Variant report

Variant	nsv872436
Chromosome Location	chr1:151357333-151413180
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1202)
CpG islands
(count:978)
Chromatin interactive
region (count:147)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1202 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:151371751-151372339	K562	blood:	n/a	chr1:151372120-151372135
2	ARID3A	chr1:151371733-151372165	HepG2	liver:	n/a	chr1:151372120-151372135
3	ATF1	chr1:151357084-151357455	K562	blood:	n/a	n/a
4	ATF1	chr1:151371742-151372196	K562	blood:	n/a	n/a
5	ATF2	chr1:151371724-151372171	GM12878	blood:	n/a	n/a
6	ATF2	chr1:151371634-151372180	GM12878	blood:	n/a	n/a
7	ATF2	chr1:151371732-151372222	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr1:151371626-151372256	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr1:151368851-151369032	K562	blood:	n/a	n/a
10	ATF3	chr1:151371725-151372346	A549	lung:	n/a	n/a
11	BACH1	chr1:151371808-151372310	H1-hESC	embryonic stem cell:	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	BCL3	chr1:151371666-151372235	A549	lung:	n/a	chr1:151372009-151372018
15	BCL3	chr1:151373524-151374156	A549	lung:	n/a	n/a
16	BCL3	chr1:151372480-151372962	GM12878	blood:	n/a	n/a
17	BCL3	chr1:151375014-151375704	A549	lung:	n/a	n/a
18	BCL3	chr1:151371693-151373473	A549	lung:	n/a	chr1:151372009-151372018
19	BCLAF1	chr1:151371705-151372350	GM12878	blood:	n/a	chr1:151372009-151372018
20	BCLAF1	chr1:151371605-151372282	GM12878	blood:	n/a	chr1:151372009-151372018
21	BRCA1	chr1:151371813-151372175	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr1:151372596-151372778	H1-hESC	embryonic stem cell:	n/a	n/a
23	CBX3	chr1:151371662-151372200	K562	blood:	n/a	n/a
24	CBX3	chr1:151360096-151360428	K562	blood:	n/a	n/a
25	CBX3	chr1:151358593-151358947	K562	blood:	n/a	n/a
26	CCNT2	chr1:151357075-151357435	K562	blood:	n/a	n/a
27	CCNT2	chr1:151372277-151372477	K562	blood:	n/a	n/a
28	CEBPB	chr1:151374030-151374114	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:151372559-151372585	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:151392443-151392803	A549	lung:	n/a	chr1:151392614-151392625
31	CEBPB	chr1:151407815-151407820	K562	blood:	n/a	n/a
32	CEBPB	chr1:151371677-151372310	A549	lung:	n/a	chr1:151371884-151371895
33	CEBPB	chr1:151407559-151408104	A549	lung:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
34	CEBPB	chr1:151388726-151389184	ECC-1	luminal epithelium:	n/a	chr1:151388928-151388939
35	CEBPB	chr1:151368769-151369117	HepG2	liver:	n/a	chr1:151368942-151368953
36	CEBPB	chr1:151388780-151389091	A549	lung:	n/a	chr1:151388928-151388939
37	CEBPB	chr1:151388608-151389348	MCF-7	breast:	n/a	chr1:151388928-151388939
38	CEBPB	chr1:151371615-151372199	K562	blood:	n/a	chr1:151371884-151371895
39	CEBPB	chr1:151388780-151389068	HepG2	liver:	n/a	chr1:151388928-151388939
40	CEBPB	chr1:151371719-151372303	ECC-1	luminal epithelium:	n/a	chr1:151371884-151371895
41	CEBPB	chr1:151371694-151372147	IMR90	lung:	n/a	chr1:151371884-151371895
42	CEBPB	chr1:151372556-151372600	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:151388736-151389119	Hela-S3	cervix:	n/a	chr1:151388928-151388939
44	CEBPB	chr1:151368769-151369121	K562	blood:	n/a	chr1:151368942-151368953
45	CEBPB	chr1:151371706-151372643	MCF-7	breast:	n/a	chr1:151371884-151371895
46	CEBPB	chr1:151388769-151389110	HepG2	liver:	n/a	chr1:151388928-151388939
47	CEBPB	chr1:151392510-151392715	HepG2	liver:	n/a	chr1:151392614-151392625
48	CEBPB	chr1:151371700-151372167	Hela-S3	cervix:	n/a	chr1:151371884-151371895
49	CEBPB	chr1:151407641-151407943	MCF-7	breast:	n/a	chr1:151407813-151407824 chr1:151407813-151407826
50	CEBPB	chr1:151371745-151372043	HepG2	liver:	n/a	chr1:151371884-151371895

