Variant report

Variant	nsv1049457
Chromosome Location	chr9:72539144-72765913
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2640)
CpG islands
(count:549)
Chromatin interactive
region (count:59)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2640 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:72652942-72653681	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:72732806-72733543	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:72547942-72548142	HepG2	liver:	n/a	n/a
4	ATF1	chr9:72652915-72653683	K562	blood:	n/a	n/a
5	ATF1	chr9:72551434-72551710	K562	blood:	n/a	n/a
6	ATF2	chr9:72658141-72658540	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:72645981-72646409	GM12878	blood:	n/a	n/a
8	ATF3	chr9:72645989-72646673	HCT-116	colon:	n/a	n/a
9	ATF3	chr9:72561624-72562128	HCT-116	colon:	n/a	n/a
10	ATF3	chr9:72551440-72551684	K562	blood:	n/a	n/a
11	ATF3	chr9:72561686-72562065	K562	blood:	n/a	n/a
12	ATF3	chr9:72561761-72562186	HCT-116	colon:	n/a	n/a
13	BACH1	chr9:72659293-72659810	H1-hESC	embryonic stem cell:	n/a	chr9:72659725-72659739
14	BACH1	chr9:72635231-72635403	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:72668667-72668675	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr9:72653001-72653590	GM12878	blood:	n/a	n/a
17	BATF	chr9:72540793-72540973	GM12878	blood:	n/a	n/a
18	BATF	chr9:72653022-72653590	GM12878	blood:	n/a	n/a
19	BCL11A	chr9:72653004-72653733	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:72653027-72653579	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:72586930-72587122	K562	blood:	n/a	n/a
22	BHLHE40	chr9:72728434-72728713	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:72652915-72653599	HepG2	liver:	n/a	n/a
24	BHLHE40	chr9:72721326-72721464	K562	blood:	n/a	n/a
25	BRCA1	chr9:72653194-72653651	GM12878	blood:	n/a	n/a
26	BRCA1	chr9:72576763-72576779	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr9:72764337-72764394	GM12878	blood:	n/a	n/a
28	BRCA1	chr9:72726873-72726877	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr9:72725908-72726266	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr9:72546453-72546462	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr9:72725812-72726414	HCT-116	colon:	n/a	n/a
32	CBX3	chr9:72725818-72726415	HCT-116	colon:	n/a	n/a
33	CBX3	chr9:72561555-72562148	HCT-116	colon:	n/a	n/a
34	CBX3	chr9:72646012-72646752	HCT-116	colon:	n/a	n/a
35	CBX3	chr9:72561650-72562184	HCT-116	colon:	n/a	n/a
36	CBX3	chr9:72635788-72636290	HCT-116	colon:	n/a	n/a
37	CBX3	chr9:72548472-72548697	K562	blood:	n/a	n/a
38	CBX3	chr9:72668437-72669453	HCT-116	colon:	n/a	n/a
39	CEBPB	chr9:72712779-72713051	Hela-S3	cervix:	n/a	chr9:72712881-72712898
40	CEBPB	chr9:72552499-72552748	A549	lung:	n/a	n/a
41	CEBPB	chr9:72738680-72739024	HepG2	liver:	n/a	chr9:72738845-72738856
42	CEBPB	chr9:72583594-72583737	HepG2	liver:	n/a	chr9:72583698-72583709
43	CEBPB	chr9:72694685-72695066	HepG2	liver:	n/a	chr9:72694886-72694897 chr9:72694886-72694897 chr9:72694884-72694895 chr9:72694884-72694897 chr9:72694884-72694897
44	CEBPB	chr9:72694641-72694985	MCF-7	breast:	n/a	chr9:72694886-72694897 chr9:72694886-72694897 chr9:72694884-72694895 chr9:72694884-72694897 chr9:72694884-72694897
45	CEBPB	chr9:72712128-72712399	K562	blood:	n/a	chr9:72712276-72712289 chr9:72712278-72712287 chr9:72712278-72712287 chr9:72712276-72712287 chr9:72712278-72712287
46	CEBPB	chr9:72685336-72685345	K562	blood:	n/a	n/a
47	CEBPB	chr9:72560547-72561073	IMR90	lung:	n/a	n/a
48	CEBPB	chr9:72735499-72736157	IMR90	lung:	n/a	n/a
49	CEBPB	chr9:72712129-72712477	Hela-S3	cervix:	n/a	chr9:72712276-72712289 chr9:72712278-72712287 chr9:72712278-72712287 chr9:72712276-72712287 chr9:72712278-72712287
50	CEBPB	chr9:72748315-72748670	IMR90	lung:	n/a	chr9:72748483-72748494

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72658837-72658887	HCF	heart:	n/a
2	chr9:72658837-72658887	A549	lung:	n/a
3	chr9:72658358-72658408	HCPEpiC	choroid plexus:	n/a
