Variant report

Variant	nsv1025896
Chromosome Location	chr5:60190594-60255004
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:757)
CpG islands
(count:977)
Chromatin interactive
region (count:44)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60224933-60225228	K562	blood:	n/a	n/a
2	ARID3A	chr5:60227642-60227690	K562	blood:	n/a	n/a
3	ARID3A	chr5:60240718-60241241	HepG2	liver:	n/a	n/a
4	ATF2	chr5:60240675-60241129	GM12878	blood:	n/a	n/a
5	BACH1	chr5:60241238-60241531	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCLAF1	chr5:60241147-60241621	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:60240872-60241581	K562	blood:	n/a	chr5:60241008-60241024
8	BHLHE40	chr5:60240684-60241301	GM12878	blood:	n/a	chr5:60241008-60241024
9	BHLHE40	chr5:60241820-60242140	K562	blood:	n/a	n/a
10	BRCA1	chr5:60242705-60242764	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr5:60251024-60251519	HCT-116	colon:	n/a	n/a
12	CBX3	chr5:60231541-60231761	K562	blood:	n/a	n/a
13	CBX3	chr5:60240930-60241613	K562	blood:	n/a	n/a
14	CCNT2	chr5:60241747-60241947	K562	blood:	n/a	n/a
15	CCNT2	chr5:60240705-60241024	K562	blood:	n/a	n/a
16	CEBPB	chr5:60249109-60249119	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:60239556-60240203	HepG2	liver:	n/a	chr5:60239733-60239744
18	CEBPB	chr5:60239553-60239813	A549	lung:	n/a	chr5:60239733-60239744
19	CEBPB	chr5:60240711-60242121	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:60239532-60239892	K562	blood:	n/a	chr5:60239733-60239744
21	CEBPB	chr5:60239540-60239884	Hela-S3	cervix:	n/a	chr5:60239733-60239744
22	CEBPB	chr5:60240741-60241412	IMR90	lung:	n/a	n/a
23	CEBPB	chr5:60236700-60237001	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:60240799-60241057	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:60239558-60239890	IMR90	lung:	n/a	chr5:60239733-60239744
26	CEBPB	chr5:60241137-60241281	K562	blood:	n/a	n/a
27	CEBPD	chr5:60240787-60241142	HepG2	liver:	n/a	n/a
28	CHD1	chr5:60241123-60241161	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD1	chr5:60240748-60240773	GM12878	blood:	n/a	n/a
30	CHD2	chr5:60240692-60241371	K562	blood:	n/a	n/a
31	CHD2	chr5:60240662-60241524	GM12878	blood:	n/a	n/a
32	CHD2	chr5:60241056-60241063	HepG2	liver:	n/a	n/a
33	CHD2	chr5:60241795-60241842	GM12878	blood:	n/a	n/a
34	CHD2	chr5:60241804-60241993	K562	blood:	n/a	n/a
35	CHD2	chr5:60240697-60241779	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr5:60240689-60241539	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr5:60241159-60241375	A549	lung:	n/a	n/a
38	CREB1	chr5:60240714-60241128	A549	lung:	n/a	n/a
39	CTCF	chr5:60254980-60255130	HPAF	blood vessel:	n/a	chr5:60255087-60255103 chr5:60255088-60255109 chr5:60255086-60255104
40	CTCF	chr5:60224940-60225090	WI-38	lung:	n/a	n/a
41	CTCF	chr5:60254942-60255213	A549	lung:	n/a	chr5:60255087-60255103 chr5:60255088-60255109 chr5:60255086-60255104
42	CTCF	chr5:60225020-60225170	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr5:60224940-60225090	HUVEC	blood vessel:	n/a	n/a
44	CTCF	chr5:60225000-60225150	HPF	lung:	n/a	n/a
45	CTCF	chr5:60224980-60225130	BJ	skin:	n/a	n/a
46	CTCF	chr5:60224960-60225110	HCFaa	heart:	n/a	n/a
47	CTCF	chr5:60241109-60241118	GM12891	blood:	n/a	n/a
48	CTCF	chr5:60224787-60225309	HCT-116	colon:	n/a	n/a
49	CTCF	chr5:60225000-60225150	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:60224850-60225231	IMR90	lung:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60240838-60240888	HEK293	kidney:	embryo
2	chr5:60240838-60240888	HEK293	kidney:	embryo
3	chr5:60241019-60241069	GM06990	blood:	n/a
4	chr5:60241019-60241069	NHBE	bronchial:	n/a
5	chr5:60240568-60240618	SK-N-SH_RA	brain:	n/a
6	chr5:60240926-60240976	PFSK-1	brain:	n/a
7	chr5:60241424-60241474	SK-N-SH	brain:	n/a
8	chr5:60241003-60241053	LNCaP	prostate:	n/a
9	chr5:60240568-60240618	ovcar-3	ovarian:	n/a
10	chr5:60240952-60241002	GM06990	blood:	n/a
11	chr5:60240952-60241002	U87	brain:	n/a
12	chr5:60240670-60240720	Jurkat	blood:	n/a
13	chr5:60241003-60241053	RPTEC	kidney:	n/a
14	chr5:60240891-60240941	AG09309	skin:	n/a
15	chr5:60240838-60240888	K562	blood:	n/a
16	chr5:60240870-60240920	ProgFib	skin:	n/a
17	chr5:60240870-60240920	PFSK-1	brain:	n/a
18	chr5:60240891-60240941	HEEpiC	esophagus:	n/a
19	chr5:60240926-60240976	ProgFib	skin:	n/a
20	chr5:60241003-60241053	Jurkat	blood:	n/a
21	chr5:60241424-60241474	GM12878	blood:	n/a
