Variant report

Variant	nsv892163
Chromosome Location	chr9:6523056-6632061
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1499)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1499 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6568252-6568419	K562	blood:	n/a	n/a
2	ARID3A	chr9:6542871-6542968	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6590416-6591246	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6585226-6585461	K562	blood:	n/a	n/a
5	ARID3A	chr9:6552110-6552393	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6530270-6530987	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6592072-6592556	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:6585150-6585539	HepG2	liver:	n/a	n/a
9	ATF1	chr9:6594559-6594926	K562	blood:	n/a	n/a
10	ATF2	chr9:6605130-6605645	GM12878	blood:	n/a	n/a
11	ATF2	chr9:6598244-6598868	GM12878	blood:	n/a	n/a
12	ATF2	chr9:6630782-6631440	GM12878	blood:	n/a	n/a
13	ATF2	chr9:6620437-6621001	GM12878	blood:	n/a	n/a
14	ATF2	chr9:6575185-6575710	GM12878	blood:	n/a	n/a
15	ATF2	chr9:6566455-6566850	GM12878	blood:	n/a	n/a
16	ATF2	chr9:6597976-6598892	GM12878	blood:	n/a	n/a
17	BATF	chr9:6566437-6566727	GM12878	blood:	n/a	n/a
18	BATF	chr9:6598357-6598887	GM12878	blood:	n/a	chr9:6598659-6598670
19	BATF	chr9:6630698-6631421	GM12878	blood:	n/a	chr9:6630833-6630842
20	BATF	chr9:6598389-6598834	GM12878	blood:	n/a	chr9:6598659-6598670
21	BATF	chr9:6592868-6593086	GM12878	blood:	n/a	n/a
22	BATF	chr9:6620458-6620655	GM12878	blood:	n/a	n/a
23	BCL11A	chr9:6598313-6598874	GM12878	blood:	n/a	n/a
24	BCL11A	chr9:6605232-6605584	GM12878	blood:	n/a	n/a
25	BCL11A	chr9:6575318-6575518	GM12878	blood:	n/a	n/a
26	BCL11A	chr9:6598377-6598720	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:6605220-6605551	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:6594611-6594793	GM12878	blood:	n/a	n/a
29	BCL3	chr9:6598339-6598796	GM12878	blood:	n/a	n/a
30	BCL3	chr9:6575300-6575684	GM12878	blood:	n/a	n/a
31	BCL3	chr9:6558003-6558364	GM12878	blood:	n/a	n/a
32	BCL3	chr9:6566337-6566811	GM12878	blood:	n/a	n/a
33	BCLAF1	chr9:6575167-6575735	GM12878	blood:	n/a	n/a
34	BCLAF1	chr9:6598356-6598906	GM12878	blood:	n/a	n/a
35	BCLAF1	chr9:6598022-6598904	GM12878	blood:	n/a	n/a
36	BCLAF1	chr9:6605192-6605673	GM12878	blood:	n/a	n/a
37	BCLAF1	chr9:6630775-6631290	GM12878	blood:	n/a	n/a
38	BHLHE40	chr9:6605262-6605585	GM12878	blood:	n/a	n/a
39	BHLHE40	chr9:6565465-6565665	K562	blood:	n/a	chr9:6565520-6565533 chr9:6565522-6565531 chr9:6565523-6565532 chr9:6565522-6565531
40	BHLHE40	chr9:6590771-6591126	HepG2	liver:	n/a	n/a
41	BHLHE40	chr9:6598319-6598809	GM12878	blood:	n/a	n/a
42	BHLHE40	chr9:6575351-6575622	GM12878	blood:	n/a	n/a
43	BHLHE40	chr9:6549190-6549255	K562	blood:	n/a	n/a
44	BHLHE40	chr9:6590791-6591226	HepG2	liver:	n/a	n/a
45	BHLHE40	chr9:6630905-6631327	GM12878	blood:	n/a	n/a
46	BHLHE40	chr9:6620810-6621062	GM12878	blood:	n/a	n/a
47	BRCA1	chr9:6566427-6567569	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr9:6594553-6594752	GM12878	blood:	n/a	n/a
49	BRF1	chr9:6594560-6594923	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr9:6566237-6567676	HCT-116	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6552115-6552165	HL-60	blood:	n/a
2	chr9:6552115-6552165	HAEpiC	amniotic membrane:	n/a
3	chr9:6552115-6552165	ProgFib	skin:	n/a
4	chr9:6532828-6532878	AG09319	gingival:	n/a
5	chr9:6552115-6552165	NB4	blood:	n/a
6	chr9:6552115-6552165	NHDF-neo	bronchial:	n/a
7	chr9:6552115-6552165	ovcar-3	ovarian:	n/a
8	chr9:6532828-6532878	Hela-S3	cervix:	n/a
9	chr9:6552115-6552165	SK-N-SH_RA	brain:	n/a
10	chr9:6552115-6552165	SKMC	muscle:	n/a
11	chr9:6532828-6532878	IMR90	lung:	fetal
12	chr9:6552115-6552165	HMEC	breast:	n/a
13	chr9:6532828-6532878	HCT-116	colon:	n/a
14	chr9:6552115-6552165	AG09309	skin:	n/a
15	chr9:6552115-6552165	BJ	skin:	n/a
16	chr9:6552115-6552165	GM19239	blood:	n/a
17	chr9:6552115-6552165	NH-A	brain:	n/a
