Variant report

Variant	nsv829878
Chromosome Location	chr4:20966047-21138626
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	chr4:20985747-20986024	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:21132270-21132579	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:21132290-21132590	K562	blood:	n/a	n/a
4	BHLHE40	chr4:21091805-21092242	GM12878	blood:	n/a	n/a
5	CCNT2	chr4:21050255-21050426	K562	blood:	n/a	n/a
6	CEBPB	chr4:20995636-20995925	HepG2	liver:	n/a	chr4:20995796-20995807
7	CEBPB	chr4:21007405-21007666	ECC-1	luminal epithelium:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
8	CEBPB	chr4:21016084-21016366	H1-hESC	embryonic stem cell:	n/a	chr4:21016190-21016201
9	CEBPB	chr4:21047845-21048111	HepG2	liver:	n/a	chr4:21047991-21048002 chr4:21047990-21048001 chr4:21047990-21048003 chr4:21047990-21048003 chr4:21047990-21048003 chr4:21047989-21048006
10	CEBPB	chr4:21007300-21007662	H1-hESC	embryonic stem cell:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
11	CEBPB	chr4:21007315-21007659	HepG2	liver:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
12	CEBPB	chr4:21007296-21007654	K562	blood:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
13	CEBPB	chr4:20995666-20995866	A549	lung:	n/a	chr4:20995796-20995807
14	CEBPB	chr4:21016058-21016322	IMR90	lung:	n/a	chr4:21016190-21016201
15	CEBPB	chr4:21004945-21004966	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:21007300-21007669	IMR90	lung:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
17	CEBPB	chr4:21007301-21007644	A549	lung:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
18	CEBPB	chr4:21016698-21016997	IMR90	lung:	n/a	chr4:21016833-21016844
19	CEBPB	chr4:21016036-21016344	K562	blood:	n/a	chr4:21016190-21016201
20	CEBPB	chr4:21078163-21078442	HepG2	liver:	n/a	chr4:21078293-21078304
21	CEBPB	chr4:21016039-21016354	HepG2	liver:	n/a	chr4:21016190-21016201
22	CEBPB	chr4:21016785-21016985	HepG2	liver:	n/a	chr4:21016833-21016844
23	CEBPB	chr4:21079594-21079818	HepG2	liver:	n/a	n/a
24	CEBPB	chr4:21065859-21066502	HepG2	liver:	n/a	chr4:21065976-21065987 chr4:21065974-21065985
25	CEBPB	chr4:21016074-21016346	A549	lung:	n/a	chr4:21016190-21016201
26	CEBPB	chr4:21007324-21007642	Hela-S3	cervix:	n/a	chr4:21007478-21007489 chr4:21007479-21007488 chr4:21007479-21007488 chr4:21007477-21007490 chr4:21007479-21007488
27	CHD2	chr4:21091717-21092028	GM12878	blood:	n/a	n/a
28	CTCF	chr4:21136760-21136910	NHDF-neo	bronchial:	n/a	chr4:21136808-21136826
29	CTCF	chr4:21136740-21136890	HMF	breast:	n/a	chr4:21136808-21136826
30	CTCF	chr4:21136699-21136935	Medullo	brain:	n/a	chr4:21136808-21136826
31	CTCF	chr4:21136740-21136890	NHEK	skin:	n/a	chr4:21136808-21136826
32	CTCF	chr4:21136740-21136890	HRPEpiC	eye:	n/a	chr4:21136808-21136826
33	CTCF	chr4:21136603-21136980	GM12878	blood:	n/a	chr4:21136808-21136826
34	CTCF	chr4:21136774-21136883	Spleen_OC	spleen:	n/a	chr4:21136808-21136826
35	CTCF	chr4:21136725-21136932	LNCaP	prostate:	n/a	chr4:21136808-21136826
36	CTCF	chr4:21136720-21136870	HMEC	breast:	n/a	chr4:21136808-21136826
37	CTCF	chr4:21036460-21036610	HepG2	liver:	n/a	n/a
38	CTCF	chr4:21036469-21036568	NHEK	skin:	n/a	n/a
39	CTCF	chr4:21136406-21137176	SK-N-SH	brain:	n/a	chr4:21136808-21136826
40	CTCF	chr4:21136700-21136850	MCF-7	breast:	n/a	chr4:21136808-21136826
41	CTCF	chr4:20988900-20989050	MCF-7	breast:	n/a	chr4:20989007-20989028
42	CTCF	chr4:21136780-21136930	HVMF	connective:	n/a	chr4:21136808-21136826
43	CTCF	chr4:21136820-21136970	HAc	cerebellar:	n/a	n/a
44	CTCF	chr4:21136800-21136950	NHDF-neo	bronchial:	n/a	chr4:21136808-21136826
45	CTCF	chr4:21136760-21136910	HCPEpiC	choroid plexus:	n/a	chr4:21136808-21136826
46	CTCF	chr4:21136720-21136870	AG10803	skin:	n/a	chr4:21136808-21136826
47	CTCF	chr4:21136700-21136850	AG10803	skin:	n/a	chr4:21136808-21136826
48	CTCF	chr4:21136684-21136900	SK-N-SH_RA	brain:	n/a	chr4:21136808-21136826
49	CTCF	chr4:21136700-21136850	HBMEC	blood vessel:	n/a	chr4:21136808-21136826
50	CTCF	chr4:21136820-21136970	HCFaa	heart:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:21004400-21004450	HMEC	breast:	n/a
2	chr4:21004400-21004450	HMEC	breast:	n/a
3	chr4:20985984-20986034	GM19239	blood:	n/a
4	chr4:20988275-20988325	MCF-7	breast:	n/a
5	chr4:20985623-20985673	AG09309	skin:	n/a
6	chr4:20985696-20985746	SK-N-MC	brain:	n/a
7	chr4:20985696-20985746	Hepatocyte	liver:	n/a
8	chr4:20985623-20985673	HEK293	kidney:	embryo
9	chr4:20985927-20985977	IMR90	lung:	fetal
10	chr4:20986246-20986296	BJ	skin:	n/a
11	chr4:20985696-20985746	NH-A	brain:	n/a
12	chr4:20985984-20986034	SAEC	small airway:	n/a
13	chr4:20986246-20986296	SK-N-SH_RA	brain:	n/a
14	chr4:20985696-20985746	MCF10A-Er-Src	breast:	n/a
15	chr4:21004400-21004450	HCPEpiC	choroid plexus:	n/a
16	chr4:21004400-21004450	H1-hESC	embryonic stem cell:	embryo
17	chr4:20988275-20988325	HL-60	blood:	n/a
18	chr4:21039877-21039927	BJ	skin:	n/a
19	chr4:21039877-21039927	IMR90	lung:	fetal
20	chr4:20985696-20985746	NHBE	bronchial:	n/a
21	chr4:20985696-20985746	BJ	skin:	n/a
22	chr4:21004400-21004450	NB4	blood:	n/a
23	chr4:21004400-21004450	BJ	skin:	n/a
24	chr4:21039877-21039927	NB4	blood:	n/a