22	chr5:60240568-60240618	HMEC	breast:	n/a
23	chr5:60240891-60240941	LNCaP	prostate:	n/a
24	chr5:60240926-60240976	HRE	kidney:	n/a
25	chr5:60239580-60239630	BE2_C	brain:	n/a
26	chr5:60240952-60241002	K562	blood:	n/a
27	chr5:60240870-60240920	A549	lung:	n/a
28	chr5:60240938-60240988	PrEC	prostate:	n/a
29	chr5:60240926-60240976	GM12891	blood:	n/a
30	chr5:60240568-60240618	BJ	skin:	n/a
31	chr5:60241324-60241374	HAEpiC	amniotic membrane:	n/a
32	chr5:60240891-60240941	SK-N-SH_RA	brain:	n/a
33	chr5:60240891-60240941	GM06990	blood:	n/a
34	chr5:60240952-60241002	SK-N-SH	brain:	n/a
35	chr5:60241428-60241478	AG10803	skin:	n/a
36	chr5:60241019-60241069	MCF-7	breast:	n/a
37	chr5:60241424-60241474	BJ	skin:	n/a
38	chr5:60241424-60241474	AG10803	skin:	n/a
39	chr5:60240870-60240920	NHDF-neo	bronchial:	n/a
40	chr5:60240670-60240720	AoSMC	blood vessel:	n/a
41	chr5:60239580-60239630	HEEpiC	esophagus:	n/a
42	chr5:60240952-60241002	H1-hESC	embryonic stem cell:	embryo
43	chr5:60239580-60239630	H1-hESC	embryonic stem cell:	embryo
44	chr5:60240838-60240888	U87	brain:	n/a
45	chr5:60241003-60241053	NT2-D1	testis:	n/a
46	chr5:60241424-60241474	GM12891	blood:	n/a
47	chr5:60241424-60241474	ECC-1	luminal epithelium:	n/a
48	chr5:60240952-60241002	SAEC	small airway:	n/a
49	chr5:60240952-60241002	HUVEC	blood vessel:	n/a
50	chr5:60240891-60240941	HEK293	kidney:	embryo

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
2	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
3	chr5:60254798..60255532-chr5:60954065..60954863,2	K562	blood:
4	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
5	chr5:60238903..60240533-chr5:60255101..60257245,2	K562	blood:
6	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
7	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
8	chr5:60248322..60251287-chr5:60256158..60258205,2	K562	blood:
9	chr5:60231929..60237280-chr5:60239098..60242865,6	MCF-7	breast:
10	chr5:60242359..60244736-chr5:60254537..60257581,3	K562	blood:
11	chr5:60234928..60236588-chr5:60398367..60400919,2	K562	blood:
12	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
13	chr5:60199382..60201400-chr5:60201974..60203709,2	MCF-7	breast:
14	chr5:59973247..59973801-chr5:60224508..60225118,3	K562	blood:
15	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
16	chr5:60238110..60240722-chr5:60956482..60958434,2	MCF-7	breast:
17	chr5:59995886..59998322-chr5:60239584..60242446,2	MCF-7	breast:
18	chr5:10761355..10761920-chr5:60240758..60241387,2	NB4	blood:
19	chr5:59995721..59997582-chr5:60231998..60233519,2	K562	blood:
20	chr5:59995106..59997535-chr5:60240120..60242292,3	K562	blood:
21	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
22	chr5:60239573..60241896-chr5:60245590..60248548,2	K562	blood:
23	chr5:60244730..60246591-chr5:60250985..60252968,2	MCF-7	breast:
24	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:
25	chr5:59973332..59975337-chr5:60224481..60226392,2	MCF-7	breast:
26	chr5:60249583..60251720-chr5:60253693..60255301,2	K562	blood:
27	chr5:60242359..60244736-chr5:60254537..60257581,3	K562	blood:
28	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:
29	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
30	chr5:60248420..60251083-chr5:60253409..60255301,2	K562	blood:
31	chr5:60239789..60242454-chr5:60245834..60249187,6	MCF-7	breast:
32	chr5:60246470..60249444-chr5:60252320..60255288,2	K562	blood:
33	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
34	chr5:60241626..60243235-chr5:60252135..60253778,2	K562	blood:
35	chr5:60232184..60235811-chr5:60236501..60239833,3	K562	blood:
36	chr1:156698013..156698560-chr5:60240745..60241454,2	Hela-S3	cervix:
37	chr5:60234642..60236205-chr5:60241471..60243288,2	MCF-7	breast:
38	chr5:60234534..60237256-chr5:60239004..60241956,3	K562	blood:
39	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
40	chr2:25194755..25195595-chr5:60240745..60241487,2	Hela-S3	cervix:
41	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
42	chr5:60138467..60140103-chr5:60240605..60242461,2	MCF-7	breast:
43	chr5:60221265..60223618-chr5:60225710..60228290,2	MCF-7	breast:
44	chr5:60244987..60247970-chr5:60252320..60254157,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFAF2-1	chr5:60215204-60215400	ENSG00000233847.1
2	lnc-ZSWIM6-4	chr5:60241056-60241209	NONHSAT101655
3	lnc-NDUFAF2-1	chr5:60214122-60214254	ENSG00000233847.1
