Variant report

Variant	nsv916660
Chromosome Location	chr7:33272493-33506384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1472)
CpG islands
(count:549)
Chromatin interactive
region (count:51)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1472 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:33282922-33283297	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:33397641-33397646	K562	blood:	n/a	n/a
3	ATF1	chr7:33294366-33294457	K562	blood:	n/a	n/a
4	ATF1	chr7:33282670-33283260	K562	blood:	n/a	n/a
5	BACH1	chr7:33495168-33495210	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr7:33492456-33492655	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr7:33492541-33492768	K562	blood:	n/a	n/a
8	BATF	chr7:33463182-33463442	GM12878	blood:	n/a	n/a
9	BATF	chr7:33301181-33301540	GM12878	blood:	n/a	n/a
10	BATF	chr7:33301171-33301471	GM12878	blood:	n/a	n/a
11	BATF	chr7:33346807-33347032	GM12878	blood:	n/a	n/a
12	BCL11A	chr7:33301252-33301500	GM12878	blood:	n/a	n/a
13	BCL11A	chr7:33301242-33301503	GM12878	blood:	n/a	n/a
14	BHLHE40	chr7:33273222-33273621	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:33376469-33376855	GM12878	blood:	n/a	n/a
16	BRCA1	chr7:33274663-33274752	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr7:33374025-33374217	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:33278923-33279002	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr7:33489448-33489725	HepG2	liver:	n/a	chr7:33489558-33489569
20	CEBPB	chr7:33329609-33329873	K562	blood:	n/a	chr7:33329729-33329740
21	CEBPB	chr7:33400743-33400980	HepG2	liver:	n/a	n/a
22	CEBPB	chr7:33385688-33385938	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr7:33455450-33455468	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:33278972-33279036	K562	blood:	n/a	n/a
25	CEBPB	chr7:33475778-33476051	A549	lung:	n/a	chr7:33475910-33475921
26	CEBPB	chr7:33397437-33397913	MCF-7	breast:	n/a	n/a
27	CEBPB	chr7:33489436-33489697	IMR90	lung:	n/a	chr7:33489558-33489569
28	CEBPB	chr7:33298165-33298788	IMR90	lung:	n/a	chr7:33298503-33298515
29	CEBPB	chr7:33431614-33431774	HepG2	liver:	n/a	chr7:33431668-33431677 chr7:33431667-33431678 chr7:33431668-33431677 chr7:33431668-33431677 chr7:33431666-33431677 chr7:33431668-33431677 chr7:33431666-33431679
30	CEBPB	chr7:33329567-33329912	HepG2	liver:	n/a	chr7:33329729-33329740
31	CEBPB	chr7:33386182-33386511	ECC-1	luminal epithelium:	n/a	chr7:33386259-33386272 chr7:33386320-33386331 chr7:33386321-33386332 chr7:33386258-33386275 chr7:33386322-33386331
32	CEBPB	chr7:33386273-33386398	H1-hESC	embryonic stem cell:	n/a	chr7:33386320-33386331 chr7:33386321-33386332 chr7:33386322-33386331
33	CEBPB	chr7:33461052-33461367	IMR90	lung:	n/a	chr7:33461216-33461227
34	CEBPB	chr7:33489521-33489594	Hela-S3	cervix:	n/a	chr7:33489558-33489569
35	CEBPB	chr7:33468209-33468226	A549	lung:	n/a	n/a
36	CEBPB	chr7:33485981-33486050	HepG2	liver:	n/a	chr7:33485988-33486001 chr7:33485989-33486000
37	CEBPB	chr7:33329562-33329894	IMR90	lung:	n/a	chr7:33329729-33329740
38	CEBPB	chr7:33400672-33400966	IMR90	lung:	n/a	n/a
39	CEBPB	chr7:33495619-33495622	A549	lung:	n/a	n/a
40	CEBPB	chr7:33329623-33329910	A549	lung:	n/a	chr7:33329729-33329740
41	CEBPB	chr7:33455461-33455617	IMR90	lung:	n/a	n/a
42	CEBPB	chr7:33386213-33386490	A549	lung:	n/a	chr7:33386259-33386272 chr7:33386320-33386331 chr7:33386321-33386332 chr7:33386258-33386275 chr7:33386322-33386331
43	CEBPB	chr7:33475790-33476059	HepG2	liver:	n/a	chr7:33475910-33475921
44	CEBPB	chr7:33400718-33400968	A549	lung:	n/a	n/a
45	CEBPB	chr7:33329578-33329864	H1-hESC	embryonic stem cell:	n/a	chr7:33329729-33329740
