Variant report

Variant	nsv8380
Chromosome Location	chr1:151329887-151410346
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1619)
CpG islands
(count:1649)
Chromatin interactive
region (count:227)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:1619 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

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	chr1:151357084-151357455	K562	blood:	n/a	n/a
5	ATF1	chr1:151371742-151372196	K562	blood:	n/a	n/a
6	ATF2	chr1:151371732-151372222	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr1:151371626-151372256	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:151371634-151372180	GM12878	blood:	n/a	n/a
9	ATF2	chr1:151371724-151372171	GM12878	blood:	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	chr1:151345733-151346070	GM12878	blood:	n/a	n/a
16	BCL3	chr1:151371666-151372235	A549	lung:	n/a	chr1:151372009-151372018
17	BCL3	chr1:151373524-151374156	A549	lung:	n/a	n/a
18	BCL3	chr1:151371693-151373473	A549	lung:	n/a	chr1:151372009-151372018
19	BCL3	chr1:151372480-151372962	GM12878	blood:	n/a	n/a
20	BCL3	chr1:151375014-151375704	A549	lung:	n/a	n/a
21	BCLAF1	chr1:151371705-151372350	GM12878	blood:	n/a	chr1:151372009-151372018
22	BCLAF1	chr1:151371605-151372282	GM12878	blood:	n/a	chr1:151372009-151372018
23	BHLHE40	chr1:151344946-151345289	K562	blood:	n/a	n/a
24	BHLHE40	chr1:151345650-151345906	HepG2	liver:	n/a	n/a
25	BHLHE40	chr1:151356747-151357326	K562	blood:	n/a	n/a
26	BHLHE40	chr1:151342372-151343265	K562	blood:	n/a	n/a
27	BRCA1	chr1:151371813-151372175	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr1:151372596-151372778	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr1:151345169-151345211	HepG2	liver:	n/a	n/a
30	CBX3	chr1:151342983-151343411	K562	blood:	n/a	n/a
31	CBX3	chr1:151334672-151335188	K562	blood:	n/a	n/a
32	CBX3	chr1:151360096-151360428	K562	blood:	n/a	n/a
33	CBX3	chr1:151371662-151372200	K562	blood:	n/a	n/a
34	CBX3	chr1:151358593-151358947	K562	blood:	n/a	n/a
35	CBX3	chr1:151334633-151335302	K562	blood:	n/a	n/a
36	CCNT2	chr1:151357075-151357435	K562	blood:	n/a	n/a
37	CCNT2	chr1:151372277-151372477	K562	blood:	n/a	n/a
38	CCNT2	chr1:151343082-151343282	K562	blood:	n/a	n/a
39	CEBPB	chr1:151351919-151352047	HepG2	liver:	n/a	chr1:151351985-151351996
40	CEBPB	chr1:151371720-151372181	ECC-1	luminal epithelium:	n/a	chr1:151371884-151371895
41	CEBPB	chr1:151368769-151369117	HepG2	liver:	n/a	chr1:151368942-151368953
42	CEBPB	chr1:151371816-151372137	GM12878	blood:	n/a	chr1:151371884-151371895
43	CEBPB	chr1:151371734-151372082	K562	blood:	n/a	chr1:151371884-151371895
44	CEBPB	chr1:151392464-151392882	MCF-7	breast:	n/a	chr1:151392614-151392625
45	CEBPB	chr1:151351943-151352012	H1-hESC	embryonic stem cell:	n/a	chr1:151351985-151351996
46	CEBPB	chr1:151407534-151408096	MCF-7	breast:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
