Variant report

Variant	esv3388509
Chromosome Location	chr11:46763105-46818814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:324)
CpG islands
(count:366)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:5)

(count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:46798485-46798816	A549	lung:	n/a	chr11:46798626-46798637 chr11:46798624-46798637
2	CEBPB	chr11:46798463-46798747	H1-hESC	embryonic stem cell:	n/a	chr11:46798626-46798637 chr11:46798624-46798637
3	CEBPB	chr11:46782031-46782373	HepG2	liver:	n/a	n/a
4	CEBPB	chr11:46781975-46782351	MCF-7	breast:	n/a	n/a
5	CEBPB	chr11:46771719-46772049	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:46798458-46798777	A549	lung:	n/a	chr11:46798626-46798637 chr11:46798624-46798637
7	CEBPB	chr11:46769511-46769609	HepG2	liver:	n/a	chr11:46769544-46769555
8	CEBPB	chr11:46782125-46782300	K562	blood:	n/a	n/a
9	CEBPB	chr11:46782090-46782099	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr11:46782029-46782342	A549	lung:	n/a	n/a
11	CEBPB	chr11:46798480-46798778	K562	blood:	n/a	chr11:46798626-46798637 chr11:46798624-46798637
12	CEBPB	chr11:46778630-46778790	IMR90	lung:	n/a	chr11:46778677-46778688
13	CEBPB	chr11:46798464-46798814	HepG2	liver:	n/a	chr11:46798626-46798637 chr11:46798624-46798637
14	CEBPB	chr11:46771686-46772054	MCF-7	breast:	n/a	n/a
15	CEBPB	chr11:46778620-46778714	HepG2	liver:	n/a	chr11:46778677-46778688
16	CEBPB	chr11:46771815-46771951	IMR90	lung:	n/a	n/a
17	CEBPB	chr11:46771753-46772011	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:46798460-46798816	IMR90	lung:	n/a	chr11:46798626-46798637 chr11:46798624-46798637
19	CEBPB	chr11:46798412-46798916	A549	lung:	n/a	chr11:46798626-46798637 chr11:46798624-46798637
20	CEBPB	chr11:46782033-46782344	IMR90	lung:	n/a	n/a
21	CHD2	chr11:46765662-46765819	HepG2	liver:	n/a	n/a
22	CTCF	chr11:46799920-46800070	MCF-7	breast:	n/a	n/a
23	CTCF	chr11:46778560-46778710	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr11:46773840-46773990	GM12865	blood:	n/a	n/a
25	CTCF	chr11:46816779-46816817	GM13976	blood:	n/a	n/a
26	CTCF	chr11:46803020-46803170	NHLF	lung:	n/a	n/a
27	CTCF	chr11:46774720-46774870	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr11:46765320-46765470	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr11:46815960-46816110	GM12865	blood:	n/a	n/a
30	CTCF	chr11:46789483-46789507	GM20000	blood:	n/a	n/a
31	CTCF	chr11:46808420-46808570	GM06990	blood:	n/a	n/a
32	E2F4	chr11:46773047-46773236	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr11:46813273-46813276	MCF10A-Er-Src	breast:	n/a	n/a
34	EP300	chr11:46777034-46777309	HepG2	liver:	n/a	n/a
35	FOS	chr11:46777092-46777179	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr11:46777107-46777121	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:46777071-46777295	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr11:46777075-46777355	MCF10A-Er-Src	breast:	n/a	n/a