4	chr9:72659163-72659213	NH-A	brain:	n/a
5	chr9:72658358-72658408	HRE	kidney:	n/a
6	chr9:72560940-72560990	NT2-D1	testis:	n/a
7	chr9:72560940-72560990	SK-N-MC	brain:	n/a
8	chr9:72659163-72659213	HRE	kidney:	n/a
9	chr9:72658747-72658797	HNPCEpiC	eye:	n/a
10	chr9:72658747-72658797	A549	lung:	n/a
11	chr9:72665127-72665177	NT2-D1	testis:	n/a
12	chr9:72665127-72665177	SK-N-SH_RA	brain:	n/a
13	chr9:72658358-72658408	HEK293	kidney:	embryo
14	chr9:72660082-72660132	AG04450	lung:	fetal
15	chr9:72655401-72655451	ovcar-3	ovarian:	n/a
16	chr9:72658837-72658887	SKMC	muscle:	n/a
17	chr9:72665127-72665177	HCF	heart:	n/a
18	chr9:72659163-72659213	HCT-116	colon:	n/a
19	chr9:72735830-72735880	AoSMC	blood vessel:	n/a
20	chr9:72655401-72655451	Hela-S3	cervix:	n/a
21	chr9:72660082-72660132	HRE	kidney:	n/a
22	chr9:72659163-72659213	ProgFib	skin:	n/a
23	chr9:72655401-72655451	SK-N-SH	brain:	n/a
24	chr9:72560940-72560990	BJ	skin:	n/a
25	chr9:72735830-72735880	AG10803	skin:	n/a
26	chr9:72658358-72658408	SK-N-SH_RA	brain:	n/a
27	chr9:72658747-72658797	HRCEpiC	kidney:	n/a
28	chr9:72660082-72660132	GM12891	blood:	n/a
29	chr9:72658358-72658408	SK-N-MC	brain:	n/a
30	chr9:72655401-72655451	K562	blood:	n/a
31	chr9:72560940-72560990	SKMC	muscle:	n/a
32	chr9:72560940-72560990	AG04449	skin:	fetal
33	chr9:72660082-72660132	U87	brain:	n/a
34	chr9:72658837-72658887	LNCaP	prostate:	n/a
35	chr9:72658837-72658887	NT2-D1	testis:	n/a
36	chr9:72655401-72655451	Jurkat	blood:	n/a
37	chr9:72658747-72658797	PrEC	prostate:	n/a
38	chr9:72560940-72560990	GM19239	blood:	n/a
39	chr9:72658747-72658797	K562	blood:	n/a
40	chr9:72735830-72735880	H1-hESC	embryonic stem cell:	embryo
41	chr9:72659163-72659213	Hela-S3	cervix:	n/a
42	chr9:72735830-72735880	AG09319	gingival:	n/a
43	chr9:72658358-72658408	HMEC	breast:	n/a
44	chr9:72665127-72665177	HNPCEpiC	eye:	n/a
45	chr9:72658837-72658887	HMEC	breast:	n/a
46	chr9:72560940-72560990	PANC-1	pancreas:	n/a
47	chr9:72655401-72655451	NT2-D1	testis:	n/a
48	chr9:72660082-72660132	HEEpiC	esophagus:	n/a
49	chr9:72735830-72735880	AG04450	lung:	fetal
50	chr9:72658747-72658797	HepG2	liver:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:72625669..72627256-chr9:72629721..72631306,2	MCF-7	breast:
2	chr9:72723556..72726029-chr9:72727042..72729559,2	K562	blood:
3	chr9:72683149..72684713-chr9:72696505..72698897,2	K562	blood:
4	chr9:72586975..72587497-chr9:73124835..73125760,2	K562	blood:
5	chr9:72748535..72750686-chr9:72751248..72753868,2	MCF-7	breast:
6	chr9:72586692..72587617-chr9:72725591..72726665,4	MCF-7	breast:
7	chr9:72586526..72587567-chr9:72725652..72726529,9	MCF-7	breast:
8	chr9:72552090..72553965-chr9:72554095..72555858,2	K562	blood:
9	chr9:72762270..72763345-chr9:72843683..72845020,7	MCF-7	breast:
10	chr9:72602857..72604672-chr9:72606319..72607860,2	K562	blood:
11	chr9:72625560..72627184-chr9:72663529..72666454,2	MCF-7	breast:
12	chr9:72602857..72604672-chr9:72606319..72607860,2	K562	blood:
13	chr9:72649187..72651651-chr9:72654412..72657228,3	K562	blood:
14	chr9:72625669..72627256-chr9:72629721..72631306,2	MCF-7	breast:
15	chr9:72579585..72583057-chr9:72584421..72588172,5	K562	blood:
16	chr9:72707394..72709089-chr9:72720199..72722050,2	K562	blood:
17	chr9:72649187..72651016-chr9:72654412..72657228,2	K562	blood:
18	chr9:72611748..72614537-chr9:72726027..72728626,2	MCF-7	breast:
19	chr9:72733654..72736603-chr9:72737665..72741649,3	MCF-7	breast:
20	chr9:72649187..72651651-chr9:72654412..72657228,3	K562	blood:
21	chr6:30582912..30585021-chr9:72685079..72686915,2	MCF-7	breast:
22	chr9:72586692..72587617-chr9:72725591..72726665,4	MCF-7	breast:
23	chr9:72579585..72583057-chr9:72584421..72588172,5	K562	blood:
24	chr9:72748007..72750453-chr9:72808216..72811141,2	MCF-7	breast:
25	chr9:72738878..72740762-chr9:72748344..72751164,2	MCF-7	breast:
26	chr9:72735746..72736503-chr9:72844295..72845240,3	MCF-7	breast:
27	chr9:72655440..72657664-chr9:72659271..72661535,2	MCF-7	breast:
28	chr9:72637007..72638664-chr9:72645208..72646717,2	MCF-7	breast:
