Variant report

Variant	nsv596449
Chromosome Location	chr4:188317381-188844211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1474)
CpG islands
(count:2077)
Chromatin interactive
region (count:23)
LncRNA
region (count:87)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1474 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

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	ATF3	chr4:188527774-188527903	K562	blood:	n/a	n/a
5	BACH1	chr4:188413248-188413433	K562	blood:	n/a	chr4:188413338-188413352
6	BHLHE40	chr4:188534744-188534930	K562	blood:	n/a	n/a
7	BHLHE40	chr4:188343966-188344142	K562	blood:	n/a	n/a
8	BHLHE40	chr4:188533400-188533687	K562	blood:	n/a	n/a
9	BHLHE40	chr4:188527838-188527964	K562	blood:	n/a	n/a
10	BHLHE40	chr4:188519650-188519830	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:188538740-188538867	K562	blood:	n/a	n/a
12	BRCA1	chr4:188570315-188570361	GM12878	blood:	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	CBX3	chr4:188665981-188666555	HCT-116	colon:	n/a	n/a
16	CEBPB	chr4:188735771-188736121	A549	lung:	n/a	n/a
17	CEBPB	chr4:188337413-188337766	Hela-S3	cervix:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
18	CEBPB	chr4:188591052-188591273	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:188632761-188633106	HepG2	liver:	n/a	chr4:188632937-188632948
20	CEBPB	chr4:188587766-188588125	IMR90	lung:	n/a	chr4:188587944-188587955
21	CEBPB	chr4:188517628-188517892	HepG2	liver:	n/a	chr4:188517748-188517759
22	CEBPB	chr4:188337464-188337763	HepG2	liver:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
23	CEBPB	chr4:188538269-188538668	IMR90	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
24	CEBPB	chr4:188569010-188569242	IMR90	lung:	n/a	chr4:188569144-188569155
25	CEBPB	chr4:188839840-188839977	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:188405582-188405932	A549	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
27	CEBPB	chr4:188752270-188752506	HepG2	liver:	n/a	chr4:188752367-188752378
28	CEBPB	chr4:188317704-188317987	IMR90	lung:	n/a	chr4:188317842-188317853 chr4:188317842-188317855 chr4:188317839-188317856
29	CEBPB	chr4:188405581-188406417	HepG2	liver:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
30	CEBPB	chr4:188399632-188400363	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:188769115-188769241	A549	lung:	n/a	chr4:188769178-188769189
32	CEBPB	chr4:188570725-188570925	K562	blood:	n/a	chr4:188570868-188570879
33	CEBPB	chr4:188608883-188609243	HepG2	liver:	n/a	chr4:188609058-188609071 chr4:188609058-188609069 chr4:188609060-188609069
34	CEBPB	chr4:188538148-188538851	HCT-116	colon:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
35	CEBPB	chr4:188504954-188505154	HepG2	liver:	n/a	chr4:188504994-188505011
36	CEBPB	chr4:188538314-188538633	A549	lung:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
37	CEBPB	chr4:188538294-188538645	K562	blood:	n/a	chr4:188538447-188538458 chr4:188538481-188538492
38	CEBPB	chr4:188529058-188529739	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:188735860-188736134	MCF-7	breast:	n/a	n/a
40	CEBPB	chr4:188405573-188406437	IMR90	lung:	n/a	chr4:188405878-188405889 chr4:188405683-188405696 chr4:188405685-188405696 chr4:188405877-188405890
41	CEBPB	chr4:188440289-188440620	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:188690637-188690931	HepG2	liver:	n/a	chr4:188690750-188690761
43	CEBPB	chr4:188735766-188736145	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:188474103-188474183	K562	blood:	n/a	n/a
45	CEBPB	chr4:188600607-188601013	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr4:188570745-188571038	IMR90	lung:	n/a	chr4:188570868-188570879
47	CEBPB	chr4:188632788-188633066	K562	blood:	n/a	chr4:188632937-188632948
48	CEBPB	chr4:188735760-188736147	K562	blood:	n/a	n/a
49	CEBPB	chr4:188337469-188337769	A549	lung:	n/a	chr4:188337610-188337621 chr4:188337669-188337677
50	CEBPB	chr4:188529114-188529530	Hela-S3	cervix:	n/a	n/a

