Variant report

Variant	nsv1023461
Chromosome Location	chr9:6774993-7022554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2524)
CpG islands
(count:427)
Chromatin interactive
region (count:50)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2524 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6845117-6845374	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6899014-6899731	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6896614-6898522	HepG2	liver:	n/a	chr9:6897723-6897739 chr9:6897724-6897740
4	ARID3A	chr9:6927709-6928185	K562	blood:	n/a	n/a
5	ARID3A	chr9:6986412-6986867	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6931921-6932276	K562	blood:	n/a	n/a
7	ARID3A	chr9:6787981-6788483	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:6779378-6780217	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:6871154-6871863	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:6779811-6780274	K562	blood:	n/a	n/a
11	ARID3A	chr9:6955127-6955771	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:6932065-6932168	HepG2	liver:	n/a	n/a
13	ARID3A	chr9:6819233-6819386	HepG2	liver:	n/a	n/a
14	ARID3A	chr9:6896535-6896910	K562	blood:	n/a	n/a
15	ARID3A	chr9:6781433-6781998	HepG2	liver:	n/a	n/a
16	ARID3A	chr9:6900480-6901015	HepG2	liver:	n/a	n/a
17	ARID3A	chr9:6910048-6910291	K562	blood:	n/a	n/a
18	ARID3A	chr9:6788815-6789003	HepG2	liver:	n/a	n/a
19	ARID3A	chr9:6877521-6878180	HepG2	liver:	n/a	n/a
20	ARID3A	chr9:6845932-6846244	HepG2	liver:	n/a	n/a
21	ATF1	chr9:7011743-7011938	K562	blood:	n/a	n/a
22	ATF1	chr9:6896588-6896942	K562	blood:	n/a	n/a
23	ATF1	chr9:6779901-6780225	K562	blood:	n/a	n/a
24	ATF1	chr9:6931877-6932320	K562	blood:	n/a	n/a
25	ATF1	chr9:6927695-6928152	K562	blood:	n/a	n/a
26	ATF1	chr9:6894414-6894608	K562	blood:	n/a	n/a
27	ATF2	chr9:6973498-6974318	GM12878	blood:	n/a	n/a
28	ATF2	chr9:6893660-6894746	GM12878	blood:	n/a	n/a
29	ATF2	chr9:6902404-6902842	GM12878	blood:	n/a	n/a
30	ATF2	chr9:6917103-6917695	GM12878	blood:	n/a	n/a
31	ATF2	chr9:6777168-6777670	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr9:6893949-6894575	GM12878	blood:	n/a	n/a
33	ATF2	chr9:6960665-6961260	GM12878	blood:	n/a	n/a
34	ATF2	chr9:6973706-6974207	GM12878	blood:	n/a	n/a
35	ATF3	chr9:6779898-6780160	K562	blood:	n/a	n/a
36	ATF3	chr9:6931886-6932304	K562	blood:	n/a	n/a
37	ATF3	chr9:6896530-6896937	K562	blood:	n/a	n/a
38	BACH1	chr9:6854906-6854915	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr9:6955248-6955617	H1-hESC	embryonic stem cell:	n/a	chr9:6955424-6955438
40	BATF	chr9:6973758-6974189	GM12878	blood:	n/a	chr9:6973978-6973989
41	BATF	chr9:6894106-6894608	GM12878	blood:	n/a	n/a
42	BATF	chr9:6894207-6894592	GM12878	blood:	n/a	n/a
43	BATF	chr9:6973808-6974185	GM12878	blood:	n/a	chr9:6973978-6973989
44	BATF	chr9:6816627-6816816	GM12878	blood:	n/a	n/a
45	BATF	chr9:6923191-6923398	GM12878	blood:	n/a	n/a
46	BCL11A	chr9:6973811-6974164	GM12878	blood:	n/a	n/a
47	BCL11A	chr9:6893817-6893964	GM12878	blood:	n/a	n/a