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:151375993-151376043	NHDF-neo	bronchial:	n/a
2	chr1:151371944-151371994	SK-N-SH_RA	brain:	n/a
3	chr1:151375993-151376043	NHDF-neo	bronchial:	n/a
4	chr1:151371944-151371994	SK-N-SH_RA	brain:	n/a
5	chr1:151372335-151372385	LNCaP	prostate:	n/a
6	chr1:151372147-151372197	PrEC	prostate:	n/a
7	chr1:151372335-151372385	HRE	kidney:	n/a
8	chr1:151372335-151372385	BE2_C	brain:	n/a
9	chr1:151372652-151372702	HRE	kidney:	n/a
10	chr1:151372147-151372197	SK-N-MC	brain:	n/a
11	chr1:151399683-151399733	RPTEC	kidney:	n/a
12	chr1:151369469-151369519	SKMC	muscle:	n/a
13	chr1:151371309-151371359	NB4	blood:	n/a
14	chr1:151402121-151402171	GM19239	blood:	n/a
15	chr1:151371285-151371335	GM12878	blood:	n/a
16	chr1:151399683-151399733	NHDF-neo	bronchial:	n/a
17	chr1:151399683-151399733	HCPEpiC	choroid plexus:	n/a
18	chr1:151372228-151372278	RPTEC	kidney:	n/a
19	chr1:151372581-151372631	HRCEpiC	kidney:	n/a
20	chr1:151371944-151371994	ECC-1	luminal epithelium:	n/a
21	chr1:151372147-151372197	AoSMC	blood vessel:	n/a
22	chr1:151372581-151372631	PANC-1	pancreas:	n/a
23	chr1:151372572-151372622	PANC-1	pancreas:	n/a
24	chr1:151399683-151399733	SAEC	small airway:	n/a
25	chr1:151371944-151371994	ProgFib	skin:	n/a
26	chr1:151372581-151372631	HL-60	blood:	n/a
27	chr1:151369469-151369519	IMR90	lung:	fetal
28	chr1:151370645-151370695	K562	blood:	n/a
29	chr1:151371972-151372022	LNCaP	prostate:	n/a
30	chr1:151375993-151376043	AoSMC	blood vessel:	n/a
31	chr1:151371944-151371994	GM06990	blood:	n/a
32	chr1:151371309-151371359	PrEC	prostate:	n/a
33	chr1:151372652-151372702	GM06990	blood:	n/a
34	chr1:151372147-151372197	HepG2	liver:	n/a
35	chr1:151369469-151369519	U87	brain:	n/a
36	chr1:151402121-151402171	BJ	skin:	n/a
37	chr1:151402121-151402171	HCM	heart:	n/a
38	chr1:151372581-151372631	LNCaP	prostate:	n/a
39	chr1:151372652-151372702	AG04449	skin:	fetal
40	chr1:151371285-151371335	SK-N-SH_RA	brain:	n/a
41	chr1:151371944-151371994	CMK	blood:	n/a
42	chr1:151370645-151370695	Hela-S3	cervix:	n/a
43	chr1:151372581-151372631	HRE	kidney:	n/a
44	chr1:151371944-151371994	MCF-7	breast:	n/a
45	chr1:151370645-151370695	A549	lung:	n/a
46	chr1:151372335-151372385	T-47D	breast:	n/a
47	chr1:151371285-151371335	LNCaP	prostate:	n/a
48	chr1:151371944-151371994	PANC-1	pancreas:	n/a
49	chr1:151375993-151376043	NHBE	bronchial:	n/a
50	chr1:151371944-151371994	BJ	skin:	n/a

