Variant report

Variant	nsv7507
Chromosome Location	chr10:99031233-99070690
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1139)
CpG islands
(count:919)
Chromatin interactive
region (count:57)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1139 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:99051614-99052821	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:99053811-99054111	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:99052299-99052770	K562	blood:	n/a	n/a
4	ARID3A	chr10:99057363-99057743	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:99057466-99058100	K562	blood:	n/a	n/a
6	ARID3A	chr10:99038222-99039608	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:99068141-99068401	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:99053920-99054039	K562	blood:	n/a	n/a
9	ARID3A	chr10:99038171-99038699	K562	blood:	n/a	n/a
10	ATF1	chr10:99057474-99058065	K562	blood:	n/a	n/a
11	ATF1	chr10:99052266-99052723	K562	blood:	n/a	n/a
12	ATF2	chr10:99052194-99052756	GM12878	blood:	n/a	n/a
13	ATF3	chr10:99039088-99039522	K562	blood:	n/a	n/a
14	ATF3	chr10:99039246-99039441	K562	blood:	n/a	n/a
15	BACH1	chr10:99052348-99052837	K562	blood:	n/a	chr10:99052752-99052766
16	BACH1	chr10:99039478-99039637	K562	blood:	n/a	n/a
17	BACH1	chr10:99051579-99051818	K562	blood:	n/a	n/a
18	BCLAF1	chr10:99052363-99052864	GM12878	blood:	n/a	n/a
19	BCLAF1	chr10:99051689-99052353	GM12878	blood:	n/a	chr10:99052184-99052197 chr10:99052097-99052110
20	BHLHE40	chr10:99051884-99052413	K562	blood:	n/a	n/a
21	BHLHE40	chr10:99057423-99057534	HepG2	liver:	n/a	n/a
22	BHLHE40	chr10:99051944-99052578	HepG2	liver:	n/a	n/a
23	BHLHE40	chr10:99057702-99057972	K562	blood:	n/a	n/a
24	BHLHE40	chr10:99051765-99052726	GM12878	blood:	n/a	n/a
25	BRCA1	chr10:99052170-99052216	HepG2	liver:	n/a	n/a
26	BRCA1	chr10:99038906-99039407	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr10:99051994-99052658	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr10:99051745-99052768	K562	blood:	n/a	n/a
29	CBX3	chr10:99057566-99058055	K562	blood:	n/a	n/a
30	CCNT2	chr10:99051900-99052431	K562	blood:	n/a	n/a
31	CCNT2	chr10:99057509-99058010	K562	blood:	n/a	n/a
32	CEBPB	chr10:99039168-99039528	HepG2	liver:	n/a	chr10:99039305-99039316
33	CEBPB	chr10:99046182-99046360	HepG2	liver:	n/a	chr10:99046299-99046310
34	CEBPB	chr10:99057205-99057918	K562	blood:	n/a	n/a
35	CEBPB	chr10:99039139-99039498	HepG2	liver:	n/a	chr10:99039305-99039316
36	CEBPB	chr10:99051672-99052054	K562	blood:	n/a	n/a
37	CEBPB	chr10:99057269-99057525	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr10:99039133-99039448	H1-hESC	embryonic stem cell:	n/a	chr10:99039305-99039316
39	CEBPB	chr10:99039132-99039525	MCF-7	breast:	n/a	chr10:99039305-99039316
40	CEBPB	chr10:99057249-99057566	MCF-7	breast:	n/a	n/a
41	CEBPB	chr10:99057315-99057445	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:99053204-99053404	K562	blood:	n/a	n/a
43	CEBPB	chr10:99068119-99068533	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:99039120-99039504	HepG2	liver:	n/a	chr10:99039305-99039316
45	CEBPB	chr10:99039156-99039429	ECC-1	luminal epithelium:	n/a	chr10:99039305-99039316
46	CEBPB	chr10:99057237-99057538	HepG2	liver:	n/a	n/a
47	CEBPB	chr10:99051545-99052583	A549	lung:	n/a	n/a
48	CEBPB	chr10:99057230-99057761	A549	lung:	n/a	n/a
49	CEBPB	chr10:99068265-99068420	HepG2	liver:	n/a	n/a
50	CEBPB	chr10:99057027-99057729	A549	lung:	n/a	n/a

