Variant report

Variant	nsv892576
Chromosome Location	chr9:12925921-13093345
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1266)
CpG islands
(count:61)
Chromatin interactive
region (count:49)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1266 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:13034076-13034447	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:13088757-13089016	K562	blood:	n/a	n/a
3	BATF	chr9:12954486-12954757	GM12878	blood:	n/a	chr9:12954660-12954671
4	CEBPB	chr9:13084074-13084457	MCF-7	breast:	n/a	n/a
5	CEBPB	chr9:13078170-13078464	IMR90	lung:	n/a	n/a
6	CEBPB	chr9:13089847-13090081	A549	lung:	n/a	chr9:13089932-13089943
7	CEBPB	chr9:13064015-13064567	MCF-7	breast:	n/a	n/a
8	CEBPB	chr9:13078187-13078444	HepG2	liver:	n/a	n/a
9	CEBPB	chr9:13072021-13072288	HepG2	liver:	n/a	chr9:13072118-13072129
10	CEBPB	chr9:13089796-13090099	HepG2	liver:	n/a	chr9:13089932-13089943
11	CEBPB	chr9:13078156-13078473	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr9:13088129-13088153	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:13089783-13090083	IMR90	lung:	n/a	chr9:13089932-13089943
14	CEBPB	chr9:13017938-13018130	HepG2	liver:	n/a	n/a
15	CEBPB	chr9:13082699-13083256	MCF-7	breast:	n/a	n/a
16	CEBPB	chr9:12993478-12993785	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:13023407-13023862	MCF-7	breast:	n/a	chr9:13023441-13023452
18	CEBPB	chr9:13078159-13078455	A549	lung:	n/a	n/a
19	CEBPB	chr9:12973769-12974074	IMR90	lung:	n/a	chr9:12973911-12973922
20	CEBPB	chr9:13082785-13083206	MCF-7	breast:	n/a	n/a
21	CEBPB	chr9:12933878-12934366	HCT-116	colon:	n/a	n/a
22	CEBPB	chr9:12961066-12961594	IMR90	lung:	n/a	chr9:12961125-12961136 chr9:12961125-12961138 chr9:12961125-12961138
23	CEBPB	chr9:12939987-12940115	A549	lung:	n/a	chr9:12940029-12940040
24	CEBPB	chr9:13017970-13018214	A549	lung:	n/a	n/a
25	CEBPB	chr9:13023462-13023889	MCF-7	breast:	n/a	n/a
26	CEBPB	chr9:13022910-13023041	A549	lung:	n/a	n/a
27	CEBPB	chr9:12939943-12940204	HepG2	liver:	n/a	chr9:12940029-12940040
28	CHD2	chr9:13034283-13034375	HepG2	liver:	n/a	n/a
29	CREB1	chr9:13034239-13034529	A549	lung:	n/a	n/a
30	CTCF	chr9:13034133-13034560	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr9:13089200-13089350	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr9:12972582-12972718	MCF-7	breast:	n/a	chr9:12972596-12972617
33	CTCF	chr9:13088773-13089071	HepG2	liver:	n/a	chr9:13088919-13088940 chr9:13088929-13088937 chr9:13088924-13088942 chr9:13088925-13088941
34	CTCF	chr9:13088880-13089030	AG10803	skin:	n/a	chr9:13088919-13088940 chr9:13088929-13088937 chr9:13088924-13088942 chr9:13088925-13088941
35	CTCF	chr9:13089240-13089390	HPF	lung:	n/a	n/a
36	CTCF	chr9:13034260-13034410	HAc	cerebellar:	n/a	n/a
37	CTCF	chr9:13034280-13034430	GM12872	blood:	n/a	n/a
38	CTCF	chr9:13088860-13089010	HMF	breast:	n/a	chr9:13088919-13088940 chr9:13088929-13088937 chr9:13088924-13088942 chr9:13088925-13088941
39	CTCF	chr9:13089267-13089385	GM19240	blood:	n/a	n/a
40	CTCF	chr9:13089240-13089390	AG09319	gingival:	n/a	n/a
41	CTCF	chr9:13056861-13056962	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr9:13034260-13034410	HRE	kidney:	n/a	n/a
43	CTCF	chr9:13034179-13034555	ECC-1	luminal epithelium:	n/a	n/a
44	CTCF	chr9:13089220-13089370	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr9:12977140-12977290	BE2_C	brain:	n/a	n/a
46	CTCF	chr9:13034280-13034430	HMF	breast:	n/a	n/a
47	CTCF	chr9:13034200-13034350	A549	lung:	n/a	n/a
48	CTCF	chr9:13089280-13089430	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr9:13089220-13089370	HCFaa	heart:	n/a	n/a
50	CTCF	chr9:13088860-13089010	RPTEC	kidney:	n/a	chr9:13088919-13088940 chr9:13088929-13088937 chr9:13088924-13088942 chr9:13088925-13088941

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:13038210-13038260	Hela-S3	cervix:	n/a
2	chr9:13038210-13038260	SAEC	small airway:	n/a
3	chr9:13038210-13038260	NB4	blood:	n/a
4	chr9:13038210-13038260	HIPEpiC	eye:	n/a
5	chr9:13038210-13038260	HCF	heart:	n/a
6	chr9:13038210-13038260	NHBE	bronchial:	n/a
7	chr9:13038210-13038260	NH-A	brain:	n/a
8	chr9:13038210-13038260	ECC-1	luminal epithelium:	n/a
9	chr9:13038210-13038260	LNCaP	prostate:	n/a
10	chr9:13038210-13038260	Jurkat	blood:	n/a
11	chr9:13038210-13038260	AG10803	skin:	n/a
12	chr9:13038210-13038260	BJ	skin:	n/a
13	chr9:13038210-13038260	HepG2	liver:	n/a
14	chr9:13038210-13038260	AG09319	gingival:	n/a
15	chr9:13038210-13038260	HRPEpiC	eye:	n/a
16	chr9:13038210-13038260	HMEC	breast:	n/a
