Variant report

Variant	nsv482662
Chromosome Location	chr9:571838-722561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2017)
CpG islands
(count:366)
Chromatin interactive
region (count:53)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2017 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:672953-673149	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:592251-592433	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:673768-674544	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:716213-716255	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:685087-685396	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:613790-614724	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:682346-683925	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:676651-678350	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:696723-696891	HepG2	liver:	n/a	n/a
10	ARID3A	chr9:706757-707182	HepG2	liver:	n/a	chr9:706927-706943
11	ARID3A	chr9:710020-710338	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:706038-706477	HepG2	liver:	n/a	n/a
13	BACH1	chr9:706737-707111	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:652937-653241	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:674115-674612	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr9:674204-674357	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr9:674131-674488	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr9:694616-695281	A549	lung:	n/a	n/a
19	BHLHE40	chr9:682623-683064	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:614452-614687	HepG2	liver:	n/a	n/a
21	BHLHE40	chr9:682578-683474	HepG2	liver:	n/a	n/a
22	BHLHE40	chr9:706697-706897	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:694893-695215	A549	lung:	n/a	n/a
24	BHLHE40	chr9:629150-629515	GM12878	blood:	n/a	n/a
25	BRCA1	chr9:613818-614198	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr9:614887-615070	H1-hESC	embryonic stem cell:	n/a	chr9:614996-615007
27	CEBPB	chr9:618469-618742	A549	lung:	n/a	chr9:618588-618601 chr9:618588-618601 chr9:618588-618599 chr9:618590-618601
28	CEBPB	chr9:650441-650784	IMR90	lung:	n/a	chr9:650606-650617
29	CEBPB	chr9:650475-650734	HepG2	liver:	n/a	chr9:650606-650617
30	CEBPB	chr9:647176-647333	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr9:599948-600356	MCF-7	breast:	n/a	chr9:600087-600098 chr9:600123-600134
32	CEBPB	chr9:693275-695253	IMR90	lung:	n/a	n/a
33	CEBPB	chr9:599971-600359	ECC-1	luminal epithelium:	n/a	chr9:600087-600098 chr9:600123-600134
34	CEBPB	chr9:694779-695136	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr9:650454-650746	H1-hESC	embryonic stem cell:	n/a	chr9:650606-650617
36	CEBPB	chr9:710023-710247	HepG2	liver:	n/a	n/a
37	CEBPB	chr9:614904-615126	HepG2	liver:	n/a	chr9:614996-615007
38	CEBPB	chr9:682501-683161	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:694718-695117	A549	lung:	n/a	n/a
40	CEBPB	chr9:599943-600381	IMR90	lung:	n/a	chr9:600087-600098 chr9:600123-600134
41	CEBPB	chr9:709974-710470	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:602928-603376	MCF-7	breast:	n/a	n/a
43	CEBPB	chr9:710003-710250	A549	lung:	n/a	n/a
44	CEBPB	chr9:673758-673927	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:710012-710271	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:706925-707259	IMR90	lung:	n/a	n/a
47	CEBPB	chr9:602628-603112	MCF-7	breast:	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	chr9:650489-650689	A549	lung:	n/a	chr9:650606-650617
50	CEBPB	chr9:573656-573820	H1-hESC	embryonic stem cell:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:707166-707216	HCT-116	colon:	n/a
2	chr9:707166-707216	U87	brain:	n/a
3	chr9:707387-707437	Jurkat	blood:	n/a
4	chr9:705143-705193	HCPEpiC	choroid plexus:	n/a
5	chr9:705143-705193	HEK293	kidney:	embryo
6	chr9:707410-707460	HMEC	breast:	n/a
7	chr9:714269-714319	A549	lung:	n/a
8	chr9:707410-707460	PrEC	prostate:	n/a
9	chr9:714269-714319	HEEpiC	esophagus:	n/a
10	chr9:707410-707460	Hepatocyte	liver:	n/a
11	chr9:705143-705193	Jurkat	blood:	n/a
12	chr9:707387-707437	BE2_C	brain:	n/a
13	chr9:574312-574362	BJ	skin:	n/a
14	chr9:714269-714319	Caco-2	colon:	n/a
15	chr9:707410-707460	H1-hESC	embryonic stem cell:	embryo
16	chr9:574312-574362	HMEC	breast:	n/a
17	chr9:707166-707216	T-47D	breast:	n/a
18	chr9:707410-707460	SAEC	small airway:	n/a