39	FOSL1	chr11:46776983-46777349	HCT-116	colon:	n/a	n/a
40	FOSL1	chr11:46776898-46777365	HCT-116	colon:	n/a	n/a
41	FOSL2	chr11:46762721-46766216	HepG2	liver:	n/a	n/a
42	FOSL2	chr11:46766233-46767942	HepG2	liver:	n/a	n/a
43	FOSL2	chr11:46767944-46770007	HepG2	liver:	n/a	n/a
44	FOXA1	chr11:46782875-46783152	T-47D	breast:	n/a	n/a
45	FOXA1	chr11:46782939-46783134	T-47D	breast:	n/a	n/a
46	FOXA1	chr11:46800090-46800420	HepG2	liver:	n/a	n/a
47	FOXA1	chr11:46774672-46774967	T-47D	breast:	n/a	n/a
48	FOXA2	chr11:46800092-46800305	HepG2	liver:	n/a	n/a
49	FOXA2	chr11:46765246-46765545	HepG2	liver:	n/a	n/a
50	FOXA2	chr11:46776997-46777262	HepG2	liver:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46784275-46784325	HCPEpiC	choroid plexus:	n/a
2	chr11:46784427-46784477	NT2-D1	testis:	n/a
3	chr11:46784979-46785029	HEEpiC	esophagus:	n/a
4	chr11:46784427-46784477	SAEC	small airway:	n/a
5	chr11:46818454-46818504	LNCaP	prostate:	n/a
6	chr11:46784979-46785029	AG09309	skin:	n/a
7	chr11:46765391-46765441	MCF10A-Er-Src	breast:	n/a
8	chr11:46787299-46787349	GM12892	blood:	n/a
9	chr11:46784979-46785029	ECC-1	luminal epithelium:	n/a
10	chr11:46818454-46818504	NH-A	brain:	n/a
11	chr11:46818454-46818504	HRPEpiC	eye:	n/a
12	chr11:46787299-46787349	HCPEpiC	choroid plexus:	n/a
13	chr11:46787299-46787349	BJ	skin:	n/a
14	chr11:46818454-46818504	HPAEpiC	pulmonary alveolar:	n/a
15	chr11:46784427-46784477	HMEC	breast:	n/a
16	chr11:46784427-46784477	Jurkat	blood:	n/a
17	chr11:46787299-46787349	AG09309	skin:	n/a
18	chr11:46784275-46784325	K562	blood:	n/a
19	chr11:46784979-46785029	HCT-116	colon:	n/a
20	chr11:46784275-46784325	BJ	skin:	n/a
21	chr11:46818454-46818504	NB4	blood:	n/a
22	chr11:46784275-46784325	GM12892	blood:	n/a
23	chr11:46784427-46784477	GM12891	blood:	n/a
24	chr11:46784979-46785029	NH-A	brain:	n/a
25	chr11:46784979-46785029	HAEpiC	amniotic membrane:	n/a
26	chr11:46765391-46765441	AG04450	lung:	fetal
27	chr11:46818454-46818504	HCM	heart:	n/a
28	chr11:46765391-46765441	AG10803	skin:	n/a
29	chr11:46784427-46784477	GM19239	blood:	n/a
30	chr11:46818454-46818504	PANC-1	pancreas:	n/a
31	chr11:46787299-46787349	RPTEC	kidney:	n/a
32	chr11:46765391-46765441	HEEpiC	esophagus:	n/a
33	chr11:46818454-46818504	HAEpiC	amniotic membrane:	n/a
34	chr11:46818454-46818504	AG09319	gingival:	n/a
35	chr11:46784275-46784325	IMR90	lung:	fetal
36	chr11:46784275-46784325	MCF10A-Er-Src	breast:	n/a
37	chr11:46784275-46784325	SK-N-SH_RA	brain:	n/a
38	chr11:46784427-46784477	SK-N-SH	brain:	n/a
39	chr11:46784979-46785029	HRCEpiC	kidney:	n/a
40	chr11:46765391-46765441	Hepatocyte	liver:	n/a
41	chr11:46784427-46784477	Hepatocyte	liver:	n/a
42	chr11:46818454-46818504	ovcar-3	ovarian:	n/a
43	chr11:46784275-46784325	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:46818454-46818504	PrEC	prostate:	n/a
45	chr11:46818454-46818504	K562	blood:	n/a
46	chr11:46784427-46784477	AG09319	gingival:	n/a
