Variant report

Variant	nsv1024695
Chromosome Location	chr4:188483183-188856843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1209)
CpG islands
(count:1526)
Chromatin interactive
region (count:11)
LncRNA
region (count:57)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr4:188735920-188736251	K562	blood:	n/a	n/a
3	ATF1	chr4:188538300-188538599	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	chr4:188534744-188534930	K562	blood:	n/a	n/a
8	BHLHE40	chr4:188538740-188538867	K562	blood:	n/a	n/a
9	BHLHE40	chr4:188533400-188533687	K562	blood:	n/a	n/a
10	BHLHE40	chr4:188527838-188527964	K562	blood:	n/a	n/a
11	BRCA1	chr4:188570315-188570361	GM12878	blood:	n/a	n/a
12	CBX3	chr4:188660869-188661415	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:188507537-188508612	HCT-116	colon:	n/a	n/a
15	CEBPB	chr4:188735851-188736097	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:188632768-188633111	IMR90	lung:	n/a	chr4:188632937-188632948
17	CEBPB	chr4:188608828-188609265	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
18	CEBPB	chr4:188608897-188609217	Hela-S3	cervix:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
19	CEBPB	chr4:188520953-188521275	IMR90	lung:	n/a	chr4:188521110-188521121
20	CEBPB	chr4:188538269-188538668	IMR90	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
21	CEBPB	chr4:188735766-188736151	K562	blood:	n/a	n/a
22	CEBPB	chr4:188529114-188529530	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:188735860-188736134	MCF-7	breast:	n/a	n/a
24	CEBPB	chr4:188540170-188540484	A549	lung:	n/a	n/a
25	CEBPB	chr4:188632817-188633098	Hela-S3	cervix:	n/a	chr4:188632937-188632948
26	CEBPB	chr4:188538314-188538633	A549	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
27	CEBPB	chr4:188608874-188609254	IMR90	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
28	CEBPB	chr4:188829199-188829608	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:188538086-188538843	HCT-116	colon:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
30	CEBPB	chr4:188570695-188571039	A549	lung:	n/a	chr4:188570868-188570879
31	CEBPB	chr4:188591052-188591273	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:188728718-188728984	HepG2	liver:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
33	CEBPB	chr4:188632761-188633106	HepG2	liver:	n/a	chr4:188632937-188632948
34	CEBPB	chr4:188572787-188573018	HepG2	liver:	n/a	chr4:188572900-188572911
35	CEBPB	chr4:188569034-188569253	A549	lung:	n/a	chr4:188569144-188569155
36	CEBPB	chr4:188610953-188611148	IMR90	lung:	n/a	chr4:188610998-188611011
37	CEBPB	chr4:188735841-188736022	K562	blood:	n/a	n/a
38	CEBPB	chr4:188504954-188505154	HepG2	liver:	n/a	chr4:188504994-188505011
39	CEBPB	chr4:188538301-188538611	HepG2	liver:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
40	CEBPB	chr4:188728733-188729010	IMR90	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
41	CEBPB	chr4:188728777-188728937	A549	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
42	CEBPB	chr4:188570725-188570925	K562	blood:	n/a	chr4:188570868-188570879
43	CEBPB	chr4:188608883-188609243	HepG2	liver:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
44	CEBPB	chr4:188540074-188540575	A549	lung:	n/a	n/a
45	CEBPB	chr4:188552483-188552484	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:188769070-188769319	IMR90	lung:	n/a	chr4:188769178-188769189
47	CEBPB	chr4:188517628-188517892	HepG2	liver:	n/a	chr4:188517748-188517759
48	CEBPB	chr4:188539805-188540519	IMR90	lung:	n/a	n/a
49	CEBPB	chr4:188570202-188570305	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:188690722-188690811	A549	lung:	n/a	chr4:188690750-188690761

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188829287-188829337	HUVEC	blood vessel:	n/a
2	chr4:188829287-188829337	HUVEC	blood vessel:	n/a
3	chr4:188854221-188854271	PFSK-1	brain:	n/a
4	chr4:188736172-188736222	Hela-S3	cervix:	n/a
5	chr4:188530842-188530892	AG09309	skin:	n/a
6	chr4:188829287-188829337	HEK293	kidney:	embryo
7	chr4:188534509-188534559	ECC-1	luminal epithelium:	n/a
8	chr4:188534448-188534498	HAEpiC	amniotic membrane:	n/a
9	chr4:188533158-188533208	GM06990	blood:	n/a
10	chr4:188539183-188539233	HCM	heart:	n/a
11	chr4:188736172-188736222	HRE	kidney:	n/a
12	chr4:188843522-188843572	HRE	kidney:	n/a
13	chr4:188539183-188539233	GM12892	blood:	n/a
14	chr4:188534776-188534826	T-47D	breast:	n/a