48	BCL11A	chr9:6894214-6894574	GM12878	blood:	n/a	n/a
49	BCL11A	chr9:6917243-6917586	GM12878	blood:	n/a	n/a
50	BCL11A	chr9:6973797-6974200	GM12878	blood:	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	chr9:6835001-6835051	AG04449	skin:	fetal
2	chr9:6932042-6932092	HPAEpiC	pulmonary alveolar:	n/a
3	chr9:6779450-6779500	HIPEpiC	eye:	n/a
4	chr9:6779450-6779500	PrEC	prostate:	n/a
5	chr9:6955559-6955609	SK-N-SH	brain:	n/a
6	chr9:6955559-6955609	ovcar-3	ovarian:	n/a
7	chr9:6779450-6779500	GM12891	blood:	n/a
8	chr9:6779450-6779500	AG10803	skin:	n/a
9	chr9:6835001-6835051	NB4	blood:	n/a
10	chr9:6835001-6835051	NH-A	brain:	n/a
11	chr9:6869699-6869749	NT2-D1	testis:	n/a
12	chr9:6921930-6921980	K562	blood:	n/a
13	chr9:6921930-6921980	HCM	heart:	n/a
14	chr9:6779450-6779500	HMEC	breast:	n/a
15	chr9:6835001-6835051	U87	brain:	n/a
16	chr9:6921930-6921980	HepG2	liver:	n/a
17	chr9:6779450-6779500	HL-60	blood:	n/a
18	chr9:6835001-6835051	NT2-D1	testis:	n/a
19	chr9:6955559-6955609	RPTEC	kidney:	n/a
20	chr9:6836634-6836684	Hela-S3	cervix:	n/a
21	chr9:6955559-6955609	NH-A	brain:	n/a
22	chr9:6955559-6955609	ProgFib	skin:	n/a
23	chr9:6869699-6869749	IMR90	lung:	fetal
24	chr9:6955559-6955609	HIPEpiC	eye:	n/a
25	chr9:6955559-6955609	HEEpiC	esophagus:	n/a
26	chr9:6836634-6836684	U87	brain:	n/a
27	chr9:6836634-6836684	SK-N-SH_RA	brain:	n/a
28	chr9:6835001-6835051	PrEC	prostate:	n/a
29	chr9:6836634-6836684	SAEC	small airway:	n/a
30	chr9:6955559-6955609	GM12891	blood:	n/a
31	chr9:6932042-6932092	PrEC	prostate:	n/a
32	chr9:6836634-6836684	HEK293	kidney:	embryo
33	chr9:6836634-6836684	PFSK-1	brain:	n/a
34	chr9:6869699-6869749	ECC-1	luminal epithelium:	n/a
35	chr9:6836634-6836684	ovcar-3	ovarian:	n/a
36	chr9:6955559-6955609	HAEpiC	amniotic membrane:	n/a
37	chr9:6932042-6932092	HUVEC	blood vessel:	n/a
38	chr9:6932042-6932092	HMEC	breast:	n/a
39	chr9:6779450-6779500	SKMC	muscle:	n/a
40	chr9:6836634-6836684	MCF-7	breast:	n/a
41	chr9:6869699-6869749	SK-N-MC	brain:	n/a
42	chr9:6779450-6779500	RPTEC	kidney:	n/a
43	chr9:6836634-6836684	AG04450	lung:	fetal
44	chr9:6836634-6836684	NHBE	bronchial:	n/a
45	chr9:6779450-6779500	H1-hESC	embryonic stem cell:	embryo
46	chr9:6779450-6779500	HCF	heart:	n/a
47	chr9:6869699-6869749	BJ	skin:	n/a
48	chr9:6921930-6921980	GM12891	blood:	n/a
49	chr9:6869699-6869749	RPTEC	kidney:	n/a
50	chr9:6869699-6869749	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
2	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
3	chr9:6845574..6847293-chr9:6858590..6860659,2	K562	blood:
4	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
5	chr9:6845574..6847293-chr9:6858590..6860659,2	K562	blood:
6	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
7	chr9:6890515..6892207-chr9:6893663..6895984,2	K562	blood:
8	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
9	chr9:6902386..6904166-chr9:6906939..6908570,2	K562	blood:
10	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
