG2	liver:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
17	CEBPB	chr7:104433566-104433846	K562	blood:	n/a	chr7:104433674-104433687 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685 chr7:104433676-104433685
18	CHD2	chr7:104412777-104413428	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr7:104412793-104413342	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr7:104412648-104413476	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTBP2	chr7:104412772-104413767	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:104467627-104467677	Fibrobl	skin:	n/a	n/a
23	CTCF	chr7:104434868-104434889	Lung_OC	lung:	n/a	n/a
24	CTCF	chr7:104483780-104483930	HCFaa	heart:	n/a	n/a
25	CTCF	chr7:104412735-104413130	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr7:104412845-104412952	A549	lung:	n/a	n/a
27	CTCF	chr7:104483800-104483950	NHEK	skin:	n/a	n/a
28	CTCF	chr7:104483700-104483850	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr7:104483774-104483858	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:104483740-104483890	HRPEpiC	eye:	n/a	n/a
31	CTCF	chr7:104412820-104412970	Caco-2	colon:	n/a	n/a
32	CTCF	chr7:104453040-104453190	GM12864	blood:	n/a	n/a
33	CTCF	chr7:104483785-104483856	MCF-7	breast:	n/a	n/a
34	CTCF	chr7:104412800-104412950	GM12872	blood:	n/a	n/a
35	CTCF	chr7:104412700-104412850	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr7:104483720-104483870	NHEK	skin:	n/a	n/a
37	CTCF	chr7:104483784-104483868	Gliobla	brain:	n/a	n/a
38	CTCF	chr7:104483740-104483890	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr7:104412825-104412978	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:104483785-104483871	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:104412846-104412909	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr7:104483775-104483871	K562	blood:	n/a	n/a
43	CTCF	chr7:104483764-104483899	Fibrobl	skin:	n/a	n/a
44	CTCF	chr7:104483759-104483864	ProgFib	skin:	n/a	n/a
45	CTCF	chr7:104483780-104483930	RPTEC	kidney:	n/a	n/a
46	CTCF	chr7:104483700-104483850	HMEC	breast:	n/a	n/a
47	CTCF	chr7:104483745-104483896	MCF-7	breast:	n/a	n/a
48	EBF1	chr7:104479101-104479640	GM12878	blood:	n/a	chr7:104479511-104479522
49	EBF1	chr7:104479099-104479731	GM12878	blood:	n/a	chr7:104479511-104479522
50	EGR1	chr7:104412826-104413187	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:104445585-104445635	NHDF-neo	bronchial:	n/a
2	chr7:104459130-104459180	BJ	skin:	n/a
3	chr7:104460407-104460457	HRE	kidney:	n/a
4	chr7:104460407-104460457	HCT-116	colon:	n/a
5	chr7:104444707-104444757	HL-60	blood:	n/a
6	chr7:104413036-104413086	GM12892	blood:	n/a
7	chr7:104444687-104444737	GM19239	blood:	n/a
8	chr7:104444687-104444737	NHDF-neo	bronchial:	n/a
9	chr7:104445585-104445635	SK-N-SH_RA	brain:	n/a
10	chr7:104444687-104444737	BJ	skin:	n/a
11	chr7:104460407-104460457	Hepatocyte	liver:	n/a
12	chr7:104413036-104413086	HCM	heart:	n/a
13	chr7:104459130-104459180	SK-N-MC	brain:	n/a
14	chr7:104413036-104413086	CMK	blood:	n/a
15	chr7:104444707-104444757	MCF-7	breast:	n/a
16	chr7:104445402-104445452	SAEC	small airway:	n/a
17	chr7:104444707-104444757	GM12892	blood:	n/a
18	chr7:104459130-104459180	Jurkat	blood:	n/a
19	chr7:104460407-104460457	SK-N-MC	brain:	n/a
20	chr7:104444707-104444757	NHBE	bronchial:	n/a
21	chr7:104413036-104413086	IMR90	lung:	fetal
22	chr7:104444687-104444737	AG09309	skin:	n/a
23	chr7:104444707-104444757	AoSMC	blood vessel:	n/a
24	chr7:104445402-104445452	SK-N-MC	brain:	n/a
25	chr7:104444687-104444737	Hela-S3	cervix:	n/a
26	chr7:104459130-104459180	AG04450	lung:	fetal
27	chr7:104445402-104445452	HEEpiC	esophagus:	n/a
28	chr7:104459130-104459180	HRCEpiC	kidney:	n/a
29	chr7:104413036-104413086	HCF	heart:	n/a
30	chr7:104444687-104444737	RPTEC	kidney:	n/a
31	chr7:104444687-104444737	AG09319	gingival:	n/a
32	chr7:104444707-104444757	HRPEpiC	eye:	n/a
33	chr7:104445585-104445635	Hepatocyte	liver:	n/a
34	chr7:104444687-104444737	HRE	kidney:	n/a
35	chr7:104413036-104413086	AoSMC	blood vessel:	n/a
36	chr7:104445585-104445635	LNCaP	prostate:	n/a
37	chr7:104460407-104460457	U87	brain:	n/a
38	chr7:104459130-104459180	HCT-116	colon:	n/a
39	chr7:104445585-104445635	T-47D	breast:	n/a
40	chr7:104459130-104459180	HRE	kidney:	n/a
41	chr7:104413036-104413086	HAEpiC	amniotic membrane:	n/a
42	chr7:104444707-104444757	HEEpiC	esophagus:	n/a
43	chr7:104445585-104445635	HMEC	breast:	n/a
44	chr7:104444687-104444737	HCM	heart:	n/a
45	chr7:104413036-104413086	HIPEpiC	eye:	n/a
46	chr7:104460407-104460457	HEK293	kidney:	embryo
47	chr7:104444707-104444757	Hela-S3	cervix:	n/a
48	chr7:104445402-104445452	IMR90	lung:	fetal
