Variant report

Variant	nsv538780
Chromosome Location	chr7:19153407-19163309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:527)
CpG islands
(count:2260)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:527 , 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	chr7:19156793-19156902	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr7:19157965-19157974	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr7:19155559-19156240	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr7:19156545-19156550	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	chr7:19161644-19161957	K562	blood:	n/a	n/a
9	CTCF	chr7:19161700-19161850	NHLF	lung:	n/a	n/a
10	CTCF	chr7:19161680-19161905	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr7:19161760-19161910	BE2_C	brain:	n/a	n/a
12	CTCF	chr7:19157993-19158231	ProgFib	skin:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
13	CTCF	chr7:19161720-19161870	K562	blood:	n/a	n/a
14	CTCF	chr7:19158020-19158170	NB4	blood:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
15	CTCF	chr7:19161680-19161830	GM12868	blood:	n/a	n/a
16	CTCF	chr7:19157980-19158130	AoAF	blood vessel:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
17	CTCF	chr7:19158020-19158170	A549	lung:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
18	CTCF	chr7:19161740-19161890	AoAF	blood vessel:	n/a	n/a
19	CTCF	chr7:19161740-19161890	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr7:19161714-19161827	NHEK	skin:	n/a	n/a
21	CTCF	chr7:19161668-19161922	A549	lung:	n/a	n/a
22	CTCF	chr7:19156855-19156908	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:19161740-19161890	GM12870	blood:	n/a	n/a
24	CTCF	chr7:19161704-19161873	A549	lung:	n/a	n/a
25	CTCF	chr7:19161716-19161886	HepG2	liver:	n/a	n/a
26	CTCF	chr7:19161720-19161870	GM12864	blood:	n/a	n/a
27	CTCF	chr7:19158060-19158210	HCFaa	heart:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
28	CTCF	chr7:19161674-19161911	MCF-7	breast:	n/a	n/a
29	CTCF	chr7:19159080-19159230	AG10803	skin:	n/a	n/a
30	CTCF	chr7:19157200-19157350	HMF	breast:	n/a	n/a
31	CTCF	chr7:19159400-19159550	AG09319	gingival:	n/a	n/a
32	CTCF	chr7:19158000-19158150	HRE	kidney:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
33	CTCF	chr7:19157559-19157633	ProgFib	skin:	n/a	n/a
34	CTCF	chr7:19157860-19158010	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr7:19157989-19158227	Fibrobl	skin:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
36	CTCF	chr7:19158940-19159090	AG04449	skin:	n/a	n/a
37	CTCF	chr7:19157520-19157670	SK-N-SH_RA	brain:	n/a	chr7:19157529-19157542
38	CTCF	chr7:19161740-19161890	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr7:19161595-19161977	T-47D	breast:	n/a	n/a
40	CTCF	chr7:19161720-19161870	HepG2	liver:	n/a	n/a
41	CTCF	chr7:19158640-19158790	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr7:19161720-19161870	HEK293	kidney:	n/a	n/a
43	CTCF	chr7:19156720-19156870	AG04449	skin:	n/a	n/a
44	CTCF	chr7:19157240-19157390	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr7:19161720-19161870	GM12870	blood:	n/a	n/a
46	CTCF	chr7:19161720-19161870	Caco-2	colon:	n/a	n/a
47	CTCF	chr7:19161700-19161850	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr7:19158020-19158170	AG04449	skin:	n/a	chr7:19158101-19158119 chr7:19158104-19158117
49	CTCF	chr7:19161660-19161810	A549	lung:	n/a	n/a
50	CTCF	chr7:19161720-19161870	HRE	kidney:	n/a	n/a

(count:2260 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:19157339-19157389	GM06990	blood:	n/a
2	chr7:19157263-19157313	HUVEC	blood vessel:	n/a
3	chr7:19157263-19157313	PANC-1	pancreas:	n/a
4	chr7:19157339-19157389	GM06990	blood:	n/a
5	chr7:19157263-19157313	HUVEC	blood vessel:	n/a
6	chr7:19157263-19157313	PANC-1	pancreas:	n/a
7	chr7:19158349-19158399	HEK293	kidney:	embryo
8	chr7:19154096-19154146	SKMC	muscle:	n/a
9	chr7:19158378-19158428	GM12892	blood:	n/a
10	chr7:19160621-19160671	HCF	heart:	n/a
11	chr7:19157739-19157789	HCT-116	colon:	n/a
12	chr7:19157650-19157700	Hela-S3	cervix:	n/a
13	chr7:19157839-19157889	ECC-1	luminal epithelium:	n/a
14	chr7:19158666-19158716	ProgFib	skin:	n/a
15	chr7:19158954-19159004	ProgFib	skin:	n/a
16	chr7:19158001-19158051	MCF10A-Er-Src	breast:	n/a
17	chr7:19158664-19158714	HUVEC	blood vessel:	n/a
18	chr7:19157710-19157760	A549	lung:	n/a