18	chr9:6552115-6552165	A549	lung:	n/a
19	chr9:6552115-6552165	ECC-1	luminal epithelium:	n/a
20	chr9:6532828-6532878	ovcar-3	ovarian:	n/a
21	chr9:6532828-6532878	NH-A	brain:	n/a
22	chr9:6552115-6552165	IMR90	lung:	fetal
23	chr9:6552115-6552165	SAEC	small airway:	n/a
24	chr9:6552115-6552165	Jurkat	blood:	n/a
25	chr9:6552115-6552165	PFSK-1	brain:	n/a
26	chr9:6552115-6552165	AoSMC	blood vessel:	n/a
27	chr9:6552115-6552165	CMK	blood:	n/a
28	chr9:6532828-6532878	GM06990	blood:	n/a
29	chr9:6532828-6532878	HPAEpiC	pulmonary alveolar:	n/a
30	chr9:6552115-6552165	Hepatocyte	liver:	n/a
31	chr9:6532828-6532878	GM12878	blood:	n/a
32	chr9:6552115-6552165	PANC-1	pancreas:	n/a
33	chr9:6552115-6552165	HCPEpiC	choroid plexus:	n/a
34	chr9:6552115-6552165	Hela-S3	cervix:	n/a
35	chr9:6532828-6532878	MCF10A-Er-Src	breast:	n/a
36	chr9:6552115-6552165	NT2-D1	testis:	n/a
37	chr9:6532828-6532878	HIPEpiC	eye:	n/a
38	chr9:6532828-6532878	HL-60	blood:	n/a
39	chr9:6552115-6552165	HEEpiC	esophagus:	n/a
40	chr9:6532828-6532878	HepG2	liver:	n/a
41	chr9:6552115-6552165	HNPCEpiC	eye:	n/a
42	chr9:6552115-6552165	HCT-116	colon:	n/a
43	chr9:6532828-6532878	HRE	kidney:	n/a
44	chr9:6532828-6532878	ProgFib	skin:	n/a
45	chr9:6552115-6552165	T-47D	breast:	n/a
46	chr9:6532828-6532878	SKMC	muscle:	n/a
47	chr9:6532828-6532878	HRPEpiC	eye:	n/a
48	chr9:6552115-6552165	BE2_C	brain:	n/a
49	chr9:6552115-6552165	MCF10A-Er-Src	breast:	n/a
50	chr9:6532828-6532878	BE2_C	brain:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6593764..6596429-chr9:6597405..6599828,2	MCF-7	breast:
2	chr9:6627812..6629680-chr9:6632614..6635740,3	MCF-7	breast:
3	chr9:6562859..6565330-chr9:6565433..6569047,3	K562	blood:
4	chr9:6615911..6617907-chr9:6681150..6682978,2	MCF-7	breast:
5	chr9:6605288..6608151-chr9:6611363..6613701,3	K562	blood:
6	chr9:6411889..6413422-chr9:6565833..6568598,2	K562	blood:
7	chr9:6579960..6582259-chr9:6679731..6681701,2	MCF-7	breast:
8	chr9:6593764..6596429-chr9:6597405..6599828,2	MCF-7	breast:
9	chr9:6584834..6585802-chr9:6667386..6668426,5	MCF-7	breast:
10	chr9:6354058..6354828-chr9:6567905..6568745,4	MCF-7	breast:
11	chr9:6624229..6626158-chr9:6679853..6681433,2	MCF-7	breast:
12	chr9:6570923..6573857-chr9:6574160..6576030,2	K562	blood:
13	chr9:6516849..6518888-chr9:6521453..6523458,2	K562	blood:
14	chr9:6354258..6354771-chr9:6567896..6568668,2	MCF-7	breast:
15	chr9:6588736..6590830-chr9:6680231..6682699,2	MCF-7	breast:
16	chr9:6410972..6413613-chr9:6564070..6565701,2	MCF-7	breast:
17	chr9:6623651..6625727-chr9:6679924..6681530,2	MCF-7	breast:
18	chr9:6585232..6587306-chr9:6664888..6666750,2	MCF-7	breast:
19	chr9:6533272..6535800-chr9:6681069..6683891,2	K562	blood:
20	chr9:6550978..6552657-chr9:6561789..6563568,2	K562	blood:
21	chr9:6590828..6592705-chr9:6679350..6681430,2	MCF-7	breast:
22	chr9:6523722..6524445-chr9:6667595..6668159,2	K562	blood:
23	chr9:6605288..6608151-chr9:6611363..6613701,3	K562	blood:
24	chr9:6570923..6573857-chr9:6574160..6576030,2	K562	blood:
25	chr9:6550978..6552657-chr9:6561789..6563568,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-3	chr9:6529539-6529917	NONHSAT130138
2	lnc-UHRF2-4	chr9:6542094-6542350	NONHSAT130139
3	lnc-UHRF2-5	chr9:6568844-6569360	NONHSAT130143

No data

Variant related genes	Relation type
ENSG00000252110	TF binding region
ENSG00000237158	TF binding region
RN7SL25P	TF binding region
GLDC	TF binding region
ENSG00000252110	CpG island
ENSG00000237158	CpG island
RN7SL25P	CpG island
GLDC	CpG island
ENSG00000147854	chromatin interactions
ENSG00000237158	chromatin interactions
ENSG00000252110	chromatin interactions

Extended variants
