Variant report

Variant	esv3440556
Chromosome Location	chr4:119272654-119275202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:119274135-119274146	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:119273220-119273579	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr4:119273963-119274383	GM12878	blood:	n/a	chr4:119274073-119274086 chr4:119274079-119274092
4	BHLHE40	chr4:119274055-119274318	K562	blood:	n/a	chr4:119274073-119274089 chr4:119274300-119274316 chr4:119274075-119274091
5	BHLHE40	chr4:119274124-119274292	A549	lung:	n/a	n/a
6	BHLHE40	chr4:119274032-119274393	GM12878	blood:	n/a	chr4:119274308-119274324 chr4:119274073-119274089 chr4:119274300-119274316 chr4:119274075-119274091
7	BHLHE40	chr4:119274138-119274294	HepG2	liver:	n/a	n/a
8	BHLHE40	chr4:119274053-119274379	HepG2	liver:	n/a	chr4:119274308-119274324 chr4:119274073-119274089 chr4:119274300-119274316 chr4:119274075-119274091
9	BRCA1	chr4:119274099-119274232	H1-hESC	embryonic stem cell:	n/a	n/a
10	BRCA1	chr4:119273423-119273462	HepG2	liver:	n/a	n/a
11	CCNT2	chr4:119274018-119274408	K562	blood:	n/a	n/a
12	CEBPB	chr4:119274097-119274344	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr4:119274041-119274247	Hela-S3	cervix:	n/a	chr4:119274085-119274098
14	CHD1	chr4:119274185-119274208	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr4:119274090-119274333	Hela-S3	cervix:	n/a	n/a
16	CHD2	chr4:119274142-119274306	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr4:119274043-119274406	A549	lung:	n/a	n/a
18	CTBP2	chr4:119274019-119274543	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr4:119273320-119273470	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr4:119273380-119273530	SAEC	small airway:	n/a	n/a
21	CTCF	chr4:119274140-119274290	SAEC	small airway:	n/a	n/a
22	CTCF	chr4:119274120-119274270	GM12875	blood:	n/a	n/a
23	CTCF	chr4:119274160-119274310	HAc	cerebellar:	n/a	n/a
24	CTCF	chr4:119274140-119274290	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr4:119274080-119274230	NHEK	skin:	n/a	chr4:119274112-119274125
26	CTCF	chr4:119274420-119274570	GM06990	blood:	n/a	n/a
27	CTCF	chr4:119273640-119273790	GM12871	blood:	n/a	n/a
28	CTCF	chr4:119274500-119274650	HCFaa	heart:	n/a	n/a
29	CTCF	chr4:119273240-119273390	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr4:119274140-119274290	AG04450	lung:	n/a	n/a
31	CTCF	chr4:119274140-119274290	HL-60	blood:	n/a	n/a
32	CTCF	chr4:119274071-119274364	Lung_OC	lung:	n/a	chr4:119274304-119274317 chr4:119274112-119274125
33	CTCF	chr4:119274000-119274150	HFF-Myc	foreskin:	n/a	chr4:119274068-119274077 chr4:119274062-119274080 chr4:119274029-119274042 chr4:119274112-119274125
34	CTCF	chr4:119273707-119273775	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr4:119274140-119274290	BJ	skin:	n/a	n/a
36	CTCF	chr4:119274120-119274270	Caco-2	colon:	n/a	n/a
37	CTCF	chr4:119274047-119274405	K562	blood:	n/a	chr4:119274068-119274077 chr4:119274304-119274317 chr4:119274062-119274080 chr4:119274112-119274125
38	CTCF	chr4:119273983-119274324	HepG2	liver:	n/a	chr4:119274068-119274077 chr4:119274304-119274317 chr4:119274062-119274080 chr4:119274029-119274042 chr4:119274112-119274125
39	CTCF	chr4:119274120-119274270	AG04449	skin:	n/a	n/a
40	CTCF	chr4:119274019-119274453	GM12891	blood:	n/a	chr4:119274068-119274077 chr4:119274304-119274317 chr4:119274062-119274080 chr4:119274029-119274042 chr4:119274112-119274125
41	CTCF	chr4:119273220-119273370	HA-sp	spinal cord:	n/a	n/a
42	CTCF	chr4:119274140-119274290	HMF	breast:	n/a	n/a
43	CTCF	chr4:119274060-119274210	NHLF	lung:	n/a	chr4:119274068-119274077 chr4:119274062-119274080 chr4:119274112-119274125
44	CTCF	chr4:119274112-119274363	MCF-7	breast:	n/a	chr4:119274304-119274317 chr4:119274112-119274125
45	CTCF	chr4:119274100-119274250	GM12801	blood:	n/a	chr4:119274112-119274125
46	CTCF	chr4:119273340-119273490	HRE	kidney:	n/a	n/a
47	CTCF	chr4:119274140-119274290	GM12875	blood:	n/a	n/a
48	CTCF	chr4:119274120-119274270	BJ	skin:	n/a	n/a
49	CTCF	chr4:119273994-119274426	MCF-7	breast:	n/a	chr4:119274068-119274077 chr4:119274304-119274317 chr4:119274062-119274080 chr4:119274029-119274042 chr4:119274112-119274125
50	CTCF	chr4:119274111-119274299	MCF-7	breast:	n/a	chr4:119274112-119274125

