Variant report

Variant	nsv1016686
Chromosome Location	chr4:188292185-188908622
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1873)
CpG islands
(count:2564)
Chromatin interactive
region (count:26)
LncRNA
region (count:96)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1873 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

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	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
7	BATF	chr4:188896133-188896354	GM12878	blood:	n/a	chr4:188896272-188896283
8	BHLHE40	chr4:188519650-188519830	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:188534744-188534930	K562	blood:	n/a	n/a
10	BHLHE40	chr4:188533400-188533687	K562	blood:	n/a	n/a
11	BHLHE40	chr4:188527838-188527964	K562	blood:	n/a	n/a
12	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
13	BHLHE40	chr4:188538740-188538867	K562	blood:	n/a	n/a
14	BRCA1	chr4:188570315-188570361	GM12878	blood:	n/a	n/a
15	CBX3	chr4:188660869-188661415	HCT-116	colon:	n/a	n/a
16	CBX3	chr4:188301159-188301792	HCT-116	colon:	n/a	n/a
17	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
18	CBX3	chr4:188507537-188508612	HCT-116	colon:	n/a	n/a
19	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
20	CEBPB	chr4:188376676-188376735	HepG2	liver:	n/a	chr4:188376676-188376689 chr4:188376676-188376687 chr4:188376678-188376689
21	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
22	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:188632833-188633099	H1-hESC	embryonic stem cell:	n/a	chr4:188632937-188632948
24	CEBPB	chr4:188538148-188538851	HCT-116	colon:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
25	CEBPB	chr4:188608883-188609243	HepG2	liver:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
26	CEBPB	chr4:188540074-188540575	A549	lung:	n/a	n/a
27	CEBPB	chr4:188538307-188538573	K562	blood:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
28	CEBPB	chr4:188608874-188609254	IMR90	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
29	CEBPB	chr4:188540170-188540484	A549	lung:	n/a	n/a
30	CEBPB	chr4:188538269-188538668	IMR90	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
31	CEBPB	chr4:188301254-188301597	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:188632761-188633106	HepG2	liver:	n/a	chr4:188632937-188632948
33	CEBPB	chr4:188728718-188728984	HepG2	liver:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
34	CEBPB	chr4:188735851-188736097	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:188538314-188538633	A549	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
36	CEBPB	chr4:188337419-188337771	IMR90	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
37	CEBPB	chr4:188538294-188538645	K562	blood:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
38	CEBPB	chr4:188735766-188736151	K562	blood:	n/a	n/a
39	CEBPB	chr4:188529058-188529739	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:188479534-188479869	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:188504954-188505154	HepG2	liver:	n/a	chr4:188504994-188505011
42	CEBPB	chr4:188839840-188839977	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
44	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
45	CEBPB	chr4:188632788-188633066	K562	blood:	n/a	chr4:188632937-188632948
46	CEBPB	chr4:188608828-188609265	A549	lung:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
47	CEBPB	chr4:188539916-188540476	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:188735771-188736121	A549	lung:	n/a	n/a
49	CEBPB	chr4:188552350-188552627	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:188317722-188317931	HepG2	liver:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856