4	lnc-NDUFAF2-1	chr5:60213317-60213394	ENSG00000233847.1

No data

Variant related genes	Relation type
NDUFAF2	TF binding region
ERCC8	TF binding region
GNL3LP1	TF binding region
ENSG00000233847	TF binding region
NDUFAF2	CpG island
ERCC8	CpG island
GNL3LP1	CpG island
ENSG00000233847	CpG island
ENSG00000164181	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000224165	chromatin interactions
ENSG00000164182	chromatin interactions
ENSG00000112977	chromatin interactions
ENSG00000035499	chromatin interactions
ENSG00000143319	chromatin interactions
ENSG00000115137	chromatin interactions
ENSG00000049167	chromatin interactions
ENSG00000143303	chromatin interactions

Extended variants
information (count: 2307 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2307 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7726671	chr5:60190594-60190595	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529176390	chr5:60190609-60190610	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs549227876	chr5:60190618-60190619	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs573487213	chr5:60190638-60190639	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs540608260	chr5:60190656-60190657	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs565470569	chr5:60190680-60190681	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs567608321	chr5:60190681-60190682	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs538383560	chr5:60190726-60190727	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs558229326	chr5:60190735-60190736	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs117098869	chr5:60190764-60190765	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs200839942	chr5:60190770-60190771	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs534206877	chr5:60190779-60190780	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs553846642	chr5:60190788-60190789	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs375562475	chr5:60190830-60190831	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs574013950	chr5:60190866-60190867	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs532622783	chr5:60190885-60190886	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs1644463	chr5:60190907-60190908	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs1644462	chr5:60190928-60190929	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs542888926	chr5:60190930-60190931	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192626	chr5:60190948-60190949	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs5868257	chr5:60191016-60191017	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188775861	chr5:60191068-60191069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556371267	chr5:60191123-60191124	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190439270	chr5:60191195-60191196	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544263367	chr5:60191200-60191201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78317809	chr5:60191214-60191215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372684577	chr5:60191216-60191217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564219176	chr5:60191266-60191267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369027137	chr5:60191275-60191276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532856522	chr5:60191281-60191282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117415642	chr5:60191330-60191331	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182582204	chr5:60191338-60191339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs562595947	chr5:60191424-60191425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529239440	chr5:60191431-60191432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs549291137	chr5:60191440-60191441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1021005	chr5:60191460-60191461	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs186837413	chr5:60191624-60191625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145033374	chr5:60191638-60191639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571729609	chr5:60191651-60191652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75006130	chr5:60191719-60191720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146821208	chr5:60191745-60191746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569044081	