Variant report

Variant	nsv516951
Chromosome Location	chr9:569992-704075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1669)
CpG islands
(count:61)
Chromatin interactive
region (count:42)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1669 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
9	BACH1	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:652937-653241	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
14	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
15	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
16	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
17	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
18	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
19	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:650454-650746	H1-hESC	embryonic stem cell:	n/a	chr9:650606-650617
21	CEBPB	chr9:589772-590180	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr9:694779-695136	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr9:677054-677465	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:650527-650679	HepG2	liver:	n/a	chr9:650606-650617
25	CEBPB	chr9:599936-600319	K562	blood:	n/a	chr9:600087-600098 chr9:600123-600134
26	CEBPB	chr9:674165-674905	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr9:683597-683939	HepG2	liver:	n/a	chr9:683771-683782
28	CEBPB	chr9:647225-647438	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr9:687423-687597	HepG2	liver:	n/a	chr9:687549-687562
30	CEBPB	chr9:677101-677415	A549	lung:	n/a	n/a
31	CEBPB	chr9:599936-600484	Hela-S3	cervix:	n/a	chr9:600087-600098 chr9:600123-600134
32	CEBPB	chr9:647176-647333	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:614904-615126	HepG2	liver:	n/a	chr9:614996-615007
34	CEBPB	chr9:694718-695117	A549	lung:	n/a	n/a
35	CEBPB	chr9:599971-600359	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
36	CEBPB	chr9:653004-653086	K562	blood:	n/a	n/a
37	CEBPB	chr9:602628-603112	MCF-7	breast:	n/a	n/a
38	CEBPB	chr9:614887-615070	H1-hESC	embryonic stem cell:	n/a	chr9:614996-615007
39	CEBPB	chr9:573616-573837	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr9:652997-653155	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr9:702920-703098	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:599889-600308	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
43	CEBPB	chr9:618469-618742	A549	lung:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
44	CEBPB	chr9:694740-695175	A549	lung:	n/a	n/a
45	CEBPB	chr9:650489-650689	A549	lung:	n/a	chr9:650606-650617
46	CEBPB	chr9:693275-695253	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:673657-674592	HepG2	liver:	n/a	n/a
48	CEBPB	chr9:618492-618642	H1-hESC	embryonic stem cell:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
49	CEBPB	chr9:599921-600405	A549	lung:	n/a	chr9:600087-600098 chr9:600123-600134
50	CEBPB	chr9:647187-647486	HepG2	liver:	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	A549	lung:	n/a
2	chr9:574312-574362	SK-N-SH_RA	brain:	n/a
3	chr9:574312-574362	ECC-1	luminal epithelium:	n/a
4	chr9:574312-574362	GM19239	blood:	n/a
5	chr9:574312-574362	HCF	heart:	n/a
6	chr9:574312-574362	Hepatocyte	liver:	n/a
7	chr9:574312-574362	HCPEpiC	choroid plexus:	n/a
8	chr9:574312-574362	H1-hESC	embryonic stem cell:	embryo
9	chr9:574312-574362	Caco-2	colon:	n/a
10	chr9:574312-574362	AG04449	skin:	fetal
11	chr9:574312-574362	Hela-S3	cervix:	n/a
12	chr9:574312-574362	HRE	kidney:	n/a
13	chr9:574312-574362	NB4	blood:	n/a
14	chr9:574312-574362	ProgFib	skin:	n/a
15	chr9:574312-574362	HCT-116	colon:	n/a
16	chr9:574312-574362	RPTEC	kidney:	n/a
17	chr9:574312-574362	SK-N-SH	brain:	n/a
18	chr9:574312-574362	HRCEpiC	kidney:	n/a
19	chr9:574312-574362	HPAEpiC	pulmonary alveolar:	n/a
20	chr9:574312-574362	CMK	blood:	n/a
21	chr9:574312-574362	U87	brain:	n/a
22	chr9:574312-574362	GM12891	blood:	n/a
23	chr9:574312-574362	PFSK-1	brain:	n/a
24	chr9:574312-574362	HepG2	liver:	n/a
25	chr9:574312-574362	ovcar-3	ovarian:	n/a
