Variant report

Variant	nsv892740
Chromosome Location	chr9:21471499-21551513
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	BCL3	chr9:21508689-21509632	A549	lung:	n/a	n/a
2	BCL3	chr9:21500520-21501100	A549	lung:	n/a	n/a
3	BCL3	chr9:21501977-21502583	A549	lung:	n/a	n/a
4	BCL3	chr9:21499752-21501285	A549	lung:	n/a	n/a
5	BCL3	chr9:21519608-21520690	A549	lung:	n/a	chr9:21519928-21519937
6	BCL3	chr9:21498490-21499615	A549	lung:	n/a	n/a
7	BCL3	chr9:21548899-21550745	A549	lung:	n/a	n/a
8	BCL3	chr9:21499921-21500395	A549	lung:	n/a	n/a
9	BCL3	chr9:21506616-21507704	A549	lung:	n/a	n/a
10	BCL3	chr9:21501331-21508410	A549	lung:	n/a	chr9:21506204-21506213
11	BCL3	chr9:21549187-21550089	A549	lung:	n/a	n/a
12	BCL3	chr9:21503475-21506429	A549	lung:	n/a	chr9:21506204-21506213
13	BRCA1	chr9:21548988-21549868	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr9:21548534-21548634	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr9:21520811-21522028	HCT-116	colon:	n/a	n/a
16	CBX3	chr9:21526174-21527163	HCT-116	colon:	n/a	n/a
17	CBX3	chr9:21519763-21526025	HCT-116	colon:	n/a	n/a
18	CBX3	chr9:21522147-21524471	HCT-116	colon:	n/a	n/a
19	CEBPB	chr9:21506792-21507249	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:21549314-21550172	A549	lung:	n/a	chr9:21549692-21549703
21	CEBPB	chr9:21519556-21521968	HCT-116	colon:	n/a	n/a
22	CEBPB	chr9:21549112-21550105	A549	lung:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
23	CEBPB	chr9:21549163-21550161	HCT-116	colon:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
24	CEBPB	chr9:21495278-21495540	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:21549459-21550071	A549	lung:	n/a	chr9:21549692-21549703
26	CEBPB	chr9:21493662-21493841	A549	lung:	n/a	n/a
27	CEBPB	chr9:21501197-21501480	A549	lung:	n/a	n/a
28	CEBPB	chr9:21549213-21550026	IMR90	lung:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
29	CEBPB	chr9:21506492-21507694	HCT-116	colon:	n/a	chr9:21507245-21507257
30	CEBPB	chr9:21551365-21551981	A549	lung:	n/a	n/a
31	CEBPB	chr9:21513524-21513835	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:21519283-21525730	HCT-116	colon:	n/a	n/a
33	CEBPB	chr9:21495325-21495569	A549	lung:	n/a	n/a
34	CEBPB	chr9:21495286-21495543	HepG2	liver:	n/a	n/a
35	CEBPB	chr9:21549138-21550039	Hela-S3	cervix:	n/a	chr9:21549276-21549287 chr9:21549692-21549703
36	CEBPB	chr9:21506801-21507249	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr9:21478670-21478870	A549	lung:	n/a	chr9:21478675-21478688
38	CHD2	chr9:21549127-21549911	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr9:21549503-21549856	A549	lung:	n/a	n/a
40	CREB1	chr9:21549320-21549833	A549	lung:	n/a	n/a
41	CTCF	chr9:21527780-21527930	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr9:21473340-21473490	HPAF	blood vessel:	n/a	chr9:21473366-21473387
43	CTCF	chr9:21527700-21527850	HepG2	liver:	n/a	n/a
44	CTCF	chr9:21549623-21549631	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr9:21527771-21527883	GM10248	blood:	n/a	n/a
46	CTCF	chr9:21473280-21473430	HRE	kidney:	n/a	chr9:21473366-21473387
47	CTCF	chr9:21473300-21473450	GM12871	blood:	n/a	chr9:21473366-21473387
48	CTCF	chr9:21527680-21527830	GM12864	blood:	n/a	n/a
49	CTCF	chr9:21473320-21473470	HCM	heart:	n/a	chr9:21473366-21473387
50	CTCF	chr9:21473340-21473490	HVMF	connective:	n/a	chr9:21473366-21473387

