Variant report

Variant	nsv527072
Chromosome Location	chr11:121448090-121486552
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:658)
CpG islands
(count:611)
Chromatin interactive
region (count:6)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:658 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:121456665-121456680	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:121462057-121462420	HepG2	liver:	n/a	n/a
3	ATF1	chr11:121462166-121462512	K562	blood:	n/a	n/a
4	ATF2	chr11:121461996-121462649	GM12878	blood:	n/a	n/a
5	ATF2	chr11:121460309-121461845	GM12878	blood:	n/a	n/a
6	ATF2	chr11:121463338-121463847	GM12878	blood:	n/a	n/a
7	ATF2	chr11:121460260-121461812	GM12878	blood:	n/a	n/a
8	ATF2	chr11:121463443-121463810	GM12878	blood:	n/a	n/a
9	BATF	chr11:121460536-121461472	GM12878	blood:	n/a	chr11:121461005-121461016
10	BATF	chr11:121460641-121461440	GM12878	blood:	n/a	chr11:121461005-121461016
11	BATF	chr11:121463471-121463715	GM12878	blood:	n/a	n/a
12	BATF	chr11:121463446-121463715	GM12878	blood:	n/a	n/a
13	BCL11A	chr11:121460569-121461315	GM12878	blood:	n/a	n/a
14	BCL11A	chr11:121460541-121461528	GM12878	blood:	n/a	n/a
15	BCL3	chr11:121460476-121461344	GM12878	blood:	n/a	n/a
16	BCL3	chr11:121460618-121461380	GM12878	blood:	n/a	n/a
17	BCLAF1	chr11:121462089-121462535	GM12878	blood:	n/a	n/a
18	BCLAF1	chr11:121460453-121461855	GM12878	blood:	n/a	n/a
19	BCLAF1	chr11:121461910-121462508	GM12878	blood:	n/a	n/a
20	BCLAF1	chr11:121460517-121461846	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:121462129-121462470	GM12878	blood:	n/a	n/a
22	BHLHE40	chr11:121466496-121466728	A549	lung:	n/a	n/a
23	BHLHE40	chr11:121460369-121461611	GM12878	blood:	n/a	n/a
24	BHLHE40	chr11:121462175-121462424	K562	blood:	n/a	n/a
25	CEBPB	chr11:121466349-121466833	A549	lung:	n/a	n/a
26	CEBPB	chr11:121466347-121466933	A549	lung:	n/a	n/a
27	CEBPB	chr11:121474954-121475312	HepG2	liver:	n/a	chr11:121475135-121475146
28	CEBPB	chr11:121466388-121466905	MCF-7	breast:	n/a	n/a
29	CEBPB	chr11:121466364-121467020	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr11:121466403-121466792	MCF-7	breast:	n/a	n/a
31	CEBPB	chr11:121466389-121466938	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr11:121466449-121466737	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:121460457-121461948	GM12878	blood:	n/a	n/a
34	CEBPB	chr11:121474109-121474344	IMR90	lung:	n/a	chr11:121474263-121474274
35	CEBPB	chr11:121448924-121449101	IMR90	lung:	n/a	chr11:121448997-121449006
36	CEBPB	chr11:121456493-121456764	HepG2	liver:	n/a	chr11:121456614-121456625
37	CEBPB	chr11:121466427-121466773	A549	lung:	n/a	n/a
38	CEBPB	chr11:121466339-121466997	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr11:121466324-121466873	HCT-116	colon:	n/a	n/a
40	CEBPB	chr11:121460610-121461099	GM12878	blood:	n/a	n/a
41	CEBPB	chr11:121474225-121474321	HepG2	liver:	n/a	chr11:121474263-121474274
42	CEBPB	chr11:121474996-121475222	HepG2	liver:	n/a	chr11:121475135-121475146
43	CEBPB	chr11:121466328-121466947	IMR90	lung:	n/a	n/a
44	CEBPB	chr11:121474987-121475185	HepG2	liver:	n/a	chr11:121475135-121475146
45	CEBPB	chr11:121466263-121466986	HCT-116	colon:	n/a	n/a
46	CHD1	chr11:121460745-121462563	GM12878	blood:	n/a	n/a
47	CHD2	chr11:121466467-121466832	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr11:121460563-121461490	GM12878	blood:	n/a	n/a
49	CTCF	chr11:121462120-121462270	WI-38	lung:	n/a	n/a
50	CTCF	chr11:121462196-121462448	Hela-S3	cervix:	n/a	chr11:121462294-121462315 chr11:121462304-121462312 chr11:121462299-121462317 chr11:121462300-121462316