47	CEBPB	chr1:151371703-151372202	HepG2	liver:	n/a	chr1:151371884-151371895
48	CEBPB	chr1:151371706-151372643	MCF-7	breast:	n/a	chr1:151371884-151371895
49	CEBPB	chr1:151368776-151369077	A549	lung:	n/a	chr1:151368942-151368953
50	CEBPB	chr1:151343930-151344227	ECC-1	luminal epithelium:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151336795-151336845	HL-60	blood:	n/a
2	chr1:151371285-151371335	NB4	blood:	n/a
3	chr1:151336795-151336845	HL-60	blood:	n/a
4	chr1:151371285-151371335	NB4	blood:	n/a
5	chr1:151346048-151346098	AG10803	skin:	n/a
6	chr1:151370645-151370695	GM12878	blood:	n/a
7	chr1:151346048-151346098	HNPCEpiC	eye:	n/a
8	chr1:151372581-151372631	HEEpiC	esophagus:	n/a
9	chr1:151372147-151372197	HCPEpiC	choroid plexus:	n/a
10	chr1:151372572-151372622	AG04450	lung:	fetal
11	chr1:151345173-151345223	PrEC	prostate:	n/a
12	chr1:151345771-151345821	AG09319	gingival:	n/a
13	chr1:151375993-151376043	BE2_C	brain:	n/a
14	chr1:151371309-151371359	PrEC	prostate:	n/a
15	chr1:151375993-151376043	HRE	kidney:	n/a
16	chr1:151371309-151371359	U87	brain:	n/a
17	chr1:151372652-151372702	MCF-7	breast:	n/a
18	chr1:151400745-151400795	SK-N-MC	brain:	n/a
19	chr1:151344806-151344856	MCF10A-Er-Src	breast:	n/a
20	chr1:151344806-151344856	LNCaP	prostate:	n/a
21	chr1:151371972-151372022	SAEC	small airway:	n/a
22	chr1:151372572-151372622	NHDF-neo	bronchial:	n/a
23	chr1:151346400-151346450	HCPEpiC	choroid plexus:	n/a
24	chr1:151372147-151372197	AG09319	gingival:	n/a
25	chr1:151370645-151370695	HCF	heart:	n/a
26	chr1:151343840-151343890	GM12892	blood:	n/a
27	chr1:151343840-151343890	HUVEC	blood vessel:	n/a
28	chr1:151371944-151371994	HUVEC	blood vessel:	n/a
29	chr1:151345771-151345821	NH-A	brain:	n/a
30	chr1:151400745-151400795	HAEpiC	amniotic membrane:	n/a
31	chr1:151371285-151371335	NHBE	bronchial:	n/a
32	chr1:151371944-151371994	GM12891	blood:	n/a
33	chr1:151344806-151344856	NH-A	brain:	n/a
34	chr1:151371309-151371359	HCPEpiC	choroid plexus:	n/a
35	chr1:151346048-151346098	NHDF-neo	bronchial:	n/a
36	chr1:151336795-151336845	BJ	skin:	n/a
37	chr1:151371972-151372022	AG04450	lung:	fetal
38	chr1:151345248-151345298	ProgFib	skin:	n/a
39	chr1:151370645-151370695	ECC-1	luminal epithelium:	n/a
40	chr1:151345771-151345821	AG09309	skin:	n/a
41	chr1:151372652-151372702	HUVEC	blood vessel:	n/a
42	chr1:151345248-151345298	NB4	blood:	n/a
43	chr1:151346400-151346450	ECC-1	luminal epithelium:	n/a
44	chr1:151345123-151345173	AG09319	gingival:	n/a
45	chr1:151369469-151369519	K562	blood:	n/a
46	chr1:151372228-151372278	HCF	heart:	n/a
47	chr1:151369469-151369519	AG04450	lung:	fetal
48	chr1:151369469-151369519	MCF10A-Er-Src	breast:	n/a
49	chr1:151402121-151402171	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:151402121-151402171	Caco-2	colon:	n/a