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99052489-99052539	NB4	blood:	n/a
2	chr10:99051975-99052025	NHDF-neo	bronchial:	n/a
3	chr10:99052653-99052703	A549	lung:	n/a
4	chr10:99053150-99053200	RPTEC	kidney:	n/a
5	chr10:99052489-99052539	NB4	blood:	n/a
6	chr10:99051975-99052025	NHDF-neo	bronchial:	n/a
7	chr10:99052653-99052703	A549	lung:	n/a
8	chr10:99053150-99053200	RPTEC	kidney:	n/a
9	chr10:99049020-99049070	SK-N-MC	brain:	n/a
10	chr10:99052653-99052703	SK-N-MC	brain:	n/a
11	chr10:99052489-99052539	H1-hESC	embryonic stem cell:	embryo
12	chr10:99052489-99052539	AG09309	skin:	n/a
13	chr10:99049020-99049070	HCM	heart:	n/a
14	chr10:99052468-99052518	IMR90	lung:	fetal
15	chr10:99052472-99052522	AG09309	skin:	n/a
16	chr10:99051975-99052025	NHBE	bronchial:	n/a
17	chr10:99052468-99052518	ProgFib	skin:	n/a
18	chr10:99050413-99050463	NH-A	brain:	n/a
19	chr10:99053150-99053200	ovcar-3	ovarian:	n/a
20	chr10:99052472-99052522	MCF10A-Er-Src	breast:	n/a
21	chr10:99052618-99052668	AG04450	lung:	fetal
22	chr10:99055765-99055815	HCF	heart:	n/a
23	chr10:99053150-99053200	HMEC	breast:	n/a
24	chr10:99052509-99052559	HRCEpiC	kidney:	n/a
25	chr10:99052555-99052605	CMK	blood:	n/a
26	chr10:99050413-99050463	ovcar-3	ovarian:	n/a
27	chr10:99055765-99055815	HEK293	kidney:	embryo
28	chr10:99052472-99052522	HCT-116	colon:	n/a
29	chr10:99052472-99052522	HEK293	kidney:	embryo
30	chr10:99051975-99052025	H1-hESC	embryonic stem cell:	embryo
31	chr10:99052618-99052668	AoSMC	blood vessel:	n/a
32	chr10:99049020-99049070	MCF-7	breast:	n/a
33	chr10:99052555-99052605	A549	lung:	n/a
34	chr10:99052545-99052595	A549	lung:	n/a
35	chr10:99052215-99052265	PrEC	prostate:	n/a
36	chr10:99052468-99052518	HIPEpiC	eye:	n/a
37	chr10:99052215-99052265	SK-N-MC	brain:	n/a
38	chr10:99055765-99055815	Hela-S3	cervix:	n/a
39	chr10:99055765-99055815	AG04450	lung:	fetal
40	chr10:99050413-99050463	SKMC	muscle:	n/a
41	chr10:99052468-99052518	AG10803	skin:	n/a
42	chr10:99052472-99052522	HRPEpiC	eye:	n/a
43	chr10:99052215-99052265	U87	brain:	n/a
44	chr10:99055765-99055815	HPAEpiC	pulmonary alveolar:	n/a
45	chr10:99052555-99052605	NHDF-neo	bronchial:	n/a
46	chr10:99052509-99052559	ProgFib	skin:	n/a
47	chr10:99053150-99053200	SKMC	muscle:	n/a
48	chr10:99052468-99052518	CMK	blood:	n/a
49	chr10:99052509-99052559	HIPEpiC	eye:	n/a
50	chr10:99052545-99052595	CMK	blood:	n/a

