Variant report

Variant	nsv538775
Chromosome Location	chr7:19152934-19162079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:2261)
Chromatin interactive
region (count:3)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:19155559-19156240	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:19156545-19156550	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:19157965-19157974	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:19156793-19156902	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr7:19158087-19158099	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr7:19157108-19157365	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTBP2	chr7:19155933-19159128	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr7:19155960-19156110	HMEC	breast:	n/a	n/a
9	CTCF	chr7:19161680-19161830	GM12868	blood:	n/a	n/a
10	CTCF	chr7:19159060-19159210	AG04449	skin:	n/a	n/a
11	CTCF	chr7:19158020-19158170	HEK293	kidney:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
12	CTCF	chr7:19157520-19157670	AG09319	gingival:	n/a	chr7:19157529-19157542
13	CTCF	chr7:19161758-19161838	GM20000	blood:	n/a	n/a
14	CTCF	chr7:19161740-19161890	HPF	lung:	n/a	n/a
15	CTCF	chr7:19157920-19158070	HPF	lung:	n/a	n/a
16	CTCF	chr7:19161740-19161890	WI-38	lung:	n/a	n/a
17	CTCF	chr7:19158680-19158830	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr7:19158020-19158191	SK-N-SH_RA	brain:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
19	CTCF	chr7:19161692-19161878	ProgFib	skin:	n/a	n/a
20	CTCF	chr7:19161733-19161893	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr7:19161720-19161870	GM12872	blood:	n/a	n/a
22	CTCF	chr7:19155987-19156193	Fibrobl	skin:	n/a	n/a
23	CTCF	chr7:19161720-19161870	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr7:19157960-19158110	HVMF	connective:	n/a	n/a
25	CTCF	chr7:19161720-19161870	GM12874	blood:	n/a	n/a
26	CTCF	chr7:19155520-19155670	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr7:19161675-19161892	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:19161700-19161850	GM12872	blood:	n/a	n/a
29	CTCF	chr7:19158020-19158170	BJ	skin:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
30	CTCF	chr7:19161740-19161890	GM12875	blood:	n/a	n/a
31	CTCF	chr7:19158060-19158210	AG04450	lung:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
32	CTCF	chr7:19158160-19158310	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr7:19161740-19161890	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr7:19161740-19161890	AG09319	gingival:	n/a	n/a
35	CTCF	chr7:19157220-19157370	AG04449	skin:	n/a	n/a
36	CTCF	chr7:19157860-19158010	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr7:19161668-19161922	A549	lung:	n/a	n/a
38	CTCF	chr7:19161720-19161870	HVMF	connective:	n/a	n/a
39	CTCF	chr7:19161740-19161890	HA-sp	spinal cord:	n/a	n/a
40	CTCF	chr7:19161740-19161890	GM12867	blood:	n/a	n/a
41	CTCF	chr7:19161731-19161901	K562	blood:	n/a	n/a
42	CTCF	chr7:19157980-19158130	AoAF	blood vessel:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
43	CTCF	chr7:19159520-19159670	AG09319	gingival:	n/a	n/a
44	CTCF	chr7:19157980-19158130	HCPEpiC	choroid plexus:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
45	CTCF	chr7:19161760-19161910	HCT-116	colon:	n/a	n/a
46	CTCF	chr7:19158940-19159090	AG04449	skin:	n/a	n/a
47	CTCF	chr7:19161720-19161870	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr7:19161765-19161856	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr7:19158020-19158170	HMF	breast:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
50	CTCF	chr7:19161501-19162045	HCT-116	colon:	n/a	n/a

