Variant report

Variant	nsv613613
Chromosome Location	chr9:12641987-12773263
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:12719466-12719806	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:12702242-12702514	HepG2	liver:	n/a	n/a
3	ATF2	chr9:12735567-12735964	GM12878	blood:	n/a	n/a
4	ATF2	chr9:12735544-12735972	GM12878	blood:	n/a	n/a
5	ATF3	chr9:12708586-12708908	HCT-116	colon:	n/a	n/a
6	BACH1	chr9:12653013-12653212	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr9:12771808-12772164	A549	lung:	n/a	n/a
8	BRCA1	chr9:12666817-12666918	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr9:12734440-12734884	HCT-116	colon:	n/a	n/a
10	CBX3	chr9:12708489-12709018	HCT-116	colon:	n/a	n/a
11	CEBPB	chr9:12723645-12724015	IMR90	lung:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
12	CEBPB	chr9:12656603-12657162	IMR90	lung:	n/a	chr9:12656979-12656988 chr9:12656681-12656694 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656681-12656692 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988 chr9:12656681-12656694
13	CEBPB	chr9:12690305-12690523	IMR90	lung:	n/a	chr9:12690390-12690401 chr9:12690390-12690403 chr9:12690390-12690403 chr9:12690390-12690403
14	CEBPB	chr9:12708603-12708891	IMR90	lung:	n/a	n/a
15	CEBPB	chr9:12765440-12765779	IMR90	lung:	n/a	chr9:12765544-12765555 chr9:12765557-12765570 chr9:12765559-12765570 chr9:12765545-12765556 chr9:12765557-12765568 chr9:12765557-12765570
16	CEBPB	chr9:12681521-12681770	A549	lung:	n/a	chr9:12681604-12681615
17	CEBPB	chr9:12766377-12766715	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:12760728-12761077	IMR90	lung:	n/a	chr9:12760880-12760891 chr9:12760880-12760889
19	CEBPB	chr9:12749002-12749232	H1-hESC	embryonic stem cell:	n/a	chr9:12749138-12749149
20	CEBPB	chr9:12656840-12657079	H1-hESC	embryonic stem cell:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
21	CEBPB	chr9:12676985-12677220	HepG2	liver:	n/a	chr9:12677146-12677157 chr9:12677068-12677076
22	CEBPB	chr9:12698242-12698670	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:12723662-12724016	HepG2	liver:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
24	CEBPB	chr9:12702155-12702522	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr9:12681514-12681726	HepG2	liver:	n/a	chr9:12681604-12681615
26	CEBPB	chr9:12723472-12724107	A549	lung:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
27	CEBPB	chr9:12723615-12723923	MCF-7	breast:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
28	CEBPB	chr9:12759658-12760086	IMR90	lung:	n/a	n/a
29	CEBPB	chr9:12718687-12719000	H1-hESC	embryonic stem cell:	n/a	chr9:12718859-12718870
30	CEBPB	chr9:12756864-12756989	A549	lung:	n/a	n/a
31	CEBPB	chr9:12702101-12702516	A549	lung:	n/a	n/a
32	CEBPB	chr9:12723659-12723959	MCF-7	breast:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
33	CEBPB	chr9:12723634-12723995	A549	lung:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
34	CEBPB	chr9:12690390-12690469	K562	blood:	n/a	chr9:12690390-12690401 chr9:12690390-12690403 chr9:12690390-12690403 chr9:12690390-12690403
35	CEBPB	chr9:12765407-12765699	HepG2	liver:	n/a	chr9:12765544-12765555 chr9:12765557-12765570 chr9:12765559-12765570 chr9:12765545-12765556 chr9:12765557-12765568 chr9:12765557-12765570
36	CEBPB	chr9:12723546-12724141	HCT-116	colon:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
37	CEBPB	chr9:12723705-12723977	H1-hESC	embryonic stem cell:	n/a	chr9:12723826-12723837 chr9:12723826-12723839
38	CEBPB	chr9:12708437-12709072	HCT-116	colon:	n/a	chr9:12708963-12708975 chr9:12708893-12708906
39	CEBPB	chr9:12748962-12749329	IMR90	lung:	n/a	chr9:12749138-12749149
40	CEBPB	chr9:12643730-12643980	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:12702160-12702495	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:12765486-12765694	A549	lung:	n/a	chr9:12765544-12765555 chr9:12765557-12765570 chr9:12765559-12765570 chr9:12765545-12765556 chr9:12765557-12765568 chr9:12765557-12765570
43	CEBPB	chr9:12702152-12702503	A549	lung:	n/a	n/a
44	CEBPB	chr9:12656816-12657170	A549	lung:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
45	CEBPB	chr9:12766470-12766670	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:12656586-12657172	HepG2	liver:	n/a	chr9:12656979-12656988 chr9:12656681-12656694 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656681-12656692 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988 chr9:12656681-12656694
47	CEBPB	chr9:12681471-12681796	Hela-S3	cervix:	n/a	chr9:12681604-12681615
