Variant report

Variant	esv1851383
Chromosome Location	chr15:52501831-52534344
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:678)
CpG islands
(count:122)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:678 , 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	ATF1	chr15:52519613-52520042	K562	blood:	n/a	n/a
2	ATF1	chr15:52521191-52521433	K562	blood:	n/a	n/a
3	ATF3	chr15:52521129-52521393	K562	blood:	n/a	chr15:52521286-52521294 chr15:52521286-52521306 chr15:52521283-52521296
4	BATF	chr15:52528218-52528426	GM12878	blood:	n/a	chr15:52528346-52528357 chr15:52528347-52528357
5	BATF	chr15:52528131-52528521	GM12878	blood:	n/a	chr15:52528346-52528357 chr15:52528347-52528357
6	BATF	chr15:52524542-52524809	GM12878	blood:	n/a	n/a
7	BATF	chr15:52524517-52524811	GM12878	blood:	n/a	n/a
8	BCLAF1	chr15:52524426-52524843	GM12878	blood:	n/a	chr15:52524688-52524697
9	BCLAF1	chr15:52524483-52524882	GM12878	blood:	n/a	chr15:52524688-52524697
10	BHLHE40	chr15:52524604-52524900	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:52519702-52519947	K562	blood:	n/a	n/a
12	BHLHE40	chr15:52521190-52521472	K562	blood:	n/a	n/a
13	BHLHE40	chr15:52513178-52513477	GM12878	blood:	n/a	n/a
14	BHLHE40	chr15:52519627-52519979	GM12878	blood:	n/a	n/a
15	BHLHE40	chr15:52514128-52514368	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:52509494-52509574	K562	blood:	n/a	n/a
17	BHLHE40	chr15:52521163-52521374	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:52531157-52531525	A549	lung:	n/a	chr15:52531338-52531349
19	CEBPB	chr15:52532946-52533267	HepG2	liver:	n/a	chr15:52533073-52533084 chr15:52533072-52533083 chr15:52533072-52533085
20	CEBPB	chr15:52533008-52533234	K562	blood:	n/a	chr15:52533073-52533084 chr15:52533072-52533083 chr15:52533072-52533085
21	CEBPB	chr15:52521130-52521446	A549	lung:	n/a	n/a
22	CEBPB	chr15:52521093-52521468	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:52521128-52521388	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr15:52531170-52531525	HepG2	liver:	n/a	chr15:52531338-52531349
25	CEBPB	chr15:52521094-52521542	MCF-7	breast:	n/a	n/a
26	CEBPB	chr15:52521142-52521427	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:52532958-52533223	A549	lung:	n/a	chr15:52533073-52533084 chr15:52533072-52533083 chr15:52533072-52533085
28	CEBPB	chr15:52520073-52520168	A549	lung:	n/a	n/a
29	CEBPB	chr15:52531183-52531370	K562	blood:	n/a	chr15:52531338-52531349
30	CEBPB	chr15:52531322-52531465	Hela-S3	cervix:	n/a	chr15:52531338-52531349
31	CEBPB	chr15:52521115-52521578	MCF-7	breast:	n/a	n/a
32	CEBPB	chr15:52521128-52521449	K562	blood:	n/a	n/a
33	CEBPB	chr15:52505734-52505930	IMR90	lung:	n/a	n/a
34	CEBPB	chr15:52521123-52521515	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr15:52531168-52531517	IMR90	lung:	n/a	chr15:52531338-52531349
36	CEBPB	chr15:52520982-52521540	A549	lung:	n/a	n/a
37	CEBPB	chr15:52532960-52533203	IMR90	lung:	n/a	chr15:52533073-52533084 chr15:52533072-52533083 chr15:52533072-52533085
38	CEBPB	chr15:52531303-52531355	H1-hESC	embryonic stem cell:	n/a	chr15:52531338-52531349
39	CHD1	chr15:52525651-52525840	GM12878	blood:	n/a	n/a
40	CHD1	chr15:52519469-52520061	IMR90	lung:	n/a	n/a
41	CHD1	chr15:52513614-52514379	GM12878	blood:	n/a	n/a
42	CHD2	chr15:52524624-52524874	GM12878	blood:	n/a	n/a
43	CHD2	chr15:52525607-52525887	GM12878	blood:	n/a	n/a
44	CHD2	chr15:52519736-52519928	GM12878	blood:	n/a	n/a
45	CHD2	chr15:52513389-52513577	GM12878	blood:	n/a	n/a
46	CREB1	chr15:52521082-52521574	ECC-1	luminal epithelium:	n/a	n/a
47	CREB1	chr15:52521139-52521569	GM12878	blood:	n/a	n/a
48	CTCF	chr15:52509900-52510050	GM12870	blood:	n/a	n/a
49	CTCF	chr15:52509420-52509570	HRPEpiC	eye:	n/a	chr15:52509509-52509530 chr15:52509507-52509525 chr15:52509510-52509523 chr15:52509510-52509523 chr15:52509508-52509524
50	CTCF	chr15:52519639-52519932	Spleen_OC	spleen:	n/a	chr15:52519755-52519773 chr15:52519756-52519772 chr15:52519750-52519771

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:52526871-52526921	GM19239	blood:	n/a
2	chr15:52506363-52506413	HRCEpiC	kidney:	n/a
3	chr15:52506363-52506413	HEEpiC	esophagus:	n/a
4	chr15:52506363-52506413	A549	lung:	n/a
5	chr15:52526871-52526921	PANC-1	pancreas:	n/a
6	chr15:52506363-52506413	Hepatocyte	liver:	n/a
7	chr15:52506363-52506413	AG09309	skin:	n/a
8	chr15:52526871-52526921	Hepatocyte	liver:	n/a
9	chr15:52526871-52526921	SK-N-MC	brain:	n/a
10	chr15:52506363-52506413	HCM	heart:	n/a
11	chr15:52526871-52526921	HepG2	liver:	n/a
12	chr15:52526871-52526921	K562	blood:	n/a
13	chr15:52506363-52506413	LNCaP	prostate:	n/a
