Variant report

Variant	nsv892164
Chromosome Location	chr9:6555079-6664282
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1945)
CpG islands
(count:367)
Chromatin interactive
region (count:36)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1945 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

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	chr9:6585150-6585539	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:6592072-6592556	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6641775-6641951	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6645695-6646211	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6590416-6591246	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6585226-6585461	K562	blood:	n/a	n/a
8	ATF1	chr9:6594559-6594926	K562	blood:	n/a	n/a
9	ATF2	chr9:6654995-6655416	GM12878	blood:	n/a	n/a
10	ATF2	chr9:6575185-6575710	GM12878	blood:	n/a	n/a
11	ATF2	chr9:6566455-6566850	GM12878	blood:	n/a	n/a
12	ATF2	chr9:6597976-6598892	GM12878	blood:	n/a	n/a
13	ATF2	chr9:6598244-6598868	GM12878	blood:	n/a	n/a
14	ATF2	chr9:6654912-6655463	GM12878	blood:	n/a	n/a
15	ATF2	chr9:6630782-6631440	GM12878	blood:	n/a	n/a
16	ATF2	chr9:6605130-6605645	GM12878	blood:	n/a	n/a
17	ATF2	chr9:6632332-6633189	GM12878	blood:	n/a	n/a
18	ATF2	chr9:6620437-6621001	GM12878	blood:	n/a	n/a
19	BACH1	chr9:6645623-6645968	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr9:6644871-6645230	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr9:6598389-6598834	GM12878	blood:	n/a	chr9:6598659-6598670
22	BATF	chr9:6620458-6620655	GM12878	blood:	n/a	n/a
23	BATF	chr9:6598357-6598887	GM12878	blood:	n/a	chr9:6598659-6598670
24	BATF	chr9:6632442-6633016	GM12878	blood:	n/a	n/a
25	BATF	chr9:6566437-6566727	GM12878	blood:	n/a	n/a
26	BATF	chr9:6630698-6631421	GM12878	blood:	n/a	chr9:6630833-6630842
27	BATF	chr9:6592868-6593086	GM12878	blood:	n/a	n/a
28	BATF	chr9:6655058-6655371	GM12878	blood:	n/a	n/a
29	BATF	chr9:6656332-6656632	GM12878	blood:	n/a	n/a
30	BCL11A	chr9:6594611-6594793	GM12878	blood:	n/a	n/a
31	BCL11A	chr9:6605220-6605551	GM12878	blood:	n/a	n/a
32	BCL11A	chr9:6655034-6655412	GM12878	blood:	n/a	n/a
33	BCL11A	chr9:6632471-6632972	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:6605232-6605584	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:6632584-6632927	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:6575318-6575518	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:6598377-6598720	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:6598313-6598874	GM12878	blood:	n/a	n/a
39	BCL3	chr9:6566337-6566811	GM12878	blood:	n/a	n/a
40	BCL3	chr9:6632539-6633018	GM12878	blood:	n/a	n/a
41	BCL3	chr9:6575300-6575684	GM12878	blood:	n/a	n/a
42	BCL3	chr9:6558003-6558364	GM12878	blood:	n/a	n/a
