Variant report

Variant	nsv1034085
Chromosome Location	chr9:519256-617804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1100)
CpG islands
(count:61)
Chromatin interactive
region (count:37)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
3	ATF3	chr9:557723-558324	A549	lung:	n/a	n/a
4	BACH1	chr9:561382-561724	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:557912-558114	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr9:561341-561682	GM12878	blood:	n/a	n/a
7	BCL3	chr9:557812-558394	A549	lung:	n/a	n/a
8	BCL3	chr9:561269-561869	A549	lung:	n/a	n/a
9	BHLHE40	chr9:567560-567673	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:546835-547287	K562	blood:	n/a	n/a
11	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
12	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:599921-600405	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
14	CEBPB	chr9:614887-615070	H1-hESC	embryonic stem cell:	n/a	chr9:614996-615007
15	CEBPB	chr9:599942-600395	HepG2	liver:	n/a	chr9:600087-600098 chr9:600123-600134
16	CEBPB	chr9:599945-600321	H1-hESC	embryonic stem cell:	n/a	chr9:600087-600098 chr9:600123-600134
17	CEBPB	chr9:561463-561714	A549	lung:	n/a	n/a
18	CEBPB	chr9:599907-600250	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
19	CEBPB	chr9:561371-561765	A549	lung:	n/a	n/a
20	CEBPB	chr9:530695-530959	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr9:573656-573820	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr9:530749-531005	A549	lung:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
23	CEBPB	chr9:563605-564145	A549	lung:	n/a	n/a
24	CEBPB	chr9:530652-530956	A549	lung:	n/a	n/a
25	CEBPB	chr9:561219-561918	A549	lung:	n/a	n/a
26	CEBPB	chr9:614904-615126	HepG2	liver:	n/a	chr9:614996-615007
27	CEBPB	chr9:599936-600484	Hela-S3	cervix:	n/a	chr9:600087-600098 chr9:600123-600134
28	CEBPB	chr9:530490-531138	HCT-116	colon:	n/a	chr9:530982-530993 chr9:530982-530995 chr9:530982-530995 chr9:530982-530993
29	CEBPB	chr9:599943-600381	IMR90	lung:	n/a	chr9:600087-600098 chr9:600123-600134
30	CEBPB	chr9:589772-590180	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:599844-600456	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
32	CEBPB	chr9:573616-573837	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:561474-561777	MCF-7	breast:	n/a	n/a
34	CEBPB	chr9:589903-590000	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr9:599836-600408	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
36	CEBPB	chr9:602928-603376	MCF-7	breast:	n/a	n/a
37	CEBPB	chr9:599936-600319	K562	blood:	n/a	chr9:600087-600098 chr9:600123-600134
38	CEBPB	chr9:604811-604854	A549	lung:	n/a	n/a
39	CEBPB	chr9:599889-600308	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
40	CEBPB	chr9:602628-603112	MCF-7	breast:	n/a	n/a
41	CEBPB	chr9:599948-600356	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
42	CEBPB	chr9:599971-600359	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
43	CHD1	chr9:557966-558051	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr9:567407-567657	GM12878	blood:	n/a	n/a
45	CHD2	chr9:617710-617715	HepG2	liver:	n/a	n/a
46	CHD2	chr9:591485-591533	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr9:614613-614676	HepG2	liver:	n/a	n/a
48	CREB1	chr9:557738-558028	A549	lung:	n/a	n/a
49	CREB1	chr9:591355-591625	A549	lung:	n/a	n/a
50	CREB1	chr9:591330-591688	A549	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:574312-574362	HCM	heart:	n/a
2	chr9:574312-574362	HMEC	breast:	n/a
3	chr9:574312-574362	HepG2	liver:	n/a
4	chr9:574312-574362	U87	brain:	n/a
5	chr9:574312-574362	HRPEpiC	eye:	n/a
6	chr9:574312-574362	SK-N-MC	brain:	n/a
7	chr9:574312-574362	MCF10A-Er-Src	breast:	n/a
8	chr9:574312-574362	GM19239	blood:	n/a
9	chr9:574312-574362	SK-N-SH	brain:	n/a
10	chr9:574312-574362	AG10803	skin:	n/a
11	chr9:574312-574362	BE2_C	brain:	n/a
12	chr9:574312-574362	ProgFib	skin:	n/a
13	chr9:574312-574362	GM12891	blood:	n/a
14	chr9:574312-574362	PFSK-1	brain:	n/a