(count:2077 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188423066-188423116	GM12892	blood:	n/a
2	chr4:188700879-188700929	HRPEpiC	eye:	n/a
3	chr4:188534509-188534559	HCM	heart:	n/a
4	chr4:188423066-188423116	GM12892	blood:	n/a
5	chr4:188700879-188700929	HRPEpiC	eye:	n/a
6	chr4:188534509-188534559	HCM	heart:	n/a
7	chr4:188686763-188686813	HEK293	kidney:	embryo
8	chr4:188829287-188829337	HCF	heart:	n/a
9	chr4:188538807-188538857	Hela-S3	cervix:	n/a
10	chr4:188686726-188686776	Hela-S3	cervix:	n/a
11	chr4:188428637-188428687	ECC-1	luminal epithelium:	n/a
12	chr4:188534912-188534962	NHBE	bronchial:	n/a
13	chr4:188686664-188686714	SK-N-SH	brain:	n/a
14	chr4:188534776-188534826	SKMC	muscle:	n/a
15	chr4:188700879-188700929	U87	brain:	n/a
16	chr4:188588839-188588889	ProgFib	skin:	n/a
17	chr4:188534873-188534923	MCF10A-Er-Src	breast:	n/a
18	chr4:188736336-188736386	HNPCEpiC	eye:	n/a
19	chr4:188588839-188588889	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:188736172-188736222	HUVEC	blood vessel:	n/a
21	chr4:188534509-188534559	AG09319	gingival:	n/a
22	chr4:188686664-188686714	SK-N-MC	brain:	n/a
23	chr4:188534776-188534826	PrEC	prostate:	n/a
24	chr4:188843522-188843572	AG09319	gingival:	n/a
25	chr4:188843522-188843572	Hela-S3	cervix:	n/a
26	chr4:188530842-188530892	GM12892	blood:	n/a
27	chr4:188539183-188539233	HEK293	kidney:	embryo
28	chr4:188391387-188391437	NHDF-neo	bronchial:	n/a
29	chr4:188538807-188538857	HCM	heart:	n/a
30	chr4:188534912-188534962	HCPEpiC	choroid plexus:	n/a
31	chr4:188539183-188539233	SK-N-SH_RA	brain:	n/a
32	chr4:188534509-188534559	HepG2	liver:	n/a
33	chr4:188533158-188533208	SKMC	muscle:	n/a
34	chr4:188554583-188554633	T-47D	breast:	n/a
35	chr4:188534448-188534498	HNPCEpiC	eye:	n/a
36	chr4:188534912-188534962	HUVEC	blood vessel:	n/a
37	chr4:188686726-188686776	MCF-7	breast:	n/a
38	chr4:188423066-188423116	Jurkat	blood:	n/a
39	chr4:188533158-188533208	HRCEpiC	kidney:	n/a
40	chr4:188843522-188843572	Hepatocyte	liver:	n/a
41	chr4:188426506-188426556	HRE	kidney:	n/a
42	chr4:188554583-188554633	HCT-116	colon:	n/a
43	chr4:188736112-188736162	HL-60	blood:	n/a
44	chr4:188824073-188824123	BE2_C	brain:	n/a
45	chr4:188534693-188534743	AG09309	skin:	n/a
46	chr4:188588839-188588889	AG04449	skin:	fetal
47	chr4:188534776-188534826	AG09309	skin:	n/a
48	chr4:188577176-188577226	GM12878	blood:	n/a
49	chr4:188539183-188539233	GM06990	blood:	n/a
50	chr4:188538807-188538857	HL-60	blood:	n/a

