Variant report

Variant	esv3408421
Chromosome Location	chr4:102267454-102270302
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	chr4:102268870-102269129	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:102270051-102270246	HepG2	liver:	n/a	n/a
3	BACH1	chr4:102269007-102269398	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:102268296-102268651	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr4:102269133-102269684	A549	lung:	n/a	chr4:102269314-102269327 chr4:102269500-102269508 chr4:102269334-102269347 chr4:102269310-102269323
6	BCL3	chr4:102269158-102269648	A549	lung:	n/a	chr4:102269314-102269327 chr4:102269500-102269508 chr4:102269334-102269347 chr4:102269310-102269323
7	BCLAF1	chr4:102269101-102269432	GM12878	blood:	n/a	chr4:102269314-102269327 chr4:102269334-102269347 chr4:102269310-102269323
8	BHLHE40	chr4:102266870-102267476	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:102268204-102268609	K562	blood:	n/a	n/a
10	BHLHE40	chr4:102268827-102269533	K562	blood:	n/a	chr4:102269313-102269329 chr4:102269324-102269340 chr4:102269316-102269332
11	BHLHE40	chr4:102268064-102269557	GM12878	blood:	n/a	chr4:102269313-102269329 chr4:102269324-102269340 chr4:102269316-102269332
12	BHLHE40	chr4:102267821-102267970	K562	blood:	n/a	n/a
13	BRCA1	chr4:102267814-102267862	GM12878	blood:	n/a	n/a
14	BRCA1	chr4:102268829-102269193	HepG2	liver:	n/a	n/a
15	BRCA1	chr4:102268747-102269426	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr4:102267844-102267962	Hela-S3	cervix:	n/a	n/a
17	CBX3	chr4:102269056-102269540	K562	blood:	n/a	n/a
18	CCNT2	chr4:102267791-102269472	K562	blood:	n/a	chr4:102268917-102268926 chr4:102267808-102267817
19	CEBPB	chr4:102267603-102267949	H1-hESC	embryonic stem cell:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
20	CEBPB	chr4:102267624-102267995	A549	lung:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
21	CEBPB	chr4:102267568-102267963	HepG2	liver:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
22	CEBPB	chr4:102267360-102267953	A549	lung:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
23	CEBPB	chr4:102267592-102267975	K562	blood:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
24	CEBPB	chr4:102267668-102267854	HepG2	liver:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
25	CEBPB	chr4:102267589-102267957	HepG2	liver:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
26	CEBPB	chr4:102269028-102269244	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:102267513-102269351	Hela-S3	cervix:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102268839-102268847 chr4:102267750-102267761
28	CEBPB	chr4:102267344-102268145	IMR90	lung:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
29	CEBPB	chr4:102267606-102268054	A549	lung:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
30	CEBPB	chr4:102268910-102269318	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:102267523-102268008	ECC-1	luminal epithelium:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
32	CEBPB	chr4:102267513-102268017	MCF-7	breast:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
33	CEBPB	chr4:102267624-102267908	ECC-1	luminal epithelium:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
34	CEBPB	chr4:102268920-102269278	HepG2	liver:	n/a	n/a
35	CEBPB	chr4:102267616-102267982	HepG2	liver:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
36	CEBPB	chr4:102267632-102267853	K562	blood:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
37	CEBPB	chr4:102267620-102267920	K562	blood:	n/a	chr4:102267752-102267763 chr4:102267752-102267761 chr4:102267750-102267761
38	CEBPD	chr4:102267582-102267921	HepG2	liver:	n/a	chr4:102267751-102267762
39	CEBPD	chr4:102267609-102267818	HepG2	liver:	n/a	chr4:102267751-102267762
40	CEBPD	chr4:102268454-102269260	HepG2	liver:	n/a	n/a
41	CHD1	chr4:102269015-102269384	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr4:102267832-102268002	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr4:102267025-102267486	K562	blood:	n/a	n/a
44	CHD2	chr4:102266600-102267961	HepG2	liver:	n/a	n/a
45	CHD2	chr4:102268188-102269502	HepG2	liver:	n/a	n/a
46	CHD2	chr4:102267248-102269843	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr4:102267781-102267981	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:102268260-102268460	K562	blood:	n/a	n/a
49	CHD2	chr4:102266540-102269492	GM12878	blood:	n/a	n/a
50	CHD2	chr4:102268704-102269446	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:102269425-102269475	NB4	blood:	n/a
2	chr4:102269425-102269475	NB4	blood:	n/a
3	chr4:102267974-102268024	HEK293	kidney:	embryo
4	chr4:102269779-102269829	AG09319	gingival:	n/a
5	chr4:102268075-102268125	CMK	blood:	n/a
6	chr4:102269779-102269829	PrEC	prostate:	n/a
7	chr4:102268821-102268871	NHDF-neo	bronchial:	n/a
8	chr4:102268949-102268999	PANC-1	pancreas:	n/a
9	chr4:102268821-102268871	K562	blood:	n/a
10	chr4:102268949-102268999	HUVEC	blood vessel:	n/a
11	chr4:102268957-102269007	SKMC	muscle:	n/a
12	chr4:102268622-102268672	Hepatocyte	liver:	n/a
13	chr4:102268821-102268871	HRE	kidney:	n/a
14	chr4:102268799-102268849	BJ	skin:	n/a
15	chr4:102268854-102268904	HNPCEpiC	eye:	n/a
16	chr4:102268622-102268672	HPAEpiC	pulmonary alveolar:	n/a
