Variant report

Variant	nsv1027962
Chromosome Location	chr4:188463111-188874675
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1273)
CpG islands
(count:1649)
Chromatin interactive
region (count:13)
LncRNA
region (count:68)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:188527707-188527965	HepG2	liver:	n/a	n/a
2	ATF1	chr4:188538300-188538599	K562	blood:	n/a	n/a
3	ATF1	chr4:188735920-188736251	K562	blood:	n/a	n/a
4	ATF2	chr4:188850148-188850549	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:188527774-188527903	K562	blood:	n/a	n/a
6	BHLHE40	chr4:188519650-188519830	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:188527838-188527964	K562	blood:	n/a	n/a
8	BHLHE40	chr4:188533400-188533687	K562	blood:	n/a	n/a
9	BHLHE40	chr4:188534744-188534930	K562	blood:	n/a	n/a
10	BHLHE40	chr4:188538740-188538867	K562	blood:	n/a	n/a
11	BRCA1	chr4:188570315-188570361	GM12878	blood:	n/a	n/a
12	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:188507537-188508612	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:188660869-188661415	HCT-116	colon:	n/a	n/a
15	CEBPB	chr4:188735860-188736134	MCF-7	breast:	n/a	n/a
16	CEBPB	chr4:188610953-188611148	IMR90	lung:	n/a	chr4:188610998-188611011
17	CEBPB	chr4:188538269-188538668	IMR90	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
18	CEBPB	chr4:188474103-188474183	K562	blood:	n/a	n/a
19	CEBPB	chr4:188600607-188601013	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:188600657-188600937	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:188728733-188729010	IMR90	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
22	CEBPB	chr4:188578082-188578310	HepG2	liver:	n/a	chr4:188578218-188578229
23	CEBPB	chr4:188769070-188769319	IMR90	lung:	n/a	chr4:188769178-188769189
24	CEBPB	chr4:188735851-188736097	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:188538310-188538620	H1-hESC	embryonic stem cell:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
26	CEBPB	chr4:188608874-188609254	IMR90	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
27	CEBPB	chr4:188524161-188524444	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:188621538-188621620	HepG2	liver:	n/a	chr4:188621582-188621599 chr4:188621587-188621598
29	CEBPB	chr4:188509334-188509409	HepG2	liver:	n/a	chr4:188509373-188509384
30	CEBPB	chr4:188569034-188569253	A549	lung:	n/a	chr4:188569144-188569155
31	CEBPB	chr4:188569010-188569242	IMR90	lung:	n/a	chr4:188569144-188569155
32	CEBPB	chr4:188608959-188609177	K562	blood:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
33	CEBPB	chr4:188608892-188609208	H1-hESC	embryonic stem cell:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
34	CEBPB	chr4:188538314-188538633	A549	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
35	CEBPB	chr4:188735766-188736151	K562	blood:	n/a	n/a
36	CEBPB	chr4:188735771-188736121	A549	lung:	n/a	n/a
37	CEBPB	chr4:188570725-188570925	K562	blood:	n/a	chr4:188570868-188570879
38	CEBPB	chr4:188529058-188529739	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:188632802-188633082	A549	lung:	n/a	chr4:188632937-188632948
40	CEBPB	chr4:188520953-188521275	IMR90	lung:	n/a	chr4:188521110-188521121
41	CEBPB	chr4:188769115-188769241	A549	lung:	n/a	chr4:188769178-188769189
42	CEBPB	chr4:188632817-188633098	Hela-S3	cervix:	n/a	chr4:188632937-188632948
43	CEBPB	chr4:188570719-188571283	HepG2	liver:	n/a	chr4:188570868-188570879
44	CEBPB	chr4:188569020-188569256	HepG2	liver:	n/a	chr4:188569144-188569155
45	CEBPB	chr4:188728777-188728937	A549	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
46	CEBPB	chr4:188538148-188538851	HCT-116	colon:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
47	CEBPB	chr4:188735766-188736145	IMR90	lung:	n/a	n/a
48	CEBPB	chr4:188608883-188609243	HepG2	liver:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
49	CEBPB	chr4:188608897-188609217	Hela-S3	cervix:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
50	CEBPB	chr4:188529114-188529530	Hela-S3	cervix:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188686763-188686813	GM19239	blood:	n/a
2	chr4:188736172-188736222	Jurkat	blood:	n/a
3	chr4:188686763-188686813	GM19239	blood:	n/a
4	chr4:188736172-188736222	Jurkat	blood:	n/a
5	chr4:188534873-188534923	PANC-1	pancreas:	n/a
6	chr4:188539183-188539233	HCM	heart:	n/a
7	chr4:188700879-188700929	PANC-1	pancreas:	n/a
8	chr4:188686664-188686714	HCF	heart:	n/a
9	chr4:188577176-188577226	AG04449	skin:	fetal
10	chr4:188534873-188534923	HAEpiC	amniotic membrane:	n/a
11	chr4:188577176-188577226	SK-N-SH	brain:	n/a
12	chr4:188686726-188686776	ProgFib	skin:	n/a
13	chr4:188533158-188533208	GM12892	blood:	n/a
14	chr4:188534912-188534962	AG04450	lung:	fetal
