Variant report

Variant	nsv553454
Chromosome Location	chr11:9059192-9125301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1006)
CpG islands
(count:1590)
Chromatin interactive
region (count:62)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1006 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:9114802-9115029	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:9099950-9100188	K562	blood:	n/a	n/a
3	ARID3A	chr11:9124983-9125402	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:9121165-9121443	K562	blood:	n/a	n/a
5	ATF1	chr11:9095458-9095507	K562	blood:	n/a	n/a
6	ATF2	chr11:9082081-9082804	GM12878	blood:	n/a	n/a
7	ATF2	chr11:9082226-9082802	GM12878	blood:	n/a	n/a
8	BACH1	chr11:9087974-9088007	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr11:9082271-9082786	GM12878	blood:	n/a	chr11:9082572-9082580 chr11:9082463-9082474
10	BATF	chr11:9110264-9110538	GM12878	blood:	n/a	n/a
11	BATF	chr11:9082154-9082811	GM12878	blood:	n/a	chr11:9082572-9082580 chr11:9082463-9082474
12	BATF	chr11:9093262-9093527	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:9082240-9082819	GM12878	blood:	n/a	chr11:9082575-9082584 chr11:9082803-9082816
14	BCL11A	chr11:9082283-9082676	GM12878	blood:	n/a	chr11:9082575-9082584
15	BCL3	chr11:9082229-9082703	GM12878	blood:	n/a	chr11:9082575-9082584
16	BCLAF1	chr11:9082128-9082821	GM12878	blood:	n/a	chr11:9082575-9082584 chr11:9082803-9082816
17	BCLAF1	chr11:9082182-9082786	GM12878	blood:	n/a	chr11:9082575-9082584
18	BHLHE40	chr11:9082262-9082778	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:9125237-9125593	HepG2	liver:	n/a	n/a
20	BHLHE40	chr11:9121342-9121417	K562	blood:	n/a	n/a
21	BHLHE40	chr11:9118076-9118298	K562	blood:	n/a	n/a
22	CCNT2	chr11:9121300-9121539	K562	blood:	n/a	n/a
23	CEBPB	chr11:9124886-9125445	MCF-7	breast:	n/a	n/a
24	CEBPB	chr11:9123705-9123864	K562	blood:	n/a	chr11:9123758-9123769
25	CEBPB	chr11:9092718-9093049	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:9087105-9087540	HepG2	liver:	n/a	chr11:9087368-9087379
27	CEBPB	chr11:9104352-9104551	K562	blood:	n/a	n/a
28	CEBPB	chr11:9107388-9107527	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr11:9123679-9123884	HepG2	liver:	n/a	chr11:9123758-9123769
30	CEBPB	chr11:9064009-9064191	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:9062311-9062315	HepG2	liver:	n/a	n/a
32	CEBPB	chr11:9060216-9060260	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:9124934-9125493	MCF-7	breast:	n/a	n/a
34	CEBPB	chr11:9092763-9093022	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:9082257-9082691	GM12878	blood:	n/a	n/a
36	CEBPB	chr11:9087146-9087794	A549	lung:	n/a	chr11:9087368-9087379
37	CEBPB	chr11:9087155-9087685	IMR90	lung:	n/a	chr11:9087368-9087379
38	CEBPB	chr11:9104308-9104498	IMR90	lung:	n/a	n/a
39	CEBPB	chr11:9092803-9092992	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr11:9087187-9087527	Hela-S3	cervix:	n/a	chr11:9087368-9087379
41	CEBPB	chr11:9063984-9064045	A549	lung:	n/a	n/a
42	CEBPB	chr11:9060575-9061210	HCT-116	colon:	n/a	n/a
43	CEBPB	chr11:9087128-9087934	A549	lung:	n/a	chr11:9087368-9087379
44	CEBPB	chr11:9060161-9060294	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:9125054-9125525	HepG2	liver:	n/a	n/a
46	CEBPB	chr11:9121240-9121382	K562	blood:	n/a	n/a
47	CEBPB	chr11:9060183-9060257	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr11:9060786-9061097	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr11:9092774-9093033	A549	lung:	n/a	n/a
50	CEBPB	chr11:9120038-9120281	K562	blood:	n/a	n/a

(count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9119437-9119487	GM12892	blood:	n/a
2	chr11:9113406-9113456	HEEpiC	esophagus:	n/a
3	chr11:9113184-9113234	HRE	kidney:	n/a
4	chr11:9112989-9113039	PFSK-1	brain:	n/a
5	chr11:9119437-9119487	GM12892	blood:	n/a
6	chr11:9113406-9113456	HEEpiC	esophagus:	n/a
7	chr11:9113184-9113234	HRE	kidney:	n/a
8	chr11:9112989-9113039	PFSK-1	brain:	n/a
9	chr11:9113146-9113196	HCF	heart:	n/a
10	chr11:9112989-9113039	MCF10A-Er-Src	breast:	n/a
11	chr11:9113370-9113420	Hepatocyte	liver:	n/a
12	chr11:9112989-9113039	HRCEpiC	kidney:	n/a
13	chr11:9115009-9115059	HCPEpiC	choroid plexus:	n/a
14	chr11:9113146-9113196	MCF10A-Er-Src	breast:	n/a
15	chr11:9075898-9075948	SK-N-SH	brain:	n/a
16	chr11:9114431-9114481	SK-N-MC	brain:	n/a
17	chr11:9113179-9113229	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:9113167-9113217	BJ	skin:	n/a
19	chr11:9115107-9115157	SKMC	muscle:	n/a
20	chr11:9113152-9113202	NB4	blood:	n/a
21	chr11:9115009-9115059	K562	blood:	n/a
22	chr11:9115107-9115157	HRPEpiC	eye:	n/a
