Variant report

Variant	nsv1024324
Chromosome Location	chr9:6308178-6408875
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	ATF1	chr9:6408431-6408699	K562	blood:	n/a	n/a
2	ATF3	chr9:6408408-6408659	K562	blood:	n/a	n/a
3	BATF	chr9:6355807-6355988	GM12878	blood:	n/a	chr9:6355904-6355915
4	BHLHE40	chr9:6355818-6355946	HepG2	liver:	n/a	n/a
5	BHLHE40	chr9:6408385-6408658	K562	blood:	n/a	n/a
6	BHLHE40	chr9:6355705-6356113	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:6408412-6408647	HepG2	liver:	n/a	n/a
8	BRCA1	chr9:6354191-6354410	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr9:6382717-6383026	IMR90	lung:	n/a	n/a
10	CEBPB	chr9:6356965-6357266	HepG2	liver:	n/a	chr9:6357095-6357108 chr9:6357095-6357108 chr9:6357095-6357106 chr9:6357097-6357108
11	CEBPB	chr9:6356584-6357272	Hela-S3	cervix:	n/a	chr9:6357095-6357108 chr9:6357095-6357108 chr9:6357095-6357106 chr9:6357097-6357108
12	CEBPB	chr9:6405496-6405697	K562	blood:	n/a	chr9:6405557-6405570 chr9:6405619-6405630 chr9:6405559-6405570
13	CEBPB	chr9:6405472-6405788	IMR90	lung:	n/a	chr9:6405557-6405570 chr9:6405619-6405630 chr9:6405559-6405570
14	CEBPB	chr9:6357011-6357239	A549	lung:	n/a	chr9:6357095-6357108 chr9:6357095-6357108 chr9:6357095-6357106 chr9:6357097-6357108
15	CEBPB	chr9:6405482-6405699	A549	lung:	n/a	chr9:6405557-6405570 chr9:6405619-6405630 chr9:6405559-6405570
16	CEBPB	chr9:6357057-6357205	H1-hESC	embryonic stem cell:	n/a	chr9:6357095-6357108 chr9:6357095-6357108 chr9:6357095-6357106 chr9:6357097-6357108
17	CEBPB	chr9:6405490-6405703	HepG2	liver:	n/a	chr9:6405557-6405570 chr9:6405619-6405630 chr9:6405559-6405570
18	CEBPB	chr9:6383754-6384293	IMR90	lung:	n/a	n/a
19	CTCF	chr9:6317080-6317230	HMEC	breast:	n/a	n/a
20	CTCF	chr9:6353818-6354972	A549	lung:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
21	CTCF	chr9:6353980-6354130	GM12874	blood:	n/a	n/a
22	CTCF	chr9:6354220-6354370	GM12869	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
23	CTCF	chr9:6317120-6317270	HPF	lung:	n/a	n/a
24	CTCF	chr9:6354141-6354454	Medullo	brain:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
25	CTCF	chr9:6354240-6354390	GM12867	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
26	CTCF	chr9:6353940-6354090	AG04449	skin:	n/a	n/a
27	CTCF	chr9:6317136-6317275	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr9:6317140-6317290	HFF	foreskin:	n/a	n/a
29	CTCF	chr9:6354169-6354405	GM10266	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
30	CTCF	chr9:6353968-6354502	IMR90	lung:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
31	CTCF	chr9:6354200-6354350	SK-N-SH_RA	brain:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
32	CTCF	chr9:6354172-6354399	GM19239	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
33	CTCF	chr9:6354240-6354390	GM12868	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
34	CTCF	chr9:6318809-6318833	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr9:6354220-6354370	GM12878	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
36	CTCF	chr9:6354122-6354510	H1-hESC	embryonic stem cell:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
37	CTCF	chr9:6371625-6371655	LNCaP	prostate:	n/a	n/a
38	CTCF	chr9:6354017-6354522	MCF-7	breast:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
39	CTCF	chr9:6354180-6354330	AoAF	blood vessel:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
40	CTCF	chr9:6378214-6378271	GM20000	blood:	n/a	n/a
41	CTCF	chr9:6354200-6354350	GM12871	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
42	CTCF	chr9:6354155-6354433	Hela-S3	cervix:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
43	CTCF	chr9:6354180-6354330	GM12870	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
44	CTCF	chr9:6354180-6354330	HFF	foreskin:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
45	CTCF	chr9:6354200-6354350	HEK293	kidney:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
46	CTCF	chr9:6354144-6354398	SK-N-SH_RA	brain:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
47	CTCF	chr9:6354200-6354350	GM12870	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
48	CTCF	chr9:6354180-6354330	GM12875	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301
49	CTCF	chr9:6317140-6317290	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr9:6354172-6354376	GM19238	blood:	n/a	chr9:6354284-6354300 chr9:6354285-6354306 chr9:6354283-6354301

