Variant report

Variant	nsv832079
Chromosome Location	chr11:17927967-18047743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2413)
CpG islands
(count:1589)
Chromatin interactive
region (count:110)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2413 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18001373-18001689	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:18034536-18035062	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:18013367-18013709	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:18017674-18017711	K562	blood:	n/a	n/a
5	ARID3A	chr11:18008127-18009064	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:18022189-18022780	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:17955322-17956057	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:18038365-18038633	K562	blood:	n/a	n/a
9	ATF1	chr11:17943616-17943908	K562	blood:	n/a	n/a
10	ATF2	chr11:18034384-18035237	GM12878	blood:	n/a	n/a
11	BACH1	chr11:17974425-17974426	K562	blood:	n/a	n/a
12	BACH1	chr11:17942849-17942895	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:17943518-17943811	K562	blood:	n/a	n/a
14	BACH1	chr11:18034402-18035041	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCLAF1	chr11:18034335-18035247	GM12878	blood:	n/a	chr11:18034593-18034606 chr11:18034600-18034613 chr11:18034598-18034607 chr11:18034815-18034828 chr11:18034791-18034804
16	BCLAF1	chr11:18034310-18035318	GM12878	blood:	n/a	chr11:18034593-18034606 chr11:18034600-18034613 chr11:18034598-18034607 chr11:18034815-18034828 chr11:18034791-18034804
17	BHLHE40	chr11:18034402-18035008	K562	blood:	n/a	chr11:18034597-18034613 chr11:18034468-18034484 chr11:18034427-18034443
18	BHLHE40	chr11:18033341-18034043	K562	blood:	n/a	n/a
19	BHLHE40	chr11:18022314-18022673	HepG2	liver:	n/a	n/a
20	BHLHE40	chr11:18001343-18001643	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:18034452-18035194	HepG2	liver:	n/a	chr11:18034597-18034613 chr11:18035168-18035184 chr11:18034468-18034484
22	BHLHE40	chr11:18032561-18032935	K562	blood:	n/a	n/a
23	BHLHE40	chr11:18034369-18035221	GM12878	blood:	n/a	chr11:18034597-18034613 chr11:18035168-18035184 chr11:18034468-18034484 chr11:18034427-18034443
24	BHLHE40	chr11:18038361-18038654	K562	blood:	n/a	n/a
25	BRCA1	chr11:18035249-18035449	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr11:17939960-17940160	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr11:18034478-18034552	HepG2	liver:	n/a	n/a
28	BRCA1	chr11:18034643-18034854	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr11:18030248-18030257	GM12878	blood:	n/a	n/a
30	BRCA1	chr11:17927752-17928284	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr11:18033259-18034075	K562	blood:	n/a	n/a
32	CBX3	chr11:18034325-18035026	K562	blood:	n/a	n/a
33	CCNT2	chr11:18033938-18035241	K562	blood:	n/a	n/a
34	CEBPB	chr11:18029083-18029287	HepG2	liver:	n/a	chr11:18029221-18029232
35	CEBPB	chr11:17954110-17954310	HepG2	liver:	n/a	chr11:17954212-17954223
36	CEBPB	chr11:18019456-18019539	HepG2	liver:	n/a	chr11:18019507-18019518 chr11:18019466-18019477
37	CEBPB	chr11:18036992-18037258	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:17969669-17969895	A549	lung:	n/a	chr11:17969791-17969802
39	CEBPB	chr11:18008243-18008825	HepG2	liver:	n/a	chr11:18008644-18008655
40	CEBPB	chr11:17928047-17928099	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr11:18027260-18027609	H1-hESC	embryonic stem cell:	n/a	chr11:18027442-18027453
42	CEBPB	chr11:18034874-18035074	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr11:18019369-18019659	K562	blood:	n/a	chr11:18019507-18019518 chr11:18019466-18019477
44	CEBPB	chr11:18027275-18027776	IMR90	lung:	n/a	chr11:18027442-18027453
45	CEBPB	chr11:18008282-18008494	HepG2	liver:	n/a	n/a
46	CEBPB	chr11:18027391-18027543	A549	lung:	n/a	chr11:18027442-18027453
47	CEBPB	chr11:18032902-18032961	K562	blood:	n/a	n/a
48	CEBPB	chr11:18037040-18037193	A549	lung:	n/a	n/a
49	CEBPB	chr11:18027304-18027609	Hela-S3	cervix:	n/a	chr11:18027442-18027453
50	CEBPB	chr11:17999086-17999242	A549	lung:	n/a	n/a