14	chr15:52526871-52526921	HEK293	kidney:	embryo
15	chr15:52526871-52526921	HUVEC	blood vessel:	n/a
16	chr15:52506363-52506413	HCPEpiC	choroid plexus:	n/a
17	chr15:52526871-52526921	HCM	heart:	n/a
18	chr15:52526871-52526921	HL-60	blood:	n/a
19	chr15:52506363-52506413	HRE	kidney:	n/a
20	chr15:52506363-52506413	AG09319	gingival:	n/a
21	chr15:52526871-52526921	HPAEpiC	pulmonary alveolar:	n/a
22	chr15:52526871-52526921	AG09309	skin:	n/a
23	chr15:52526871-52526921	GM12892	blood:	n/a
24	chr15:52526871-52526921	GM12891	blood:	n/a
25	chr15:52506363-52506413	HCF	heart:	n/a
26	chr15:52506363-52506413	HRPEpiC	eye:	n/a
27	chr15:52526871-52526921	AG10803	skin:	n/a
28	chr15:52506363-52506413	SAEC	small airway:	n/a
29	chr15:52526871-52526921	PFSK-1	brain:	n/a
30	chr15:52506363-52506413	SK-N-SH_RA	brain:	n/a
31	chr15:52526871-52526921	HNPCEpiC	eye:	n/a
32	chr15:52526871-52526921	AoSMC	blood vessel:	n/a
33	chr15:52506363-52506413	HEK293	kidney:	embryo
34	chr15:52506363-52506413	GM12891	blood:	n/a
35	chr15:52526871-52526921	HAEpiC	amniotic membrane:	n/a
36	chr15:52506363-52506413	ovcar-3	ovarian:	n/a
37	chr15:52526871-52526921	HIPEpiC	eye:	n/a
38	chr15:52526871-52526921	NHDF-neo	bronchial:	n/a
39	chr15:52526871-52526921	PrEC	prostate:	n/a
40	chr15:52526871-52526921	Jurkat	blood:	n/a
41	chr15:52506363-52506413	NT2-D1	testis:	n/a
42	chr15:52506363-52506413	NHBE	bronchial:	n/a
43	chr15:52506363-52506413	NH-A	brain:	n/a
44	chr15:52506363-52506413	AG10803	skin:	n/a
45	chr15:52506363-52506413	MCF-7	breast:	n/a
46	chr15:52526871-52526921	GM06990	blood:	n/a
47	chr15:52526871-52526921	NH-A	brain:	n/a
48	chr15:52506363-52506413	GM19239	blood:	n/a
49	chr15:52506363-52506413	HAEpiC	amniotic membrane:	n/a
50	chr15:52526871-52526921	CMK	blood:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:52530481..52532321-chr15:52539248..52541574,2	MCF-7	breast:
2	chr15:52469037..52470714-chr15:52511840..52513591,2	MCF-7	breast:
3	chr15:52500850..52502666-chr15:52514026..52515788,2	MCF-7	breast:
4	chr15:52531482..52533056-chr15:52536199..52538626,2	MCF-7	breast:
5	chr15:52509455..52510001-chr15:52755530..52756071,2	MCF-7	breast:
6	chr15:52529228..52532090-chr15:52537433..52540764,3	MCF-7	breast:
7	chr15:52311257..52313666-chr15:52519365..52521577,2	MCF-7	breast:
8	chr15:52473218..52475845-chr15:52500048..52503534,3	MCF-7	breast:
9	chr15:52486663..52491950-chr15:52497424..52502756,7	MCF-7	breast:
10	chr15:52216346..52217850-chr15:52500229..52502926,2	MCF-7	breast:
11	chr15:52532630..52535359-chr15:52579231..52581828,3	MCF-7	breast:
12	chr15:52519699..52521506-chr15:52579377..52581027,2	MCF-7	breast:
13	chr15:52508008..52509939-chr15:53026331..53028847,2	MCF-7	breast:
14	chr15:52520877..52522858-chr15:52523295..52525074,3	MCF-7	breast:
15	chr15:52521161..52523907-chr15:52528053..52529733,2	MCF-7	breast:
16	chr15:52509233..52510844-chr15:52512535..52515103,2	K562	blood:
17	chr15:52500676..52501391-chr15:52509036..52509975,2	K562	blood:
18	chr15:52466781..52469103-chr15:52500146..52502200,2	MCF-7	breast:
19	chr15:52470561..52473090-chr15:52500221..52502576,3	MCF-7	breast:
20	chr15:52526628..52528365-chr15:52537492..52540150,2	MCF-7	breast:
21	chr15:52505827..52511235-chr15:52516876..52519875,7	MCF-7	breast:
22	chr15:52509010..52510015-chr15:52519316..52520083,4	MCF-7	breast:
23	chr15:52500850..52502666-chr15:52514026..52515788,2	MCF-7	breast:
24	chr15:52499920..52501518-chr15:52503207..52505042,2	MCF-7	breast:
25	chr15:52510129..52510638-chr15:52519361..52520037,2	MCF-7	breast:
26	chr15:52514548..52516962-chr15:52580174..52582493,2	MCF-7	breast:
27	chr15:52529115..52532047-chr15:52992666..52994402,2	K562	blood:
28	chr15:52509083..52509697-chr15:53027309..53027962,2	MCF-7	breast:
29	chr15:52510129..52510638-chr15:52519361..52520037,2	MCF-7	breast:
30	chr15:52513190..52514784-chr15:52519152..52521403,2	MCF-7	breast:
31	chr15:52532801..52535731-chr15:52601515..52603297,2	MCF-7	breast:
32	chr15:52520877..52522858-chr15:52523295..52525074,3	MCF-7	breast:
33	chr15:52509010..52510015-chr15:52519316..52520083,4	MCF-7	breast:
34	chr15:52471929..52473457-chr15:52519200..52522069,2	MCF-7	breast:
35	chr15:51942260..51942806-chr15:52519301..52520236,2	K562	blood:
36	chr15:52509089..52509941-chr15:53027516..53028325,2	MCF-7	breast:
37	chr15:52505827..52511235-chr15:52516876..52519875,7	MCF-7	breast:
38	chr15:52498552..52502035-chr15:52503246..52505472,3	MCF-7	breast:
39	chr15:52513190..52514784-chr15:52519152..52521403,2	MCF-7	breast:
40	chr15:52521390..52524844-chr15:52525282..52528513,3	MCF-7	breast:
41	chr15:52475563..52476065-chr15:52509089..52509975,2	MCF-7	breast:
42	chr15:52498552..52502035-chr15:52503246..52505472,3	MCF-7	breast:
43	chr15:52271043..52273593-chr15:52500641..52502378,2	MCF-7	breast:
44	chr15:52521390..52524844-chr15:52525282..52528513,3	MCF-7	breast:
45	chr15:52521161..52523907-chr15:52528053..52529733,2	MCF-7	breast:
46	chr15:52521470..52523349-chr15:52580283..52582342,2	MCF-7	breast:
47	chr15:52509233..52510844-chr15:52512535..52515103,2	K562	blood:
48	chr15:52505434..52507299-chr15:52513137..52515697,2	MCF-7	breast:

No data

Variant related genes	Relation type
MYO5C	TF binding region
MYO5C	CpG island
ENSG00000128833	chromatin interactions
ENSG00000069966	chromatin interactions
ENSG00000259577	chromatin interactions
ENSG00000259438	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000138594	chromatin interactions

Extended variants
information (count: 1337 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1337 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11070884	chr15:52501831-52501832	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74940475	chr15:52501850-52501851	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs11070885	chr15:52501856-52501857	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs11632189	chr15:52501894-52501895	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs374449330	chr15:52501895-52501896	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs143882311	chr15:52501901-52501902	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs34415872	chr15:52501932-52501933	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs569676556	chr15:52501963-52501964	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs77858124	chr15:52501968-52501969	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs187072134	chr15:52501973-52501974	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs11632174	chr15:52502128-52502129	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs538844833	chr15:52502147-52502148	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs554362421	chr15:52502148-52502149	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs572179526	chr15:52502149-52502150	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs76734578	chr15:52502160-52502161	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs8031893	chr15:52502164-52502165	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs553985494	chr15:52502168-52502169	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs148163504	chr15:52502224-52502225	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs373873585	chr15:52502227-52502228	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs565017098	chr15:52502291-52502292	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs192233580	chr15:52502315-52502316	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs540839839	chr15:52502316-52502317	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs372888467	chr15:52502329-52502330	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs559588579	chr15:52502468-52502469	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs376170751	chr15:52502502-52502503	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs376394929	chr15:52502510-52502511	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs74015631	chr15:52502622-52502623	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs563418393	chr15:52502633-52502634	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143092958	chr15:52502696-52502697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs565916408	chr15:52502710-52502711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376465109	chr15:52502727-52502728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571816320	chr15:52502756-52502757	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs11638716	chr15:52502783-52502784	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs554386089	chr15:52502818-52502819	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184385745	chr15:52502826-52502827	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs78711125	chr15:52502852-52502853	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536490274	chr15:52502853-52502854	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190404842	chr15:52502873-52502874	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs576162118	chr15:52502882-52502883	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537015616	chr15:52502893-52502894	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573136900	