Variant report

Variant	nsv1040065
Chromosome Location	chr11:17556031-17753467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2489)
CpG islands
(count:3670)
Chromatin interactive
region (count:114)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2489 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17671968-17672201	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:17752734-17752850	HepG2	liver:	n/a	n/a
3	ATF1	chr11:17738453-17738597	K562	blood:	n/a	n/a
4	ATF1	chr11:17628235-17628622	K562	blood:	n/a	n/a
5	ATF1	chr11:17572084-17572296	K562	blood:	n/a	n/a
6	ATF2	chr11:17620484-17620848	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr11:17725592-17725911	GM12878	blood:	n/a	n/a
8	ATF3	chr11:17628163-17628526	K562	blood:	n/a	n/a
9	ATF3	chr11:17721100-17721405	K562	blood:	n/a	n/a
10	ATF3	chr11:17725652-17725838	K562	blood:	n/a	n/a
11	BACH1	chr11:17717654-17717769	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr11:17735827-17736024	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr11:17743740-17743870	K562	blood:	n/a	n/a
14	BACH1	chr11:17740034-17740383	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr11:17566012-17566149	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr11:17743545-17743911	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:17620619-17620801	K562	blood:	n/a	n/a
18	BACH1	chr11:17741849-17741864	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr11:17705029-17705295	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:17752607-17752898	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:17721100-17721426	K562	blood:	n/a	chr11:17721107-17721123
22	BHLHE40	chr11:17620615-17620804	K562	blood:	n/a	n/a
23	BHLHE40	chr11:17656958-17657152	K562	blood:	n/a	chr11:17657012-17657025 chr11:17657008-17657029
24	BHLHE40	chr11:17620457-17620819	GM12878	blood:	n/a	n/a
25	BHLHE40	chr11:17597341-17597624	K562	blood:	n/a	chr11:17597468-17597477
26	BHLHE40	chr11:17597349-17597729	HepG2	liver:	n/a	chr11:17597468-17597477
27	BRCA1	chr11:17620579-17620779	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr11:17752729-17752836	HepG2	liver:	n/a	n/a
29	BRCA1	chr11:17741781-17741867	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr11:17705053-17705514	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr11:17752601-17752887	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr11:17752773-17752833	GM12878	blood:	n/a	n/a
33	CBX3	chr11:17721090-17721463	K562	blood:	n/a	n/a
34	CCNT2	chr11:17593825-17594070	K562	blood:	n/a	n/a
35	CCNT2	chr11:17738413-17738634	K562	blood:	n/a	n/a
36	CEBPB	chr11:17741695-17741950	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:17641102-17641317	K562	blood:	n/a	chr11:17641178-17641189
38	CEBPB	chr11:17603008-17603337	HepG2	liver:	n/a	chr11:17603166-17603177
39	CEBPB	chr11:17628173-17628529	K562	blood:	n/a	chr11:17628357-17628368
40	CEBPB	chr11:17666681-17666736	HepG2	liver:	n/a	chr11:17666696-17666707 chr11:17666694-17666707 chr11:17666694-17666707 chr11:17666694-17666705
41	CEBPB	chr11:17752652-17752914	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr11:17680490-17680658	H1-hESC	embryonic stem cell:	n/a	chr11:17680586-17680597
43	CEBPB	chr11:17602986-17603307	H1-hESC	embryonic stem cell:	n/a	chr11:17603166-17603177
44	CEBPB	chr11:17602990-17603355	IMR90	lung:	n/a	chr11:17603166-17603177
45	CEBPB	chr11:17588780-17589028	HepG2	liver:	n/a	chr11:17588880-17588889 chr11:17588878-17588889
46	CEBPB	chr11:17568597-17569010	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr11:17680479-17680725	HepG2	liver:	n/a	chr11:17680586-17680597
48	CEBPB	chr11:17641053-17641205	A549	lung:	n/a	chr11:17641178-17641189
49	CEBPB	chr11:17725586-17725830	K562	blood:	n/a	n/a
50	CEBPB	chr11:17752607-17752941	Hela-S3	cervix:	n/a	n/a

(count:3670 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17566591-17566641	NB4	blood:	n/a
2	chr11:17738031-17738081	HMEC	breast:	n/a
