Variant report

Variant	nsv975329
Chromosome Location	chr11:58767290-58907813
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2462)
CpG islands
(count:2323)
Chromatin interactive
region (count:34)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2462 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58903414-58903708	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:58874268-58874746	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
4	ATF1	chr11:58864804-58864948	K562	blood:	n/a	n/a
5	ATF1	chr11:58779639-58779652	K562	blood:	n/a	n/a
6	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
7	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
8	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
9	ATF2	chr11:58869726-58870352	GM12878	blood:	n/a	n/a
10	ATF2	chr11:58874286-58874870	GM12878	blood:	n/a	n/a
11	ATF2	chr11:58903346-58903784	GM12878	blood:	n/a	n/a
12	ATF2	chr11:58874015-58875031	GM12878	blood:	n/a	n/a
13	ATF2	chr11:58869606-58870352	GM12878	blood:	n/a	n/a
14	ATF2	chr11:58874367-58874899	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
16	ATF2	chr11:58903427-58903758	GM12878	blood:	n/a	n/a
17	ATF2	chr11:58874344-58874770	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr11:58869743-58869963	K562	blood:	n/a	n/a
19	BACH1	chr11:58869800-58870060	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:58873974-58874757	H1-hESC	embryonic stem cell:	n/a	chr11:58874543-58874557
21	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr11:58903471-58903671	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr11:58875555-58875818	GM12878	blood:	n/a	chr11:58875662-58875670
24	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
25	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
26	BATF	chr11:58869559-58870293	GM12878	blood:	n/a	n/a
27	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
28	BATF	chr11:58875256-58875548	GM12878	blood:	n/a	n/a
29	BATF	chr11:58874419-58874727	GM12878	blood:	n/a	chr11:58874543-58874553 chr11:58874547-58874557 chr11:58874542-58874553
30	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
31	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
32	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
34	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
35	BCL11A	chr11:58869760-58870216	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
37	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
39	BCL11A	chr11:58875271-58875606	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:58869844-58870260	GM12878	blood:	n/a	n/a
42	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
43	BCL3	chr11:58869751-58870129	GM12878	blood:	n/a	n/a
44	BCL3	chr11:58903396-58903768	GM12878	blood:	n/a	n/a
45	BCLAF1	chr11:58903341-58903724	GM12878	blood:	n/a	n/a
46	BCLAF1	chr11:58869650-58870315	GM12878	blood:	n/a	n/a
47	BCLAF1	chr11:58873883-58874436	GM12878	blood:	n/a	chr11:58874084-58874097
48	BCLAF1	chr11:58869623-58870275	GM12878	blood:	n/a	n/a
49	BHLHE40	chr11:58874518-58874815	A549	lung:	n/a	n/a
50	BHLHE40	chr11:58903395-58903676	K562	blood:	n/a	n/a

(count:2323 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58826110-58826160	MCF-7	breast:	n/a
2	chr11:58874723-58874773	A549	lung:	n/a
3	chr11:58904869-58904919	BE2_C	brain:	n/a
4	chr11:58830424-58830474	T-47D	breast:	n/a
5	chr11:58904869-58904919	HMEC	breast:	n/a
6	chr11:58826110-58826160	MCF-7	breast:	n/a
7	chr11:58874723-58874773	A549	lung:	n/a
8	chr11:58904869-58904919	BE2_C	brain:	n/a
9	chr11:58830424-58830474	T-47D	breast:	n/a
10	chr11:58904869-58904919	HMEC	breast:	n/a
11	chr11:58874207-58874257	SK-N-MC	brain:	n/a
12	chr11:58874733-58874783	AoSMC	blood vessel:	n/a
13	chr11:58826475-58826525	AG04449	skin:	fetal
14	chr11:58904869-58904919	AG09319	gingival:	n/a
15	chr11:58892585-58892635	SK-N-MC	brain:	n/a
16	chr11:58874637-58874687	SK-N-MC	brain:	n/a
17	chr11:58870075-58870125	AG04449	skin:	fetal
18	chr11:58873955-58874005	Jurkat	blood:	n/a
19	chr11:58877370-58877420	HMEC	breast:	n/a
20	chr11:58874348-58874398	HNPCEpiC	eye:	n/a
21	chr11:58825870-58825920	HMEC	breast:	n/a
22	chr11:58830424-58830474	HRCEpiC	kidney:	n/a
23	chr11:58874637-58874687	LNCaP	prostate:	n/a
24	chr11:58874723-58874773	MCF10A-Er-Src	breast:	n/a
25	chr11:58874635-58874685	SK-N-SH	brain:	n/a
26	chr11:58877370-58877420	PFSK-1	brain:	n/a
27	chr11:58874641-58874691	HCPEpiC	choroid plexus:	n/a
28	chr11:58874608-58874658	IMR90	lung:	fetal
29	chr11:58830355-58830405	NHDF-neo	bronchial:	n/a
30	chr11:58866721-58866771	AG04450	lung:	fetal
31	chr11:58907379-58907429	A549	lung:	n/a
32	chr11:58830355-58830405	HUVEC	blood vessel:	n/a
33	chr11:58825870-58825920	MCF10A-Er-Src	breast:	n/a
34	chr11:58873823-58873873	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:58892585-58892635	T-47D	breast:	n/a