46	CEBPB	chr7:33386192-33386493	ECC-1	luminal epithelium:	n/a	chr7:33386259-33386272 chr7:33386320-33386331 chr7:33386321-33386332 chr7:33386258-33386275 chr7:33386322-33386331
47	CEBPB	chr7:33498960-33499280	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr7:33386210-33386447	HepG2	liver:	n/a	chr7:33386259-33386272 chr7:33386320-33386331 chr7:33386321-33386332 chr7:33386258-33386275 chr7:33386322-33386331
49	CEBPB	chr7:33391358-33391654	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr7:33502039-33502212	GM12878	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:33301429-33301479	NHDF-neo	bronchial:	n/a
2	chr7:33301429-33301479	BE2_C	brain:	n/a
3	chr7:33301429-33301479	BJ	skin:	n/a
4	chr7:33462512-33462562	HCT-116	colon:	n/a
5	chr7:33389294-33389344	SKMC	muscle:	n/a
6	chr7:33383025-33383075	PANC-1	pancreas:	n/a
7	chr7:33462512-33462562	NT2-D1	testis:	n/a
8	chr7:33462512-33462562	ECC-1	luminal epithelium:	n/a
9	chr7:33457940-33457990	CMK	blood:	n/a
10	chr7:33389294-33389344	HCF	heart:	n/a
11	chr7:33343842-33343892	ECC-1	luminal epithelium:	n/a
12	chr7:33343842-33343892	RPTEC	kidney:	n/a
13	chr7:33301429-33301479	HCF	heart:	n/a
14	chr7:33389821-33389871	MCF10A-Er-Src	breast:	n/a
15	chr7:33343842-33343892	HCM	heart:	n/a
16	chr7:33384022-33384072	HMEC	breast:	n/a
17	chr7:33389885-33389935	NHDF-neo	bronchial:	n/a
18	chr7:33462512-33462562	H1-hESC	embryonic stem cell:	embryo
19	chr7:33457940-33457990	AG10803	skin:	n/a
20	chr7:33389885-33389935	HMEC	breast:	n/a
21	chr7:33383025-33383075	HRCEpiC	kidney:	n/a
22	chr7:33384022-33384072	Caco-2	colon:	n/a
23	chr7:33389885-33389935	A549	lung:	n/a
24	chr7:33457940-33457990	H1-hESC	embryonic stem cell:	embryo
25	chr7:33389294-33389344	AG04449	skin:	fetal
26	chr7:33383025-33383075	GM12891	blood:	n/a
27	chr7:33389821-33389871	NHDF-neo	bronchial:	n/a
28	chr7:33389294-33389344	HEK293	kidney:	embryo
29	chr7:33383025-33383075	GM06990	blood:	n/a
30	chr7:33343842-33343892	U87	brain:	n/a
31	chr7:33384022-33384072	SK-N-SH	brain:	n/a
32	chr7:33457940-33457990	AG09319	gingival:	n/a
33	chr7:33389885-33389935	T-47D	breast:	n/a
34	chr7:33383025-33383075	GM12892	blood:	n/a
35	chr7:33384022-33384072	ovcar-3	ovarian:	n/a
36	chr7:33389885-33389935	SKMC	muscle:	n/a
37	chr7:33457940-33457990	HRCEpiC	kidney:	n/a
38	chr7:33301429-33301479	HCPEpiC	choroid plexus:	n/a
39	chr7:33389821-33389871	MCF-7	breast:	n/a
40	chr7:33389294-33389344	GM12892	blood:	n/a
41	chr7:33343842-33343892	HCPEpiC	choroid plexus:	n/a
42	chr7:33301429-33301479	AoSMC	blood vessel:	n/a
43	chr7:33389821-33389871	AG09309	skin:	n/a
44	chr7:33389821-33389871	HepG2	liver:	n/a
45	chr7:33457940-33457990	T-47D	breast:	n/a
46	chr7:33384022-33384072	Jurkat	blood:	n/a
47	chr7:33301429-33301479	HEEpiC	esophagus:	n/a
48	chr7:33457940-33457990	Hela-S3	cervix:	n/a
49	chr7:33301429-33301479	AG09319	gingival:	n/a
50	chr7:33389821-33389871	HCT-116	colon:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:33374003..33374685-chr7:33972197..33973188,2	MCF-7	breast:
2	chr7:33354992..33357519-chr7:33360634..33362706,2	K562	blood:
3	chr7:33417630..33419879-chr7:33421037..33423794,2	K562	blood:
4	chr17:41462282..41463821-chr7:33291335..33292857,2	K562	blood:
5	chr7:33407715..33410648-chr7:33411444..33414144,2	K562	blood:
6	chr7:33373710..33374867-chr7:33498631..33499702,4	MCF-7	breast:
7	chr7:33438887..33440911-chr7:33449255..33451707,2	K562	blood:
8	chr17:41462939..41465367-chr7:33292835..33294355,2	MCF-7	breast:
9	chr7:33498720..33499554-chr7:33783613..33784456,2	MCF-7	breast:
10	chr7:33369970..33372614-chr7:33374377..33376090,2	K562	blood:
11	chr17:41463874..41467729-chr7:33291332..33294337,4	K562	blood:
12	chr7:33438887..33440911-chr7:33449255..33451707,2	K562	blood:
13	chr7:33306418..33309708-chr7:33313851..33316308,3	K562	blood:
14	chr7:33407715..33410648-chr7:33411444..33414144,2	K562	blood:
15	chr7:33288159..33290734-chr7:33296118..33297688,2	K562	blood:
16	chr7:33288330..33291319-chr7:33303929..33306157,2	K562	blood:
17	chr7:33417630..33419879-chr7:33421037..33423794,2	K562	blood:
18	chr7:33381826..33383987-chr7:33388092..33389898,2	MCF-7	breast:
19	chr7:33480819..33483351-chr7:33485248..33487940,2	K562	blood:
20	chr17:41380292..41383703-chr7:33291335..33294335,6	K562	blood:
21	chr7:33462937..33463514-chr7:33783854..33784554,2	MCF-7	breast:
22	chr7:33282661..33283550-chr7:33499199..33499750,2	MCF-7	breast:
23	chr7:33448405..33450851-chr7:33456089..33457716,2	MCF-7	breast:
24	chr7:33299351..33301852-chr7:33302490..33303993,2	K562	blood:
25	chr7:33354992..33357519-chr7:33360634..33362706,2	K562	blood:
26	chr7:33369970..33372614-chr7:33374377..33376090,2	K562	blood:
27	chr7:33387307..33390007-chr7:33559029..33560942,2	K562	blood:
28	chr17:41398797..41401165-chr7:33291335..33294355,5	MCF-7	breast:
29	chr17:41398400..41401723-chr7:33291352..33294335,3	K562	blood:
30	chr17:41380127..41383362-chr7:33291332..33294355,8	K562	blood:
31	chr7:33225227..33225941-chr7:33282574..33283336,3	MCF-7	breast:
32	chr7:33499224..33499840-chr7:33756036..33756556,2	MCF-7	breast:
33	chr17:41380387..41382197-chr7:33292837..33294355,4	MCF-7	breast:
34	chr7:33381826..33383987-chr7:33388092..33389898,2	MCF-7	breast:
35	chr7:33373710..33374867-chr7:33498631..33499702,4	MCF-7	breast:
36	chr7:33448405..33450851-chr7:33456089..33457716,2	MCF-7	breast:
37	chr7:33480819..33483351-chr7:33485248..33487940,2	K562	blood:
38	chr7:33288330..33291319-chr7:33303929..33306157,2	K562	blood:
39	chr7:33347526..33349125-chr7:33353046..33355911,2	K562	blood:
40	chr7:33225084..33225594-chr7:33499029..33499648,2	MCF-7	breast:
41	chr7:33282661..33283550-chr7:33499199..33499750,2	MCF-7	breast:
42	chr7:33314204..33317885-chr7:33320684..33323971,3	K562	blood:
43	chr7:33299351..33301852-chr7:33302490..33303993,2	K562	blood:
44	chr17:41380312..41383401-chr7:33291355..33294353,3	MCF-7	breast:
45	chr17:41398400..41402313-chr7:33292833..33294335,3	K562	blood:
46	chr7:33283153..33284693-chr7:33295167..33297777,2	K562	blood:
47	chr7:33288159..33290734-chr7:33296118..33297688,2	K562	blood:
48	chr7:33347526..33349125-chr7:33353046..33355911,2	K562	blood:
49	chr7:33283153..33284693-chr7:33295167..33297777,2	K562	blood:
50	chr7:33306418..33309708-chr7:33313851..33316308,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AVL9-4	chr7:33419576-33420498	NONHSAT120025

No data

Variant related genes	Relation type
ENSG00000224946	TF binding region
BBS9	TF binding region
ENSG00000238090	TF binding region
ENSG00000224946	CpG island
BBS9	CpG island
ENSG00000238090	CpG island
ENSG00000224946	chromatin interactions
ENSG00000122507	chromatin interactions
ENSG00000238090	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 8352 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:8352 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541740190	chr7:33272517-33272518	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370125907	chr7:33272529-33272530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545642223	chr7:33272534-33272535	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12666753	chr7:33272555-33272556	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs551914763	chr7:33272575-33272576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145381011	chr7:33272589-33272590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531304017	chr7:33272609-33272610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34992704	chr7:33272623-33272624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549507666	