(count:227 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type	Cell Stage
1	1:151219411-151234038..1:151329948-151333184	Hela-S3	cervix:
2	chr1:151372236..151373964-chr20:46129058..46130747,2	MCF-7	breast:
3	chr1:151319574..151321193-chr1:151343801..151346115,3	MCF-7	breast:
4	chr1:151348976..151351066-chr1:151352472..151354650,2	K562	blood:
5	chr1:151318180..151322621-chr1:151370786..151375600,7	K562	blood:
6	chr1:151161951..151163611-chr1:151344546..151346783,2	MCF-7	breast:
7	chr1:151353527..151355666-chr1:151374191..151375959,2	K562	blood:
8	chr1:151344490..151346113-chr1:151376702..151378922,2	K562	blood:
9	chr1:151370751..151375455-chr1:151387327..151390376,6	MCF-7	breast:
10	1:151368336-151375897..1:151592347-151603110	Hela-S3	cervix:
11	chr1:151298919..151301179-chr1:151402872..151405310,2	MCF-7	breast:
12	chr1:151298391..151300174-chr1:151343656..151346785,4	MCF-7	breast:
13	chr1:151332835..151334750-chr1:151336636..151339074,2	K562	blood:
14	chr1:151332835..151334750-chr1:151336636..151339074,2	K562	blood:
15	chr1:151162193..151163907-chr1:151370731..151372764,2	MCF-7	breast:
16	1:151324693-151329948..1:151368336-151375897	GM12878	blood:
17	1:151254384-151268403..1:151402394-151411623	GM12878	blood:
18	chr1:151317585..151319121-chr1:151341611..151344384,2	MCF-7	breast:
19	1:151158061-151171193..1:151358657-151368243	K562	blood:
20	chr1:151341989..151348019-chr1:151370228..151376359,14	MCF-7	breast:
21	1:151180715-151199990..1:151352394-151353564	K562	blood:
22	chr1:151392368..151395124-chr1:151396162..151399523,3	K562	blood:
23	chr1:151313664..151315822-chr1:151337463..151339471,3	MCF-7	breast:
24	chr1:151225665..151228952-chr1:151371435..151373604,4	MCF-7	breast:
25	chr1:151370719..151373828-chr1:151394792..151398021,4	MCF-7	breast:
26	1:151393910-151394636..1:151516085-151535167	GM12878	blood:
27	chr1:151371973..151373501-chr1:151810861..151813533,2	MCF-7	breast:
28	chr1:151273322..151275078-chr1:151370486..151372389,2	MCF-7	breast:
29	chr1:151160213..151162825-chr1:151370506..151372060,2	K562	blood:
30	chr1:151311947..151315930-chr1:151341715..151344576,4	K562	blood:
31	chr1:151320179..151321696-chr1:151331665..151333678,2	MCF-7	breast:
32	chr1:151298795..151301346-chr1:151338740..151340960,2	MCF-7	breast:
33	chr1:151368568..151371370-chr1:151392039..151394565,2	K562	blood:
34	1:151180715-151199990..1:151324693-151329948	GM12878	blood:
35	chr1:151397867..151399867-chr1:151430315..151432145,2	MCF-7	breast:
36	1:151270864-151283078..1:151324693-151329948	Hela-S3	cervix:
37	chr1:151373885..151375953-chr1:151382352..151386017,5	K562	blood:
38	chr1:151377630..151380310-chr1:151382827..151386169,3	K562	blood:
39	chr1:151298715..151300740-chr1:151336029..151338584,2	K562	blood:
40	chr1:151317375..151319614-chr1:151336795..151338993,2	K562	blood:
41	chr1:151318199..151320967-chr1:151371516..151373553,2	K562	blood:
42	chr1:151341812..151345526-chr1:151348590..151351097,4	K562	blood:
43	1:151180715-151199990..1:151378579-151379560	H1-hESC	embryonic stem cell:	embryo
44	chr1:151319505..151321169-chr1:151370320..151372349,2	MCF-7	breast:
45	chr1:151401923..151403617-chr1:151404854..151407788,2	MCF-7	breast:
46	1:151352394-151353564..1:151411623-151426875	Hela-S3	cervix:
47	chr1:151319407..151322212-chr1:151384935..151387557,2	K562	blood:
48	chr1:151379379..151381233-chr1:151511239..151513051,2	MCF-7	breast:
49	1:151402394-151411623..1:151618750-151636526	GM12878	blood:
50	1:151382407-151385079..1:151516085-151535167	Hela-S3	cervix:

No data

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

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

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
ENSG00000143376	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000265753	chromatin interactions
ENSG00000143416	chromatin interactions
ENSG00000206635	chromatin interactions
ENSG00000163159	chromatin interactions
ENSG00000119878	chromatin interactions
ENSG00000143436	chromatin interactions
ENSG00000159352	chromatin interactions
ENSG00000252840	chromatin interactions
ENSG00000124151	chromatin interactions
ENSG00000197622	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000143375	chromatin interactions
ENSG00000237976	chromatin interactions
ENSG00000143450	chromatin interactions
ENSG00000143393	chromatin interactions
ENSG00000273481	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000151665	chromatin interactions
ENSG00000223861	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000224645	chromatin interactions
ENSG00000207606	chromatin interactions
ENSG00000143390	chromatin interactions
ENSG00000143398	chromatin interactions
ENSG00000238711	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000163141	chromatin interactions
ENSG00000225556	chromatin interactions
ENSG00000159377	chromatin interactions

Extended variants
information (count: 3184 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:3184 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528123693	chr1:151329910-151329911	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
2	rs548180601	chr1:151329925-151329926	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
3	rs182464094	chr1:151329938-151329939	Weak transcription	Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
4	rs147221741	chr1:151330017-151330018	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs368275253	chr1:151330044-151330045	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs550323371	chr1:151330049-151330050	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs148701946	chr1:151330064-151330065	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs187935574	chr1:151330073-151330074	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs570158419	chr1:151330079-151330080	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs552665004	chr1:151330098-151330099	Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs193022897	chr1:151330161-151330162	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs142219770	chr1:151330187-151330188	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs111586482	chr1:151330212-151330213	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs2800951	chr1:151330289-151330290	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575139403	chr1:151330303-151330304	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs537750182	chr1:151330337-151330338	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs371659497	chr1:151330359-151330360	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs548752201	chr1:151330361-151330362	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs577396206	chr1:151330386-151330387	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs113218370	chr1:151330435-151330436	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs140283539	chr1:151330439-151330440	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs559440804	chr1:151330507-151330508	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs572749174	chr1:151330508-151330509	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs541380041	chr1:151330511-151330512	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs561359301	chr1:151330512-151330513	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs537626351	chr1:151330517-151330518	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs562486675	chr1:151330533-151330534	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs530680384	chr1:151330571-151330572	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs144052181	chr1:151330578-151330579	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs372852754	chr1:151330599-151330600	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs564107974	chr1:151330610-151330611	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs146439382	chr1:151330626-151330627	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs552381983	chr1:151330721-151330722	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs566213369	chr1:151330747-151330748	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs140808703	chr1:151330756-151330757	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs549148950	chr1:151330782-151330783	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs548562585	chr1:151330795-151330796	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs541578215	chr1:151330797-151330798	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs560304527	chr1:151330838-151330839	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs112570628	chr1:151330852-151330853	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs563761606	chr1:151330893-151330894	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs116705100	chr1:151330918-151330919	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs377179925	chr1:151330939-151330940	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs540070332	chr1:151330943-151330944	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs553293138	chr1:151331022-151331023	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs376912570	chr1:151331086-151331087	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs370021622	chr1:151331096-151331097	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs144625862	chr1:151331106-151331107	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs574925811	chr1:151331107-151331108	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs184929675	chr1:151331148-151331149	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	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:2156 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151328400-151334600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:151328400-151336000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:151328600-151334800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:151329400-151340600	Weak transcription	Osteobl	bone
5	chr1:151329600-151336600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr1:151329600-151336800	Weak transcription	Colonic Mucosa	Colon
7	chr1:151329800-151334400	Weak transcription	K562	blood
8	chr1:151329800-151334600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr1:151331400-151334600	Weak transcription	Lung	lung
10	chr1:151331600-151334600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr1:151331600-151334800	Weak transcription	Right Ventricle	heart
12	chr1:151332200-151334600	Weak transcription	Fetal Intestine Small	intestine
13	chr1:151332200-151334800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:151332200-151340000	Weak transcription	Fetal Heart	heart
15	chr1:151332600-151334400	Weak transcription	Fetal Lung	lung
16	chr1:151332600-151336200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:151333200-151336800	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr1:151333400-151333600	Enhancers	Spleen	Spleen
19	chr1:151333600-151334600	Weak transcription	Spleen	Spleen
20	chr1:151333800-151334400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr1:151333800-151335400	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr1:151334000-151336000	Weak transcription	Left Ventricle	heart
23	chr1:151334000-151336000	Weak transcription	Stomach Smooth Muscle	stomach
24	chr1:151334400-151335600	ZNF genes & repeats	K562	blood
25	chr1:151334400-151336400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr1:151334400-151341600	Strong transcription	Fetal Lung	lung
27	chr1:151334600-151335000	ZNF genes & repeats	Fetal Kidney	kidney
28	chr1:151334600-151335200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
29	chr1:151334600-151335200	ZNF genes & repeats	Brain Substantia Nigra	brain
30	chr1:151334600-151335200	ZNF genes & repeats	Pancreas	Pancrea
31	chr1:151334600-151335200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
32	chr1:151334600-151335400	ZNF genes & repeats	Gastric	stomach
33	chr1:151334600-151335400	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr1:151334600-151335400	ZNF genes & repeats	Spleen	Spleen
35	chr1:151334600-151335600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:151334600-151335600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:151334600-151335600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:151334600-151335600	ZNF genes & repeats	Adipose Nuclei	Adipose
39	chr1:151334600-151335600	ZNF genes & repeats	Esophagus	oesophagus
40	chr1:151334600-151335600	ZNF genes & repeats	Lung	lung
41	chr1:151334600-151335800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr1:151334600-151335800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr1:151334600-151336000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr1:151334600-151336200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
45	chr1:151334600-151337000	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr1:151334600-151337200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
47	chr1:151334600-151340000	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr1:151334800-151335000	Weak transcription	Aorta	Aorta
49	chr1:151334800-151335200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:151334800-151335200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain

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