Variant report

Variant	nsv1026487
Chromosome Location	chr4:188457879-189060610
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2425)
CpG islands
(count:5067)
Chromatin interactive
region (count:27)
LncRNA
region (count:79)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2425 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

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	chr4:189002649-189002842	K562	blood:	n/a	n/a
3	ATF1	chr4:188538300-188538599	K562	blood:	n/a	n/a
4	ATF1	chr4:188735920-188736251	K562	blood:	n/a	n/a
5	ATF2	chr4:188850148-188850549	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:188917657-188917951	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:188915055-188915396	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:189029405-189029911	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:188916764-188917071	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr4:189028935-189029785	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:188926433-188926974	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:188916749-188917170	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:188953244-188953886	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr4:188527774-188527903	K562	blood:	n/a	n/a
15	ATF3	chr4:189032216-189032636	A549	lung:	n/a	n/a
16	BACH1	chr4:188936288-188936488	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr4:188964645-188964695	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:188952989-188953975	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:188916526-188917174	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr4:188989551-188989709	GM12878	blood:	n/a	n/a
21	BATF	chr4:188896133-188896354	GM12878	blood:	n/a	chr4:188896272-188896283
22	BCL11A	chr4:188953306-188953649	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL3	chr4:189032156-189032852	A549	lung:	n/a	chr4:189032779-189032788 chr4:189032795-189032804
24	BHLHE40	chr4:188538740-188538867	K562	blood:	n/a	n/a
25	BHLHE40	chr4:188534744-188534930	K562	blood:	n/a	n/a
26	BHLHE40	chr4:188923505-188923772	K562	blood:	n/a	n/a
27	BHLHE40	chr4:188533400-188533687	K562	blood:	n/a	n/a
28	BHLHE40	chr4:188527838-188527964	K562	blood:	n/a	n/a
29	BHLHE40	chr4:188929455-188929456	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:189032318-189032600	A549	lung:	n/a	n/a
31	BHLHE40	chr4:188519650-188519830	GM12878	blood:	n/a	n/a
32	BRCA1	chr4:188936021-188936859	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr4:188917816-188917938	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr4:189031951-189032705	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr4:189030619-189031448	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr4:188570315-188570361	GM12878	blood:	n/a	n/a
37	BRCA1	chr4:188909297-188909449	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr4:188923496-188923905	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr4:188660869-188661415	HCT-116	colon:	n/a	n/a
40	CBX3	chr4:188507537-188508612	HCT-116	colon:	n/a	n/a
41	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
42	CBX3	chr4:189032628-189033133	HCT-116	colon:	n/a	n/a
43	CBX3	chr4:189048292-189049092	HCT-116	colon:	n/a	n/a
44	CBX3	chr4:189048248-189049169	HCT-116	colon:	n/a	n/a
45	CEBPB	chr4:188479534-188479869	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:188474103-188474183	K562	blood:	n/a	n/a
47	CEBPB	chr4:188916852-188917179	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:188529058-188529739	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:188873517-188873689	Hela-S3	cervix:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
50	CEBPB	chr4:188929463-188929848	IMR90	lung:	n/a	n/a