chr7:33272626-33272627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183861162	chr7:33272634-33272635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113424823	chr7:33272639-33272640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567949177	chr7:33272707-33272708	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572651340	chr7:33272712-33272713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374716958	chr7:33272730-33272731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs186284314	chr7:33272793-33272794	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1861298	chr7:33272797-33272798	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs561411829	chr7:33272809-33272810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138018127	chr7:33272814-33272815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534504857	chr7:33272816-33272817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568428691	chr7:33272844-33272845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559145008	chr7:33272850-33272851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571101769	chr7:33272875-33272876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1019301	chr7:33272922-33272923	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs1019300	chr7:33272948-33272949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs574717911	chr7:33272965-33272966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75824604	chr7:33272996-33272997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553891174	chr7:33273012-33273013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532830139	chr7:33273088-33273089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572259332	chr7:33273125-33273126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs545741569	chr7:33273167-33273168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563930536	chr7:33273188-33273189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535053300	chr7:33273190-33273191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543093062	chr7:33273209-33273210	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs561793975	chr7:33273210-33273211	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs551170206	chr7:33273211-33273212	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs191036007	chr7:33273223-33273224	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs7789007	chr7:33273277-33273278	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs565542449	chr7:33273312-33273313	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs1420158	chr7:33273347-33273348	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs370710306	chr7:33273353-33273354	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs374908354	chr7:33273451-33273452	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs143161210	chr7:33273454-33273455	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs571039065	chr7:33273518-33273519	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs182185045	chr7:33273528-33273529	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs556498579	chr7:33273533-33273534	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs372533868	chr7:33273572-33273573	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs535583158	chr7:33273573-33273574	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs554135492	chr7:33273585-33273586	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs186783275	chr7:33273619-33273620	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs58756850	chr7:33273620-33273621	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
Melanoma	18172304	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
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