15	chr4:188534776-188534826	NB4	blood:	n/a
16	chr4:188534448-188534498	HepG2	liver:	n/a
17	chr4:188534448-188534498	HEEpiC	esophagus:	n/a
18	chr4:188700879-188700929	HL-60	blood:	n/a
19	chr4:188533158-188533208	MCF-7	breast:	n/a
20	chr4:188588839-188588889	AoSMC	blood vessel:	n/a
21	chr4:188686726-188686776	HAEpiC	amniotic membrane:	n/a
22	chr4:188736336-188736386	GM12878	blood:	n/a
23	chr4:188824073-188824123	NT2-D1	testis:	n/a
24	chr4:188736112-188736162	GM06990	blood:	n/a
25	chr4:188858971-188859021	SAEC	small airway:	n/a
26	chr4:188843522-188843572	RPTEC	kidney:	n/a
27	chr4:188534912-188534962	AG09319	gingival:	n/a
28	chr4:188736172-188736222	NT2-D1	testis:	n/a
29	chr4:188588839-188588889	PrEC	prostate:	n/a
30	chr4:188686726-188686776	SAEC	small airway:	n/a
31	chr4:188534912-188534962	HCM	heart:	n/a
32	chr4:188533158-188533208	HCM	heart:	n/a
33	chr4:188858709-188858759	HAEpiC	amniotic membrane:	n/a
34	chr4:188858971-188859021	NB4	blood:	n/a
35	chr4:188588839-188588889	AG09319	gingival:	n/a
36	chr4:188534873-188534923	AG09319	gingival:	n/a
37	chr4:188538807-188538857	H1-hESC	embryonic stem cell:	embryo
38	chr4:188736112-188736162	SAEC	small airway:	n/a
39	chr4:188530842-188530892	NH-A	brain:	n/a
40	chr4:188533158-188533208	SK-N-SH_RA	brain:	n/a
41	chr4:188539183-188539233	Caco-2	colon:	n/a
42	chr4:188530842-188530892	HRPEpiC	eye:	n/a
43	chr4:188858971-188859021	HRPEpiC	eye:	n/a
44	chr4:188577176-188577226	AG10803	skin:	n/a
45	chr4:188736172-188736222	NH-A	brain:	n/a
46	chr4:188700879-188700929	HCT-116	colon:	n/a
47	chr4:188700879-188700929	NB4	blood:	n/a
48	chr4:188736172-188736222	NHDF-neo	bronchial:	n/a
49	chr4:188736336-188736386	AoSMC	blood vessel:	n/a
50	chr4:188736336-188736386	ECC-1	luminal epithelium:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
2	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
3	chr4:188587219..188588049-chr4:189293834..189294448,2	MCF-7	breast:
4	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
5	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:
6	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
7	chr1:149223042..149224634-chr4:188652998..188654518,2	MCF-7	breast:
8	chr1:149223776..149224611-chr4:188652518..188653518,3	MCF-7	breast:
9	chr1:149223872..149224384-chr4:188652498..188652998,2	MCF-7	breast:
10	chr4:188807826..188808346-chr6:74078319..74078839,2	MCF-7	breast:
11	chr1:149223786..149225310-chr4:188651498..188652998,2	MCF-7	breast:
12	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
13	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:

(count:68 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-2	chr4:188626502-188626577	XLOC_003829
2	lnc-ZFP42-2	chr4:188626129-188626577	NONHSAT099717
3	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
4	lnc-TRIML2-4	chr4:188567364-188567526	NONHSAT099706
5	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
6	lnc-TRIML2-4	chr4:188567364-188567526	NONHSAT099704
7	lnc-ZFP42-2	chr4:188571727-188571815	XLOC_003829
8	lnc-TRIML2-11	chr4:188532415-188533775	l_2818_chr4:188532414-188535272_placenta
9	lnc-TRIML2-4	chr4:188586916-188586992	NR_110436
10	lnc-TRIML2-9	chr4:188804358-188804581	l_2820_chr4:188691027-188804581_testes
11	lnc-TRIML2-11	chr4:188535229-188535272	l_2818_chr4:188532414-188535272_placenta
12	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
13	lnc-TRIML2-4	chr4:188513897-188514081	NONHSAT099704
14	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099719
15	lnc-ZFP42-2	chr4:188632898-188633111	NONHSAT099719
16	lnc-ZFP42-2	chr4:188543796-188543894	XLOC_003829
17	lnc-TRIML2-3	chr4:188534640-188534713	XLOC_004221
18	lnc-ZFP42-2	chr4:188553805-188553988	XLOC_003829
19	lnc-TRIML2-4	chr4:188593716-188593795	NR_110436
20	lnc-ZFP42-9	chr4:188779825-188780051	l_2821_chr4:188771633-188780051_testes
21	lnc-ZFP42-8	chr4:188863112-188863571	l_2822_chr4:188790794-188818331_testes
22	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
23	lnc-ZFP42-1	chr4:188735822-188736272	NONHSAT099722
24	lnc-ZFP42-2	chr4:188581291-188581523	XLOC_003829
25	lnc-ZFP42-8	chr4:188808721-188808809	l_2822_chr4:188790794-188818331_testes
26	lnc-ZFP42-2	chr4:188635490-188635540	NONHSAT099719
27	lnc-TRIML2-9	chr4:188771044-188771493	l_2820_chr4:188691027-188804581_testes
28	lnc-TRIML2-4	chr4:188503575-188503684	ENSG00000250590
29	lnc-TRIML2-2	chr4:188866817-188867016	NONHSAT099725
30	lnc-ZFP42-2	chr4:188554100-188554300	XLOC_003829
31	lnc-TRIML2-4	chr4:188513797-188514081	NONHSAT099706
32	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
33	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
34	lnc-TRIML2-4	chr4:188586916-188586992	ENSG00000250590