17	chr4:102268957-102269007	ProgFib	skin:	n/a
18	chr4:102269779-102269829	IMR90	lung:	fetal
19	chr4:102267974-102268024	MCF10A-Er-Src	breast:	n/a
20	chr4:102268957-102269007	GM12878	blood:	n/a
21	chr4:102268125-102268175	HRPEpiC	eye:	n/a
22	chr4:102268075-102268125	H1-hESC	embryonic stem cell:	embryo
23	chr4:102269779-102269829	K562	blood:	n/a
24	chr4:102267974-102268024	AG09309	skin:	n/a
25	chr4:102268799-102268849	AG04450	lung:	fetal
26	chr4:102267974-102268024	AG09319	gingival:	n/a
27	chr4:102267974-102268024	GM12891	blood:	n/a
28	chr4:102268957-102269007	HEEpiC	esophagus:	n/a
29	chr4:102268245-102268295	AG10803	skin:	n/a
30	chr4:102268799-102268849	NHDF-neo	bronchial:	n/a
31	chr4:102268854-102268904	HRPEpiC	eye:	n/a
32	chr4:102268821-102268871	HRCEpiC	kidney:	n/a
33	chr4:102268957-102269007	A549	lung:	n/a
34	chr4:102268821-102268871	Caco-2	colon:	n/a
35	chr4:102268957-102269007	AG09309	skin:	n/a
36	chr4:102268949-102268999	SK-N-SH	brain:	n/a
37	chr4:102268799-102268849	PFSK-1	brain:	n/a
38	chr4:102268957-102269007	ECC-1	luminal epithelium:	n/a
39	chr4:102268622-102268672	H1-hESC	embryonic stem cell:	embryo
40	chr4:102268799-102268849	AG09309	skin:	n/a
41	chr4:102268854-102268904	HAEpiC	amniotic membrane:	n/a
42	chr4:102268949-102268999	MCF10A-Er-Src	breast:	n/a
43	chr4:102268125-102268175	RPTEC	kidney:	n/a
44	chr4:102268799-102268849	NT2-D1	testis:	n/a
45	chr4:102268821-102268871	HCM	heart:	n/a
46	chr4:102268949-102268999	A549	lung:	n/a
47	chr4:102269425-102269475	HNPCEpiC	eye:	n/a
48	chr4:102268075-102268125	AG09319	gingival:	n/a
49	chr4:102268799-102268849	HCM	heart:	n/a
50	chr4:102269374-102269424	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:100869383..100871934-chr4:102267599..102271042,3	K562	blood:
2	chr4:102249081..102251620-chr4:102269591..102272220,2	MCF-7	breast:
3	chr4:102265718..102267485-chr4:103187307..103189886,2	MCF-7	breast:
4	chr4:102269774..102272032-chr4:102277264..102279804,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP001816.1.1-1	chr4:102269481-102270040	NR_033874
2	lnc-AP001816.1.1-1	chr4:102268934-102269166	NR_033874

Variant related genes	Relation type
ENSG00000254531	TF binding region
PPP3CA	TF binding region
ENSG00000254531	CpG island
PPP3CA	CpG island
ENSG00000245322	chromatin interactions
ENSG00000164032	chromatin interactions
ENSG00000221265	chromatin interactions

Extended variants
information (count: 106 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113086344	chr4:102267507-102267508	Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs541866054	chr4:102267512-102267513	Active TSS Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs578105720	chr4:102267691-102267692	Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs200427644	chr4:102267816-102267817	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs201159854	chr4:102267818-102267819	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs368445098	chr4:102267821-102267822	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs2583390	chr4:102267822-102267823	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs530528856	chr4:102267829-102267830	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs548951833	chr4:102267832-102267833	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs560862822	chr4:102267912-102267913	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs140003651	chr4:102267942-102267943	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs376661307	chr4:102267945-102267946	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs199920410	chr4:102267962-102267963	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs202209525	chr4:102267971-102267972	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs571381637	chr4:102267977-102267978	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs546755954	chr4:102268034-102268035	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs376443800	chr4:102268035-102268036	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs45441997	chr4:102268036-102268037	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs3974660	chr4:102268061-102268062	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs3730248	chr4:102268113-102268114	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs371830308	chr4:102268116-102268117	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs149278688	chr4:102268146-102268147	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs569776674	chr4:102268284-102268285	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs537052902	chr4:102268312-102268313	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs115296173	chr4:102268342-102268343	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs114272959	chr4:102268343-102268344	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs117015016	chr4:102268393-102268394	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs78822234	chr4:102268570-102268571	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs553600798	chr4:102268588-102268589	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs578119207	chr4:102268652-102268653	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs545578591	chr4:102268655-102268656	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs557095690	