Variant report

Variant	esv3444781
Chromosome Location	chr4:166127852-166130050
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	ARID3A	chr4:166128689-166128731	K562	blood:	n/a	n/a
2	ARID3A	chr4:166128621-166128911	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:166129030-166129091	K562	blood:	n/a	n/a
4	ARID3A	chr4:166129222-166129239	HepG2	liver:	n/a	n/a
5	ATF1	chr4:166128531-166128845	K562	blood:	n/a	n/a
6	ATF3	chr4:166128608-166128920	K562	blood:	n/a	n/a
7	ATF3	chr4:166128654-166128843	GM12878	blood:	n/a	n/a
8	BACH1	chr4:166129092-166129306	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr4:166128688-166129218	K562	blood:	n/a	chr4:166129145-166129161 chr4:166128730-166128746 chr4:166129150-166129166 chr4:166128955-166128971 chr4:166128910-166128926 chr4:166128729-166128745 chr4:166129099-166129115 chr4:166129142-166129158
10	BHLHE40	chr4:166128304-166129269	GM12878	blood:	n/a	chr4:166129145-166129161 chr4:166128730-166128746 chr4:166129150-166129166 chr4:166128955-166128971 chr4:166128910-166128926 chr4:166128729-166128745 chr4:166129099-166129115 chr4:166129142-166129158
11	BRCA1	chr4:166127967-166128035	GM12878	blood:	n/a	n/a
12	BRCA1	chr4:166128391-166128400	GM12878	blood:	n/a	n/a
13	CCNT2	chr4:166128393-166129240	K562	blood:	n/a	n/a
14	CEBPD	chr4:166128437-166128893	HepG2	liver:	n/a	n/a
15	CHD1	chr4:166129054-166129055	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD1	chr4:166128216-166128360	GM12878	blood:	n/a	n/a
17	CHD2	chr4:166128381-166129193	Hela-S3	cervix:	n/a	chr4:166129156-166129166
18	CHD2	chr4:166128187-166128254	GM12878	blood:	n/a	n/a
19	CHD2	chr4:166129167-166129331	K562	blood:	n/a	n/a
20	CREB1	chr4:166128426-166128913	K562	blood:	n/a	n/a
21	CREB1	chr4:166128418-166128980	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr4:166128473-166128990	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr4:166128056-166129241	HepG2	liver:	n/a	n/a
24	CREB1	chr4:166128401-166129030	K562	blood:	n/a	n/a
25	CREB1	chr4:166128405-166128979	A549	lung:	n/a	n/a
26	CREB1	chr4:166128471-166128989	HepG2	liver:	n/a	n/a
27	CREB1	chr4:166128422-166129405	GM12878	blood:	n/a	n/a
28	CREB1	chr4:166128572-166128887	A549	lung:	n/a	n/a
29	CTBP2	chr4:166128291-166129366	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr4:166128820-166128970	GM12866	blood:	n/a	chr4:166128909-166128922
31	CTCF	chr4:166128800-166128950	SAEC	small airway:	n/a	chr4:166128909-166128922
32	CTCF	chr4:166128860-166129010	GM12874	blood:	n/a	chr4:166128909-166128922
33	CTCF	chr4:166128853-166129001	GM12892	blood:	n/a	chr4:166128909-166128922
34	CTCF	chr4:166128844-166129001	GM19238	blood:	n/a	chr4:166128909-166128922
35	CTCF	chr4:166128756-166128978	HepG2	liver:	n/a	chr4:166128909-166128922
36	CTCF	chr4:166128850-166128981	GM12891	blood:	n/a	chr4:166128909-166128922
37	CTCF	chr4:166129260-166129410	HBMEC	blood vessel:	n/a	chr4:166129334-166129342
38	CTCF	chr4:166128850-166129012	GM10266	blood:	n/a	chr4:166128909-166128922
39	CTCF	chr4:166128780-166128930	AG04449	skin:	n/a	chr4:166128909-166128922
40	CTCF	chr4:166129023-166129028	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:166128860-166129010	GM12873	blood:	n/a	chr4:166128909-166128922
42	CTCF	chr4:166128858-166128986	MCF-7	breast:	n/a	chr4:166128909-166128922
43	CTCF	chr4:166128885-166128977	MCF-7	breast:	n/a	chr4:166128909-166128922
44	CTCF	chr4:166129040-166129190	AG04449	skin:	n/a	chr4:166129154-166129167
45	CTCF	chr4:166128860-166129010	GM12871	blood:	n/a	chr4:166128909-166128922
46	CTCF	chr4:166128868-166129001	Fibrobl	skin:	n/a	chr4:166128909-166128922
47	CTCF	chr4:166128780-166128930	GM12869	blood:	n/a	chr4:166128909-166128922
48	CTCF	chr4:166128860-166129010	GM12865	blood:	n/a	chr4:166128909-166128922
49	CTCF	chr4:166128638-166129084	GM12878	blood:	n/a	chr4:166128909-166128922
50	CTCF	chr4:166128900-166129050	K562	blood:	n/a	chr4:166128909-166128922

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:166128178-166128228	HCT-116	colon:	n/a
2	chr4:166128178-166128228	HCT-116	colon:	n/a
3	chr4:166128394-166128444	AG04450	lung:	fetal
4	chr4:166128178-166128228	AG09309	skin:	n/a
5	chr4:166129605-166129655	NHDF-neo	bronchial:	n/a
6	chr4:166128480-166128530	HL-60	blood:	n/a
7	chr4:166128394-166128444	NT2-D1	testis:	n/a
8	chr4:166129241-166129291	GM06990	blood:	n/a
9	chr4:166129605-166129655	ProgFib	skin:	n/a
10	chr4:166128394-166128444	A549	lung:	n/a
11	chr4:166129241-166129291	AG04449	skin:	fetal
12	chr4:166128394-166128444	Hela-S3	cervix:	n/a
13	chr4:166129561-166129611	AG10803	skin:	n/a
14	chr4:166129003-166129053	HCM	heart:	n/a
15	chr4:166129605-166129655	HRE	kidney:	n/a
16	chr4:166128480-166128530	GM12891	blood:	n/a
17	chr4:166128480-166128530	Caco-2	colon:	n/a
18	chr4:166128394-166128444	IMR90	lung:	fetal
19	chr4:166129003-166129053	LNCaP	prostate:	n/a
20	chr4:166128480-166128530	U87	brain:	n/a
21	chr4:166129605-166129655	GM06990	blood:	n/a
22	chr4:166129561-166129611	GM12878	blood:	n/a
23	chr4:166129241-166129291	T-47D	breast:	n/a
24	chr4:166128394-166128444	HEEpiC	esophagus:	n/a
25	chr4:166129640-166129690	MCF-7	breast:	n/a
26	chr4:166129561-166129611	IMR90	lung:	fetal
27	chr4:166129605-166129655	Hepatocyte	liver:	n/a
28	chr4:166129003-166129053	GM12878	blood:	n/a
29	chr4:166129241-166129291	HEK293	kidney:	embryo
