Variant report

Variant	nsv540945
Chromosome Location	chr11:6652513-6679974
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:445)
CpG islands
(count:917)
Chromatin interactive
region (count:58)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:6659700-6660020	K562	blood:	n/a	n/a
2	ATF1	chr11:6656532-6657078	K562	blood:	n/a	n/a
3	ATF1	chr11:6672191-6672588	K562	blood:	n/a	n/a
4	ATF2	chr11:6668226-6668603	GM12878	blood:	n/a	n/a
5	ATF2	chr11:6668141-6668709	GM12878	blood:	n/a	n/a
6	ATF3	chr11:6672143-6672531	K562	blood:	n/a	n/a
7	BACH1	chr11:6652724-6652770	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr11:6668240-6668630	GM12878	blood:	n/a	n/a
9	BATF	chr11:6668309-6668594	GM12878	blood:	n/a	n/a
10	BCL11A	chr11:6668266-6668622	GM12878	blood:	n/a	chr11:6668417-6668426
11	BCL11A	chr11:6668309-6668572	GM12878	blood:	n/a	chr11:6668417-6668426
12	BCL3	chr11:6676139-6676571	GM12878	blood:	n/a	n/a
13	BCL3	chr11:6676125-6676580	GM12878	blood:	n/a	n/a
14	BCLAF1	chr11:6668095-6668639	GM12878	blood:	n/a	chr11:6668230-6668243 chr11:6668417-6668426
15	BHLHE40	chr11:6668194-6668608	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:6675830-6676659	HepG2	liver:	n/a	chr11:6676109-6676125
17	BHLHE40	chr11:6672233-6672728	K562	blood:	n/a	n/a
18	BHLHE40	chr11:6667310-6667971	K562	blood:	n/a	chr11:6667509-6667525
19	BHLHE40	chr11:6656636-6657104	K562	blood:	n/a	n/a
20	BHLHE40	chr11:6667292-6667668	GM12878	blood:	n/a	chr11:6667509-6667525
21	BHLHE40	chr11:6661731-6661972	HepG2	liver:	n/a	n/a
22	BRCA1	chr11:6667929-6668007	GM12878	blood:	n/a	n/a
23	CBX3	chr11:6672180-6672534	K562	blood:	n/a	n/a
24	CBX3	chr11:6667254-6667657	K562	blood:	n/a	n/a
25	CBX3	chr11:6656543-6657182	K562	blood:	n/a	n/a
26	CCNT2	chr11:6672265-6672540	K562	blood:	n/a	n/a
27	CEBPB	chr11:6675663-6675907	HepG2	liver:	n/a	n/a
28	CEBPB	chr11:6661760-6661960	HepG2	liver:	n/a	chr11:6661843-6661854
29	CEBPB	chr11:6656559-6657048	HepG2	liver:	n/a	n/a
30	CHD1	chr11:6668385-6668585	GM12878	blood:	n/a	n/a
31	CHD1	chr11:6656475-6656498	GM12878	blood:	n/a	n/a
32	CHD2	chr11:6667421-6668657	GM12878	blood:	n/a	chr11:6668146-6668156
33	CHD2	chr11:6675961-6676109	HepG2	liver:	n/a	n/a
34	CHD2	chr11:6656745-6656917	K562	blood:	n/a	n/a
35	CHD2	chr11:6676301-6676392	GM12878	blood:	n/a	n/a
36	CHD2	chr11:6668967-6669076	GM12878	blood:	n/a	n/a
37	CHD2	chr11:6676335-6676521	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTBP2	chr11:6677224-6677701	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr11:6667384-6667487	GM19239	blood:	n/a	n/a
40	CTCF	chr11:6659760-6659910	HepG2	liver:	n/a	n/a
41	CTCF	chr11:6659736-6659995	Medullo	brain:	n/a	n/a
42	CTCF	chr11:6659780-6659930	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr11:6659800-6659950	NB4	blood:	n/a	n/a
44	CTCF	chr11:6659820-6659970	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr11:6659681-6659983	K562	blood:	n/a	n/a
46	CTCF	chr11:6659680-6660018	K562	blood:	n/a	n/a
47	CTCF	chr11:6659738-6660049	HepG2	liver:	n/a	n/a
48	CTCF	chr11:6659780-6659930	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr11:6659820-6659970	K562	blood:	n/a	n/a
50	CTCF	chr11:6667920-6668070	SK-N-SH_RA	brain:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:6677919-6677969	NHDF-neo	bronchial:	n/a
2	chr11:6676597-6676647	HCT-116	colon:	n/a
3	chr11:6677919-6677969	NHDF-neo	bronchial:	n/a
4	chr11:6676597-6676647	HCT-116	colon:	n/a
5	chr11:6677087-6677137	HPAEpiC	pulmonary alveolar:	n/a
6	chr11:6661968-6662018	HEK293	kidney:	embryo
7	chr11:6677919-6677969	CMK	blood:	n/a
8	chr11:6655429-6655479	GM12892	blood:	n/a
9	chr11:6676597-6676647	GM06990	blood:	n/a
10	chr11:6662141-6662191	H1-hESC	embryonic stem cell:	embryo
11	chr11:6668214-6668264	NH-A	brain:	n/a
12	chr11:6661968-6662018	NHBE	bronchial:	n/a
13	chr11:6677087-6677137	SKMC	muscle:	n/a
14	chr11:6677919-6677969	HMEC	breast:	n/a
15	chr11:6662324-6662374	HL-60	blood:	n/a
16	chr11:6676366-6676416	HRCEpiC	kidney:	n/a
17	chr11:6677965-6678015	SAEC	small airway:	n/a
18	chr11:6662141-6662191	HRPEpiC	eye:	n/a
19	chr11:6668214-6668264	AG10803	skin:	n/a
20	chr11:6662324-6662374	SKMC	muscle:	n/a
21	chr11:6676366-6676416	SK-N-MC	brain:	n/a
22	chr11:6676515-6676565	HEEpiC	esophagus:	n/a
23	chr11:6655429-6655479	AG10803	skin:	n/a
24	chr11:6662141-6662191	HAEpiC	amniotic membrane:	n/a
25	chr11:6662324-6662374	GM12892	blood:	n/a
26	chr11:6677965-6678015	NB4	blood:	n/a