(count:23 , 50 per page) page: 1

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

(count:87 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-12	chr4:188371277-188372335	l_2817_chr4:188360138-188372335_testes
2	lnc-ZFP42-4	chr4:188351216-188351539	XLOC_003828
3	lnc-ZFP42-2	chr4:188534800-188535153	XLOC_003829
4	lnc-ZFP42-5	chr4:188334716-188334865	NONHSAT099694
5	lnc-ZFP42-9	chr4:188771634-188772147	l_2821_chr4:188771633-188780051_testes
6	lnc-ZFP42-11	chr4:188419171-188419708	NONHSAT099698
7	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
8	lnc-ZFP42-5	chr4:188329695-188330053	NONHSAT099694
9	lnc-ZFP42-4	chr4:188351172-188352018	NONHSAT099695
10	lnc-ZFP42-8	chr4:188808721-188808809	l_2822_chr4:188790794-188818331_testes
11	lnc-ZFP42-11	chr4:188419753-188420210	NONHSAT099698
12	lnc-ZFP42-2	chr4:188543796-188543894	XLOC_003829
13	lnc-ZFP42-2	chr4:188632898-188633228	XLOC_003829
14	lnc-ZFP42-2	chr4:188534919-188535153	XLOC_003829
15	lnc-TRIML2-4	chr4:188454036-188454357	ENSG00000250590
16	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722
17	lnc-ZFP42-2	chr4:188553805-188553988	XLOC_003829
18	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
19	lnc-ZFP42-2	chr4:188543796-188543871	XLOC_003829
20	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
21	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
22	lnc-TRIML2-4	chr4:188593716-188593795	NR_110436
23	lnc-ZFP42-2	chr4:188542831-188543333	XLOC_003829
24	lnc-TRIML2-4	chr4:188503575-188503684	ENSG00000250590
25	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
26	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590
27	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
28	lnc-TRIML2-5	chr4:188437307-188437878	XLOC_004219
29	lnc-TRIML2-12	chr4:188364965-188365452	NONHSAT099697
30	lnc-TRIML2-5	chr4:188438236-188438362	XLOC_004219
31	lnc-TRIML2-4	chr4:188586916-188586992	NR_110436
32	lnc-ZFP42-5	chr4:188336464-188336851	ENSG00000250620
33	lnc-ZFP42-2	chr4:188571621-188571815	XLOC_003829
34	lnc-TRIML2-4	chr4:188514038-188514081	ENSG00000250590
35	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
36	lnc-TRIML2-3	chr4:188534640-188534713	XLOC_004221
37	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
38	lnc-TRIML2-3	chr4:188534050-188534499	XLOC_004221
39	lnc-TRIML2-12	chr4:188364017-188364135	NONHSAT099697
40	lnc-ZFP42-12	chr4:188370524-188371133	l_2817_chr4:188360138-188372335_testes
41	lnc-ZFP42-1	chr4:188735823-188736246	XLOC_003831
42	lnc-TRIML2-9	chr4:188771634-188772347	l_2820_chr4:188691027-188804581_testes
43	lnc-ZFP42-2	chr4:188571727-188571815	XLOC_003829
44	lnc-TRIML2-9	chr4:188804358-188804581	l_2820_chr4:188691027-188804581_testes
45	lnc-TRIML2-11	chr4:188532415-188533775	l_2818_chr4:188532414-188535272_placenta
46	lnc-TRIML2-11	chr4:188535229-188535272	l_2818_chr4:188532414-188535272_placenta
47	lnc-TRIML2-9	chr4:188716229-188716412	l_2820_chr4:188691027-188804581_testes
48	lnc-ZFP42-2	chr4:188581291-188581337	XLOC_003829
49	lnc-ZFP42-2	chr4:188626118-188626433	XLOC_003829
50	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590

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
ENSG00000251490	CpG island
ENSG00000251643	CpG island
ENSG00000250620	CpG island
ADAM20P3	CpG island
ENSG00000249642	CpG island
ENSG00000250590	CpG island
ENSG00000251643	chromatin interactions
ENSG00000029993	chromatin interactions
ENSG00000206737	chromatin interactions
TIMP3	miRNA target sites
ANP32E	miRNA target sites
NDP	miRNA target sites
KLF12	miRNA target sites
CDC42	miRNA target sites
MED20	miRNA target sites
FSCN1	miRNA target sites
MCL1	miRNA target sites
PHF6	miRNA target sites
ANTXR1	miRNA target sites
TAGLN2	miRNA target sites
KIF13B	miRNA target sites

Extended variants
information (count: 9122 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:9122 , 50 per page) page: 1 2 3 4 5 6 7 ... 183