15	chr9:574312-574362	HRCEpiC	kidney:	n/a
16	chr9:574312-574362	HNPCEpiC	eye:	n/a
17	chr9:574312-574362	HCPEpiC	choroid plexus:	n/a
18	chr9:574312-574362	AG09309	skin:	n/a
19	chr9:574312-574362	GM06990	blood:	n/a
20	chr9:574312-574362	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:574312-574362	GM12892	blood:	n/a
22	chr9:574312-574362	AG09319	gingival:	n/a
23	chr9:574312-574362	SAEC	small airway:	n/a
24	chr9:574312-574362	A549	lung:	n/a
25	chr9:574312-574362	K562	blood:	n/a
26	chr9:574312-574362	RPTEC	kidney:	n/a
27	chr9:574312-574362	HEK293	kidney:	embryo
28	chr9:574312-574362	AG04450	lung:	fetal
29	chr9:574312-574362	NB4	blood:	n/a
30	chr9:574312-574362	HCF	heart:	n/a
31	chr9:574312-574362	NHBE	bronchial:	n/a
32	chr9:574312-574362	HL-60	blood:	n/a
33	chr9:574312-574362	Jurkat	blood:	n/a
34	chr9:574312-574362	SKMC	muscle:	n/a
35	chr9:574312-574362	IMR90	lung:	fetal
36	chr9:574312-574362	PrEC	prostate:	n/a
37	chr9:574312-574362	GM12878	blood:	n/a
38	chr9:574312-574362	SK-N-SH_RA	brain:	n/a
39	chr9:574312-574362	Caco-2	colon:	n/a
40	chr9:574312-574362	H1-hESC	embryonic stem cell:	embryo
41	chr9:574312-574362	ECC-1	luminal epithelium:	n/a
42	chr9:574312-574362	NH-A	brain:	n/a
43	chr9:574312-574362	LNCaP	prostate:	n/a
44	chr9:574312-574362	HIPEpiC	eye:	n/a
45	chr9:574312-574362	HEEpiC	esophagus:	n/a
46	chr9:574312-574362	BJ	skin:	n/a
47	chr9:574312-574362	HAEpiC	amniotic membrane:	n/a
48	chr9:574312-574362	ovcar-3	ovarian:	n/a
49	chr9:574312-574362	AG04449	skin:	fetal
50	chr9:574312-574362	HUVEC	blood vessel:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
2	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
3	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
4	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
5	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
6	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
7	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
8	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
9	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
10	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
11	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
12	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
13	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
14	chr9:469326..471004-chr9:547085..549851,2	MCF-7	breast:
15	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
16	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
17	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
18	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
19	chr9:530586..533539-chr9:534026..536380,2	MCF-7	breast:
20	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
21	chr9:535330..537087-chr9:549296..551126,2	K562	blood:
22	chr9:555602..557901-chr9:561314..563396,2	K562	blood:
23	chr9:385596..386468-chr9:546637..547164,2	MCF-7	breast:
24	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
25	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
26	chr9:385789..386423-chr9:612104..612846,2	K562	blood:
27	chr9:523311..524277-chr9:542856..543632,2	MCF-7	breast:
28	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
29	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
30	chr9:518740..521510-chr9:531283..533605,2	MCF-7	breast:
31	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
32	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
33	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
34	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
35	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
36	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
37	chr9:582031..585321-chr9:586707..590039,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK8-2	chr9:547317-547341	ENSG00000226403.1
2	lnc-DOCK8-2	chr9:549107-549525	NONHSAT129931
3	lnc-DOCK8-2	chr9:547038-547341	NONHSAT129931
4	lnc-DOCK8-2	chr9:549107-549531	ENSG00000226403.1
5	lnc-DOCK8-2	chr9:549190-549531	ENSG00000226403.1
6	lnc-DOCK8-2	chr9:547318-547341	ENSG00000226403.1

