Variant report

Variant	esv3345645
Chromosome Location	chr5:113697478-113700026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:976)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:113697353-113697984	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:113697450-113697904	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr5:113697128-113697759	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr5:113699684-113700046	GM12878	blood:	n/a	n/a
5	BHLHE40	chr5:113696584-113698264	GM12878	blood:	n/a	chr5:113697876-113697892 chr5:113696876-113696892 chr5:113698067-113698083 chr5:113696801-113696817 chr5:113698011-113698027 chr5:113697882-113697898 chr5:113697210-113697226 chr5:113697879-113697895
6	CEBPB	chr5:113697556-113697924	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:113697525-113697886	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr5:113697619-113698066	MCF-7	breast:	n/a	n/a
9	CHD1	chr5:113697758-113698338	H1-hESC	embryonic stem cell:	n/a	chr5:113698112-113698122 chr5:113698145-113698155
10	CHD1	chr5:113697499-113697930	GM12878	blood:	n/a	n/a
11	CHD2	chr5:113697500-113698251	GM12878	blood:	n/a	chr5:113698112-113698122 chr5:113698145-113698155
12	CHD2	chr5:113697586-113698120	H1-hESC	embryonic stem cell:	n/a	n/a
13	CREB1	chr5:113697565-113697845	A549	lung:	n/a	n/a
14	CREB1	chr5:113697244-113698442	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr5:113697225-113698021	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr5:113697493-113697908	GM12878	blood:	n/a	n/a
17	CREB1	chr5:113697368-113697960	ECC-1	luminal epithelium:	n/a	n/a
18	CREB1	chr5:113697448-113697884	ECC-1	luminal epithelium:	n/a	n/a
19	CTBP2	chr5:113696255-113699679	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr5:113698020-113698170	GM12878	blood:	n/a	chr5:113698068-113698081
21	CTCF	chr5:113697936-113698251	MCF-7	breast:	n/a	chr5:113698068-113698081
22	CTCF	chr5:113697740-113697890	BJ	skin:	n/a	n/a
23	CTCF	chr5:113697600-113697750	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:113697940-113698090	GM12878	blood:	n/a	chr5:113698068-113698081
25	CTCF	chr5:113699680-113699830	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:113697680-113697830	MCF-7	breast:	n/a	n/a
27	CTCF	chr5:113697733-113697834	MCF-7	breast:	n/a	n/a
28	CTCF	chr5:113697878-113698315	MCF-7	breast:	n/a	chr5:113698068-113698081
29	CTCF	chr5:113697553-113698292	GM12878	blood:	n/a	chr5:113698068-113698081
30	CTCF	chr5:113699640-113699790	GM12878	blood:	n/a	n/a
31	CTCF	chr5:113697736-113697775	GM12891	blood:	n/a	n/a
32	CTCF	chr5:113699500-113699650	GM12866	blood:	n/a	n/a
33	CTCF	chr5:113697945-113698236	MCF-7	breast:	n/a	chr5:113698068-113698081
34	CTCF	chr5:113699700-113699850	GM12869	blood:	n/a	n/a
35	CTCF	chr5:113697880-113698030	GM12866	blood:	n/a	n/a
36	CTCF	chr5:113697945-113698208	H1-hESC	embryonic stem cell:	n/a	chr5:113698068-113698081
37	CTCF	chr5:113697718-113697816	MCF-7	breast:	n/a	n/a
38	CTCF	chr5:113698090-113698189	NHEK	skin:	n/a	n/a
39	CTCF	chr5:113699459-113699906	GM12878	blood:	n/a	n/a
40	CTCF	chr5:113697660-113697810	AG04449	skin:	n/a	n/a
41	CTCF	chr5:113697997-113698119	GM12891	blood:	n/a	chr5:113698068-113698081
42	CTCF	chr5:113697971-113698185	GM19238	blood:	n/a	chr5:113698068-113698081
43	CTCF	chr5:113698098-113698101	LNCaP	prostate:	n/a	n/a
44	CTCF	chr5:113699600-113699750	GM12874	blood:	n/a	n/a
45	CTCF	chr5:113698040-113698190	GM12870	blood:	n/a	chr5:113698068-113698081
46	CTCF	chr5:113698100-113698250	GM12874	blood:	n/a	n/a
47	CTCF	chr5:113697960-113698110	AG04449	skin:	n/a	chr5:113698068-113698081
48	CTCF	chr5:113698020-113698170	GM12869	blood:	n/a	chr5:113698068-113698081
49	CTCF	chr5:113697720-113697870	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr5:113697703-113697737	Kidney_OC	kidney:	n/a	n/a