19	chr7:19158747-19158797	AG09319	gingival:	n/a
20	chr7:19156621-19156671	HCF	heart:	n/a
21	chr7:19155806-19155856	HRE	kidney:	n/a
22	chr7:19158954-19159004	GM19239	blood:	n/a
23	chr7:19157296-19157346	BJ	skin:	n/a
24	chr7:19156621-19156671	HEK293	kidney:	embryo
25	chr7:19157263-19157313	HCF	heart:	n/a
26	chr7:19157263-19157313	PrEC	prostate:	n/a
27	chr7:19157263-19157313	AG10803	skin:	n/a
28	chr7:19158747-19158797	ProgFib	skin:	n/a
29	chr7:19158566-19158616	NHBE	bronchial:	n/a
30	chr7:19157296-19157346	HRCEpiC	kidney:	n/a
31	chr7:19157634-19157684	HCPEpiC	choroid plexus:	n/a
32	chr7:19155806-19155856	HCT-116	colon:	n/a
33	chr7:19155806-19155856	HUVEC	blood vessel:	n/a
34	chr7:19157739-19157789	PFSK-1	brain:	n/a
35	chr7:19156621-19156671	HPAEpiC	pulmonary alveolar:	n/a
36	chr7:19158041-19158091	GM19239	blood:	n/a
37	chr7:19155806-19155856	H1-hESC	embryonic stem cell:	embryo
38	chr7:19158210-19158260	NH-A	brain:	n/a
39	chr7:19158030-19158080	PrEC	prostate:	n/a
40	chr7:19157710-19157760	SK-N-SH_RA	brain:	n/a
41	chr7:19158954-19159004	HCM	heart:	n/a
42	chr7:19158747-19158797	SK-N-SH	brain:	n/a
43	chr7:19154096-19154146	NH-A	brain:	n/a
44	chr7:19158123-19158173	NHBE	bronchial:	n/a
45	chr7:19160621-19160671	PFSK-1	brain:	n/a
46	chr7:19158664-19158714	HRCEpiC	kidney:	n/a
47	chr7:19158030-19158080	GM12878	blood:	n/a
48	chr7:19157420-19157470	GM06990	blood:	n/a
49	chr7:19157650-19157700	NHBE	bronchial:	n/a
50	chr7:19158666-19158716	ovcar-3	ovarian:	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	chr7:19161315..19162333-chr7:19661177..19662063,3	MCF-7	breast:
3	chr7:19161360..19162323-chr7:19704757..19705725,5	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDAC9-9	chr7:19156130-19156172	NONHSAT119382
2	lnc-HDAC9-8	chr7:19155207-19155609	NONHSAT119381
3	lnc-HDAC9-2	chr7:19152378-19153894	ENSG00000232821.1
4	lnc-HDAC9-8	chr7:19154854-19155484	NONHSAT119380
5	lnc-TWIST1-3	chr7:19162607-19162812	NONHSAT119384
6	lnc-HDAC9-3	chr7:19161404-19161539	ENSG00000236536.1
7	lnc-HDAC9-3	chr7:19159556-19160111	ENSG00000236536.1
8	lnc-HDAC9-9	chr7:19156379-19156637	NONHSAT119382
9	lnc-HDAC9-2	chr7:19152378-19153891	XLOC_006001

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: 450 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:450 , 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	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
2	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
3	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
4	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
5	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
6	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
7	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
8	rs376130922	chr7:19153602-19153603	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
9	rs183024374	chr7:19153633-19153634	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
10	rs548978712	chr7:19153700-19153701	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
11	rs369514359	chr7:19153715-19153716	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
12	rs560902865	chr7:19153725-19153726	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
13	rs376670936	chr7:19153765-19153766	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	lncRNA	n/a	Overlapped CNVs	n/a
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	rs182422950	chr7:19154339-19154340	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
32	rs568198446	chr7:19154342-19154343	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
33	rs554436517	chr7:19154343-19154344	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
34	rs533657156	chr7:19154373-19154374	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
35	rs572157601	chr7:19154378-19154379	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
36	rs542712713	chr7:19154395-19154396	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