No.	Distal block	Cell Line	Cell type
1	chr14:68668658..68669180-chr9:21520044..21520625,2	HCT-116	colon:
2	chr9:21491433..21492444-chr9:21789127..21790263,7	MCF-7	breast:
3	chr14:74955326..74955958-chr9:21530738..21531280,2	HCT-116	colon:
4	chr9:21496297..21498448-chr9:21802383..21804700,2	MCF-7	breast:
5	chr11:61583818..61584553-chr9:21518322..21519322,2	HCT-116	colon:
6	chr9:21492643..21493283-chr9:21789425..21789929,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130385
2	lnc-IFNE-1	chr9:21477168-21477292	NONHSAT130388
3	lnc-IFNE-1	chr9:21476873-21477034	NONHSAT130389
4	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130388
5	lnc-IFNE-1	chr9:21476898-21477034	ENSG00000171889
6	lnc-IFNE-1	chr9:21476898-21477034	NONHSAT130386
7	lnc-IFNE-1	chr9:21477168-21477291	NONHSAT130385
8	lnc-IFNE-1	chr9:21477168-21477291	NONHSAT130386
9	lnc-IFNE-1	chr9:21477168-21477292	NONHSAT130389
10	lnc-IFNE-1	chr9:21477168-21477291	ENSG00000171889

miRNA name	Chromosome Location	mirBase accession
hsa-miR-31-3p	chr9:21512120-21512141	MIMAT0004504
hsa-miR-31-5p	chr9:21512157-21512177	MIMAT0000089

Variant related genes	Relation type
MIR31	TF binding region
ENSG00000264379	TF binding region
IFNE	TF binding region
ENSG00000264545	chromatin interactions
ENSG00000149485	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000099810	chromatin interactions
RICTOR	Mature miRNA region
NDFIP2	Mature miRNA region
MED12	Mature miRNA region
EXOSC5	Mature miRNA region
NFAT5	Mature miRNA region
ATP2A2	Mature miRNA region
FZD3	Mature miRNA region
ZC3H12C	Mature miRNA region
TNKS2	Mature miRNA region
PCSK1N	Mature miRNA region
MET	Mature miRNA region
ACADVL	Mature miRNA region
MMP16	Mature miRNA region
C1orf198	Mature miRNA region
DBR1	Mature miRNA region
CYP27B1	Mature miRNA region
TIAM1	Mature miRNA region
YY1	Mature miRNA region
DKK1	Mature miRNA region
FAM134C	Mature miRNA region
ZC3H18	Mature miRNA region
DMD	Mature miRNA region
HOXC13	Mature miRNA region
PTPRJ	Mature miRNA region
UBA6	Mature miRNA region
LATS2	Mature miRNA region
EXOC6	Mature miRNA region
FOXP3	Mature miRNA region
TRIB3	Mature miRNA region
PPP2R5C	Mature miRNA region
LRRC59	Mature miRNA region
DDX19A	Mature miRNA region
SATB2	Mature miRNA region
CDK1	Mature miRNA region
ITGA5	Mature miRNA region
ICAM1	Mature miRNA region
C2CD5	Mature miRNA region
MLH1	Mature miRNA region
DACT3	Mature miRNA region
JAZF1	Mature miRNA region
NUS1	Mature miRNA region
XK	Mature miRNA region
SELE	Mature miRNA region
SMEK2	Mature miRNA region
NFATC2IP	Mature miRNA region
NUP188	Mature miRNA region
DNAJC5	Mature miRNA region
MPRIP	Mature miRNA region
ARL6IP5	Mature miRNA region
NOP56	Mature miRNA region
AGO1	Mature miRNA region
ETS1	Mature miRNA region
RPL37A	Mature miRNA region
SRRM2	Mature miRNA region
HIST1H2BK	Mature miRNA region
TNRC6B	Mature miRNA region
TRRAP	Mature miRNA region
TXNDC5	Mature miRNA region
MYO1D	Mature miRNA region
INHBA	Mature miRNA region
HIF1AN	Mature miRNA region
RET	Mature miRNA region
SFXN1	Mature miRNA region
FLNA	Mature miRNA region
RPA1	Mature miRNA region
GLI2	Mature miRNA region
ARPC5	Mature miRNA region
PRKCE	Mature miRNA region
PPP2R2A	Mature miRNA region
HIST1H2BI	Mature miRNA region
NUMB	Mature miRNA region
STK40	Mature miRNA region
RAN	Mature miRNA region
EDC3	Mature miRNA region
CXCL12	Mature miRNA region
NOL9	Mature miRNA region
STOML2	Mature miRNA region
RASA1	Mature miRNA region
RANGAP1	Mature miRNA region
SLC9A6	Mature miRNA region
ZNF275	Mature miRNA region
MCM2	Mature miRNA region
HOXA7	Mature miRNA region
PPIA	Mature miRNA region
PPIL2	Mature miRNA region
GYG1	Mature miRNA region
RDX	Mature miRNA region
CIPC	Mature miRNA region
KLF13	Mature miRNA region
CASR	Mature miRNA region
AKAP8L	Mature miRNA region
RPS7	Mature miRNA region
CREG1	Mature miRNA region
RHOA	Mature miRNA region
MCM4	Mature miRNA region
ILF2	Mature miRNA region
RPS4Y1	Mature miRNA region
HEATR2	Mature miRNA region
PEX19	Mature miRNA region
HIST1H2BJ	Mature miRNA region
GHITM	Mature miRNA region
EEF1A1	miRNA target sites
RPP40	miRNA target sites

