Variant report

Variant	esv3427855
Chromosome Location	chr10:98590262-98594060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1036)
CpG islands
(count:671)
Chromatin interactive
region (count:27)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1036 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:98591206-98591623	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:98590374-98590581	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:98591492-98591766	K562	blood:	n/a	n/a
4	ARID3A	chr10:98593511-98594264	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:98590315-98590687	K562	blood:	n/a	n/a
6	ATF2	chr10:98592222-98592986	GM12878	blood:	n/a	n/a
7	BACH1	chr10:98590236-98590603	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr10:98591622-98591908	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:98592404-98592938	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr10:98592412-98592953	GM12878	blood:	n/a	chr10:98592735-98592744 chr10:98592599-98592612
11	BCLAF1	chr10:98591455-98591980	GM12878	blood:	n/a	chr10:98591814-98591827 chr10:98591715-98591728
12	BCLAF1	chr10:98591417-98591827	GM12878	blood:	n/a	chr10:98591814-98591827 chr10:98591715-98591728
13	BCLAF1	chr10:98590196-98590741	GM12878	blood:	n/a	chr10:98590416-98590425
14	BCLAF1	chr10:98592459-98592950	GM12878	blood:	n/a	chr10:98592735-98592744 chr10:98592599-98592612
15	BHLHE40	chr10:98592051-98592980	HepG2	liver:	n/a	chr10:98592672-98592688 chr10:98592830-98592846 chr10:98592802-98592818 chr10:98592683-98592699 chr10:98592247-98592263 chr10:98592805-98592821
16	BHLHE40	chr10:98592578-98592790	A549	lung:	n/a	chr10:98592672-98592688 chr10:98592683-98592699
17	BHLHE40	chr10:98591522-98593138	K562	blood:	n/a	chr10:98592672-98592688 chr10:98592830-98592846 chr10:98592802-98592818 chr10:98592683-98592699 chr10:98592247-98592263 chr10:98591808-98591824 chr10:98592805-98592821
18	BHLHE40	chr10:98590391-98590582	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:98593411-98593520	GM12878	blood:	n/a	n/a
20	BHLHE40	chr10:98591578-98593027	GM12878	blood:	n/a	chr10:98592672-98592688 chr10:98592830-98592846 chr10:98592802-98592818 chr10:98592683-98592699 chr10:98592247-98592263 chr10:98591808-98591824 chr10:98592805-98592821
21	CBX3	chr10:98591336-98591934	K562	blood:	n/a	n/a
22	CCNT2	chr10:98591490-98593481	K562	blood:	n/a	chr10:98592292-98592301 chr10:98592362-98592371 chr10:98592630-98592639
23	CEBPB	chr10:98591449-98592124	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr10:98591445-98591802	K562	blood:	n/a	n/a
25	CEBPB	chr10:98591464-98591821	A549	lung:	n/a	n/a
26	CEBPB	chr10:98591484-98591817	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:98591514-98591779	HepG2	liver:	n/a	n/a
28	CEBPB	chr10:98591640-98591714	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr10:98591420-98591789	K562	blood:	n/a	n/a
30	CEBPD	chr10:98591479-98591854	K562	blood:	n/a	n/a
31	CEBPD	chr10:98591419-98591875	K562	blood:	n/a	n/a
32	CEBPD	chr10:98591622-98592779	HepG2	liver:	n/a	n/a
33	CHD1	chr10:98592049-98592261	GM12878	blood:	n/a	n/a
34	CHD1	chr10:98592660-98594046	GM12878	blood:	n/a	n/a
35	CHD2	chr10:98592090-98592820	HepG2	liver:	n/a	chr10:98592561-98592571
36	CHD2	chr10:98591669-98591708	K562	blood:	n/a	n/a
37	CHD2	chr10:98591619-98591657	HepG2	liver:	n/a	n/a
38	CHD2	chr10:98593326-98593570	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr10:98591458-98593045	GM12878	blood:	n/a	chr10:98592561-98592571
40	CHD2	chr10:98591482-98592963	Hela-S3	cervix:	n/a	chr10:98592561-98592571
41	CHD2	chr10:98592018-98592815	K562	blood:	n/a	chr10:98592561-98592571
42	CHD2	chr10:98592510-98592836	H1-hESC	embryonic stem cell:	n/a	chr10:98592561-98592571
43	CHD2	chr10:98593304-98593863	GM12878	blood:	n/a	n/a
44	CREB1	chr10:98592563-98593056	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr10:98591504-98593074	GM12878	blood:	n/a	n/a
46	CREB1	chr10:98592431-98592944	K562	blood:	n/a	n/a
47	CREB1	chr10:98591549-98593169	A549	lung:	n/a	n/a
48	CREB1	chr10:98591561-98593301	HepG2	liver:	n/a	n/a
49	CTBP2	chr10:98592341-98592973	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr10:98590800-98590950	HRPEpiC	eye:	n/a	chr10:98590851-98590864

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:98591780-98591830	HNPCEpiC	eye:	n/a
2	chr10:98592168-98592218	SAEC	small airway:	n/a
3	chr10:98593167-98593217	BJ	skin:	n/a