23	chr11:9099393-9099443	GM12891	blood:	n/a
24	chr11:9112989-9113039	NHDF-neo	bronchial:	n/a
25	chr11:9113194-9113244	NT2-D1	testis:	n/a
26	chr11:9113152-9113202	Hepatocyte	liver:	n/a
27	chr11:9114431-9114481	IMR90	lung:	fetal
28	chr11:9112214-9112264	HMEC	breast:	n/a
29	chr11:9108982-9109032	HL-60	blood:	n/a
30	chr11:9068984-9069034	AG09309	skin:	n/a
31	chr11:9113458-9113508	HCPEpiC	choroid plexus:	n/a
32	chr11:9113152-9113202	HL-60	blood:	n/a
33	chr11:9108982-9109032	PANC-1	pancreas:	n/a
34	chr11:9113167-9113217	HCPEpiC	choroid plexus:	n/a
35	chr11:9119437-9119487	HRE	kidney:	n/a
36	chr11:9087524-9087574	SKMC	muscle:	n/a
37	chr11:9113167-9113217	HEEpiC	esophagus:	n/a
38	chr11:9114431-9114481	Caco-2	colon:	n/a
39	chr11:9112471-9112521	IMR90	lung:	fetal
40	chr11:9113190-9113240	AG09309	skin:	n/a
41	chr11:9113194-9113244	HCPEpiC	choroid plexus:	n/a
42	chr11:9113152-9113202	GM19239	blood:	n/a
43	chr11:9112471-9112521	HCT-116	colon:	n/a
44	chr11:9113184-9113234	H1-hESC	embryonic stem cell:	embryo
45	chr11:9068984-9069034	K562	blood:	n/a
46	chr11:9112214-9112264	ovcar-3	ovarian:	n/a
47	chr11:9112715-9112765	K562	blood:	n/a
48	chr11:9113152-9113202	HEK293	kidney:	embryo
49	chr11:9116583-9116633	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:9116583-9116633	HAEpiC	amniotic membrane:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:9109700..9116224-chr11:9155740..9163743,14	MCF-7	breast:
2	chr11:9109535..9113708-chr11:9115640..9120311,8	MCF-7	breast:
3	chr11:9109432..9111291-chr11:9117498..9119505,2	K562	blood:
4	chr11:9063917..9065926-chr11:9066926..9068759,2	K562	blood:
5	chr11:9079042..9082011-chr11:9084095..9086895,2	MCF-7	breast:
6	chr11:9096772..9098814-chr11:9159653..9161311,2	MCF-7	breast:
7	chr11:9088886..9093572-chr11:9094471..9099536,5	MCF-7	breast:
8	chr11:9090840..9093994-chr11:9109730..9112612,4	MCF-7	breast:
9	chr11:9023989..9026905-chr11:9075078..9077579,2	K562	blood:
10	chr11:9088310..9090421-chr11:9092696..9094493,2	K562	blood:
11	chr11:9088886..9093572-chr11:9094471..9099536,5	MCF-7	breast:
12	chr11:9011525..9013427-chr11:9074733..9076584,2	K562	blood:
13	chr11:9104158..9106515-chr11:9110510..9112401,2	K562	blood:
14	chr11:9114505..9115469-chr11:9158990..9159883,2	MCF-7	breast:
15	chr11:9079563..9082027-chr11:9110788..9112419,2	K562	blood:
16	chr11:9075149..9076918-chr11:9084166..9086058,2	K562	blood:
17	chr11:9088310..9090421-chr11:9092696..9094493,2	K562	blood:
18	chr11:9081414..9083188-chr11:9094934..9097421,2	MCF-7	breast:
19	chr11:9098428..9102271-chr11:9102420..9106613,4	MCF-7	breast:
20	chr11:9094776..9100228-chr11:9109116..9115745,9	MCF-7	breast:
21	chr11:9075127..9077709-chr11:9146787..9148861,2	MCF-7	breast:
22	chr11:9060449..9064388-chr11:9064769..9066551,3	MCF-7	breast:
23	chr11:9070098..9074605-chr11:9077166..9080417,4	K562	blood:
24	chr11:9123650..9128342-chr11:9129047..9134546,16	MCF-7	breast:
25	chr11:9110779..9112949-chr14:50359771..50361759,2	MCF-7	breast:
26	chr11:9057967..9060899-chr11:9063796..9066670,2	MCF-7	breast:
27	chr11:9112943..9114701-chr11:9593377..9596594,3	MCF-7	breast:
28	chr11:9060449..9064388-chr11:9064769..9066551,3	MCF-7	breast:
29	chr11:9078089..9081038-chr11:9097785..9099533,2	K562	blood:
30	chr11:9063917..9065926-chr11:9066926..9068759,2	K562	blood:
31	chr11:9096453..9100009-chr11:9109171..9113548,7	MCF-7	breast:
32	chr11:9108004..9116385-chr11:9156452..9162678,21	MCF-7	breast:
33	chr11:9069483..9071598-chr11:9076073..9078809,2	K562	blood:
34	chr11:9104308..9107322-chr11:9124502..9128223,3	MCF-7	breast:
35	chr11:9097322..9098871-chr11:9128931..9130944,2	MCF-7	breast:
36	chr11:9109535..9113708-chr11:9115640..9120311,8	MCF-7	breast:
37	chr11:9099703..9100633-chr11:9159006..9159677,3	K562	blood:
38	chr11:9062855..9067296-chr11:9070515..9073195,4	K562	blood:
39	chr11:9098428..9102271-chr11:9102420..9106613,4	MCF-7	breast:
40	chr11:9081414..9083188-chr11:9094934..9097421,2	MCF-7	breast:
41	chr11:9079042..9082011-chr11:9084095..9086895,2	MCF-7	breast:
42	chr11:9108929..9110845-chr11:9168410..9170250,2	MCF-7	breast:
43	chr11:9097322..9099854-chr11:9158017..9160893,2	MCF-7	breast:
44	chr11:9125247..9126912-chr11:9158309..9160456,2	MCF-7	breast:
45	chr11:9070098..9074605-chr11:9077166..9080417,4	K562	blood:
46	chr11:9093993..9096683-chr11:9129654..9132296,2	MCF-7	breast:
47	chr11:9085105..9088993-chr11:9089153..9093371,4	K562	blood:
48	chr11:9078071..9079689-chr9:92219545..92221105,2	MCF-7	breast:
49	chr11:9092833..9094684-chr11:9112419..9114154,2	MCF-7	breast:
50	chr11:9072036..9074888-chr11:9076818..9079933,4	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKIP1-2	chr11:9078786-9078831	ENSG00000253973.2
2	lnc-AKIP1-2	chr11:9080767-9081286	NONHSAT017906
3	lnc-AKIP1-7	chr11:9060362-9060963	NONHSAT017903
4	lnc-AKIP1-2	chr11:9086079-9086701	ENSG00000253973.2
5	lnc-AKIP1-2	chr11:9078798-9079002	ENSG00000253973.2
6	lnc-NRIP3-4	chr11:9071446-9071944	NONHSAT017904
7	lnc-AKIP1-2	chr11:9081155-9081286	ENSG00000253973.2
8	lnc-AKIP1-7	chr11:9078045-9078561	NONHSAT017903
9	lnc-NRIP3-4	chr11:9069620-9069645	NONHSAT017904
10	lnc-AKIP1-2	chr11:9086079-9088694	NONHSAT017906

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5691	chr11:9111897-9111918	MIMAT0022483

No data

Variant related genes	Relation type
ENSG00000253973	TF binding region
MIR5691	TF binding region
KRT8P41	TF binding region
SCUBE2	TF binding region
ENSG00000253973	CpG island
MIR5691	CpG island
KRT8P41	CpG island
SCUBE2	CpG island
ENSG00000253973	chromatin interactions
ENSG00000165527	chromatin interactions
ENSG00000166483	chromatin interactions
ENSG00000130222	chromatin interactions
ENSG00000264984	chromatin interactions
ENSG00000175352	chromatin interactions
ENSG00000175356	chromatin interactions
ENSG00000213538	chromatin interactions

Extended variants
information (count: 2631 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:2631 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1883100	chr11:9059192-9059193	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532358048	chr11:9059200-9059201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552163650	chr11:9059395-9059396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141765510	chr11:9059401-9059402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192803920	chr11:9059416-9059417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541990558	chr11:9059539-9059540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs10743098	chr11:9059550-9059551	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs567382712	chr11:9059604-9059605	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529912241	chr11:9059622-9059623	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568308751	chr11:9059646-9059647	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10668342	chr11:9059669-9059670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34984187	chr11:9059670-9059671	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371379323	chr11:9059673-9059674	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs397724530	chr11:9059674-9059675	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549580036	chr11:9059677-9059678	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370693988	chr11:9059707-9059708	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs184650603	chr11:9059736-9059737	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146231713	chr11:9059778-9059779	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373990404	chr11:9059794-9059795	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78651583	chr11:9059803-9059804	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78408706	chr11:9059804-9059805	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs566356594	chr11:9059881-9059882	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7124182	chr11:9059943-9059944	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs114059404	chr11:9059955-9059956	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs574908525	chr11:9059962-9059963	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543999065	chr11:9059965-9059966	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545845898	chr11:9059980-9059981	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs58032533	chr11:9059992-9059993	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs577309383	chr11:9060014-9060015	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs545788846	chr11:9060017-9060018	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571444297	chr11:9060037-9060038	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535598711	chr11:9060050-9060051	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527566379	chr11:9060061-9060062	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540893203	chr11:9060128-9060129	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200488741	chr11:9060164-9060165	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139205074	chr11:9060171-9060172	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7124472	chr11:9060179-9060180	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs373867805	chr11:9060182-9060183	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7130454	