Extended variants
information (count: 3370 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:3370 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1412395	chr9:21471499-21471500	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs78588252	chr9:21471531-21471532	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537421800	chr9:21471540-21471541	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs111914895	chr9:21471593-21471594	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566098811	chr9:21471603-21471604	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs115668153	chr9:21471615-21471616	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372427909	chr9:21471625-21471626	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs181866358	chr9:21471638-21471639	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs570543130	chr9:21471648-21471649	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539545512	chr9:21471707-21471708	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs117832159	chr9:21471721-21471722	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2383192	chr9:21471726-21471727	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs371853805	chr9:21471776-21471777	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149279271	chr9:21471798-21471799	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554822118	chr9:21471839-21471840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574661103	chr9:21471844-21471845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537278310	chr9:21471859-21471860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543735424	chr9:21471861-21471862	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139270998	chr9:21471881-21471882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs144102204	chr9:21471933-21471934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10965009	chr9:21471957-21471958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190184338	chr9:21471996-21471997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs117346827	chr9:21471997-21471998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548517183	chr9:21472015-21472016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562368929	chr9:21472041-21472042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376420609	chr9:21472062-21472063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375376673	chr9:21472095-21472096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370718826	chr9:21472099-21472100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531092068	chr9:21472119-21472120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550912402	chr9:21472136-21472137	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181802349	chr9:21472160-21472161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539458659	chr9:21472165-21472166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376224894	chr9:21472355-21472356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146016304	chr9:21472364-21472365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538369883	chr9:21472373-21472374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs75135358	chr9:21472392-21472393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10965010	chr9:21472419-21472420	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs148702974	chr9:21472475-21472476	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537340271	chr9:21472478-21472479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186304195	chr9:21472492-21472493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371268098	chr9:21472503-21472504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191218595	chr9:21472518-21472519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114127183	chr9:21472594-21472595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181407502	chr9:21472596-21472597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572864222	chr9:21472681-21472682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374383371	chr9:21472701-21472702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541939666	chr9:21472744-21472745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185289265	chr9:21472779-21472780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117633264	chr9:21472828-21472829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557876156	chr9:21472852-21472853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:158)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Oral squamous cell carcinoma	17134496	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
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	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
Chronic myeloid leukemia	21384125	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
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Glioblastoma multiforme	21569311	CNVD
Myelofibrosis	22110671	CNVD
Ewing''s sarcoma	22429812	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	19435819	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Lung cancer	21911935	CNVD
Primary central nervous system lymphoma	21088137	CNVD
head and neck squamous cell carcinoma	21798897	CNVD
Cancer	21253487	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Leukemia	19602459	CNVD
Acute monocytic leukemia	16498392	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Leukemia	18688285	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Glioma	20126413	CNVD
Melanoma	17363583	CNVD
Glioblastoma multiforme	19115005	CNVD
Glioblastoma multiforme	21525872	CNVD
Glioblastoma multiforme	21138945	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Cancer	20581869	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Oral cancer	22144094	CNVD
Lung cancer	21569311	CNVD
Epilepsy	20502679	CNVD
Barrett''s syndrome	19417022	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:933 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:21454800-21474400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr9:21454800-21481600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr9:21455200-21481000	Weak transcription	NHDF-Ad	bronchial
4	chr9:21455800-21481000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr9:21456000-21476600	Weak transcription	NHLF	lung
6	chr9:21462600-21474600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr9:21463000-21502200	Weak transcription	HSMM	muscle
8	chr9:21465400-21474600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr9:21466000-21473600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:21466000-21527600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:21467000-21478600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr9:21468600-21477600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:21468800-21473400	Weak transcription	NHEK	skin
14	chr9:21469000-21476400	Weak transcription	A549	lung
15	chr9:21469000-21478200	Strong transcription	Osteobl	bone
16	chr9:21469200-21477800	Strong transcription	HMEC	breast
17	chr9:21469400-21471800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr9:21470200-21472000	Strong transcription	Muscle Satellite Cultured Cells	--
19	chr9:21470200-21477800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:21470800-21471600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr9:21470800-21473400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr9:21471000-21471600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:21471000-21471800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr9:21471400-21477800	Strong transcription	NH-A	brain
25	chr9:21471600-21505600	Weak transcription	HUVEC	blood vessel
26	chr9:21471800-21473400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr9:21472000-21472800	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr9:21472800-21473800	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr9:21473400-21473600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr9:21473400-21475400	Strong transcription	NHEK	skin
31	chr9:21473400-21475800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr9:21473600-21474200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr9:21473600-21475000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr9:21473800-21476400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr9:21474200-21474600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr9:21474400-21477000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr9:21474600-21475000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr9:21474600-21475400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr9:21474600-21475800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr9:21475000-21481000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr9:21475000-21485600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr9:21475400-21478000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr9:21475400-21481000	Weak transcription	NHEK	skin
44	chr9:21475800-21476600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr9:21475800-21477400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr9:21476400-21477200	Strong transcription	A549	lung
47	chr9:21476400-21478400	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr9:21476600-21477400	Strong transcription	NHLF	lung
49	chr9:21476600-21477800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:21476600-21481200	Weak transcription	Stomach Mucosa	stomach

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