Variant report

Variant	nsv1041462
Chromosome Location	chr10:89518729-89584284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1494)
CpG islands
(count:1162)
Chromatin interactive
region (count:56)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:89576584-89576789	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:89521839-89521939	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:89578025-89578152	K562	blood:	n/a	n/a
4	ARID3A	chr10:89577794-89578166	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:89575959-89576196	K562	blood:	n/a	n/a
6	ATF2	chr10:89553899-89554469	GM12878	blood:	n/a	n/a
7	ATF2	chr10:89577688-89578901	GM12878	blood:	n/a	n/a
8	ATF2	chr10:89521575-89522015	GM12878	blood:	n/a	n/a
9	ATF2	chr10:89577542-89579031	GM12878	blood:	n/a	n/a
10	ATF2	chr10:89553980-89554369	GM12878	blood:	n/a	n/a
11	ATF3	chr10:89577934-89578140	K562	blood:	n/a	n/a
12	ATF3	chr10:89577503-89578236	A549	lung:	n/a	n/a
13	BACH1	chr10:89577656-89578527	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr10:89521578-89522033	GM12878	blood:	n/a	chr10:89521778-89521789
15	BATF	chr10:89554077-89554440	GM12878	blood:	n/a	n/a
16	BATF	chr10:89557834-89558102	GM12878	blood:	n/a	n/a
17	BATF	chr10:89557799-89558125	GM12878	blood:	n/a	n/a
18	BATF	chr10:89521676-89521955	GM12878	blood:	n/a	chr10:89521778-89521789
19	BCL11A	chr10:89554123-89554473	GM12878	blood:	n/a	n/a
20	BCL11A	chr10:89557888-89558020	GM12878	blood:	n/a	n/a
21	BCL3	chr10:89577582-89578224	A549	lung:	n/a	chr10:89578059-89578068 chr10:89577998-89578007
22	BCL3	chr10:89577655-89578553	A549	lung:	n/a	chr10:89578059-89578068 chr10:89577998-89578007
23	BCLAF1	chr10:89577438-89578340	GM12878	blood:	n/a	chr10:89578059-89578068 chr10:89577998-89578007
24	BCLAF1	chr10:89553969-89554431	GM12878	blood:	n/a	n/a
25	BCLAF1	chr10:89553969-89554407	GM12878	blood:	n/a	n/a
26	BCLAF1	chr10:89577048-89578841	GM12878	blood:	n/a	chr10:89578059-89578068 chr10:89577998-89578007
27	BHLHE40	chr10:89577136-89578791	K562	blood:	n/a	n/a
28	BHLHE40	chr10:89554104-89554496	GM12878	blood:	n/a	n/a
29	BHLHE40	chr10:89577315-89578823	GM12878	blood:	n/a	n/a
30	BRCA1	chr10:89577508-89578339	HepG2	liver:	n/a	n/a
31	BRCA1	chr10:89577177-89578810	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr10:89565130-89565165	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr10:89577939-89578300	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr10:89535534-89535672	Hela-S3	cervix:	n/a	n/a
35	CBX3	chr10:89561649-89561958	K562	blood:	n/a	n/a
36	CBX3	chr10:89561589-89561972	K562	blood:	n/a	n/a
37	CBX3	chr10:89577739-89578512	K562	blood:	n/a	n/a
38	CCNT2	chr10:89577563-89578598	K562	blood:	n/a	n/a
39	CCNT2	chr10:89523109-89523475	K562	blood:	n/a	n/a
40	CEBPB	chr10:89521794-89521943	HepG2	liver:	n/a	n/a
41	CEBPB	chr10:89575851-89578965	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:89522365-89522511	A549	lung:	n/a	n/a
43	CEBPB	chr10:89521744-89522006	IMR90	lung:	n/a	n/a
44	CEBPB	chr10:89575901-89576688	K562	blood:	n/a	n/a
45	CEBPB	chr10:89559688-89559845	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr10:89576318-89576503	K562	blood:	n/a	n/a
47	CEBPB	chr10:89577832-89578135	IMR90	lung:	n/a	n/a
48	CEBPB	chr10:89527191-89527193	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr10:89576008-89576594	HepG2	liver:	n/a	n/a
50	CEBPB	chr10:89575911-89576619	A549	lung:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:89578165-89578215	SAEC	small airway:	n/a
2	chr10:89578113-89578163	U87	brain:	n/a
3	chr10:89578176-89578226	CMK	blood:	n/a
4	chr10:89578165-89578215	SAEC	small airway:	n/a
5	chr10:89578113-89578163	U87	brain:	n/a
6	chr10:89578176-89578226	CMK	blood:	n/a
7	chr10:89578072-89578122	SK-N-MC	brain:	n/a
8	chr10:89577906-89577956	CMK	blood:	n/a
9	chr10:89578111-89578161	GM12891	blood:	n/a
10	chr10:89577736-89577786	AG09309	skin:	n/a
11	chr10:89577788-89577838	NT2-D1	testis:	n/a
12	chr10:89578176-89578226	AG09309	skin:	n/a
13	chr10:89577399-89577449	Caco-2	colon:	n/a
14	chr10:89578165-89578215	HMEC	breast:	n/a
15	chr10:89577736-89577786	ProgFib	skin:	n/a
16	chr10:89577882-89577932	HRE	kidney:	n/a
17	chr10:89577906-89577956	HEEpiC	esophagus:	n/a
18	chr10:89577882-89577932	CMK	blood:	n/a
19	chr10:89580388-89580438	BE2_C	brain:	n/a
20	chr10:89580388-89580438	AG09309	skin:	n/a
21	chr10:89578165-89578215	AoSMC	blood vessel:	n/a
22	chr10:89578165-89578215	GM19239	blood:	n/a
23	chr10:89578165-89578215	GM12878	blood:	n/a
24	chr10:89577906-89577956	SKMC	muscle:	n/a
25	chr10:89578111-89578161	HNPCEpiC	eye:	n/a
26	chr10:89578072-89578122	HepG2	liver:	n/a
27	chr10:89578187-89578237	NHDF-neo	bronchial:	n/a
28	chr10:89577736-89577786	AG09319	gingival:	n/a
29	chr10:89578111-89578161	HUVEC	blood vessel:	n/a
30	chr10:89577399-89577449	SKMC	muscle:	n/a
