Variant report

Variant	nsv1046213
Chromosome Location	chr10:4059937-4144692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:544)
CpG islands
(count:488)
Chromatin interactive
region (count:44)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:544 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:4086139-4086362	K562	blood:	n/a	n/a
2	ATF1	chr10:4109970-4110365	K562	blood:	n/a	n/a
3	ATF1	chr10:4096326-4096755	K562	blood:	n/a	n/a
4	ATF2	chr10:4075507-4076001	GM12878	blood:	n/a	n/a
5	ATF3	chr10:4095993-4096241	K562	blood:	n/a	n/a
6	BACH1	chr10:4066201-4066516	H1-hESC	embryonic stem cell:	n/a	chr10:4066369-4066383
7	BATF	chr10:4075558-4075962	GM12878	blood:	n/a	n/a
8	BATF	chr10:4075474-4076041	GM12878	blood:	n/a	n/a
9	BATF	chr10:4060448-4060652	GM12878	blood:	n/a	n/a
10	BCL3	chr10:4108679-4108933	GM12878	blood:	n/a	n/a
11	BCL3	chr10:4115040-4115270	GM12878	blood:	n/a	n/a
12	BCLAF1	chr10:4075509-4076019	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:4144171-4144395	GM12878	blood:	n/a	n/a
14	BHLHE40	chr10:4077169-4077389	K562	blood:	n/a	n/a
15	BHLHE40	chr10:4068987-4069334	K562	blood:	n/a	chr10:4069162-4069175 chr10:4069158-4069179
16	BHLHE40	chr10:4075602-4076018	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:4103542-4103893	K562	blood:	n/a	n/a
18	BHLHE40	chr10:4088337-4088593	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:4086160-4086223	K562	blood:	n/a	n/a
20	BHLHE40	chr10:4060167-4060681	GM12878	blood:	n/a	n/a
21	CBX3	chr10:4083805-4084053	K562	blood:	n/a	n/a
22	CBX3	chr10:4083717-4084062	K562	blood:	n/a	n/a
23	CBX3	chr10:4083718-4084299	HCT-116	colon:	n/a	n/a
24	CCNT2	chr10:4103887-4103958	K562	blood:	n/a	n/a
25	CEBPB	chr10:4090572-4090780	K562	blood:	n/a	n/a
26	CEBPB	chr10:4092330-4092568	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr10:4137075-4137362	K562	blood:	n/a	chr10:4137230-4137241
28	CEBPB	chr10:4112594-4112832	A549	lung:	n/a	n/a
29	CEBPB	chr10:4071025-4071398	MCF-7	breast:	n/a	chr10:4071241-4071250 chr10:4071241-4071250 chr10:4071239-4071250 chr10:4071241-4071250 chr10:4071241-4071250 chr10:4071239-4071252 chr10:4071239-4071252 chr10:4071241-4071252 chr10:4071239-4071252
30	CEBPB	chr10:4092282-4092621	A549	lung:	n/a	n/a
31	CEBPB	chr10:4079164-4079328	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:4099948-4101307	A549	lung:	n/a	chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101119-4101132 chr10:4101119-4101130 chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101121-4101132
33	CEBPB	chr10:4095995-4096296	K562	blood:	n/a	chr10:4096135-4096146
34	CEBPB	chr10:4100935-4101240	MCF-7	breast:	n/a	chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101119-4101132 chr10:4101119-4101130 chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101121-4101132
35	CEBPB	chr10:4072354-4072356	A549	lung:	n/a	n/a
36	CEBPB	chr10:4095996-4096246	HepG2	liver:	n/a	chr10:4096135-4096146
37	CEBPB	chr10:4092298-4092604	K562	blood:	n/a	n/a
38	CEBPB	chr10:4090508-4090776	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:4092279-4092607	HepG2	liver:	n/a	n/a
40	CEBPB	chr10:4112598-4112798	K562	blood:	n/a	n/a
41	CEBPB	chr10:4095997-4096297	IMR90	lung:	n/a	chr10:4096135-4096146
42	CEBPB	chr10:4100959-4101257	A549	lung:	n/a	chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101119-4101132 chr10:4101119-4101130 chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101121-4101132
43	CEBPB	chr10:4144461-4144796	Hela-S3	cervix:	n/a	chr10:4144620-4144633
44	CEBPB	chr10:4137062-4137359	IMR90	lung:	n/a	chr10:4137230-4137241
45	CEBPB	chr10:4085577-4085652	A549	lung:	n/a	n/a
46	CEBPB	chr10:4100979-4101255	IMR90	lung:	n/a	chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101119-4101132 chr10:4101119-4101130 chr10:4101121-4101130 chr10:4101121-4101130 chr10:4101121-4101132