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:113698140-113698190	HCF	heart:	n/a
2	chr5:113697649-113697699	HL-60	blood:	n/a
3	chr5:113699342-113699392	HCF	heart:	n/a
4	chr5:113697895-113697945	NB4	blood:	n/a
5	chr5:113697946-113697996	HEK293	kidney:	embryo
6	chr5:113697861-113697911	SKMC	muscle:	n/a
7	chr5:113697946-113697996	PrEC	prostate:	n/a
8	chr5:113698445-113698495	AG10803	skin:	n/a
9	chr5:113698291-113698341	GM12891	blood:	n/a
10	chr5:113697861-113697911	PrEC	prostate:	n/a
11	chr5:113699604-113699654	HIPEpiC	eye:	n/a
12	chr5:113697897-113697947	T-47D	breast:	n/a
13	chr5:113698847-113698897	AG04449	skin:	fetal
14	chr5:113699683-113699733	NHBE	bronchial:	n/a
15	chr5:113699683-113699733	HCF	heart:	n/a
16	chr5:113698140-113698190	K562	blood:	n/a
17	chr5:113699194-113699244	HCF	heart:	n/a
18	chr5:113697897-113697947	H1-hESC	embryonic stem cell:	embryo
19	chr5:113698506-113698556	GM06990	blood:	n/a
20	chr5:113697632-113697682	HUVEC	blood vessel:	n/a
21	chr5:113697861-113697911	HAEpiC	amniotic membrane:	n/a
22	chr5:113697861-113697911	A549	lung:	n/a
23	chr5:113697946-113697996	ovcar-3	ovarian:	n/a
24	chr5:113699194-113699244	GM19239	blood:	n/a
25	chr5:113697946-113697996	HRE	kidney:	n/a
26	chr5:113697632-113697682	Jurkat	blood:	n/a
27	chr5:113697632-113697682	A549	lung:	n/a
28	chr5:113699604-113699654	GM19239	blood:	n/a
29	chr5:113697861-113697911	ProgFib	skin:	n/a
30	chr5:113697895-113697945	LNCaP	prostate:	n/a
31	chr5:113699683-113699733	NT2-D1	testis:	n/a
32	chr5:113699683-113699733	NB4	blood:	n/a
33	chr5:113698847-113698897	NB4	blood:	n/a
34	chr5:113698506-113698556	NHDF-neo	bronchial:	n/a
35	chr5:113697632-113697682	HRCEpiC	kidney:	n/a
36	chr5:113697946-113697996	HRPEpiC	eye:	n/a
37	chr5:113697895-113697945	MCF-7	breast:	n/a
38	chr5:113697897-113697947	NT2-D1	testis:	n/a
39	chr5:113697895-113697945	PrEC	prostate:	n/a
40	chr5:113699683-113699733	HCT-116	colon:	n/a
41	chr5:113699194-113699244	HMEC	breast:	n/a
42	chr5:113698847-113698897	HRCEpiC	kidney:	n/a
43	chr5:113698291-113698341	GM19239	blood:	n/a
44	chr5:113699194-113699244	AoSMC	blood vessel:	n/a
45	chr5:113697897-113697947	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:113698506-113698556	HAEpiC	amniotic membrane:	n/a
47	chr5:113697895-113697945	HUVEC	blood vessel:	n/a
48	chr5:113697632-113697682	HCF	heart:	n/a
49	chr5:113699604-113699654	BE2_C	brain:	n/a
50	chr5:113699683-113699733	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:113697099..113699226-chr5:113699378..113701050,2	MCF-7	breast:

No data

Variant related genes	Relation type
KCNN2	TF binding region
KCNN2	CpG island
ENSG00000080709	chromatin interactions