29	chr9:72726384..72729356-chr9:72732064..72734127,2	MCF-7	breast:
30	chr9:72611748..72614537-chr9:72726027..72728626,2	MCF-7	breast:
31	chr9:72690045..72693021-chr9:72707849..72710235,2	MCF-7	breast:
32	chr9:72586559..72587592-chr9:72844298..72845151,6	K562	blood:
33	chr9:72655440..72657664-chr9:72659271..72661535,2	MCF-7	breast:
34	chr9:72738878..72740762-chr9:72748344..72751164,2	MCF-7	breast:
35	chr9:72649187..72651016-chr9:72654412..72657228,2	K562	blood:
36	chr17:62496286..62496984-chr9:72617693..72618495,2	MCF-7	breast:
37	chr9:72650886..72653009-chr9:72653069..72655464,2	MCF-7	breast:
38	chr9:72552090..72553965-chr9:72554095..72555858,2	K562	blood:
39	chr9:72638407..72640762-chr9:72642071..72643641,2	K562	blood:
40	chr9:72637007..72638664-chr9:72645208..72646717,2	MCF-7	breast:
41	chr9:72748535..72750686-chr9:72751248..72753868,2	MCF-7	breast:
42	chr9:72596256..72598713-chr9:72601006..72603750,3	K562	blood:
43	chr9:72638407..72640762-chr9:72642071..72643641,2	K562	blood:
44	chr9:72588649..72589350-chr9:72728157..72729028,2	MCF-7	breast:
45	chr9:72586588..72587213-chr9:72844309..72845161,2	MCF-7	breast:
46	chr9:72586536..72587505-chr9:72725613..72726553,4	K562	blood:
47	chr9:72733654..72736603-chr9:72737665..72741649,3	MCF-7	breast:
48	chr9:72726692..72728267-chr9:72871219..72873032,2	MCF-7	breast:
49	chr9:72625560..72627184-chr9:72663529..72666454,2	MCF-7	breast:
50	chr9:72650886..72653009-chr9:72653069..72655464,2	MCF-7	breast:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLF9-1	chr9:72724124-72724260	ENSG00000204706.10
2	lnc-KLF9-2	chr9:72728671-72728782	ENSG00000237778.1
3	lnc-KLF9-1	chr9:72728671-72728782	NONHSAT131797
4	lnc-KLF9-1	chr9:72703235-72703410	ENSG00000204706.10
5	lnc-KLF9-1	chr9:72703235-72703913	ENSG00000204706.10
6	lnc-KLF9-1	chr9:72703235-72703410	ENSG00000204706.10
7	lnc-KLF9-1	chr9:72703235-72703410	NONHSAT131795
8	lnc-KLF9-1	chr9:72703235-72703410	NONHSAT131793
9	lnc-KLF9-1	chr9:72708693-72708878	ENSG00000204706.10
10	lnc-KLF9-1	chr9:72700732-72702546	NONHSAT131793
11	lnc-KLF9-1	chr9:72703235-72703410	ENSG00000204706.10
12	lnc-KLF9-1	chr9:72707616-72707661	ENSG00000204706.10
13	lnc-KLF9-1	chr9:72705522-72705706	ENSG00000204706.10
14	lnc-KLF9-1	chr9:72702335-72702546	NONHSAT131795
15	lnc-KLF9-1	chr9:72702335-72702546	ENSG00000204706.10
16	lnc-KLF9-1	chr9:72702506-72702546	ENSG00000204706.10
17	lnc-KLF9-2	chr9:72702213-72702546	ENSG00000237778.1
18	lnc-KLF9-1	chr9:72728671-72728776	ENSG00000204706.10
19	lnc-KLF9-1	chr9:72707167-72707622	ENSG00000204706.10
20	lnc-KLF9-2	chr9:72703235-72703410	ENSG00000237778.1
21	lnc-KLF9-1	chr9:72703235-72703410	ENSG00000204706.10
22	lnc-KLF9-1	chr9:72720832-72720958	ENSG00000204706.10
23	lnc-KLF9-1	chr9:72728671-72728776	ENSG00000204706.10
24	lnc-KLF9-1	chr9:72705522-72705710	NONHSAT131795
25	lnc-KLF9-1	chr9:72702335-72702546	ENSG00000204706.10
26	lnc-KLF9-1	chr9:72728671-72728782	NONHSAT131793
27	lnc-KLF9-1	chr9:72703219-72703410	NONHSAT131797
28	lnc-KLF9-1	chr9:72702335-72702546	ENSG00000204706.10
29	lnc-KLF9-1	chr9:72762897-72762994	ENSG00000204706.10
30	lnc-KLF9-1	chr9:72700732-72702546	ENSG00000204706.10

No data

Variant related genes	Relation type
MAMDC2-AS1	TF binding region
MAMDC2	TF binding region
MAMDC2-AS1	CpG island
MAMDC2	CpG island
ENSG00000222894	chromatin interactions
ENSG00000265695	chromatin interactions
ENSG00000261447	chromatin interactions
ENSG00000204706	chromatin interactions

Extended variants