31	chr10:89577882-89577932	SAEC	small airway:	n/a
32	chr10:89580388-89580438	AG04450	lung:	fetal
33	chr10:89578168-89578218	GM06990	blood:	n/a
34	chr10:89577850-89577900	HIPEpiC	eye:	n/a
35	chr10:89578168-89578218	BJ	skin:	n/a
36	chr10:89574331-89574381	Caco-2	colon:	n/a
37	chr10:89578165-89578215	NHDF-neo	bronchial:	n/a
38	chr10:89578019-89578069	SKMC	muscle:	n/a
39	chr10:89577850-89577900	SKMC	muscle:	n/a
40	chr10:89574331-89574381	PANC-1	pancreas:	n/a
41	chr10:89577736-89577786	Hepatocyte	liver:	n/a
42	chr10:89578165-89578215	SK-N-SH	brain:	n/a
43	chr10:89536166-89536216	MCF10A-Er-Src	breast:	n/a
44	chr10:89577399-89577449	AG09319	gingival:	n/a
45	chr10:89536166-89536216	HCPEpiC	choroid plexus:	n/a
46	chr10:89577850-89577900	HCT-116	colon:	n/a
47	chr10:89578019-89578069	GM12878	blood:	n/a
48	chr10:89536166-89536216	SAEC	small airway:	n/a
49	chr10:89577850-89577900	NB4	blood:	n/a
50	chr10:89578168-89578218	AG09309	skin:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:89531576..89533907-chr10:89541046..89543285,2	MCF-7	breast:
2	chr10:89526081..89527597-chr10:89531587..89533299,2	K562	blood:
3	chr10:89526081..89527597-chr10:89531587..89533299,2	K562	blood:
4	chr10:89523125..89525014-chr10:89530627..89532236,2	MCF-7	breast:
5	chr10:89578063..89578573-chr7:77166206..77166939,2	Hela-S3	cervix:
6	chr10:89572839..89574816-chr10:89578225..89580021,2	K562	blood:
7	chr10:89539239..89541985-chr10:89576945..89578679,2	MCF-7	breast:
8	chr10:89581988..89583906-chr10:89620816..89623644,2	MCF-7	breast:
9	chr10:89578473..89580973-chr10:89716614..89719298,2	K562	blood:
10	chr10:89517545..89520078-chr10:89524489..89526607,2	MCF-7	breast:
11	chr10:89418532..89421056-chr10:89521556..89523639,2	MCF-7	breast:
12	chr10:89543639..89545668-chr10:89555412..89557312,2	MCF-7	breast:
13	chr10:89577120..89579087-chr10:89622150..89625835,3	MCF-7	breast:
14	chr10:89531576..89533907-chr10:89541046..89543285,2	MCF-7	breast:
15	chr10:89522883..89524581-chr10:89525481..89528269,2	K562	blood:
16	chr1:78444381..78445068-chr10:89577628..89578293,2	HCT-116	colon:
17	chr10:89403582..89405804-chr10:89575405..89577517,2	K562	blood:
18	chr10:89566431..89568592-chr10:89569858..89571983,2	MCF-7	breast:
19	chr10:89548477..89550357-chr10:89552346..89554969,2	K562	blood:
20	chr10:89545916..89549076-chr10:89574795..89578314,3	K562	blood:
21	chr10:89577213..89577931-chr12:120729063..120729972,2	HCT-116	colon:
22	chr10:89523125..89525014-chr10:89530627..89532236,2	MCF-7	breast:
23	chr10:89575517..89578014-chr10:89580293..89583592,3	K562	blood:
24	chr10:89560023..89562647-chr10:89574852..89577669,2	MCF-7	breast:
25	chr10:89579775..89581930-chr10:89585369..89587872,2	MCF-7	breast:
26	chr10:89557779..89559626-chr10:89565125..89566841,2	MCF-7	breast:
27	chr10:89577445..89577987-chr19:680043..680972,2	Hela-S3	cervix:
28	chr10:89566431..89568592-chr10:89569858..89571983,2	MCF-7	breast:
29	chr10:89577659..89578611-chr5:78907933..78908541,2	Hela-S3	cervix:
30	chr10:89577320..89579545-chr10:89584211..89586148,2	K562	blood:
31	chr10:89571592..89573409-chr10:89582904..89584628,2	K562	blood:
32	chr10:89517545..89520078-chr10:89524489..89526607,2	MCF-7	breast:
33	chr10:89522883..89524581-chr10:89525481..89528269,2	K562	blood:
34	chr10:89416173..89416867-chr10:89531418..89532343,5	K562	blood:
35	chr10:89577385..89578083-chr11:61559882..61560539,2	Hela-S3	cervix:
36	chr10:89575333..89578815-chr10:89619388..89623763,5	K562	blood:
37	chr1:44116091..44116658-chr10:89577728..89578268,2	HCT-116	colon:
38	chr10:89575231..89578479-chr10:89619975..89624868,8	K562	blood:
39	chr10:89293288..89293802-chr10:89531355..89532198,2	MCF-7	breast:
40	chr10:89542324..89546194-chr10:89549829..89553311,3	K562	blood:
41	chr10:89576079..89578102-chr10:89621664..89623913,2	MCF-7	breast:
42	chr10:89565566..89567376-chr10:89574790..89577127,2	K562	blood:
43	chr10:89543639..89545668-chr10:89555412..89557312,2	MCF-7	breast:
44	chr10:89527650..89529882-chr10:89533805..89535747,2	K562	blood:
45	chr10:89531718..89534084-chr10:89536520..89538723,2	K562	blood:
46	chr10:89560023..89562647-chr10:89574852..89577669,2	MCF-7	breast:
47	chr10:89564584..89567110-chr10:89568918..89570948,2	K562	blood:
48	chr10:89531718..89534084-chr10:89536520..89538723,2	K562	blood:
49	chr10:89564584..89567110-chr10:89568918..89570948,2	K562	blood:
50	chr10:89527650..89529882-chr10:89533805..89535747,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTEN-6	chr10:89578659-89578838	NONHSAT015451
2	lnc-PTEN-6	chr10:89578182-89578471	NONHSAT015451
3	lnc-PTEN-6	chr10:89577685-89577746	NONHSAT015450
4	lnc-PTEN-6	chr10:89578659-89579020	NONHSAT015450

No data

Variant related genes	Relation type
ATAD1	TF binding region
CFL1P1	TF binding region
ATAD1	CpG island
CFL1P1	CpG island
ENSG00000198682	chromatin interactions