37	rs2857550	chr7:19154479-19154480	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs560844069	chr7:19154501-19154502	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs35677062	chr7:19154506-19154507	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs531290698	chr7:19154509-19154510	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs543059785	chr7:19154530-19154531	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs2522197	chr7:19154535-19154536	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs146381514	chr7:19154549-19154550	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs187813644	chr7:19154552-19154553	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs547165705	chr7:19154558-19154559	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs2857551	chr7:19154563-19154564	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs576846140	chr7:19154570-19154571	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs565572232	chr7:19154573-19154574	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs529852661	chr7:19154605-19154606	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs138498449	chr7:19154618-19154619	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	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:526 , 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	chr7:19150800-19157200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:19151400-19155200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr7:19151800-19158800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:19152200-19155600	Transcr. at gene 5' and 3'	NHDF-Ad	bronchial
7	chr7:19152400-19155400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:19152600-19154000	Weak transcription	Placenta	Placenta
9	chr7:19152600-19154000	Weak transcription	NHLF	lung
10	chr7:19152600-19154600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr7:19152800-19153600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:19152800-19153600	Weak transcription	Right Atrium	heart
13	chr7:19152800-19154200	Weak transcription	Aorta	Aorta
14	chr7:19153000-19153600	Enhancers	NH-A	brain
15	chr7:19153000-19154800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr7:19153200-19155800	Active TSS	Adipose Nuclei	Adipose
17	chr7:19153400-19154000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr7:19153400-19154000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
19	chr7:19153400-19154000	Transcr. at gene 5' and 3'	HSMM	muscle
20	chr7:19153400-19155200	Flanking Active TSS	Osteobl	bone
21	chr7:19153600-19153800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:19153600-19154800	Flanking Active TSS	NH-A	brain
23	chr7:19153600-19158600	Active TSS	Right Atrium	heart
24	chr7:19153800-19158000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr7:19154000-19154400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:19154000-19156000	Active TSS	Placenta	Placenta
27	chr7:19154000-19157800	Active TSS	NHLF	lung
28	chr7:19154000-19158000	Active TSS	Muscle Satellite Cultured Cells	--
29	chr7:19154000-19158600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:19154000-19159000	Active TSS	HSMM	muscle
31	chr7:19154200-19154400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:19154200-19158200	Active TSS	Aorta	Aorta
33	chr7:19154400-19154600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr7:19154400-19155400	Active TSS	Fetal Muscle Leg	muscle
35	chr7:19154400-19155400	Active TSS	Fetal Stomach	stomach
36	chr7:19154600-19154800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:19154600-19154800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
38	chr7:19154600-19154800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:19154600-19156000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
40	chr7:19154800-19155000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:19154800-19155000	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:19154800-19155000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
43	chr7:19154800-19155000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr7:19154800-19155000	Bivalent Enhancer	Rectal Smooth Muscle	rectum
45	chr7:19154800-19155200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr7:19154800-19157800	Active TSS	NH-A	brain
47	chr7:19154800-19158200	Active TSS	HSMMtube	muscle
48	chr7:19155000-19155800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:19155000-19157400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr7:19155000-19158400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell

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