Variant report

Variant	nsv551841
Chromosome Location	chr10:90759724-90775756
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:56)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:90760753-90761157	GM12878	blood:	n/a	n/a
2	BATF	chr10:90760821-90761075	GM12878	blood:	n/a	n/a
3	BRCA1	chr10:90761692-90761695	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr10:90759470-90759805	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr10:90761205-90761688	IMR90	lung:	n/a	chr10:90761385-90761396
6	CEBPB	chr10:90761305-90761535	Hela-S3	cervix:	n/a	chr10:90761385-90761396
7	CEBPB	chr10:90761264-90761545	A549	lung:	n/a	chr10:90761385-90761396
8	CEBPB	chr10:90761233-90761569	HepG2	liver:	n/a	chr10:90761385-90761396
9	CEBPB	chr10:90761248-90761518	H1-hESC	embryonic stem cell:	n/a	chr10:90761385-90761396
10	CEBPB	chr10:90759451-90759765	IMR90	lung:	n/a	n/a
11	CTCF	chr10:90760853-90760908	GM20000	blood:	n/a	n/a
12	CTCF	chr10:90770840-90770990	GM12865	blood:	n/a	n/a
13	CTCF	chr10:90774860-90775010	GM12872	blood:	n/a	n/a
14	CUX1	chr10:90764662-90764697	K562	blood:	n/a	n/a
15	CUX1	chr10:90763559-90763609	GM12878	blood:	n/a	n/a
16	E2F4	chr10:90768791-90769041	MCF10A-Er-Src	breast:	n/a	n/a
17	EBF1	chr10:90760902-90761014	GM12878	blood:	n/a	n/a
18	ELK1	chr10:90761767-90761773	GM12878	blood:	n/a	n/a
19	EP300	chr10:90763058-90763458	SK-N-SH_RA	brain:	n/a	chr10:90763228-90763237 chr10:90763227-90763236
20	EP300	chr10:90763098-90763473	SK-N-SH_RA	brain:	n/a	chr10:90763228-90763237 chr10:90763227-90763236
21	EP300	chr10:90763252-90763281	GM12878	blood:	n/a	n/a
22	FOS	chr10:90762988-90763480	HUVEC	blood vessel:	n/a	chr10:90763227-90763236 chr10:90763227-90763237 chr10:90763228-90763236 chr10:90763228-90763235
23	FOS	chr10:90763197-90763295	MCF10A-Er-Src	breast:	n/a	chr10:90763227-90763236 chr10:90763227-90763237 chr10:90763228-90763236 chr10:90763228-90763235
24	FOS	chr10:90759397-90759814	MCF10A-Er-Src	breast:	n/a	chr10:90759541-90759550
25	FOSL2	chr10:90763036-90763454	SK-N-SH	brain:	n/a	chr10:90763227-90763236 chr10:90763227-90763237 chr10:90763228-90763236 chr10:90763228-90763235
26	GATA2	chr10:90762704-90763574	HUVEC	blood vessel:	n/a	chr10:90763247-90763263
27	GATA3	chr10:90762832-90763646	SK-N-SH	brain:	n/a	chr10:90763247-90763263
28	GATA3	chr10:90762950-90763640	SK-N-SH	brain:	n/a	chr10:90763247-90763263
29	IRF1	chr10:90760276-90760352	K562	blood:	n/a	chr10:90760323-90760330
30	JUN	chr10:90763082-90763431	HUVEC	blood vessel:	n/a	chr10:90763227-90763236 chr10:90763227-90763237 chr10:90763228-90763236 chr10:90763228-90763235
31	JUND	chr10:90761243-90761541	HepG2	liver:	n/a	n/a
32	JUND	chr10:90762954-90763493	SK-N-SH	brain:	n/a	chr10:90763227-90763236 chr10:90763227-90763237 chr10:90763228-90763236 chr10:90763228-90763235
33	MAFK	chr10:90773139-90773370	HepG2	liver:	n/a	n/a
34	MXI1	chr10:90760827-90761182	GM12878	blood:	n/a	n/a
35	NFIC	chr10:90762951-90763484	SK-N-SH	brain:	n/a	n/a
36	NFIC	chr10:90762195-90762670	GM12878	blood:	n/a	n/a
37	NFYB	chr10:90761289-90761523	GM12878	blood:	n/a	n/a
38	PBX3	chr10:90762949-90763584	SK-N-SH	brain:	n/a	n/a
39	PBX3	chr10:90762983-90763595	SK-N-SH	brain:	n/a	n/a
40	POLR2A	chr10:90767208-90767270	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr10:90760783-90760972	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr10:90775755-90776719	GM12892	blood:	n/a	n/a
43	POLR2A	chr10:90774532-90774538	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr10:90772389-90772467	ProgFib	skin:	n/a	n/a
45	POLR2A	chr10:90763089-90763359	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr10:90771202-90771342	GM12878	blood:	n/a	n/a
47	POLR2A	chr10:90758942-90760270	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr10:90762475-90763156	GM12878	blood:	n/a	n/a
49	POLR2A	chr10:90761448-90761482	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr10:90766186-90766524	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:90761751-90761801	MCF10A-Er-Src	breast:	n/a
2	chr10:90761751-90761801	H1-hESC	embryonic stem cell:	embryo
3	chr10:90761751-90761801	HRCEpiC	kidney:	n/a
4	chr10:90761751-90761801	U87	brain:	n/a
5	chr10:90761751-90761801	PrEC	prostate:	n/a
6	chr10:90761751-90761801	Caco-2	colon:	n/a
7	chr10:90761751-90761801	Hela-S3	cervix:	n/a
8	chr10:90761751-90761801	LNCaP	prostate:	n/a
9	chr10:90761751-90761801	AG04450	lung:	fetal
10	chr10:90761751-90761801	Hepatocyte	liver:	n/a
11	chr10:90761751-90761801	HIPEpiC	eye:	n/a
12	chr10:90761751-90761801	K562	blood:	n/a