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564520670	chr4:188319626-188319627	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561470741	chr4:188319673-188319674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530290172	chr4:188319685-188319686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370199699	chr4:188319733-188319734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546827315	chr4:188319746-188319747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560332320	chr4:188319753-188319754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs116448727	chr4:188321433-188321434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs199807765	chr4:188321453-188321454	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564399350	chr4:188321462-188321463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77048246	chr4:188321468-188321469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7676864	chr4:188321485-188321486	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs549672132	chr4:188321512-188321513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148144636	chr4:188321514-188321515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537908124	chr4:188321515-188321516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556919525	chr4:188321538-188321539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375741491	chr4:188321586-188321587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568106200	chr4:188321625-188321626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372431721	chr4:188321724-188321725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553339120	chr4:188321853-188321854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181952254	chr4:188321920-188321921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554022638	chr4:188321923-188321924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536749584	chr4:188321931-188321932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs547628036	chr4:188321966-188321967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs375123692	chr4:188321967-188321968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576587341	chr4:188321976-188321977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147183168	chr4:188323213-188323214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148669683	chr4:188323240-188323241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528760360	chr4:188323246-188323247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577564507	chr4:188323259-188323260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs142087965	chr4:188323282-188323283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188379767	chr4:188323305-188323306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556961765	chr4:188323343-188323344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573846190	chr4:188323347-188323348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192032392	chr4:188323356-188323357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183419673	chr4:188323378-188323379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528310182	chr4:188323379-188323380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541122449	chr4:188323471-188323472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549020184	chr4:188323510-188323511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188020534	chr4:188323557-188323558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559315554	chr4:188323567-188323568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs200749322	chr4:188323605-188323606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2376244	chr4:188323649-188323650	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs12510956	chr4:188323665-188323666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs12503162	chr4:188323670-188323671	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs2376245	chr4:188323688-188323689	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs140700081	chr4:188323692-188323693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs12499680	chr4:188323706-188323707	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370680713	chr4:188323827-188323828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557865406	chr4:188323828-188323829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570714628	chr4:188323857-188323858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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

Chromatin state (count:826 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188319600-188319800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:188321400-188322000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:188323200-188338800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:188329000-188329600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:188329400-188330000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:188335600-188337800	Enhancers	Fetal Brain Male	brain
7	chr4:188335800-188336000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr4:188335800-188336200	Enhancers	Fetal Muscle Leg	muscle
9	chr4:188335800-188339400	Enhancers	Fetal Lung	lung
10	chr4:188336000-188336800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr4:188336000-188337800	Enhancers	Fetal Heart	heart
12	chr4:188336200-188336800	Enhancers	Adipose Nuclei	Adipose
13	chr4:188336200-188336800	Enhancers	HSMM	muscle
14	chr4:188336800-188338800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:188336800-188339000	Weak transcription	Adipose Nuclei	Adipose
16	chr4:188337800-188338800	Weak transcription	Fetal Brain Male	brain
17	chr4:188337800-188343800	Weak transcription	Fetal Heart	heart
18	chr4:188338800-188339000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:188338800-188339800	Enhancers	Fetal Brain Male	brain
20	chr4:188338800-188340600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr4:188339000-188339200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:188339000-188339200	Enhancers	Adipose Nuclei	Adipose
23	chr4:188339200-188339600	Weak transcription	Adipose Nuclei	Adipose
24	chr4:188339400-188339600	Flanking Active TSS	Fetal Lung	lung
25	chr4:188339400-188342200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:188339600-188340000	Enhancers	Fetal Lung	lung
27	chr4:188339600-188340400	Enhancers	Adipose Nuclei	Adipose
28	chr4:188340000-188340400	Flanking Active TSS	Fetal Lung	lung
29	chr4:188342200-188342400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:188342400-188342600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:188342400-188342800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:188342600-188342800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr4:188342800-188346000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:188343800-188344400	Enhancers	Fetal Heart	heart
35	chr4:188345400-188346000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr4:188345600-188346200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr4:188346000-188346400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:188351800-188352000	Enhancers	Aorta	Aorta
39	chr4:188352000-188357000	Weak transcription	Aorta	Aorta
40	chr4:188353400-188353800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:188353400-188355400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr4:188353600-188355200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr4:188353800-188354800	Enhancers	HMEC	breast
44	chr4:188354400-188355400	Enhancers	Fetal Heart	heart
45	chr4:188354800-188355000	Flanking Active TSS	HMEC	breast
46	chr4:188355000-188355200	Active TSS	HMEC	breast
47	chr4:188355400-188357200	Weak transcription	Fetal Heart	heart
48	chr4:188357200-188357600	Enhancers	Fetal Heart	heart
49	chr4:188357200-188357600	Enhancers	Stomach Smooth Muscle	stomach
50	chr4:188357200-188357800	Enhancers	Cortex derived primary cultured neurospheres	brain

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