information (count: 7873 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:7873 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35506524	chr9:72539229-72539230	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554020443	chr9:72539230-72539231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10780705	chr9:72539240-72539241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10746756	chr9:72539262-72539263	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs148871825	chr9:72539279-72539280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564456954	chr9:72539294-72539295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576411190	chr9:72539333-72539334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544239869	chr9:72539353-72539354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543930452	chr9:72539403-72539404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143725964	chr9:72539456-72539457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190641099	chr9:72539463-72539464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7044593	chr9:72539486-72539487	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs71356150	chr9:72539516-72539517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559353099	chr9:72539548-72539549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs529702504	chr9:72539552-72539553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542110281	chr9:72539554-72539555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs55732918	chr9:72539555-72539556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578013260	chr9:72539612-72539613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577092440	chr9:72539615-72539616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376755291	chr9:72539621-72539622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530561980	chr9:72539627-72539628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77670566	chr9:72539644-72539645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562716540	chr9:72539652-72539653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532538905	chr9:72539672-72539673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs73446732	chr9:72539709-72539710	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs140577500	chr9:72539721-72539722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536652766	chr9:72539758-72539759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548340590	chr9:72539769-72539770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs570021617	chr9:72539797-72539798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531366982	chr9:72539798-72539799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188539253	chr9:72547589-72547590	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148224175	chr9:72547617-72547618	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs546224037	chr9:72547625-72547626	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112600424	chr9:72547626-72547627	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs11788737	chr9:72547631-72547632	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs141181240	chr9:72547655-72547656	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372947321	chr9:72547673-72547674	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557917778	chr9:72547679-72547680	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs181293161	chr9:72547680-72547681	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs150297899	chr9:72547682-72547683	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12338191	chr9:72547704-72547705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs12238457	chr9:72547729-72547730	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs562562093	chr9:72547730-72547731	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185888561	chr9:72547733-72547734	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533909280	chr9:72547756-72547757	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555467549	chr9:72547877-72547878	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs373613033	chr9:72547883-72547884	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189314088	chr9:72547889-72547890	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536005398	chr9:72547912-72547913	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557583448	chr9:72547914-72547915	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD
Autism	21484199	CNVD
Breast cancer	22737080	CNVD
Malignant peripheral nerve sheath tumor	22811580	CNVD
Leprosy	22719964	CNVD
Primary ovarian insufficiency	22879975	CNVD
Malignant melanoma	17260012	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3585 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72514000-72539600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr9:72537800-72539200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:72538000-72539600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr9:72538600-72539200	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr9:72538600-72539200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr9:72538800-72539200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:72538800-72539400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr9:72539200-72539400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:72539600-72539800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr9:72548000-72549400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr9:72548200-72548800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:72548400-72549200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
13	chr9:72548800-72549000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr9:72548800-72549200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:72548800-72550800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr9:72549000-72549800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr9:72549200-72549400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr9:72549400-72551000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr9:72550800-72553000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr9:72551000-72551600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr9:72551000-72552800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr9:72551200-72553000	Enhancers	HMEC	breast
23	chr9:72551400-72552800	Enhancers	Muscle Satellite Cultured Cells	--
24	chr9:72551400-72553000	Enhancers	NHDF-Ad	bronchial
25	chr9:72551400-72553600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr9:72551600-72552600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr9:72551800-72552000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr9:72551800-72553600	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr9:72552000-72552200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
30	chr9:72552000-72552800	Enhancers	K562	blood
31	chr9:72552000-72552800	Enhancers	Osteobl	bone
32	chr9:72552200-72552600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr9:72552200-72553000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:72552600-72553000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
35	chr9:72552600-72553200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr9:72552800-72558200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr9:72553000-72553600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr9:72553000-72553800	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr9:72553200-72558400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr9:72553600-72555000	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr9:72553600-72558000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr9:72553800-72554800	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr9:72554800-72555000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr9:72555000-72555800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr9:72555000-72556200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr9:72555200-72555600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr9:72555800-72556200	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr9:72556200-72556400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr9:72556200-72556400	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr9:72556400-72559800	Weak transcription	Primary monocytes fromperipheralblood	blood

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