36	chr11:58907379-58907429	HRPEpiC	eye:	n/a
37	chr11:58874723-58874773	ProgFib	skin:	n/a
38	chr11:58873955-58874005	H1-hESC	embryonic stem cell:	embryo
39	chr11:58828174-58828224	HCPEpiC	choroid plexus:	n/a
40	chr11:58870494-58870544	HL-60	blood:	n/a
41	chr11:58907379-58907429	HepG2	liver:	n/a
42	chr11:58874207-58874257	CMK	blood:	n/a
43	chr11:58877370-58877420	GM12892	blood:	n/a
44	chr11:58874637-58874687	ECC-1	luminal epithelium:	n/a
45	chr11:58874207-58874257	H1-hESC	embryonic stem cell:	embryo
46	chr11:58904901-58904951	RPTEC	kidney:	n/a
47	chr11:58874733-58874783	GM12878	blood:	n/a
48	chr11:58869663-58869713	HRE	kidney:	n/a
49	chr11:58874637-58874687	GM19239	blood:	n/a
50	chr11:58870494-58870544	HMEC	breast:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
2	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
3	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
4	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
5	chr11:58873708..58874686-chr11:63448916..63449711,2	Hela-S3	cervix:
6	chr11:58726086..58726653-chr11:58902781..58903961,3	K562	blood:
7	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:
8	chr11:58884380..58886693-chr11:58887312..58889287,2	K562	blood:
9	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
10	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
11	chr11:58869192..58871421-chr11:58911598..58913836,2	MCF-7	breast:
12	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
13	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
14	chr11:58892733..58893477-chr11:58901491..58902182,2	K562	blood:
15	chr11:58884380..58886693-chr11:58887312..58889287,2	K562	blood:
16	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
17	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
18	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
19	chr11:58875233..58875940-chr12:49657802..49658323,2	Hela-S3	cervix:
20	chr11:58896273..58898836-chr11:58901279..58902925,2	K562	blood:
21	chr11:58873805..58876804-chr17:41466274..41467888,2	K562	blood:
22	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
23	chr11:58896273..58898836-chr11:58901279..58902925,2	K562	blood:
24	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:
25	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
26	chr11:58873861..58874546-chr5:111496427..111496981,2	Hela-S3	cervix:
27	chr11:58890846..58893267-chr11:58894892..58896437,2	MCF-7	breast:
28	chr11:58904183..58908174-chr11:58910132..58913359,4	MCF-7	breast:
29	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
30	chr11:58890846..58893267-chr11:58894892..58896437,2	MCF-7	breast:
31	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
32	chr11:58873805..58875305-chr17:41466179..41467880,2	MCF-7	breast:
33	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
34	chr11:58892733..58893477-chr11:58901491..58902182,2	K562	blood:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MPEG1-2	chr11:58897606-58897784	NONHSAT021502
2	lnc-MPEG1-2	chr11:58902051-58902156	XLOC_009445
3	lnc-MPEG1-2	chr11:58902051-58903061	XLOC_009445
4	lnc-MPEG1-2	chr11:58900752-58901122	XLOC_009445
5	lnc-FAM111A-1	chr11:58874709-58874769	NONHSAT021500
6	lnc-FAM111A-1	chr11:58876141-58876185	NONHSAT021500
7	lnc-MPEG1-2	chr11:58903530-58903557	XLOC_009445
8	lnc-MPEG1-2	chr11:58903530-58903754	NONHSAT021502
9	lnc-MPEG1-2	chr11:58903530-58903754	XLOC_009445
10	lnc-MPEG1-2	chr11:58897610-58901122	XLOC_009445
11	lnc-MPEG1-2	chr11:58902763-58903061	ENSG00000245571
12	lnc-FAM111A-1	chr11:58877013-58877480	NONHSAT021500
13	lnc-MPEG1-2	chr11:58901712-58903061	NONHSAT021502
14	lnc-MPEG1-2	chr11:58901132-58902156	XLOC_009445
15	lnc-MPEG1-2	chr11:58903398-58903754	ENSG00000245571
16	lnc-MPEG1-2	chr11:58903530-58903754	ENSG00000245571
17	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
18	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
19	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
20	lnc-MPEG1-2	chr11:58897606-58897773	ENSG00000245571
21	lnc-MPEG1-2	chr11:58901446-58903061	NR_110184
22	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
23	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
24	lnc-MPEG1-2	chr11:58907430-58907640	NR_110184
25	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
26	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
27	lnc-MPEG1-2	chr11:58907430-58907588	ENSG00000245571
28	lnc-MPEG1-2	chr11:58907430-58907640	ENSG00000245571
29	lnc-MPEG1-2	chr11:58907188-58907564	ENSG00000245571
30	lnc-MPEG1-2	chr11:58903530-58903754	NR_110184
31	lnc-MPEG1-2	chr11:58903530-58903754	ENSG00000245571
32	lnc-MPEG1-2	chr11:58907430-58907640	ENSG00000245571
33	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
34	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