17	chr9:13038210-13038260	NT2-D1	testis:	n/a
18	chr9:13038210-13038260	MCF10A-Er-Src	breast:	n/a
19	chr9:13038210-13038260	HRE	kidney:	n/a
20	chr9:13038210-13038260	HPAEpiC	pulmonary alveolar:	n/a
21	chr9:13038210-13038260	PFSK-1	brain:	n/a
22	chr9:13038210-13038260	HNPCEpiC	eye:	n/a
23	chr9:13038210-13038260	IMR90	lung:	fetal
24	chr9:13038210-13038260	HCPEpiC	choroid plexus:	n/a
25	chr9:13038210-13038260	MCF-7	breast:	n/a
26	chr9:13038210-13038260	ovcar-3	ovarian:	n/a
27	chr9:13038210-13038260	HEK293	kidney:	embryo
28	chr9:13038210-13038260	BE2_C	brain:	n/a
29	chr9:13038210-13038260	HRCEpiC	kidney:	n/a
30	chr9:13038210-13038260	GM12878	blood:	n/a
31	chr9:13038210-13038260	U87	brain:	n/a
32	chr9:13038210-13038260	AG04450	lung:	fetal
33	chr9:13038210-13038260	SKMC	muscle:	n/a
34	chr9:13038210-13038260	NHDF-neo	bronchial:	n/a
35	chr9:13038210-13038260	HCT-116	colon:	n/a
36	chr9:13038210-13038260	HCM	heart:	n/a
37	chr9:13038210-13038260	PrEC	prostate:	n/a
38	chr9:13038210-13038260	RPTEC	kidney:	n/a
39	chr9:13038210-13038260	GM12891	blood:	n/a
40	chr9:13038210-13038260	HEEpiC	esophagus:	n/a
41	chr9:13038210-13038260	HL-60	blood:	n/a
42	chr9:13038210-13038260	K562	blood:	n/a
43	chr9:13038210-13038260	Caco-2	colon:	n/a
44	chr9:13038210-13038260	HAEpiC	amniotic membrane:	n/a
45	chr9:13038210-13038260	H1-hESC	embryonic stem cell:	embryo
46	chr9:13038210-13038260	ProgFib	skin:	n/a
47	chr9:13038210-13038260	AG09309	skin:	n/a
48	chr9:13038210-13038260	T-47D	breast:	n/a
49	chr9:13038210-13038260	PANC-1	pancreas:	n/a
50	chr9:13038210-13038260	Hepatocyte	liver:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:13083897..13086773-chr9:13277976..13279924,2	MCF-7	breast:
2	chr9:13034942..13035837-chr9:13088355..13089237,4	MCF-7	breast:
3	chr9:13034942..13035837-chr9:13088355..13089237,4	MCF-7	breast:
4	chr9:13085685..13087546-chr9:13092734..13094499,2	MCF-7	breast:
5	chr9:12776384..12777092-chr9:12988313..12988856,2	MCF-7	breast:
6	chr9:13033916..13034844-chr9:13088403..13089550,10	MCF-7	breast:
7	chr9:13056729..13057438-chr9:13089019..13089759,2	MCF-7	breast:
8	chr9:13046311..13049119-chr9:13049415..13051985,2	MCF-7	breast:
9	chr9:13020387..13022064-chr9:13024360..13026782,2	K562	blood:
10	chr9:13074973..13076495-chr9:13082888..13084585,2	MCF-7	breast:
11	chr9:13008470..13010567-chr9:13018005..13020586,2	MCF-7	breast:
12	chr9:12723685..12724314-chr9:12988034..12988919,3	MCF-7	breast:
13	chr9:13008470..13010567-chr9:13018005..13020586,2	MCF-7	breast:
14	chr9:13033933..13036265-chr9:13080318..13084279,3	MCF-7	breast:
15	chr9:12922589..12925309-chr9:12932316..12933934,2	MCF-7	breast:
16	chr9:12708111..12711033-chr9:13076014..13078647,2	MCF-7	breast:
17	chr9:12774582..12776386-chr9:12976678..12978992,2	MCF-7	breast:
18	chr9:13020387..13022064-chr9:13024360..13026782,2	K562	blood:
19	chr9:12719485..12720037-chr9:12987933..12988498,2	MCF-7	breast:
20	chr9:13074973..13076495-chr9:13082888..13084585,2	MCF-7	breast:
21	chr9:13002424..13004560-chr9:13006872..13008431,2	MCF-7	breast:
22	chr9:12964990..12966933-chr9:12968548..12971225,2	MCF-7	breast:
23	chr9:13033734..13035793-chr9:13280439..13283221,2	K562	blood:
24	chr9:13033933..13036265-chr9:13080318..13084279,3	MCF-7	breast:
25	chr9:13092848..13095853-chr9:14312583..14315715,3	MCF-7	breast:
26	chr9:13050118..13051990-chr9:13062072..13064345,2	MCF-7	breast:
27	chr9:13034030..13034837-chr9:13088503..13089360,4	K562	blood:
28	chr9:13034030..13034837-chr9:13088503..13089360,4	K562	blood:
29	chr9:12964990..12966933-chr9:12968548..12971225,2	MCF-7	breast:
30	chr9:13085685..13087546-chr9:13092734..13094499,2	MCF-7	breast:
31	chr9:13056729..13057438-chr9:13089019..13089759,2	MCF-7	breast:
32	chr9:13013683..13015999-chr9:13017070..13019514,2	MCF-7	breast:
33	chr9:13033929..13034651-chr9:14400323..14400953,2	MCF-7	breast:
34	chr9:13050118..13051990-chr9:13062072..13064345,2	MCF-7	breast:
35	chr9:13036362..13039283-chr9:13086631..13088810,2	K562	blood:
36	chr9:13013683..13015999-chr9:13017070..13019514,2	MCF-7	breast:
37	chr9:13033916..13034844-chr9:13088403..13089550,10	MCF-7	breast:
38	chr9:12955347..12957519-chr9:12959298..12960920,2	MCF-7	breast:
39	chr9:13058767..13060767-chr9:13068798..13070825,2	MCF-7	breast:
40	chr9:13091674..13093219-chr9:13093470..13095334,2	MCF-7	breast:
41	chr9:13046311..13049119-chr9:13049415..13051985,2	MCF-7	breast:
42	chr9:13044695..13047159-chr9:13050621..13052940,2	K562	blood:
43	chr9:13002424..13004560-chr9:13006872..13008431,2	MCF-7	breast:
44	chr9:13058767..13060767-chr9:13068798..13070825,2	MCF-7	breast:
45	chr9:13036362..13039283-chr9:13086631..13088810,2	K562	blood:
46	chr9:12794502..12796197-chr9:13084693..13086368,2	MCF-7	breast:
47	chr9:13089285..13089789-chr9:13424262..13424942,2	MCF-7	breast:
48	chr9:13044695..13047159-chr9:13050621..13052940,2	K562	blood:
49	chr9:12955347..12957519-chr9:12959298..12960920,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPDZ-6	chr9:12968103-12968512	NONHSAT130231
2	lnc-MPDZ-4	chr9:13021693-13022891	NONHSAT130232
3	lnc-MPDZ-7	chr9:12950565-12950844	NONHSAT130230
4	lnc-MPDZ-6	chr9:12951763-12951838	NONHSAT130231
5	lnc-MPDZ-7	chr9:12956371-12956378	NONHSAT130230

No data

Variant related genes	Relation type
ENSG00000234586	TF binding region
TDPX2	TF binding region
ENSG00000234586	CpG island
TDPX2	CpG island
ENSG00000147862	chromatin interactions
ENSG00000234740	chromatin interactions
ENSG00000153714	chromatin interactions
ENSG00000107186	chromatin interactions

Extended variants
information (count: 5836 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5836 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10511576	chr9:12925921-12925922	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538368865	chr9:12925928-12925929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116911867	chr9:12926008-12926009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs16929933	chr9:12926043-12926044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534503186	chr9:12926059-12926060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554171458	chr9:12926066-12926067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189010352	chr9:12926081-12926082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539679614	chr9:12926200-12926201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555817683	chr9:12926223-12926224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs148272362	chr9:12926267-12926268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34852390	chr9:12926287-12926288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs541539674	chr9:12926291-12926292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs561304975	chr9:12926311-12926312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571946660	chr9:12926345-12926346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181791460	chr9:12926348-12926349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564261416	chr9:12926353-12926354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1412294	chr9:12926360-12926361	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs186408840	chr9:12926372-12926373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2382375	chr9:12926377-12926378	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560540087	chr9:12926383-12926384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371448591	chr9:12926393-12926394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561236785	chr9:12926406-12926407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147742387	chr9:12926417-12926418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61663705	chr9:12926422-12926423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs548705654	chr9:12926432-12926433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568439519	chr9:12926435-12926436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528520049	chr9:12926438-12926439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191190608	chr9:12926460-12926461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566704217	chr9:12926469-12926470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180707012	chr9:12926473-12926474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7856080	chr9:12926478-12926479	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs185042992	chr9:12926542-12926543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs556303553	chr9:12926561-12926562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs386732800	chr9:12926563-12926564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs1412296	chr9:12926571-12926572	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs555087823	chr9:12926612-12926613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571995021	chr9:12926614-12926615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540701758	chr9:12926639-12926640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs557759888	chr9:12926640-12926641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551094690	