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18034920-18034970	Jurkat	blood:	n/a
2	chr11:18033296-18033346	HCT-116	colon:	n/a
3	chr11:18042499-18042549	HRPEpiC	eye:	n/a
4	chr11:18034920-18034970	Jurkat	blood:	n/a
5	chr11:18033296-18033346	HCT-116	colon:	n/a
6	chr11:18042499-18042549	HRPEpiC	eye:	n/a
7	chr11:18035267-18035317	AG10803	skin:	n/a
8	chr11:18035852-18035902	SKMC	muscle:	n/a
9	chr11:18034693-18034743	PrEC	prostate:	n/a
10	chr11:18035350-18035400	LNCaP	prostate:	n/a
11	chr11:18034355-18034405	Hepatocyte	liver:	n/a
12	chr11:18034688-18034738	HIPEpiC	eye:	n/a
13	chr11:18034024-18034074	HAEpiC	amniotic membrane:	n/a
14	chr11:18034662-18034712	GM12891	blood:	n/a
15	chr11:17973565-17973615	NB4	blood:	n/a
16	chr11:17973565-17973615	NHBE	bronchial:	n/a
17	chr11:17948881-17948931	HRE	kidney:	n/a
18	chr11:17928213-17928263	HCM	heart:	n/a
19	chr11:18034024-18034074	MCF-7	breast:	n/a
20	chr11:18034662-18034712	BE2_C	brain:	n/a
21	chr11:17994507-17994557	AG09309	skin:	n/a
22	chr11:18042499-18042549	HCM	heart:	n/a
23	chr11:17994507-17994557	HepG2	liver:	n/a
24	chr11:17948881-17948931	RPTEC	kidney:	n/a
25	chr11:18034757-18034807	PrEC	prostate:	n/a
26	chr11:18034693-18034743	U87	brain:	n/a
27	chr11:18034693-18034743	SK-N-SH	brain:	n/a
28	chr11:18008039-18008089	PrEC	prostate:	n/a
29	chr11:18034355-18034405	GM12892	blood:	n/a
30	chr11:17944560-17944610	HNPCEpiC	eye:	n/a
31	chr11:18038904-18038954	LNCaP	prostate:	n/a
32	chr11:17952483-17952533	MCF10A-Er-Src	breast:	n/a
33	chr11:18034662-18034712	CMK	blood:	n/a
34	chr11:17952483-17952533	HEEpiC	esophagus:	n/a
35	chr11:18031127-18031177	Caco-2	colon:	n/a
36	chr11:18034626-18034676	AG04450	lung:	fetal
37	chr11:18034664-18034714	NT2-D1	testis:	n/a
38	chr11:18034024-18034074	NH-A	brain:	n/a
39	chr11:18035350-18035400	CMK	blood:	n/a
40	chr11:17973565-17973615	BE2_C	brain:	n/a
41	chr11:18035136-18035186	HUVEC	blood vessel:	n/a
42	chr11:18034688-18034738	RPTEC	kidney:	n/a
43	chr11:17939679-17939729	AG09319	gingival:	n/a
44	chr11:18034664-18034714	GM12891	blood:	n/a
45	chr11:17994507-17994557	AG04450	lung:	fetal
46	chr11:18034920-18034970	BJ	skin:	n/a
47	chr11:18035267-18035317	PrEC	prostate:	n/a
48	chr11:18034626-18034676	Hepatocyte	liver:	n/a
49	chr11:18034662-18034712	BJ	skin:	n/a
50	chr11:17994507-17994557	HRCEpiC	kidney:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:18013361..18015172-chr11:18032256..18034056,2	K562	blood:
2	chr11:17752292..17753246-chr11:17999986..18000903,4	K562	blood:
3	chr11:17781836..17782575-chr11:17999957..18000865,3	MCF-7	breast:
4	chr11:17783547..17784473-chr11:18000133..18001470,5	MCF-7	breast:
5	chr11:17986603..17989181-chr11:17992411..17994723,3	MCF-7	breast:
6	chr10:123687232..123687760-chr11:18034020..18034616,2	HCT-116	colon:
7	chr11:17426991..17427860-chr11:17946039..17946557,2	MCF-7	breast:
8	chr11:18024725..18026485-chr11:18033759..18035414,2	MCF-7	breast:
9	chr11:17788319..17789007-chr11:17994351..17995171,2	MCF-7	breast:
10	chr11:17228155..17229875-chr11:18033843..18035455,2	K562	blood:
11	chr11:17987462..17990448-chr11:17991474..17994357,2	K562	blood:
12	chr11:18000487..18002989-chr11:18006898..18009156,2	MCF-7	breast:
13	chr11:17941038..17943989-chr11:17944479..17947250,2	MCF-7	breast:
14	chr11:18013613..18016047-chr11:18016241..18018614,3	K562	blood:
15	chr11:18023740..18027348-chr11:18028955..18031128,4	K562	blood:
16	chr11:18033935..18034483-chr6:41748410..41748911,2	HCT-116	colon:
17	chr11:17781862..17782597-chr11:17994721..17995346,2	K562	blood:
18	chr11:18034152..18035903-chr11:18125561..18127722,2	MCF-7	breast:
19	chr11:18007709..18010705-chr11:18020081..18022716,2	MCF-7	breast:
20	chr11:17781675..17782374-chr11:17994338..17995285,3	MCF-7	breast:
21	chr11:17990720..17992274-chr11:17994760..17996286,2	K562	blood:
22	chr11:17752483..17753383-chr11:17994354..17995164,3	MCF-7	breast:
23	chr11:18034385..18036192-chr11:18040931..18043541,2	MCF-7	breast:
24	chr11:17935767..17938091-chr11:17939422..17941128,2	MCF-7	breast:
25	chr11:17620278..17621149-chr11:18000256..18000759,2	MCF-7	breast:
26	chr11:18025939..18028718-chr11:18036280..18038941,2	K562	blood:
27	chr11:17752325..17753223-chr11:18001001..18001982,6	K562	blood:
28	chr11:18013361..18015172-chr11:18032256..18034056,2	K562	blood:
29	chr11:17427284..17427815-chr11:17946414..17946944,2	MCF-7	breast:
30	chr11:17942173..17945463-chr11:17948339..17951076,3	MCF-7	breast:
31	chr11:18034918..18037858-chr11:18041029..18043888,2	K562	blood:
32	chr11:17944503..17947787-chr11:17948470..17951111,3	K562	blood:
33	chr11:18007256..18009129-chr11:18025177..18027765,2	MCF-7	breast:
34	chr11:17999269..18002828-chr11:18002925..18007406,4	K562	blood:
35	chr11:18013093..18014057-chr11:18027034..18027551,2	MCF-7	breast:
36	chr11:18033238..18034907-chr11:18042629..18045446,2	MCF-7	breast:
37	chr11:17987462..17990448-chr11:17991474..17994357,2	K562	blood:
38	chr11:18029427..18031734-chr11:18032905..18035754,2	MCF-7	breast:
39	chr11:18013193..18013909-chr11:18166278..18166794,2	MCF-7	breast:
40	chr11:18013093..18014057-chr11:18027034..18027551,2	MCF-7	breast:
41	chr11:18033853..18039770-chr11:18040771..18045725,5	K562	blood:
42	chr11:17751795..17753232-chr11:17999934..18001786,19	MCF-7	breast:
43	chr11:17986603..17989181-chr11:17992411..17994723,3	MCF-7	breast:
44	chr11:18033853..18039770-chr11:18040771..18045725,5	K562	blood:
45	chr11:18033238..18034907-chr11:18042629..18045446,2	MCF-7	breast:
46	chr11:17977063..17978660-chr11:17979586..17982551,2	K562	blood:
47	chr11:17751864..17753212-chr11:17999973..18001949,7	MCF-7	breast:
48	chr11:17942744..17945115-chr11:17945670..17947778,2	K562	blood:
49	chr11:17868099..17868883-chr11:17927786..17928302,2	MCF-7	breast:
50	chr11:17752064..17753282-chr11:17994336..17995305,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERGEF-1	chr11:17961024-17961179	NONHSAT018249

