Variant report

Variant	nsv818888
Chromosome Location	chr1:10719645-10750432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:407)
CpG islands
(count:2934)
Chromatin interactive
region (count:58)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10746020-10747010	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:10739699-10740090	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:10739738-10739938	K562	blood:	n/a	n/a
4	ATF2	chr1:10739666-10740097	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:10739634-10740012	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr1:10722400-10722952	GM12878	blood:	n/a	n/a
7	BCL3	chr1:10722391-10722933	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:10745752-10746071	K562	blood:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
9	BHLHE40	chr1:10739818-10739897	K562	blood:	n/a	n/a
10	BHLHE40	chr1:10745723-10746597	HepG2	liver:	n/a	chr1:10745933-10745942 chr1:10745934-10745943 chr1:10746013-10746029 chr1:10745934-10745943 chr1:10745935-10745944
11	BHLHE40	chr1:10722323-10722716	K562	blood:	n/a	n/a
12	BRCA1	chr1:10737875-10737890	HepG2	liver:	n/a	n/a
13	CBX3	chr1:10739625-10740024	K562	blood:	n/a	n/a
14	CEBPB	chr1:10739750-10739932	K562	blood:	n/a	n/a
15	CEBPB	chr1:10739707-10739926	K562	blood:	n/a	n/a
16	CEBPB	chr1:10746636-10747091	HepG2	liver:	n/a	chr1:10746910-10746923
17	CEBPB	chr1:10737782-10737942	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr1:10739719-10739976	HepG2	liver:	n/a	n/a
19	CEBPD	chr1:10745991-10746333	HepG2	liver:	n/a	n/a
20	CHD2	chr1:10746764-10746893	K562	blood:	n/a	n/a
21	CHD2	chr1:10744588-10744881	K562	blood:	n/a	n/a
22	CHD2	chr1:10739793-10739993	HepG2	liver:	n/a	n/a
23	CHD2	chr1:10746469-10747098	HepG2	liver:	n/a	n/a
24	CREB1	chr1:10739595-10740096	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr1:10739587-10740043	HepG2	liver:	n/a	n/a
26	CREB1	chr1:10739569-10740154	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr1:10741440-10741590	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr1:10746880-10747030	HMEC	breast:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
29	CTCF	chr1:10746899-10746952	GM12892	blood:	n/a	n/a
30	CTCF	chr1:10746937-10747045	K562	blood:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
31	CTCF	chr1:10725480-10725630	K562	blood:	n/a	n/a
32	CTCF	chr1:10746860-10747010	SAEC	small airway:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
33	CTCF	chr1:10746820-10746970	HBMEC	blood vessel:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
34	CTCF	chr1:10746866-10747078	Gliobla	brain:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
35	CTCF	chr1:10746940-10747090	MCF-7	breast:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
36	CTCF	chr1:10746900-10747050	K562	blood:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
37	CTCF	chr1:10725502-10725539	K562	blood:	n/a	n/a
38	CTCF	chr1:10746859-10747076	MCF-7	breast:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
39	CTCF	chr1:10746930-10747020	MCF-7	breast:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
40	CTCF	chr1:10722570-10722625	GM19239	blood:	n/a	n/a
41	CTCF	chr1:10739400-10739550	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr1:10719500-10719650	GM12874	blood:	n/a	n/a
43	CTCF	chr1:10721500-10721579	GM19239	blood:	n/a	n/a
44	CTCF	chr1:10746900-10747050	WERI-Rb-1	eye:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
45	CTCF	chr1:10746800-10746950	BJ	skin:	n/a	n/a
46	CTCF	chr1:10746889-10747048	MCF-7	breast:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
47	CTCF	chr1:10746680-10746830	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:10747360-10747414	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:10746920-10747070	SAEC	small airway:	n/a	chr1:10746953-10746966 chr1:10746951-10746969
50	CTCF	chr1:10741340-10741490	HepG2	liver:	n/a	n/a

(count:2934 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10732912-10732962	Jurkat	blood:	n/a
2	chr1:10726865-10726915	HIPEpiC	eye:	n/a
3	chr1:10732290-10732340	HCM	heart:	n/a
4	chr1:10731250-10731300	NH-A	brain:	n/a
5	chr1:10733477-10733527	SAEC	small airway:	n/a
6	chr1:10733030-10733080	K562	blood:	n/a
7	chr1:10732912-10732962	Jurkat	blood:	n/a
8	chr1:10726865-10726915	HIPEpiC	eye:	n/a
9	chr1:10732290-10732340	HCM	heart:	n/a
10	chr1:10731250-10731300	NH-A	brain:	n/a
11	chr1:10733477-10733527	SAEC	small airway:	n/a
12	chr1:10733030-10733080	K562	blood:	n/a