47	CEBPB	chr10:4127816-4128066	HepG2	liver:	n/a	chr10:4127967-4127978
48	CEBPB	chr10:4127846-4127993	A549	lung:	n/a	chr10:4127967-4127978
49	CEBPB	chr10:4072286-4072517	HepG2	liver:	n/a	chr10:4072432-4072443
50	CEBPB	chr10:4103780-4104113	MCF-7	breast:	n/a	chr10:4103932-4103943

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:4076396-4076446	Caco-2	colon:	n/a
2	chr10:4117248-4117298	GM12878	blood:	n/a
3	chr10:4066442-4066492	BJ	skin:	n/a
4	chr10:4093925-4093975	ProgFib	skin:	n/a
5	chr10:4117248-4117298	PANC-1	pancreas:	n/a
6	chr10:4069749-4069799	NHBE	bronchial:	n/a
7	chr10:4066442-4066492	LNCaP	prostate:	n/a
8	chr10:4066499-4066549	HPAEpiC	pulmonary alveolar:	n/a
9	chr10:4076396-4076446	SK-N-MC	brain:	n/a
10	chr10:4066531-4066581	IMR90	lung:	fetal
11	chr10:4066442-4066492	HPAEpiC	pulmonary alveolar:	n/a
12	chr10:4117248-4117298	RPTEC	kidney:	n/a
13	chr10:4066499-4066549	Jurkat	blood:	n/a
14	chr10:4066442-4066492	T-47D	breast:	n/a
15	chr10:4066442-4066492	HCM	heart:	n/a
16	chr10:4069749-4069799	NT2-D1	testis:	n/a
17	chr10:4066442-4066492	HAEpiC	amniotic membrane:	n/a
18	chr10:4076396-4076446	HNPCEpiC	eye:	n/a
19	chr10:4125518-4125568	GM12892	blood:	n/a
20	chr10:4066531-4066581	NB4	blood:	n/a
21	chr10:4066531-4066581	HUVEC	blood vessel:	n/a
22	chr10:4066499-4066549	MCF-7	breast:	n/a
23	chr10:4066442-4066492	IMR90	lung:	fetal
24	chr10:4117248-4117298	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:4066499-4066549	Hepatocyte	liver:	n/a
26	chr10:4076396-4076446	GM12892	blood:	n/a
27	chr10:4066442-4066492	HUVEC	blood vessel:	n/a
28	chr10:4076396-4076446	AoSMC	blood vessel:	n/a
29	chr10:4066442-4066492	HCF	heart:	n/a
30	chr10:4066499-4066549	K562	blood:	n/a
31	chr10:4093925-4093975	ovcar-3	ovarian:	n/a
32	chr10:4117248-4117298	SK-N-MC	brain:	n/a
33	chr10:4069749-4069799	PFSK-1	brain:	n/a
34	chr10:4066499-4066549	HCM	heart:	n/a
35	chr10:4117248-4117298	U87	brain:	n/a
36	chr10:4117248-4117298	HepG2	liver:	n/a
37	chr10:4125518-4125568	NHBE	bronchial:	n/a
38	chr10:4066499-4066549	U87	brain:	n/a
39	chr10:4093925-4093975	PFSK-1	brain:	n/a
40	chr10:4076396-4076446	ProgFib	skin:	n/a
41	chr10:4066531-4066581	HRCEpiC	kidney:	n/a
42	chr10:4125518-4125568	PrEC	prostate:	n/a
43	chr10:4117248-4117298	SK-N-SH_RA	brain:	n/a
44	chr10:4066499-4066549	RPTEC	kidney:	n/a
45	chr10:4066442-4066492	HRE	kidney:	n/a
46	chr10:4066499-4066549	AG04450	lung:	fetal
47	chr10:4066531-4066581	HNPCEpiC	eye:	n/a
48	chr10:4069749-4069799	LNCaP	prostate:	n/a
49	chr10:4066531-4066581	Jurkat	blood:	n/a
50	chr10:4117248-4117298	HRPEpiC	eye:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:4122248..4124500-chr10:4135012..4136575,2	MCF-7	breast:
2	chr10:3827665..3830357-chr10:4102508..4105467,3	K562	blood:
3	chr10:4122248..4124500-chr10:4135012..4136575,2	MCF-7	breast:
4	chr10:4089131..4091223-chr10:4129721..4132308,2	K562	blood:
5	chr10:3827062..3828607-chr10:4093523..4096614,3	MCF-7	breast:
6	chr10:4087454..4089060-chr10:4095096..4097134,2	K562	blood:
7	chr10:4104934..4107897-chr10:4109686..4112440,3	K562	blood:
8	chr10:3827197..3829936-chr10:4065952..4068460,2	K562	blood:
9	chr10:4104934..4107897-chr10:4109686..4112440,3	K562	blood:
10	chr10:4063549..4065847-chr10:4069623..4072057,2	K562	blood:
11	chr10:4087454..4089060-chr10:4095096..4097134,2	K562	blood:
12	chr10:4117313..4119775-chr10:4122866..4124506,2	K562	blood:
13	chr10:3825543..3829712-chr10:4097460..4102174,5	K562	blood:
14	chr10:3826070..3828691-chr10:4114442..4117278,2	MCF-7	breast:
15	chr10:4068902..4073609-chr10:4074396..4078715,6	MCF-7	breast:
16	chr10:4124093..4126058-chr10:4126935..4129373,2	K562	blood:
17	chr10:3826418..3828432-chr10:4130532..4132999,2	K562	blood:
18	chr10:4099803..4101448-chr10:4116645..4119570,2	MCF-7	breast:
19	chr10:4059523..4061369-chr10:4062560..4064462,2	MCF-7	breast:
20	chr10:4089131..4091223-chr10:4129721..4132308,2	K562	blood:
21	chr10:4068902..4073609-chr10:4074396..4078715,6	MCF-7	breast:
22	chr10:4101159..4103691-chr10:4170864..4173275,2	MCF-7	breast:
23	chr10:3827101..3828753-chr10:4060844..4063751,2	MCF-7	breast:
24	chr10:4088826..4091869-chr10:4093004..4096419,3	MCF-7	breast:
25	chr10:4124093..4126058-chr10:4126935..4129373,2	K562	blood:
26	chr10:4116566..4118827-chr10:4119100..4121820,2	K562	blood:
27	chr10:4063549..4065847-chr10:4069623..4072057,2	K562	blood:
28	chr10:4100357..4102296-chr10:4102463..4105433,2	K562	blood:
29	chr10:3827043..3829153-chr10:4097911..4099652,2	K562	blood:
30	chr10:3827376..3829863-chr10:4088234..4090529,2	K562	blood:
31	chr10:4059523..4061369-chr10:4062560..4064462,2	MCF-7	breast:
32	chr10:4099803..4101448-chr10:4116645..4119570,2	MCF-7	breast:
33	chr10:3827232..3829993-chr10:4098770..4104169,5	MCF-7	breast:
34	chr10:4108012..4110673-chr10:4118999..4120974,2	K562	blood:
35	chr10:4107010..4110673-chr10:4118999..4120974,3	K562	blood:
36	chr10:4100357..4102296-chr10:4102463..4105433,2	K562	blood:
37	chr10:4107010..4110673-chr10:4118999..4120974,3	K562	blood:
38	chr10:4116566..4118827-chr10:4119100..4121820,2	K562	blood:
39	chr10:3825444..3830395-chr10:4144658..4149398,6	MCF-7	breast:
40	chr10:4117313..4119775-chr10:4122866..4124506,2	K562	blood:
41	chr10:4034845..4036569-chr10:4064234..4066048,2	MCF-7	breast:
42	chr10:3967575..3969364-chr10:4091525..4093516,2	MCF-7	breast:
43	chr10:4108012..4110673-chr10:4118999..4120974,2	K562	blood:
44	chr10:4032476..4035285-chr10:4060007..4062185,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKR1E2-11	chr10:4119551-4121205	NONHSAT011077
2	lnc-AKR1E2-5	chr10:4067130-4067548	XLOC_008358
3	lnc-AKR1E2-5	chr10:4127798-4127900	XLOC_008358
4	lnc-AKR1E2-5	chr10:4093909-4093948	XLOC_008358
5	lnc-AKR1E2-5	chr10:4075198-4075386	NONHSAT011074
6	lnc-AKR1E2-5	chr10:4094838-4095197	XLOC_008358
7	lnc-AKR1E2-11	chr10:4117389-4117485	NONHSAT011077
8	lnc-AKR1E2-5	chr10:4067130-4067548	XLOC_008358
9	lnc-AKR1E2-11	chr10:4117798-4117900	NONHSAT011077
10	lnc-AKR1E2-5	chr10:4093918-4094349	XLOC_008358
11	lnc-AKR1E2-5	chr10:4067130-4067548	XLOC_008358
12	lnc-AKR1E2-5	chr10:4073718-4073895	XLOC_008358
13	lnc-AKR1E2-11	chr10:4083918-4084349	NONHSAT011077
14	lnc-AKR1E2-5	chr10:4069101-4069180	XLOC_008358
15	lnc-AKR1E2-5	chr10:4070371-4070586	XLOC_008358
16	lnc-AKR1E2-5	chr10:4129551-4131205	XLOC_008358
17	lnc-AKR1E2-5	chr10:4093909-4094349	XLOC_008358
18	lnc-AKR1E2-5	chr10:4073718-4073895	XLOC_008358
19	lnc-AKR1E2-5	chr10:4067109-4067548	XLOC_008358
20	lnc-AKR1E2-5	chr10:4089273-4089346	XLOC_008358
21	lnc-AKR1E2-5	chr10:4067130-4067548	NONHSAT011073
22	lnc-AKR1E2-5	chr10:4067130-4067548	NONHSAT011074
23	lnc-AKR1E2-12	chr10:4060371-4060586	NONHSAT011070
24	lnc-AKR1E2-5	chr10:4067132-4067548	XLOC_008358
25	lnc-AKR1E2-5	chr10:4131983-4132028	XLOC_008358
26	lnc-AKR1E2-5	chr10:4070371-4070715	NONHSAT011073
27	lnc-AKR1E2-5	chr10:4094065-4094349	XLOC_008358
28	lnc-AKR1E2-5	chr10:4127389-4127485	XLOC_008358

No data

Variant related genes	Relation type
ENSG00000236990	TF binding region
ENSG00000227101	TF binding region
ENSG00000236990	CpG island
ENSG00000227101	CpG island
ENSG00000236990	chromatin interactions
ENSG00000067082	chromatin interactions
DISC1	miRNA target sites
LRP4	miRNA target sites
FGF7	miRNA target sites
CDK4	miRNA target sites
NT5E	miRNA target sites

Extended variants