43	BCL3	chr9:6598339-6598796	GM12878	blood:	n/a	n/a
44	BCLAF1	chr9:6630775-6631290	GM12878	blood:	n/a	n/a
45	BCLAF1	chr9:6646220-6646693	GM12878	blood:	n/a	n/a
46	BCLAF1	chr9:6632431-6632955	GM12878	blood:	n/a	n/a
47	BCLAF1	chr9:6605192-6605673	GM12878	blood:	n/a	n/a
48	BCLAF1	chr9:6632444-6633343	GM12878	blood:	n/a	n/a
49	BCLAF1	chr9:6654844-6655458	GM12878	blood:	n/a	n/a
50	BCLAF1	chr9:6598356-6598906	GM12878	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6644603-6644653	Caco-2	colon:	n/a
2	chr9:6644603-6644653	Caco-2	colon:	n/a
3	chr9:6645686-6645736	PrEC	prostate:	n/a
4	chr9:6644603-6644653	GM06990	blood:	n/a
5	chr9:6645468-6645518	NHDF-neo	bronchial:	n/a
6	chr9:6644369-6644419	LNCaP	prostate:	n/a
7	chr9:6644603-6644653	SK-N-MC	brain:	n/a
8	chr9:6645686-6645736	GM06990	blood:	n/a
9	chr9:6644603-6644653	MCF10A-Er-Src	breast:	n/a
10	chr9:6645736-6645786	AG09319	gingival:	n/a
11	chr9:6646386-6646436	GM12878	blood:	n/a
12	chr9:6645736-6645786	NHDF-neo	bronchial:	n/a
13	chr9:6644369-6644419	GM12891	blood:	n/a
14	chr9:6644369-6644419	HRPEpiC	eye:	n/a
15	chr9:6645468-6645518	NT2-D1	testis:	n/a
16	chr9:6644369-6644419	HEEpiC	esophagus:	n/a
17	chr9:6644369-6644419	GM12892	blood:	n/a
18	chr9:6645468-6645518	PrEC	prostate:	n/a
19	chr9:6646386-6646436	AG09319	gingival:	n/a
20	chr9:6645468-6645518	LNCaP	prostate:	n/a
21	chr9:6644369-6644419	H1-hESC	embryonic stem cell:	embryo
22	chr9:6645686-6645736	LNCaP	prostate:	n/a
23	chr9:6645468-6645518	HCM	heart:	n/a
24	chr9:6645736-6645786	AG10803	skin:	n/a
25	chr9:6645686-6645736	ECC-1	luminal epithelium:	n/a
26	chr9:6645686-6645736	BJ	skin:	n/a
27	chr9:6646386-6646436	NB4	blood:	n/a
28	chr9:6644603-6644653	NT2-D1	testis:	n/a
29	chr9:6645736-6645786	RPTEC	kidney:	n/a
30	chr9:6645468-6645518	HAEpiC	amniotic membrane:	n/a
31	chr9:6646386-6646436	BJ	skin:	n/a
32	chr9:6645686-6645736	NT2-D1	testis:	n/a
33	chr9:6645686-6645736	CMK	blood:	n/a
34	chr9:6644603-6644653	HIPEpiC	eye:	n/a
35	chr9:6645736-6645786	GM12878	blood:	n/a
36	chr9:6644369-6644419	PrEC	prostate:	n/a
37	chr9:6645736-6645786	NT2-D1	testis:	n/a
38	chr9:6646386-6646436	HRE	kidney:	n/a
39	chr9:6644369-6644419	SAEC	small airway:	n/a
40	chr9:6644603-6644653	BE2_C	brain:	n/a
41	chr9:6644369-6644419	NT2-D1	testis:	n/a
42	chr9:6644603-6644653	Jurkat	blood:	n/a
43	chr9:6644369-6644419	HRE	kidney:	n/a
44	chr9:6644603-6644653	PANC-1	pancreas:	n/a
45	chr9:6645468-6645518	Caco-2	colon:	n/a
46	chr9:6645468-6645518	BE2_C	brain:	n/a
47	chr9:6644369-6644419	K562	blood:	n/a
48	chr9:6645468-6645518	SKMC	muscle:	n/a
49	chr9:6644603-6644653	AG04450	lung:	fetal
50	chr9:6645686-6645736	SK-N-MC	brain:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6410972..6413613-chr9:6564070..6565701,2	MCF-7	breast:
2	chr9:6615911..6617907-chr9:6681150..6682978,2	MCF-7	breast:
3	chr9:6639721..6642651-chr9:6680043..6682884,2	MCF-7	breast:
4	chr9:6662765..6664429-chr9:6666367..6668579,2	MCF-7	breast:
5	chr9:6663029..6667664-chr9:6679639..6683357,9	MCF-7	breast:
6	chr9:6639393..6643031-chr9:6644244..6646064,4	MCF-7	breast:
7	chr9:6585232..6587306-chr9:6664888..6666750,2	MCF-7	breast:
8	chr9:6627812..6629680-chr9:6632614..6635740,3	MCF-7	breast:
9	chr9:6663663..6666675-chr9:6715678..6718421,3	MCF-7	breast:
10	chr9:6354258..6354771-chr9:6567896..6568668,2	MCF-7	breast:
11	chr9:6641084..6643158-chr9:6652442..6654682,2	MCF-7	breast:
12	chr9:6643546..6649129-chr9:6652921..6657149,5	MCF-7	breast:
13	chr9:6570923..6573857-chr9:6574160..6576030,2	K562	blood:
14	chr9:6579960..6582259-chr9:6679731..6681701,2	MCF-7	breast:
15	chr9:6656639..6659482-chr9:6662780..6664665,3	MCF-7	breast:
16	chr9:6593764..6596429-chr9:6597405..6599828,2	MCF-7	breast:
17	chr9:6640659..6642824-chr9:6643049..6645706,2	MCF-7	breast:
18	chr9:6590828..6592705-chr9:6679350..6681430,2	MCF-7	breast:
19	chr9:6654607..6656764-chr9:6663214..6664911,2	K562	blood:
20	chr9:6588736..6590830-chr9:6680231..6682699,2	MCF-7	breast:
21	chr9:6605288..6608151-chr9:6611363..6613701,3	K562	blood:
22	chr9:6641084..6643158-chr9:6652442..6654682,2	MCF-7	breast:
23	chr9:6570923..6573857-chr9:6574160..6576030,2	K562	blood:
24	chr9:6605288..6608151-chr9:6611363..6613701,3	K562	blood:
25	chr9:6656639..6659482-chr9:6662780..6664665,3	MCF-7	breast:
26	chr9:6562859..6565330-chr9:6565433..6569047,3	K562	blood:
27	chr9:6354058..6354828-chr9:6567905..6568745,4	MCF-7	breast:
28	chr9:6623651..6625727-chr9:6679924..6681530,2	MCF-7	breast:
29	chr9:6654607..6656764-chr9:6663214..6664911,2	K562	blood:
30	chr9:6411889..6413422-chr9:6565833..6568598,2	K562	blood:
31	chr9:6584834..6585802-chr9:6667386..6668426,5	MCF-7	breast:
32	chr9:6550978..6552657-chr9:6561789..6563568,2	K562	blood:
33	chr9:6627812..6629680-chr9:6632614..6635740,3	MCF-7	breast:
34	chr9:6593764..6596429-chr9:6597405..6599828,2	MCF-7	breast:
35	chr9:6624229..6626158-chr9:6679853..6681433,2	MCF-7	breast:
36	chr9:6652273..6654630-chr9:6673766..6675385,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KDM4C-13	chr9:6663156-6663366	NONHSAT130148
2	lnc-UHRF2-5	chr9:6568844-6569360	NONHSAT130143
3	lnc-KDM4C-14	chr9:6661651-6661936	NONHSAT130147
4	lnc-KDM4C-5	chr9:6645882-6646085	NONHSAT130145
5	lnc-KDM4C-5	chr9:6645956-6646085	ENSG00000236924.1
6	lnc-KDM4C-13	chr9:6662424-6662810	NONHSAT130148
7	lnc-KDM4C-13	chr9:6663657-6663792	NONHSAT130148
8	lnc-KDM4C-14	chr9:6660407-6661044	NONHSAT130146
9	lnc-KDM4C-14	chr9:6661783-6661845	NONHSAT130146
10	lnc-KDM4C-14	chr9:6661291-6661345	NONHSAT130146