No data

Variant related genes	Relation type
ENSG00000226403	TF binding region
RNU6-1327P	TF binding region
ENSG00000226403	CpG island
RNU6-1327P	CpG island
ENSG00000227155	chromatin interactions
ENSG00000107104	chromatin interactions

Extended variants
information (count: 5731 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:5731 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371796582	chr9:519319-519320	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539456313	chr9:519323-519324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188844934	chr9:519339-519340	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573276009	chr9:519361-519362	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536010554	chr9:519372-519373	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148887728	chr9:519412-519413	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575986184	chr9:519419-519420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544966219	chr9:519425-519426	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141124662	chr9:519429-519430	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191777614	chr9:519451-519452	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576862574	chr9:519473-519474	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536030591	chr9:519484-519485	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs34794396	chr9:519507-519508	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117200309	chr9:519519-519520	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559365748	chr9:519541-519542	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528212236	chr9:519574-519575	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184373228	chr9:519594-519595	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555887310	chr9:519631-519632	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201866439	chr9:519643-519644	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72705668	chr9:519666-519667	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs143543102	chr9:519678-519679	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189306185	chr9:519693-519694	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112753046	chr9:519694-519695	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182198842	chr9:519717-519718	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112982642	chr9:519724-519725	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72705669	chr9:519732-519733	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76229240	chr9:519773-519774	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540885652	chr9:519782-519783	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558541841	chr9:519792-519793	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535603085	chr9:519807-519808	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79137374	chr9:519808-519809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569511986	chr9:519814-519815	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538444891	chr9:519818-519819	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558463443	chr9:519823-519824	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187576006	chr9:519825-519826	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74960756	chr9:519897-519898	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs552724999	chr9:519941-519942	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572894286	chr9:519942-519943	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544266215	chr9:519943-519944	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189257965	chr9:520028-520029	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs561152445	chr9:520060-520061	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561458212	chr9:520064-520065	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs145786107	chr9:520085-520086	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs28560187	chr9:520159-520160	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544022703	chr9:520190-520191	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564002343	chr9:520195-520196	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1976260	chr9:520211-520212	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369897843	chr9:520222-520223	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112567592	chr9:520228-520229	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540018562	chr9:520241-520242	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	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
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
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
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
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-small cell lung cancer	16651412	CNVD

Chromatin state (count:2030 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:506000-520000	Weak transcription	Aorta	Aorta
2	chr9:506000-520200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr9:506400-519600	Weak transcription	Colon Smooth Muscle	Colon
4	chr9:507000-532600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr9:508400-522400	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:512400-522400	Weak transcription	Right Ventricle	heart
7	chr9:513400-520800	Weak transcription	Fetal Lung	lung
8	chr9:513400-521000	Weak transcription	Brain Substantia Nigra	brain
9	chr9:513400-522400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr9:513600-522800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr9:514000-532200	Weak transcription	Fetal Muscle Trunk	muscle
12	chr9:514800-519400	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr9:516000-521400	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr9:516200-520800	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr9:517000-522400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr9:517400-520600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr9:517400-522200	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr9:517600-519400	Enhancers	Fetal Intestine Large	intestine
19	chr9:517600-520800	Weak transcription	Brain Hippocampus Middle	brain
20	chr9:517800-520000	Enhancers	Primary T cells from cord blood	blood
21	chr9:518000-522000	Weak transcription	Colonic Mucosa	Colon
22	chr9:518000-522400	Weak transcription	Lung	lung
23	chr9:518200-519400	Enhancers	Right Atrium	heart
24	chr9:518200-522400	Enhancers	Fetal Heart	heart
25	chr9:518400-519400	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr9:518400-519600	Enhancers	Brain Anterior Caudate	brain
27	chr9:518600-519400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr9:518600-520000	Enhancers	Stomach Mucosa	stomach
29	chr9:518600-522400	Weak transcription	Fetal Kidney	kidney
30	chr9:518600-522400	Weak transcription	Stomach Smooth Muscle	stomach
31	chr9:518800-520000	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr9:518800-520000	Weak transcription	Left Ventricle	heart
33	chr9:518800-520000	Weak transcription	Pancreas	Pancrea
34	chr9:518800-520200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr9:518800-520200	Enhancers	Duodenum Mucosa	Duodenum
36	chr9:518800-520200	Strong transcription	A549	lung
37	chr9:518800-528800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr9:518800-529400	Weak transcription	NHEK	skin
39	chr9:518800-529600	Weak transcription	HMEC	breast
40	chr9:519000-519400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr9:519000-520200	Weak transcription	Small Intestine	intestine
42	chr9:519000-520600	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr9:519000-525400	Weak transcription	Fetal Intestine Small	intestine
44	chr9:519200-519400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr9:519200-522800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr9:519400-519600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr9:519400-519800	Weak transcription	Right Atrium	heart
48	chr9:519400-520400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr9:519400-521000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr9:519400-527000	Weak transcription	Fetal Intestine Large	intestine

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