13	chr10:90761751-90761801	AG10803	skin:	n/a
14	chr10:90761751-90761801	PANC-1	pancreas:	n/a
15	chr10:90761751-90761801	HNPCEpiC	eye:	n/a
16	chr10:90761751-90761801	SK-N-SH_RA	brain:	n/a
17	chr10:90761751-90761801	HCM	heart:	n/a
18	chr10:90761751-90761801	ovcar-3	ovarian:	n/a
19	chr10:90761751-90761801	ECC-1	luminal epithelium:	n/a
20	chr10:90761751-90761801	RPTEC	kidney:	n/a
21	chr10:90761751-90761801	BJ	skin:	n/a
22	chr10:90761751-90761801	HAEpiC	amniotic membrane:	n/a
23	chr10:90761751-90761801	AG04449	skin:	fetal
24	chr10:90761751-90761801	T-47D	breast:	n/a
25	chr10:90761751-90761801	HMEC	breast:	n/a
26	chr10:90761751-90761801	NT2-D1	testis:	n/a
27	chr10:90761751-90761801	NH-A	brain:	n/a
28	chr10:90761751-90761801	GM19239	blood:	n/a
29	chr10:90761751-90761801	HRPEpiC	eye:	n/a
30	chr10:90761751-90761801	HPAEpiC	pulmonary alveolar:	n/a
31	chr10:90761751-90761801	GM12891	blood:	n/a
32	chr10:90761751-90761801	AG09309	skin:	n/a
33	chr10:90761751-90761801	HRE	kidney:	n/a
34	chr10:90761751-90761801	ProgFib	skin:	n/a
35	chr10:90761751-90761801	Jurkat	blood:	n/a
36	chr10:90761751-90761801	HepG2	liver:	n/a
37	chr10:90761751-90761801	A549	lung:	n/a
38	chr10:90761751-90761801	HCF	heart:	n/a
39	chr10:90761751-90761801	HUVEC	blood vessel:	n/a
40	chr10:90761751-90761801	PFSK-1	brain:	n/a
41	chr10:90761751-90761801	SK-N-SH	brain:	n/a
42	chr10:90761751-90761801	NB4	blood:	n/a
43	chr10:90761751-90761801	CMK	blood:	n/a
44	chr10:90761751-90761801	GM12878	blood:	n/a
45	chr10:90761751-90761801	HEK293	kidney:	embryo
46	chr10:90761751-90761801	HEEpiC	esophagus:	n/a
47	chr10:90761751-90761801	MCF-7	breast:	n/a
48	chr10:90761751-90761801	SAEC	small airway:	n/a
49	chr10:90761751-90761801	HL-60	blood:	n/a
50	chr10:90761751-90761801	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:90682113..90684969-chr10:90763834..90765980,2	K562	blood:
2	chr10:90760115..90762878-chr10:90763662..90767506,4	K562	blood:
3	chr10:90760115..90762878-chr10:90763662..90767506,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STAMBPL1-1	chr10:90773876-90775542	NR_028036
2	lnc-STAMBPL1-1	chr10:90768646-90768754	NONHSAT015488
3	lnc-STAMBPL1-1	chr10:90773876-90773973	NONHSAT015492
4	lnc-STAMBPL1-1	chr10:90768646-90768754	NONHSAT015487
5	lnc-STAMBPL1-1	chr10:90773876-90775542	NR_028033
6	lnc-STAMBPL1-1	chr10:90762786-90762951	NR_028035
7	lnc-STAMBPL1-1	chr10:90770296-90770357	NR_028033
8	lnc-STAMBPL1-1	chr10:90767457-90767594	NONHSAT015488
9	lnc-STAMBPL1-1	chr10:90770296-90770357	NONHSAT015493
10	lnc-STAMBPL1-1	chr10:90767457-90767594	NONHSAT015491
11	lnc-STAMBPL1-1	chr10:90771756-90771838	NONHSAT015492
12	lnc-STAMBPL1-1	chr10:90773876-90775542	NR_028035
13	lnc-STAMBPL1-1	chr10:90773876-90775542	NR_028034
14	lnc-STAMBPL1-1	chr10:90770510-90770572	NR_028035
15	lnc-STAMBPL1-1	chr10:90773100-90773124	NR_028036
16	lnc-STAMBPL1-1	chr10:90773100-90773124	NONHSAT015492
17	lnc-STAMBPL1-1	chr10:90771756-90771838	NONHSAT015488
18	lnc-STAMBPL1-1	chr10:90771756-90771838	NR_028034
19	lnc-STAMBPL1-1	chr10:90773876-90773934	NONHSAT015488
20	lnc-STAMBPL1-1	chr10:90762786-90762951	NONHSAT015493
21	lnc-STAMBPL1-1	chr10:90770296-90770357	NONHSAT015492
22	lnc-STAMBPL1-1	chr10:90762786-90762951	NONHSAT015488
23	lnc-STAMBPL1-1	chr10:90762786-90762951	NR_028034
24	lnc-STAMBPL1-1	chr10:90770296-90770357	NR_028036
25	lnc-STAMBPL1-1	chr10:90762786-90762951	NONHSAT015490
26	lnc-STAMBPL1-1	chr10:90762786-90762951	NONHSAT015491
27	lnc-STAMBPL1-1	chr10:90768646-90768754	NONHSAT015493
28	lnc-STAMBPL1-1	chr10:90770510-90770572	NONHSAT015492
29	lnc-STAMBPL1-1	chr10:90771756-90771838	NR_028035
30	lnc-STAMBPL1-1	chr10:90771756-90771838	NR_028036
31	lnc-STAMBPL1-1	chr10:90771756-90771838	NONHSAT015493
32	lnc-STAMBPL1-1	chr10:90762786-90762951	NR_028033
33	lnc-STAMBPL1-1	chr10:90767457-90767594	NR_028036
34	lnc-STAMBPL1-1	chr10:90770510-90770572	NR_028036
35	lnc-STAMBPL1-1	chr10:90773100-90773124	NONHSAT015488
36	lnc-STAMBPL1-1	chr10:90767457-90767594	NONHSAT015493
37	lnc-STAMBPL1-1	chr10:90768646-90768754	NONHSAT015491
38	lnc-STAMBPL1-1	chr10:90762786-90762951	NONHSAT015492
39	lnc-STAMBPL1-1	chr10:90767457-90767594	NR_028033
40	lnc-FAS-1	chr10:90775593-90776816	ENSG00000261438.1
41	lnc-STAMBPL1-1	chr10:90770296-90770357	NR_028034
42	lnc-STAMBPL1-1	chr10:90770296-90770417	NONHSAT015490
43	lnc-STAMBPL1-1	chr10:90770510-90770572	NONHSAT015488
44	lnc-STAMBPL1-1	chr10:90773100-90773124	NR_028033
45	lnc-STAMBPL1-1	chr10:90767457-90767594	NONHSAT015487