11	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
12	chr9:7001163..7002731-chr9:7004777..7006309,2	K562	blood:
13	chr9:6757938..6759489-chr9:6817335..6820629,3	MCF-7	breast:
14	chr9:6928105..6930890-chr9:6932209..6935061,3	K562	blood:
15	chr9:6921809..6924418-chr9:6928929..6932002,3	MCF-7	breast:
16	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
17	chr9:6881706..6883676-chr9:6890777..6893621,2	K562	blood:
18	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
19	chr9:6978865..6981054-chr9:6982708..6984588,2	K562	blood:
20	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
21	chr9:6876130..6878078-chr9:6891371..6893102,2	K562	blood:
22	chr9:6921809..6924418-chr9:6928929..6932002,3	MCF-7	breast:
23	chr9:6996659..6998506-chr9:6999056..7001855,2	K562	blood:
24	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
25	chr9:6920289..6921801-chr9:7142294..7145025,2	K562	blood:
26	chr9:6986135..6988312-chr9:6992816..6995034,2	MCF-7	breast:
27	chr9:6755920..6758663-chr9:6904149..6906669,2	K562	blood:
28	chr9:6756573..6759030-chr9:6894279..6896008,2	K562	blood:
29	chr9:6967812..6970366-chr9:6971584..6973778,2	K562	blood:
30	chr9:6766833..6770674-chr9:6780008..6783723,3	K562	blood:
31	chr9:6896046..6898374-chr9:6899883..6901481,2	K562	blood:
32	chr9:6923976..6925853-chr9:6926210..6927942,2	K562	blood:
33	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
34	chr9:6954682..6956612-chr9:6970287..6972358,2	MCF-7	breast:
35	chr9:6909294..6911452-chr9:6925149..6926696,2	K562	blood:
36	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:
37	chr9:6888137..6890891-chr9:6891909..6894488,2	K562	blood:
38	chr9:6896445..6898374-chr9:6899981..6902743,2	K562	blood:
39	chr9:6931770..6934269-chr9:6942265..6944921,2	MCF-7	breast:
40	chr9:6972707..6974430-chr9:6976948..6979606,2	K562	blood:
41	chr9:6896046..6898374-chr9:6899883..6901481,2	K562	blood:
42	chr9:6890515..6892207-chr9:6893663..6895984,2	K562	blood:
43	chr9:6892256..6893815-chr9:6903780..6905360,2	MCF-7	breast:
44	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:
45	chr9:6680103..6682666-chr9:6784102..6786978,2	K562	blood:
46	chr9:6952608..6955450-chr9:6959103..6961194,2	K562	blood:
47	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
48	chr5:35003633..35004245-chr9:7020432..7021432,2	K562	blood:
49	chr9:6876130..6878078-chr9:6891371..6893102,2	K562	blood:
50	chr9:6919963..6921657-chr9:6923857..6925524,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-2	chr9:6978625-6978859	ENSG00000224972.1
2	lnc-UHRF2-1	chr9:6780333-6780490	ENSG00000236563.1
3	lnc-UHRF2-2	chr9:6974766-6974939	ENSG00000224972.1
4	lnc-UHRF2-6	chr9:6948033-6948214	NONHSAT130166
5	lnc-UHRF2-6	chr9:6942460-6942634	NONHSAT130166
6	lnc-UHRF2-2	chr9:6973827-6973887	ENSG00000224972.1
7	lnc-UHRF2-6	chr9:6941586-6941815	NONHSAT130166
8	lnc-UHRF2-1	chr9:6785601-6785929	ENSG00000236563.1
9	lnc-UHRF2-2	chr9:6902670-6902752	ENSG00000224972.1
10	lnc-UHRF2-6	chr9:6893123-6893232	NONHSAT130166