No data

Variant related genes	Relation type
SERGEF	TF binding region
TPH1	TF binding region
ENSG00000255448	TF binding region
SERGEF	CpG island
TPH1	CpG island
ENSG00000255448	CpG island
ENSG00000166787	chromatin interactions
ENSG00000151116	chromatin interactions
ENSG00000166788	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000011405	chromatin interactions
ENSG00000107669	chromatin interactions
ENSG00000129158	chromatin interactions
ENSG00000129159	chromatin interactions
ENSG00000129167	chromatin interactions
ENSG00000124593	chromatin interactions
ENSG00000070081	chromatin interactions
ENSG00000255448	chromatin interactions

Extended variants
information (count: 3829 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3829 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549142763	chr11:17928066-17928067	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs12577747	chr11:17928069-17928070	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528745583	chr11:17928070-17928071	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547281934	chr11:17928105-17928106	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571505360	chr11:17928131-17928132	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140148738	chr11:17928213-17928214	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs551037625	chr11:17928285-17928286	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569516019	chr11:17928339-17928340	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35732861	chr11:17928348-17928349	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75994019	chr11:17928370-17928371	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375079027	chr11:17928373-17928374	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs56102467	chr11:17928389-17928390	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113715185	chr11:17928398-17928399	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs536775135	chr11:17928454-17928455	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185944601	chr11:17928522-17928523	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554780208	chr11:17928524-17928525	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573001403	chr11:17928562-17928563	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs36033475	chr11:17928571-17928572	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533796809	chr11:17928597-17928598	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192034338	chr11:17928598-17928599	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs475737	chr11:17928617-17928618	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144032406	chr11:17928627-17928628	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12281092	chr11:17928708-17928709	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374395976	chr11:17928710-17928711	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs200442630	chr11:17928711-17928712	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577102206	chr11:17928801-17928802	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543789578	chr11:17928879-17928880	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73426284	chr11:17928906-17928907	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs73426285	chr11:17928931-17928932	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs140698506	chr11:17928934-17928935	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150076625	chr11:17929010-17929011	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182197265	chr11:17929029-17929030	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs34549618	chr11:17929048-17929049	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78983017	chr11:17929093-17929094	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567186733	chr11:17929108-17929109	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186785337	chr11:17929123-17929124	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557119194	chr11:17929128-17929129	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532882831	chr11:17929277-17929278	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555252537	chr11:17929320-17929321	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550976424	chr11:17929323-17929324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190591377	chr11:17929327-17929328	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536700763	chr11:17929330-17929331	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548675756	chr11:17929335-17929336	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567018639	chr11:17929368-17929369	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76528741	chr11:17929393-17929394	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533990346	chr11:17929460-17929461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145461654	chr11:17929483-17929484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371743851	chr11:17929540-17929541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576711986	chr11:17929571-17929572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537765491	chr11:17929584-17929585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD

Chromatin state (count:2701 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17838400-17971600	Weak transcription	Gastric	stomach
2	chr11:17863800-17939200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr11:17864400-17944800	Weak transcription	Ovary	ovary
4	chr11:17882800-17943800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr11:17885800-17939200	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr11:17886000-17965200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr11:17895200-17939000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:17895800-17937200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:17895800-17943400	Weak transcription	Pancreas	Pancrea
10	chr11:17896000-17944600	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr11:17896000-17968000	Weak transcription	Duodenum Mucosa	Duodenum
12	chr11:17896400-17939200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr11:17896400-17968000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr11:17896800-17939200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr11:17897400-17939400	Weak transcription	Adipose Nuclei	Adipose
16	chr11:17897600-17928400	Weak transcription	Primary B cells from cord blood	blood
17	chr11:17898800-17944200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr11:17899000-17930600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr11:17899200-17943400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr11:17906000-17970200	Weak transcription	Lung	lung
21	chr11:17910600-17947000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr11:17913400-17928400	Weak transcription	Fetal Brain Male	brain
23	chr11:17914400-17938800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr11:17914400-17939200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr11:17914600-17965400	Weak transcription	Primary hematopoietic stem cells	blood
26	chr11:17914800-17928400	Weak transcription	Primary B cells from peripheral blood	blood
27	chr11:17914800-17934600	Weak transcription	Aorta	Aorta
28	chr11:17914800-17939000	Weak transcription	Dnd41	blood
29	chr11:17914800-17939200	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:17915400-17943000	Weak transcription	Spleen	Spleen
31	chr11:17915600-17939400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr11:17915800-17966000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr11:17917000-17943200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr11:17917000-17944600	Weak transcription	Brain Angular Gyrus	brain
35	chr11:17917000-17947600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr11:17917200-17938800	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr11:17920600-17976000	Weak transcription	Esophagus	oesophagus
38	chr11:17923600-17939600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:17924200-17937200	Weak transcription	Psoas Muscle	Psoas
40	chr11:17925600-17932000	Weak transcription	HepG2	liver
41	chr11:17927000-17928000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:17927000-17928000	Enhancers	Brain Hippocampus Middle	brain
43	chr11:17927000-17928400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr11:17927000-17929200	Enhancers	GM12878-XiMat	blood
45	chr11:17927000-17939200	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr11:17927200-17929200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr11:17927400-17928200	Enhancers	Right Atrium	heart
48	chr11:17927400-17928400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr11:17927400-17928600	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr11:17927400-17928600	Enhancers	Thymus	Thymus

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