Variant report

Variant	esv1836264
Chromosome Location	chr1:10473200-10483456
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:365)
CpG islands
(count:122)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr1:10475540-10475782	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:10475375-10475878	K562	blood:	n/a	n/a
6	BCL3	chr1:10475010-10475874	A549	lung:	n/a	n/a
7	BCL3	chr1:10480357-10481022	A549	lung:	n/a	n/a
8	BCL3	chr1:10481065-10485114	A549	lung:	n/a	n/a
9	BCL3	chr1:10475047-10475833	A549	lung:	n/a	n/a
10	BCL3	chr1:10481151-10483619	A549	lung:	n/a	n/a
11	BHLHE40	chr1:10481691-10481732	K562	blood:	n/a	n/a
12	BHLHE40	chr1:10475286-10475924	K562	blood:	n/a	n/a
13	CBX3	chr1:10475082-10475901	K562	blood:	n/a	n/a
14	CCNT2	chr1:10480614-10480901	K562	blood:	n/a	n/a
15	CEBPB	chr1:10475191-10475915	K562	blood:	n/a	n/a
16	CEBPB	chr1:10475437-10475803	IMR90	lung:	n/a	n/a
17	CEBPB	chr1:10480685-10480898	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	chr1:10475168-10475828	A549	lung:	n/a	n/a
21	CEBPB	chr1:10475190-10475808	K562	blood:	n/a	n/a
22	CEBPB	chr1:10475439-10475759	K562	blood:	n/a	n/a
23	CEBPB	chr1:10475062-10475971	A549	lung:	n/a	n/a
24	CHD2	chr1:10475464-10475664	K562	blood:	n/a	n/a
25	CREB1	chr1:10481782-10482246	A549	lung:	n/a	n/a
26	CREB1	chr1:10475400-10475729	A549	lung:	n/a	n/a
27	CTCF	chr1:10475480-10475630	HPAF	blood vessel:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
28	CTCF	chr1:10479560-10479710	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr1:10474854-10474955	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr1:10481900-10482050	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr1:10482012-10482081	A549	lung:	n/a	n/a
32	CTCF	chr1:10482024-10482095	MCF-7	breast:	n/a	n/a
33	CTCF	chr1:10478175-10478239	Lung_OC	lung:	n/a	n/a
34	CTCF	chr1:10475400-10475550	BJ	skin:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
35	CTCF	chr1:10482013-10482084	MCF-7	breast:	n/a	n/a
36	CTCF	chr1:10475460-10475610	HUVEC	blood vessel:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
37	CTCF	chr1:10475420-10475570	SAEC	small airway:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
38	CTCF	chr1:10475420-10475570	BJ	skin:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
39	CTCF	chr1:10482036-10482066	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr1:10475380-10475530	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr1:10482014-10482089	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:10475361-10475810	K562	blood:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
43	CTCF	chr1:10475420-10475570	HCPEpiC	choroid plexus:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
44	CTCF	chr1:10475420-10475570	HPAF	blood vessel:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
45	CTCF	chr1:10481940-10482090	NHEK	skin:	n/a	n/a
46	CTCF	chr1:10475500-10475650	HepG2	liver:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
47	CTCF	chr1:10475340-10475490	K562	blood:	n/a	n/a
48	CTCF	chr1:10479583-10479670	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:10475500-10475650	HCM	heart:	n/a	chr1:10475523-10475536 chr1:10475521-10475539 chr1:10475527-10475536
50	CTCF	chr1:10475360-10475510	HCM	heart:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10475318-10475368	NHDF-neo	bronchial:	n/a
2	chr1:10475318-10475368	PrEC	prostate:	n/a
3	chr1:10475318-10475368	HRCEpiC	kidney:	n/a
4	chr1:10475318-10475368	AoSMC	blood vessel:	n/a
5	chr1:10480153-10480203	PrEC	prostate:	n/a
6	chr1:10480153-10480203	MCF10A-Er-Src	breast:	n/a
7	chr1:10475318-10475368	HMEC	breast:	n/a
8	chr1:10480153-10480203	MCF-7	breast:	n/a
9	chr1:10475318-10475368	HRPEpiC	eye:	n/a
10	chr1:10480153-10480203	NHDF-neo	bronchial:	n/a
11	chr1:10475318-10475368	HAEpiC	amniotic membrane:	n/a
12	chr1:10480153-10480203	T-47D	breast:	n/a
13	chr1:10475318-10475368	HL-60	blood:	n/a
14	chr1:10475318-10475368	AG09309	skin:	n/a
15	chr1:10475318-10475368	HUVEC	blood vessel:	n/a
16	chr1:10475318-10475368	HCT-116	colon:	n/a
17	chr1:10475318-10475368	HCM	heart:	n/a
18	chr1:10480153-10480203	HRCEpiC	kidney:	n/a
19	chr1:10480153-10480203	GM12878	blood:	n/a
20	chr1:10480153-10480203	HUVEC	blood vessel:	n/a
21	chr1:10480153-10480203	A549	lung:	n/a
22	chr1:10480153-10480203	ovcar-3	ovarian:	n/a
23	chr1:10480153-10480203	SK-N-SH_RA	brain:	n/a
24	chr1:10480153-10480203	AG04449	skin:	fetal
25	chr1:10475318-10475368	ProgFib	skin:	n/a
26	chr1:10480153-10480203	PFSK-1	brain:	n/a
27	chr1:10475318-10475368	SKMC	muscle:	n/a
28	chr1:10480153-10480203	NH-A	brain:	n/a
29	chr1:10480153-10480203	HEEpiC	esophagus:	n/a
30	chr1:10480153-10480203	ECC-1	luminal epithelium:	n/a