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:99051571..99052405-chr19:12273845..12274393,2	Hela-S3	cervix:
2	chr10:99050343..99055587-chr10:99077475..99082102,7	MCF-7	breast:
3	chr10:99038998..99042436-chr10:99050729..99053109,4	K562	blood:
4	chr10:99057981..99059481-chr10:99078317..99080380,2	K562	blood:
5	chr10:99066210..99068899-chr10:99092992..99095167,2	K562	blood:
6	chr10:99044514..99046643-chr10:99048334..99050746,3	K562	blood:
7	chr10:99052215..99054143-chr10:99055411..99058552,4	K562	blood:
8	chr10:99067120..99069373-chr10:99092057..99094640,2	MCF-7	breast:
9	chr10:99029216..99031729-chr10:99037036..99038703,2	K562	blood:
10	chr10:99028447..99031711-chr10:99092744..99094330,3	MCF-7	breast:
11	chr10:99037958..99038944-chr10:99092338..99093941,8	MCF-7	breast:
12	chr10:99048545..99053546-chr10:99092341..99096465,6	K562	blood:
13	chr10:99049975..99053832-chr10:99093402..99096465,5	K562	blood:
14	chr10:99040683..99043669-chr10:99044105..99045670,2	MCF-7	breast:
15	chr10:99051590..99052388-chr10:101380641..101381344,2	Hela-S3	cervix:
16	chr10:99043100..99045603-chr10:99092696..99094572,2	MCF-7	breast:
17	chr10:99065771..99067454-chr10:99080586..99083013,2	MCF-7	breast:
18	chr10:99036931..99039171-chr10:99085750..99087329,2	K562	blood:
19	chr10:99040697..99043641-chr10:99044330..99048505,4	K562	blood:
20	chr10:99051532..99052217-chr11:65270337..65271200,2	Hela-S3	cervix:
21	chr10:99066273..99068879-chr10:99069326..99071417,2	K562	blood:
22	chr10:99038038..99038854-chr10:99093284..99094248,2	K562	blood:
23	chr10:99036915..99039794-chr10:99077195..99080138,2	MCF-7	breast:
24	chr10:99050239..99051953-chr10:99089208..99091250,2	K562	blood:
25	chr10:99051546..99052354-chr2:55843946..55844595,2	Hela-S3	cervix:
26	chr10:99055451..99057876-chr10:99084798..99087346,2	MCF-7	breast:
27	chr10:99052064..99052648-chr10:99078773..99079491,2	NB4	blood:
28	chr10:99052531..99053031-chr12:32259435..32260354,2	Hela-S3	cervix:
29	chr10:99052581..99054143-chr10:99054832..99057681,2	K562	blood:
30	chr10:99066690..99071389-chr10:99076606..99080814,5	MCF-7	breast:
31	chr10:99051705..99053713-chr10:99056526..99058710,2	MCF-7	breast:
32	chr10:99065882..99067668-chr10:99093705..99096433,2	MCF-7	breast:
33	chr10:99063544..99065067-chr10:99093063..99094830,2	K562	blood:
34	chr10:99051582..99054067-chr10:99077169..99079188,3	K562	blood:
35	chr10:99059557..99062005-chr10:99076805..99079632,3	K562	blood:
36	chr10:99051058..99054984-chr10:99078319..99082092,7	MCF-7	breast:
37	chr10:99051045..99053385-chr10:99092824..99094336,2	MCF-7	breast:
38	chr10:99050912..99053751-chr10:99091766..99095025,5	MCF-7	breast:
39	chr10:99040697..99043641-chr10:99044330..99048505,4	K562	blood:
40	chr10:99067399..99070806-chr10:99092978..99095924,3	K562	blood:
41	chr10:99051582..99055310-chr10:99077169..99083058,6	K562	blood:
42	chr10:99040683..99043669-chr10:99044105..99045670,2	MCF-7	breast:
43	chr10:99034381..99036020-chr10:99036062..99037985,2	K562	blood:
44	chr10:99069668..99072343-chr10:99094033..99096294,2	MCF-7	breast:
45	chr10:99052282..99052884-chr5:41870193..41871067,2	Hela-S3	cervix:
46	chr10:99050735..99053520-chr16:284621..286236,2	MCF-7	breast:
47	chr10:99052581..99054143-chr10:99054832..99057681,2	K562	blood:
48	chr10:99051863..99052445-chr4:76439211..76440158,2	HCT-116	colon:
49	chr10:99031855..99035094-chr10:99036519..99039061,3	K562	blood:
50	chr10:99044514..99046643-chr10:99048334..99050746,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRAT1-3	chr10:99037705-99037854	NONHSAT015852
2	lnc-FRAT1-3	chr10:99037396-99037514	NONHSAT015852
3	lnc-FRAT1-3	chr10:99034769-99034864	NONHSAT015852

No data

Variant related genes	Relation type
ARHGAP19	TF binding region
ENSG00000231398	TF binding region
ARHGAP19-SLIT1	TF binding region
ENSG00000237169	TF binding region
ARHGAP19	CpG island
ENSG00000231398	CpG island
ARHGAP19-SLIT1	CpG island
ENSG00000237169	CpG island
ENSG00000163743	chromatin interactions
ENSG00000167930	chromatin interactions
ENSG00000231398	chromatin interactions
ENSG00000196646	chromatin interactions
ENSG00000174796	chromatin interactions
ENSG00000151746	chromatin interactions
ENSG00000213390	chromatin interactions
ENSG00000248668	chromatin interactions
ENSG00000165879	chromatin interactions
ENSG00000083720	chromatin interactions
ENSG00000225850	chromatin interactions
ENSG00000269891	chromatin interactions
ENSG00000181274	chromatin interactions
ENSG00000237169	chromatin interactions
ENSG00000260475	chromatin interactions