(count:5067 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188953969-188954019	HRE	kidney:	n/a
2	chr4:189027935-189027985	HepG2	liver:	n/a
3	chr4:188917251-188917301	Caco-2	colon:	n/a
4	chr4:188916865-188916915	CMK	blood:	n/a
5	chr4:188953969-188954019	HRE	kidney:	n/a
6	chr4:189027935-189027985	HepG2	liver:	n/a
7	chr4:188917251-188917301	Caco-2	colon:	n/a
8	chr4:188916865-188916915	CMK	blood:	n/a
9	chr4:189059677-189059727	SAEC	small airway:	n/a
10	chr4:188916581-188916631	BE2_C	brain:	n/a
11	chr4:188918072-188918122	A549	lung:	n/a
12	chr4:188736112-188736162	HRPEpiC	eye:	n/a
13	chr4:189042690-189042740	HCM	heart:	n/a
14	chr4:188916865-188916915	NH-A	brain:	n/a
15	chr4:188953527-188953577	AG04450	lung:	fetal
16	chr4:188700879-188700929	NT2-D1	testis:	n/a
17	chr4:188916726-188916776	NHDF-neo	bronchial:	n/a
18	chr4:189024495-189024545	HL-60	blood:	n/a
19	chr4:188528319-188528369	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:188916814-188916864	AG09319	gingival:	n/a
21	chr4:188916865-188916915	HL-60	blood:	n/a
22	chr4:188917173-188917223	NH-A	brain:	n/a
23	chr4:188953092-188953142	U87	brain:	n/a
24	chr4:188533158-188533208	AG04449	skin:	fetal
25	chr4:188554583-188554633	HRPEpiC	eye:	n/a
26	chr4:188539183-188539233	K562	blood:	n/a
27	chr4:188895407-188895457	HAEpiC	amniotic membrane:	n/a
28	chr4:189059510-189059560	MCF10A-Er-Src	breast:	n/a
29	chr4:188534912-188534962	Hepatocyte	liver:	n/a
30	chr4:188895407-188895457	SK-N-MC	brain:	n/a
31	chr4:188916726-188916776	PFSK-1	brain:	n/a
32	chr4:188858971-188859021	HCM	heart:	n/a
33	chr4:188916814-188916864	HUVEC	blood vessel:	n/a
34	chr4:188577176-188577226	PANC-1	pancreas:	n/a
35	chr4:189012434-189012484	LNCaP	prostate:	n/a
36	chr4:188916814-188916864	AG04449	skin:	fetal
37	chr4:188533158-188533208	HRCEpiC	kidney:	n/a
38	chr4:188916726-188916776	HIPEpiC	eye:	n/a
39	chr4:189026860-189026910	NT2-D1	testis:	n/a
40	chr4:189026682-189026732	NH-A	brain:	n/a
41	chr4:188462685-188462735	HCF	heart:	n/a
42	chr4:188963260-188963310	CMK	blood:	n/a
43	chr4:189059677-189059727	NB4	blood:	n/a
44	chr4:189028032-189028082	HEEpiC	esophagus:	n/a
45	chr4:188895421-188895471	ovcar-3	ovarian:	n/a
46	chr4:188963260-188963310	HMEC	breast:	n/a
47	chr4:188953092-188953142	Hela-S3	cervix:	n/a
48	chr4:188963260-188963310	SK-N-MC	brain:	n/a
49	chr4:188963260-188963310	Hela-S3	cervix:	n/a
50	chr4:188736112-188736162	HMEC	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188914670..188915671-chr4:189167438..189168869,4	MCF-7	breast:
2	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
3	chr4:189039532..189042082-chr4:189115720..189117330,2	MCF-7	breast:
4	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
5	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
6	chr1:149223042..149224634-chr4:188652998..188654518,2	MCF-7	breast:
7	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
8	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:
9	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
10	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
11	chr4:188807826..188808346-chr6:74078319..74078839,2	MCF-7	breast:
12	chr1:149223872..149224384-chr4:188652498..188652998,2	MCF-7	breast:
13	chr1:149223786..149225310-chr4:188651498..188652998,2	MCF-7	breast:
14	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
15	chr4:188955745..188958212-chr4:188967134..188969834,2	K562	blood:
16	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
17	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:
18	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
19	chr4:188959730..188961356-chr4:188968354..188971076,2	MCF-7	breast:
20	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
21	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
22	chr1:149223776..149224611-chr4:188652518..188653518,3	MCF-7	breast:
23	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
24	chr4:188587219..188588049-chr4:189293834..189294448,2	MCF-7	breast:
25	chr4:188959730..188961356-chr4:188968354..188971076,2	MCF-7	breast:
26	chr4:188955745..188958212-chr4:188967134..188969834,2	K562	blood:
27	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:

(count:79 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAT1-6	chr4:189026861-189027193	NONHSAT099727
2	lnc-ZFP42-2	chr4:188581291-188581337	XLOC_003829
3	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099725
4	lnc-TRIML2-3	chr4:188534640-188534713	XLOC_004221
5	lnc-TRIML2-4	chr4:188513897-188514081	NONHSAT099704
6	lnc-ZFP42-8	chr4:188818285-188818331	l_2822_chr4:188790794-188818331_testes
7	lnc-ZFP42-2	chr4:188626129-188626577	NONHSAT099717
8	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
9	lnc-ZFP42-2	chr4:188571621-188571815	XLOC_003829
10	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099720
11	lnc-ZFP42-2	chr4:188543796-188543894	XLOC_003829
12	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
13	lnc-ZFP42-10	chr4:188493477-188493987	NONHSAT099705
14	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
15	lnc-TRIML2-4	chr4:188567364-188567526	NONHSAT099704
16	lnc-ZFP42-8	chr4:188808721-188808809	l_2822_chr4:188790794-188818331_testes
17	lnc-TRIML2-3	chr4:188534050-188534499	XLOC_004221
18	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
19	lnc-TRIML2-2	chr4:188866788-188867016	XLOC_004222
20	lnc-ZFP42-2	chr4:188581291-188581521	XLOC_003829
21	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
22	lnc-ZFP42-2	chr4:188632898-188633273	NONHSAT099720
23	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
24	lnc-TRIML2-9	chr4:188716229-188716412	l_2820_chr4:188691027-188804581_testes
25	lnc-ZFP42-2	chr4:188534086-188535153	XLOC_003829
26	lnc-ZFP42-1	chr4:188735822-188736272	NONHSAT099722
27	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
28	lnc-ZFP42-2	chr4:188542831-188543333	XLOC_003829
29	lnc-ZFP42-2	chr4:188543796-188543871	XLOC_003829
30	lnc-TRIML2-11	chr4:188535229-188535272	l_2818_chr4:188532414-188535272_placenta
31	lnc-ZFP42-8	chr4:188863112-188863571	l_2822_chr4:188790794-188818331_testes
32	lnc-ZFP42-2	chr4:188581291-188581523	XLOC_003829
33	lnc-ZFP42-2	chr4:188632897-188633241	NONHSAT099717
34	lnc-FAT1-6	chr4:189030397-189030757	NONHSAT099728
35	lnc-TRIML2-4	chr4:188513797-188514081	NONHSAT099706
36	lnc-TRIML2-9	chr4:188771044-188771493	l_2820_chr4:188691027-188804581_testes
37	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722
38	lnc-ZFP42-2	chr4:188534800-188535153	XLOC_003829
39	lnc-ZFP42-2	chr4:188553805-188553988	XLOC_003829
40	lnc-ZFP42-2	chr4:188553703-188553988	XLOC_003829
41	lnc-TRIML2-2	chr4:188908697-188908733	NONHSAT099726
42	lnc-TRIML2-4	chr4:188514038-188514081	ENSG00000250590
43	lnc-FAT1-6	chr4:189026567-189026741	NONHSAT099728
44	lnc-ZFP42-8	chr4:188869892-188870239	l_2822_chr4:188790794-188818331_testes
45	lnc-TRIML2-2	chr4:188881751-188881835	NONHSAT099725
46	lnc-ZFP42-2	chr4:188632898-188633111	NONHSAT099719
47	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
48	lnc-ZFP42-2	chr4:188571727-188571815	XLOC_003829
49	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
50	lnc-ZFP42-2	chr4:188632898-188633228	XLOC_003829

No data

Variant related genes	Relation type
TRIML2	TF binding region
ZFP42	TF binding region
ADAM20P3	TF binding region
ENSG00000213331	TF binding region
TRIML1	TF binding region
RNU6-173P	TF binding region
ENSG00000249642	TF binding region
ENSG00000250590	TF binding region
ENSG00000241011	TF binding region
TRIML2	CpG island
ZFP42	CpG island
ADAM20P3	CpG island
ENSG00000213331	CpG island
TRIML1	CpG island
RNU6-173P	CpG island
ENSG00000249642	CpG island
ENSG00000250590	CpG island
ENSG00000241011	CpG island
ENSG00000206737	chromatin interactions
MCL1	miRNA target sites
KIF13B	miRNA target sites
TAGLN2	miRNA target sites
MED20	miRNA target sites
PHF6	miRNA target sites
CDC42	miRNA target sites
FSCN1	miRNA target sites
NDP	miRNA target sites
KLF12	miRNA target sites
TIMP3	miRNA target sites

Extended variants
information (count: 13301 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:13301 , 50 per page) page: 1 2 3 4 5 6 7 ... 267