15	chr4:188686726-188686776	AG10803	skin:	n/a
16	chr4:188528319-188528369	HCT-116	colon:	n/a
17	chr4:188843522-188843572	LNCaP	prostate:	n/a
18	chr4:188530842-188530892	Hepatocyte	liver:	n/a
19	chr4:188686763-188686813	HEK293	kidney:	embryo
20	chr4:188686763-188686813	AG04449	skin:	fetal
21	chr4:188538807-188538857	GM12891	blood:	n/a
22	chr4:188533158-188533208	SK-N-MC	brain:	n/a
23	chr4:188534873-188534923	ECC-1	luminal epithelium:	n/a
24	chr4:188824073-188824123	GM19239	blood:	n/a
25	chr4:188534912-188534962	BE2_C	brain:	n/a
26	chr4:188533158-188533208	HRPEpiC	eye:	n/a
27	chr4:188538807-188538857	GM19239	blood:	n/a
28	chr4:188577176-188577226	ECC-1	luminal epithelium:	n/a
29	chr4:188686664-188686714	BE2_C	brain:	n/a
30	chr4:188736112-188736162	H1-hESC	embryonic stem cell:	embryo
31	chr4:188533158-188533208	HNPCEpiC	eye:	n/a
32	chr4:188588839-188588889	Caco-2	colon:	n/a
33	chr4:188854221-188854271	Hela-S3	cervix:	n/a
34	chr4:188854221-188854271	HCT-116	colon:	n/a
35	chr4:188534873-188534923	Hepatocyte	liver:	n/a
36	chr4:188530842-188530892	CMK	blood:	n/a
37	chr4:188534776-188534826	LNCaP	prostate:	n/a
38	chr4:188686726-188686776	SAEC	small airway:	n/a
39	chr4:188588839-188588889	AG04449	skin:	fetal
40	chr4:188686763-188686813	GM12892	blood:	n/a
41	chr4:188530842-188530892	Jurkat	blood:	n/a
42	chr4:188533158-188533208	MCF-7	breast:	n/a
43	chr4:188824073-188824123	ECC-1	luminal epithelium:	n/a
44	chr4:188686763-188686813	K562	blood:	n/a
45	chr4:188530842-188530892	MCF10A-Er-Src	breast:	n/a
46	chr4:188829287-188829337	GM19239	blood:	n/a
47	chr4:188854221-188854271	HCPEpiC	choroid plexus:	n/a
48	chr4:188528319-188528369	LNCaP	prostate:	n/a
49	chr4:188700879-188700929	HCPEpiC	choroid plexus:	n/a
50	chr4:188686763-188686813	AG10803	skin:	n/a

(count:11 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-2	chr4:188543796-188543871	XLOC_003829
2	lnc-TRIML2-4	chr4:188586916-188586992	NR_110436
3	lnc-ZFP42-2	chr4:188632898-188633273	NONHSAT099720
4	lnc-ZFP42-8	chr4:188808721-188808809	l_2822_chr4:188790794-188818331_testes
5	lnc-TRIML2-4	chr4:188567364-188567526	NONHSAT099704
6	lnc-ZFP42-2	chr4:188571727-188571815	XLOC_003829
7	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099720
8	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
9	lnc-ZFP42-2	chr4:188571621-188571815	XLOC_003829
10	lnc-TRIML2-4	chr4:188567364-188567526	NONHSAT099706
11	lnc-ZFP42-8	chr4:188818285-188818331	l_2822_chr4:188790794-188818331_testes
12	lnc-TRIML2-4	chr4:188513797-188514081	NONHSAT099706
13	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
14	lnc-ZFP42-2	chr4:188581291-188581337	XLOC_003829
15	lnc-ZFP42-1	chr4:188735823-188736246	XLOC_003831
16	lnc-ZFP42-2	chr4:188581291-188581521	XLOC_003829
17	lnc-TRIML2-3	chr4:188534050-188534499	XLOC_004221
18	lnc-ZFP42-2	chr4:188554100-188554300	XLOC_003829
19	lnc-TRIML2-9	chr4:188771044-188771493	l_2820_chr4:188691027-188804581_testes
20	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
21	lnc-ZFP42-1	chr4:188735822-188736272	NONHSAT099722
22	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
23	lnc-TRIML2-9	chr4:188804358-188804581	l_2820_chr4:188691027-188804581_testes
24	lnc-TRIML2-4	chr4:188503575-188503684	ENSG00000250590
25	lnc-TRIML2-3	chr4:188534640-188534713	XLOC_004221
26	lnc-TRIML2-4	chr4:188593716-188593795	NR_110436
27	lnc-TRIML2-11	chr4:188532415-188533775	l_2818_chr4:188532414-188535272_placenta
28	lnc-TRIML2-4	chr4:188514038-188514081	ENSG00000250590
29	lnc-ZFP42-2	chr4:188632897-188633241	NONHSAT099717
30	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099719
31	lnc-TRIML2-9	chr4:188771634-188772347	l_2820_chr4:188691027-188804581_testes
32	lnc-ZFP42-2	chr4:188647752-188647874	NONHSAT099717
33	lnc-ZFP42-2	chr4:188632898-188633228	XLOC_003829
34	lnc-ZFP42-2	chr4:188581291-188581523	XLOC_003829
35	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
36	lnc-ZFP42-2	chr4:188553703-188553988	XLOC_003829
37	lnc-ZFP42-2	chr4:188632898-188633111	NONHSAT099719
38	lnc-ZFP42-2	chr4:188626129-188626577	NONHSAT099717
39	lnc-ZFP42-2	chr4:188635490-188635540	NONHSAT099719
40	lnc-ZFP42-9	chr4:188771634-188772147	l_2821_chr4:188771633-188780051_testes
41	lnc-ZFP42-9	chr4:188779825-188780051	l_2821_chr4:188771633-188780051_testes
42	lnc-TRIML2-9	chr4:188716229-188716412	l_2820_chr4:188691027-188804581_testes