3	chr11:17717629-17717679	RPTEC	kidney:	n/a
4	chr11:17717280-17717330	LNCaP	prostate:	n/a
5	chr11:17591822-17591872	HCPEpiC	choroid plexus:	n/a
6	chr11:17741243-17741293	Jurkat	blood:	n/a
7	chr11:17564696-17564746	LNCaP	prostate:	n/a
8	chr11:17713884-17713934	NHBE	bronchial:	n/a
9	chr11:17742502-17742552	AoSMC	blood vessel:	n/a
10	chr11:17566163-17566213	Jurkat	blood:	n/a
11	chr11:17566591-17566641	NB4	blood:	n/a
12	chr11:17738031-17738081	HMEC	breast:	n/a
13	chr11:17717629-17717679	RPTEC	kidney:	n/a
14	chr11:17717280-17717330	LNCaP	prostate:	n/a
15	chr11:17591822-17591872	HCPEpiC	choroid plexus:	n/a
16	chr11:17741243-17741293	Jurkat	blood:	n/a
17	chr11:17564696-17564746	LNCaP	prostate:	n/a
18	chr11:17713884-17713934	NHBE	bronchial:	n/a
19	chr11:17742502-17742552	AoSMC	blood vessel:	n/a
20	chr11:17566163-17566213	Jurkat	blood:	n/a
21	chr11:17738031-17738081	BJ	skin:	n/a
22	chr11:17743667-17743717	HL-60	blood:	n/a
23	chr11:17741243-17741293	HRPEpiC	eye:	n/a
24	chr11:17742502-17742552	T-47D	breast:	n/a
25	chr11:17599691-17599741	HNPCEpiC	eye:	n/a
26	chr11:17743080-17743130	HPAEpiC	pulmonary alveolar:	n/a
27	chr11:17566591-17566641	GM19239	blood:	n/a
28	chr11:17745835-17745885	NT2-D1	testis:	n/a
29	chr11:17740430-17740480	H1-hESC	embryonic stem cell:	embryo
30	chr11:17745835-17745885	PrEC	prostate:	n/a
31	chr11:17599715-17599765	AG09309	skin:	n/a
32	chr11:17566591-17566641	HCM	heart:	n/a
33	chr11:17747289-17747339	GM06990	blood:	n/a
34	chr11:17720071-17720121	HUVEC	blood vessel:	n/a
35	chr11:17565769-17565819	PFSK-1	brain:	n/a
36	chr11:17743610-17743660	ovcar-3	ovarian:	n/a
37	chr11:17720071-17720121	HAEpiC	amniotic membrane:	n/a
38	chr11:17717818-17717868	SKMC	muscle:	n/a
39	chr11:17713884-17713934	HIPEpiC	eye:	n/a
40	chr11:17740967-17741017	LNCaP	prostate:	n/a
41	chr11:17741070-17741120	NH-A	brain:	n/a
42	chr11:17565744-17565794	HIPEpiC	eye:	n/a
43	chr11:17713884-17713934	MCF-7	breast:	n/a
44	chr11:17602053-17602103	HEK293	kidney:	embryo
45	chr11:17565878-17565928	GM06990	blood:	n/a
46	chr11:17566048-17566098	Hepatocyte	liver:	n/a
47	chr11:17598735-17598785	U87	brain:	n/a
48	chr11:17565878-17565928	RPTEC	kidney:	n/a
49	chr11:17598735-17598785	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:17740430-17740480	MCF-7	breast:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:17598332..17600155-chr11:17601959..17604145,2	MCF-7	breast:
2	chr11:17579575..17581891-chr11:17582600..17585148,3	K562	blood:
3	chr11:17620215..17621250-chr11:17751773..17752935,12	MCF-7	breast:
4	chr11:17652276..17654406-chr11:17655549..17657899,2	K562	blood:
5	chr11:17564338..17566127-chr11:17572702..17576571,3	K562	blood:
6	chr11:17573988..17575798-chr11:17578729..17580759,2	K562	blood:
7	chr11:17619891..17621109-chr11:17743288..17744431,5	MCF-7	breast:
8	chr11:17661202..17663655-chr11:17664754..17666769,2	MCF-7	breast:
9	chr11:17652276..17654406-chr11:17655549..17657899,2	K562	blood:
10	chr11:17658918..17660836-chr11:17665440..17668031,2	MCF-7	breast:
11	chr11:17405649..17406157-chr11:17617828..17618472,2	MCF-7	breast:
12	chr11:17567943..17569861-chr11:17577683..17579553,2	K562	blood:
13	chr11:17628448..17630427-chr11:17632737..17634648,2	MCF-7	breast:
14	chr11:17710093..17712652-chr11:17715299..17717332,2	K562	blood:
15	chr11:17622327..17624526-chr11:17631868..17633701,2	K562	blood:
16	chr11:17520408..17522288-chr11:17583277..17586222,2	K562	blood:
17	chr11:17751795..17753232-chr11:17999934..18001786,19	MCF-7	breast:
18	chr11:17620217..17621179-chr11:17742829..17744247,6	MCF-7	breast:
19	chr11:17752308..17752866-chr11:17774705..17775593,2	MCF-7	breast:
20	chr11:17620453..17621194-chr11:17656903..17657523,2	K562	blood:
21	chr11:17710440..17715421-chr11:17715832..17719362,5	K562	blood:
22	chr11:17554291..17557125-chr11:17558715..17560348,2	MCF-7	breast:
23	chr11:17752308..17753219-chr11:18785582..18786221,2	K562	blood:
24	chr11:17573695..17575515-chr11:17575864..17578594,2	K562	blood:
25	chr11:17622678..17623570-chr11:17743313..17743816,2	MCF-7	breast:
26	chr11:17597969..17599564-chr11:17601245..17604128,2	K562	blood:
27	chr11:17594662..17597692-chr11:17599938..17601708,3	K562	blood:
28	chr11:17622618..17623441-chr11:17752027..17752742,2	K562	blood:
29	chr11:17726249..17728928-chr11:17732573..17735083,2	MCF-7	breast:
30	chr11:17674426..17676272-chr11:17704010..17706690,2	K562	blood:
31	chr11:17701946..17705746-chr11:17707792..17711044,3	K562	blood:
32	chr11:17595636..17597692-chr11:17599938..17601981,3	K562	blood:
33	chr11:17622618..17623441-chr11:17752027..17752742,2	K562	blood:
34	chr11:17735220..17735764-chr11:17743713..17744525,2	MCF-7	breast:
35	chr11:17649369..17651435-chr11:17694889..17696565,2	MCF-7	breast:
36	chr11:17612630..17615852-chr11:17618211..17621966,5	K562	blood:
37	chr11:17752076..17753447-chr11:17867688..17868717,4	MCF-7	breast:
38	chr11:17622678..17623570-chr11:17743313..17743816,2	MCF-7	breast:
39	chr11:17752325..17753223-chr11:18001001..18001982,6	K562	blood:
40	chr11:17735220..17735764-chr11:17743713..17744525,2	MCF-7	breast:
41	chr11:17705084..17707821-chr11:17711837..17714694,2	K562	blood:
42	chr11:17620278..17621149-chr11:18000256..18000759,2	MCF-7	breast:
43	chr11:17620244..17621142-chr11:17752157..17753016,5	MCF-7	breast:
44	chr11:17628448..17630427-chr11:17632737..17634648,2	MCF-7	breast:
45	chr11:17661202..17663655-chr11:17664754..17666769,2	MCF-7	breast:
46	chr11:17733888..17735691-chr11:17739053..17741610,3	K562	blood:
47	chr11:17578365..17580159-chr11:17580246..17582171,2	MCF-7	breast:
48	chr11:17578365..17580159-chr11:17580246..17582171,2	MCF-7	breast:
49	chr11:17573988..17575798-chr11:17578729..17580759,2	K562	blood:
50	chr11:17722486..17724717-chr11:17727954..17730842,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOD1-1	chr11:17716569-17716597	ENSG00000254586
2	lnc-USH1C-1	chr11:17673394-17673887	l_441_chr11:17673393-17675099_testes
3	lnc-MYOD1-1	chr11:17718516-17718844	ENSG00000254586
4	lnc-SERGEF-2	chr11:17718366-17718523	XLOC_009385
5	lnc-MYOD1-1	chr11:17716600-17716913	ENSG00000254586
6	lnc-SERGEF-2	chr11:17718366-17719033	XLOC_009385
7	lnc-SERGEF-2	chr11:17716814-17717247	ENSG00000255335.1
8	lnc-SERGEF-2	chr11:17716827-17717247	XLOC_009385
9	lnc-SERGEF-2	chr11:17718427-17718751	NONHSAT018242
10	lnc-SERGEF-2	chr11:17716823-17717247	NONHSAT018243
11	lnc-SERGEF-2	chr11:17716823-17717247	NONHSAT018242
12	lnc-MYOD1-1	chr11:17716844-17716913	ENSG00000254586
13	lnc-SERGEF-2	chr11:17718366-17718487	ENSG00000255335.1
14	lnc-SERGEF-2	chr11:17718366-17718751	NONHSAT018243
15	lnc-SERGEF-2	chr11:17717579-17717919	XLOC_009385
16	lnc-SERGEF-2	chr11:17716818-17717247	XLOC_009385
17	lnc-USH1C-1	chr11:17674942-17675179	l_441_chr11:17673393-17675099_testes
18	lnc-SERGEF-2	chr11:17716827-17717311	XLOC_009385
19	lnc-MYOD1-1	chr11:17718516-17719018	ENSG00000254586

No data

Variant related genes	Relation type
OTOG	TF binding region
ENSG00000255335	TF binding region
KCNC1	TF binding region
USH1C	TF binding region
ENSG00000254586	TF binding region
MYOD1	TF binding region
OTOG	CpG island
ENSG00000255335	CpG island
KCNC1	CpG island
USH1C	CpG island
ENSG00000254586	CpG island
MYOD1	CpG island
ENSG00000129152	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000254586	chromatin interactions
ENSG00000188162	chromatin interactions
ENSG00000006611	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000129158	chromatin interactions
ENSG00000255335	chromatin interactions
ZNF644	miRNA target sites

Extended variants
