Variant report

Variant	nsv524849
Chromosome Location	chr9:15299590-15362057
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	ARID3A	chr9:15351035-15351548	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15333319-15333669	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:15306129-15306386	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15350374-15350711	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:15357028-15357575	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:15307077-15307551	HepG2	liver:	n/a	n/a
7	ATF1	chr9:15299673-15299858	K562	blood:	n/a	n/a
8	BACH1	chr9:15328520-15328827	K562	blood:	n/a	n/a
9	BACH1	chr9:15306339-15306925	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:15328555-15328874	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr9:15299577-15299867	GM12878	blood:	n/a	chr9:15299785-15299794
12	BATF	chr9:15306084-15306387	GM12878	blood:	n/a	n/a
13	BCL3	chr9:15331510-15331929	GM12878	blood:	n/a	n/a
14	BCL3	chr9:15331480-15331831	GM12878	blood:	n/a	n/a
15	BCLAF1	chr9:15299556-15300027	GM12878	blood:	n/a	chr9:15299645-15299654
16	BHLHE40	chr9:15315454-15315624	K562	blood:	n/a	n/a
17	BHLHE40	chr9:15351043-15351484	HepG2	liver:	n/a	n/a
18	BHLHE40	chr9:15318021-15318086	K562	blood:	n/a	n/a
19	BHLHE40	chr9:15307159-15307687	K562	blood:	n/a	n/a
20	BHLHE40	chr9:15306190-15306323	K562	blood:	n/a	n/a
21	BHLHE40	chr9:15307178-15307437	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:15357545-15357594	GM12878	blood:	n/a	n/a
23	BRCA1	chr9:15307498-15307506	HepG2	liver:	n/a	n/a
24	CBX3	chr9:15323298-15323578	K562	blood:	n/a	n/a
25	CCNT2	chr9:15307181-15307674	K562	blood:	n/a	n/a
26	CEBPB	chr9:15357066-15357440	HepG2	liver:	n/a	chr9:15357245-15357256
27	CEBPB	chr9:15305959-15306418	A549	lung:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
28	CEBPB	chr9:15331605-15331805	HepG2	liver:	n/a	chr9:15331667-15331678
29	CEBPB	chr9:15305868-15306420	MCF-7	breast:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
30	CEBPB	chr9:15328741-15329330	K562	blood:	n/a	chr9:15329145-15329156
31	CEBPB	chr9:15305925-15306284	ECC-1	luminal epithelium:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
32	CEBPB	chr9:15305937-15306278	K562	blood:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
33	CEBPB	chr9:15357064-15357692	H1-hESC	embryonic stem cell:	n/a	chr9:15357245-15357256
34	CEBPB	chr9:15357101-15357372	HepG2	liver:	n/a	chr9:15357245-15357256
35	CEBPB	chr9:15357075-15357432	K562	blood:	n/a	chr9:15357245-15357256
36	CEBPB	chr9:15308517-15308964	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:15350420-15351443	HepG2	liver:	n/a	chr9:15350602-15350613
38	CEBPB	chr9:15357187-15357345	Hela-S3	cervix:	n/a	chr9:15357245-15357256
39	CEBPB	chr9:15306044-15306211	HepG2	liver:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
40	CEBPB	chr9:15307255-15307554	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:15305930-15306387	IMR90	lung:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
42	CEBPB	chr9:15357133-15357334	IMR90	lung:	n/a	chr9:15357245-15357256
43	CEBPB	chr9:15361869-15362048	H1-hESC	embryonic stem cell:	n/a	chr9:15361911-15361922
44	CEBPB	chr9:15305937-15306330	H1-hESC	embryonic stem cell:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
45	CEBPB	chr9:15328968-15329272	A549	lung:	n/a	chr9:15329145-15329156
46	CEBPB	chr9:15305873-15306429	MCF-7	breast:	n/a	chr9:15306113-15306126 chr9:15306113-15306124 chr9:15306115-15306126
47	CEBPB	chr9:15357103-15357439	MCF-7	breast:	n/a	chr9:15357245-15357256
48	CEBPB	chr9:15357101-15357410	A549	lung:	n/a	chr9:15357245-15357256
49	CEBPB	chr9:15350243-15350844	A549	lung:	n/a	chr9:15350602-15350613
50	CEBPB	chr9:15307236-15307631	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15307873-15307923	HMEC	breast:	n/a
2	chr9:15307873-15307923	HMEC	breast:	n/a
3	chr9:15306736-15306786	Jurkat	blood:	n/a
4	chr9:15305873-15305923	AG04449	skin:	fetal
5	chr9:15306736-15306786	GM06990	blood:	n/a
6	chr9:15305873-15305923	HNPCEpiC	eye:	n/a
7	chr9:15305873-15305923	ovcar-3	ovarian:	n/a
8	chr9:15305873-15305923	SAEC	small airway:	n/a
9	chr9:15307376-15307426	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:15305873-15305923	IMR90	lung:	fetal
11	chr9:15307376-15307426	T-47D	breast:	n/a
12	chr9:15310979-15311029	Hepatocyte	liver:	n/a
13	chr9:15305873-15305923	PFSK-1	brain:	n/a
14	chr9:15307873-15307923	HUVEC	blood vessel:	n/a
15	chr9:15305873-15305923	BE2_C	brain:	n/a
16	chr9:15306736-15306786	ProgFib	skin:	n/a
17	chr9:15306736-15306786	GM12891	blood:	n/a
18	chr9:15305873-15305923	ProgFib	skin:	n/a
19	chr9:15305873-15305923	MCF10A-Er-Src	breast:	n/a
20	chr9:15307376-15307426	BJ	skin:	n/a
21	chr9:15306337-15306387	SK-N-MC	brain:	n/a
22	chr9:15306736-15306786	HCT-116	colon:	n/a
23	chr9:15310979-15311029	HMEC	breast:	n/a
24	chr9:15306337-15306387	BE2_C	brain:	n/a
25	chr9:15310979-15311029	HRCEpiC	kidney:	n/a
26	chr9:15310979-15311029	PANC-1	pancreas:	n/a
27	chr9:15307873-15307923	AG09309	skin:	n/a
28	chr9:15310979-15311029	NHDF-neo	bronchial:	n/a
29	chr9:15306337-15306387	Hepatocyte	liver:	n/a
30	chr9:15306736-15306786	SK-N-MC	brain:	n/a
31	chr9:15306337-15306387	K562	blood:	n/a
32	chr9:15306736-15306786	HEK293	kidney:	embryo
33	chr9:15307376-15307426	HCF	heart:	n/a
34	chr9:15306736-15306786	HEEpiC	esophagus:	n/a