4	chr10:98590849-98590899	SK-N-SH	brain:	n/a
5	chr10:98591780-98591830	PANC-1	pancreas:	n/a
6	chr10:98593167-98593217	AG04450	lung:	fetal
7	chr10:98591602-98591652	HCF	heart:	n/a
8	chr10:98591602-98591652	AG09309	skin:	n/a
9	chr10:98592168-98592218	ovcar-3	ovarian:	n/a
10	chr10:98592837-98592887	PANC-1	pancreas:	n/a
11	chr10:98591780-98591830	HPAEpiC	pulmonary alveolar:	n/a
12	chr10:98592837-98592887	Jurkat	blood:	n/a
13	chr10:98591758-98591808	NHDF-neo	bronchial:	n/a
14	chr10:98593247-98593297	AoSMC	blood vessel:	n/a
15	chr10:98591758-98591808	HAEpiC	amniotic membrane:	n/a
16	chr10:98592168-98592218	AG09309	skin:	n/a
17	chr10:98590849-98590899	MCF-7	breast:	n/a
18	chr10:98590797-98590847	MCF10A-Er-Src	breast:	n/a
19	chr10:98591602-98591652	Jurkat	blood:	n/a
20	chr10:98591602-98591652	AG10803	skin:	n/a
21	chr10:98593167-98593217	HUVEC	blood vessel:	n/a
22	chr10:98593167-98593217	ECC-1	luminal epithelium:	n/a
23	chr10:98590574-98590624	GM19239	blood:	n/a
24	chr10:98592104-98592154	BE2_C	brain:	n/a
25	chr10:98592168-98592218	HL-60	blood:	n/a
26	chr10:98593247-98593297	Jurkat	blood:	n/a
27	chr10:98590797-98590847	HUVEC	blood vessel:	n/a
28	chr10:98593167-98593217	NH-A	brain:	n/a
29	chr10:98593247-98593297	AG04450	lung:	fetal
30	chr10:98593167-98593217	SKMC	muscle:	n/a
31	chr10:98590797-98590847	HRE	kidney:	n/a
32	chr10:98590849-98590899	HEK293	kidney:	embryo
33	chr10:98592168-98592218	AG09319	gingival:	n/a
34	chr10:98591758-98591808	HNPCEpiC	eye:	n/a
35	chr10:98592168-98592218	SK-N-MC	brain:	n/a
36	chr10:98592104-98592154	K562	blood:	n/a
37	chr10:98593167-98593217	SK-N-SH	brain:	n/a
38	chr10:98590574-98590624	HRPEpiC	eye:	n/a
39	chr10:98590574-98590624	A549	lung:	n/a
40	chr10:98592168-98592218	HCF	heart:	n/a
41	chr10:98591780-98591830	SK-N-SH	brain:	n/a
42	chr10:98592837-98592887	Hela-S3	cervix:	n/a
43	chr10:98592837-98592887	HCM	heart:	n/a
44	chr10:98590574-98590624	HUVEC	blood vessel:	n/a
45	chr10:98591780-98591830	HCF	heart:	n/a
46	chr10:98591602-98591652	GM12878	blood:	n/a
47	chr10:98590797-98590847	NHDF-neo	bronchial:	n/a
48	chr10:98591758-98591808	RPTEC	kidney:	n/a
49	chr10:98591602-98591652	HUVEC	blood vessel:	n/a
50	chr10:98590574-98590624	NH-A	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:98591566..98592141-chr12:52449274..52450124,2	Hela-S3	cervix:
2	chr10:98590420..98592007-chr10:98615843..98619097,3	K562	blood:
3	chr10:98272672..98275170-chr10:98590720..98593680,2	MCF-7	breast:
4	chr10:98133863..98136449-chr10:98590863..98592811,2	MCF-7	breast:
5	chr10:98592013..98592977-chr3:143690256..143690764,2	Hela-S3	cervix:
6	chr10:98398475..98400373-chr10:98590281..98591916,2	MCF-7	breast:
7	chr10:98591738..98592804-chr16:29973157..29974128,3	Hela-S3	cervix:
8	chr10:98392223..98394189-chr10:98590324..98593027,3	MCF-7	breast:
9	chr10:98592217..98593132-chr9:91925720..91926664,2	Hela-S3	cervix:
10	chr10:98524912..98526111-chr10:98589792..98591303,11	MCF-7	breast:
11	chr10:98345052..98347789-chr10:98590945..98593407,3	K562	blood:
12	chr10:98549134..98550000-chr10:98589983..98590943,3	K562	blood:
13	chr1:224622290..224622794-chr10:98591846..98592614,2	Hela-S3	cervix:
14	chr10:98592149..98592649-chr14:55493692..55494488,2	Hela-S3	cervix:
15	chr10:98588526..98590444-chr10:98592117..98594559,3	K562	blood:
16	chr10:98345733..98347828-chr10:98591279..98593531,2	MCF-7	breast:
17	chr10:98523538..98526378-chr10:98589191..98591883,2	MCF-7	breast:
18	chr10:98591262..98592221-chr5:108083306..108084137,2	Hela-S3	cervix:
19	chr10:98592030..98592614-chr3:101405121..101405644,2	Hela-S3	cervix:
20	chr10:98584665..98586917-chr10:98589906..98591474,2	K562	blood:
21	chr10:98400341..98400974-chr10:98590389..98590915,2	MCF-7	breast:
22	chr10:98591605..98592442-chr19:55628620..55629157,2	Hela-S3	cervix:
23	chr10:98591909..98592710-chr6:33678934..33679670,2	Hela-S3	cervix:
24	chr10:98593714..98596338-chr10:98621792..98624067,2	K562	blood:
25	chr10:98402475..98403373-chr10:98589917..98590679,3	MCF-7	breast:
26	chr10:98591162..98592122-chr7:106809872..106810661,2	Hela-S3	cervix:
27	chr10:98525204..98525891-chr10:98589963..98590854,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PIK3AP1-6	chr10:98590424-98592003	NONHSAT015837

No data

Variant related genes	Relation type
LCOR	TF binding region
MIR607	TF binding region
LCOR	CpG island
MIR607	CpG island
ENSG00000123358	chromatin interactions
ENSG00000143786	chromatin interactions