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:121466463-121466513	HEEpiC	esophagus:	n/a
2	chr11:121466463-121466513	HEEpiC	esophagus:	n/a
3	chr11:121474197-121474247	RPTEC	kidney:	n/a
4	chr11:121460973-121461023	SK-N-SH_RA	brain:	n/a
5	chr11:121477737-121477787	AoSMC	blood vessel:	n/a
6	chr11:121460973-121461023	Hela-S3	cervix:	n/a
7	chr11:121460973-121461023	AG09319	gingival:	n/a
8	chr11:121474197-121474247	GM12878	blood:	n/a
9	chr11:121460778-121460828	GM12891	blood:	n/a
10	chr11:121474197-121474247	HIPEpiC	eye:	n/a
11	chr11:121466629-121466679	HCF	heart:	n/a
12	chr11:121466463-121466513	HIPEpiC	eye:	n/a
13	chr11:121460793-121460843	BJ	skin:	n/a
14	chr11:121460793-121460843	T-47D	breast:	n/a
15	chr11:121477737-121477787	HCT-116	colon:	n/a
16	chr11:121466430-121466480	HNPCEpiC	eye:	n/a
17	chr11:121477655-121477705	HRE	kidney:	n/a
18	chr11:121485684-121485734	NT2-D1	testis:	n/a
19	chr11:121460973-121461023	Hepatocyte	liver:	n/a
20	chr11:121485684-121485734	MCF-7	breast:	n/a
21	chr11:121466629-121466679	A549	lung:	n/a
22	chr11:121477737-121477787	HEK293	kidney:	embryo
23	chr11:121466629-121466679	HRCEpiC	kidney:	n/a
24	chr11:121460973-121461023	NT2-D1	testis:	n/a
25	chr11:121460793-121460843	NH-A	brain:	n/a
26	chr11:121466629-121466679	NT2-D1	testis:	n/a
27	chr11:121474197-121474247	Hela-S3	cervix:	n/a
28	chr11:121477655-121477705	HUVEC	blood vessel:	n/a
29	chr11:121466629-121466679	MCF-7	breast:	n/a
30	chr11:121477737-121477787	HRPEpiC	eye:	n/a
31	chr11:121466629-121466679	H1-hESC	embryonic stem cell:	embryo
32	chr11:121460778-121460828	ECC-1	luminal epithelium:	n/a
33	chr11:121460973-121461023	GM12878	blood:	n/a
34	chr11:121485684-121485734	HRE	kidney:	n/a
35	chr11:121460793-121460843	CMK	blood:	n/a
36	chr11:121466430-121466480	GM12891	blood:	n/a
37	chr11:121460973-121461023	ovcar-3	ovarian:	n/a
38	chr11:121477655-121477705	RPTEC	kidney:	n/a
39	chr11:121460793-121460843	RPTEC	kidney:	n/a
40	chr11:121460973-121461023	HUVEC	blood vessel:	n/a
41	chr11:121474197-121474247	K562	blood:	n/a
42	chr11:121477655-121477705	GM12878	blood:	n/a
43	chr11:121477737-121477787	AG04449	skin:	fetal
44	chr11:121460973-121461023	SK-N-MC	brain:	n/a
45	chr11:121477737-121477787	HRE	kidney:	n/a
46	chr11:121460973-121461023	HEEpiC	esophagus:	n/a
47	chr11:121460778-121460828	AG10803	skin:	n/a
48	chr11:121460973-121461023	BE2_C	brain:	n/a
49	chr11:121474197-121474247	PANC-1	pancreas:	n/a
50	chr11:121460778-121460828	NH-A	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:121316893..121318248-chr11:121461711..121462415,3	MCF-7	breast:
2	chr11:121192033..121192612-chr11:121461567..121462290,2	MCF-7	breast:
3	chr11:120381894..120382837-chr11:121461399..121462390,3	K562	blood:
4	chr11:121189831..121190442-chr11:121461888..121462730,2	MCF-7	breast:
5	chr11:120975216..120977193-chr11:121456635..121459591,2	K562	blood:
6	chr11:121192094..121192920-chr11:121461877..121462689,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BLID-7	chr11:121465023-121467658	ucscGeneNc_uc001pya_2
2	lnc-BLID-6	chr11:121471818-121474271	ucscGeneNc_uc001pye_1
3	lnc-BLID-7	chr11:121476292-121476369	ucscGeneNc_uc001pya_2

No data

Variant related genes	Relation type
SORL1	TF binding region
SORL1	CpG island
ENSG00000149403	chromatin interactions
ENSG00000204306	chromatin interactions