35	chr9:15305873-15305923	Hepatocyte	liver:	n/a
36	chr9:15307873-15307923	HEK293	kidney:	embryo
37	chr9:15306337-15306387	MCF-7	breast:	n/a
38	chr9:15310979-15311029	HCPEpiC	choroid plexus:	n/a
39	chr9:15305873-15305923	U87	brain:	n/a
40	chr9:15306337-15306387	MCF10A-Er-Src	breast:	n/a
41	chr9:15310979-15311029	HIPEpiC	eye:	n/a
42	chr9:15305873-15305923	HMEC	breast:	n/a
43	chr9:15310979-15311029	PFSK-1	brain:	n/a
44	chr9:15306736-15306786	NH-A	brain:	n/a
45	chr9:15305873-15305923	SK-N-MC	brain:	n/a
46	chr9:15306736-15306786	Hepatocyte	liver:	n/a
47	chr9:15307376-15307426	HEK293	kidney:	embryo
48	chr9:15305873-15305923	NHBE	bronchial:	n/a
49	chr9:15307873-15307923	AG09319	gingival:	n/a
50	chr9:15307873-15307923	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:15332011..15334775-chr9:15347128..15349228,2	MCF-7	breast:
2	chr9:15306963..15308773-chr9:15314988..15318754,3	MCF-7	breast:
3	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
4	chr9:15305088..15306661-chr9:15415103..15416933,2	MCF-7	breast:
5	chr9:15356402..15356902-chr9:134721602..134722134,2	NB4	blood:
6	chr9:15298942..15301605-chr9:15420446..15422025,2	MCF-7	breast:
7	chr9:15306135..15309581-chr9:15420818..15425516,6	MCF-7	breast:
8	chr9:15305128..15307154-chr9:15417021..15419951,2	MCF-7	breast:
9	chr9:15298408..15301257-chr9:15344895..15347811,2	MCF-7	breast:
10	chr9:15211338..15211919-chr9:15356761..15357369,2	MCF-7	breast:
11	chr9:15357011..15359248-chr9:15422187..15424051,2	MCF-7	breast:
12	chr9:15305709..15307336-chr9:15348928..15350627,2	MCF-7	breast:
13	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:
14	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
15	chr9:15277443..15278337-chr9:15356714..15357650,2	MCF-7	breast:
16	chr9:15352501..15354066-chr9:15419261..15422025,2	MCF-7	breast:
17	chr9:15303560..15305523-chr9:15350040..15352891,2	MCF-7	breast:
18	chr9:15300090..15302521-chr9:15304681..15306725,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-2	chr9:15348166-15348453	NONHSAT130262

Variant related genes	Relation type
RPL7P33	TF binding region
RN7SL157P	TF binding region
TTC39B	TF binding region
RPL7P33	CpG island
RN7SL157P	CpG island
TTC39B	CpG island
ENSG00000164975	chromatin interactions
ENSG00000155158	chromatin interactions
ENSG00000263817	chromatin interactions

Extended variants
information (count: 2972 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2972 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11792305	chr9:15299590-15299591	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566172296	chr9:15299613-15299614	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145021997	chr9:15299672-15299673	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138679320	chr9:15299678-15299679	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs16932971	chr9:15299699-15299700	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs583204	chr9:15299715-15299716	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs16932979	chr9:15299735-15299736	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
8	rs371868450	chr9:15299769-15299770	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs16932980	chr9:15299791-15299792	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs149377311	chr9:15299811-15299812	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs538382523	chr9:15299863-15299864	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553853879	chr9:15299869-15299870	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572137073	chr9:15299907-15299908	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185853702	chr9:15299940-15299941	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192361560	chr9:15299968-15299969	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182254770	chr9:15299969-15299970	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs5896670	chr9:15299972-15299973	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs386414506	chr9:15299973-15299974	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs397739209	chr9:15299974-15299975	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144716123	chr9:15300011-15300012	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs570913340	chr9:15300021-15300022	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186175587	chr9:15300030-15300031	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148459524	chr9:15300052-15300053	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369645518	chr9:15300073-15300074	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372644154	chr9:15300087-15300088	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571856603	chr9:15300113-15300114	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs3866794	chr9:15300116-15300117	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs190688638	chr9:15300156-15300157	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77950724	chr9:15300160-15300161	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs182854616	chr9:15300165-15300166	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567746256	chr9:15300202-15300203	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548419248	chr9:15300206-15300207	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563529596	chr9:15300211-15300212	