ENSG00000164329	chromatin interactions
ENSG00000162613	chromatin interactions
ENSG00000127947	chromatin interactions
ENSG00000134824	chromatin interactions
ENSG00000223820	chromatin interactions
ENSG00000168496	chromatin interactions
ENSG00000196566	chromatin interactions
ENSG00000227268	chromatin interactions
ENSG00000138138	chromatin interactions
ENSG00000207601	chromatin interactions
ENSG00000171862	chromatin interactions
ENSG00000070404	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000134825	chromatin interactions
ENSG00000066135	chromatin interactions

Extended variants
information (count: 2210 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2210 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202117291	chr10:89518781-89518782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs186784713	chr10:89518819-89518820	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565881907	chr10:89518853-89518854	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563946197	chr10:89518855-89518856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536114757	chr10:89518902-89518903	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554851095	chr10:89518977-89518978	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368244602	chr10:89519030-89519031	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569898667	chr10:89519064-89519065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536634388	chr10:89519075-89519076	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558158566	chr10:89519094-89519095	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576503776	chr10:89519112-89519113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531925723	chr10:89519183-89519184	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143558599	chr10:89519191-89519192	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559884317	chr10:89519225-89519226	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12772164	chr10:89519252-89519253	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527957459	chr10:89519260-89519261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540744058	chr10:89519371-89519372	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10509411	chr10:89519376-89519377	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs572604773	chr10:89519529-89519530	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145544119	chr10:89519535-89519536	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148877109	chr10:89519604-89519605	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs34836939	chr10:89519616-89519617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531162366	chr10:89519636-89519637	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs193245811	chr10:89519713-89519714	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370875464	chr10:89519721-89519722	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547476421	chr10:89519744-89519745	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543815127	chr10:89519759-89519760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs386746286	chr10:89519766-89519767	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs150190807	chr10:89519777-89519778	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565299862	chr10:89519821-89519822	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73352850	chr10:89519876-89519877	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs66863455	chr10:89519880-89519881	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs565690033	chr10:89519922-89519923	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529895724	chr10:89519930-89519931	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556641591	chr10:89519969-89519970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116189599	chr10:89520055-89520056	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34325090	chr10:89520138-89520139	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs184092841	chr10:89520143-89520144	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34466534	chr10:89520188-89520189	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs558097145	chr10:89520217-89520218	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs11592130	chr10:89520241-89520242	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs188467017	chr10:89520293-89520294	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs537754736	chr10:89520298-89520299	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs140626507	chr10:89520301-89520302	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs574490392	chr10:89520307-89520308	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs55886446	chr10:89520313-89520314	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548364898	chr10:89520381-89520382	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs375234599	chr10:89520392-89520393	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs576780386	chr10:89520428-89520429	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs544141355	chr10:89520429-89520430	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Thoracic aortic aneurysm	21092924	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