chr11:9060199-9060200	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs75461375	chr11:9060203-9060204	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569650778	chr11:9060229-9060230	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79902325	chr11:9060236-9060237	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568288780	chr11:9060274-9060275	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552189176	chr11:9060286-9060287	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145817950	chr11:9060418-9060419	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs565648705	chr11:9060439-9060440	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs199871691	chr11:9060440-9060441	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
48	rs370341579	chr11:9060442-9060443	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
49	rs367543556	chr11:9060447-9060448	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs534624790	chr11:9060455-9060456	Weak transcription Enhancers Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1134 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9038200-9064000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr11:9043400-9059200	Weak transcription	Right Atrium	heart
3	chr11:9047200-9068600	Weak transcription	Fetal Intestine Large	intestine
4	chr11:9052400-9067800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr11:9052800-9060400	Weak transcription	Lung	lung
6	chr11:9052800-9060600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:9052800-9069800	Weak transcription	Gastric	stomach
8	chr11:9053000-9060600	Weak transcription	Fetal Stomach	stomach
9	chr11:9055200-9060200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr11:9055600-9059600	Weak transcription	Pancreas	Pancrea
11	chr11:9055600-9060800	Weak transcription	Adipose Nuclei	Adipose
12	chr11:9056000-9060800	Weak transcription	Fetal Muscle Leg	muscle
13	chr11:9057800-9059400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr11:9057800-9059600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr11:9057800-9059600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr11:9057800-9059600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:9057800-9060000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr11:9058200-9059200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr11:9058200-9059200	Enhancers	Brain Angular Gyrus	brain
20	chr11:9058200-9059200	Enhancers	Brain Hippocampus Middle	brain
21	chr11:9058200-9059200	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr11:9058200-9059400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr11:9058200-9059400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr11:9058200-9059400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:9058200-9059400	Enhancers	Brain Anterior Caudate	brain
26	chr11:9058200-9059400	Enhancers	Brain Cingulate Gyrus	brain
27	chr11:9058200-9059400	Enhancers	Brain Substantia Nigra	brain
28	chr11:9058200-9059600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr11:9058200-9059600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:9058200-9060400	Enhancers	Fetal Lung	lung
31	chr11:9058400-9059200	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr11:9058400-9059600	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr11:9058400-9099800	Weak transcription	Aorta	Aorta
34	chr11:9058600-9059200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:9058600-9060600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr11:9058800-9059200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:9058800-9059400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr11:9058800-9059400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:9058800-9063000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr11:9059000-9059400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr11:9059000-9060600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr11:9059000-9060800	Enhancers	Placenta	Placenta
43	chr11:9059000-9061000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr11:9059000-9061800	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr11:9059200-9059400	Enhancers	Right Atrium	heart
46	chr11:9059200-9059600	Enhancers	Fetal Kidney	kidney
47	chr11:9059200-9063400	Weak transcription	Brain Hippocampus Middle	brain
48	chr11:9059200-9074000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:9059400-9059600	Weak transcription	Right Atrium	heart
50	chr11:9059400-9060200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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