31	chr1:10475318-10475368	Jurkat	blood:	n/a
32	chr1:10480153-10480203	HEK293	kidney:	embryo
33	chr1:10480153-10480203	HNPCEpiC	eye:	n/a
34	chr1:10480153-10480203	ProgFib	skin:	n/a
35	chr1:10480153-10480203	NT2-D1	testis:	n/a
36	chr1:10480153-10480203	PANC-1	pancreas:	n/a
37	chr1:10475318-10475368	HPAEpiC	pulmonary alveolar:	n/a
38	chr1:10475318-10475368	MCF-7	breast:	n/a
39	chr1:10480153-10480203	U87	brain:	n/a
40	chr1:10480153-10480203	GM12892	blood:	n/a
41	chr1:10480153-10480203	SAEC	small airway:	n/a
42	chr1:10480153-10480203	HCF	heart:	n/a
43	chr1:10480153-10480203	GM06990	blood:	n/a
44	chr1:10475318-10475368	AG09319	gingival:	n/a
45	chr1:10475318-10475368	GM12878	blood:	n/a
46	chr1:10480153-10480203	SK-N-MC	brain:	n/a
47	chr1:10475318-10475368	HepG2	liver:	n/a
48	chr1:10480153-10480203	H1-hESC	embryonic stem cell:	embryo
49	chr1:10475318-10475368	HEK293	kidney:	embryo
50	chr1:10475318-10475368	H1-hESC	embryonic stem cell:	embryo

(count:26 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 470 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:470 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41289075	chr1:10473200-10473201	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
2	rs150181821	chr1:10473202-10473203	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
3	rs200998486	chr1:10473204-10473205	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
4	rs202134777	chr1:10473219-10473220	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
5	rs375996998	chr1:10473222-10473223	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
6	rs61736950	chr1:10473238-10473239	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573041776	chr1:10473263-10473264	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
8	rs369275295	chr1:10473265-10473266	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
9	rs11547610	chr1:10473266-10473267	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs143540325	chr1:10473275-10473276	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
11	rs200238924	chr1:10473286-10473287	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
12	rs199582637	chr1:10473287-10473288	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
13	rs112301623	chr1:10473326-10473327	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
14	rs201584341	chr1:10473327-10473328	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
15	rs375650373	chr1:10473332-10473333	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
16	rs370257596	chr1:10473340-10473341	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
17	rs35645432	chr1:10473362-10473363	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
18	rs542953749	chr1:10473373-10473374	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
19	rs149000470	chr1:10473445-10473446	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
20	rs574128004	chr1:10473493-10473494	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
21	rs191525655	chr1:10473522-10473523	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
22	rs377101939	chr1:10473685-10473686	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs545624383	chr1:10473711-10473712	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541044393	chr1:10473733-10473734	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560519176	chr1:10473734-10473735	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs527842474	chr1:10473777-10473778	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs74795675	chr1:10473814-10473815	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs111337927	chr1:10473822-10473823	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs147118951	chr1:10473832-10473833	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs374273424	chr1:10473833-10473834	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs138581801	chr1:10473902-10473903	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs549486065	chr1:10473948-10473949	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs35827044	chr1:10473961-10473962	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs57709995	chr1:10473962-10473963	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs143972735	chr1:10474084-10474085	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs2847346	chr1:10474087-10474088	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs538546539	chr1:10474102-10474103	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs182607524	chr1:10474172-10474173	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs377629737	chr1:10474193-10474194	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs565541590	chr1:10474237-10474238	