chr15:52502921-52502922	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146122767	chr15:52502967-52502968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193248572	chr15:52502975-52502976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140151620	chr15:52503020-52503021	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1011050	chr15:52503082-52503083	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs574679283	chr15:52503188-52503189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1011051	chr15:52503257-52503258	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs563358187	chr15:52503266-52503267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545324736	chr15:52503273-52503274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530648775	chr15:52503277-52503278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:846 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52473200-52513600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr15:52473600-52512400	Weak transcription	Primary B cells from cord blood	blood
3	chr15:52475800-52505600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr15:52479800-52532800	Weak transcription	Brain Angular Gyrus	brain
5	chr15:52484200-52503200	Weak transcription	Lung	lung
6	chr15:52484400-52503800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:52486000-52505800	Weak transcription	Psoas Muscle	Psoas
8	chr15:52487400-52505200	Weak transcription	Thymus	Thymus
9	chr15:52488600-52509800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr15:52488800-52505600	Weak transcription	Fetal Kidney	kidney
11	chr15:52489200-52520800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:52489200-52523800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr15:52490400-52503000	Weak transcription	Brain Hippocampus Middle	brain
14	chr15:52495600-52519000	Strong transcription	HepG2	liver
15	chr15:52496000-52505000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:52496200-52505400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:52497200-52505200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr15:52497400-52503000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:52497400-52505000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr15:52497400-52509400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:52497400-52510400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:52497400-52514600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr15:52497400-52535600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr15:52497600-52502800	Weak transcription	Adipose Nuclei	Adipose
25	chr15:52497600-52503200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr15:52497600-52503200	Weak transcription	Esophagus	oesophagus
27	chr15:52497600-52503200	Weak transcription	Fetal Intestine Small	intestine
28	chr15:52497600-52503200	Weak transcription	Fetal Muscle Leg	muscle
29	chr15:52497600-52503200	Weak transcription	Spleen	Spleen
30	chr15:52497600-52503400	Weak transcription	Fetal Intestine Large	intestine
31	chr15:52497600-52503600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:52497600-52503600	Weak transcription	Primary T cells from cord blood	blood
33	chr15:52497600-52503600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr15:52497600-52503600	Weak transcription	Colonic Mucosa	Colon
35	chr15:52497600-52504000	Weak transcription	Right Ventricle	heart
36	chr15:52497600-52508800	Weak transcription	Stomach Mucosa	stomach
37	chr15:52497800-52549000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr15:52498400-52503000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr15:52498600-52502000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr15:52499000-52502800	Weak transcription	H9 Cell Line	embryonic stem cell
41	chr15:52499000-52503800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr15:52499000-52504400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr15:52499000-52505200	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr15:52499000-52515600	Weak transcription	Left Ventricle	heart
45	chr15:52499200-52503000	Weak transcription	Liver	Liver
46	chr15:52499200-52512600	Strong transcription	A549	lung
47	chr15:52499600-52502000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr15:52500000-52512000	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr15:52500000-52519000	Strong transcription	Rectal Mucosa Donor 31	rectum
50	chr15:52500200-52502000	Strong transcription	Duodenum Mucosa	Duodenum

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