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6328493-6328543	HL-60	blood:	n/a
2	chr9:6328493-6328543	HL-60	blood:	n/a
3	chr9:6328386-6328436	Hela-S3	cervix:	n/a
4	chr9:6328010-6328060	HNPCEpiC	eye:	n/a
5	chr9:6328386-6328436	SAEC	small airway:	n/a
6	chr9:6326904-6326954	MCF-7	breast:	n/a
7	chr9:6328010-6328060	HepG2	liver:	n/a
8	chr9:6328386-6328436	AG04449	skin:	fetal
9	chr9:6326904-6326954	GM19239	blood:	n/a
10	chr9:6328010-6328060	HCPEpiC	choroid plexus:	n/a
11	chr9:6326904-6326954	T-47D	breast:	n/a
12	chr9:6328386-6328436	IMR90	lung:	fetal
13	chr9:6328493-6328543	NH-A	brain:	n/a
14	chr9:6328493-6328543	HCM	heart:	n/a
15	chr9:6328493-6328543	Caco-2	colon:	n/a
16	chr9:6328386-6328436	HRCEpiC	kidney:	n/a
17	chr9:6328493-6328543	ovcar-3	ovarian:	n/a
18	chr9:6328386-6328436	NHDF-neo	bronchial:	n/a
19	chr9:6326904-6326954	HCT-116	colon:	n/a
20	chr9:6328010-6328060	GM06990	blood:	n/a
21	chr9:6326904-6326954	K562	blood:	n/a
22	chr9:6328493-6328543	LNCaP	prostate:	n/a
23	chr9:6328010-6328060	GM12891	blood:	n/a
24	chr9:6326904-6326954	MCF10A-Er-Src	breast:	n/a
25	chr9:6326904-6326954	HAEpiC	amniotic membrane:	n/a
26	chr9:6328010-6328060	ovcar-3	ovarian:	n/a
27	chr9:6328010-6328060	HRCEpiC	kidney:	n/a
28	chr9:6328010-6328060	HIPEpiC	eye:	n/a
29	chr9:6326904-6326954	IMR90	lung:	fetal
30	chr9:6328386-6328436	SK-N-SH	brain:	n/a
31	chr9:6328386-6328436	HRE	kidney:	n/a
32	chr9:6328493-6328543	Hela-S3	cervix:	n/a
33	chr9:6326904-6326954	SAEC	small airway:	n/a
34	chr9:6326904-6326954	HepG2	liver:	n/a
35	chr9:6326904-6326954	NHDF-neo	bronchial:	n/a
36	chr9:6328010-6328060	Hepatocyte	liver:	n/a
37	chr9:6326904-6326954	HEEpiC	esophagus:	n/a
38	chr9:6328386-6328436	HUVEC	blood vessel:	n/a
39	chr9:6328010-6328060	AG04449	skin:	fetal
40	chr9:6328386-6328436	Hepatocyte	liver:	n/a
41	chr9:6328386-6328436	HCF	heart:	n/a
42	chr9:6328493-6328543	IMR90	lung:	fetal
43	chr9:6328010-6328060	IMR90	lung:	fetal
44	chr9:6326904-6326954	HNPCEpiC	eye:	n/a
45	chr9:6326904-6326954	AG04449	skin:	fetal
46	chr9:6328386-6328436	GM06990	blood:	n/a
47	chr9:6328493-6328543	K562	blood:	n/a
48	chr9:6328386-6328436	K562	blood:	n/a
49	chr9:6328386-6328436	MCF10A-Er-Src	breast:	n/a
50	chr9:6326904-6326954	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:6354258..6354771-chr9:6567896..6568668,2	MCF-7	breast:
2	chr9:6354058..6354828-chr9:6567905..6568745,4	MCF-7	breast:
3	chr9:6352849..6355311-chr9:6679612..6682199,2	MCF-7	breast:
4	chr9:6398344..6401128-chr9:6407574..6409551,2	K562	blood:
5	chr9:6307810..6309784-chr9:6311496..6314006,2	K562	blood:
6	chr9:6398344..6401128-chr9:6407574..6409551,2	K562	blood:
7	chr9:6305170..6307719-chr9:6307772..6310215,2	K562	blood:
8	chr9:6389667..6391498-chr9:6396973..6399114,2	MCF-7	breast:
9	chr1:11968667..11972683-chr9:6399248..6402268,5	K562	blood:
10	chr9:6329167..6331675-chr9:6333759..6336639,2	K562	blood:
11	chr9:6307810..6309784-chr9:6311496..6314006,2	K562	blood:
12	chr9:6354241..6354767-chr9:6667295..6668097,2	K562	blood:
13	chr1:11969564..11971245-chr9:6400768..6402268,2	K562	blood:
14	chr9:6389667..6391498-chr9:6396973..6399114,2	MCF-7	breast:
15	chr9:6408551..6411662-chr9:6412630..6415165,4	MCF-7	breast:
16	chr9:6354073..6354743-chr9:6738989..6739892,3	K562	blood:
17	chr9:6329167..6331675-chr9:6333759..6336639,2	K562	blood:
18	chr9:6408168..6410435-chr9:6411394..6414242,2	K562	blood:
19	chr9:6054942..6055457-chr9:6353907..6354484,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf38-2	chr9:6408524-6408756	NONHSAT130128
2	lnc-C9orf38-2	chr9:6408525-6408756	XLOC_007638