48	CEBPB	chr9:12712576-12712881	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr9:12656839-12657163	K562	blood:	n/a	chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656990 chr9:12656979-12656988 chr9:12656979-12656988 chr9:12656977-12656988
50	CEBPB	chr9:12712648-12712865	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:12704964-12705014	A549	lung:	n/a
2	chr9:12693326-12693376	H1-hESC	embryonic stem cell:	embryo
3	chr9:12693326-12693376	HPAEpiC	pulmonary alveolar:	n/a
4	chr9:12693326-12693376	HMEC	breast:	n/a
5	chr9:12693326-12693376	ovcar-3	ovarian:	n/a
6	chr9:12693326-12693376	SKMC	muscle:	n/a
7	chr9:12704964-12705014	NHBE	bronchial:	n/a
8	chr9:12704964-12705014	HL-60	blood:	n/a
9	chr9:12704964-12705014	ProgFib	skin:	n/a
10	chr9:12704964-12705014	GM12891	blood:	n/a
11	chr9:12693326-12693376	AG09309	skin:	n/a
12	chr9:12704964-12705014	Jurkat	blood:	n/a
13	chr9:12693326-12693376	AG04449	skin:	fetal
14	chr9:12693326-12693376	PANC-1	pancreas:	n/a
15	chr9:12704964-12705014	AoSMC	blood vessel:	n/a
16	chr9:12693694-12693744	NB4	blood:	n/a
17	chr9:12693326-12693376	HCM	heart:	n/a
18	chr9:12704964-12705014	HUVEC	blood vessel:	n/a
19	chr9:12693694-12693744	SAEC	small airway:	n/a
20	chr9:12704964-12705014	IMR90	lung:	fetal
21	chr9:12693326-12693376	MCF-7	breast:	n/a
22	chr9:12693326-12693376	SK-N-SH_RA	brain:	n/a
23	chr9:12693694-12693744	AG10803	skin:	n/a
24	chr9:12693694-12693744	HUVEC	blood vessel:	n/a
25	chr9:12693326-12693376	RPTEC	kidney:	n/a
26	chr9:12693694-12693744	GM19239	blood:	n/a
27	chr9:12693326-12693376	SK-N-MC	brain:	n/a
28	chr9:12693326-12693376	HRCEpiC	kidney:	n/a
29	chr9:12693326-12693376	GM12892	blood:	n/a
30	chr9:12693326-12693376	T-47D	breast:	n/a
31	chr9:12693694-12693744	T-47D	breast:	n/a
32	chr9:12693694-12693744	U87	brain:	n/a
33	chr9:12693326-12693376	NB4	blood:	n/a
34	chr9:12693694-12693744	HL-60	blood:	n/a
35	chr9:12693326-12693376	HAEpiC	amniotic membrane:	n/a
36	chr9:12704964-12705014	HRPEpiC	eye:	n/a
37	chr9:12704964-12705014	HRCEpiC	kidney:	n/a
38	chr9:12693694-12693744	AG09319	gingival:	n/a
39	chr9:12693694-12693744	HCF	heart:	n/a
40	chr9:12704964-12705014	GM12892	blood:	n/a
41	chr9:12693326-12693376	K562	blood:	n/a
42	chr9:12693694-12693744	HMEC	breast:	n/a
43	chr9:12693694-12693744	Caco-2	colon:	n/a
44	chr9:12693694-12693744	HRPEpiC	eye:	n/a
45	chr9:12693326-12693376	ECC-1	luminal epithelium:	n/a
46	chr9:12693694-12693744	HRE	kidney:	n/a
47	chr9:12693694-12693744	A549	lung:	n/a
48	chr9:12693326-12693376	PFSK-1	brain:	n/a
49	chr9:12704964-12705014	K562	blood:	n/a
50	chr9:12693694-12693744	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:12748565..12752577-chr9:12774636..12778893,4	MCF-7	breast:
2	chr9:12728162..12729688-chr9:12774800..12776867,2	MCF-7	breast:
3	chr9:12719485..12720037-chr9:12987933..12988498,2	MCF-7	breast:
4	chr9:12716514..12718700-chr9:12776478..12778096,2	MCF-7	breast:
5	chr9:12722041..12725292-chr9:12774361..12778280,6	MCF-7	breast:
6	chr9:12752690..12755433-chr9:12775370..12778156,2	MCF-7	breast:
7	chr9:12607055..12609983-chr9:12671838..12674027,2	K562	blood:
8	chr9:12736141..12737643-chr9:12774520..12776197,2	MCF-7	breast:
9	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
10	chr9:12771458..12774120-chr9:12775878..12777874,2	K562	blood:
11	chr9:12723429..12724424-chr9:12884471..12885741,6	MCF-7	breast:
12	chr9:12719062..12719862-chr9:12884578..12885277,2	MCF-7	breast:
13	chr9:12708111..12711033-chr9:13076014..13078647,2	MCF-7	breast:
14	chr9:12723856..12726602-chr9:12884690..12886916,2	MCF-7	breast:
15	chr9:12694806..12696732-chr9:12696808..12698503,2	MCF-7	breast:
16	chr9:12733476..12735004-chr9:12774992..12776567,2	MCF-7	breast:
17	chr9:12737180..12738894-chr9:12739213..12741322,2	MCF-7	breast:
18	chr9:12750217..12752763-chr9:12757622..12759170,2	MCF-7	breast:
19	chr9:12770939..12774696-chr9:12774747..12779041,5	MCF-7	breast:
20	chr9:12723685..12724314-chr9:12988034..12988919,3	MCF-7	breast:
21	chr9:12729225..12731478-chr9:12790178..12792905,2	MCF-7	breast:
22	chr9:12750217..12752763-chr9:12757622..12759170,2	MCF-7	breast:
23	chr9:12715023..12717622-chr9:12718396..12720573,2	MCF-7	breast:
24	chr9:12768044..12770724-chr9:12775061..12776621,2	MCF-7	breast:
25	chr9:12732393..12734244-chr9:12774652..12776497,2	MCF-7	breast:
26	chr9:12737180..12738894-chr9:12739213..12741322,2	MCF-7	breast:
27	chr9:12709414..12711296-chr9:14429666..14432393,2	MCF-7	breast:
28	chr9:12723451..12724539-chr9:12884675..12885414,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf150-1	chr9:12768922-12770158	XLOC_007283
