Variant report

Variant	nsv872425
Chromosome Location	chr1:151325055-151413790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1684)
CpG islands
(count:1650)
Chromatin interactive
region (count:244)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:1684 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151371733-151372165	HepG2	liver:	n/a	chr1:151372120-151372135
2	ARID3A	chr1:151371751-151372339	K562	blood:	n/a	chr1:151372120-151372135
3	ARID3A	chr1:151345015-151345215	HepG2	liver:	n/a	n/a
4	ATF1	chr1:151371742-151372196	K562	blood:	n/a	n/a
5	ATF1	chr1:151357084-151357455	K562	blood:	n/a	n/a
6	ATF2	chr1:151371724-151372171	GM12878	blood:	n/a	n/a
7	ATF2	chr1:151371732-151372222	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:151371634-151372180	GM12878	blood:	n/a	n/a
9	ATF2	chr1:151371626-151372256	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr1:151371725-151372346	A549	lung:	n/a	n/a
11	ATF3	chr1:151368851-151369032	K562	blood:	n/a	n/a
12	BACH1	chr1:151405126-151405250	K562	blood:	n/a	n/a
13	BACH1	chr1:151405549-151405676	K562	blood:	n/a	n/a
14	BACH1	chr1:151371808-151372310	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr1:151375014-151375704	A549	lung:	n/a	n/a
16	BCL3	chr1:151345733-151346070	GM12878	blood:	n/a	n/a
17	BCL3	chr1:151372480-151372962	GM12878	blood:	n/a	n/a
18	BCL3	chr1:151371666-151372235	A549	lung:	n/a	chr1:151372009-151372018
19	BCL3	chr1:151371693-151373473	A549	lung:	n/a	chr1:151372009-151372018
20	BCL3	chr1:151373524-151374156	A549	lung:	n/a	n/a
21	BCLAF1	chr1:151371605-151372282	GM12878	blood:	n/a	chr1:151372009-151372018
22	BCLAF1	chr1:151371705-151372350	GM12878	blood:	n/a	chr1:151372009-151372018
23	BHLHE40	chr1:151345650-151345906	HepG2	liver:	n/a	n/a
24	BHLHE40	chr1:151342372-151343265	K562	blood:	n/a	n/a
25	BHLHE40	chr1:151344946-151345289	K562	blood:	n/a	n/a
26	BHLHE40	chr1:151356747-151357326	K562	blood:	n/a	n/a
27	BRCA1	chr1:151345169-151345211	HepG2	liver:	n/a	n/a
28	BRCA1	chr1:151371813-151372175	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr1:151372596-151372778	H1-hESC	embryonic stem cell:	n/a	n/a
30	CBX3	chr1:151334672-151335188	K562	blood:	n/a	n/a
31	CBX3	chr1:151324469-151325208	K562	blood:	n/a	n/a
32	CBX3	chr1:151358593-151358947	K562	blood:	n/a	n/a
33	CBX3	chr1:151371662-151372200	K562	blood:	n/a	n/a
34	CBX3	chr1:151360096-151360428	K562	blood:	n/a	n/a
35	CBX3	chr1:151324783-151325152	K562	blood:	n/a	n/a
36	CBX3	chr1:151342983-151343411	K562	blood:	n/a	n/a
37	CBX3	chr1:151334633-151335302	K562	blood:	n/a	n/a
38	CCNT2	chr1:151357075-151357435	K562	blood:	n/a	n/a
39	CCNT2	chr1:151372277-151372477	K562	blood:	n/a	n/a
40	CCNT2	chr1:151343082-151343282	K562	blood:	n/a	n/a
41	CEBPB	chr1:151343887-151344177	A549	lung:	n/a	n/a
42	CEBPB	chr1:151342723-151343113	K562	blood:	n/a	n/a
43	CEBPB	chr1:151371698-151372133	A549	lung:	n/a	chr1:151371884-151371895
44	CEBPB	chr1:151372556-151372600	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:151343870-151344239	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr1:151371684-151372272	GM12878	blood:	n/a	chr1:151371884-151371895
47	CEBPB	chr1:151388726-151389184	ECC-1	luminal epithelium:	n/a	chr1:151388928-151388939
48	CEBPB	chr1:151407654-151407997	IMR90	lung:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
49	CEBPB	chr1:151388780-151389068	HepG2	liver:	n/a	chr1:151388928-151388939
50	CEBPB	chr1:151372559-151372585	Hela-S3	cervix:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151345771-151345821	AG04450	lung:	fetal
2	chr1:151372228-151372278	HPAEpiC	pulmonary alveolar:	n/a
3	chr1:151370645-151370695	GM19239	blood:	n/a
4	chr1:151345771-151345821	AG04450	lung:	fetal
5	chr1:151372228-151372278	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:151370645-151370695	GM19239	blood:	n/a
7	chr1:151371285-151371335	HL-60	blood:	n/a
8	chr1:151345123-151345173	GM19239	blood:	n/a
9	chr1:151372581-151372631	HL-60	blood:	n/a
10	chr1:151372228-151372278	Hela-S3	cervix:	n/a