No data

Variant related genes	Relation type
ENSG00000236924	TF binding region
ENSG00000237158	TF binding region
ENSG00000206147	TF binding region
ENSG00000229057	TF binding region
ENSG00000252110	TF binding region
RN7SL123P	TF binding region
GLDC	TF binding region
ENSG00000236924	CpG island
ENSG00000237158	CpG island
ENSG00000206147	CpG island
ENSG00000229057	CpG island
ENSG00000252110	CpG island
RN7SL123P	CpG island
GLDC	CpG island
ENSG00000236924	chromatin interactions
ENSG00000252110	chromatin interactions
ENSG00000237158	chromatin interactions
ENSG00000178445	chromatin interactions
ENSG00000147854	chromatin interactions
ENSG00000232946	chromatin interactions
ENSG00000225489	chromatin interactions

Extended variants
information (count: 6318 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:6318 , 50 per page) page: 1 2 3 4 5 6 7 ... 127

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1929933	chr9:6555079-6555080	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs529337742	chr9:6555128-6555129	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370770448	chr9:6555136-6555137	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs17499965	chr9:6555172-6555173	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565868941	chr9:6555178-6555179	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10815443	chr9:6555183-6555184	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
7	rs114667156	chr9:6555194-6555195	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370465540	chr9:6555211-6555212	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537759037	chr9:6555222-6555223	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556376061	chr9:6555226-6555227	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568259255	chr9:6555234-6555235	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs117388658	chr9:6555242-6555243	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374451230	chr9:6555264-6555265	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572194134	chr9:6555283-6555284	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs11998836	chr9:6555290-6555291	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs558081251	chr9:6555296-6555297	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs10125618	chr9:6555311-6555312	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs543653470	chr9:6555313-6555314	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs562446574	chr9:6555319-6555320	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140349396	chr9:6555321-6555322	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12379309	chr9:6555329-6555330	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116529655	chr9:6555359-6555360	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59993571	chr9:6555361-6555362	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533264063	chr9:6555362-6555363	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551421913	chr9:6555371-6555372	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185307878	chr9:6555383-6555384	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138132424	chr9:6555392-6555393	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10975640	chr9:6555417-6555418	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537435761	chr9:6555474-6555475	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139223689	chr9:6555475-6555476	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549700305	chr9:6555487-6555488	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112376419	chr9:6555556-6555557	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs535719278	chr9:6555562-6555563	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189009725	chr9:6555620-6555621	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565638809	chr9:6555636-6555637	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539544639	chr9:6555642-6555643	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557884502	chr9:6555672-6555673	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576049257	chr9:6555687-6555688	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544031279	chr9:6555702-6555703	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555658242	chr9:6555741-6555742	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572178367	chr9:6555747-6555748	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181100274	chr9:6555763-6555764	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541289970	chr9:6555771-6555772	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370794001	chr9:6555813-6555814	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs185487940	chr9:6555818-6555819	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs16924687	chr9:6555850-6555851	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs150835843	chr9:6555897-6555898	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs563844813	chr9:6555900-6555901	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs530888639	chr9:6555911-6555912	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs187996774	chr9:6555923-6555924	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1752 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6510400-6558800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr9:6528600-6558000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr9:6530800-6563200	Weak transcription	A549	lung
4	chr9:6532000-6570400	Strong transcription	Liver	Liver
5	chr9:6533200-6559800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr9:6534600-6558200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr9:6544400-6558000	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr9:6547000-6557800	Weak transcription	Brain Hippocampus Middle	brain
9	chr9:6547200-6560600	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:6548000-6558000	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr9:6548400-6557800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr9:6549000-6557800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr9:6549600-6558200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:6550000-6557600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:6550200-6556800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:6550200-6557600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:6550400-6557800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr9:6551400-6557800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr9:6552800-6556400	Strong transcription	GM12878-XiMat	blood
20	chr9:6553000-6557600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr9:6553000-6557800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr9:6553000-6557800	Weak transcription	Fetal Brain Female	brain
23	chr9:6553000-6560400	Weak transcription	Placenta	Placenta
24	chr9:6553200-6555600	Strong transcription	H9 Cell Line	embryonic stem cell
25	chr9:6553200-6557800	Weak transcription	Brain Anterior Caudate	brain
26	chr9:6553400-6555200	Enhancers	HUVEC	blood vessel
27	chr9:6553400-6556200	Weak transcription	Brain Germinal Matrix	brain
28	chr9:6553400-6557600	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr9:6553400-6561600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr9:6553400-6563000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr9:6553800-6555200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr9:6553800-6556600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:6553800-6557800	Weak transcription	NH-A	brain
34	chr9:6553800-6558400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr9:6554000-6557200	Weak transcription	Fetal Brain Male	brain
36	chr9:6554400-6556000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
37	chr9:6554400-6556000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr9:6554400-6556600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:6554400-6561800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr9:6554600-6556000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr9:6554600-6556000	Strong transcription	HepG2	liver
42	chr9:6554600-6568600	Weak transcription	Fetal Intestine Small	intestine
43	chr9:6555200-6555400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr9:6555200-6556200	Weak transcription	HUVEC	blood vessel
45	chr9:6555600-6557600	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr9:6556000-6557800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr9:6556000-6557800	Weak transcription	HepG2	liver
48	chr9:6556000-6563200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr9:6556000-6566800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr9:6556200-6556400	Enhancers	Brain Germinal Matrix	brain

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