27	chr11:6661968-6662018	PFSK-1	brain:	n/a
28	chr11:6668214-6668264	GM12878	blood:	n/a
29	chr11:6677965-6678015	GM19239	blood:	n/a
30	chr11:6676366-6676416	HCM	heart:	n/a
31	chr11:6677919-6677969	A549	lung:	n/a
32	chr11:6677919-6677969	HCT-116	colon:	n/a
33	chr11:6677965-6678015	H1-hESC	embryonic stem cell:	embryo
34	chr11:6657194-6657244	BJ	skin:	n/a
35	chr11:6668214-6668264	GM19239	blood:	n/a
36	chr11:6677087-6677137	PFSK-1	brain:	n/a
37	chr11:6677965-6678015	RPTEC	kidney:	n/a
38	chr11:6657194-6657244	A549	lung:	n/a
39	chr11:6661968-6662018	RPTEC	kidney:	n/a
40	chr11:6657194-6657244	Hepatocyte	liver:	n/a
41	chr11:6662324-6662374	HUVEC	blood vessel:	n/a
42	chr11:6676366-6676416	HCF	heart:	n/a
43	chr11:6661968-6662018	SKMC	muscle:	n/a
44	chr11:6677919-6677969	IMR90	lung:	fetal
45	chr11:6678143-6678193	BJ	skin:	n/a
46	chr11:6655429-6655479	RPTEC	kidney:	n/a
47	chr11:6655429-6655479	HIPEpiC	eye:	n/a
48	chr11:6678143-6678193	PFSK-1	brain:	n/a
49	chr11:6676597-6676647	HIPEpiC	eye:	n/a
50	chr11:6661968-6662018	A549	lung:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:6658451..6661437-chr11:6662516..6665841,4	K562	blood:
2	chr11:6625119..6628109-chr11:6677478..6680311,2	K562	blood:
3	chr11:6671564..6673124-chr11:6685521..6687390,2	K562	blood:
4	chr11:6642401..6645177-chr11:6674156..6676379,2	K562	blood:
5	chr11:6653503..6655020-chr11:6655234..6657015,2	MCF-7	breast:
6	chr11:6641899..6643962-chr11:6651822..6653980,2	K562	blood:
7	chr11:6661578..6664296-chr11:6676405..6678394,2	K562	blood:
8	chr11:6656547..6659365-chr11:6666285..6668794,2	K562	blood:
9	chr11:6632773..6634316-chr11:6656599..6658208,2	K562	blood:
10	chr11:6655611..6658760-chr11:6664581..6666992,3	K562	blood:
11	chr11:6552223..6553419-chr11:6659519..6660386,4	K562	blood:
12	chr11:6638642..6641377-chr11:6671039..6674008,2	K562	blood:
13	chr11:6672344..6673946-chr11:6674107..6675922,2	K562	blood:
14	chr11:6632176..6635139-chr11:6668951..6671645,3	MCF-7	breast:
15	chr11:6655611..6658760-chr11:6664581..6666992,3	K562	blood:
16	chr11:6639505..6641485-chr11:6656272..6658184,2	K562	blood:
17	chr11:6654578..6657843-chr11:6703066..6706154,4	K562	blood:
18	chr11:6624901..6626426-chr11:6658015..6660451,2	MCF-7	breast:
19	chr11:6673046..6675996-chr11:6697602..6699173,2	K562	blood:
20	chr11:6667612..6669318-chr11:6678887..6680520,2	K562	blood:
21	chr11:6631935..6636002-chr11:6669789..6672430,3	K562	blood:
22	chr11:6659598..6661282-chr11:6662662..6665078,2	MCF-7	breast:
23	chr11:6660854..6663363-chr11:6666895..6669145,2	MCF-7	breast:
24	chr11:6650671..6652738-chr11:6656023..6657936,2	K562	blood:
25	chr11:6657432..6659673-chr11:6702962..6704488,2	MCF-7	breast:
26	chr11:6662316..6664531-chr11:6673542..6676066,2	K562	blood:
27	chr11:6631323..6635025-chr11:6655682..6658099,3	K562	blood:
28	chr11:6549341..6550863-chr11:6658993..6661562,2	MCF-7	breast:
29	chr11:6550497..6552523-chr11:6668338..6670273,2	K562	blood:
30	chr11:6643075..6645177-chr11:6673470..6675656,2	K562	blood:
31	chr11:6667612..6669318-chr11:6678887..6680520,2	K562	blood:
32	chr11:6677320..6679632-chr11:6685201..6687162,3	K562	blood:
33	chr11:6659598..6661282-chr11:6662662..6665078,2	MCF-7	breast:
34	chr11:6654750..6657029-chr11:6703066..6704825,2	K562	blood:
35	chr11:6660854..6663363-chr11:6666895..6669145,2	MCF-7	breast:
36	chr11:6646749..6649566-chr11:6656604..6660574,4	K562	blood:
37	chr11:6639337..6641377-chr11:6671039..6672968,2	K562	blood:
38	chr11:6678471..6681926-chr11:6700369..6702976,3	K562	blood:
39	chr11:6647467..6650354-chr11:6655499..6658337,3	K562	blood:
40	chr11:6655101..6657094-chr11:6659773..6662365,3	K562	blood:
41	chr11:6658451..6661437-chr11:6662516..6665841,4	K562	blood:
42	chr11:6674078..6676312-chr11:6677846..6681354,3	K562	blood:
43	chr11:6638833..6641485-chr11:6656272..6659369,4	K562	blood:
44	chr11:6662316..6664531-chr11:6673542..6676066,2	K562	blood:
45	chr11:6658482..6660687-chr11:6661991..6663928,2	MCF-7	breast:
46	chr11:6647293..6652436-chr11:6674078..6677379,4	K562	blood:
47	chr11:6672344..6673946-chr11:6674107..6675922,2	K562	blood:
48	chr11:6660452..6662091-chr11:6701041..6703575,2	K562	blood:
49	chr11:6655101..6657094-chr11:6659773..6662365,3	K562	blood:
50	chr11:6674078..6676312-chr11:6677846..6681354,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ILK-4	chr11:6678138-6678468	XLOC_009046