43	lnc-TRIML2-11	chr4:188535229-188535272	l_2818_chr4:188532414-188535272_placenta
44	lnc-TRIML2-4	chr4:188513897-188514081	NONHSAT099704
45	lnc-ZFP42-10	chr4:188501769-188501890	NONHSAT099705
46	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
47	lnc-ZFP42-2	chr4:188534086-188535153	XLOC_003829
48	lnc-ZFP42-2	chr4:188534800-188535153	XLOC_003829
49	lnc-ZFP42-2	chr4:188534919-188535153	XLOC_003829
50	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722

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
MED20	miRNA target sites
PHF6	miRNA target sites
CDC42	miRNA target sites
TIMP3	miRNA target sites
KLF12	miRNA target sites
FSCN1	miRNA target sites
NDP	miRNA target sites
MCL1	miRNA target sites
TAGLN2	miRNA target sites
KIF13B	miRNA target sites

Extended variants
information (count: 5710 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:5710 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138313332	chr4:188483189-188483190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367642173	chr4:188483254-188483255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541227859	chr4:188483277-188483278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs573693298	chr4:188483345-188483346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536326711	chr4:188483361-188483362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72710413	chr4:188483384-188483385	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs72710415	chr4:188483385-188483386	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs190880349	chr4:188483407-188483408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182318780	chr4:188483422-188483423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575514316	chr4:188483542-188483543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559565068	chr4:188483567-188483568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186685664	chr4:188483571-188483572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs561127668	chr4:188483572-188483573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs28477117	chr4:188483573-188483574	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs191246963	chr4:188483632-188483633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112812467	chr4:188483649-188483650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559346157	chr4:188483662-188483663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528435850	chr4:188483664-188483665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35900728	chr4:188483667-188483668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76343733	chr4:188483676-188483677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537737702	chr4:188483731-188483732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs2376278	chr4:188483754-188483755	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs567823929	chr4:188483758-188483759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183407317	chr4:188483761-188483762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7663622	chr4:188483773-188483774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572884939	chr4:188483790-188483791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187897339	chr4:188483792-188483793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs193202432	chr4:188483811-188483812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571372914	chr4:188483821-188483822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575491617	chr4:188483858-188483859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184194728	chr4:188483882-188483883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs368154417	chr4:188483912-188483913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149641604	chr4:188483925-188483926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs574549071	chr4:188483949-188483950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144317099	chr4:188483980-188483981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs28595562	chr4:188483999-188484000	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs374637365	chr4:188484036-188484037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375709360	chr4:188484044-188484045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551401453	chr4:188484080-188484081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1505508	