ENSG00000077147	chromatin interactions
ENSG00000095587	chromatin interactions
ENSG00000198554	chromatin interactions
ENSG00000181744	chromatin interactions
ENSG00000125503	chromatin interactions
ENSG00000105856	chromatin interactions
ENSG00000155629	chromatin interactions
ENSG00000196233	chromatin interactions
ENSG00000114391	chromatin interactions
ENSG00000137288	chromatin interactions
ENSG00000149932	chromatin interactions
ENSG00000180008	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000123975	chromatin interactions

Extended variants
information (count: 114 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571738182	chr10:98590279-98590280	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs538838920	chr10:98590289-98590290	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs557570352	chr10:98590341-98590342	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs544464237	chr10:98590355-98590356	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs569569010	chr10:98590379-98590380	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs2851	chr10:98590439-98590440	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs373575230	chr10:98590479-98590480	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs77613888	chr10:98590486-98590487	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs555310331	chr10:98590496-98590497	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs573643954	chr10:98590538-98590539	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs562367441	chr10:98590562-98590563	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs541043918	chr10:98590574-98590575	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs189405955	chr10:98590590-98590591	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs192153605	chr10:98590598-98590599	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs61858077	chr10:98590625-98590626	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs184234582	chr10:98590655-98590656	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs563192974	chr10:98590662-98590663	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs543191976	chr10:98590664-98590665	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs148233619	chr10:98590728-98590729	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs542475440	chr10:98590785-98590786	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs560865986	chr10:98590786-98590787	Active TSS Flanking Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs189427851	chr10:98590800-98590801	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs547003725	chr10:98590858-98590859	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs12769505	chr10:98590888-98590889	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs35660482	chr10:98590918-98590919	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs553507897	chr10:98590927-98590928	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs565222512	chr10:98590930-98590931	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs141357221	chr10:98590933-98590934	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs181824658	chr10:98590934-98590935	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs569433104	chr10:98590957-98590958	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs369294038	chr10:98590959-98590960	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
32	rs536851911	chr10:98591075-98591076	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
33	rs548872856	chr10:98591080-98591081	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
34	rs370549595	chr10:98591248-98591249	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs567200287	chr10:98591283-98591284	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
36	rs560327542	chr10:98591286-98591287	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
37	rs150788945	chr10:98591295-98591296	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
38	rs116096267	chr10:98591307-98591308	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
39	rs114762962	chr10:98591371-98591372	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
40	rs538683730	chr10:98591381-98591382	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
41	rs139050852	chr10:98591390-98591391	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
42	rs200771126	chr10:98591407-98591408	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