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs372872292	chr1:10474312-10474313	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs369288046	chr1:10474332-10474333	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs61775983	chr1:10474352-10474353	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs186940184	chr1:10474398-10474399	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs533279948	chr1:10474415-10474416	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs573775267	chr1:10474417-10474418	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs35759975	chr1:10474430-10474431	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs373032794	chr1:10474440-10474441	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs563541954	chr1:10474454-10474455	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs58014725	chr1:10474457-10474458	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:115)

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
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:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr1:10460400-10475200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr1:10460600-10481200	Strong transcription	H1 Cell Line	embryonic stem cell
5	chr1:10460800-10480400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr1:10460800-10482000	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr1:10460800-10482400	Strong transcription	Fetal Stomach	stomach
8	chr1:10460800-10483400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:10461000-10474600	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr1:10461000-10475200	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr1:10461000-10476800	Weak transcription	Fetal Heart	heart
12	chr1:10461000-10482000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr1:10461200-10482000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr1:10461200-10482000	Strong transcription	Fetal Muscle Leg	muscle
15	chr1:10461200-10490000	Weak transcription	Right Atrium	heart
16	chr1:10461400-10475200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:10461400-10483000	Strong transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:10461400-10483000	Strong transcription	Fetal Intestine Small	intestine
19	chr1:10461400-10483400	Strong transcription	Fetal Muscle Trunk	muscle
20	chr1:10461600-10481800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr1:10461600-10482800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr1:10461800-10473600	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr1:10461800-10473600	Strong transcription	Primary hematopoietic stem cells	blood
24	chr1:10461800-10473600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr1:10461800-10473600	Strong transcription	Rectal Smooth Muscle	rectum
26	chr1:10461800-10474200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
27	chr1:10461800-10475200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:10461800-10482000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:10461800-10482000	Strong transcription	Dnd41	blood
30	chr1:10462000-10475200	Strong transcription	H9 Cell Line	embryonic stem cell
31	chr1:10462000-10482000	Strong transcription	Fetal Intestine Large	intestine
32	chr1:10462000-10482200	Strong transcription	Brain Germinal Matrix	brain
33	chr1:10462000-10483000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:10462200-10473200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:10462200-10475000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
36	chr1:10462200-10475200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
37	chr1:10462200-10475400	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr1:10462200-10475400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr1:10462200-10481600	Strong transcription	Liver	Liver
40	chr1:10462200-10481600	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr1:10462200-10482000	Strong transcription	Sigmoid Colon	Sigmoid Colon
42	chr1:10462200-10483200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:10462400-10476000	Strong transcription	Ovary	ovary
44	chr1:10462600-10473600	Strong transcription	Esophagus	oesophagus
45	chr1:10462600-10482000	Strong transcription	Duodenum Mucosa	Duodenum
46	chr1:10462800-10473400	Strong transcription	Primary B cells from cord blood	blood
47	chr1:10462800-10473400	Strong transcription	Lung	lung
48	chr1:10462800-10473400	Strong transcription	Right Ventricle	heart
49	chr1:10462800-10473800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr1:10462800-10474800	Strong transcription	Primary T cells fromperipheralblood	blood

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