49	chr7:104445585-104445635	HL-60	blood:	n/a
50	chr7:104413036-104413086	SKMC	muscle:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:104427635..104430340-chr7:104433804..104436120,2	K562	blood:
2	chr7:104455637..104457503-chr7:104461736..104463277,2	K562	blood:
3	chr7:104412687..104414288-chr7:104414612..104417316,2	K562	blood:
4	chr7:104455637..104457503-chr7:104461736..104463277,2	K562	blood:
5	chr7:104189213..104191693-chr7:104438258..104440897,2	K562	blood:
6	chr7:104414380..104416720-chr7:104418892..104421394,2	K562	blood:
7	chr7:104415972..104418312-chr7:104418747..104420588,2	K562	blood:
8	chr7:104409406..104411368-chr7:104413418..104415967,2	K562	blood:
9	chr7:104453530..104456071-chr7:104485897..104488742,2	K562	blood:
10	chr7:104451035..104453878-chr7:104454466..104456364,2	K562	blood:
11	chr7:103848353..103851254-chr7:104459006..104460903,2	K562	blood:
12	chr7:104415740..104417803-chr7:104432798..104435671,2	K562	blood:
13	chr7:104435065..104437773-chr7:104442766..104444672,2	K562	blood:
14	chr7:104415740..104417803-chr7:104432798..104435671,2	K562	blood:
15	chr7:104419886..104422032-chr7:104422359..104424194,2	K562	blood:
16	chr7:104412687..104414288-chr7:104414612..104417316,2	K562	blood:
17	chr7:104435065..104439363-chr7:104442614..104444965,4	K562	blood:
18	chr7:104408013..104410317-chr7:104422818..104425471,2	K562	blood:
19	chr7:104438743..104441735-chr7:104443965..104445982,2	K562	blood:
20	chr7:104451035..104453878-chr7:104454466..104456364,2	K562	blood:
21	chr7:104427635..104430340-chr7:104433804..104436120,2	K562	blood:
22	chr7:104458052..104460838-chr7:104463968..104465824,2	K562	blood:
23	chr7:104419886..104422032-chr7:104422359..104424194,2	K562	blood:
24	chr7:104421671..104423208-chr7:104427462..104429131,2	K562	blood:
25	chr7:104421671..104423208-chr7:104427462..104429131,2	K562	blood:
26	chr7:104415972..104418312-chr7:104418747..104420588,2	K562	blood:
27	chr7:104458052..104460838-chr7:104463968..104465824,2	K562	blood:
28	chr7:104409406..104411368-chr7:104413418..104415967,2	K562	blood:
29	chr7:104414380..104416720-chr7:104418892..104421394,2	K562	blood:
30	chr7:104423057..104424601-chr7:104428990..104431789,2	MCF-7	breast:
31	chr7:104345772..104348271-chr7:104471773..104473637,2	MCF-7	breast:
32	chr7:104443017..104446705-chr7:104447012..104450843,4	K562	blood:
33	chr7:104453530..104456071-chr7:104485897..104488742,2	K562	blood:
34	chr7:104302642..104305367-chr7:104448713..104450769,2	K562	blood:
35	chr7:104432454..104433087-chrX:39058476..39059438,2	MCF-7	breast:
36	chr7:104423057..104424601-chr7:104428990..104431789,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SRPK2-4	chr7:104409432-104411609	ucscGeneNc_uc003vcj_1
2	lnc-SRPK2-4	chr7:104443286-104443410	NONHSAT122568
3	lnc-SRPK2-4	chr7:104436954-104437396	NONHSAT122568
4	lnc-SRPK2-4	chr7:104436963-104437396	ENSG00000226869.2
5	lnc-SRPK2-4	chr7:104444403-104444539	NONHSAT122568
6	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
7	lnc-SRPK2-4	chr7:104439840-104440516	ENSG00000226869.2
8	lnc-SRPK2-4	chr7:104444403-104444554	ENSG00000226869.2
9	lnc-SRPK2-4	chr7:104444403-104444554	ENSG00000226869.2
10	lnc-SRPK2-4	chr7:104438784-104438854	ENSG00000226869.2
11	lnc-MLL5-10	chr7:104442608-104443160	expReg_chr7_7212_+
12	lnc-SRPK2-4	chr7:104426178-104426232	ENSG00000226869.2
13	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
14	lnc-SRPK2-4	chr7:104438784-104438854	ENSG00000226869.2
15	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
16	lnc-SRPK2-4	chr7:104443899-104443986	ENSG00000226869.2
17	lnc-SRPK2-4	chr7:104444403-104444531	ENSG00000226869.2
18	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
19	lnc-SRPK2-4	chr7:104444403-104444535	ENSG00000226869.2
20	lnc-MLL5-8	chr7:104456917-104457497	expReg_chr7_7241_+
21	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
22	lnc-MLL5-9	chr7:104443904-104444763	expReg_chr7_7219_+
23	lnc-SRPK2-4	chr7:104426965-104427028	ENSG00000226869.2
24	lnc-SRPK2-4	chr7:104444403-104444539	NONHSAT122570
25	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
26	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
27	lnc-MLL5-7	chr7:104466783-104467243	NONHSAT122572
28	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
29	lnc-SRPK2-4	chr7:104436953-104437396	ENSG00000226869.2
30	lnc-SRPK2-4	chr7:104444403-104444533	ENSG00000226869.2
31	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
32	lnc-SRPK2-4	chr7:104439447-104440516	NONHSAT122570
33	lnc-SRPK2-4	chr7:104440265-104440516	NONHSAT122568
34	lnc-SRPK2-4	chr7:104443286-104443410	ENSG00000226869.2