11	chr1:151369469-151369519	HUVEC	blood vessel:	n/a
12	chr1:151369469-151369519	HAEpiC	amniotic membrane:	n/a
13	chr1:151372652-151372702	LNCaP	prostate:	n/a
14	chr1:151346400-151346450	HNPCEpiC	eye:	n/a
15	chr1:151372581-151372631	HRCEpiC	kidney:	n/a
16	chr1:151371944-151371994	CMK	blood:	n/a
17	chr1:151336795-151336845	BJ	skin:	n/a
18	chr1:151343840-151343890	SAEC	small airway:	n/a
19	chr1:151372572-151372622	IMR90	lung:	fetal
20	chr1:151372228-151372278	HNPCEpiC	eye:	n/a
21	chr1:151371285-151371335	SK-N-SH_RA	brain:	n/a
22	chr1:151372652-151372702	GM19239	blood:	n/a
23	chr1:151370645-151370695	HEK293	kidney:	embryo
24	chr1:151345123-151345173	Hela-S3	cervix:	n/a
25	chr1:151370645-151370695	ECC-1	luminal epithelium:	n/a
26	chr1:151346122-151346172	K562	blood:	n/a
27	chr1:151372572-151372622	SK-N-SH	brain:	n/a
28	chr1:151344806-151344856	HEK293	kidney:	embryo
29	chr1:151371285-151371335	AG09319	gingival:	n/a
30	chr1:151399683-151399733	GM19239	blood:	n/a
31	chr1:151372147-151372197	BJ	skin:	n/a
32	chr1:151372581-151372631	Jurkat	blood:	n/a
33	chr1:151372581-151372631	AG09319	gingival:	n/a
34	chr1:151402121-151402171	NB4	blood:	n/a
35	chr1:151371944-151371994	BJ	skin:	n/a
36	chr1:151344806-151344856	NHDF-neo	bronchial:	n/a
37	chr1:151346048-151346098	IMR90	lung:	fetal
38	chr1:151371309-151371359	T-47D	breast:	n/a
39	chr1:151336795-151336845	NH-A	brain:	n/a
40	chr1:151345771-151345821	HAEpiC	amniotic membrane:	n/a
41	chr1:151369469-151369519	NHBE	bronchial:	n/a
42	chr1:151402121-151402171	AG09309	skin:	n/a
43	chr1:151346122-151346172	PFSK-1	brain:	n/a
44	chr1:151372652-151372702	H1-hESC	embryonic stem cell:	embryo
45	chr1:151372147-151372197	HCF	heart:	n/a
46	chr1:151346122-151346172	HRE	kidney:	n/a
47	chr1:151345248-151345298	NHBE	bronchial:	n/a
48	chr1:151345248-151345298	PANC-1	pancreas:	n/a
49	chr1:151369469-151369519	NHDF-neo	bronchial:	n/a
50	chr1:151372581-151372631	SKMC	muscle:	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type	Cell Stage
1	1:151171193-151178589..1:151411623-151426875	GM12878	blood:
2	chr1:151351127..151353952-chr1:151357831..151359391,2	K562	blood:
3	chr1:151340911..151342650-chr1:151344414..151346132,2	K562	blood:
4	chr1:151344758..151345571-chr1:151371234..151372258,3	MCF-7	breast:
5	chr1:151400148..151402604-chr1:151403204..151405612,2	MCF-7	breast:
6	chr1:151332835..151334750-chr1:151336636..151339074,2	K562	blood:
7	chr1:151394927..151396962-chr1:151399900..151402085,2	K562	blood:
8	chr1:151319532..151321750-chr1:151328271..151330103,3	K562	blood:
9	chr1:151370719..151373828-chr1:151394792..151398021,4	MCF-7	breast:
10	chr1:151272157..151273670-chr1:151373944..151376221,2	MCF-7	breast:
11	1:151270864-151283078..1:151378579-151379560	H1-hESC	embryonic stem cell:	embryo
12	1:151393910-151394636..1:151516085-151535167	GM12878	blood:
13	1:151333184-151350267..1:151592347-151603110	K562	blood:
14	chr1:151351127..151353952-chr1:151357831..151359391,2	K562	blood:
15	chr1:151319634..151321435-chr1:151323050..151325074,3	K562	blood:
16	1:151402394-151411623..1:151516085-151535167	GM12878	blood:
17	chr1:151211452..151213818-chr1:151375380..151378253,2	K562	blood:
18	1:151158061-151171193..1:151375897-151378579	K562	blood:
19	chr1:151380793..151382979-chr1:151735863..151737514,2	K562	blood:
20	chr1:151334136..151338213-chr1:151347669..151350682,3	MCF-7	breast:
21	chr1:151370915..151372636-chr1:151386697..151388263,2	K562	blood:
22	chr1:151352995..151355687-chr1:151371966..151374635,2	MCF-7	breast:
23	1:151329948-151333184..1:151516085-151535167	Hela-S3	cervix:
24	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
25	chr1:151371234..151374091-chr1:151403253..151406283,3	K562	blood:
26	chr1:151324405..151326399-chr1:151329640..151331142,2	MCF-7	breast:
27	chr1:151313664..151315822-chr1:151337463..151339471,3	MCF-7	breast:
28	chr1:151404848..151406397-chr1:151409975..151412744,2	MCF-7	breast:
29	chr1:151317450..151322791-chr1:151370457..151374000,10	MCF-7	breast:
30	chr1:151370990..151372636-chr1:151386252..151388197,2	K562	blood:
31	chr1:151328228..151331162-chr1:151332669..151334329,2	MCF-7	breast:
32	chr1:151373766..151375598-chr1:151437855..151440411,2	K562	blood:
33	chr1:151318199..151320967-chr1:151371516..151373553,2	K562	blood:
34	chr1:151341829..151344340-chr1:151348347..151350090,2	K562	blood:
35	1:151180715-151199990..1:151402394-151411623	GM12878	blood:
36	chr1:151348976..151351066-chr1:151352472..151354650,2	K562	blood:
37	chr1:151343171..151345745-chr1:151364677..151366498,2	MCF-7	breast:
38	chr1:151363150..151367072-chr1:151371054..151375745,5	MCF-7	breast:
39	chr1:151353527..151355666-chr1:151374191..151375959,2	K562	blood:
40	chr1:151318980..151319798-chr1:151371884..151372449,2	MCF-7	breast:
41	chr1:151379590..151381378-chr1:151394172..151396237,2	MCF-7	breast:
42	chr1:151377630..151380310-chr1:151382827..151386169,3	K562	blood:
43	1:151411623-151426875..1:151592347-151603110	GM12878	blood:
44	1:151270864-151283078..1:151358657-151368243	K562	blood:
45	chr1:151161951..151163611-chr1:151344546..151346783,2	MCF-7	breast:
46	chr1:151318180..151322621-chr1:151370786..151375600,7	K562	blood:
47	chr1:151298277..151300050-chr1:151330058..151331618,2	MCF-7	breast:
48	chr1:151273322..151275078-chr1:151370486..151372389,2	MCF-7	breast:
49	chr1:151337000..151339561-chr1:151374303..151377046,2	MCF-7	breast:
50	chr1:151268846..151270969-chr1:151374087..151376100,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSMB4-2	chr1:151413618-151413745	NONHSAT006396

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	POGZ	hsa-miR-9-5p	chr1:151377089-151377112
2	SELENBP1	hsa-miR-335-5p	chr1:151336816-151336837
3	SELENBP1	hsa-miR-92a-3p	chr1:151336887-151336908
4	POGZ	hsa-miR-19b-3p	chr1:151376496-151376518
5	POGZ	hsa-miR-221-3p	chr1:151376785-151376779
6	POGZ	hsa-miR-34a-5p	chr1:151376091-151376084
7	POGZ	hsa-miR-221-3p	chr1:151376779-151376802
8	POGZ	hsa-miR-34a-5p	chr1:151376085-151376106
9	POGZ	hsa-miR-17-5p	chr1:151376717-151376739
10	POGZ	hsa-miR-20a-5p	chr1:151376717-151376739
11	POGZ	hsa-miR-130b-3p	chr1:151376495-151376516

Variant related genes	Relation type
SELENBP1	TF binding region
POGZ	TF binding region
PSMB4	TF binding region
RNY4P25	TF binding region
SELENBP1	CpG island
POGZ	CpG island
PSMB4	CpG island
RNY4P25	CpG island
ENSG00000143450	chromatin interactions
ENSG00000265753	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000143393	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000252840	chromatin interactions
ENSG00000119878	chromatin interactions
ENSG00000163159	chromatin interactions
ENSG00000143436	chromatin interactions
ENSG00000225556	chromatin interactions
ENSG00000159377	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000163141	chromatin interactions
ENSG00000197622	chromatin interactions
ENSG00000224645	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000151665	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000143416	chromatin interactions
ENSG00000237976	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000238711	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000143375	chromatin interactions
ENSG00000143376	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000273481	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000159352	chromatin interactions

Extended variants
information (count: 3458 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:3458 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2800946	chr1:151325055-151325056	Weak transcription	Chromatin interactive region	17 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553492075	chr1:151325056-151325057	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
3	rs573839820	chr1:151325059-151325060	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs542573344	chr1:151325094-151325095	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
5	rs562646734	chr1:151325097-151325098	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