35	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
36	lnc-ZFP42-1	chr4:188735823-188736246	XLOC_003831
37	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
38	lnc-ZFP42-2	chr4:188534919-188535153	XLOC_003829
39	lnc-ZFP42-2	chr4:188534800-188535153	XLOC_003829
40	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722
41	lnc-TRIML2-9	chr4:188771634-188772347	l_2820_chr4:188691027-188804581_testes
42	lnc-ZFP42-2	chr4:188553703-188553988	XLOC_003829
43	lnc-TRIML2-3	chr4:188534050-188534499	XLOC_004221
44	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
45	lnc-TRIML2-4	chr4:188514038-188514081	ENSG00000250590
46	lnc-TRIML2-2	chr4:188866788-188867016	XLOC_004222
47	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
48	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
49	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
50	lnc-ZFP42-2	chr4:188543796-188543871	XLOC_003829

No data

Variant related genes	Relation type
ADAM20P3	TF binding region
ENSG00000249642	TF binding region
ENSG00000250590	TF binding region
ADAM20P3	CpG island
ENSG00000249642	CpG island
ENSG00000250590	CpG island
ENSG00000206737	chromatin interactions
FSCN1	miRNA target sites
KLF12	miRNA target sites
MED20	miRNA target sites
TAGLN2	miRNA target sites
NDP	miRNA target sites
KIF13B	miRNA target sites
TIMP3	miRNA target sites
CDC42	miRNA target sites
MCL1	miRNA target sites
PHF6	miRNA target sites

Extended variants
information (count: 6465 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:6465 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7666852	chr4:188463111-188463112	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs368360875	chr4:188463183-188463184	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs138807270	chr4:188463211-188463212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558564729	chr4:188463291-188463292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571221593	chr4:188463310-188463311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536987987	chr4:188463330-188463331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs557209071	chr4:188463350-188463351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369404990	chr4:188463374-188463375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573784998	chr4:188463425-188463426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs371651021	chr4:188463451-188463452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs28488057	chr4:188463511-188463512	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs529063962	chr4:188463513-188463514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375230327	chr4:188463514-188463515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555910190	chr4:188463516-188463517	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577201267	chr4:188463540-188463541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141992187	chr4:188463623-188463624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572530821	chr4:188463628-188463629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150791848	chr4:188463640-188463641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs541003979	chr4:188463650-188463651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564517115	chr4:188463652-188463653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs577961425	chr4:188463666-188463667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139217440	chr4:188463694-188463695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563981263	chr4:188463704-188463705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529480101	chr4:188463714-188463715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542774232	chr4:188463739-188463740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559026536	chr4:188463779-188463780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149921408	chr4:188463780-188463781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112242032	chr4:188463806-188463807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551053755	chr4:188463811-188463812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77939007	chr4:188463851-188463852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571192567	chr4:188463867-188463868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62800560	chr4:188463870-188463871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs397709732	chr4:188463873-188463874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550620650	chr4:188463876-188463877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567514116	chr4:188463877-188463878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144058567	chr4:188463951-188463952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs553154902	