35	lnc-SRPK2-4	chr7:104425659-104425805	ENSG00000226869.2
36	lnc-SRPK2-4	chr7:104443286-104443410	NONHSAT122570
37	lnc-SRPK2-4	chr7:104440265-104440516	ENSG00000226869.2
38	lnc-SRPK2-4	chr7:104438225-104441824	l_3463_NR_024586

No data

Variant related genes	Relation type
LHFPL3-AS1	TF binding region
ENSG00000237606	TF binding region
LHFPL3-AS1	CpG island
ENSG00000237606	CpG island
ENSG00000164815	chromatin interactions
ENSG00000226869	chromatin interactions

Extended variants
information (count: 2784 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2784 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13221774	chr7:104411273-104411274	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553463410	chr7:104411306-104411307	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs35222096	chr7:104411326-104411327	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs76548316	chr7:104411345-104411346	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs139607881	chr7:104411361-104411362	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs562582418	chr7:104411394-104411395	Weak transcription Enhancers Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs12705274	chr7:104411420-104411421	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs57276252	chr7:104411433-104411434	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs373371792	chr7:104411449-104411450	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs188249680	chr7:104411466-104411467	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs527534678	chr7:104411473-104411474	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs6969954	chr7:104411547-104411548	Enhancers Weak transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs145109250	chr7:104411612-104411613	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561089697	chr7:104411628-104411629	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530088311	chr7:104411653-104411654	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs549932082	chr7:104411732-104411733	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6950059	chr7:104411736-104411737	Enhancers Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs147579503	chr7:104411738-104411739	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539147744	chr7:104411753-104411754	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561177698	chr7:104411757-104411758	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140730061	chr7:104411782-104411783	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566301330	chr7:104411822-104411823	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534973639	chr7:104411853-104411854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs17141483	chr7:104411872-104411873	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs575059375	chr7:104411899-104411900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4730044	chr7:104411900-104411901	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs35239668	chr7:104411917-104411918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555780837	chr7:104411942-104411943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs386716462	chr7:104411976-104411977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs6950832	chr7:104411977-104411978	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564709119	chr7:104412003-104412004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77408145	chr7:104412009-104412010	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540901074	chr7:104412022-104412023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561210932	chr7:104412039-104412040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs4481520	chr7:104412066-104412067	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs74378298	chr7:104412081-104412082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191344095	chr7:104412104-104412105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551277435	chr7:104412150-104412151	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs532626323	chr7:104412179-104412180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150075062	chr7:104412190-104412191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145633900	chr7:104412222-104412223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62484641	chr7:104412258-104412259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144226748	chr7:104412262-104412263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376380716	chr7:104412264-104412265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558513010	chr7:104412283-104412284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs398005687	chr7:104412289-104412290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368399212	chr7:104412295-104412296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563126000	chr7:104412301-104412302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548545867	chr7:104412309-104412310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568728435	chr7:104412351-104412352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	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