47	chr11:46784979-46785029	AG04449	skin:	fetal
48	chr11:46765391-46765441	HEK293	kidney:	embryo
49	chr11:46784275-46784325	CMK	blood:	n/a
50	chr11:46784275-46784325	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:46775438..46777025-chr11:46785365..46787825,2	K562	blood:
2	chr11:46742083..46744335-chr11:46763243..46766196,2	K562	blood:
3	chr11:46785964..46788289-chr11:46809938..46811766,2	K562	blood:
4	chr11:46771022..46772971-chr11:46779196..46781590,2	MCF-7	breast:
5	chr11:46800078..46802503-chr11:47181465..47183295,2	MCF-7	breast:
6	chr11:46785236..46787820-chr11:46798096..46801052,2	MCF-7	breast:
7	chr11:46777860..46782157-chr11:46783052..46787711,4	K562	blood:
8	chr11:46812144..46815531-chr11:46816972..46819757,4	K562	blood:
9	chr11:46760225..46762619-chr11:46766210..46768757,2	MCF-7	breast:
10	chr11:46798348..46800815-chr11:46802877..46805320,2	MCF-7	breast:
11	chr11:46769655..46771244-chr11:46773585..46775802,2	K562	blood:
12	chr11:46798348..46800815-chr11:46802877..46805320,2	MCF-7	breast:
13	chr11:46802857..46804523-chr11:46805186..46807970,2	K562	blood:
14	chr11:46787403..46789216-chr11:46830914..46832486,2	K562	blood:
15	chr11:46812144..46813760-chr11:46816972..46819757,2	K562	blood:
16	chr11:46719204..46720865-chr11:46763113..46765630,2	K562	blood:
17	chr11:46785236..46787820-chr11:46798096..46801052,2	MCF-7	breast:
18	chr11:46771294..46774103-chr11:46776539..46778054,2	MCF-7	breast:
19	chr11:46709487..46711426-chr11:46765477..46767414,2	K562	blood:
20	chr11:46763360..46766169-chr11:46766734..46769498,4	K562	blood:
21	chr11:46785313..46788117-chr11:46804478..46806472,2	MCF-7	breast:
22	chr11:46761363..46764873-chr11:46765216..46768275,3	K562	blood:
23	chr11:46774947..46777617-chr11:46782047..46783769,2	K562	blood:
24	chr11:46777860..46782157-chr11:46783052..46787711,4	K562	blood:
25	chr11:46753339..46754886-chr11:46762231..46764899,2	K562	blood:
26	chr11:46785964..46788289-chr11:46809938..46811766,2	K562	blood:
27	chr11:46761363..46764873-chr11:46765216..46768275,3	K562	blood:
28	chr11:46756420..46758070-chr11:46763484..46765200,2	MCF-7	breast:
29	chr11:46815521..46817270-chr11:46825873..46827721,2	K562	blood:
30	chr11:46812144..46813760-chr11:46816972..46819757,2	K562	blood:
31	chr11:46763360..46766169-chr11:46766734..46769498,4	K562	blood:
32	chr11:46776239..46779172-chr11:46803736..46805304,2	K562	blood:
33	chr11:46776239..46779172-chr11:46803736..46805304,2	K562	blood:
34	chr11:46812144..46815531-chr11:46816972..46819757,4	K562	blood:
35	chr11:46800295..46801836-chr11:46805253..46808228,2	MCF-7	breast:
36	chr11:46771022..46772971-chr11:46779196..46781590,2	MCF-7	breast:
37	chr11:46775438..46777025-chr11:46785365..46787825,2	K562	blood:
38	chr11:46774351..46777025-chr11:46785365..46788115,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5582-3p	chr11:46774675-46774696	MIMAT0022280
hsa-miR-5582-5p	chr11:46774721-46774742	MIMAT0022279