Endometrioid adenocarcinoma	16974079	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Colorectal cancer	18645599	CNVD
Polyposis syndrome	18645599	CNVD
Prostate cancer	17245344	CNVD
Glioblastoma multiforme	17369134	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Autism	22241247	CNVD
Intracranial ependymoma	16609018	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21569311	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Colorectal cancer	19359472	CNVD
Neurocytoma	17123091	CNVD
Prostate cancer	16461572	CNVD
Basal-like breast cancer	18066063	CNVD
Effusion lymphoma	18079361	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Glioblastoma multiforme	19115005	CNVD
Prostate cancer	21147910	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2375 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89463000-89541400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr10:89473000-89577200	Weak transcription	Gastric	stomach
3	chr10:89476200-89542400	Weak transcription	Pancreas	Pancrea
4	chr10:89495000-89541400	Weak transcription	Right Ventricle	heart
5	chr10:89495000-89576400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr10:89495200-89530600	Weak transcription	Brain Cingulate Gyrus	brain
7	chr10:89495200-89542600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr10:89495200-89544600	Weak transcription	Brain Substantia Nigra	brain
9	chr10:89495200-89559200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr10:89495200-89577400	Weak transcription	Spleen	Spleen
11	chr10:89495400-89525600	Weak transcription	Brain Hippocampus Middle	brain
12	chr10:89498200-89519400	Weak transcription	Stomach Smooth Muscle	stomach
13	chr10:89498200-89541400	Weak transcription	Aorta	Aorta
14	chr10:89498800-89536200	Weak transcription	Small Intestine	intestine
15	chr10:89503200-89521200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:89503400-89523200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr10:89503400-89528400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr10:89504200-89551800	Weak transcription	Psoas Muscle	Psoas
19	chr10:89505000-89520000	Weak transcription	Fetal Stomach	stomach
20	chr10:89506800-89520000	Weak transcription	Fetal Intestine Small	intestine
21	chr10:89507000-89525600	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr10:89507000-89557600	Weak transcription	Lung	lung
23	chr10:89509000-89527000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr10:89510200-89553800	Weak transcription	Esophagus	oesophagus
25	chr10:89510400-89525800	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr10:89510800-89519800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr10:89510800-89523000	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr10:89511000-89519800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:89511000-89576800	Weak transcription	Colonic Mucosa	Colon
30	chr10:89511200-89521400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr10:89511200-89526800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr10:89511400-89521200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr10:89511600-89525600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr10:89512000-89520200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr10:89512000-89520400	Strong transcription	Dnd41	blood
36	chr10:89512000-89522200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr10:89512400-89521400	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr10:89512400-89521800	Weak transcription	NHLF	lung
39	chr10:89512600-89519200	Strong transcription	HUES64 Cell Line	embryonic stem cell
40	chr10:89512600-89520200	Weak transcription	Thymus	Thymus
41	chr10:89512600-89525600	Weak transcription	Fetal Brain Female	brain
42	chr10:89512800-89560400	Weak transcription	Fetal Brain Male	brain
43	chr10:89513000-89520200	Strong transcription	GM12878-XiMat	blood
44	chr10:89513000-89521400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr10:89513200-89520200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:89513200-89520600	Strong transcription	HSMM	muscle
47	chr10:89513400-89577000	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr10:89513600-89520400	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr10:89513800-89521200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr10:89514000-89520600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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