Variant report

Variant	esv1831760
Chromosome Location	chr1:10467074-10483456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:482)
CpG islands
(count:123)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:482 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10475422-10475837	K562	blood:	n/a	n/a
2	ATF1	chr1:10475249-10475812	K562	blood:	n/a	n/a
3	ATF3	chr1:10475138-10475859	A549	lung:	n/a	n/a
4	BACH1	chr1:10475375-10475878	K562	blood:	n/a	n/a
5	BACH1	chr1:10475540-10475782	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr1:10481151-10483619	A549	lung:	n/a	n/a
7	BCL3	chr1:10471483-10472321	A549	lung:	n/a	n/a
8	BCL3	chr1:10480357-10481022	A549	lung:	n/a	n/a
9	BCL3	chr1:10475047-10475833	A549	lung:	n/a	n/a
10	BCL3	chr1:10481065-10485114	A549	lung:	n/a	n/a
11	BCL3	chr1:10475010-10475874	A549	lung:	n/a	n/a
12	BHLHE40	chr1:10481691-10481732	K562	blood:	n/a	n/a
13	BHLHE40	chr1:10475286-10475924	K562	blood:	n/a	n/a
14	CBX3	chr1:10475082-10475901	K562	blood:	n/a	n/a
15	CCNT2	chr1:10470366-10470554	K562	blood:	n/a	n/a
16	CCNT2	chr1:10480614-10480901	K562	blood:	n/a	n/a
17	CEBPB	chr1:10475439-10475759	K562	blood:	n/a	n/a
18	CEBPB	chr1:10475531-10475738	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:10475402-10475859	A549	lung:	n/a	n/a
20	CEBPB	chr1:10475191-10475915	K562	blood:	n/a	n/a
21	CEBPB	chr1:10467083-10467119	A549	lung:	n/a	n/a
22	CEBPB	chr1:10480685-10480898	K562	blood:	n/a	n/a
23	CEBPB	chr1:10475190-10475808	K562	blood:	n/a	n/a
24	CEBPB	chr1:10475168-10475828	A549	lung:	n/a	n/a
25	CEBPB	chr1:10475062-10475971	A549	lung:	n/a	n/a
26	CEBPB	chr1:10475437-10475803	IMR90	lung:	n/a	n/a
27	CHD2	chr1:10475464-10475664	K562	blood:	n/a	n/a
28	CHD2	chr1:10469477-10469498	HepG2	liver:	n/a	n/a
29	CREB1	chr1:10475400-10475729	A549	lung:	n/a	n/a
30	CREB1	chr1:10468061-10468309	A549	lung:	n/a	n/a
31	CREB1	chr1:10481782-10482246	A549	lung:	n/a	n/a
32	CTCF	chr1:10479583-10479670	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:10481900-10482050	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr1:10475480-10475630	HPAF	blood vessel:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
35	CTCF	chr1:10467260-10467410	GM12865	blood:	n/a	n/a
36	CTCF	chr1:10475360-10475510	HCM	heart:	n/a	n/a
37	CTCF	chr1:10482012-10482081	A549	lung:	n/a	n/a
38	CTCF	chr1:10475380-10475530	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr1:10475420-10475570	SAEC	small airway:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
40	CTCF	chr1:10482036-10482066	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr1:10475420-10475570	BJ	skin:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
42	CTCF	chr1:10478175-10478239	Lung_OC	lung:	n/a	n/a
43	CTCF	chr1:10475340-10475490	K562	blood:	n/a	n/a
44	CTCF	chr1:10475420-10475570	HCPEpiC	choroid plexus:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
45	CTCF	chr1:10472960-10473110	A549	lung:	n/a	n/a
46	CTCF	chr1:10475500-10475650	HCM	heart:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
47	CTCF	chr1:10474854-10474955	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr1:10475361-10475810	K562	blood:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
49	CTCF	chr1:10479871-10480198	T-47D	breast:	n/a	n/a
50	CTCF	chr1:10481940-10482090	NHEK	skin:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10475318-10475368	MCF10A-Er-Src	breast:	n/a
2	chr1:10475318-10475368	MCF10A-Er-Src	breast:	n/a
3	chr1:10475318-10475368	GM12891	blood:	n/a
4	chr1:10480153-10480203	GM06990	blood:	n/a
5	chr1:10475318-10475368	HCF	heart:	n/a
6	chr1:10475318-10475368	HMEC	breast:	n/a
7	chr1:10480153-10480203	GM12891	blood:	n/a
8	chr1:10480153-10480203	HNPCEpiC	eye:	n/a
9	chr1:10475318-10475368	AG10803	skin:	n/a
10	chr1:10480153-10480203	HL-60	blood:	n/a
11	chr1:10475318-10475368	BJ	skin:	n/a
12	chr1:10480153-10480203	AoSMC	blood vessel:	n/a
13	chr1:10475318-10475368	AG09319	gingival:	n/a
14	chr1:10480153-10480203	BJ	skin:	n/a
15	chr1:10480153-10480203	H1-hESC	embryonic stem cell:	embryo
16	chr1:10475318-10475368	HEEpiC	esophagus:	n/a
17	chr1:10475318-10475368	HAEpiC	amniotic membrane:	n/a
18	chr1:10480153-10480203	Jurkat	blood:	n/a