25	chr4:20985623-20985673	ECC-1	luminal epithelium:	n/a
26	chr4:20988275-20988325	ProgFib	skin:	n/a
27	chr4:21004400-21004450	U87	brain:	n/a
28	chr4:20985696-20985746	PANC-1	pancreas:	n/a
29	chr4:20985623-20985673	GM06990	blood:	n/a
30	chr4:20985696-20985746	GM19239	blood:	n/a
31	chr4:20985984-20986034	T-47D	breast:	n/a
32	chr4:20985927-20985977	H1-hESC	embryonic stem cell:	embryo
33	chr4:20985623-20985673	K562	blood:	n/a
34	chr4:20985984-20986034	BE2_C	brain:	n/a
35	chr4:21120300-21120350	HIPEpiC	eye:	n/a
36	chr4:20985623-20985673	HUVEC	blood vessel:	n/a
37	chr4:20985696-20985746	AoSMC	blood vessel:	n/a
38	chr4:20985696-20985746	U87	brain:	n/a
39	chr4:20988275-20988325	HRCEpiC	kidney:	n/a
40	chr4:20985927-20985977	AG10803	skin:	n/a
41	chr4:20986246-20986296	HMEC	breast:	n/a
42	chr4:20985984-20986034	AG09319	gingival:	n/a
43	chr4:21120300-21120350	HUVEC	blood vessel:	n/a
44	chr4:20985927-20985977	BE2_C	brain:	n/a
45	chr4:21039877-21039927	NT2-D1	testis:	n/a
46	chr4:20985623-20985673	T-47D	breast:	n/a
47	chr4:20985927-20985977	ProgFib	skin:	n/a
48	chr4:20985623-20985673	GM12892	blood:	n/a
49	chr4:21120300-21120350	AG04450	lung:	fetal
50	chr4:21120300-21120350	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
2	chr4:20774939..20775520-chr4:21136553..21137202,2	MCF-7	breast:
3	chr4:21099804..21101899-chr4:21102257..21105155,2	K562	blood:
4	chr1:217085881..217086616-chr4:21121511..21122023,2	MCF-7	breast:
5	chr4:20774749..20775678-chr4:21136384..21137379,5	MCF-7	breast:
6	chr4:21099804..21101899-chr4:21102257..21105155,2	K562	blood:
7	chr4:21002667..21005415-chr4:21005443..21008347,2	K562	blood:
8	chr1:147804723..147806420-chr4:20979153..20981320,2	MCF-7	breast:
9	chr4:20966569..20968200-chr4:20971149..20973804,2	K562	blood:
10	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
11	chr4:20971332..20974110-chr4:20975805..20978136,2	K562	blood:
12	chr4:21002667..21005415-chr4:21005443..21008347,2	K562	blood:

Variant related genes	Relation type
KCNIP4	TF binding region
KCNIP4	CpG island

Extended variants
information (count: 3135 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3135 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572468338	chr4:20984808-20984809	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs12643593	chr4:20984833-20984834	Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs75028503	chr4:20984859-20984860	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs538966320	chr4:20984915-20984916	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs555189255	chr4:20984930-20984931	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs577029956	chr4:20984944-20984945	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs76335412	chr4:20984965-20984966	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs77805910	chr4:20984992-20984993	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529837354	chr4:20984994-20984995	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs201949257	chr4:20984996-20984997	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs142375861	chr4:20984997-20984998	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs150872869	chr4:20985018-20985019	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs551719020	chr4:20985055-20985056	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs192908105	chr4:20985070-20985071	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs184940600	chr4:20985111-20985112	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs139377548	chr4:20985137-20985138	Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs6841954	chr4:20985138-20985139	Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs535994545	chr4:20985208-20985209	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs554311579	chr4:20985210-20985211	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs566138496	chr4:20985222-20985223	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs116251508	chr4:20985234-20985235	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs558157908	chr4:20985256-20985257	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs150040463	chr4:20985272-20985273	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs146628229	chr4:20985338-20985339	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs531040759	chr4:20985351-20985352	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs551241769	chr4:20985378-20985379	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs199583869	chr4:20985468-20985469	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
28	rs200719857	chr4:20985469-20985470	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