13	chr1:10723174-10723224	MCF10A-Er-Src	breast:	n/a
14	chr1:10725254-10725304	SK-N-MC	brain:	n/a
15	chr1:10730684-10730734	Hepatocyte	liver:	n/a
16	chr1:10731250-10731300	Jurkat	blood:	n/a
17	chr1:10745727-10745777	SK-N-MC	brain:	n/a
18	chr1:10732900-10732950	NHDF-neo	bronchial:	n/a
19	chr1:10733511-10733561	ProgFib	skin:	n/a
20	chr1:10735169-10735219	HepG2	liver:	n/a
21	chr1:10732290-10732340	HPAEpiC	pulmonary alveolar:	n/a
22	chr1:10720368-10720418	HL-60	blood:	n/a
23	chr1:10733477-10733527	HUVEC	blood vessel:	n/a
24	chr1:10731250-10731300	IMR90	lung:	fetal
25	chr1:10728270-10728320	ovcar-3	ovarian:	n/a
26	chr1:10739980-10740030	GM12878	blood:	n/a
27	chr1:10725571-10725621	AG04450	lung:	fetal
28	chr1:10737562-10737612	HAEpiC	amniotic membrane:	n/a
29	chr1:10719929-10719979	Hepatocyte	liver:	n/a
30	chr1:10725237-10725287	NT2-D1	testis:	n/a
31	chr1:10743216-10743266	NT2-D1	testis:	n/a
32	chr1:10739980-10740030	NT2-D1	testis:	n/a
33	chr1:10732464-10732514	Hela-S3	cervix:	n/a
34	chr1:10732912-10732962	SK-N-SH_RA	brain:	n/a
35	chr1:10732900-10732950	AG09309	skin:	n/a
36	chr1:10720269-10720319	GM12878	blood:	n/a
37	chr1:10720466-10720516	SK-N-MC	brain:	n/a
38	chr1:10732744-10732794	AoSMC	blood vessel:	n/a
39	chr1:10732464-10732514	RPTEC	kidney:	n/a
40	chr1:10729216-10729266	AG04449	skin:	fetal
41	chr1:10732558-10732608	HRE	kidney:	n/a
42	chr1:10738664-10738714	PrEC	prostate:	n/a
43	chr1:10732912-10732962	AG10803	skin:	n/a
44	chr1:10732519-10732569	CMK	blood:	n/a
45	chr1:10732464-10732514	HRE	kidney:	n/a
46	chr1:10739184-10739234	SK-N-SH_RA	brain:	n/a
47	chr1:10725254-10725304	HNPCEpiC	eye:	n/a
48	chr1:10725237-10725287	Hela-S3	cervix:	n/a
49	chr1:10735169-10735219	HCPEpiC	choroid plexus:	n/a
50	chr1:10725237-10725287	HL-60	blood:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:10738788..10740418-chr1:10744263..10746556,2	MCF-7	breast:
2	chr1:10744408..10746422-chr1:10754548..10756295,2	MCF-7	breast:
3	chr1:10742610..10744196-chr1:10755434..10757046,2	K562	blood:
4	chr1:10659595..10662178-chr1:10730395..10732793,2	MCF-7	breast:
5	chr1:10733635..10735480-chr1:10745613..10747198,2	K562	blood:
6	chr1:10725635..10727609-chr1:10737981..10739512,2	K562	blood:
7	chr1:10736438..10738952-chr1:10740834..10743683,3	K562	blood:
8	chr1:10731829..10734631-chr1:10737455..10739630,2	K562	blood:
9	chr1:10741683..10743188-chr1:10744761..10747734,2	MCF-7	breast:
10	chr1:10717594..10722225-chr1:10722686..10725044,4	K562	blood:
11	chr1:10744767..10746959-chr1:10754994..10757049,2	K562	blood:
12	chr1:10749491..10752032-chr1:10752294..10754052,2	K562	blood:
13	chr1:10732310..10734082-chr1:10748973..10751556,2	K562	blood:
14	chr1:10742297..10745036-chr1:10749705..10751341,3	MCF-7	breast:
15	chr1:10739929..10741898-chr1:10854079..10856532,2	MCF-7	breast:
16	chr1:10733440..10737843-chr1:10738072..10740756,3	K562	blood:
17	chr1:10725435..10726303-chr1:10810964..10811494,2	MCF-7	breast:
18	chr1:10742297..10745036-chr1:10749705..10751341,3	MCF-7	breast:
19	chr1:10723769..10726210-chr1:10728292..10729827,2	MCF-7	breast:
20	chr1:10736438..10738952-chr1:10740834..10743683,3	K562	blood:
21	chr1:10738788..10740418-chr1:10744263..10746556,2	MCF-7	breast:
22	chr1:10730915..10733198-chr1:10740298..10742012,2	K562	blood:
23	chr1:10731586..10734308-chr1:10735752..10737991,2	MCF-7	breast:
24	chr1:10722706..10724721-chr1:10733970..10736738,2	MCF-7	breast:
25	chr1:10735100..10736602-chr1:10738947..10741483,2	MCF-7	breast:
26	chr1:10731829..10734631-chr1:10737455..10739630,2	K562	blood:
27	chr1:10705750..10708723-chr1:10731868..10733988,2	K562	blood:
28	chr1:10741683..10743188-chr1:10744761..10747734,2	MCF-7	breast:
29	chr1:10735100..10736602-chr1:10738947..10741483,2	MCF-7	breast:
30	chr1:10738789..10740392-chr1:10741913..10744233,2	MCF-7	breast:
31	chr1:10746225..10747873-chr1:10749821..10751374,2	K562	blood:
32	chr1:10725635..10727609-chr1:10737981..10739512,2	K562	blood:
33	chr1:10738789..10740392-chr1:10741913..10744233,2	MCF-7	breast:
34	chr1:10716711..10719662-chr1:10722945..10725596,2	MCF-7	breast:
35	chr1:10731586..10734308-chr1:10735752..10737991,2	MCF-7	breast:
36	chr1:10746278..10748730-chr1:10764916..10766801,2	K562	blood:
37	chr1:10722706..10724721-chr1:10733970..10736738,2	MCF-7	breast:
38	chr1:10733440..10737843-chr1:10738072..10740756,3	K562	blood:
39	chr1:10728805..10730887-chr1:10732213..10735865,3	MCF-7	breast:
40	chr1:10730026..10731880-chr1:10732441..10734858,2	MCF-7	breast:
41	chr1:10746225..10747873-chr1:10749821..10751374,2	K562	blood:
42	chr1:10739997..10741906-chr1:10786836..10789661,2	MCF-7	breast:
43	chr1:10733635..10735480-chr1:10745613..10747198,2	K562	blood:
44	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
45	chr1:10723769..10726210-chr1:10728292..10729827,2	MCF-7	breast:
46	chr1:10716711..10719662-chr1:10722945..10725596,2	MCF-7	breast:
47	chr1:10738414..10740371-chr1:10749837..10752208,2	MCF-7	breast:
48	chr1:10738414..10740371-chr1:10749837..10752208,2	MCF-7	breast:
49	chr1:10739770..10741770-chr1:10741804..10744517,2	K562	blood:
50	chr1:10730915..10733198-chr1:10740298..10742012,2	K562	blood:

No data

Variant related genes	Relation type
CASZ1	TF binding region
CASZ1	CpG island
ENSG00000130940	chromatin interactions

Extended variants
information (count: 1399 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:1399 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs475980	chr1:10719645-10719646	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74052160	chr1:10719649-10719650	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs117450756	chr1:10719657-10719658	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs187202763	chr1:10719679-10719680	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs76451128	chr1:10719694-10719695	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs192819208	chr1:10719751-10719752	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs369998591	chr1:10719752-10719753	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs371271451	chr1:10719812-10719813	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146116942	chr1:10719818-10719819	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs373574627	chr1:10719877-10719878	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530151570	chr1:10719892-10719893	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370703881	chr1:10719893-10719894	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373804665	chr1:10719897-10719898	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs184530993	chr1:10719905-10719906	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141586663	chr1:10719908-10719909	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375499155	chr1:10719923-10719924	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530829402	chr1:10719929-10719930	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145422074	chr1:10719934-10719935	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570411712	chr1:10719935-10719936	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs534628168	chr1:10719940-10719941	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143375182	chr1:10719941-10719942	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370358970	chr1:10719944-10719945	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs142093239	chr1:10719964-10719965	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs137936205	chr1:10719967-10719968	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140148473	chr1:10719968-10719969	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374982298	chr1:10719970-10719971	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535551834	chr1:10719971-10719972	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371246046	chr1:10719993-10719994	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375136047	chr1:10720001-10720002	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574244333	chr1:10720010-10720011	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149330108	chr1:10720012-10720013	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371486958	chr1:10720027-10720028	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs374997815	chr1:10720030-10720031	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111908315	chr1:10720064-10720065	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368475799	chr1:10720100-10720101	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs71645003	chr1:10720103-10720104	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs377360245	chr1:10720112-10720113	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367590246	chr1:10720118-10720119	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372248785	chr1:10720122-10720123	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200719150	chr1:10720123-10720124	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141628348	