19	chr1:10480153-10480203	AG09319	gingival:	n/a
20	chr1:10475318-10475368	ECC-1	luminal epithelium:	n/a
21	chr1:10480153-10480203	SAEC	small airway:	n/a
22	chr1:10475318-10475368	NHBE	bronchial:	n/a
23	chr1:10480153-10480203	BE2_C	brain:	n/a
24	chr1:10480153-10480203	CMK	blood:	n/a
25	chr1:10475318-10475368	HCM	heart:	n/a
26	chr1:10480153-10480203	HepG2	liver:	n/a
27	chr1:10475318-10475368	HIPEpiC	eye:	n/a
28	chr1:10480153-10480203	U87	brain:	n/a
29	chr1:10475318-10475368	RPTEC	kidney:	n/a
30	chr1:10475318-10475368	HEK293	kidney:	embryo
31	chr1:10480153-10480203	HIPEpiC	eye:	n/a
32	chr1:10475318-10475368	HRE	kidney:	n/a
33	chr1:10480153-10480203	ECC-1	luminal epithelium:	n/a
34	chr1:10480153-10480203	ProgFib	skin:	n/a
35	chr1:10475318-10475368	SK-N-SH	brain:	n/a
36	chr1:10480153-10480203	GM12878	blood:	n/a
37	chr1:10475318-10475368	HepG2	liver:	n/a
38	chr1:10480153-10480203	AG04449	skin:	fetal
39	chr1:10480153-10480203	A549	lung:	n/a
40	chr1:10475318-10475368	HUVEC	blood vessel:	n/a
41	chr1:10475318-10475368	IMR90	lung:	fetal
42	chr1:10475318-10475368	CMK	blood:	n/a
43	chr1:10480153-10480203	LNCaP	prostate:	n/a
44	chr1:10475318-10475368	ovcar-3	ovarian:	n/a
45	chr1:10475318-10475368	SAEC	small airway:	n/a
46	chr1:10475318-10475368	NT2-D1	testis:	n/a
47	chr1:10480153-10480203	HRPEpiC	eye:	n/a
48	chr1:10475318-10475368	Hela-S3	cervix:	n/a
49	chr1:10480153-10480203	NT2-D1	testis:	n/a
50	chr1:10480153-10480203	RPTEC	kidney:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10437408..10438442-chr1:10475501..10476423,3	K562	blood:
2	chr1:10458613..10460935-chr1:10466143..10469098,3	K562	blood:
3	chr1:10458252..10460577-chr1:10480549..10482459,3	K562	blood:
4	chr1:10417330..10419820-chr1:10480235..10483214,2	K562	blood:
5	chr1:10474196..10477325-chr1:10477463..10484153,8	K562	blood:
6	chr1:10457799..10462480-chr1:10462835..10469512,11	MCF-7	breast:
7	chr1:10469567..10472179-chr1:10478906..10481569,2	MCF-7	breast:
8	chr1:10475618..10478486-chr1:10479191..10481866,2	MCF-7	breast:
9	chr1:10449520..10451785-chr1:10471449..10473119,2	K562	blood:
10	chr1:10457797..10461098-chr1:10474071..10478087,9	K562	blood:
11	chr1:10475618..10478486-chr1:10479191..10481866,2	MCF-7	breast:
12	chr1:10437214..10438077-chr1:10475535..10476340,2	MCF-7	breast:
13	chr1:10479306..10481846-chr1:10534906..10536972,2	K562	blood:
14	chr1:9969356..9971879-chr1:10474323..10477073,2	K562	blood:
15	chr1:10458301..10460577-chr1:10466868..10469882,3	MCF-7	breast:
16	chr1:10474880..10479716-chr1:10481883..10486910,5	K562	blood:
17	chr1:10474109..10477987-chr1:10478782..10481616,9	K562	blood:
18	chr1:10480824..10482719-chr1:10531236..10533762,2	K562	blood:
19	chr1:10474196..10477325-chr1:10477463..10484153,8	K562	blood:
20	chr1:10475480..10478071-chr1:10488933..10491824,2	K562	blood:
21	chr1:10479206..10481807-chr1:10489257..10490879,3	K562	blood:
22	chr1:10469567..10472179-chr1:10478906..10481569,2	MCF-7	breast:
23	chr1:10458949..10460563-chr1:10481035..10483154,2	MCF-7	breast:
24	chr1:10477766..10478549-chr8:87566020..87566871,2	MCF-7	breast:
25	chr1:10467177..10469031-chr1:10471099..10473310,2	MCF-7	breast:
26	chr1:10475041..10475642-chr1:10489986..10490702,2	K562	blood:
27	chr1:10467907..10472174-chr1:10473763..10477621,4	MCF-7	breast:
28	chr1:10473903..10475499-chr1:10533435..10536154,2	K562	blood:
29	chr1:10483316..10484984-chr1:10487772..10489866,2	K562	blood:
30	chr1:10456065..10459752-chr1:10480399..10483247,3	K562	blood:
31	chr1:10473791..10476777-chr1:10490511..10492354,2	K562	blood:
32	chr1:10457490..10461716-chr1:10469511..10473951,6	K562	blood:
33	chr1:10474109..10477987-chr1:10478782..10481616,9	K562	blood:

No data

Variant related genes	Relation type
PGD	TF binding region
PGD	CpG island
ENSG00000265945	chromatin interactions
ENSG00000251503	chromatin interactions
ENSG00000175279	chromatin interactions
ENSG00000178585	chromatin interactions
ENSG00000271989	chromatin interactions
ENSG00000142655	chromatin interactions
ENSG00000160049	chromatin interactions
ENSG00000142657	chromatin interactions

Extended variants