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531142037	chr9:15300243-15300244	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs3866795	chr9:15300263-15300264	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs111562225	chr9:15300265-15300266	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538643562	chr9:15300285-15300286	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547037412	chr9:15300288-15300289	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553399417	chr9:15300324-15300325	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs187042629	chr9:15300330-15300331	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs373393811	chr9:15300401-15300402	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183258330	chr9:15300435-15300436	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554845910	chr9:15300450-15300451	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576290855	chr9:15300457-15300458	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143664122	chr9:15300464-15300465	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558837766	chr9:15300465-15300466	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577032003	chr9:15300475-15300476	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188732111	chr9:15300486-15300487	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541415431	chr9:15300534-15300535	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190992149	chr9:15300539-15300540	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	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
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	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
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	19835627	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15287400-15303600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr9:15290800-15305600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:15290800-15306000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:15291200-15305600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:15294400-15306200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:15296600-15301200	Enhancers	Primary B cells from peripheral blood	blood
7	chr9:15296800-15305600	Weak transcription	Left Ventricle	heart
8	chr9:15297000-15299600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr9:15297000-15305200	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr9:15297200-15300800	Enhancers	Primary hematopoietic stem cells	blood
11	chr9:15297200-15305600	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr9:15297200-15305600	Weak transcription	Brain Cingulate Gyrus	brain
13	chr9:15297200-15305600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr9:15297400-15299600	Weak transcription	HUVEC	blood vessel
15	chr9:15297400-15300200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr9:15297400-15300200	Weak transcription	Spleen	Spleen
17	chr9:15297400-15304800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr9:15297400-15305200	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr9:15297400-15305600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr9:15297400-15305600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr9:15297400-15305600	Weak transcription	NHEK	skin
22	chr9:15297400-15305600	Weak transcription	NHLF	lung
23	chr9:15297400-15306000	Weak transcription	HSMM	muscle
24	chr9:15297600-15299800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr9:15297600-15300000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr9:15297600-15300200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr9:15297600-15300200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr9:15297600-15300200	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr9:15297600-15300200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr9:15297600-15300200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr9:15297600-15301000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr9:15297600-15301000	Strong transcription	Fetal Stomach	stomach
33	chr9:15297600-15304600	Weak transcription	Stomach Mucosa	stomach
34	chr9:15297600-15305200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr9:15297600-15305200	Weak transcription	HMEC	breast
36	chr9:15297600-15305400	Weak transcription	Fetal Lung	lung
37	chr9:15297600-15305400	Weak transcription	Osteobl	bone
38	chr9:15297600-15305600	Weak transcription	Adipose Nuclei	Adipose
39	chr9:15297600-15305600	Weak transcription	Colon Smooth Muscle	Colon
40	chr9:15297600-15305600	Weak transcription	Esophagus	oesophagus
41	chr9:15297600-15305600	Weak transcription	Lung	lung
42	chr9:15297600-15305600	Weak transcription	Rectal Smooth Muscle	rectum
43	chr9:15297600-15305800	Weak transcription	Gastric	stomach
44	chr9:15297600-15305800	Weak transcription	Right Atrium	heart
45	chr9:15297800-15299600	Strong transcription	Fetal Intestine Large	intestine
46	chr9:15297800-15304800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr9:15297800-15305600	Weak transcription	NHDF-Ad	bronchial
48	chr9:15297800-15306000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr9:15298000-15300600	Flanking Active TSS	Primary T cells from cord blood	blood
50	chr9:15298000-15305400	Weak transcription	Stomach Smooth Muscle	stomach

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