Extended variants
information (count: 124 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:124 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554513257	chr5:113697495-113697496	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs561967878	chr5:113697504-113697505	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs533688948	chr5:113697505-113697506	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs545168758	chr5:113697529-113697530	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs529251812	chr5:113697534-113697535	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs544067371	chr5:113697561-113697562	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs562739460	chr5:113697562-113697563	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs36945	chr5:113697587-113697588	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs141306235	chr5:113697597-113697598	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs566312467	chr5:113697636-113697637	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs527292555	chr5:113697649-113697650	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs548612300	chr5:113697731-113697732	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs568403425	chr5:113697811-113697812	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs113199942	chr5:113697845-113697846	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557251457	chr5:113697849-113697850	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs566655645	chr5:113697880-113697881	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs370841646	chr5:113697911-113697912	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs201373959	chr5:113697936-113697937	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs539513321	chr5:113698027-113698028	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs558239519	chr5:113698086-113698087	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs371232510	chr5:113698136-113698137	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540629332	chr5:113698137-113698138	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs555838803	chr5:113698152-113698153	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs567706065	chr5:113698168-113698169	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs184147412	chr5:113698171-113698172	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs544525765	chr5:113698189-113698190	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs562518388	chr5:113698198-113698199	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs533170154	chr5:113698258-113698259	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs373945997	chr5:113698264-113698265	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs116711658	chr5:113698276-113698277	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs527423415	chr5:113698322-113698323	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs548552236	chr5:113698349-113698350	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs1058999	chr5:113698372-113698373	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs368225575	chr5:113698374-113698375	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs551270514	chr5:113698379-113698380	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs574507059	chr5:113698383-113698384	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs569310374	chr5:113698393-113698394	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs540027916	chr5:113698401-113698402	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs373053308	chr5:113698431-113698432	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs376306073	chr5:113698447-113698448	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs551736281	chr5:113698463-113698464	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs376269746	chr5:113698477-113698478	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs144037213	chr5:113698484-113698485	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs368172006	chr5:113698493-113698494	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs370364781	chr5:113698502-113698503	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs370311843	chr5:113698503-113698504	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs139352881	chr5:113698537-113698538	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs76109643	chr5:113698542-113698543	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs40179	chr5:113698544-113698545	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148619065	chr5:113698572-113698573	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Autism	22495309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113695200-113698000	Active TSS	HUES6 Cell Line	embryonic stem cell
2	chr5:113695200-113698400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr5:113695200-113698800	Active TSS	HUES64 Cell Line	embryonic stem cell
4	chr5:113695200-113699400	Active TSS	H1 Cell Line	embryonic stem cell
5	chr5:113695400-113699400	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr5:113695600-113698800	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr5:113695600-113699200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr5:113695600-113700200	Active TSS	H9 Cell Line	embryonic stem cell
9	chr5:113695600-113701000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
10	chr5:113695800-113698800	Active TSS	HUES48 Cell Line	embryonic stem cell
11	chr5:113695800-113700000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr5:113696000-113699000	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr5:113696000-113699000	Active TSS	Brain Inferior Temporal Lobe	brain
14	chr5:113696000-113699600	Active TSS	Brain Anterior Caudate	brain
15	chr5:113696200-113697600	Active TSS	Colon Smooth Muscle	Colon
16	chr5:113696200-113698400	Bivalent/Poised TSS	Fetal Stomach	stomach
17	chr5:113696200-113698600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:113696200-113698800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr5:113696200-113698800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
20	chr5:113696200-113698800	Active TSS	Right Ventricle	heart
21	chr5:113696200-113699200	Active TSS	Brain Substantia Nigra	brain
22	chr5:113696200-113699800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:113696200-113700200	Active TSS	Brain Angular Gyrus	brain
24	chr5:113696400-113697600	Flanking Active TSS	Liver	Liver
25	chr5:113696400-113697600	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
26	chr5:113696400-113697600	Flanking Bivalent TSS/Enh	Ovary	ovary
27	chr5:113696400-113697800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
28	chr5:113696400-113698000	Bivalent Enhancer	Placenta	Placenta
29	chr5:113696400-113698200	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:113696400-113698600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr5:113696400-113698800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr5:113696400-113698800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
33	chr5:113696400-113699200	Active TSS	Fetal Kidney	kidney
34	chr5:113696400-113699200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
35	chr5:113696400-113699400	Active TSS	Left Ventricle	heart
36	chr5:113696400-113699400	Active TSS	Right Atrium	heart
37	chr5:113696600-113697600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr5:113696600-113697600	Bivalent/Poised TSS	Esophagus	oesophagus
39	chr5:113696600-113698000	Bivalent/Poised TSS	Fetal Thymus	thymus
40	chr5:113696600-113698200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
41	chr5:113696600-113698400	Bivalent/Poised TSS	A549	lung
42	chr5:113696600-113698600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:113696600-113698600	Active TSS	Fetal Brain Female	brain
44	chr5:113696600-113698800	Bivalent/Poised TSS	Brain Germinal Matrix	brain
45	chr5:113696600-113699200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr5:113696600-113699400	Active TSS	Brain Cingulate Gyrus	brain
47	chr5:113696600-113699400	Bivalent/Poised TSS	NHLF	lung
48	chr5:113696600-113699600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr5:113696600-113699800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr5:113696800-113698000	Bivalent Enhancer	Primary B cells from peripheral blood	blood

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