26	chr9:574312-574362	HAEpiC	amniotic membrane:	n/a
27	chr9:574312-574362	BE2_C	brain:	n/a
28	chr9:574312-574362	PANC-1	pancreas:	n/a
29	chr9:574312-574362	MCF-7	breast:	n/a
30	chr9:574312-574362	GM06990	blood:	n/a
31	chr9:574312-574362	AG04450	lung:	fetal
32	chr9:574312-574362	AG10803	skin:	n/a
33	chr9:574312-574362	NH-A	brain:	n/a
34	chr9:574312-574362	NT2-D1	testis:	n/a
35	chr9:574312-574362	IMR90	lung:	fetal
36	chr9:574312-574362	AG09309	skin:	n/a
37	chr9:574312-574362	GM12892	blood:	n/a
38	chr9:574312-574362	HCM	heart:	n/a
39	chr9:574312-574362	NHDF-neo	bronchial:	n/a
40	chr9:574312-574362	HMEC	breast:	n/a
41	chr9:574312-574362	SAEC	small airway:	n/a
42	chr9:574312-574362	HL-60	blood:	n/a
43	chr9:574312-574362	HNPCEpiC	eye:	n/a
44	chr9:574312-574362	HRPEpiC	eye:	n/a
45	chr9:574312-574362	Jurkat	blood:	n/a
46	chr9:574312-574362	HEEpiC	esophagus:	n/a
47	chr9:574312-574362	AG09319	gingival:	n/a
48	chr9:574312-574362	HUVEC	blood vessel:	n/a
49	chr9:574312-574362	HIPEpiC	eye:	n/a
50	chr9:574312-574362	PrEC	prostate:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
2	chr9:613814..614512-chr9:1017801..1018342,2	MCF-7	breast:
3	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
4	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
5	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
6	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
7	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
8	chr9:697287..699295-chr9:705065..707332,2	K562	blood:
9	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
10	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
11	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
12	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
13	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
14	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
15	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
16	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
17	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
18	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
19	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
20	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
21	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
22	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
23	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
24	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
25	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
26	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
27	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
28	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
29	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
30	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
31	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
32	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
33	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
34	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
35	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
36	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
37	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
38	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
39	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
40	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
41	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
42	chr9:385789..386423-chr9:612104..612846,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf66-3	chr9:673817-674379	ENSG00000227914.1
2	lnc-C9orf66-3	chr9:674124-674379	ENSG00000227914.3
3	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.3
4	lnc-DMRT1-3	chr9:659986-660326	NONHSAT129934
5	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.3
6	lnc-C9orf66-3	chr9:680857-681046	ENSG00000227914.1
7	lnc-C9orf66-3	chr9:673478-674379	ENSG00000227914.3
8	lnc-C9orf66-3	chr9:685528-685555	ENSG00000227914.1
9	lnc-C9orf66-3	chr9:677542-677628	ENSG00000227914.3