2	lnc-ILK-4	chr11:6677940-6677988	XLOC_009046

No data

Variant related genes	Relation type
DCHS1	TF binding region
DCHS1	CpG island
ENSG00000166340	chromatin interactions
ENSG00000254641	chromatin interactions
ENSG00000255680	chromatin interactions
ENSG00000179532	chromatin interactions
ENSG00000255410	chromatin interactions
ENSG00000254400	chromatin interactions
ENSG00000158042	chromatin interactions
ENSG00000255390	chromatin interactions
ENSG00000166341	chromatin interactions
ENSG00000166337	chromatin interactions
ENSG00000166333	chromatin interactions

Extended variants
information (count: 1107 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1107 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561000514	chr11:6652521-6652522	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs143368111	chr11:6652545-6652546	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147152025	chr11:6652550-6652551	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs371857669	chr11:6652566-6652567	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs376478104	chr11:6652576-6652577	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201076402	chr11:6652592-6652593	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs112445976	chr11:6652603-6652604	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142768745	chr11:6652604-6652605	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs2659871	chr11:6652618-6652619	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs200997946	chr11:6652627-6652628	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs139849372	chr11:6652628-6652629	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565376353	chr11:6652629-6652630	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs374415969	chr11:6652636-6652637	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs377750047	chr11:6652653-6652654	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567796598	chr11:6652695-6652696	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs536821033	chr11:6652713-6652714	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556527197	chr11:6652736-6652737	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs560122816	chr11:6652739-6652740	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576666420	chr11:6652780-6652781	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs545387501	chr11:6652806-6652807	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149828248	chr11:6652851-6652852	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368728632	chr11:6652928-6652929	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs373116509	chr11:6652932-6652933	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs376375338	chr11:6652950-6652951	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557707384	chr11:6652955-6652956	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs577234399	chr11:6652970-6652971	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs138559226	chr11:6652976-6652977	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200372389	chr11:6652984-6652985	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547827281	chr11:6653010-6653011	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs370729666	chr11:6653015-6653016	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529000213	chr11:6653019-6653020	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs373525271	chr11:6653058-6653059	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs140289438	chr11:6653068-6653069	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369754083	chr11:6653069-6653070	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373965759	chr11:6653085-6653086	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs562547836	chr11:6653115-6653116	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186090878	chr11:6653128-6653129	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190500158	chr11:6653138-6653139	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs571637317	chr11:6653147-6653148	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs145239157	chr11:6653167-6653168	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147991846	chr11:6653169-6653170	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs536785069	chr11:6653172-6653173	ZNF genes & repeats Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2555164	chr11:6653229-6653230	