30	chr4:166128178-166128228	AG04450	lung:	fetal
31	chr4:166129561-166129611	NHDF-neo	bronchial:	n/a
32	chr4:166129003-166129053	AG09319	gingival:	n/a
33	chr4:166129640-166129690	HRE	kidney:	n/a
34	chr4:166128394-166128444	NB4	blood:	n/a
35	chr4:166129241-166129291	RPTEC	kidney:	n/a
36	chr4:166129605-166129655	H1-hESC	embryonic stem cell:	embryo
37	chr4:166128178-166128228	NB4	blood:	n/a
38	chr4:166129640-166129690	IMR90	lung:	fetal
39	chr4:166129241-166129291	HRPEpiC	eye:	n/a
40	chr4:166128178-166128228	HMEC	breast:	n/a
41	chr4:166129241-166129291	HL-60	blood:	n/a
42	chr4:166128480-166128530	HCT-116	colon:	n/a
43	chr4:166129003-166129053	NT2-D1	testis:	n/a
44	chr4:166128394-166128444	Hepatocyte	liver:	n/a
45	chr4:166129640-166129690	BJ	skin:	n/a
46	chr4:166129640-166129690	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:166128394-166128444	RPTEC	kidney:	n/a
48	chr4:166129640-166129690	AG09319	gingival:	n/a
49	chr4:166129561-166129611	Caco-2	colon:	n/a
50	chr4:166129003-166129053	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:166114045..166117632-chr4:166124756..166128607,4	K562	blood:
2	chr4:166126423..166128941-chr4:166299614..166301287,2	MCF-7	breast:
3	chr4:166031817..166034229-chr4:166129496..166132218,3	K562	blood:
4	chr4:166127276..166130366-chr4:166247405..166250443,3	K562	blood:
5	chr4:166126308..166130366-chr4:166247405..166251145,5	K562	blood:
6	chr4:166128531..166130929-chr4:166246215..166249595,5	MCF-7	breast:
7	chr4:166127800..166130090-chr4:166130347..166132969,2	MCF-7	breast:
8	chr4:166127386..166130072-chr4:166247171..166250406,6	MCF-7	breast:
9	chr4:166032812..166034984-chr4:166128697..166130341,2	K562	blood:

Variant related genes	Relation type
TMEM192	TF binding region
KLHL2	TF binding region
TMEM192	CpG island
KLHL2	CpG island
ENSG00000170088	chromatin interactions
ENSG00000109466	chromatin interactions
ENSG00000109472	chromatin interactions
ENSG00000052802	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575256025	chr4:166127861-166127862	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs553000642	chr4:166127870-166127871	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs114095469	chr4:166127875-166127876	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs190447965	chr4:166127887-166127888	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs541789822	chr4:166127946-166127947	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs563366632	chr4:166127948-166127949	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs530966515	chr4:166127967-166127968	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs193225108	chr4:166127991-166127992	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs200259849	chr4:166128032-166128033	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs564840632	chr4:166128039-166128040	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs73875504	chr4:166128087-166128088	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs547219931	chr4:166128094-166128095	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs551344455	chr4:166128104-166128105	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs529836441	chr4:166128113-166128114	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs548332208	chr4:166128150-166128151	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs149651087	chr4:166128196-166128197	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs116348803	chr4:166128204-166128205	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs114736033	chr4:166128233-166128234	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs552183466	chr4:166128234-166128235	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs144381831	chr4:166128235-166128236	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs148724963	chr4:166128245-166128246	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs201177168	chr4:166128290-166128291	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs534475728	chr4:166128325-166128326	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs552762746	chr4:166128450-166128451	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs375966230	chr4:166128509-166128510	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs535535177	chr4:166128544-166128545	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs557068904	chr4:166128554-166128555	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs575541480	chr4:166128634-166128635	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs546637520	chr4:166128640-166128641	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs546226453	chr4:166128653-166128654	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs564577526	chr4:166128726-166128727	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs573491209	chr4:166128741-166128742	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs540795869	chr4:166128773-166128774	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs562245862	chr4:166128793-166128794	Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs529545669	chr4:166128833-166128834	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs548295917	chr4:166128877-166128878	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs190204099	chr4:166128911-166128912	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs11547096	