6	rs143092977	chr1:151325105-151325106	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
7	rs61818010	chr1:151325122-151325123	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
8	rs372998883	chr1:151325144-151325145	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
9	rs368349357	chr1:151325150-151325151	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
10	rs564613883	chr1:151325174-151325175	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
11	rs533167290	chr1:151325203-151325204	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
12	rs575930649	chr1:151325219-151325220	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
13	rs191507361	chr1:151325240-151325241	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
14	rs576518727	chr1:151325254-151325255	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
15	rs529555309	chr1:151325255-151325256	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
16	rs146142083	chr1:151325322-151325323	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
17	rs543121117	chr1:151325325-151325326	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
18	rs140139570	chr1:151325344-151325345	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
19	rs116042514	chr1:151325375-151325376	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
20	rs576888011	chr1:151325396-151325397	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
21	rs35517466	chr1:151325397-151325398	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
22	rs570116267	chr1:151325421-151325422	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
23	rs375392987	chr1:151325427-151325428	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
24	rs7531495	chr1:151325472-151325473	Weak transcription	Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs182528487	chr1:151325562-151325563	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
26	rs11588030	chr1:151325595-151325596	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
27	rs7517408	chr1:151325600-151325601	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
28	rs7531658	chr1:151325612-151325613	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
29	rs7531663	chr1:151325617-151325618	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
30	rs553696389	chr1:151325645-151325646	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
31	rs187175721	chr1:151325748-151325749	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
32	rs573578231	chr1:151325805-151325806	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
33	rs145860590	chr1:151325811-151325812	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
34	rs573178928	chr1:151325858-151325859	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
35	rs369263729	chr1:151325861-151325862	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
36	rs72710106	chr1:151325879-151325880	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
37	rs556534479	chr1:151325936-151325937	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
38	rs2800947	chr1:151325947-151325948	Weak transcription	Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs149390763	chr1:151325991-151325992	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
40	rs531561586	chr1:151326017-151326018	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
41	rs565074510	chr1:151326040-151326041	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs191255948	chr1:151326065-151326066	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs374176200	chr1:151326087-151326088	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs540384820	chr1:151326107-151326108	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
45	rs560509593	chr1:151326143-151326144	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
46	rs529297008	chr1:151326159-151326160	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
47	rs549249063	chr1:151326182-151326183	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