(count:2261 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19157839-19157889	IMR90	lung:	fetal
2	chr7:19157739-19157789	HMEC	breast:	n/a
3	chr7:19160621-19160671	HCF	heart:	n/a
4	chr7:19157634-19157684	ProgFib	skin:	n/a
5	chr7:19157839-19157889	IMR90	lung:	fetal
6	chr7:19157739-19157789	HMEC	breast:	n/a
7	chr7:19160621-19160671	HCF	heart:	n/a
8	chr7:19157634-19157684	ProgFib	skin:	n/a
9	chr7:19158692-19158742	HRE	kidney:	n/a
10	chr7:19158378-19158428	HEEpiC	esophagus:	n/a
11	chr7:19158134-19158184	GM12878	blood:	n/a
12	chr7:19155785-19155835	SK-N-MC	brain:	n/a
13	chr7:19157339-19157389	RPTEC	kidney:	n/a
14	chr7:19158349-19158399	GM12878	blood:	n/a
15	chr7:19156550-19156600	ProgFib	skin:	n/a
16	chr7:19158666-19158716	NHDF-neo	bronchial:	n/a
17	chr7:19158123-19158173	HRPEpiC	eye:	n/a
18	chr7:19158134-19158184	ProgFib	skin:	n/a
19	chr7:19156550-19156600	BJ	skin:	n/a
20	chr7:19157813-19157863	AG10803	skin:	n/a
21	chr7:19158692-19158742	PrEC	prostate:	n/a
22	chr7:19157739-19157789	GM12892	blood:	n/a
23	chr7:19157813-19157863	ECC-1	luminal epithelium:	n/a
24	chr7:19158210-19158260	AG10803	skin:	n/a
25	chr7:19156621-19156671	HCM	heart:	n/a
26	chr7:19156086-19156136	HepG2	liver:	n/a
27	chr7:19158747-19158797	Hepatocyte	liver:	n/a
28	chr7:19157839-19157889	BE2_C	brain:	n/a
29	chr7:19158666-19158716	ovcar-3	ovarian:	n/a
30	chr7:19156621-19156671	HEK293	kidney:	embryo
31	chr7:19156902-19156952	PrEC	prostate:	n/a
32	chr7:19157938-19157988	SK-N-MC	brain:	n/a
33	chr7:19156086-19156136	IMR90	lung:	fetal
34	chr7:19158647-19158697	PrEC	prostate:	n/a
35	chr7:19158666-19158716	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:19158647-19158697	HEEpiC	esophagus:	n/a
37	chr7:19158692-19158742	IMR90	lung:	fetal
38	chr7:19157634-19157684	T-47D	breast:	n/a
39	chr7:19157193-19157243	A549	lung:	n/a
40	chr7:19157420-19157470	K562	blood:	n/a
41	chr7:19158134-19158184	HUVEC	blood vessel:	n/a
42	chr7:19158041-19158091	ProgFib	skin:	n/a
43	chr7:19157813-19157863	HCPEpiC	choroid plexus:	n/a
44	chr7:19156902-19156952	T-47D	breast:	n/a
45	chr7:19158041-19158091	HAEpiC	amniotic membrane:	n/a
46	chr7:19158566-19158616	H1-hESC	embryonic stem cell:	embryo
47	chr7:19157296-19157346	GM12892	blood:	n/a
48	chr7:19158030-19158080	MCF10A-Er-Src	breast:	n/a
49	chr7:19158664-19158714	Hepatocyte	liver:	n/a
50	chr7:19158647-19158697	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:19161356..19162289-chr7:19481424..19482541,6	MCF-7	breast:
2	chr7:19161360..19162323-chr7:19704757..19705725,5	MCF-7	breast:
3	chr7:19161315..19162333-chr7:19661177..19662063,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC9-3	chr7:19161404-19161539	ENSG00000236536.1
2	lnc-HDAC9-9	chr7:19156379-19156637	NONHSAT119382
3	lnc-HDAC9-8	chr7:19155207-19155609	NONHSAT119381
4	lnc-HDAC9-2	chr7:19152378-19153894	ENSG00000232821.1
5	lnc-HDAC9-3	chr7:19159556-19160111	ENSG00000236536.1
6	lnc-HDAC9-8	chr7:19154854-19155484	NONHSAT119380
7	lnc-HDAC9-2	chr7:19152378-19153891	XLOC_006001
8	lnc-HDAC9-9	chr7:19156130-19156172	NONHSAT119382

No data

Variant related genes	Relation type
TWIST1	TF binding region
ENSG00000236536	TF binding region
TWIST1	CpG island
ENSG00000236536	CpG island
NEDD4	miRNA target sites

