Variant report

Variant	nsv972781
Chromosome Location	chr9:95639258-95671744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:122)
Chromatin interactive
region (count:8)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:559 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:95640133-95640654	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:95640345-95640576	K562	blood:	n/a	n/a
3	ARID3A	chr9:95639498-95639870	K562	blood:	n/a	n/a
4	ATF1	chr9:95640164-95640573	K562	blood:	n/a	n/a
5	BATF	chr9:95655088-95655280	GM12878	blood:	n/a	chr9:95655210-95655221
6	BCLAF1	chr9:95639994-95640627	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:95640126-95640568	GM12878	blood:	n/a	n/a
8	BHLHE40	chr9:95640211-95640530	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:95640109-95640567	K562	blood:	n/a	n/a
10	BRCA1	chr9:95640437-95640595	GM12878	blood:	n/a	n/a
11	BRCA1	chr9:95640113-95640490	HepG2	liver:	n/a	n/a
12	BRCA1	chr9:95640228-95640696	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr9:95639931-95640800	K562	blood:	n/a	n/a
14	CEBPB	chr9:95644651-95644836	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr9:95655537-95655586	A549	lung:	n/a	n/a
16	CEBPB	chr9:95655555-95655570	IMR90	lung:	n/a	n/a
17	CEBPB	chr9:95641168-95641468	A549	lung:	n/a	n/a
18	CEBPB	chr9:95640145-95640539	MCF-7	breast:	n/a	chr9:95640369-95640380
19	CEBPB	chr9:95655562-95655694	HepG2	liver:	n/a	n/a
20	CEBPB	chr9:95640206-95640652	A549	lung:	n/a	chr9:95640369-95640380
21	CEBPB	chr9:95641222-95641432	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:95654712-95654828	HepG2	liver:	n/a	chr9:95654753-95654764
23	CEBPB	chr9:95640233-95640590	K562	blood:	n/a	chr9:95640369-95640380
24	CEBPB	chr9:95640124-95640611	Hela-S3	cervix:	n/a	chr9:95640369-95640380
25	CEBPD	chr9:95640080-95640537	K562	blood:	n/a	n/a
26	CHD1	chr9:95639460-95639644	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr9:95640061-95640434	GM12878	blood:	n/a	n/a
28	CHD2	chr9:95640049-95640583	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr9:95644664-95644871	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr9:95640045-95640575	K562	blood:	n/a	n/a
31	CHD2	chr9:95640033-95640685	GM12878	blood:	n/a	n/a
32	CHD2	chr9:95640298-95640514	HepG2	liver:	n/a	n/a
33	CREB1	chr9:95640143-95640541	GM12878	blood:	n/a	n/a
34	CREB1	chr9:95640236-95640498	A549	lung:	n/a	n/a
35	CREB1	chr9:95640110-95640518	A549	lung:	n/a	n/a
36	CTCF	chr9:95646412-95646530	GM10266	blood:	n/a	n/a
37	CTCF	chr9:95646294-95646530	K562	blood:	n/a	n/a
38	CTCF	chr9:95646344-95646572	K562	blood:	n/a	n/a
39	CTCF	chr9:95646405-95646530	GM12892	blood:	n/a	n/a
40	CTCF	chr9:95646040-95646190	WI-38	lung:	n/a	n/a
41	CTCF	chr9:95646200-95646728	K562	blood:	n/a	n/a
42	CTCF	chr9:95646460-95646610	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr9:95646401-95646547	NHEK	skin:	n/a	n/a
44	CTCF	chr9:95646480-95646630	K562	blood:	n/a	n/a
45	CTCF	chr9:95667540-95667657	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr9:95646286-95646571	K562	blood:	n/a	n/a
47	CTCF	chr9:95646373-95646563	MCF-7	breast:	n/a	n/a
48	CTCF	chr9:95646363-95646542	GM19240	blood:	n/a	n/a
49	CTCF	chr9:95639954-95639964	MCF-7	breast:	n/a	n/a
50	CTCF	chr9:95646520-95646670	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:95640366-95640416	NT2-D1	testis:	n/a
2	chr9:95640366-95640416	BE2_C	brain:	n/a
3	chr9:95640659-95640709	PANC-1	pancreas:	n/a
4	chr9:95640659-95640709	HIPEpiC	eye:	n/a