information (count: 714 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:714 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6541094	chr1:10467074-10467075	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571257865	chr1:10467076-10467077	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538209323	chr1:10467090-10467091	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs577726592	chr1:10467105-10467106	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35603742	chr1:10467111-10467112	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs186336687	chr1:10467113-10467114	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs565800356	chr1:10467184-10467185	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536467630	chr1:10467210-10467211	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545328585	chr1:10467234-10467235	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573838486	chr1:10467242-10467243	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563435611	chr1:10467243-10467244	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs537947019	chr1:10467252-10467253	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556191509	chr1:10467274-10467275	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs35206132	chr1:10467306-10467307	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs577979769	chr1:10467381-10467382	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190785728	chr1:10467418-10467419	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs1300646	chr1:10467456-10467457	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572630778	chr1:10467462-10467463	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543275885	chr1:10467472-10467473	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561455560	chr1:10467478-10467479	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs35155032	chr1:10467488-10467489	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145443149	chr1:10467513-10467514	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs183165854	chr1:10467520-10467521	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs564932165	chr1:10467558-10467559	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs146486561	chr1:10467579-10467580	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547049346	chr1:10467581-10467582	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565990900	chr1:10467597-10467598	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs536147510	chr1:10467609-10467610	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548029874	chr1:10467637-10467638	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187489036	chr1:10467644-10467645	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536467178	chr1:10467698-10467699	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536809689	chr1:10467770-10467771	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556256837	chr1:10467783-10467784	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs117040016	chr1:10467800-10467801	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191812790	chr1:10467801-10467802	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553863143	chr1:10467819-10467820	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs183227227	chr1:10467821-10467822	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543337229	chr1:10467878-10467879	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561515952	chr1:10467889-10467890	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12739210	chr1:10467897-10467898	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs550183622	chr1:10467904-10467905	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576719236	chr1:10467918-10467919	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543997451	chr1:10467930-10467931	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs565011879	chr1:10467988-10467989	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs562029200	chr1:10467991-10467992	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs532085994	chr1:10467997-10467998	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs71583867	chr1:10468005-10468006	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs77784060	chr1:10468006-10468007	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs76522364	chr1:10468019-10468020	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs144558011	chr1:10468020-10468021	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Basal cell lymphoma	21115979	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
