Variant report

Variant	nsv519429
Chromosome Location	chr1:242807999-243338216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2904)
CpG islands
(count:1589)
Chromatin interactive
region (count:32)
LncRNA
region (count:68)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2904 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:243265016-243265233	K562	blood:	n/a	n/a
2	ARID3A	chr1:243088083-243088303	K562	blood:	n/a	n/a
3	ARID3A	chr1:243269320-243269342	K562	blood:	n/a	n/a
4	ATF1	chr1:243148543-243148578	K562	blood:	n/a	n/a
5	ATF1	chr1:243264723-243265401	K562	blood:	n/a	n/a
6	ATF1	chr1:243265917-243265988	K562	blood:	n/a	n/a
7	ATF1	chr1:243314340-243314430	K562	blood:	n/a	n/a
8	ATF1	chr1:243269266-243269450	K562	blood:	n/a	n/a
9	ATF2	chr1:243264845-243265326	GM12878	blood:	n/a	n/a
10	ATF2	chr1:242976778-242977056	GM12878	blood:	n/a	n/a
11	ATF3	chr1:243264891-243265281	K562	blood:	n/a	n/a
12	ATF3	chr1:243268452-243268665	K562	blood:	n/a	n/a
13	ATF3	chr1:243264888-243265345	GM12878	blood:	n/a	n/a
14	ATF3	chr1:243264834-243265328	K562	blood:	n/a	n/a
15	ATF3	chr1:243264822-243265305	K562	blood:	n/a	n/a
16	ATF3	chr1:243265013-243265180	GM12878	blood:	n/a	n/a
17	BACH1	chr1:242918799-242919176	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
19	BACH1	chr1:242848092-242848258	K562	blood:	n/a	n/a
20	BACH1	chr1:242996994-242996997	K562	blood:	n/a	n/a
21	BACH1	chr1:242907415-242907671	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr1:242908535-242908689	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr1:243264659-243265193	GM12878	blood:	n/a	n/a
24	BATF	chr1:243186903-243187203	GM12878	blood:	n/a	chr1:243187183-243187192
25	BATF	chr1:243178561-243178941	GM12878	blood:	n/a	n/a
26	BATF	chr1:243171378-243171664	GM12878	blood:	n/a	n/a
27	BATF	chr1:243225276-243225613	GM12878	blood:	n/a	n/a
28	BATF	chr1:243174180-243174389	GM12878	blood:	n/a	n/a
29	BATF	chr1:243182370-243182587	GM12878	blood:	n/a	n/a
30	BATF	chr1:243263835-243263995	GM12878	blood:	n/a	n/a
31	BATF	chr1:243186946-243187196	GM12878	blood:	n/a	chr1:243187183-243187192
32	BATF	chr1:243225252-243225590	GM12878	blood:	n/a	n/a
33	BATF	chr1:243178503-243178928	GM12878	blood:	n/a	n/a
34	BCL11A	chr1:243264570-243265004	GM12878	blood:	n/a	n/a
35	BCL11A	chr1:243169760-243169972	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:243153505-243153675	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:242976721-242977165	GM12878	blood:	n/a	chr1:242976959-242976968
38	BCL11A	chr1:243264959-243265161	GM12878	blood:	n/a	n/a
39	BCL11A	chr1:243178625-243178904	GM12878	blood:	n/a	chr1:243178799-243178808
40	BCL11A	chr1:243182297-243182573	GM12878	blood:	n/a	chr1:243182520-243182528 chr1:243182526-243182535
41	BCL11A	chr1:243172627-243172798	GM12878	blood:	n/a	n/a
42	BCL11A	chr1:243186357-243186528	GM12878	blood:	n/a	n/a
43	BCL11A	chr1:243171382-243171573	GM12878	blood:	n/a	n/a
44	BCL11A	chr1:243189520-243189781	GM12878	blood:	n/a	n/a
45	BCL11A	chr1:242976760-242977140	GM12878	blood:	n/a	chr1:242976959-242976968
46	BCL11A	chr1:243174177-243174356	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:243178550-243178986	GM12878	blood:	n/a	chr1:243178799-243178808
48	BCL3	chr1:242843399-242843681	GM12878	blood:	n/a	n/a
49	BCL3	chr1:242843343-242843676	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:243264981-243265237	K562	blood:	n/a	n/a