(count:2564 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188426437-188426487	SK-N-MC	brain:	n/a
2	chr4:188895421-188895471	Caco-2	colon:	n/a
3	chr4:188426437-188426487	SK-N-MC	brain:	n/a
4	chr4:188895421-188895471	Caco-2	colon:	n/a
5	chr4:188686664-188686714	AG09319	gingival:	n/a
6	chr4:188426437-188426487	Jurkat	blood:	n/a
7	chr4:188736336-188736386	SK-N-SH	brain:	n/a
8	chr4:188426506-188426556	SK-N-SH_RA	brain:	n/a
9	chr4:188462685-188462735	HPAEpiC	pulmonary alveolar:	n/a
10	chr4:188824073-188824123	H1-hESC	embryonic stem cell:	embryo
11	chr4:188895390-188895440	SK-N-MC	brain:	n/a
12	chr4:188427966-188428016	HEK293	kidney:	embryo
13	chr4:188858709-188858759	GM19239	blood:	n/a
14	chr4:188426506-188426556	IMR90	lung:	fetal
15	chr4:188398437-188398487	HNPCEpiC	eye:	n/a
16	chr4:188554583-188554633	AG10803	skin:	n/a
17	chr4:188824073-188824123	GM06990	blood:	n/a
18	chr4:188398437-188398487	HEK293	kidney:	embryo
19	chr4:188854221-188854271	H1-hESC	embryonic stem cell:	embryo
20	chr4:188530842-188530892	Hela-S3	cervix:	n/a
21	chr4:188686664-188686714	T-47D	breast:	n/a
22	chr4:188700879-188700929	H1-hESC	embryonic stem cell:	embryo
23	chr4:188829287-188829337	AG09309	skin:	n/a
24	chr4:188736112-188736162	LNCaP	prostate:	n/a
25	chr4:188534776-188534826	Jurkat	blood:	n/a
26	chr4:188736172-188736222	AG04450	lung:	fetal
27	chr4:188534448-188534498	AG09309	skin:	n/a
28	chr4:188401038-188401088	SK-N-MC	brain:	n/a
29	chr4:188824073-188824123	HUVEC	blood vessel:	n/a
30	chr4:188401038-188401088	HL-60	blood:	n/a
31	chr4:188554583-188554633	GM06990	blood:	n/a
32	chr4:188534873-188534923	AG04449	skin:	fetal
33	chr4:188686763-188686813	ECC-1	luminal epithelium:	n/a
34	chr4:188534693-188534743	SK-N-SH_RA	brain:	n/a
35	chr4:188736172-188736222	HEEpiC	esophagus:	n/a
36	chr4:188577176-188577226	Hela-S3	cervix:	n/a
37	chr4:188854221-188854271	HCT-116	colon:	n/a
38	chr4:188428637-188428687	AG09319	gingival:	n/a
39	chr4:188534912-188534962	Caco-2	colon:	n/a
40	chr4:188858971-188859021	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:188462685-188462735	AG10803	skin:	n/a
42	chr4:188533158-188533208	PFSK-1	brain:	n/a
43	chr4:188534776-188534826	U87	brain:	n/a
44	chr4:188895407-188895457	BE2_C	brain:	n/a
45	chr4:188577176-188577226	A549	lung:	n/a
46	chr4:188895421-188895471	HCF	heart:	n/a
47	chr4:188530842-188530892	MCF-7	breast:	n/a
48	chr4:188401038-188401088	Jurkat	blood:	n/a
49	chr4:188401038-188401088	HRPEpiC	eye:	n/a
50	chr4:188824073-188824123	HNPCEpiC	eye:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:
2	chr4:188807826..188808346-chr6:74078319..74078839,2	MCF-7	breast:
3	chr4:188426813..188429681-chrX:150150480..150152156,2	MCF-7	breast:
4	chr1:149223042..149224634-chr4:188652998..188654518,2	MCF-7	breast:
5	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
6	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
7	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
8	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
9	chr4:188527128..188528286-chr4:189293970..189294660,4	MCF-7	breast:
10	chr1:149223776..149224611-chr4:188652518..188653518,3	MCF-7	breast:
11	chr1:149223786..149225310-chr4:188651498..188652998,2	MCF-7	breast:
12	chr4:188424251..188426259-chr4:188431828..188433769,2	MCF-7	breast:
13	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
14	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
15	chr1:149223872..149224384-chr4:188652498..188652998,2	MCF-7	breast:
16	chr4:188527681..188530400-chr4:188530916..188532601,2	K562	blood:
17	chr4:188587219..188588049-chr4:189293834..189294448,2	MCF-7	breast:
18	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
19	chr4:188343831..188346613-chr4:188349550..188352474,2	K562	blood:
20	chr4:188360438..188363227-chr4:188363317..188366717,3	K562	blood:
21	chr4:188391078..188391578-chr8:43092429..43092931,2	MCF-7	breast:
22	chr4:188390078..188391598-chr8:43091410..43092931,3	MCF-7	breast:
23	chr4:188361387..188363227-chr4:188363317..188365027,2	K562	blood:
24	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
25	chr4:188638802..188641142-chr4:188661839..188664453,2	K562	blood:
26	chr4:188379432..188382221-chr4:188385756..188387515,2	K562	blood:

(count:96 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-4	chr4:188514038-188514081	ENSG00000250590
2	lnc-TRIML2-4	chr4:188503575-188503684	ENSG00000250590
3	lnc-ZFP42-2	chr4:188581291-188581337	XLOC_003829
4	lnc-ZFP42-6	chr4:188292838-188293075	XLOC_003826
5	lnc-ZFP42-1	chr4:188735822-188736272	NONHSAT099722
6	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
7	lnc-ZFP42-2	chr4:188632898-188633111	NONHSAT099719
8	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
9	lnc-ZFP42-6	chr4:188292449-188292580	XLOC_003826
10	lnc-ZFP42-2	chr4:188647752-188647874	NONHSAT099717
11	lnc-ZFP42-2	chr4:188534919-188535153	XLOC_003829
12	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
13	lnc-TRIML2-4	chr4:188513897-188514081	NONHSAT099704
14	lnc-ZFP42-2	chr4:188632898-188633273	NONHSAT099720
15	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
16	lnc-ZFP42-4	chr4:188343853-188344622	NONHSAT099695
17	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
18	lnc-ZFP42-2	chr4:188581291-188581523	XLOC_003829
19	lnc-TRIML2-5	chr4:188438236-188438362	XLOC_004219
20	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
21	lnc-TRIML2-4	chr4:188454036-188454357	ENSG00000250590
22	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
23	lnc-ZFP42-2	chr4:188571621-188571815	XLOC_003829
24	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
25	lnc-ZFP42-12	chr4:188360139-188360290	l_2817_chr4:188360138-188372335_testes
26	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
27	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
28	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099719
29	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
30	lnc-TRIML2-12	chr4:188362831-188363446	NONHSAT099697
31	lnc-TRIML2-4	chr4:188513797-188514081	NONHSAT099706
32	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
33	lnc-TRIML2-9	chr4:188771044-188771493	l_2820_chr4:188691027-188804581_testes
34	lnc-ZFP42-5	chr4:188336464-188337128	NONHSAT099694
35	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
36	lnc-TRIML2-2	chr4:188881751-188881835	NONHSAT099725
37	lnc-TRIML2-2	chr4:188881466-188881649	NONHSAT099725
38	lnc-ZFP42-2	chr4:188626207-188626577	NONHSAT099720
39	lnc-TRIML2-11	chr4:188535229-188535272	l_2818_chr4:188532414-188535272_placenta
40	lnc-TRIML2-9	chr4:188716229-188716412	l_2820_chr4:188691027-188804581_testes
41	lnc-ZFP42-10	chr4:188501769-188501890	NONHSAT099705
42	lnc-TRIML2-4	chr4:188593716-188593795	ENSG00000250590
43	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
44	lnc-ZFP42-2	chr4:188632898-188633228	XLOC_003829
45	lnc-ZFP42-2	chr4:188635490-188635540	NONHSAT099719
46	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
47	lnc-ZFP42-1	chr4:188735823-188736246	XLOC_003831
48	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
49	lnc-ZFP42-2	chr4:188626502-188626577	XLOC_003829
50	lnc-ZFP42-2	chr4:188553703-188553988	XLOC_003829

No data

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000251643	TF binding region
ENSG00000250620	TF binding region
ADAM20P3	TF binding region
ENSG00000249642	TF binding region
ENSG00000250590	TF binding region
ENSG00000213331	TF binding region
ENSG00000251490	CpG island
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ADAM20P3	CpG island
ENSG00000249642	CpG island
ENSG00000250590	CpG island
ENSG00000213331	CpG island
ENSG00000251643	chromatin interactions
ENSG00000029993	chromatin interactions
ENSG00000206737	chromatin interactions
TAGLN2	miRNA target sites
KIF13B	miRNA target sites
KLF12	miRNA target sites
NDP	miRNA target sites
ANTXR1	miRNA target sites
PHF6	miRNA target sites
FSCN1	miRNA target sites
MED20	miRNA target sites
TIMP3	miRNA target sites
CDC42	miRNA target sites
ANP32E	miRNA target sites
MCL1	miRNA target sites

Extended variants
information (count: 11230 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:11230 , 50 per page) page: 1 2 3 4 5 6 7 ... 225