information (count: 3936 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3936 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74507386	chr10:4059947-4059948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138921432	chr10:4059948-4059949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184803033	chr10:4059967-4059968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs571356937	chr10:4060047-4060048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148834194	chr10:4060054-4060055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553911782	chr10:4060097-4060098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs143443816	chr10:4060101-4060102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111342878	chr10:4060126-4060127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554826448	chr10:4060144-4060145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs148015030	chr10:4060145-4060146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543401500	chr10:4060175-4060176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543685444	chr10:4060178-4060179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs189245836	chr10:4060180-4060181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs74114594	chr10:4060181-4060182	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576831118	chr10:4060195-4060196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150045714	chr10:4060196-4060197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs66789085	chr10:4060246-4060247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541087462	chr10:4060266-4060267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2478062	chr10:4060269-4060270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74114596	chr10:4060290-4060291	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs199964350	chr10:4060308-4060309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530290131	chr10:4060331-4060332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544078349	chr10:4060337-4060338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs563867022	chr10:4060355-4060356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs576843472	chr10:4060388-4060389	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs531274387	chr10:4060414-4060415	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs180721709	chr10:4060425-4060426	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
28	rs568117737	chr10:4060444-4060445	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs368181514	chr10:4060452-4060453	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs17131879	chr10:4060495-4060496	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs532157616	chr10:4060522-4060523	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs547438777	chr10:4060536-4060537	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs138832323	chr10:4060618-4060619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536431307	chr10:4060622-4060623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12244341	chr10:4060624-4060625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs142784366	chr10:4060630-4060631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536900684	chr10:4060641-4060642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs150808905	chr10:4060649-4060650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140500834	chr10:4060704-4060705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76126041	chr10:4060705-4060706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79908098	chr10:4060706-4060707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76232397	chr10:4060707-4060708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34563119	chr10:4060719-4060720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372312500	chr10:4060720-4060721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576793512	chr10:4060731-4060732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541048838	