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243219082-243219132	GM19239	blood:	n/a
2	chr1:243053425-243053475	Caco-2	colon:	n/a
3	chr1:243218706-243218756	HRE	kidney:	n/a
4	chr1:243219082-243219132	GM19239	blood:	n/a
5	chr1:243053425-243053475	Caco-2	colon:	n/a
6	chr1:243218706-243218756	HRE	kidney:	n/a
7	chr1:243265016-243265066	HCPEpiC	choroid plexus:	n/a
8	chr1:243053934-243053984	RPTEC	kidney:	n/a
9	chr1:243057080-243057130	A549	lung:	n/a
10	chr1:243217947-243217997	HEK293	kidney:	embryo
11	chr1:243270834-243270884	K562	blood:	n/a
12	chr1:243053425-243053475	MCF10A-Er-Src	breast:	n/a
13	chr1:243217947-243217997	ProgFib	skin:	n/a
14	chr1:243053865-243053915	NHDF-neo	bronchial:	n/a
15	chr1:243267966-243268016	AG04450	lung:	fetal
16	chr1:243217776-243217826	HRPEpiC	eye:	n/a
17	chr1:243053865-243053915	HIPEpiC	eye:	n/a
18	chr1:243270834-243270884	HEEpiC	esophagus:	n/a
19	chr1:243263770-243263820	BJ	skin:	n/a
20	chr1:243054071-243054121	SK-N-SH	brain:	n/a
21	chr1:243288625-243288675	H1-hESC	embryonic stem cell:	embryo
22	chr1:243218706-243218756	A549	lung:	n/a
23	chr1:243053425-243053475	MCF-7	breast:	n/a
24	chr1:243053425-243053475	BJ	skin:	n/a
25	chr1:243326617-243326667	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:242937866-242937916	CMK	blood:	n/a
27	chr1:243138527-243138577	SK-N-SH	brain:	n/a
28	chr1:243270834-243270884	HAEpiC	amniotic membrane:	n/a
29	chr1:243267966-243268016	ECC-1	luminal epithelium:	n/a
30	chr1:243265317-243265367	PANC-1	pancreas:	n/a
31	chr1:243139525-243139575	GM06990	blood:	n/a
32	chr1:243219047-243219097	HMEC	breast:	n/a
33	chr1:243053934-243053984	HEEpiC	esophagus:	n/a
34	chr1:243053934-243053984	NH-A	brain:	n/a
35	chr1:243265317-243265367	ECC-1	luminal epithelium:	n/a
36	chr1:243053934-243053984	HCPEpiC	choroid plexus:	n/a
37	chr1:243053673-243053723	ovcar-3	ovarian:	n/a
38	chr1:243217776-243217826	K562	blood:	n/a
39	chr1:243138527-243138577	H1-hESC	embryonic stem cell:	embryo
40	chr1:243266520-243266570	RPTEC	kidney:	n/a
41	chr1:243053425-243053475	HCF	heart:	n/a
42	chr1:243139525-243139575	HCM	heart:	n/a
43	chr1:243267966-243268016	LNCaP	prostate:	n/a
44	chr1:243219082-243219132	PANC-1	pancreas:	n/a
45	chr1:243265317-243265367	HEK293	kidney:	embryo
46	chr1:243265317-243265367	AG09319	gingival:	n/a
47	chr1:243264842-243264892	Caco-2	colon:	n/a
48	chr1:243050875-243050925	K562	blood:	n/a
49	chr1:242874219-242874269	NB4	blood:	n/a
50	chr1:243053673-243053723	Jurkat	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:243278397..243280968-chr1:243284785..243287288,2	K562	blood:
2	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
3	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
4	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
5	chr1:243174257..243175773-chr22:20004723..20006804,2	K562	blood:
6	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
7	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
8	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
9	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
10	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:
11	chr1:242907367..242907987-chr1:242917774..242918489,2	MCF-7	breast:
12	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:
13	chr1:243278397..243280968-chr1:243284785..243287288,2	K562	blood:
14	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
15	chr1:242817323..242819787-chr1:242897350..242900264,2	K562	blood:
16	chr1:242989477..242991101-chr1:242991941..242994002,2	K562	blood:
17	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
18	chr1:242617838..242618342-chr1:242955947..242956813,2	MCF-7	breast:
19	chr1:243338186..243340389-chr1:243416495..243418782,3	K562	blood:
20	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
21	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:
22	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
23	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
24	chr1:243003845..243005366-chr1:243007691..243009298,2	K562	blood:
25	chr1:242938370..242940205-chr1:242949135..242951746,2	K562	blood:
26	chr1:243028922..243031643-chr1:243036505..243039074,2	K562	blood:
27	chr1:242998388..243001295-chr1:243002456..243004745,2	K562	blood:
28	chr1:243019974..243021671-chr1:243028235..243030687,2	K562	blood:
29	chr1:243028092..243030417-chr1:243031884..243034309,2	K562	blood:
30	chr1:243303841..243304368-chr4:119460604..119461246,3	MCF-7	breast:
31	chr1:242867321..242869149-chr1:242869227..242872156,2	MCF-7	breast:
32	chr1:242868996..242871474-chr1:242872273..242874608,2	K562	blood:

(count:68 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-1	chr1:243252623-243252681	ENSG00000214837.3
2	lnc-SDCCAG8-2	chr1:243331589-243331712	ENSG00000232085.1
3	lnc-CEP170-2	chr1:243202216-243202794	ENSG00000231512
4	lnc-CEP170-1	chr1:243259293-243259424	ENSG00000214837.3
5	lnc-CEP170-1	chr1:243230382-243230589	NONHSAT010586
6	lnc-AKT3-7	chr1:243289680-243289796	NONHSAT010597
7	lnc-CEP170-3	chr1:243170676-243170770	XLOC_001282
8	lnc-SDCCAG8-2	chr1:243327940-243327968	ENSG00000232085.1
9	lnc-CEP170-1	chr1:243255781-243255900	ENSG00000214837.3
10	lnc-CEP170-1	chr1:243222780-243222970	ENSG00000214837.3
11	lnc-CEP170-1	chr1:243232883-243233006	NONHSAT010586
12	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-
13	lnc-CEP170-1	chr1:243229479-243229543	NONHSAT010586
14	lnc-CEP170-3	chr1:243169714-243169980	XLOC_001282
15	lnc-CEP170-1	chr1:243245192-243245427	ENSG00000214837.3
16	lnc-CEP170-1	chr1:243222780-243222970	NONHSAT010586
17	lnc-CEP170-1	chr1:243239872-243239934	ENSG00000214837.3
18	lnc-SDCCAG8-2	chr1:243332528-243332747	ENSG00000232085.1
19	lnc-CEP170-1	chr1:243254833-243254898	ENSG00000214837.3
20	lnc-CEP170-1	chr1:243254693-243254898	ENSG00000214837.3
21	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-
22	lnc-CEP170-1	chr1:243230927-243231043	NONHSAT010586
23	lnc-CEP170-1	chr1:243255781-243255860	ENSG00000214837.3
24	lnc-CEP170-1	chr1:243220495-243220572	NONHSAT010586
25	lnc-CEP170-1	chr1:243232883-243233006	ENSG00000214837.3
26	lnc-CEP170-1	chr1:243254692-243254816	ENSG00000214837.3
27	lnc-CEP170-1	chr1:243220178-243220301	ENSG00000214837.3
28	lnc-CEP170-1	chr1:243229479-243229543	ENSG00000214837.3
29	lnc-CEP170-2	chr1:243194574-243194678	ENSG00000231512
30	lnc-SDCCAG8-3	chr1:243303255-243303890	ENSG00000227230.1
31	lnc-CEP170-1	chr1:243242290-243242354	ENSG00000214837.3
32	lnc-CEP170-1	chr1:243242159-243242354	ENSG00000214837.3
33	lnc-CEP170-2	chr1:243211014-243211171	ENSG00000231512
34	lnc-CEP170-1	chr1:243220666-243220723	NONHSAT010586
35	lnc-CEP170-3	chr1:243169147-243169576	XLOC_001282
36	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
37	lnc-CEP170-1	chr1:243239939-243239968	ENSG00000214837.3
38	lnc-CEP170-1	chr1:243230927-243231043	ENSG00000214837.3
39	lnc-CEP170-1	chr1:243220314-243220381	ENSG00000214837.3
40	lnc-CEP170-1	chr1:243230382-243230589	ENSG00000214837.3
41	lnc-CEP170-1	chr1:243220495-243220572	ENSG00000214837.3
42	lnc-CEP170-1	chr1:243245192-243245427	ENSG00000214837.3
43	lnc-CEP170-2	chr1:243211747-243211826	ENSG00000231512
44	lnc-AKT3-7	chr1:243289220-243289436	NONHSAT010597
45	lnc-CEP170-1	chr1:243220666-243220723	ENSG00000214837.3
46	lnc-CEP170-1	chr1:243230115-243230172	ENSG00000214837.3
47	lnc-CEP170-2	chr1:243192814-243193218	ENSG00000231512
48	lnc-CEP170-1	chr1:243254768-243254898	ENSG00000214837.3
49	lnc-SDCCAG8-3	chr1:243299200-243299257	ENSG00000227230.1
50	lnc-CEP170-1	chr1:243220533-243220572	ENSG00000214837.3