(count:147 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:151318482..151320695-chr1:151375632..151377570,2	MCF-7	breast:
2	1:151358657-151368243..1:151516085-151535167	Hela-S3	cervix:
3	1:151353564-151358657..1:151411623-151426875	Hela-S3	cervix:
4	1:151203965-151215310..1:151402394-151411623	GM12878	blood:
5	chr1:151299305..151301447-chr1:151370337..151372394,3	MCF-7	breast:
6	chr1:151371234..151374091-chr1:151403253..151406283,3	K562	blood:
7	chr1:151363150..151367072-chr1:151371054..151375745,5	MCF-7	breast:
8	chr1:151368568..151371370-chr1:151392039..151394565,2	K562	blood:
9	chr1:151409926..151411809-chr1:151413476..151415968,2	MCF-7	breast:
10	chr1:151211452..151213818-chr1:151375380..151378253,2	K562	blood:
11	chr1:151388224..151390291-chr1:151485508..151488200,2	MCF-7	breast:
12	chr1:151370719..151373828-chr1:151394792..151398021,4	MCF-7	breast:
13	chr1:151344758..151345571-chr1:151371234..151372258,3	MCF-7	breast:
14	chr1:151272157..151273670-chr1:151373944..151376221,2	MCF-7	breast:
15	chr1:151387420..151389134-chr1:151433019..151434724,2	K562	blood:
16	chr1:151396850..151398414-chr1:151401158..151402735,2	MCF-7	breast:
17	1:151375897-151378579..1:151618750-151636526	Hela-S3	cervix:
18	chr1:151370990..151372636-chr1:151386252..151388197,2	K562	blood:
19	chr1:151318980..151319798-chr1:151371884..151372449,2	MCF-7	breast:
20	chr1:151253607..151256454-chr1:151374853..151377670,2	MCF-7	breast:
21	chr1:151392368..151395124-chr1:151396162..151399523,3	K562	blood:
22	chr1:151394927..151396962-chr1:151399900..151402085,2	K562	blood:
23	chr1:151160213..151162825-chr1:151370506..151372060,2	K562	blood:
24	chr1:151410628..151413374-chr1:151426124..151427883,2	MCF-7	breast:
25	1:151402394-151411623..1:151496437-151509688	K562	blood:
26	1:151411623-151426875..1:151592347-151603110	GM12878	blood:
27	1:151402394-151411623..1:151516085-151535167	GM12878	blood:
28	chr1:151273322..151275078-chr1:151370486..151372389,2	MCF-7	breast:
29	chr1:151394927..151396962-chr1:151399900..151402085,2	K562	blood:
30	chr1:151319505..151321169-chr1:151370320..151372349,2	MCF-7	breast:
31	chr1:151372236..151373964-chr20:46129058..46130747,2	MCF-7	breast:
32	chr1:151373885..151375953-chr1:151382352..151386017,5	K562	blood:
33	chr1:151402390..151403923-chr1:151409370..151412245,2	MCF-7	breast:
34	1:151358657-151368243..1:151411623-151426875	Hela-S3	cervix:
35	1:151378579-151379560..1:151411623-151426875	H1-hESC	embryonic stem cell:	embryo
36	1:151381232-151382407..1:151411623-151426875	Hela-S3	cervix:
37	1:151270864-151283078..1:151378579-151379560	H1-hESC	embryonic stem cell:	embryo
38	1:151375897-151378579..1:151516085-151535167	H1-hESC	embryonic stem cell:	embryo
39	chr1:151252229..151256416-chr1:151370480..151373573,6	MCF-7	breast:
40	1:151158061-151171193..1:151358657-151368243	K562	blood:
41	chr1:151373885..151375953-chr1:151382352..151386017,5	K562	blood:
42	1:151368336-151375897..1:151592347-151603110	Hela-S3	cervix:
43	chr1:151041688..151044395-chr1:151373966..151376267,2	K562	blood:
44	chr1:151297425..151301136-chr1:151370895..151373723,5	MCF-7	breast:
45	chr1:151371851..151372388-chr2:46843826..46844603,2	HCT-116	colon:
46	1:151393910-151394636..1:151516085-151535167	GM12878	blood:
47	chr1:151371427..151373843-chr1:151402656..151405068,2	MCF-7	breast:
48	chr1:151318007..151320260-chr1:151384925..151386522,2	MCF-7	breast:
49	chr1:151373766..151375598-chr1:151437855..151440411,2	K562	blood:
50	chr1:151371684..151372560-chr17:57915184..57915738,2	MCF-7	breast:

No data

(count:9 , 50 per page) page: 1

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

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

Extended variants
information (count: 2120 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:2120 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6684085	chr1:151357333-151357334	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532986193	chr1:151357351-151357352	Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs533977083	chr1:151357415-151357416	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs558530249	chr1:151357465-151357466	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546264397	chr1:151357466-151357467	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs566801531	chr1:151357477-151357478	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs551392535	chr1:151357489-151357490	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs147998625	chr1:151357490-151357491	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs549213765	chr1:151357507-151357508	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs11582860	chr1:151357561-151357562	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs569032474	chr1:151357576-151357577	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs537544005	chr1:151357583-151357584	Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557474910	chr1:151357601-151357602	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs570845879	chr1:151357630-151357631	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs56857451	chr1:151357744-151357745	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs539853585	chr1:151357752-151357753	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs191527383	chr1:151357773-151357774	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs140769246	chr1:151357802-151357803	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542080118	chr1:151357909-151357910	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs77166397	chr1:151357963-151357964	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs78510316	chr1:151357965-151357966	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs6702368	chr1:151358032-151358033	Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575482401	chr1:151358097-151358098	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs544471936	chr1:151358149-151358150	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150095256	chr1:151358163-151358164	Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs138379953	chr1:151358209-151358210	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs370505966	chr1:151358365-151358366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566886327	chr1:151358398-151358399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs142287548	chr1:151358401-151358402	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560155600	chr1:151358417-151358418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78757683	chr1:151358418-151358419	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs549250568	chr1:151358432-151358433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569168754	chr1:151358458-151358459	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs531572545	chr1:151358586-151358587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs551269751	chr1:151358599-151358600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549468725	chr1:151358633-151358634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539517390	chr1:151358634-151358635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553343692	chr1:151358649-151358650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566484019	chr1:151358717-151358718	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs182154119	chr1:151358720-151358721	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs76614102	chr1:151358764-151358765	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs575518094	chr1:151358799-151358800	Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs142926121	chr1:151358836-151358837	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs377449332	chr1:151358837-151358838	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs558040814	chr1:151358893-151358894	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs544123301	chr1:151358951-151358952	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs577684261	chr1:151358975-151358976	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs539907435	chr1:151358983-151358984	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs144293262	chr1:151359016-151359017	Enhancers	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs562522482	chr1:151359026-151359027	Enhancers	Chromatin interactive region	11 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
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
Breast cancer	22522925	CNVD

Chromatin state (count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:151356800-151357600	Flanking Active TSS	K562	blood
2	chr1:151357000-151358000	Enhancers	HMEC	breast
3	chr1:151357200-151357400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:151357200-151357600	Enhancers	NHEK	skin
5	chr1:151357200-151357800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:151357400-151358000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:151357600-151358200	Enhancers	K562	blood
8	chr1:151358200-151358800	Weak transcription	K562	blood
9	chr1:151358800-151360600	Enhancers	K562	blood
10	chr1:151362000-151362600	Enhancers	Rectal Mucosa Donor 29	rectum
11	chr1:151362200-151362400	Enhancers	Placenta	Placenta
12	chr1:151362200-151362400	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr1:151362400-151363600	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr1:151362600-151363200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr1:151363400-151364000	Enhancers	Liver	Liver
16	chr1:151363600-151365600	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr1:151365600-151371200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr1:151370200-151370400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:151370200-151370800	Enhancers	Fetal Kidney	kidney
20	chr1:151370200-151370800	Enhancers	HepG2	liver
21	chr1:151370400-151371200	Enhancers	A549	lung
22	chr1:151370600-151370800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr1:151370600-151371200	Enhancers	Dnd41	blood
24	chr1:151370800-151371400	Enhancers	Primary B cells from peripheral blood	blood
25	chr1:151370800-151371400	Weak transcription	Fetal Kidney	kidney
26	chr1:151370800-151371400	Weak transcription	HepG2	liver
27	chr1:151371000-151371200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr1:151371000-151371200	Enhancers	Primary T helper cells PMA-I stimulated	--
29	chr1:151371000-151371400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr1:151371000-151371400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr1:151371200-151371400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr1:151371200-151371400	Enhancers	Primary T cells from cord blood	blood
33	chr1:151371200-151371400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr1:151371200-151371400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr1:151371200-151371400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr1:151371200-151371400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
37	chr1:151371200-151371400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr1:151371200-151371400	Enhancers	Brain Hippocampus Middle	brain
39	chr1:151371200-151371400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr1:151371200-151371400	Enhancers	Fetal Muscle Leg	muscle
41	chr1:151371200-151371400	Enhancers	Placenta	Placenta
42	chr1:151371200-151371400	Enhancers	Fetal Thymus	thymus
43	chr1:151371200-151371400	Enhancers	Thymus	Thymus
44	chr1:151371200-151371400	Flanking Active TSS	A549	lung
45	chr1:151371200-151371400	Active TSS	Monocytes-CD14+_RO01746	blood
46	chr1:151371200-151371600	Enhancers	Primary B cells from cord blood	blood
47	chr1:151371200-151371600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
48	chr1:151371200-151371600	Enhancers	Fetal Stomach	stomach
49	chr1:151371200-151371600	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr1:151371200-151371600	Flanking Active TSS	Dnd41	blood

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