No data

Variant related genes	Relation type
ENSG00000230581	TF binding region
ENSG00000224972	TF binding region
KDM4C	TF binding region
ENSG00000230581	CpG island
ENSG00000224972	CpG island
KDM4C	CpG island
ENSG00000224972	chromatin interactions
ENSG00000107077	chromatin interactions

Extended variants
information (count: 13275 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:13275 , 50 per page) page: 1 2 3 4 5 6 7 ... 266

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7875468	chr9:6774993-6774994	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568829346	chr9:6775010-6775011	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs536127739	chr9:6775038-6775039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554173624	chr9:6775072-6775073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368031740	chr9:6775080-6775081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182871097	chr9:6775081-6775082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533682043	chr9:6775095-6775096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs7849183	chr9:6775098-6775099	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs536281014	chr9:6775106-6775107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576835718	chr9:6775147-6775148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs187787161	chr9:6775174-6775175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs562923755	chr9:6775180-6775181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs57291468	chr9:6775181-6775182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191098352	chr9:6775198-6775199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552939196	chr9:6775232-6775233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147727199	chr9:6775236-6775237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142638509	chr9:6775269-6775270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377178669	chr9:6775270-6775271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs144966444	chr9:6775296-6775297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182980478	chr9:6775297-6775298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs72699644	chr9:6775308-6775309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs147959800	chr9:6775317-6775318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536193829	chr9:6775364-6775365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548071841	chr9:6775368-6775369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187619701	chr9:6775377-6775378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533805043	chr9:6775448-6775449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192911871	chr9:6775482-6775483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140045595	chr9:6775492-6775493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150303085	chr9:6775523-6775524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577729908	chr9:6775531-6775532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs137964777	chr9:6775542-6775543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575074729	chr9:6775543-6775544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529714889	chr9:6775557-6775558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12685062	chr9:6775566-6775567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199997060	chr9:6775575-6775576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs563428920	chr9:6775576-6775577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs149068108	chr9:6775581-6775582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554506010	chr9:6775585-6775586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538359232	chr9:6775587-6775588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144753219	chr9:6775591-6775592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1759401	chr9:6775614-6775615	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs376266676	chr9:6775648-6775649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549041935	chr9:6775680-6775681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs141839868	chr9:6775682-6775683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531862977	chr9:6775706-6775707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs374160536	chr9:6775760-6775761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559389159	chr9:6775773-6775774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146259866	chr9:6775788-6775789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529848858	chr9:6775795-6775796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547934688	chr9:6775806-6775807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD

Chromatin state (count:5732 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6759600-6782200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr9:6759800-6778800	Weak transcription	Psoas Muscle	Psoas
3	chr9:6759800-6780000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:6759800-6782800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr9:6761800-6792800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:6763400-6775000	Weak transcription	Fetal Thymus	thymus
7	chr9:6763400-6775800	Weak transcription	Thymus	Thymus
8	chr9:6763600-6779200	Weak transcription	Primary B cells from cord blood	blood
9	chr9:6763600-6782800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr9:6764600-6779400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:6765000-6777400	Weak transcription	Brain Hippocampus Middle	brain
12	chr9:6765200-6779600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr9:6765200-6780400	Weak transcription	Small Intestine	intestine
14	chr9:6765400-6779200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr9:6765400-6779400	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr9:6765600-6782000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr9:6765800-6776400	Weak transcription	Primary T cells from cord blood	blood
18	chr9:6766000-6776000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr9:6767000-6775800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr9:6767000-6776200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr9:6767000-6776800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr9:6767800-6776200	Weak transcription	Gastric	stomach
23	chr9:6767800-6776800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr9:6768200-6776000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr9:6768800-6777000	Weak transcription	GM12878-XiMat	blood
26	chr9:6769400-6776000	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr9:6769800-6776400	Weak transcription	Primary B cells from peripheral blood	blood
28	chr9:6770000-6776200	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr9:6770000-6778800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr9:6770000-6779400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:6771800-6776200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr9:6771800-6776400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr9:6772000-6775200	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr9:6772000-6775800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr9:6772000-6776200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr9:6772000-6776600	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr9:6772000-6776800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr9:6772000-6777200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr9:6772000-6777200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
40	chr9:6772000-6777400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr9:6772000-6777600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr9:6772000-6779400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr9:6772000-6779400	Weak transcription	Pancreas	Pancrea
44	chr9:6772000-6779400	Weak transcription	Right Atrium	heart
45	chr9:6772000-6782600	Weak transcription	Lung	lung
46	chr9:6772000-6783400	Weak transcription	Spleen	Spleen
47	chr9:6772000-6788600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:6772200-6775800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr9:6772200-6775800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr9:6773400-6776200	Weak transcription	Fetal Intestine Small	intestine

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