19	chr9:714269-714319	NH-A	brain:	n/a
20	chr9:705143-705193	ProgFib	skin:	n/a
21	chr9:574312-574362	ProgFib	skin:	n/a
22	chr9:707410-707460	PANC-1	pancreas:	n/a
23	chr9:707410-707460	Jurkat	blood:	n/a
24	chr9:705143-705193	NH-A	brain:	n/a
25	chr9:714269-714319	AG10803	skin:	n/a
26	chr9:714269-714319	BE2_C	brain:	n/a
27	chr9:707387-707437	RPTEC	kidney:	n/a
28	chr9:707166-707216	PrEC	prostate:	n/a
29	chr9:705143-705193	GM12892	blood:	n/a
30	chr9:574312-574362	K562	blood:	n/a
31	chr9:707166-707216	SAEC	small airway:	n/a
32	chr9:714269-714319	HUVEC	blood vessel:	n/a
33	chr9:574312-574362	HCF	heart:	n/a
34	chr9:707410-707460	GM12891	blood:	n/a
35	chr9:714269-714319	SAEC	small airway:	n/a
36	chr9:714269-714319	T-47D	breast:	n/a
37	chr9:705143-705193	PrEC	prostate:	n/a
38	chr9:707410-707460	HCF	heart:	n/a
39	chr9:574312-574362	SK-N-SH_RA	brain:	n/a
40	chr9:707387-707437	AG09309	skin:	n/a
41	chr9:574312-574362	U87	brain:	n/a
42	chr9:707387-707437	SK-N-SH	brain:	n/a
43	chr9:705143-705193	PANC-1	pancreas:	n/a
44	chr9:707387-707437	PFSK-1	brain:	n/a
45	chr9:574312-574362	AG10803	skin:	n/a
46	chr9:707166-707216	HMEC	breast:	n/a
47	chr9:574312-574362	PFSK-1	brain:	n/a
48	chr9:705143-705193	GM19239	blood:	n/a
49	chr9:705143-705193	NB4	blood:	n/a
50	chr9:574312-574362	AoSMC	blood vessel:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:581769..582694-chr9:763829..764743,4	MCF-7	breast:
2	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
3	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
4	chr9:710784..713169-chr9:756222..759004,2	MCF-7	breast:
5	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
6	chr9:704209..707068-chr9:719899..721523,2	MCF-7	breast:
7	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
8	chr9:613644..614435-chr9:753933..755128,3	MCF-7	breast:
9	chr9:613518..614436-chr9:806263..806822,2	MCF-7	breast:
10	chr9:581168..581745-chr9:613579..614471,2	MCF-7	breast:
11	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
12	chr9:709767..712435-chr9:740415..742459,2	MCF-7	breast:
13	chr9:581871..582698-chr9:763741..764739,5	MCF-7	breast:
14	chr9:640721..642302-chr9:644961..647354,2	K562	blood:
15	chr9:613026..614583-chr9:763698..764753,25	MCF-7	breast:
16	chr9:719690..721572-chr9:723182..726115,2	MCF-7	breast:
17	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
18	chr9:697287..699295-chr9:705065..707332,2	K562	blood:
19	chr9:686763..689090-chr9:692801..694616,2	MCF-7	breast:
20	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
21	chr9:582031..585321-chr9:586707..590039,3	K562	blood:
22	chr9:385789..386423-chr9:612104..612846,2	K562	blood:
23	chr9:581649..582215-chr9:998516..999103,2	MCF-7	breast:
24	chr9:613569..614095-chr9:1100690..1101615,2	MCF-7	breast:
25	chr9:693477..696151-chr9:698863..701082,2	MCF-7	breast:
26	chr9:680963..683890-chr9:685859..688092,2	MCF-7	breast:
27	chr9:691921..694076-chr9:697704..699992,2	K562	blood:
28	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
29	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
30	chr9:613348..614490-chr9:763793..765061,13	MCF-7	breast:
31	chr9:613714..614307-chr9:893592..894180,2	MCF-7	breast:
32	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
33	chr9:721333..724004-chr9:738366..740594,2	MCF-7	breast:
34	chr10:14227179..14227880-chr9:613613..614133,4	MCF-7	breast:
35	chr9:707320..708881-chr9:710200..712479,2	MCF-7	breast:
36	chr9:707080..708925-chr9:715815..718212,3	MCF-7	breast:
37	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
38	chr9:581821..582545-chr9:807512..808214,2	MCF-7	breast:
39	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:
40	chr9:613586..614504-chr9:756894..758172,6	MCF-7	breast:
41	chr9:581860..582832-chr9:613640..614518,3	MCF-7	breast:
42	chr8:128752586..128753455-chr9:706903..707668,2	NB4	blood:
43	chr9:634722..638024-chr9:640128..643682,5	MCF-7	breast:
44	chr9:581438..583645-chr9:586871..590074,4	MCF-7	breast:
45	chr10:14226157..14227663-chr9:613613..615133,2	K562	blood:
46	chr9:680230..683179-chr9:683361..685450,2	MCF-7	breast:
47	chr9:613541..614622-chr9:757205..758240,10	MCF-7	breast:
48	chr9:682966..685572-chr9:709711..712587,2	MCF-7	breast:
49	chr9:613650..614569-chr9:806256..807252,7	MCF-7	breast:
50	chr9:698899..701683-chr9:703340..705392,2	MCF-7	breast:

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

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

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
ENSG00000227914	chromatin interactions

Extended variants
information (count: 8982 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:8982 , 50 per page) page: 1 2 3 4 5 6 7 ... 180

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558465416	chr9:571894-571895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs572253078	chr9:571908-571909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534523229	chr9:571914-571915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554868157	chr9:571952-571953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs2804268	chr9:571962-571963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs144435133	chr9:571979-571980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147392224	chr9:571990-571991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530470450	chr9:571998-571999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577257631	chr9:572011-572012	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191872120	chr9:572042-572043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566596031	chr9:572050-572051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559595360	chr9:572063-572064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528645900	chr9:572081-572082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548514980	chr9:572085-572086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375232904	chr9:572098-572099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs7858168	chr9:572120-572121	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7861777	chr9:572132-572133	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs79025639	chr9:572151-572152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs77351650	chr9:572170-572171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145164837	chr9:572171-572172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62531534	chr9:572173-572174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542401362	chr9:572181-572182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562258184	chr9:572219-572220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111260258	chr9:572266-572267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76115466	chr9:572269-572270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565651884	chr9:572284-572285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534786135	chr9:572302-572303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs554829393	chr9:572346-572347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs151008743	chr9:572378-572379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs578027143	chr9:572386-572387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73373075	chr9:572398-572399	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs557388256	chr9:572412-572413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs112972543	chr9:572418-572419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545886359	chr9:572420-572421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112446034	chr9:572425-572426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573279990	chr9:572458-572459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140264493	chr9:572490-572491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577127800	chr9:572501-572502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561979800	chr9:572511-572512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs539786357	chr9:572536-572537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199514904	chr9:572557-572558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs58702657	chr9:572558-572559	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs187046455	chr9:572562-572563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2804269	chr9:572563-572564	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs57076074	chr9:572564-572565	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551905558	chr9:572579-572580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190821822	chr9:572588-572589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528206172	chr9:572603-572604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145808517	chr9:572608-572609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568308543	chr9:572610-572611	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:4894 , 50 per page) page: 1 2 3 4 5 6 7 ... 98

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:549800-593800	Weak transcription	Lung	lung
2	chr9:552400-574000	Weak transcription	Right Ventricle	heart
3	chr9:559000-573600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:563000-572600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr9:565800-573800	Weak transcription	HMEC	breast
6	chr9:565800-574000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:566600-573800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr9:567000-573000	Enhancers	Fetal Intestine Large	intestine
9	chr9:567200-572400	Enhancers	Fetal Intestine Small	intestine
10	chr9:567800-573800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr9:569200-574000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:569200-574000	Weak transcription	Gastric	stomach
13	chr9:569400-572000	Enhancers	Brain Cingulate Gyrus	brain
14	chr9:569400-573600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr9:569600-574000	Weak transcription	Esophagus	oesophagus
16	chr9:570000-572000	Enhancers	Brain Angular Gyrus	brain
17	chr9:570000-572400	Enhancers	Fetal Lung	lung
18	chr9:570200-572200	Enhancers	A549	lung
19	chr9:570400-572000	Enhancers	Brain Anterior Caudate	brain
20	chr9:570400-572000	Enhancers	Stomach Mucosa	stomach
21	chr9:570400-576000	Enhancers	Brain Hippocampus Middle	brain
22	chr9:570600-574000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr9:570600-579600	Enhancers	Fetal Heart	heart
24	chr9:571000-572000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr9:571000-572200	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr9:571000-572400	Enhancers	Duodenum Mucosa	Duodenum
27	chr9:571000-572600	Enhancers	Fetal Muscle Leg	muscle
28	chr9:571000-576600	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr9:571200-572000	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr9:571200-572000	Enhancers	Fetal Kidney	kidney
31	chr9:571200-572200	Weak transcription	Pancreas	Pancrea
32	chr9:571200-573600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr9:571400-572200	Weak transcription	Left Ventricle	heart
34	chr9:571400-573000	Weak transcription	Brain Substantia Nigra	brain
35	chr9:571400-573600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:571400-573600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:571400-573600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr9:571400-573800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr9:571400-573800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr9:571400-574000	Weak transcription	Ovary	ovary
41	chr9:571600-572200	Weak transcription	Psoas Muscle	Psoas
42	chr9:571600-572600	Enhancers	Right Atrium	heart
43	chr9:571600-573600	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr9:571600-573600	Weak transcription	NHEK	skin
45	chr9:571600-573800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr9:571800-572000	Enhancers	Aorta	Aorta
47	chr9:572000-573000	Weak transcription	Brain Angular Gyrus	brain
48	chr9:572000-573000	Weak transcription	Brain Cingulate Gyrus	brain
49	chr9:572000-573600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:572000-573800	Weak transcription	Fetal Kidney	kidney

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