No data

Variant related genes	Relation type
ENSG00000231512	TF binding region
RNU6-747P	TF binding region
CEP170	TF binding region
ENSG00000214837	TF binding region
ENSG00000253326	TF binding region
ENSG00000234116	TF binding region
ENSG00000232085	TF binding region
ENSG00000230199	TF binding region
ENSG00000270859	TF binding region
ENSG00000270818	TF binding region
ENSG00000227230	TF binding region
RSL24D1P4	TF binding region
ENSG00000264972	TF binding region
ENSG00000231512	CpG island
RNU6-747P	CpG island
CEP170	CpG island
ENSG00000214837	CpG island
ENSG00000253326	CpG island
ENSG00000234116	CpG island
ENSG00000232085	CpG island
ENSG00000230199	CpG island
ENSG00000270859	CpG island
ENSG00000270818	CpG island
ENSG00000227230	CpG island
RSL24D1P4	CpG island
ENSG00000264972	CpG island
ENSG00000143702	chromatin interactions
LEPREL4	miRNA target sites
LEFTY2	miRNA target sites

Extended variants
information (count: 11169 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:11169 , 50 per page) page: 1 2 3 4 5 6 7 ... 224

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10926804	chr1:242807999-242808000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs183258304	chr1:242808005-242808006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs558920141	chr1:242808077-242808078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202240074	chr1:242808101-242808102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539107499	chr1:242808129-242808130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557593305	chr1:242808163-242808164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34031514	chr1:242808180-242808181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs202037723	chr1:242808196-242808197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376692145	chr1:242808200-242808201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544739809	chr1:242808257-242808258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143673492	chr1:242808259-242808260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369154083	chr1:242808261-242808262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs12145120	chr1:242808292-242808293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs561503698	chr1:242808297-242808298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542845141	chr1:242808298-242808299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547313246	chr1:242808302-242808303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566832148	chr1:242808321-242808322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539038527	chr1:242808326-242808327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10737883	chr1:242808341-242808342	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs10754770	chr1:242808353-242808354	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs561590689	chr1:242808374-242808375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs537989622	chr1:242808424-242808425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs192125936	chr1:242808445-242808446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12081723	chr1:242808483-242808484	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs10803065	chr1:242808496-242808497	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs532096487	chr1:242808502-242808503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552861060	chr1:242808518-242808519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145062588	chr1:242808556-242808557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184013699	chr1:242808582-242808583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545013995	chr1:242808604-242808605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79348073	chr1:242808657-242808658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575287017	chr1:242808662-242808663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544367286	chr1:242808708-242808709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373700629	chr1:242808709-242808710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72453411	chr1:242808710-242808711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111417853	chr1:242808711-242808712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71178422	chr1:242808722-242808723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs61297097	chr1:242808746-242808747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561419050	chr1:242808770-242808771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs138844498	chr1:242808794-242808795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs10803066	chr1:242808798-242808799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs56047182	chr1:242808838-242808839	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs537875688	chr1:242808930-242808931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs560788544	chr1:242808972-242808973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12184314	chr1:242808973-242808974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182596004	chr1:242809054-242809055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186872235	chr1:242809057-242809058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12184315	chr1:242809068-242809069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs192126537	chr1:242809075-242809076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs531829590	chr1:242809096-242809097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1368 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:242802200-242815400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr1:242807400-242811400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:242807600-242815600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:242809000-242809200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:242811400-242811800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:242815000-242815600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr1:242815000-242815600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr1:242815000-242816200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr1:242815400-242815800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr1:242815400-242815800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:242815400-242815800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr1:242815400-242815800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr1:242815400-242815800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:242815400-242816000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:242815400-242816200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:242815400-242816200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr1:242815600-242815800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr1:242820800-242821000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr1:242821200-242822400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr1:242822400-242823000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr1:242832600-242833000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:242833000-242834200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr1:242833400-242833600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:242835000-242836200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:242836000-242836200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr1:242836000-242836400	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr1:242836000-242836600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr1:242836000-242837000	Enhancers	Brain Substantia Nigra	brain
29	chr1:242836200-242836400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:242836200-242836400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
31	chr1:242836200-242836600	Enhancers	Brain Cingulate Gyrus	brain
32	chr1:242836200-242837000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr1:242836200-242837000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr1:242836200-242837000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr1:242836200-242837000	Enhancers	Brain Angular Gyrus	brain
36	chr1:242836200-242837200	Enhancers	Brain Hippocampus Middle	brain
37	chr1:242836400-242836600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr1:242836400-242837000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr1:242836400-242838200	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr1:242836600-242837000	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr1:242836600-242838600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr1:242837000-242837200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:242837000-242838000	Weak transcription	Brain Substantia Nigra	brain
44	chr1:242837200-242838400	Weak transcription	Brain Hippocampus Middle	brain
45	chr1:242837200-242838800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:242838000-242838800	Enhancers	Brain Substantia Nigra	brain
47	chr1:242838200-242854000	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr1:242838400-242838600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr1:242838600-242838800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr1:242838600-242838800	Enhancers	Brain Hippocampus Middle	brain

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