chr5:60191749-60191750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191314637	chr5:60191797-60191798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112804303	chr5:60191804-60191805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527580929	chr5:60191805-60191806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184641277	chr5:60191827-60191828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140432470	chr5:60191834-60191835	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535028536	chr5:60191835-60191836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187581509	chr5:60191843-60191844	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs193279626	chr5:60191876-60191877	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1357 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60167200-60192600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:60167800-60192800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr5:60167800-60228200	Weak transcription	Psoas Muscle	Psoas
4	chr5:60168400-60191000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr5:60169800-60191000	Weak transcription	NH-A	brain
6	chr5:60175800-60239400	Weak transcription	NHEK	skin
7	chr5:60176400-60220400	Weak transcription	Esophagus	oesophagus
8	chr5:60177200-60239600	Weak transcription	HSMMtube	muscle
9	chr5:60177400-60192600	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr5:60177400-60232800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr5:60177600-60213000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:60178000-60214200	Weak transcription	Fetal Kidney	kidney
13	chr5:60179000-60191200	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr5:60179400-60192800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr5:60179800-60190600	Weak transcription	Fetal Lung	lung
16	chr5:60181000-60218800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr5:60181600-60230800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:60181800-60211000	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr5:60182000-60213000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr5:60182200-60192400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr5:60182400-60212200	Weak transcription	NHDF-Ad	bronchial
22	chr5:60182800-60196000	Weak transcription	Brain Anterior Caudate	brain
23	chr5:60183000-60193800	Weak transcription	HMEC	breast
24	chr5:60183400-60213800	Weak transcription	GM12878-XiMat	blood
25	chr5:60183400-60228000	Weak transcription	Small Intestine	intestine
26	chr5:60185200-60195800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr5:60185600-60192600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr5:60185600-60221200	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr5:60186200-60212800	Weak transcription	Placenta	Placenta
30	chr5:60186600-60195400	Weak transcription	NHLF	lung
31	chr5:60187200-60192600	Weak transcription	Duodenum Mucosa	Duodenum
32	chr5:60187400-60212000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr5:60187400-60212600	Weak transcription	HepG2	liver
34	chr5:60187600-60223800	Weak transcription	HUVEC	blood vessel
35	chr5:60187600-60239600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr5:60187800-60191000	Strong transcription	Fetal Stomach	stomach
37	chr5:60187800-60191000	Strong transcription	Left Ventricle	heart
38	chr5:60187800-60193200	Strong transcription	Primary T cells from cord blood	blood
39	chr5:60187800-60195400	Weak transcription	Colon Smooth Muscle	Colon
40	chr5:60187800-60199800	Weak transcription	Brain Cingulate Gyrus	brain
41	chr5:60187800-60239600	Weak transcription	Brain Angular Gyrus	brain
42	chr5:60188000-60191000	Strong transcription	Fetal Muscle Leg	muscle
43	chr5:60188000-60193200	Strong transcription	Fetal Intestine Large	intestine
44	chr5:60188000-60194200	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr5:60188000-60194400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr5:60188000-60200800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr5:60188000-60216200	Weak transcription	Hela-S3	cervix
48	chr5:60188000-60223400	Weak transcription	Primary B cells from peripheral blood	blood
49	chr5:60188200-60190800	Strong transcription	Skeletal Muscle Female	skeletal muscle
50	chr5:60188200-60193400	Strong transcription	Breast Myoepithelial Primary Cells	Breast

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