2	lnc-MPDZ-8	chr9:12764762-12765054	NONHSAT130228
3	lnc-C9orf150-4	chr9:12693309-12693478	NONHSAT130224
4	lnc-C9orf150-2	chr9:12728519-12728662	l_3734_chr9:12728518-12759537_heart
5	lnc-C9orf150-4	chr9:12693912-12694487	NONHSAT130224
6	lnc-MPDZ-1	chr9:12700100-12700626	ENSG00000235448.1
7	lnc-MPDZ-1	chr9:12759551-12759623	ENSG00000235448.1
8	lnc-C9orf150-2	chr9:12758922-12759300	l_3734_chr9:12728518-12759537_heart
9	lnc-C9orf150-1	chr9:12738519-12738662	XLOC_007283
10	lnc-C9orf150-2	chr9:12759301-12759537	l_3734_chr9:12728518-12759537_heart

Variant related genes	Relation type
RN7SL849P	TF binding region
TYRP1	TF binding region
LURAP1L	TF binding region
RN7SL849P	CpG island
TYRP1	CpG island
LURAP1L	CpG island
ENSG00000153714	chromatin interactions
ENSG00000222658	chromatin interactions
ENSG00000107165	chromatin interactions

Extended variants
information (count: 6147 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:6147 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10960736	chr9:12641987-12641988	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529375369	chr9:12642005-12642006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549419468	chr9:12642035-12642036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140472653	chr9:12642039-12642040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs376737827	chr9:12642110-12642111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs3079505	chr9:12642111-12642112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34303491	chr9:12642122-12642123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs397838956	chr9:12642133-12642134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs386732771	chr9:12642134-12642135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61708718	chr9:12642135-12642136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552634596	chr9:12642140-12642141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535218523	chr9:12642168-12642169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201249998	chr9:12642176-12642177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10960737	chr9:12642181-12642182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs551687592	chr9:12642189-12642190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571594625	chr9:12642222-12642223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150428095	chr9:12642243-12642244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556560839	chr9:12642246-12642247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573534408	chr9:12642277-12642278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138240041	chr9:12642289-12642290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553022503	chr9:12642305-12642306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572999873	chr9:12642314-12642315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545200188	chr9:12642340-12642341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553664964	chr9:12642341-12642342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565210053	chr9:12642344-12642345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529235176	chr9:12642352-12642353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73647212	chr9:12642355-12642356	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs115139997	chr9:12642365-12642366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2031454	chr9:12642366-12642367	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs2025441	chr9:12642379-12642380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs149505992	chr9:12642440-12642441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549259495	chr9:12642454-12642455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559777538	chr9:12642471-12642472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566578136	chr9:12642482-12642483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367864703	chr9:12642483-12642484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528714813	chr9:12642519-12642520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201205359	chr9:12642537-12642538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs202176491	chr9:12642549-12642550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199736513	chr9:12642550-12642551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200394569	chr9:12642551-12642552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs55752074	chr9:12642574-12642575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576407480	