46	lnc-STAMBPL1-1	chr10:90770296-90770357	NR_028035
47	lnc-STAMBPL1-1	chr10:90770510-90770572	NONHSAT015493
48	lnc-STAMBPL1-1	chr10:90767457-90767594	NONHSAT015490
49	lnc-STAMBPL1-1	chr10:90762786-90762951	NONHSAT015487
50	lnc-STAMBPL1-1	chr10:90771756-90771838	NR_028033

No data

Variant related genes	Relation type
ENSG00000261438	TF binding region
ENSG00000261438	CpG island

Extended variants
information (count: 619 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4406737	chr10:90759724-90759725	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs2148287	chr10:90759772-90759773	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs9658715	chr10:90759836-90759837	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs532038586	chr10:90759842-90759843	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs552051107	chr10:90759846-90759847	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs9658716	chr10:90759913-90759914	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs2147419	chr10:90759916-90759917	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs2148286	chr10:90759924-90759925	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs567879661	chr10:90759958-90759959	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs2147418	chr10:90760000-90760001	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs9658717	chr10:90760001-90760002	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs4406738	chr10:90760012-90760013	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs7916814	chr10:90760025-90760026	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs554024912	chr10:90760030-90760031	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs145191969	chr10:90760031-90760032	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs2182408	chr10:90760107-90760108	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs560716156	chr10:90760127-90760128	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs539412805	chr10:90760135-90760136	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs147625460	chr10:90760136-90760137	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs543091503	chr10:90760204-90760205	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs564879997	chr10:90760208-90760209	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs113761804	chr10:90760220-90760221	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs7920305	chr10:90760225-90760226	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs537071537	chr10:90760259-90760260	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs555708194	chr10:90760274-90760275	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs112902622	chr10:90760291-90760292	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs527949679	chr10:90760297-90760298	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs1926194	chr10:90760318-90760319	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs567841630	chr10:90760387-90760388	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs538467036	chr10:90760415-90760416	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs550295261	chr10:90760448-90760449	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs571690717	chr10:90760466-90760467	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs151031681	chr10:90760491-90760492	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs182472815	chr10:90760511-90760512	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs572421971	chr10:90760526-90760527	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs536127617	chr10:90760531-90760532	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs534412674	chr10:90760552-90760553	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs9658718	chr10:90760578-90760579	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs554472180	chr10:90760583-90760584	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs1926193	chr10:90760606-90760607	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs543256907	chr10:90760619-90760620	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs1926192	chr10:90760620-90760621	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs576819299	chr10:90760633-90760634	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs541143997	chr10:90760647-90760648	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs1926191	chr10:90760651-90760652	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs4244983	chr10:90760662-90760663	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs9658719	chr10:90760664-90760665	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs9658720	chr10:90760669-90760670	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs397950071	chr10:90760670-90760671	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs563267000	chr10:90760690-90760691	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