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:119274013-119274063	ECC-1	luminal epithelium:	n/a
2	chr4:119274013-119274063	ECC-1	luminal epithelium:	n/a
3	chr4:119273361-119273411	HRPEpiC	eye:	n/a
4	chr4:119274341-119274391	GM12891	blood:	n/a
5	chr4:119274837-119274887	GM19239	blood:	n/a
6	chr4:119274192-119274242	GM12892	blood:	n/a
7	chr4:119274192-119274242	H1-hESC	embryonic stem cell:	embryo
8	chr4:119274192-119274242	LNCaP	prostate:	n/a
9	chr4:119273073-119273123	HNPCEpiC	eye:	n/a
10	chr4:119273361-119273411	NHDF-neo	bronchial:	n/a
11	chr4:119273073-119273123	ECC-1	luminal epithelium:	n/a
12	chr4:119273827-119273877	HEK293	kidney:	embryo
13	chr4:119273889-119273939	AG09309	skin:	n/a
14	chr4:119274192-119274242	AG09319	gingival:	n/a
15	chr4:119274837-119274887	BJ	skin:	n/a
16	chr4:119273073-119273123	MCF-7	breast:	n/a
17	chr4:119273889-119273939	ovcar-3	ovarian:	n/a
18	chr4:119274013-119274063	T-47D	breast:	n/a
19	chr4:119274133-119274183	HUVEC	blood vessel:	n/a
20	chr4:119273361-119273411	NT2-D1	testis:	n/a
21	chr4:119274013-119274063	GM06990	blood:	n/a
22	chr4:119274837-119274887	PFSK-1	brain:	n/a
23	chr4:119274192-119274242	HIPEpiC	eye:	n/a
24	chr4:119274133-119274183	IMR90	lung:	fetal
25	chr4:119273361-119273411	GM19239	blood:	n/a
26	chr4:119274013-119274063	SK-N-SH	brain:	n/a
27	chr4:119274837-119274887	HRE	kidney:	n/a
28	chr4:119274133-119274183	AG04449	skin:	fetal
29	chr4:119273827-119273877	ovcar-3	ovarian:	n/a
30	chr4:119273827-119273877	GM12892	blood:	n/a
31	chr4:119273827-119273877	MCF10A-Er-Src	breast:	n/a
32	chr4:119273073-119273123	NHBE	bronchial:	n/a
33	chr4:119273073-119273123	HRPEpiC	eye:	n/a
34	chr4:119274133-119274183	HRE	kidney:	n/a
35	chr4:119274837-119274887	HCM	heart:	n/a
36	chr4:119274192-119274242	HCT-116	colon:	n/a
37	chr4:119274837-119274887	HepG2	liver:	n/a
38	chr4:119273073-119273123	PrEC	prostate:	n/a
39	chr4:119273827-119273877	ECC-1	luminal epithelium:	n/a
40	chr4:119273361-119273411	BE2_C	brain:	n/a
41	chr4:119274013-119274063	HepG2	liver:	n/a
42	chr4:119274192-119274242	HCPEpiC	choroid plexus:	n/a
43	chr4:119273827-119273877	H1-hESC	embryonic stem cell:	embryo
44	chr4:119274341-119274391	HL-60	blood:	n/a
45	chr4:119273361-119273411	GM12891	blood:	n/a
46	chr4:119273827-119273877	HAEpiC	amniotic membrane:	n/a
47	chr4:119273073-119273123	HL-60	blood:	n/a
48	chr4:119274341-119274391	BE2_C	brain:	n/a
49	chr4:119274133-119274183	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:119273073-119273123	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:119199692..119204423-chr4:119272219..119275323,9	MCF-7	breast:
2	chr4:119199765..119204001-chr4:119271592..119273818,4	K562	blood:
3	chr4:119198677..119205956-chr4:119272273..119279963,18	MCF-7	breast:

Variant related genes	Relation type
PRSS12	TF binding region
PRSS12	CpG island
ENSG00000269893	chromatin interactions