chr9:12642637-12642638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551575740	chr9:12642651-12642652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571479903	chr9:12642652-12642653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537352029	chr9:12642690-12642691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs144808223	chr9:12642705-12642706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371645436	chr9:12642708-12642709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111469609	chr9:12642710-12642711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112756473	chr9:12642737-12642738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111707914	chr9:12642741-12642742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Disorders of sex development	21048976	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
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
Renal cell carcinoma	21215367	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12640200-12642000	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr9:12641400-12643600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:12643600-12644000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:12643600-12644000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:12644000-12651000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr9:12645000-12645400	Enhancers	Fetal Lung	lung
7	chr9:12648400-12649400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr9:12651000-12652000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:12652800-12653000	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr9:12653400-12654600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr9:12654600-12655400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr9:12655000-12655400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr9:12656000-12656400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr9:12656400-12656800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr9:12656800-12657400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:12658000-12659400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr9:12658000-12659400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:12658000-12659400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr9:12658800-12659800	Enhancers	HMEC	breast
20	chr9:12659000-12659600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr9:12659000-12659600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr9:12659000-12659800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:12659000-12659800	Enhancers	NHEK	skin
24	chr9:12659400-12666400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr9:12664000-12664200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:12666200-12667000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr9:12666400-12667400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr9:12666400-12669400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr9:12667200-12667600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:12667200-12667600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr9:12669400-12671200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr9:12670000-12670400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr9:12671200-12671800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr9:12671800-12672600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:12672600-12675400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr9:12674400-12676400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr9:12675400-12675600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr9:12675600-12677400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr9:12676400-12681000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr9:12677400-12677800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:12677800-12678000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:12678000-12678200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr9:12678200-12680000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr9:12679800-12682200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr9:12680000-12680200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr9:12680000-12680200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:12680000-12680800	Enhancers	Fetal Lung	lung
48	chr9:12680000-12680800	Enhancers	A549	lung
49	chr9:12680000-12681000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr9:12680000-12681200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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