T-cell acute lymphoblastic leukemia	19406988	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	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
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	22048815	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Glioblastoma multiforme	22286061	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Sezary syndrome	18413736	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Bipolar disorder	19114987	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90751800-90768200	Weak transcription	Spleen	Spleen
2	chr10:90752000-90761600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr10:90752000-90770000	Weak transcription	Placenta	Placenta
4	chr10:90752000-90770800	Weak transcription	Esophagus	oesophagus
5	chr10:90752200-90760800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr10:90752200-90768400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr10:90752800-90773400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr10:90753000-90761400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr10:90753400-90761600	Weak transcription	Aorta	Aorta
10	chr10:90753800-90760400	Weak transcription	Brain Anterior Caudate	brain
11	chr10:90754000-90760400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr10:90754000-90760800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr10:90754000-90761000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr10:90754000-90761000	Weak transcription	Colon Smooth Muscle	Colon
15	chr10:90754000-90761200	Weak transcription	NH-A	brain
16	chr10:90754000-90779400	Weak transcription	HepG2	liver
17	chr10:90754000-90789600	Weak transcription	A549	lung
18	chr10:90754200-90760400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr10:90754200-90761000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr10:90754200-90763200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr10:90754200-90767000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr10:90754400-90761200	Weak transcription	HSMM	muscle
23	chr10:90755400-90760800	Weak transcription	Fetal Thymus	thymus
24	chr10:90755400-90761200	Weak transcription	Thymus	Thymus
25	chr10:90755600-90761400	Weak transcription	Right Ventricle	heart
26	chr10:90755600-90762600	Weak transcription	Liver	Liver
27	chr10:90755600-90768200	Weak transcription	Lung	lung
28	chr10:90755600-90771400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr10:90755600-90776000	Weak transcription	Left Ventricle	heart
30	chr10:90755600-90776200	Weak transcription	Pancreas	Pancrea
31	chr10:90755800-90760200	Weak transcription	Adipose Nuclei	Adipose
32	chr10:90755800-90760400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr10:90755800-90760600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr10:90755800-90760600	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr10:90755800-90762400	Weak transcription	Hela-S3	cervix
36	chr10:90756200-90760400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr10:90756200-90781800	Weak transcription	Stomach Mucosa	stomach
38	chr10:90756800-90760400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr10:90756800-90761000	Weak transcription	Primary hematopoietic stem cells	blood
40	chr10:90756800-90769200	Weak transcription	Colonic Mucosa	Colon
41	chr10:90757000-90760400	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr10:90757000-90760800	Weak transcription	Primary T cells from cord blood	blood
43	chr10:90757000-90760800	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr10:90757000-90770800	Weak transcription	Primary B cells from cord blood	blood
45	chr10:90757200-90760400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr10:90757200-90760400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr10:90757200-90760600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr10:90757200-90760600	Weak transcription	Duodenum Mucosa	Duodenum
49	chr10:90757200-90760600	Weak transcription	Small Intestine	intestine
50	chr10:90757200-90760800	Weak transcription	Primary monocytes fromperipheralblood	blood

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