Extended variants
information (count: 110 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:110 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182482103	chr4:119272663-119272664	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs76162901	chr4:119272674-119272675	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs146179130	chr4:119272718-119272719	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563579129	chr4:119272754-119272755	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531274069	chr4:119272768-119272769	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs186824625	chr4:119272772-119272773	Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192535928	chr4:119272808-119272809	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7669243	chr4:119272813-119272814	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs115299818	chr4:119272822-119272823	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139654870	chr4:119272847-119272848	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs142981642	chr4:119272850-119272851	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs112622559	chr4:119272889-119272890	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs113944192	chr4:119272913-119272914	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537459712	chr4:119272931-119272932	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs557185163	chr4:119272939-119272940	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7674055	chr4:119272958-119272959	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs539609176	chr4:119273004-119273005	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577670835	chr4:119273007-119273008	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs553184466	chr4:119273019-119273020	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572105663	chr4:119273076-119273077	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs142733357	chr4:119273079-119273080	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111877944	chr4:119273080-119273081	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs540811046	chr4:119273089-119273090	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540524297	chr4:119273101-119273102	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561047918	chr4:119273102-119273103	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183351435	chr4:119273195-119273196	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs200649897	chr4:119273212-119273213	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200961440	chr4:119273333-119273334	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532484606	chr4:119273340-119273341	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140025726	chr4:119273362-119273363	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112651126	chr4:119273365-119273366	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs373688551	chr4:119273373-119273374	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs375198447	chr4:119273374-119273375	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559631766	chr4:119273384-119273385	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529173422	chr4:119273393-119273394	Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs267599998	chr4:119273426-119273427	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs72903215	chr4:119273436-119273437	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs369553634	chr4:119273460-119273461	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs548349152	chr4:119273494-119273495	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568541644	chr4:119273501-119273502	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs372488853	chr4:119273517-119273518	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs372089331	chr4:119273538-119273539	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375822810	chr4:119273544-119273545	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199996930	chr4:119273553-119273554	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570793078	chr4:119273560-119273561	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373311928	chr4:119273567-119273568	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs13119545	chr4:119273712-119273713	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370717747	chr4:119273747-119273748	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs573317117	chr4:119273756-119273757	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536050186	chr4:119273789-119273790	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119267400-119273000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr4:119267400-119273200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:119268000-119273000	Weak transcription	Gastric	stomach
4	chr4:119268200-119273000	Weak transcription	Pancreas	Pancrea
5	chr4:119270800-119272800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:119270800-119272800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:119271400-119272800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:119271600-119272800	Enhancers	NHEK	skin
9	chr4:119271600-119273000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr4:119271600-119273200	Bivalent/Poised TSS	Fetal Brain Male	brain
11	chr4:119271600-119274200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr4:119271600-119274400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr4:119271600-119275000	Active TSS	NHLF	lung
14	chr4:119271800-119274200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr4:119271800-119274200	Active TSS	Rectal Mucosa Donor 31	rectum
16	chr4:119271800-119274600	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr4:119271800-119274600	Active TSS	Osteobl	bone
18	chr4:119272200-119273400	Bivalent Enhancer	HUVEC	blood vessel
19	chr4:119272200-119274600	Active TSS	NHDF-Ad	bronchial
20	chr4:119272400-119272800	Active TSS	HMEC	breast
21	chr4:119272400-119274400	Active TSS	Muscle Satellite Cultured Cells	--
22	chr4:119272400-119274400	Bivalent/Poised TSS	Fetal Brain Female	brain
23	chr4:119272600-119272800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:119272600-119272800	Active TSS	Fetal Lung	lung
25	chr4:119272600-119273200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr4:119272600-119274400	Active TSS	Stomach Mucosa	stomach
27	chr4:119272800-119273000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
28	chr4:119272800-119273000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:119272800-119273000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr4:119272800-119273000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
31	chr4:119272800-119273000	Bivalent/Poised TSS	Fetal Heart	heart
32	chr4:119272800-119273000	Active TSS	Fetal Stomach	stomach
33	chr4:119272800-119273000	Active TSS	Rectal Smooth Muscle	rectum
34	chr4:119272800-119273200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
35	chr4:119272800-119273200	Active TSS	Colonic Mucosa	Colon
36	chr4:119272800-119273200	Flanking Active TSS	Fetal Lung	lung
37	chr4:119272800-119273200	Flanking Active TSS	NHEK	skin
38	chr4:119272800-119273400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:119272800-119273400	Enhancers	Liver	Liver
40	chr4:119272800-119273600	Flanking Active TSS	HMEC	breast
41	chr4:119272800-119274400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
42	chr4:119272800-119274800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:119272800-119275000	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr4:119273000-119273200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
45	chr4:119273000-119273200	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
46	chr4:119273000-119273200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:119273000-119273200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:119273000-119273200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
49	chr4:119273000-119273200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
50	chr4:119273000-119273200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell

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