chr9:12926648-12926649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375757640	chr9:12926652-12926653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577827687	chr9:12926710-12926711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141376643	chr9:12926718-12926719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563427951	chr9:12926719-12926720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs117949434	chr9:12926723-12926724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542334018	chr9:12926756-12926757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7856551	chr9:12926781-12926782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs189896599	chr9:12926838-12926839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183155930	chr9:12926900-12926901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570840410	chr9:12926916-12926917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
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
Breast cancer	21611746	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:12917000-12933600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr9:12917200-12930000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr9:12917200-12934000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr9:12917400-12933600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr9:12922800-12931000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr9:12924000-12931000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr9:12924200-12928000	Weak transcription	Adipose Nuclei	Adipose
8	chr9:12924800-12933800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:12925400-12930000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:12925400-12930200	Weak transcription	NHDF-Ad	bronchial
11	chr9:12925400-12933200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr9:12925400-12933400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:12925400-12934200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr9:12927800-12930000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:12930000-12930200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr9:12930000-12931000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr9:12930000-12932200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr9:12930200-12931400	Enhancers	NHDF-Ad	bronchial
19	chr9:12930200-12931800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr9:12930600-12931000	Weak transcription	NHLF	lung
21	chr9:12930800-12931000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr9:12930800-12931000	Enhancers	HUVEC	blood vessel
23	chr9:12930800-12931200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr9:12930800-12931400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr9:12930800-12932200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:12931000-12931200	Enhancers	NHEK	skin
27	chr9:12931000-12931200	Enhancers	NHLF	lung
28	chr9:12931000-12931200	Enhancers	Osteobl	bone
29	chr9:12931000-12931400	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr9:12931000-12931600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr9:12931000-12932200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr9:12931000-12932200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr9:12931000-12932200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:12931000-12932600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr9:12931000-12934000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr9:12931200-12932400	Weak transcription	HUVEC	blood vessel
37	chr9:12931200-12933400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr9:12931200-12933600	Weak transcription	NHLF	lung
39	chr9:12931200-12933800	Weak transcription	NHEK	skin
40	chr9:12931200-12934000	Weak transcription	Osteobl	bone
41	chr9:12931400-12933200	Weak transcription	NHDF-Ad	bronchial
42	chr9:12931400-12933400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr9:12931400-12933600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr9:12931600-12932000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr9:12931800-12932000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:12931800-12932200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr9:12932200-12933400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr9:12932200-12933400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr9:12932200-12934000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:12932200-12934000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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