5	chr9:95640366-95640416	HIPEpiC	eye:	n/a
6	chr9:95640366-95640416	GM06990	blood:	n/a
7	chr9:95640659-95640709	GM12892	blood:	n/a
8	chr9:95640659-95640709	HEEpiC	esophagus:	n/a
9	chr9:95640659-95640709	AG10803	skin:	n/a
10	chr9:95640659-95640709	GM19239	blood:	n/a
11	chr9:95640366-95640416	HPAEpiC	pulmonary alveolar:	n/a
12	chr9:95640366-95640416	HAEpiC	amniotic membrane:	n/a
13	chr9:95640659-95640709	A549	lung:	n/a
14	chr9:95640366-95640416	ProgFib	skin:	n/a
15	chr9:95640659-95640709	HCF	heart:	n/a
16	chr9:95640659-95640709	HL-60	blood:	n/a
17	chr9:95640366-95640416	HNPCEpiC	eye:	n/a
18	chr9:95640366-95640416	NHBE	bronchial:	n/a
19	chr9:95640659-95640709	AoSMC	blood vessel:	n/a
20	chr9:95640366-95640416	NH-A	brain:	n/a
21	chr9:95640659-95640709	RPTEC	kidney:	n/a
22	chr9:95640366-95640416	HL-60	blood:	n/a
23	chr9:95640366-95640416	IMR90	lung:	fetal
24	chr9:95640659-95640709	IMR90	lung:	fetal
25	chr9:95640659-95640709	HCT-116	colon:	n/a
26	chr9:95640659-95640709	ECC-1	luminal epithelium:	n/a
27	chr9:95640366-95640416	AG04450	lung:	fetal
28	chr9:95640366-95640416	SAEC	small airway:	n/a
29	chr9:95640366-95640416	PrEC	prostate:	n/a
30	chr9:95640366-95640416	HEEpiC	esophagus:	n/a
31	chr9:95640366-95640416	HMEC	breast:	n/a
32	chr9:95640659-95640709	AG04450	lung:	fetal
33	chr9:95640366-95640416	Hela-S3	cervix:	n/a
34	chr9:95640659-95640709	HUVEC	blood vessel:	n/a
35	chr9:95640659-95640709	Caco-2	colon:	n/a
36	chr9:95640659-95640709	MCF-7	breast:	n/a
37	chr9:95640659-95640709	HepG2	liver:	n/a
38	chr9:95640366-95640416	MCF10A-Er-Src	breast:	n/a
39	chr9:95640659-95640709	HEK293	kidney:	embryo
40	chr9:95640366-95640416	H1-hESC	embryonic stem cell:	embryo
41	chr9:95640659-95640709	U87	brain:	n/a
42	chr9:95640366-95640416	GM19239	blood:	n/a
43	chr9:95640366-95640416	HCF	heart:	n/a
44	chr9:95640366-95640416	K562	blood:	n/a
45	chr9:95640659-95640709	HMEC	breast:	n/a
46	chr9:95640366-95640416	Jurkat	blood:	n/a
47	chr9:95640659-95640709	MCF10A-Er-Src	breast:	n/a
48	chr9:95640366-95640416	Hepatocyte	liver:	n/a
49	chr9:95640366-95640416	AG10803	skin:	n/a
50	chr9:95640659-95640709	GM12891	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95644477..95647026-chr9:95856409..95858869,2	MCF-7	breast:
2	chr9:95632175..95634114-chr9:95643076..95644693,2	K562	blood:
3	chr9:95570373..95571952-chr9:95637590..95640500,2	MCF-7	breast:
4	chr9:95638865..95641445-chr9:95646989..95649985,2	MCF-7	breast:
5	chr9:95630810..95632810-chr9:95646965..95649484,2	MCF-7	breast:
6	chr9:95639787..95641673-chr9:95820453..95823030,2	K562	blood:
7	chr9:95630407..95632096-chr9:95638470..95640204,2	K562	blood:
8	chr9:95668983..95671268-chr9:95672944..95675033,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGD3-3	chr9:95646848-95646908	NONHSAT133209
2	lnc-FGD3-3	chr9:95644865-95645071	NONHSAT133210
3	lnc-FGD3-3	chr9:95660664-95660887	NONHSAT133210
4	lnc-FGD3-3	chr9:95647164-95647333	NONHSAT133209
5	lnc-FGD3-3	chr9:95644849-95645071	NONHSAT133209
6	lnc-FGD3-3	chr9:95661581-95661890	NONHSAT133212
7	lnc-FGD3-3	chr9:95646188-95646282	NONHSAT133209
8	lnc-FGD3-3	chr9:95647164-95648440	NONHSAT133213
9	lnc-FGD3-3	chr9:95646467-95646908	NONHSAT133213
10	lnc-FGD3-3	chr9:95646193-95646282	NONHSAT133212
11	lnc-FGD3-3	chr9:95646848-95646908	NONHSAT133212
12	lnc-FGD3-3	chr9:95646188-95646282	NONHSAT133210
13	lnc-FGD3-3	chr9:95646848-95646908	NONHSAT133210
14	lnc-FGD3-2	chr9:95659186-95659353	NONHSAT133223
15	lnc-FGD3-2	chr9:95660214-95660436	NONHSAT133223