Extended variants
information (count: 1498 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2070045	chr11:121448090-121448091	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138407235	chr11:121448108-121448109	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs373952818	chr11:121448146-121448147	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs376949268	chr11:121448147-121448148	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs369873016	chr11:121448153-121448154	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs558633208	chr11:121448165-121448166	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs535176137	chr11:121448179-121448180	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs3824966	chr11:121448183-121448184	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs3781835	chr11:121448254-121448255	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs539013421	chr11:121448282-121448283	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs558052225	chr11:121448319-121448320	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs576619899	chr11:121448337-121448338	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs3781836	chr11:121448338-121448339	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs148507485	chr11:121448342-121448343	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs141913747	chr11:121448357-121448358	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs541520468	chr11:121448469-121448470	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559848199	chr11:121448471-121448472	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs74492884	chr11:121448492-121448493	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs578084589	chr11:121448515-121448516	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182576702	chr11:121448533-121448534	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12276224	chr11:121448559-121448560	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs531499409	chr11:121448565-121448566	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147275061	chr11:121448584-121448585	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs573209239	chr11:121448609-121448610	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs373557455	chr11:121448645-121448646	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs561713390	chr11:121448673-121448674	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs140768706	chr11:121448686-121448687	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs376241223	chr11:121448691-121448692	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs185400070	chr11:121448734-121448735	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs112281549	chr11:121448794-121448795	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs532774202	chr11:121448842-121448843	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs551079774	chr11:121448855-121448856	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs144844302	chr11:121448952-121448953	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs537321105	chr11:121448957-121448958	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs3781837	chr11:121448972-121448973	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs567775871	chr11:121449013-121449014	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs386758203	chr11:121449033-121449034	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs183420853	chr11:121449034-121449035	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs189218919	chr11:121449063-121449064	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs545462265	chr11:121449106-121449107	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs557077702	chr11:121449115-121449116	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs112498993	chr11:121449132-121449133	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs543337734	chr11:121449141-121449142	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs207472417	chr11:121449152-121449153	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs561983142	chr11:121449180-121449181	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs529076040	chr11:121449200-121449201	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs193107987	chr11:121449201-121449202	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs559062183	chr11:121449259-121449260	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs373316754	chr11:121449299-121449300	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565564666	chr11:121449306-121449307	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Squamous cell cancer	20885788	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21385341	CNVD
Multiple myeloma	16461302	CNVD
Burkitt''s lymphoma	18698080	CNVD
Prostate cancer	23792589	CNVD
Effusion lymphoma	18079361	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1092 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121407200-121459000	Weak transcription	Colon Smooth Muscle	Colon
2	chr11:121414000-121452400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr11:121416400-121451800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr11:121416600-121471800	Strong transcription	Primary T cells from cord blood	blood
5	chr11:121417000-121452400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr11:121417600-121452400	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr11:121418000-121451800	Strong transcription	Primary T helper cells PMA-I stimulated	--
8	chr11:121425000-121456800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:121428200-121451400	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr11:121431000-121466400	Weak transcription	Ovary	ovary
11	chr11:121432800-121450000	Weak transcription	Aorta	Aorta
12	chr11:121434400-121451200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr11:121434600-121453200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:121434800-121451800	Strong transcription	Primary T helper naive cells from peripheral blood	blood
15	chr11:121435200-121464800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:121436200-121450400	Strong transcription	Duodenum Mucosa	Duodenum
17	chr11:121437600-121449600	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr11:121437800-121449600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr11:121437800-121450000	Strong transcription	H1 Cell Line	embryonic stem cell
20	chr11:121437800-121453600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr11:121438000-121448200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr11:121438000-121449000	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr11:121438200-121451200	Strong transcription	HepG2	liver
24	chr11:121438400-121453600	Weak transcription	Colonic Mucosa	Colon
25	chr11:121439000-121449200	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr11:121440600-121449800	Strong transcription	Dnd41	blood
27	chr11:121440600-121450400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
28	chr11:121440600-121450800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr11:121440600-121485000	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr11:121440800-121450200	Strong transcription	H9 Cell Line	embryonic stem cell
31	chr11:121440800-121450200	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr11:121440800-121452000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr11:121441400-121449800	Genic enhancers	Brain Hippocampus Middle	brain
34	chr11:121441400-121451400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
35	chr11:121442200-121456800	Weak transcription	Esophagus	oesophagus
36	chr11:121442600-121451000	Strong transcription	Stomach Smooth Muscle	stomach
37	chr11:121443000-121455000	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr11:121443200-121450200	Strong transcription	NHEK	skin
39	chr11:121443200-121452000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:121443400-121450000	Strong transcription	Primary T killer memory cells from peripheral blood	blood
41	chr11:121443400-121464600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:121443800-121450200	Enhancers	Fetal Brain Female	brain
43	chr11:121443800-121456800	Weak transcription	Lung	lung
44	chr11:121443800-121458600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:121443800-121461600	Weak transcription	Pancreas	Pancrea
46	chr11:121444400-121448600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:121444400-121450800	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:121444400-121452200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:121444800-121450000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr11:121445000-121448400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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