35	lnc-MPEG1-2	chr11:58901697-58903061	ENSG00000245571
36	lnc-MPEG1-2	chr11:58903530-58903816	XLOC_009445
37	lnc-MPEG1-2	chr11:58907430-58907640	NONHSAT021502
38	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1

No data

Variant related genes	Relation type
ENSG00000255240	TF binding region
ENSG00000245571	TF binding region
GLYATL1P3	TF binding region
GLYATL1P4	TF binding region
FAM111A	TF binding region
ENSG00000254786	TF binding region
FAM111B	TF binding region
ENSG00000255240	CpG island
ENSG00000245571	CpG island
GLYATL1P3	CpG island
GLYATL1P4	CpG island
FAM111A	CpG island
ENSG00000254786	CpG island
FAM111B	CpG island
ENSG00000224032	chromatin interactions
ENSG00000245571	chromatin interactions
ENSG00000133318	chromatin interactions
ENSG00000189057	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000166801	chromatin interactions
CNOT6	miRNA target sites
CSNK1G3	miRNA target sites
ATAD2B	miRNA target sites
AP3S1	miRNA target sites
CDK6	miRNA target sites
KIF2A	miRNA target sites
PRUNE2	miRNA target sites
ZFPM2	miRNA target sites
PDE3B	miRNA target sites
GSPT1	miRNA target sites
KIAA0831	miRNA target sites
CRKL	miRNA target sites
PRTG	miRNA target sites
POU2F1	miRNA target sites
VPS54	miRNA target sites

Extended variants
information (count: 5581 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5581 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147237575	chr11:58767347-58767348	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs535020462	chr11:58767364-58767365	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180691300	chr11:58767407-58767408	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs550427380	chr11:58767416-58767417	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541638843	chr11:58767420-58767421	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556772393	chr11:58767467-58767468	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11229723	chr11:58767505-58767506	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs544693957	chr11:58767508-58767509	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529461617	chr11:58767523-58767524	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199601537	chr11:58767556-58767557	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs185350145	chr11:58767576-58767577	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs377135616	chr11:58767600-58767601	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs548318175	chr11:58767611-58767612	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs565248258	chr11:58767636-58767637	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs374229127	chr11:58767700-58767701	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs76923289	chr11:58767710-58767711	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs564045350	chr11:58767714-58767715	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs76037867	chr11:58767744-58767745	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs528037128	chr11:58767746-58767747	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs540240472	chr11:58767748-58767749	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs12222588	chr11:58767754-58767755	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs190943391	chr11:58767757-58767758	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs374647441	chr11:58767769-58767770	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs373062571	chr11:58767784-58767785	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs377366385	chr11:58767792-58767793	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs548782194	chr11:58767806-58767807	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs570300066	chr11:58767811-58767812	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs531227069	chr11:58767834-58767835	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs565783144	chr11:58767852-58767853	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs534663480	chr11:58767897-58767898	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs552856463	chr11:58767986-58767987	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs183266448	chr11:58767989-58767990	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs59525587	chr11:58768022-58768023	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs199779978	chr11:58768114-58768115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs188096775	chr11:58768149-58768150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191768845	chr11:58768286-58768287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568447216	chr11:58768290-58768291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367696887	chr11:58768303-58768304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182935323	