29	rs35856772	chr4:20985568-20985569	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs374425466	chr4:20985579-20985580	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs190080017	chr4:20985583-20985584	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs574547298	chr4:20985616-20985617	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs541582115	chr4:20985623-20985624	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs141429011	chr4:20985624-20985625	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs192914658	chr4:20985631-20985632	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs566073586	chr4:20985772-20985773	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs5856591	chr4:20985773-20985774	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs543699998	chr4:20985774-20985775	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs2322845	chr4:20985777-20985778	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs79736481	chr4:20985778-20985779	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs113031010	chr4:20985779-20985780	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs189392649	chr4:20985786-20985787	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs532074629	chr4:20985825-20985826	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs181986472	chr4:20985845-20985846	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs550206639	chr4:20985868-20985869	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs568691655	chr4:20985884-20985885	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs4292324	chr4:20985896-20985897	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs143959721	chr4:20985916-20985917	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs184985845	chr4:20985932-20985933	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs375591141	chr4:20985941-20985942	Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	17908972	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20984800-20985400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
2	chr4:20984800-20986200	Active TSS	Rectal Smooth Muscle	rectum
3	chr4:20984800-20986400	Active TSS	Duodenum Smooth Muscle	Duodenum
4	chr4:20985000-20985200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
5	chr4:20985000-20985400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
6	chr4:20985000-20986600	Active TSS	Colon Smooth Muscle	Colon
7	chr4:20985200-20985400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
8	chr4:20985200-20985400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
9	chr4:20985200-20985400	Active TSS	Fetal Stomach	stomach
10	chr4:20985200-20985600	Active TSS	H1 Cell Line	embryonic stem cell
11	chr4:20985200-20985600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
12	chr4:20985200-20986000	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr4:20985200-20986200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
14	chr4:20985400-20985600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr4:20985400-20985600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:20985400-20985600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:20985400-20985600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
18	chr4:20985400-20985600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
19	chr4:20985400-20985600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:20985400-20985600	Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr4:20985400-20985600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr4:20985400-20985600	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr4:20985400-20985600	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
24	chr4:20985400-20985600	Active TSS	Stomach Smooth Muscle	stomach
25	chr4:20985400-20985600	Bivalent/Poised TSS	HUVEC	blood vessel
26	chr4:20985400-20985800	Active TSS	Brain Hippocampus Middle	brain
27	chr4:20985400-20985800	Bivalent/Poised TSS	Fetal Kidney	kidney
28	chr4:20985400-20986000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:20985400-20986000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr4:20985400-20986000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
31	chr4:20985400-20986000	Active TSS	Brain Anterior Caudate	brain
32	chr4:20985400-20986000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
33	chr4:20985400-20986000	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr4:20985400-20986000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr4:20985400-20986200	Active TSS	H9 Cell Line	embryonic stem cell
36	chr4:20985400-20986200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
37	chr4:20985400-20986200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
38	chr4:20985400-20986200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
39	chr4:20985400-20986200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:20985400-20986200	Active TSS	Brain Germinal Matrix	brain
41	chr4:20985400-20986200	Active TSS	Fetal Brain Female	brain
42	chr4:20985400-20986200	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
43	chr4:20985400-20986400	Bivalent Enhancer	Fetal Brain Male	brain
44	chr4:20985600-20985800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
45	chr4:20985600-20985800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr4:20985600-20985800	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr4:20985600-20985800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:20985600-20985800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr4:20985600-20985800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
50	chr4:20985600-20985800	Enhancers	Ovary	ovary

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