Endometrioid adenocarcinoma	16974079	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
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Williams-beuren syndrome	18553513	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Aortic dissecting aneurysms	22263138	CNVD

Chromatin state (count:1228 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:33269000-33273200	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:33271600-33272800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:33272400-33272600	Enhancers	Brain Angular Gyrus	brain
4	chr7:33272400-33272800	Enhancers	NHDF-Ad	bronchial
5	chr7:33272600-33276800	Weak transcription	Brain Angular Gyrus	brain
6	chr7:33272800-33277000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:33273000-33273200	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr7:33273200-33273600	Enhancers	Colon Smooth Muscle	Colon
9	chr7:33273200-33273800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:33273200-33273800	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr7:33273400-33273600	Active TSS	Stomach Smooth Muscle	stomach
12	chr7:33273400-33273800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr7:33273400-33273800	Active TSS	Duodenum Smooth Muscle	Duodenum
14	chr7:33273400-33273800	Enhancers	Fetal Lung	lung
15	chr7:33273400-33273800	Enhancers	Left Ventricle	heart
16	chr7:33273600-33273800	Flanking Active TSS	Stomach Smooth Muscle	stomach
17	chr7:33273800-33274000	Enhancers	Pancreatic Islets	Pancreatic Islet
18	chr7:33273800-33275000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr7:33273800-33276800	Weak transcription	Stomach Smooth Muscle	stomach
20	chr7:33273800-33283800	Weak transcription	Fetal Lung	lung
21	chr7:33274800-33275000	Enhancers	Brain Substantia Nigra	brain
22	chr7:33275000-33275200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr7:33275200-33275800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr7:33275800-33276800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr7:33276600-33276800	Active TSS	Liver	Liver
26	chr7:33276800-33277000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:33276800-33277000	Flanking Active TSS	Liver	Liver
28	chr7:33276800-33277200	Enhancers	Brain Angular Gyrus	brain
29	chr7:33276800-33277200	Enhancers	Stomach Smooth Muscle	stomach
30	chr7:33276800-33277200	Enhancers	A549	lung
31	chr7:33276800-33277400	Enhancers	HUVEC	blood vessel
32	chr7:33276800-33277600	Enhancers	Brain Hippocampus Middle	brain
33	chr7:33276800-33277600	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr7:33276800-33277800	Enhancers	Brain Anterior Caudate	brain
35	chr7:33276800-33277800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:33276800-33277800	Enhancers	Brain Substantia Nigra	brain
37	chr7:33277000-33277200	Enhancers	Stomach Mucosa	stomach
38	chr7:33277000-33277400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:33277000-33277400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr7:33277000-33277800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:33277000-33277800	Enhancers	Liver	Liver
42	chr7:33277000-33278000	Enhancers	HepG2	liver
43	chr7:33277200-33277800	Enhancers	Brain Cingulate Gyrus	brain
44	chr7:33277200-33281800	Weak transcription	Stomach Mucosa	stomach
45	chr7:33277200-33282800	Weak transcription	Brain Angular Gyrus	brain
46	chr7:33282600-33283400	Enhancers	Fetal Kidney	kidney
47	chr7:33282800-33283400	Enhancers	Brain Angular Gyrus	brain
48	chr7:33283400-33284400	Weak transcription	Brain Angular Gyrus	brain
49	chr7:33283400-33290800	Weak transcription	Fetal Kidney	kidney
50	chr7:33283800-33284200	Enhancers	Fetal Lung	lung

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