chr4:188484115-188484116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531135443	chr4:188484116-188484117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536046161	chr4:188484244-188484245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs112910096	chr4:188484250-188484251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567779495	chr4:188484271-188484272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140913347	chr4:188484318-188484319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs62354918	chr4:188484415-188484416	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs566618704	chr4:188484419-188484420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538729771	chr4:188484425-188484426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs115729451	chr4:188484434-188484435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs568814066	chr4:188484445-188484446	Enhancers	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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:487 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188482800-188485000	Enhancers	Fetal Heart	heart
2	chr4:188486600-188487000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr4:188492200-188492600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr4:188493600-188493800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:188499400-188499600	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
6	chr4:188499400-188500400	Enhancers	NHDF-Ad	bronchial
7	chr4:188502000-188502200	Bivalent/Poised TSS	Liver	Liver
8	chr4:188507600-188508400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr4:188507800-188508400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:188519000-188520000	Enhancers	NHDF-Ad	bronchial
11	chr4:188519200-188519600	Enhancers	HSMMtube	muscle
12	chr4:188519200-188520000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:188519600-188520000	Enhancers	HSMM	muscle
14	chr4:188519600-188520000	Enhancers	Osteobl	bone
15	chr4:188519600-188523600	Weak transcription	HSMMtube	muscle
16	chr4:188520000-188522600	Weak transcription	HSMM	muscle
17	chr4:188520000-188522800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:188520000-188522800	Weak transcription	NHDF-Ad	bronchial
19	chr4:188520000-188523200	Weak transcription	Osteobl	bone
20	chr4:188522600-188523200	Enhancers	NH-A	brain
21	chr4:188522600-188523600	Enhancers	HSMM	muscle
22	chr4:188522800-188523200	Enhancers	Muscle Satellite Cultured Cells	--
23	chr4:188522800-188523200	Enhancers	NHDF-Ad	bronchial
24	chr4:188522800-188523600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:188522800-188523600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:188522800-188523600	Enhancers	HUVEC	blood vessel
27	chr4:188522800-188523600	Enhancers	NHLF	lung
28	chr4:188522800-188523800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr4:188523000-188524000	Enhancers	Fetal Lung	lung
30	chr4:188523000-188524800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:188523000-188525000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr4:188523000-188525000	Enhancers	NHEK	skin
33	chr4:188523200-188523600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:188523200-188523600	Enhancers	Osteobl	bone
35	chr4:188523200-188524200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
36	chr4:188523200-188524200	Flanking Active TSS	NH-A	brain
37	chr4:188523200-188524200	Flanking Active TSS	NHDF-Ad	bronchial
38	chr4:188523200-188524600	Enhancers	Adipose Nuclei	Adipose
39	chr4:188523200-188524800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr4:188523200-188524800	Enhancers	HMEC	breast
41	chr4:188523400-188523600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:188523400-188524600	Enhancers	A549	lung
43	chr4:188523600-188524000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:188523600-188524000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:188523600-188524000	Enhancers	Psoas Muscle	Psoas
46	chr4:188523600-188524000	Flanking Active TSS	HSMM	muscle
47	chr4:188523600-188524000	Flanking Active TSS	HSMMtube	muscle
48	chr4:188523600-188524000	Flanking Active TSS	HUVEC	blood vessel
49	chr4:188523600-188524000	Flanking Active TSS	NHLF	lung
50	chr4:188523600-188524200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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