43	rs374629785	chr10:98591416-98591417	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs201933405	chr10:98591419-98591420	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
45	rs199497945	chr10:98591420-98591421	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
46	rs568924340	chr10:98591423-98591424	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
47	rs573129892	chr10:98591446-98591447	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
48	rs540259996	chr10:98591547-98591548	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
49	rs565236496	chr10:98591552-98591553	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
50	rs532410823	chr10:98591594-98591595	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Recurrent pregnancy loss	19789632	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98586800-98590400	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr10:98587200-98591400	Weak transcription	Left Ventricle	heart
3	chr10:98588200-98591000	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr10:98589000-98591000	Enhancers	HepG2	liver
5	chr10:98589200-98590400	Weak transcription	Fetal Intestine Large	intestine
6	chr10:98589200-98591000	Enhancers	Duodenum Mucosa	Duodenum
7	chr10:98589200-98591000	Weak transcription	HSMMtube	muscle
8	chr10:98589200-98591200	Enhancers	Primary B cells from peripheral blood	blood
9	chr10:98589800-98591000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
10	chr10:98589800-98591000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr10:98590000-98590400	Flanking Active TSS	K562	blood
12	chr10:98590000-98590800	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr10:98590000-98591000	Enhancers	Primary B cells from cord blood	blood
14	chr10:98590000-98591000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr10:98590000-98591000	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr10:98590000-98591000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:98590000-98591000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:98590000-98591000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr10:98590000-98591000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr10:98590000-98591000	Enhancers	A549	lung
21	chr10:98590000-98591000	Enhancers	Osteobl	bone
22	chr10:98590000-98591200	Enhancers	Primary T cells from cord blood	blood
23	chr10:98590000-98591200	Enhancers	Primary hematopoietic stem cells	blood
24	chr10:98590000-98591200	Enhancers	Primary T helper naive cells from peripheral blood	blood
25	chr10:98590000-98591200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr10:98590000-98591200	Enhancers	Primary T helper cells fromperipheralblood	blood
27	chr10:98590000-98591200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr10:98590000-98591400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr10:98590000-98591400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr10:98590000-98591400	Enhancers	Small Intestine	intestine
31	chr10:98590000-98591600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:98590000-98591600	Enhancers	Stomach Mucosa	stomach
33	chr10:98590200-98590400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr10:98590200-98590400	Active TSS	Liver	Liver
35	chr10:98590200-98590400	Enhancers	Fetal Kidney	kidney
36	chr10:98590200-98590400	Flanking Active TSS	GM12878-XiMat	blood
37	chr10:98590200-98590600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr10:98590200-98590600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr10:98590200-98590600	Active TSS	Rectal Mucosa Donor 29	rectum
40	chr10:98590200-98590800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr10:98590200-98590800	Enhancers	NHDF-Ad	bronchial
42	chr10:98590200-98591000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr10:98590200-98591000	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr10:98590200-98591000	Enhancers	HMEC	breast
45	chr10:98590200-98591000	Enhancers	NHEK	skin
46	chr10:98590200-98591200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr10:98590200-98591200	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr10:98590200-98591200	Enhancers	Colon Smooth Muscle	Colon
49	chr10:98590200-98591200	Enhancers	Fetal Intestine Small	intestine
50	chr10:98590200-98594600	Active TSS	HUES48 Cell Line	embryonic stem cell

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