information (count: 6048 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:6048 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1547258	chr9:6523056-6523057	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs534275451	chr9:6523067-6523068	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs115578561	chr9:6523097-6523098	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs185651593	chr9:6523148-6523149	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs544948162	chr9:6523156-6523157	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs117570261	chr9:6523160-6523161	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs569245703	chr9:6523213-6523214	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs530504864	chr9:6523220-6523221	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs549041933	chr9:6523230-6523231	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs567369218	chr9:6523244-6523245	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs570835058	chr9:6523250-6523251	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs7021093	chr9:6523260-6523261	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs200088562	chr9:6523314-6523315	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs201043601	chr9:6523318-6523319	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs546724117	chr9:6523320-6523321	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs370404440	chr9:6523322-6523323	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs374466849	chr9:6523353-6523354	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs546872104	chr9:6523386-6523387	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs367627383	chr9:6523396-6523397	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs569566376	chr9:6523414-6523415	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs536235229	chr9:6523417-6523418	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs190056051	chr9:6523426-6523427	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs572904207	chr9:6523469-6523470	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs140643894	chr9:6523473-6523474	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs143766970	chr9:6523493-6523494	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs577742679	chr9:6523519-6523520	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs78940084	chr9:6523548-6523549	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs563429336	chr9:6523585-6523586	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs114522820	chr9:6523616-6523617	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148166233	chr9:6523631-6523632	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560824099	chr9:6523641-6523642	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528105899	chr9:6523692-6523693	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546348347	chr9:6523709-6523710	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571345177	chr9:6523764-6523765	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115089014	chr9:6523765-6523766	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538830209	chr9:6523805-6523806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569204891	chr9:6523915-6523916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181753953	chr9:6523947-6523948	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200186442	chr9:6524026-6524027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554858662	chr9:6524038-6524039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566501706	chr9:6524094-6524095	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1547257	chr9:6524148-6524149	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs141120276	chr9:6524244-6524245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs1547256	chr9:6524246-6524247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs201665601	chr9:6524256-6524257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs55813275	chr9:6524259-6524260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557074272	chr9:6524263-6524264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575522357	chr9:6524267-6524268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554696903	chr9:6524270-6524271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56410409	chr9:6524271-6524272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:107)