chr10:4060739-4060740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541050374	chr10:4060750-4060751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184325107	chr10:4060801-4060802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74114600	chr10:4060809-4060810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs563778065	chr10:4060855-4060856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Cancer	21129771	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1463 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4056200-4060400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr10:4056200-4066800	Weak transcription	Adipose Nuclei	Adipose
3	chr10:4056600-4060200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr10:4056600-4068800	Weak transcription	NHDF-Ad	bronchial
5	chr10:4057200-4063800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr10:4057400-4060000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr10:4058000-4062200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:4058400-4060200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr10:4060000-4061400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr10:4060200-4061200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr10:4060400-4061000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:4060400-4061000	Enhancers	Osteobl	bone
13	chr10:4062400-4064000	Enhancers	Dnd41	blood
14	chr10:4063800-4064000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr10:4064000-4065000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:4064000-4065400	Weak transcription	Dnd41	blood
17	chr10:4064200-4067000	Weak transcription	Right Ventricle	heart
18	chr10:4064400-4064600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr10:4065000-4068200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr10:4065400-4065800	Enhancers	Dnd41	blood
21	chr10:4065600-4066400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr10:4065600-4067400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr10:4065600-4067600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr10:4065800-4067200	Weak transcription	Dnd41	blood
25	chr10:4066400-4067400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr10:4066400-4067400	Enhancers	Fetal Brain Male	brain
27	chr10:4066400-4067600	Enhancers	NH-A	brain
28	chr10:4066400-4068000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr10:4066400-4068200	Enhancers	Placenta	Placenta
30	chr10:4066400-4081200	Weak transcription	Gastric	stomach
31	chr10:4066600-4067600	Enhancers	Fetal Brain Female	brain
32	chr10:4066800-4067400	Enhancers	Fetal Muscle Leg	muscle
33	chr10:4066800-4067600	Enhancers	Adipose Nuclei	Adipose
34	chr10:4067000-4067200	Enhancers	Right Ventricle	heart
35	chr10:4067000-4067400	Enhancers	Right Atrium	heart
36	chr10:4067200-4067600	Enhancers	HSMMtube	muscle
37	chr10:4067200-4067800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr10:4067200-4067800	Enhancers	Dnd41	blood
39	chr10:4067400-4067600	Enhancers	Lung	lung
40	chr10:4067400-4067800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:4067400-4067800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr10:4067400-4077000	Weak transcription	Right Atrium	heart
43	chr10:4067600-4068000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr10:4067600-4070200	Weak transcription	Lung	lung
45	chr10:4067800-4070000	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr10:4068000-4072800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr10:4068200-4068600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr10:4068200-4071000	Weak transcription	Placenta	Placenta
49	chr10:4068600-4069200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr10:4068800-4069600	Enhancers	NHDF-Ad	bronchial

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