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs2659870	chr11:6653232-6653233	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs367892897	chr11:6653233-6653234	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201967893	chr11:6653243-6653244	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs558971402	chr11:6653248-6653249	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs372078352	chr11:6653251-6653252	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141566818	chr11:6653253-6653254	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs201595915	chr11:6653254-6653255	ZNF genes & repeats Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1477 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:6640600-6656400	Weak transcription	Small Intestine	intestine
2	chr11:6642600-6656000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:6642600-6656600	Strong transcription	Brain Germinal Matrix	brain
4	chr11:6642800-6659200	Strong transcription	Fetal Brain Female	brain
5	chr11:6643000-6656600	Strong transcription	Fetal Muscle Leg	muscle
6	chr11:6643200-6655200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:6643200-6655400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr11:6643200-6656200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:6643400-6654600	Strong transcription	Stomach Smooth Muscle	stomach
10	chr11:6643600-6655600	Strong transcription	Duodenum Smooth Muscle	Duodenum
11	chr11:6643600-6656400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:6643800-6655600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:6643800-6655800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr11:6644400-6654800	Strong transcription	Colon Smooth Muscle	Colon
15	chr11:6644400-6655200	Strong transcription	Ovary	ovary
16	chr11:6644600-6654800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:6644600-6656000	Strong transcription	Primary T cells from cord blood	blood
18	chr11:6644600-6656000	Strong transcription	Fetal Lung	lung
19	chr11:6644600-6656400	Weak transcription	NHDF-Ad	bronchial
20	chr11:6645200-6655200	Strong transcription	Aorta	Aorta
21	chr11:6647800-6655200	Strong transcription	Adipose Nuclei	Adipose
22	chr11:6647800-6656200	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr11:6648600-6654400	Weak transcription	Left Ventricle	heart
24	chr11:6648800-6652600	Weak transcription	Brain Anterior Caudate	brain
25	chr11:6648800-6673000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr11:6649000-6656600	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr11:6649000-6656600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr11:6649200-6653400	Strong transcription	Brain Hippocampus Middle	brain
29	chr11:6649200-6655200	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr11:6649200-6663200	Strong transcription	Cortex derived primary cultured neurospheres	brain
31	chr11:6649400-6654200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:6649400-6654800	Strong transcription	HUVEC	blood vessel
33	chr11:6649400-6663400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
34	chr11:6649400-6666200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr11:6649600-6652600	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr11:6649600-6652800	Strong transcription	Primary hematopoietic stem cells	blood
37	chr11:6649600-6653600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
38	chr11:6649600-6653600	Strong transcription	Spleen	Spleen
39	chr11:6649600-6656600	Weak transcription	Primary B cells from cord blood	blood
40	chr11:6649600-6660800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr11:6649800-6652800	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr11:6649800-6654200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr11:6649800-6654600	Strong transcription	Brain Angular Gyrus	brain
44	chr11:6649800-6664000	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr11:6650000-6655200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr11:6650000-6655400	Strong transcription	Thymus	Thymus
47	chr11:6650400-6653600	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr11:6650400-6654000	Weak transcription	Fetal Kidney	kidney
49	chr11:6650400-6656400	Weak transcription	Muscle Satellite Cultured Cells	--
50	chr11:6650600-6653000	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland

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