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	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
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ependymoma	20639864	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:1420 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6498800-6554400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr9:6499000-6528400	Weak transcription	Pancreas	Pancrea
3	chr9:6506400-6530600	Weak transcription	Gastric	stomach
4	chr9:6507000-6523800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr9:6507000-6524800	Weak transcription	Brain Hippocampus Middle	brain
6	chr9:6507000-6534400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:6508400-6523600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr9:6508400-6525000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr9:6508400-6526400	Weak transcription	Rectal Smooth Muscle	rectum
10	chr9:6508400-6526600	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr9:6508400-6528200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:6508400-6530600	Weak transcription	Left Ventricle	heart
13	chr9:6508600-6524200	Weak transcription	Stomach Smooth Muscle	stomach
14	chr9:6508600-6537800	Weak transcription	HMEC	breast
15	chr9:6508600-6538200	Weak transcription	NHEK	skin
16	chr9:6508800-6523800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr9:6508800-6526600	Weak transcription	HSMM	muscle
18	chr9:6509800-6525000	Weak transcription	Osteobl	bone
19	chr9:6509800-6530200	Weak transcription	A549	lung
20	chr9:6510400-6558800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:6510600-6525000	Weak transcription	NH-A	brain
22	chr9:6510600-6543000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr9:6511400-6526800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr9:6512200-6525000	Weak transcription	HSMMtube	muscle
25	chr9:6512200-6528800	Weak transcription	NHLF	lung
26	chr9:6517600-6528000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr9:6518000-6526000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr9:6518000-6530400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr9:6518200-6526000	Weak transcription	Fetal Thymus	thymus
30	chr9:6518400-6525000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr9:6521200-6523200	ZNF genes & repeats	Primary B cells from peripheral blood	blood
32	chr9:6521600-6524000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr9:6521600-6524200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr9:6521800-6523200	ZNF genes & repeats	Primary B cells from cord blood	blood
35	chr9:6521800-6523200	ZNF genes & repeats	Adipose Nuclei	Adipose
36	chr9:6521800-6523600	Strong transcription	HUVEC	blood vessel
37	chr9:6522000-6525000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr9:6522000-6528400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr9:6522000-6549200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr9:6522200-6525000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr9:6522400-6523200	ZNF genes & repeats	Primary T cells from cord blood	blood
42	chr9:6522400-6523200	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
43	chr9:6522400-6530400	Weak transcription	NHDF-Ad	bronchial
44	chr9:6522400-6531600	Weak transcription	GM12878-XiMat	blood
45	chr9:6522600-6523200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr9:6522600-6523800	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
47	chr9:6522600-6525400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr9:6522600-6526000	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr9:6522800-6523400	ZNF genes & repeats	Aorta	Aorta
50	chr9:6522800-6523800	Weak transcription	Muscle Satellite Cultured Cells	--

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