chr4:166128965-166128966	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs530377254	chr4:166128994-166128995	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs552157985	chr4:166129097-166129098	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs570618753	chr4:166129118-166129119	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs534941554	chr4:166129128-166129129	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs551192909	chr4:166129172-166129173	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs546520942	chr4:166129176-166129177	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs567900781	chr4:166129255-166129256	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs535308573	chr4:166129293-166129294	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs181431578	chr4:166129367-166129368	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs185719336	chr4:166129394-166129395	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs539410946	chr4:166129414-166129415	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs558149264	chr4:166129527-166129528	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Breast cancer	17603634	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	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
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
Congenital diaphragmatic hernia	21085971	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
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD

Chromatin state (count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166126000-166128000	Weak transcription	A549	lung
2	chr4:166127200-166128400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr4:166127400-166128400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
4	chr4:166127400-166128400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr4:166127600-166128000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:166127600-166128000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:166127600-166128000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
8	chr4:166127600-166128000	Flanking Active TSS	Brain Germinal Matrix	brain
9	chr4:166127600-166128000	Flanking Active TSS	Brain Hippocampus Middle	brain
10	chr4:166127600-166128000	Flanking Active TSS	Esophagus	oesophagus
11	chr4:166127600-166128000	Active TSS	Fetal Kidney	kidney
12	chr4:166127600-166128000	Bivalent Enhancer	Fetal Thymus	thymus
13	chr4:166127600-166128000	Flanking Active TSS	Left Ventricle	heart
14	chr4:166127600-166128000	Flanking Active TSS	Pancreas	Pancrea
15	chr4:166127600-166128000	Flanking Active TSS	Right Atrium	heart
16	chr4:166127600-166128000	Enhancers	Sigmoid Colon	Sigmoid Colon
17	chr4:166127600-166128200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr4:166127600-166128200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:166127600-166128200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:166127600-166128200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr4:166127600-166128200	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr4:166127600-166128200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:166127600-166128200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:166127600-166128200	Flanking Active TSS	Brain Anterior Caudate	brain
25	chr4:166127600-166128200	Flanking Active TSS	Brain Cingulate Gyrus	brain
26	chr4:166127600-166128200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
27	chr4:166127600-166128200	Flanking Active TSS	Colon Smooth Muscle	Colon
28	chr4:166127600-166128200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr4:166127600-166128200	Flanking Active TSS	Fetal Heart	heart
30	chr4:166127600-166128200	Flanking Active TSS	Fetal Intestine Large	intestine
31	chr4:166127600-166128200	Enhancers	Small Intestine	intestine
32	chr4:166127600-166128200	Flanking Active TSS	Thymus	Thymus
33	chr4:166127600-166128200	Flanking Active TSS	NHLF	lung
34	chr4:166127600-166128400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:166127600-166128400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr4:166127600-166128400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
37	chr4:166127600-166128400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
38	chr4:166127600-166128400	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr4:166127600-166128400	Flanking Active TSS	Primary T cells from cord blood	blood
40	chr4:166127600-166128400	Flanking Active TSS	Primary hematopoietic stem cells	blood
41	chr4:166127600-166128400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
42	chr4:166127600-166128400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr4:166127600-166128400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
44	chr4:166127600-166128400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr4:166127600-166128400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr4:166127600-166128400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:166127600-166128400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr4:166127600-166128400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr4:166127600-166128400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr4:166127600-166128400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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