Extended variants
information (count: 1516 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1516 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144065464	chr10:99031285-99031286	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541861593	chr10:99031295-99031296	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs181116296	chr10:99031299-99031300	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs146452611	chr10:99031322-99031323	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556802107	chr10:99031343-99031344	Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575050876	chr10:99031579-99031580	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555176494	chr10:99031582-99031583	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185560937	chr10:99031584-99031585	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190902699	chr10:99031587-99031588	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140678534	chr10:99031631-99031632	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs10736115	chr10:99031685-99031686	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs539838219	chr10:99031720-99031721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369055524	chr10:99031747-99031748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576534507	chr10:99031819-99031820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs11591420	chr10:99031860-99031861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200174816	chr10:99031888-99031889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs35980234	chr10:99031889-99031890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs74860616	chr10:99031907-99031908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12241049	chr10:99031913-99031914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543865803	chr10:99031923-99031924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145776927	chr10:99031950-99031951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562359688	chr10:99031955-99031956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs151080158	chr10:99031981-99031982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548495048	chr10:99032018-99032019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141108123	chr10:99032092-99032093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540427260	chr10:99032138-99032139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527729052	chr10:99032139-99032140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182615081	chr10:99032169-99032170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76774207	chr10:99032171-99032172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560345330	chr10:99032187-99032188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550269204	chr10:99032210-99032211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376529152	chr10:99032266-99032267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188878310	chr10:99032272-99032273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569037527	chr10:99032313-99032314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554491047	chr10:99032314-99032315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs572647400	chr10:99032332-99032333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540080380	chr10:99032358-99032359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs793520	chr10:99032375-99032376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs150258249	chr10:99032413-99032414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543925943	chr10:99032425-99032426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546197601	chr10:99032452-99032453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11593754	chr10:99032473-99032474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552320096	chr10:99032577-99032578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7093375	chr10:99032589-99032590	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs201846508	chr10:99032592-99032593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574612259	chr10:99032639-99032640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371127179	chr10:99032667-99032668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191960841	chr10:99032674-99032675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527598354	chr10:99032723-99032724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546042707	chr10:99032746-99032747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Ependymoma	20639864	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98978600-99037400	Weak transcription	HSMM	muscle
2	chr10:98978600-99051800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:98983000-99037600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr10:98984600-99037600	Weak transcription	Brain Hippocampus Middle	brain
5	chr10:98987200-99051200	Weak transcription	Pancreas	Pancrea
6	chr10:98989000-99034600	Weak transcription	Aorta	Aorta
7	chr10:98989600-99038000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr10:98990000-99034600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr10:98994600-99039000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr10:99004800-99037400	Weak transcription	Fetal Heart	heart
11	chr10:99005200-99046800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr10:99013200-99037600	Weak transcription	NHLF	lung
13	chr10:99015000-99038000	Weak transcription	Fetal Brain Male	brain
14	chr10:99015400-99038200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr10:99016000-99038600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr10:99016200-99038200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:99016800-99038600	Weak transcription	HUVEC	blood vessel
18	chr10:99019200-99034600	Weak transcription	Liver	Liver
19	chr10:99019400-99038200	Weak transcription	K562	blood
20	chr10:99019400-99050000	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr10:99019400-99051600	Weak transcription	Ovary	ovary
22	chr10:99021400-99051000	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr10:99023600-99051200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr10:99024000-99034400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr10:99024000-99046800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr10:99024000-99050800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr10:99024400-99050000	Weak transcription	Spleen	Spleen
28	chr10:99024800-99034600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr10:99024800-99051200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr10:99025600-99034600	Weak transcription	Primary B cells from peripheral blood	blood
31	chr10:99025800-99037200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr10:99025800-99037400	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr10:99025800-99038000	Weak transcription	Fetal Stomach	stomach
34	chr10:99025800-99039200	Weak transcription	Fetal Muscle Trunk	muscle
35	chr10:99025800-99039200	Weak transcription	Fetal Muscle Leg	muscle
36	chr10:99025800-99050800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr10:99026000-99037400	Weak transcription	Dnd41	blood
38	chr10:99026000-99037400	Weak transcription	GM12878-XiMat	blood
39	chr10:99026000-99038600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr10:99026000-99051200	Weak transcription	Primary T cells from cord blood	blood
41	chr10:99026200-99037400	Weak transcription	Primary B cells from cord blood	blood
42	chr10:99026200-99037400	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr10:99027600-99046200	Weak transcription	Thymus	Thymus
44	chr10:99027800-99045600	Weak transcription	Fetal Thymus	thymus
45	chr10:99028400-99038200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr10:99028600-99051200	Weak transcription	Small Intestine	intestine
47	chr10:99028800-99046800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr10:99029200-99033200	Weak transcription	Fetal Intestine Small	intestine
49	chr10:99029400-99037800	Weak transcription	Duodenum Mucosa	Duodenum
50	chr10:99029600-99031400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell

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