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540967038	chr4:188462031-188462032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs557610117	chr4:188462038-188462039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73874398	chr4:188462072-188462073	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs543219167	chr4:188462088-188462089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193194123	chr4:188462111-188462112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116232682	chr4:188462115-188462116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542308236	chr4:188462121-188462122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs74637746	chr4:188462165-188462166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185002109	chr4:188462171-188462172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115570336	chr4:188462252-188462253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190643085	chr4:188462258-188462259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533586633	chr4:188462289-188462290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs550065016	chr4:188462309-188462310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569734737	chr4:188462337-188462338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138981569	chr4:188462449-188462450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377156291	chr4:188462450-188462451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374705422	chr4:188462470-188462471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148975604	chr4:188462477-188462478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143783268	chr4:188462532-188462533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151272069	chr4:188462540-188462541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148104478	chr4:188462561-188462562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534292297	chr4:188462564-188462565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11132465	chr4:188462578-188462579	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs577475937	chr4:188462591-188462592	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146898765	chr4:188462628-188462629	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs536474271	chr4:188462642-188462643	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537255777	chr4:188462646-188462647	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs556925074	chr4:188462685-188462686	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs573772465	chr4:188462761-188462762	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554772064	chr4:188462786-188462787	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs142856175	chr4:188462801-188462802	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181978583	chr4:188462857-188462858	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs112157611	chr4:188462888-188462889	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs374286930	chr4:188462908-188462909	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76117731	chr4:188462910-188462911	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs541401717	chr4:188462913-188462914	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs57928561	chr4:188462918-188462919	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs533411809	chr4:188462921-188462922	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs550445389	chr4:188462922-188462923	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs563769899	chr4:188462931-188462932	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs576268739	chr4:188463010-188463011	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs79342068	chr4:188463020-188463021	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs565403430	chr4:188463103-188463104	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs7666852	chr4:188463111-188463112	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs368360875	chr4:188463183-188463184	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs138807270	chr4:188463211-188463212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558564729	chr4:188463291-188463292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571221593	chr4:188463310-188463311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536987987	chr4:188463330-188463331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557209071	chr4:188463350-188463351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Tetralogy of Fallot	22912587	CNVD
Epilepsy	21635232	CNVD

Chromatin state (count:1685 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188462000-188462600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:188462000-188462800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:188462200-188462600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr4:188462200-188462600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:188462200-188463600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr4:188462400-188462600	Enhancers	HSMM	muscle
7	chr4:188462400-188462600	Enhancers	NHDF-Ad	bronchial
8	chr4:188462400-188462800	Enhancers	HSMMtube	muscle
9	chr4:188462600-188463000	Flanking Active TSS	HSMM	muscle
10	chr4:188462600-188463000	Flanking Active TSS	NHDF-Ad	bronchial
11	chr4:188462600-188463600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:188462800-188463000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:188462800-188463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:188462800-188463200	Flanking Active TSS	HSMMtube	muscle
15	chr4:188462800-188463600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr4:188463000-188463600	Enhancers	HSMM	muscle
17	chr4:188463000-188463600	Enhancers	NHDF-Ad	bronchial
18	chr4:188463200-188463600	Enhancers	HSMMtube	muscle
19	chr4:188463200-188468600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr4:188463600-188465600	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr4:188463600-188465600	Weak transcription	HSMM	muscle
22	chr4:188463600-188465600	Weak transcription	HSMMtube	muscle
23	chr4:188463600-188465800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:188463600-188470600	Weak transcription	NHDF-Ad	bronchial
25	chr4:188465400-188465600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:188465600-188465800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:188465600-188465800	Enhancers	HSMM	muscle
28	chr4:188465600-188466000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:188465600-188466000	Enhancers	HSMMtube	muscle
30	chr4:188465600-188466200	Enhancers	Muscle Satellite Cultured Cells	--
31	chr4:188465600-188466200	Enhancers	HMEC	breast
32	chr4:188465600-188466200	Enhancers	NHEK	skin
33	chr4:188465800-188466200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:188465800-188466200	Weak transcription	HSMM	muscle
35	chr4:188465800-188468600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:188466000-188466200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:188466000-188468400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:188466200-188466400	Enhancers	HSMM	muscle
39	chr4:188466200-188468200	Weak transcription	HMEC	breast
40	chr4:188466200-188468400	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr4:188466200-188471200	Weak transcription	NHEK	skin
42	chr4:188466200-188471400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr4:188466400-188471400	Weak transcription	HSMM	muscle
44	chr4:188466600-188471200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:188467400-188469400	Enhancers	Fetal Kidney	kidney
46	chr4:188468200-188468400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr4:188468200-188469000	Enhancers	HMEC	breast
48	chr4:188468200-188469400	Enhancers	Fetal Lung	lung
49	chr4:188468400-188468800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:188468400-188468800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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