48	rs184631017	chr1:151326184-151326185	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
49	rs190307789	chr1:151326193-151326194	Weak transcription	Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
50	rs2800948	chr1:151326215-151326216	Weak transcription	Chromatin interactive region	16 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21138945	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2347 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151320600-151326800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:151325000-151325400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:151327000-151328200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:151328000-151328200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:151328200-151328400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:151328200-151328400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:151328400-151328600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr1:151328400-151328600	Enhancers	K562	blood
9	chr1:151328400-151334600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:151328400-151336000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:151328600-151329200	Weak transcription	K562	blood
12	chr1:151328600-151334800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr1:151329200-151329400	Enhancers	Osteobl	bone
14	chr1:151329200-151329800	Enhancers	K562	blood
15	chr1:151329400-151329600	Enhancers	Colonic Mucosa	Colon
16	chr1:151329400-151329800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr1:151329400-151340600	Weak transcription	Osteobl	bone
18	chr1:151329600-151336600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr1:151329600-151336800	Weak transcription	Colonic Mucosa	Colon
20	chr1:151329800-151334400	Weak transcription	K562	blood
21	chr1:151329800-151334600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:151331400-151334600	Weak transcription	Lung	lung
23	chr1:151331600-151334600	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr1:151331600-151334800	Weak transcription	Right Ventricle	heart
25	chr1:151332200-151334600	Weak transcription	Fetal Intestine Small	intestine
26	chr1:151332200-151334800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr1:151332200-151340000	Weak transcription	Fetal Heart	heart
28	chr1:151332600-151334400	Weak transcription	Fetal Lung	lung
29	chr1:151332600-151336200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:151333200-151336800	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr1:151333400-151333600	Enhancers	Spleen	Spleen
32	chr1:151333600-151334600	Weak transcription	Spleen	Spleen
33	chr1:151333800-151334400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:151333800-151335400	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr1:151334000-151336000	Weak transcription	Left Ventricle	heart
36	chr1:151334000-151336000	Weak transcription	Stomach Smooth Muscle	stomach
37	chr1:151334400-151335600	ZNF genes & repeats	K562	blood
38	chr1:151334400-151336400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr1:151334400-151341600	Strong transcription	Fetal Lung	lung
40	chr1:151334600-151335000	ZNF genes & repeats	Fetal Kidney	kidney
41	chr1:151334600-151335200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
42	chr1:151334600-151335200	ZNF genes & repeats	Brain Substantia Nigra	brain
43	chr1:151334600-151335200	ZNF genes & repeats	Pancreas	Pancrea
44	chr1:151334600-151335200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
45	chr1:151334600-151335400	ZNF genes & repeats	Gastric	stomach
46	chr1:151334600-151335400	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr1:151334600-151335400	ZNF genes & repeats	Spleen	Spleen
48	chr1:151334600-151335600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:151334600-151335600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr1:151334600-151335600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin

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