information (count: 6873 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:6873 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17715430	chr11:17556031-17556032	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs141136453	chr11:17556077-17556078	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72870330	chr11:17556145-17556146	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs537179412	chr11:17556149-17556150	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376048211	chr11:17556150-17556151	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs191827721	chr11:17556159-17556160	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531100864	chr11:17556171-17556172	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549212262	chr11:17556179-17556180	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561124860	chr11:17556182-17556183	Weak transcription Bivalent Enhancer Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528208937	chr11:17556201-17556202	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546346417	chr11:17556251-17556252	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs571246139	chr11:17556275-17556276	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538211281	chr11:17556281-17556282	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs529460829	chr11:17556285-17556286	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550539931	chr11:17556287-17556288	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569101733	chr11:17556295-17556296	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs369034043	chr11:17556316-17556317	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554835578	chr11:17556325-17556326	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573039627	chr11:17556339-17556340	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150720456	chr11:17556352-17556353	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs58422362	chr11:17556398-17556399	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs571275350	chr11:17556419-17556420	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs377081610	chr11:17556421-17556422	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397849179	chr11:17556437-17556438	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10832797	chr11:17556438-17556439	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs7109635	chr11:17556477-17556478	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs563699692	chr11:17556500-17556501	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs368146685	chr11:17556518-17556519	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375481407	chr11:17556570-17556571	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369689274	chr11:17556580-17556581	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373887996	chr11:17556585-17556586	Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542898989	chr11:17556602-17556603	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561163911	chr11:17556629-17556630	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115734308	chr11:17556702-17556703	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145999420	chr11:17556751-17556752	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs527296216	chr11:17556779-17556780	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564789088	chr11:17556795-17556796	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532229297	chr11:17556817-17556818	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191851679	chr11:17556821-17556822	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139934808	chr11:17556871-17556872	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143679278	chr11:17556901-17556902	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs146806104	chr11:17556904-17556905	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs35176543	chr11:17556914-17556915	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs375380122	chr11:17556968-17556969	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs182475182	chr11:17556969-17556970	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs187695180	chr11:17556982-17556983	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs558708576	chr11:17556994-17556995	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs2237959	chr11:17557017-17557018	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs372644519	chr11:17557040-17557041	Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs539101761	chr11:17557093-17557094	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