chr11:58768325-58768326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556735363	chr11:58768395-58768396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77480722	chr11:58768409-58768410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs187638215	chr11:58768434-58768435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201413583	chr11:58768437-58768438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112757764	chr11:58768484-58768485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs74697357	chr11:58768519-58768520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs192493407	chr11:58768528-58768529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201929464	chr11:58768532-58768533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573115576	chr11:58768537-58768538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539823859	chr11:58768544-58768545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561755220	chr11:58768547-58768548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2245 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58761000-58769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:58764800-58775200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:58765600-58767800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:58766200-58769000	Weak transcription	Primary hematopoietic stem cells	blood
5	chr11:58766400-58767600	Enhancers	Primary B cells from cord blood	blood
6	chr11:58766400-58767600	Enhancers	Primary B cells from peripheral blood	blood
7	chr11:58766600-58767400	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr11:58766600-58768000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr11:58766600-58768000	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr11:58766800-58767800	Enhancers	Liver	Liver
11	chr11:58767000-58767400	Enhancers	GM12878-XiMat	blood
12	chr11:58767200-58767400	Enhancers	Stomach Mucosa	stomach
13	chr11:58767200-58774000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr11:58767600-58770000	Weak transcription	Primary B cells from cord blood	blood
15	chr11:58767600-58776400	Weak transcription	Primary B cells from peripheral blood	blood
16	chr11:58767800-58769200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:58767800-58771200	Weak transcription	Liver	Liver
18	chr11:58769000-58770600	Enhancers	Primary hematopoietic stem cells	blood
19	chr11:58769200-58770400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:58769200-58770400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:58770000-58771600	Strong transcription	Primary B cells from cord blood	blood
22	chr11:58770400-58773600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr11:58770400-58774400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr11:58770600-58775200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr11:58771200-58772200	Enhancers	Liver	Liver
26	chr11:58771600-58776600	Weak transcription	Primary B cells from cord blood	blood
27	chr11:58772200-58772600	Weak transcription	Liver	Liver
28	chr11:58772600-58773600	Enhancers	Liver	Liver
29	chr11:58773600-58776000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:58773600-58776000	Weak transcription	Liver	Liver
31	chr11:58774000-58774200	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr11:58774200-58774600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr11:58774400-58775200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr11:58774600-58774800	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr11:58774800-58775800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr11:58775200-58778600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:58775200-58780000	Enhancers	Primary hematopoietic stem cells	blood
38	chr11:58775200-58781000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr11:58775800-58776000	Active TSS	Primary hematopoietic stem cells short term culture	blood
40	chr11:58776000-58777200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr11:58776000-58777600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:58776000-58777600	Enhancers	Liver	Liver
43	chr11:58776400-58777200	Enhancers	Adipose Nuclei	Adipose
44	chr11:58776400-58777200	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:58776400-58780400	Enhancers	Primary B cells from peripheral blood	blood
46	chr11:58776600-58780400	Enhancers	Primary B cells from cord blood	blood
47	chr11:58776600-58781200	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr11:58777200-58777400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr11:58777200-58778600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr11:58777200-58781000	Enhancers	Primary hematopoietic stem cells short term culture	blood

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