Neuroblastoma	20406844	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
Ewing''s sarcoma	17952124	CNVD
Cancer	20164919	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10460000-10490200	Weak transcription	Psoas Muscle	Psoas
2	chr1:10460200-10475400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr1:10460400-10472800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr1:10460400-10475200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:10460600-10481200	Strong transcription	H1 Cell Line	embryonic stem cell
6	chr1:10460800-10468800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr1:10460800-10480400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr1:10460800-10482000	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr1:10460800-10482400	Strong transcription	Fetal Stomach	stomach
10	chr1:10460800-10483400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr1:10461000-10474600	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr1:10461000-10475200	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr1:10461000-10476800	Weak transcription	Fetal Heart	heart
14	chr1:10461000-10482000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr1:10461200-10482000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr1:10461200-10482000	Strong transcription	Fetal Muscle Leg	muscle
17	chr1:10461200-10490000	Weak transcription	Right Atrium	heart
18	chr1:10461400-10475200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:10461400-10483000	Strong transcription	Cortex derived primary cultured neurospheres	brain
20	chr1:10461400-10483000	Strong transcription	Fetal Intestine Small	intestine
21	chr1:10461400-10483400	Strong transcription	Fetal Muscle Trunk	muscle
22	chr1:10461600-10481800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
23	chr1:10461600-10482800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:10461800-10472800	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr1:10461800-10473600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:10461800-10473600	Strong transcription	Primary hematopoietic stem cells	blood
27	chr1:10461800-10473600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:10461800-10473600	Strong transcription	Rectal Smooth Muscle	rectum
29	chr1:10461800-10474200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr1:10461800-10475200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr1:10461800-10482000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr1:10461800-10482000	Strong transcription	Dnd41	blood
33	chr1:10462000-10473000	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr1:10462000-10475200	Strong transcription	H9 Cell Line	embryonic stem cell
35	chr1:10462000-10482000	Strong transcription	Fetal Intestine Large	intestine
36	chr1:10462000-10482200	Strong transcription	Brain Germinal Matrix	brain
37	chr1:10462000-10483000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:10462200-10473200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:10462200-10475000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
40	chr1:10462200-10475200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
41	chr1:10462200-10475400	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr1:10462200-10475400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:10462200-10481600	Strong transcription	Liver	Liver
44	chr1:10462200-10481600	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr1:10462200-10482000	Strong transcription	Sigmoid Colon	Sigmoid Colon
46	chr1:10462200-10483200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr1:10462400-10470000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr1:10462400-10476000	Strong transcription	Ovary	ovary
49	chr1:10462600-10473600	Strong transcription	Esophagus	oesophagus
50	chr1:10462600-10482000	Strong transcription	Duodenum Mucosa	Duodenum

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