No data

Variant related genes	Relation type
ENSG00000227914	TF binding region
KANK1	TF binding region
ENSG00000229875	TF binding region
ENSG00000227914	CpG island
KANK1	CpG island
ENSG00000229875	CpG island
ENSG00000107104	chromatin interactions

Extended variants
information (count: 8059 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:8059 , 50 per page) page: 1 2 3 4 5 6 7 ... 162

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs881985	chr9:569992-569993	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372996482	chr9:570006-570007	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs557751362	chr9:570045-570046	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs144871037	chr9:570054-570055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs74579491	chr9:570100-570101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs116784538	chr9:570135-570136	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs149030247	chr9:570170-570171	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs536857528	chr9:570181-570182	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs556855214	chr9:570185-570186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs576826662	chr9:570206-570207	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs368620572	chr9:570215-570216	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs143102692	chr9:570272-570273	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs114871261	chr9:570274-570275	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs554606945	chr9:570279-570280	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs73639371	chr9:570306-570307	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188871444	chr9:570338-570339	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs560194420	chr9:570357-570358	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs529035882	chr9:570359-570360	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs541795544	chr9:570416-570417	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs148213795	chr9:570431-570432	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs562414993	chr9:570497-570498	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs140680695	chr9:570500-570501	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs560278984	chr9:570525-570526	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs551344599	chr9:570526-570527	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs191750852	chr9:570536-570537	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369133053	chr9:570539-570540	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs534297651	chr9:570597-570598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs547527867	chr9:570599-570600	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs183920965	chr9:570626-570627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs72689642	chr9:570649-570650	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs188207353	chr9:570652-570653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs114488355	chr9:570660-570661	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112811709	chr9:570662-570663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180766423	chr9:570683-570684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs185746132	chr9:570685-570686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs903222	chr9:570689-570690	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368654514	chr9:570733-570734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370167788	chr9:570734-570735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs114173810	chr9:570744-570745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190219921	chr9:570757-570758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117683448	chr9:570800-570801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542391517	chr9:570811-570812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs181933881	chr9:570816-570817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185853350	chr9:570822-570823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs138482782	chr9:570836-570837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs16919886	chr9:570846-570847	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs563231032	chr9:570858-570859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531908878	chr9:570871-570872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs527647627	chr9:570899-570900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547785479	chr9:570905-570906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	21272361	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:3611 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:547600-571200	Weak transcription	Aorta	Aorta
2	chr9:549800-593800	Weak transcription	Lung	lung
3	chr9:552400-574000	Weak transcription	Right Ventricle	heart
4	chr9:559000-571000	Weak transcription	Psoas Muscle	Psoas
5	chr9:559000-573600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:561800-570000	Weak transcription	Fetal Lung	lung
7	chr9:563000-572600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr9:564600-571000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr9:565800-571000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr9:565800-571000	Weak transcription	NHEK	skin
11	chr9:565800-573800	Weak transcription	HMEC	breast
12	chr9:565800-574000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:566600-571000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr9:566600-573800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr9:567000-573000	Enhancers	Fetal Intestine Large	intestine
16	chr9:567200-571800	Enhancers	Liver	Liver
17	chr9:567200-572400	Enhancers	Fetal Intestine Small	intestine
18	chr9:567800-570400	Weak transcription	Brain Anterior Caudate	brain
19	chr9:567800-570400	Weak transcription	Brain Hippocampus Middle	brain
20	chr9:567800-573800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr9:568000-571200	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr9:568600-570400	Weak transcription	Stomach Mucosa	stomach
23	chr9:569200-571000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr9:569200-574000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:569200-574000	Weak transcription	Gastric	stomach
26	chr9:569400-570400	Weak transcription	Right Atrium	heart
27	chr9:569400-571000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr9:569400-571400	Enhancers	Brain Substantia Nigra	brain
29	chr9:569400-572000	Enhancers	Brain Cingulate Gyrus	brain
30	chr9:569400-573600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr9:569600-570400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:569600-570400	Weak transcription	Left Ventricle	heart
33	chr9:569600-570400	Weak transcription	Pancreas	Pancrea
34	chr9:569600-570600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr9:569600-571000	Weak transcription	Ovary	ovary
36	chr9:569600-574000	Weak transcription	Esophagus	oesophagus
37	chr9:569800-570200	Weak transcription	A549	lung
38	chr9:569800-570600	Flanking Active TSS	Fetal Heart	heart
39	chr9:569800-571600	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr9:570000-572000	Enhancers	Brain Angular Gyrus	brain
41	chr9:570000-572400	Enhancers	Fetal Lung	lung
42	chr9:570200-572200	Enhancers	A549	lung
43	chr9:570400-570600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr9:570400-571200	Enhancers	Pancreas	Pancrea
45	chr9:570400-571400	Enhancers	Left Ventricle	heart
46	chr9:570400-571400	Enhancers	Right Atrium	heart
47	chr9:570400-572000	Enhancers	Brain Anterior Caudate	brain
48	chr9:570400-572000	Enhancers	Stomach Mucosa	stomach
49	chr9:570400-576000	Enhancers	Brain Hippocampus Middle	brain
50	chr9:570600-571200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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