Extended variants
information (count: 420 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551419394	chr7:19152955-19152956	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
2	rs181452542	chr7:19153007-19153008	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
3	rs186038476	chr7:19153073-19153074	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
4	rs549007062	chr7:19153077-19153078	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
5	rs567565512	chr7:19153102-19153103	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
6	rs538171657	chr7:19153116-19153117	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
7	rs549696656	chr7:19153139-19153140	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
8	rs571388945	chr7:19153161-19153162	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
9	rs546216130	chr7:19153182-19153183	Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
10	rs557784093	chr7:19153223-19153224	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
11	rs115126052	chr7:19153233-19153234	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
12	rs570847958	chr7:19153243-19153244	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
13	rs533924157	chr7:19153249-19153250	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
14	rs191271775	chr7:19153290-19153291	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
15	rs2522196	chr7:19153297-19153298	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
16	rs552971033	chr7:19153305-19153306	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
17	rs371556595	chr7:19153307-19153308	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
18	rs11973396	chr7:19153320-19153321	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
19	rs550177245	chr7:19153364-19153365	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
20	rs544924008	chr7:19153403-19153404	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs376237444	chr7:19153424-19153425	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
22	rs149172562	chr7:19153477-19153478	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs541926299	chr7:19153480-19153481	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs578100951	chr7:19153494-19153495	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs4721745	chr7:19153512-19153513	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs538102464	chr7:19153522-19153523	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs560247934	chr7:19153542-19153543	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs376130922	chr7:19153602-19153603	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
29	rs183024374	chr7:19153633-19153634	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
30	rs548978712	chr7:19153700-19153701	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
31	rs369514359	chr7:19153715-19153716	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
32	rs560902865	chr7:19153725-19153726	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
33	rs376670936	chr7:19153765-19153766	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
34	rs4721746	chr7:19153843-19153844	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs550021426	chr7:19153946-19153947	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs571454453	chr7:19153983-19153984	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs373978050	chr7:19154024-19154025	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs143230344	chr7:19154042-19154043	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs372093251	chr7:19154050-19154051	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs547230973	chr7:19154052-19154053	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs543627377	chr7:19154081-19154082	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs138795134	chr7:19154097-19154098	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs187764343	chr7:19154115-19154116	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs141958920	chr7:19154123-19154124	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs567616355	chr7:19154170-19154171	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs190850527	chr7:19154226-19154227	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs556766786	chr7:19154228-19154229	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs559128718	chr7:19154238-19154239	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs35252838	chr7:19154277-19154278	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs36046091	chr7:19154321-19154322	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:19148200-19154800	Weak transcription	HSMMtube	muscle
2	chr7:19148400-19155600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:19150800-19153200	Flanking Active TSS	Adipose Nuclei	Adipose
4	chr7:19150800-19157200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:19151200-19153000	Flanking Active TSS	Osteobl	bone
6	chr7:19151400-19155200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:19151600-19153400	Strong transcription	HSMM	muscle
8	chr7:19151800-19153000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:19151800-19158800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:19152200-19153000	Flanking Active TSS	NH-A	brain
11	chr7:19152200-19155600	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
12	chr7:19152400-19155400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr7:19152600-19154000	Weak transcription	Placenta	Placenta
14	chr7:19152600-19154000	Weak transcription	NHLF	lung
15	chr7:19152600-19154600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:19152800-19153400	Genic enhancers	Muscle Satellite Cultured Cells	--
17	chr7:19152800-19153600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr7:19152800-19153600	Weak transcription	Right Atrium	heart
19	chr7:19152800-19154200	Weak transcription	Aorta	Aorta
20	chr7:19153000-19153200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:19153000-19153400	Enhancers	Osteobl	bone
22	chr7:19153000-19153600	Enhancers	NH-A	brain
23	chr7:19153000-19154800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr7:19153200-19153400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr7:19153200-19155800	Active TSS	Adipose Nuclei	Adipose
26	chr7:19153400-19154000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:19153400-19154000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr7:19153400-19154000	Transcr. at gene 5' and 3'	HSMM	muscle
29	chr7:19153400-19155200	Flanking Active TSS	Osteobl	bone
30	chr7:19153600-19153800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr7:19153600-19154800	Flanking Active TSS	NH-A	brain
32	chr7:19153600-19158600	Active TSS	Right Atrium	heart
33	chr7:19153800-19158000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:19154000-19154400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr7:19154000-19156000	Active TSS	Placenta	Placenta
36	chr7:19154000-19157800	Active TSS	NHLF	lung
37	chr7:19154000-19158000	Active TSS	Muscle Satellite Cultured Cells	--
38	chr7:19154000-19158600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:19154000-19159000	Active TSS	HSMM	muscle
40	chr7:19154200-19154400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr7:19154200-19158200	Active TSS	Aorta	Aorta
42	chr7:19154400-19154600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr7:19154400-19155400	Active TSS	Fetal Muscle Leg	muscle
44	chr7:19154400-19155400	Active TSS	Fetal Stomach	stomach
45	chr7:19154600-19154800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr7:19154600-19154800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
47	chr7:19154600-19154800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:19154600-19156000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr7:19154800-19155000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:19154800-19155000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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