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CKAP5	hsa-miR-15b-5p	chr11:46765380-46765401
2	CKAP5	hsa-miR-130b-3p	chr11:46765096-46765123
3	CKAP5	hsa-miR-34a-5p	chr11:46765328-46765348
4	CKAP5	hsa-miR-16-5p	chr11:46765380-46765401
5	CKAP5	hsa-miR-155-5p	chr11:46765095-46765116

Variant related genes	Relation type
CKAP5	TF binding region
ENSG00000252427	TF binding region
SNORD67	TF binding region
MIR5582	TF binding region
CKAP5	CpG island
ENSG00000252427	CpG island
SNORD67	CpG island
MIR5582	CpG island
ENSG00000212135	chromatin interactions
ENSG00000263540	chromatin interactions
ENSG00000175216	chromatin interactions
ENSG00000252427	chromatin interactions

Extended variants
information (count: 1952 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1952 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553711758	chr11:46763146-46763147	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs139142219	chr11:46763149-46763150	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs541031482	chr11:46763150-46763151	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs563881255	chr11:46763173-46763174	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs533271402	chr11:46763180-46763181	Strong transcription Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs543335527	chr11:46763204-46763205	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76572787	chr11:46763238-46763239	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149969717	chr11:46763242-46763243	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73454083	chr11:46763276-46763277	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs565834871	chr11:46763293-46763294	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559893368	chr11:46763309-46763310	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140308445	chr11:46763331-46763332	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs534344711	chr11:46763345-46763346	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs111576392	chr11:46763440-46763441	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111615841	chr11:46763460-46763461	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189478125	chr11:46763462-46763463	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550973231	chr11:46763502-46763503	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181861894	chr11:46763505-46763506	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567570644	chr11:46763577-46763578	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376057565	chr11:46763579-46763580	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372752226	chr11:46763610-46763611	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10528775	chr11:46763611-46763612	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539203995	chr11:46763612-46763613	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536438283	chr11:46763622-46763623	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs57884747	chr11:46763623-46763624	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs398015956	chr11:46763624-46763625	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192186135	chr11:46763626-46763627	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185973622	chr11:46763638-46763639	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557295642	chr11:46763670-46763671	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553111112	chr11:46763679-46763680	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571812993	chr11:46763697-46763698	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534385315	chr11:46763732-46763733	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs577338664	chr11:46763745-46763746	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557768214	chr11:46763752-46763753	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144167822	chr11:46763772-46763773	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs543746039	chr11:46763779-46763780	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543066852	chr11:46763817-46763818	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563562788	chr11:46763833-46763834	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557280430	chr11:46763869-46763870	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184551893	chr11:46763907-46763908	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189375554	chr11:46763908-46763909	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191516438	chr11:46763925-46763926	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183538827	chr11:46763927-46763928	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559560094	chr11:46763930-46763931	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs373983931	chr11:46763951-46763952	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs66461112	chr11:46763984-46763985	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146612130	chr11:46763986-46763987	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369655074	chr11:46763988-46763989	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4388840	chr11:46764005-46764006	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551571265	chr11:46764007-46764008	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1313 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46749800-46764000	Weak transcription	Aorta	Aorta
2	chr11:46752000-46763400	Weak transcription	Esophagus	oesophagus
3	chr11:46753000-46786600	Weak transcription	Right Atrium	heart
4	chr11:46758200-46763200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr11:46758400-46763400	Strong transcription	HepG2	liver
6	chr11:46759000-46763200	Weak transcription	NHLF	lung
7	chr11:46759000-46768000	Strong transcription	Liver	Liver
8	chr11:46759400-46763200	Weak transcription	NHEK	skin
9	chr11:46760200-46763400	Weak transcription	Brain Anterior Caudate	brain
10	chr11:46760200-46763400	Weak transcription	Fetal Brain Male	brain
11	chr11:46760200-46764600	Weak transcription	Psoas Muscle	Psoas
12	chr11:46760200-46786800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr11:46760200-46794800	Strong transcription	A549	lung
14	chr11:46760400-46764600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:46760400-46765600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr11:46760400-46777400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:46760400-46781400	Weak transcription	Stomach Mucosa	stomach
18	chr11:46760400-46795600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:46760600-46763200	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr11:46760600-46785800	Strong transcription	Fetal Stomach	stomach
21	chr11:46760600-46793800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr11:46760800-46763200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr11:46760800-46763200	Weak transcription	Ovary	ovary
24	chr11:46760800-46763200	Weak transcription	Right Ventricle	heart
25	chr11:46760800-46764200	Weak transcription	Colonic Mucosa	Colon
26	chr11:46760800-46765800	Weak transcription	Fetal Heart	heart
27	chr11:46761000-46763200	Weak transcription	Primary B cells from peripheral blood	blood
28	chr11:46761000-46766200	Strong transcription	Fetal Intestine Small	intestine
29	chr11:46761200-46763400	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr11:46761200-46763400	Weak transcription	NH-A	brain
31	chr11:46761200-46772400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr11:46761200-46787000	Strong transcription	Fetal Muscle Trunk	muscle
33	chr11:46761200-46787600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:46761400-46763200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:46761400-46764400	Weak transcription	Colon Smooth Muscle	Colon
36	chr11:46761400-46786600	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr11:46761400-46795800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:46761400-46840000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:46761400-46845200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr11:46761600-46763200	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr11:46761600-46764000	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr11:46761600-46776200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:46761600-46787000	Strong transcription	Fetal Intestine Large	intestine
44	chr11:46761600-46824600	Strong transcription	Fetal Thymus	thymus
45	chr11:46761800-46763400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr11:46761800-46765400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr11:46761800-46766200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:46762000-46763600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr11:46762000-46765000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr11:46762000-46765400	Weak transcription	Fetal Kidney	kidney

The 2.0 version of rSNPBase

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