chr4:188464026-188464027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140354983	chr4:188464093-188464094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535163115	chr4:188464140-188464141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546316825	chr4:188464151-188464152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144317988	chr4:188464169-188464170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563855461	chr4:188464182-188464183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531006072	chr4:188464189-188464190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543766283	chr4:188464208-188464209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28419401	chr4:188464210-188464211	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs371181122	chr4:188464236-188464237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574229209	chr4:188464251-188464252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115630181	chr4:188464275-188464276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112147852	chr4:188464309-188464310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528648764	chr4:188464402-188464403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Autism	20808228	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188462200-188463600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr4:188462600-188463600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr4:188462800-188463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:188462800-188463200	Flanking Active TSS	HSMMtube	muscle
5	chr4:188462800-188463600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:188463000-188463600	Enhancers	HSMM	muscle
7	chr4:188463000-188463600	Enhancers	NHDF-Ad	bronchial
8	chr4:188463200-188463600	Enhancers	HSMMtube	muscle
9	chr4:188463200-188468600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr4:188463600-188465600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr4:188463600-188465600	Weak transcription	HSMM	muscle
12	chr4:188463600-188465600	Weak transcription	HSMMtube	muscle
13	chr4:188463600-188465800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:188463600-188470600	Weak transcription	NHDF-Ad	bronchial
15	chr4:188465400-188465600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:188465600-188465800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:188465600-188465800	Enhancers	HSMM	muscle
18	chr4:188465600-188466000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:188465600-188466000	Enhancers	HSMMtube	muscle
20	chr4:188465600-188466200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr4:188465600-188466200	Enhancers	HMEC	breast
22	chr4:188465600-188466200	Enhancers	NHEK	skin
23	chr4:188465800-188466200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:188465800-188466200	Weak transcription	HSMM	muscle
25	chr4:188465800-188468600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:188466000-188466200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:188466000-188468400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr4:188466200-188466400	Enhancers	HSMM	muscle
29	chr4:188466200-188468200	Weak transcription	HMEC	breast
30	chr4:188466200-188468400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr4:188466200-188471200	Weak transcription	NHEK	skin
32	chr4:188466200-188471400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:188466400-188471400	Weak transcription	HSMM	muscle
34	chr4:188466600-188471200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:188467400-188469400	Enhancers	Fetal Kidney	kidney
36	chr4:188468200-188468400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:188468200-188469000	Enhancers	HMEC	breast
38	chr4:188468200-188469400	Enhancers	Fetal Lung	lung
39	chr4:188468400-188468800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:188468400-188468800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:188468400-188469000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:188468400-188469200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr4:188468400-188469400	Enhancers	Osteobl	bone
44	chr4:188468600-188468800	Enhancers	Adipose Nuclei	Adipose
45	chr4:188468600-188469000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:188468600-188469000	Active TSS	Fetal Muscle Leg	muscle
47	chr4:188468600-188469200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr4:188468600-188469400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:188468800-188469000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:188468800-188471200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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