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541235325	chr4:188292207-188292208	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs11942521	chr4:188292264-188292265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532697250	chr4:188292292-188292293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373852584	chr4:188292300-188292301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562709400	chr4:188292356-188292357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531756747	chr4:188292380-188292381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576785451	chr4:188292406-188292407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544504327	chr4:188292435-188292436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs563034508	chr4:188292517-188292518	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs530355773	chr4:188292530-188292531	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs568746728	chr4:188292574-188292575	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs564348477	chr4:188292580-188292581	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs528723425	chr4:188292633-188292634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547632999	chr4:188292667-188292668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570191997	chr4:188292682-188292683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539181745	chr4:188292700-188292701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186795611	chr4:188292769-188292770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575919405	chr4:188292775-188292776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554401032	chr4:188292804-188292805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546908753	chr4:188292834-188292835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148931907	chr4:188292841-188292842	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs572773838	chr4:188292870-188292871	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs555331311	chr4:188292960-188292961	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
24	rs572408818	chr4:188292968-188292969	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
25	rs541222860	chr4:188292988-188292989	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs564298849	chr4:188292989-188292990	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs577399052	chr4:188293011-188293012	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs143679337	chr4:188293052-188293053	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs563005344	chr4:188293080-188293081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72723263	chr4:188293088-188293089	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191637541	chr4:188293092-188293093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562242034	chr4:188293101-188293102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148059876	chr4:188293170-188293171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183967669	chr4:188293180-188293181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570676683	chr4:188293206-188293207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188912146	chr4:188293238-188293239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191910572	chr4:188293268-188293269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182283047	chr4:188293288-188293289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535093709	chr4:188293289-188293290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186635391	chr4:188293329-188293330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375872854	chr4:188293389-188293390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs56391790	chr4:188293401-188293402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs191837944	chr4:188293416-188293417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534948372	chr4:188293442-188293443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9992540	chr4:188293457-188293458	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs577867956	chr4:188293471-188293472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569699339	chr4:188293477-188293478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183819306	chr4:188293497-188293498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188476650	chr4:188293506-188293507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs193045448	chr4:188293539-188293540	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cognitive impairment	21505072	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:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188291800-188292600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:188291800-188292800	Enhancers	Fetal Heart	heart
3	chr4:188292000-188292200	Enhancers	Fetal Intestine Large	intestine
4	chr4:188292600-188294800	Weak transcription	Fetal Intestine Large	intestine
5	chr4:188292600-188304000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:188294600-188295200	Enhancers	Adipose Nuclei	Adipose
7	chr4:188294800-188295000	Enhancers	Fetal Intestine Large	intestine
8	chr4:188294800-188295000	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr4:188295000-188295600	Weak transcription	Fetal Intestine Large	intestine
10	chr4:188295200-188299200	Weak transcription	Adipose Nuclei	Adipose
11	chr4:188295600-188295800	Enhancers	Rectal Mucosa Donor 31	rectum
12	chr4:188295600-188296600	Enhancers	Fetal Intestine Large	intestine
13	chr4:188297800-188298400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:188299200-188300000	Enhancers	Adipose Nuclei	Adipose
15	chr4:188301400-188301800	Enhancers	Pancreas	Pancrea
16	chr4:188301800-188304000	Weak transcription	Pancreas	Pancrea
17	chr4:188304000-188304600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:188304000-188304600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:188304200-188304800	Enhancers	HMEC	breast
20	chr4:188308400-188308600	Enhancers	Placenta Amnion	Placenta Amnion
21	chr4:188308400-188309000	Enhancers	A549	lung
22	chr4:188308600-188309200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr4:188309000-188309400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr4:188309000-188309400	Flanking Active TSS	A549	lung
25	chr4:188309000-188309800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr4:188309200-188310000	Enhancers	Placenta Amnion	Placenta Amnion
27	chr4:188309400-188309600	Enhancers	A549	lung
28	chr4:188309800-188311000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:188310000-188310400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr4:188310400-188310800	Enhancers	Placenta Amnion	Placenta Amnion
31	chr4:188311000-188311200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr4:188314200-188316000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:188314400-188315600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr4:188314800-188315000	Enhancers	NHLF	lung
35	chr4:188314800-188315600	Enhancers	NHDF-Ad	bronchial
36	chr4:188319600-188319800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:188321400-188322000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr4:188323200-188338800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:188329000-188329600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr4:188329400-188330000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:188335600-188337800	Enhancers	Fetal Brain Male	brain
42	chr4:188335800-188336000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:188335800-188336200	Enhancers	Fetal Muscle Leg	muscle
44	chr4:188335800-188339400	Enhancers	Fetal Lung	lung
45	chr4:188336000-188336800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr4:188336000-188337800	Enhancers	Fetal Heart	heart
47	chr4:188336200-188336800	Enhancers	Adipose Nuclei	Adipose
48	chr4:188336200-188336800	Enhancers	HSMM	muscle
49	chr4:188336800-188338800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr4:188336800-188339000	Weak transcription	Adipose Nuclei	Adipose

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