No data

Variant related genes	Relation type
ALOX15P2	TF binding region
SNX18P2	TF binding region
ENSG00000226668	TF binding region
ZNF484	TF binding region
ALOX15P2	CpG island
SNX18P2	CpG island
ENSG00000226668	CpG island
ZNF484	CpG island
ENSG00000127081	chromatin interactions
ENSG00000157303	chromatin interactions
ENSG00000165233	chromatin interactions
ENSG00000223446	chromatin interactions
ENSG00000187984	chromatin interactions

Extended variants
information (count: 1010 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1010 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537504003	chr9:95639269-95639270	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs370383478	chr9:95639321-95639322	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs62572381	chr9:95639331-95639332	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs577712114	chr9:95639356-95639357	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs61186761	chr9:95639370-95639371	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554440399	chr9:95639378-95639379	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs12336022	chr9:95639398-95639399	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs184955105	chr9:95639440-95639441	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs543364991	chr9:95639463-95639464	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561217764	chr9:95639523-95639524	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200846750	chr9:95639565-95639566	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs200130289	chr9:95639607-95639608	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs573399904	chr9:95639634-95639635	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541467710	chr9:95639655-95639656	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs187828761	chr9:95639679-95639680	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs139304319	chr9:95639717-95639718	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374910413	chr9:95639720-95639721	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs146443361	chr9:95639794-95639795	Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs200629932	chr9:95639846-95639847	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs138882117	chr9:95639847-95639848	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs372156137	chr9:95639850-95639851	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs371463128	chr9:95639885-95639886	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs374172694	chr9:95639911-95639912	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs184547239	chr9:95639918-95639919	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs114784440	chr9:95639921-95639922	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs535322358	chr9:95639929-95639930	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs545064316	chr9:95639937-95639938	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs566353685	chr9:95639941-95639942	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs527538869	chr9:95639942-95639943	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs563348072	chr9:95639963-95639964	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs548876055	chr9:95639976-95639977	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs567490206	chr9:95639984-95639985	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs138836175	chr9:95640006-95640007	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs188252608	chr9:95640032-95640033	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs182032051	chr9:95640059-95640060	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs538751425	chr9:95640069-95640070	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs554375393	chr9:95640070-95640071	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs572680712	chr9:95640102-95640103	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs373185302	chr9:95640103-95640104	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs574636765	chr9:95640134-95640135	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs371878103	chr9:95640150-95640151	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs543302343	chr9:95640160-95640161	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs117360596	chr9:95640171-95640172	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs576710288	chr9:95640215-95640216	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs543786501	chr9:95640252-95640253	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs377159713	chr9:95640312-95640313	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs565151841	chr9:95640336-95640337	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs532610725	chr9:95640337-95640338	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs184832931	chr9:95640359-95640360	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs559878063	chr9:95640366-95640367	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD

Chromatin state (count:473 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95609000-95639800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:95616200-95639800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr9:95616400-95639800	Weak transcription	Small Intestine	intestine
4	chr9:95616600-95639600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr9:95618200-95639800	Weak transcription	Colonic Mucosa	Colon
6	chr9:95622600-95639400	Weak transcription	HSMMtube	muscle
7	chr9:95622600-95639600	Weak transcription	Fetal Kidney	kidney
8	chr9:95622600-95639800	Weak transcription	Aorta	Aorta
9	chr9:95623200-95639400	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr9:95625600-95639600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr9:95628200-95639800	Weak transcription	Right Atrium	heart
12	chr9:95630600-95639400	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr9:95630600-95639600	Weak transcription	Liver	Liver
14	chr9:95631000-95639400	Weak transcription	Brain Hippocampus Middle	brain
15	chr9:95631000-95639400	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr9:95631000-95639600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr9:95631200-95639600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr9:95631200-95639800	Weak transcription	Placenta	Placenta
19	chr9:95631400-95639800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr9:95631800-95639600	Weak transcription	Primary B cells from peripheral blood	blood
21	chr9:95633200-95639400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr9:95633200-95639400	Weak transcription	Fetal Intestine Large	intestine
23	chr9:95633200-95639400	Weak transcription	Fetal Stomach	stomach
24	chr9:95633200-95639400	Weak transcription	Stomach Smooth Muscle	stomach
25	chr9:95633200-95639600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr9:95633200-95639600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr9:95633200-95639600	Weak transcription	Adipose Nuclei	Adipose
28	chr9:95633200-95639800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr9:95633200-95639800	Weak transcription	Left Ventricle	heart
30	chr9:95633200-95639800	Weak transcription	Lung	lung
31	chr9:95633200-95639800	Weak transcription	Thymus	Thymus
32	chr9:95633400-95639400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr9:95633400-95639600	Weak transcription	Fetal Thymus	thymus
34	chr9:95633400-95639800	Weak transcription	Fetal Intestine Small	intestine
35	chr9:95634200-95639400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr9:95634200-95639400	Weak transcription	Fetal Muscle Leg	muscle
37	chr9:95634400-95639400	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr9:95634400-95639600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr9:95634400-95639600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:95635000-95639600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr9:95635000-95639800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr9:95635600-95639400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr9:95635800-95639400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr9:95636600-95639600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr9:95636600-95639800	Weak transcription	HSMM	muscle
46	chr9:95637000-95639600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr9:95637200-95639400	Enhancers	Fetal Brain Male	brain
48	chr9:95637200-95639800	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr9:95637400-95639600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
50	chr9:95637600-95639400	Enhancers	Primary T helper cells fromperipheralblood	blood

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