chr4:102268673-102268674	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs575457762	chr4:102268689-102268690	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs191240896	chr4:102268690-102268691	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs553575726	chr4:102268691-102268692	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs370949347	chr4:102268692-102268693	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs560757653	chr4:102268814-102268815	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs528069146	chr4:102268820-102268821	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs532264440	chr4:102268849-102268850	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs874116	chr4:102268868-102268869	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs565156057	chr4:102268882-102268883	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs532218412	chr4:102268922-102268923	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs2850328	chr4:102268940-102268941	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs80186323	chr4:102268958-102268959	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
45	rs565512501	chr4:102268966-102268967	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
46	rs530943990	chr4:102268975-102268976	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
47	rs183156229	chr4:102269002-102269003	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs188487462	chr4:102269056-102269057	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs567570394	chr4:102269096-102269097	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs143436754	chr4:102269132-102269133	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	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
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:102265600-102269800	Active TSS	NHLF	lung
2	chr4:102265800-102269800	Active TSS	Brain Angular Gyrus	brain
3	chr4:102265800-102270000	Active TSS	Fetal Kidney	kidney
4	chr4:102266000-102269000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr4:102266200-102269800	Active TSS	Right Atrium	heart
6	chr4:102266200-102270000	Active TSS	Aorta	Aorta
7	chr4:102266200-102270000	Active TSS	Ovary	ovary
8	chr4:102266400-102268200	Active TSS	Brain Germinal Matrix	brain
9	chr4:102266400-102269600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr4:102266400-102269600	Active TSS	Fetal Stomach	stomach
11	chr4:102266400-102269600	Active TSS	Rectal Mucosa Donor 29	rectum
12	chr4:102266400-102269800	Active TSS	Brain Hippocampus Middle	brain
13	chr4:102266400-102269800	Active TSS	Small Intestine	intestine
14	chr4:102266400-102269800	Active TSS	HSMM	muscle
15	chr4:102266400-102270000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:102266400-102270000	Active TSS	Brain Cingulate Gyrus	brain
17	chr4:102266400-102270000	Active TSS	Gastric	stomach
18	chr4:102266400-102270200	Active TSS	Pancreatic Islets	Pancreatic Islet
19	chr4:102266600-102269000	Active TSS	Fetal Muscle Trunk	muscle
20	chr4:102266600-102269600	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr4:102266600-102269600	Active TSS	Colonic Mucosa	Colon
22	chr4:102266600-102269800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:102266600-102269800	Active TSS	Colon Smooth Muscle	Colon
24	chr4:102266600-102269800	Active TSS	Lung	lung
25	chr4:102266600-102270000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:102266600-102270000	Active TSS	Breast Myoepithelial Primary Cells	Breast
27	chr4:102266600-102270200	Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr4:102266600-102270200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr4:102266600-102270200	Active TSS	A549	lung
30	chr4:102266600-102270400	Active TSS	Rectal Smooth Muscle	rectum
31	chr4:102266800-102267800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:102266800-102269200	Active TSS	HepG2	liver
33	chr4:102266800-102269600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:102266800-102269600	Active TSS	Cortex derived primary cultured neurospheres	brain
35	chr4:102266800-102269800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr4:102266800-102269800	Active TSS	iPS-15b Cell Line	embryonic stem cell
37	chr4:102266800-102269800	Active TSS	iPS-18 Cell Line	embryonic stem cell
38	chr4:102266800-102269800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:102266800-102269800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:102266800-102269800	Active TSS	Brain Substantia Nigra	brain
41	chr4:102266800-102269800	Active TSS	Right Ventricle	heart
42	chr4:102266800-102269800	Active TSS	NHEK	skin
43	chr4:102266800-102270000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr4:102266800-102270000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr4:102266800-102270000	Active TSS	H9 Cell Line	embryonic stem cell
46	chr4:102266800-102270000	Active TSS	HUES6 Cell Line	embryonic stem cell
47	chr4:102266800-102270000	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr4:102266800-102270000	Active TSS	Brain Anterior Caudate	brain
49	chr4:102266800-102270000	Active TSS	Fetal Brain Female	brain
50	chr4:102266800-102270200	Active TSS	H1 Cell Line	embryonic stem cell

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