chr1:10720132-10720133	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs72858531	chr1:10720133-10720134	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs139953654	chr1:10720135-10720136	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs151040190	chr1:10720136-10720137	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs199633436	chr1:10720142-10720143	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193132440	chr1:10720157-10720158	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150271253	chr1:10720163-10720164	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145776572	chr1:10720180-10720181	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs61776296	chr1:10720187-10720188	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370082165	chr1:10720211-10720212	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10697400-10722000	Strong transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:10698800-10726400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr1:10698800-10752000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:10699000-10723000	Weak transcription	Psoas Muscle	Psoas
5	chr1:10700400-10722800	Weak transcription	Ovary	ovary
6	chr1:10702600-10721600	Strong transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:10704400-10720400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr1:10705400-10725800	Weak transcription	HMEC	breast
9	chr1:10706400-10724000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr1:10706600-10723200	Weak transcription	Right Atrium	heart
11	chr1:10707800-10731200	Weak transcription	NHEK	skin
12	chr1:10710200-10723400	Weak transcription	Brain Anterior Caudate	brain
13	chr1:10710600-10721600	Strong transcription	Esophagus	oesophagus
14	chr1:10711400-10722000	Strong transcription	Spleen	Spleen
15	chr1:10711600-10726600	Strong transcription	Duodenum Mucosa	Duodenum
16	chr1:10711600-10728400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:10711800-10720800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:10711800-10721400	Weak transcription	Fetal Kidney	kidney
19	chr1:10712000-10720600	Strong transcription	Skeletal Muscle Male	skeletal muscle
20	chr1:10712000-10721400	Strong transcription	Fetal Intestine Small	intestine
21	chr1:10712000-10721600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:10712000-10723000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr1:10712200-10723400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:10712400-10722000	Weak transcription	Fetal Lung	lung
25	chr1:10712600-10737000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr1:10713000-10722800	Weak transcription	Liver	Liver
27	chr1:10713600-10721200	Strong transcription	Pancreas	Pancrea
28	chr1:10714200-10723000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:10714200-10723400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr1:10714400-10721200	Strong transcription	Right Ventricle	heart
31	chr1:10714400-10723200	Weak transcription	HSMMtube	muscle
32	chr1:10714400-10729200	Weak transcription	Primary hematopoietic stem cells	blood
33	chr1:10714600-10730200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:10714600-10731400	Weak transcription	Small Intestine	intestine
35	chr1:10714800-10723400	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr1:10714800-10727000	Weak transcription	Dnd41	blood
37	chr1:10716200-10723200	Weak transcription	Brain Hippocampus Middle	brain
38	chr1:10716800-10719800	Enhancers	Fetal Heart	heart
39	chr1:10717000-10719800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr1:10717400-10720600	Strong transcription	Aorta	Aorta
41	chr1:10717600-10720800	Strong transcription	Colonic Mucosa	Colon
42	chr1:10717800-10723000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr1:10717800-10723000	Weak transcription	Brain Germinal Matrix	brain
44	chr1:10718200-10720600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr1:10718200-10720600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr1:10718200-10720600	Strong transcription	Left Ventricle	heart
47	chr1:10718200-10720800	Strong transcription	Thymus	Thymus
48	chr1:10718200-10722000	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr1:10718400-10719800	Strong transcription	Primary T cells from cord blood	blood
50	chr1:10718400-10720400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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