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Breast cancer	21858162	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Prostate cancer	18632612	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	19907438	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:338 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104408600-104411800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr7:104409200-104412400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:104409200-104412800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:104409400-104414200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr7:104409600-104412800	Weak transcription	Brain Anterior Caudate	brain
6	chr7:104409800-104413000	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:104410400-104411800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr7:104411200-104411400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:104411200-104411400	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr7:104411200-104411400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr7:104411200-104412800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr7:104411200-104413000	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr7:104411400-104412600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr7:104411400-104412800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr7:104411400-104414400	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:104411600-104412800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr7:104411800-104412800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr7:104411800-104412800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:104412400-104414000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr7:104412600-104413200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:104412600-104413600	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr7:104412600-104413800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr7:104412600-104414200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr7:104412600-104414400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:104412600-104414600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr7:104412800-104413000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:104412800-104413000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr7:104412800-104413000	Active TSS	Brain Anterior Caudate	brain
29	chr7:104412800-104413200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:104412800-104413400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr7:104412800-104413800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr7:104412800-104413800	Enhancers	Spleen	Spleen
33	chr7:104412800-104414200	Enhancers	Fetal Brain Female	brain
34	chr7:104412800-104414400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr7:104412800-104414800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:104412800-104415800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr7:104413000-104413200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:104413000-104413200	Flanking Active TSS	Brain Anterior Caudate	brain
39	chr7:104413000-104413400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr7:104413000-104413400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
41	chr7:104413000-104413400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr7:104413000-104414200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr7:104413000-104414400	Enhancers	Brain Hippocampus Middle	brain
44	chr7:104413000-104414600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr7:104413200-104413800	Enhancers	Fetal Brain Male	brain
46	chr7:104413200-104414600	Enhancers	Brain Anterior Caudate	brain
47	chr7:104413200-104417800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:104413400-104414400	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr7:104413400-104414400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr7:104413400-104414800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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