Variant related genes	Relation type
TPD52L3	TF binding region
UHRF2	TF binding region
TPD52L3	CpG island
UHRF2	CpG island
ENSG00000147854	chromatin interactions
ENSG00000201801	chromatin interactions

Extended variants
information (count: 2251 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:2251 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539687138	chr9:6308192-6308193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs118170243	chr9:6308203-6308204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575171600	chr9:6308222-6308223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542530607	chr9:6308252-6308253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560884485	chr9:6308291-6308292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528051600	chr9:6308319-6308320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540266973	chr9:6308353-6308354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs564817952	chr9:6308357-6308358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556310594	chr9:6308360-6308361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574404193	chr9:6308375-6308376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551148217	chr9:6308377-6308378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2019737	chr9:6308381-6308382	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs530382452	chr9:6308398-6308399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548878934	chr9:6308405-6308406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs191177770	chr9:6308446-6308447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183797254	chr9:6308449-6308450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189161128	chr9:6308458-6308459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35887877	chr9:6308481-6308482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192027747	chr9:6308496-6308497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558920951	chr9:6308501-6308502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570812947	chr9:6308522-6308523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537973645	chr9:6308523-6308524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182760792	chr9:6308532-6308533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575081636	chr9:6308542-6308543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs111366076	chr9:6308569-6308570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147990972	chr9:6308588-6308589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554563557	chr9:6308596-6308597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573129836	chr9:6308615-6308616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4512432	chr9:6308620-6308621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539803792	chr9:6308628-6308629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs368937830	chr9:6308643-6308644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553777065	chr9:6308655-6308656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564899325	chr9:6308660-6308661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187401236	chr9:6308685-6308686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141679283	chr9:6308703-6308704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555084554	chr9:6308707-6308708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10975539	chr9:6308729-6308730	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs202113621	chr9:6308741-6308742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs540621916	chr9:6308784-6308785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs191490692	chr9:6308817-6308818	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs150126958	chr9:6308818-6308819	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs545661687	chr9:6308849-6308850	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs138561231	chr9:6308850-6308851	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs61596712	chr9:6308851-6308852	Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs570844452	chr9:6308938-6308939	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs537885220	chr9:6308970-6308971	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs577383813	chr9:6314414-6314415	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182654885	chr9:6314423-6314424	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs538408347	chr9:6314463-6314464	Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs7851000	chr9:6314487-6314488	Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	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
Disorders of sex development	21048976	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
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	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
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Dyslexia	22102821	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6307200-6308400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr9:6307400-6308200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr9:6307400-6308400	Enhancers	GM12878-XiMat	blood
4	chr9:6307800-6308800	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr9:6308800-6309000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr9:6314400-6315200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr9:6314400-6315800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr9:6314600-6315200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr9:6314600-6315400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr9:6314600-6315600	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr9:6314800-6315400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr9:6315200-6315600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr9:6315200-6315800	Enhancers	Fetal Heart	heart
14	chr9:6325400-6326200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr9:6326000-6326400	Enhancers	GM12878-XiMat	blood
16	chr9:6326200-6326400	Enhancers	Primary B cells from cord blood	blood
17	chr9:6328200-6328400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:6328400-6335800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:6329000-6329400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:6329000-6329600	Enhancers	GM12878-XiMat	blood
21	chr9:6329800-6332400	Enhancers	HUVEC	blood vessel
22	chr9:6330600-6332000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr9:6335800-6336400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:6336200-6336400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:6342200-6342400	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr9:6342400-6352000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr9:6342600-6342800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr9:6342800-6343000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr9:6348000-6348400	Enhancers	HepG2	liver
30	chr9:6348600-6348800	Enhancers	GM12878-XiMat	blood
31	chr9:6351000-6355800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr9:6351400-6352800	Enhancers	Hela-S3	cervix
33	chr9:6351800-6352200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr9:6352000-6352200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr9:6352000-6352200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr9:6352000-6352200	Enhancers	HMEC	breast
37	chr9:6352000-6352400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr9:6352200-6352600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr9:6352200-6353800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr9:6352200-6354000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:6352400-6354000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr9:6352400-6354400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr9:6352600-6353000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr9:6352800-6353800	Weak transcription	Hela-S3	cervix
45	chr9:6353000-6353200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:6353200-6354000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr9:6353800-6354800	Enhancers	Hela-S3	cervix
48	chr9:6354000-6354200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr9:6354000-6354800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr9:6354000-6354800	Enhancers	Primary B cells from peripheral blood	blood

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