T-cell prolymphocytic leukemia	19278963	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17538400-17562200	Weak transcription	Small Intestine	intestine
2	chr11:17547200-17563200	Genic enhancers	Fetal Intestine Small	intestine
3	chr11:17551600-17556200	Genic enhancers	Fetal Intestine Large	intestine
4	chr11:17553600-17557000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr11:17553600-17557200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:17553600-17561800	Weak transcription	Gastric	stomach
7	chr11:17553600-17562200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr11:17553800-17556600	Weak transcription	Brain Anterior Caudate	brain
9	chr11:17553800-17556800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr11:17553800-17558200	Weak transcription	Stomach Mucosa	stomach
11	chr11:17553800-17558600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr11:17553800-17563200	Weak transcription	Colonic Mucosa	Colon
13	chr11:17555000-17556200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr11:17555400-17560400	Weak transcription	Duodenum Mucosa	Duodenum
15	chr11:17555800-17562400	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr11:17556000-17556400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:17556000-17558000	Enhancers	Hela-S3	cervix
18	chr11:17556200-17556800	Weak transcription	Fetal Intestine Large	intestine
19	chr11:17556600-17557400	Enhancers	Brain Anterior Caudate	brain
20	chr11:17556800-17557400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr11:17556800-17557600	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr11:17556800-17558800	Enhancers	Fetal Intestine Large	intestine
23	chr11:17557200-17557400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr11:17557200-17557800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr11:17557800-17558000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:17558000-17558400	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr11:17558000-17563400	Weak transcription	Hela-S3	cervix
28	chr11:17558200-17559800	Enhancers	Stomach Mucosa	stomach
29	chr11:17558400-17563200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr11:17558600-17559000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr11:17558800-17562200	Genic enhancers	Fetal Intestine Large	intestine
32	chr11:17559000-17561800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr11:17559600-17560600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr11:17559800-17560200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr11:17559800-17562000	Weak transcription	Stomach Mucosa	stomach
36	chr11:17560200-17560600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr11:17560200-17562200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr11:17560400-17562600	Enhancers	Duodenum Mucosa	Duodenum
39	chr11:17560600-17560800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr11:17560800-17562000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:17561800-17562200	Enhancers	Gastric	stomach
42	chr11:17561800-17562800	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr11:17561800-17563000	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr11:17562000-17564000	Enhancers	Stomach Mucosa	stomach
45	chr11:17562000-17565200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:17562200-17562400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr11:17562200-17562400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr11:17562200-17562400	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine
49	chr11:17562200-17564400	Weak transcription	Gastric	stomach
50	chr11:17562400-17562600	Enhancers	Small Intestine	intestine

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