Variant report

Variant	nsv442701
Chromosome Location	chr15:45737096-45748752
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:448)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:45741591-45741920	HepG2	liver:	n/a	n/a
2	ATF1	chr15:45748752-45749171	K562	blood:	n/a	n/a
3	ATF1	chr15:45747163-45747363	K562	blood:	n/a	n/a
4	ATF2	chr15:45748681-45749144	GM12878	blood:	n/a	n/a
5	ATF2	chr15:45748688-45749194	GM12878	blood:	n/a	n/a
6	ATF3	chr15:45748741-45749190	A549	lung:	n/a	chr15:45748930-45748937 chr15:45748926-45748937 chr15:45748927-45748937 chr15:45748926-45748941 chr15:45748926-45748939 chr15:45748927-45748940 chr15:45748930-45748938 chr15:45748929-45748937 chr15:45748929-45748940
7	ATF3	chr15:45748747-45749087	K562	blood:	n/a	chr15:45748930-45748937 chr15:45748926-45748937 chr15:45748927-45748937 chr15:45748926-45748941 chr15:45748926-45748939 chr15:45748927-45748940 chr15:45748930-45748938 chr15:45748929-45748937 chr15:45748929-45748940
8	BACH1	chr15:45740554-45740609	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr15:45748707-45749173	A549	lung:	n/a	n/a
10	BHLHE40	chr15:45747175-45747332	K562	blood:	n/a	n/a
11	BHLHE40	chr15:45747123-45747362	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:45746243-45746402	K562	blood:	n/a	n/a
13	BHLHE40	chr15:45737306-45737603	K562	blood:	n/a	n/a
14	BRCA1	chr15:45746901-45747361	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr15:45748714-45749487	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr15:45737453-45737961	MCF-7	breast:	n/a	chr15:45737703-45737714
17	CEBPB	chr15:45740270-45740734	IMR90	lung:	n/a	n/a
18	CEBPB	chr15:45740460-45740535	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:45737545-45737883	IMR90	lung:	n/a	chr15:45737703-45737714
20	CEBPB	chr15:45737408-45738233	Hela-S3	cervix:	n/a	chr15:45737703-45737714
21	CEBPB	chr15:45737495-45737920	A549	lung:	n/a	chr15:45737703-45737714
22	CEBPB	chr15:45737584-45737854	HepG2	liver:	n/a	chr15:45737703-45737714
23	CEBPB	chr15:45737556-45737855	K562	blood:	n/a	chr15:45737703-45737714
24	CEBPB	chr15:45737551-45737929	ECC-1	luminal epithelium:	n/a	chr15:45737703-45737714
25	CEBPB	chr15:45741605-45741973	Hela-S3	cervix:	n/a	chr15:45741789-45741800
26	CEBPB	chr15:45747026-45747448	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr15:45748531-45749143	A549	lung:	n/a	n/a
28	CEBPB	chr15:45747115-45747303	A549	lung:	n/a	n/a
29	CEBPB	chr15:45740235-45740650	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr15:45748497-45749281	IMR90	lung:	n/a	n/a
31	CEBPB	chr15:45737561-45737972	H1-hESC	embryonic stem cell:	n/a	chr15:45737703-45737714
32	CEBPB	chr15:45741614-45741930	HepG2	liver:	n/a	chr15:45741789-45741800
33	CEBPB	chr15:45748423-45749185	A549	lung:	n/a	n/a
34	CEBPB	chr15:45740352-45740607	A549	lung:	n/a	n/a
35	CEBPB	chr15:45747038-45747447	IMR90	lung:	n/a	n/a
36	CEBPB	chr15:45737515-45737933	ECC-1	luminal epithelium:	n/a	chr15:45737703-45737714
37	CEBPB	chr15:45737437-45738042	MCF-7	breast:	n/a	chr15:45737703-45737714
38	CEBPB	chr15:45737461-45737962	A549	lung:	n/a	chr15:45737703-45737714
39	CEBPB	chr15:45748675-45749120	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:45748435-45749254	Hela-S3	cervix:	n/a	n/a
41	CHD2	chr15:45747000-45747430	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr15:45747111-45747379	GM12878	blood:	n/a	n/a
43	CHD2	chr15:45740237-45740640	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr15:45737272-45737949	Hela-S3	cervix:	n/a	n/a
45	CHD2	chr15:45748507-45749426	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr15:45748720-45749237	K562	blood:	n/a	chr15:45748927-45748940
47	CREB1	chr15:45748742-45749210	GM12878	blood:	n/a	chr15:45748927-45748940
48	CREB1	chr15:45748658-45749191	K562	blood:	n/a	chr15:45748927-45748940
49	CREB1	chr15:45748713-45749169	A549	lung:	n/a	chr15:45748927-45748940
50	CREB1	chr15:45748694-45749221	HepG2	liver:	n/a	chr15:45748927-45748940

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:45740677-45740727	HRE	kidney:	n/a
2	chr15:45740677-45740727	GM12892	blood:	n/a
3	chr15:45740677-45740727	SK-N-SH_RA	brain:	n/a
4	chr15:45740677-45740727	IMR90	lung:	fetal
5	chr15:45740677-45740727	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:45740677-45740727	ECC-1	luminal epithelium:	n/a
7	chr15:45740677-45740727	HL-60	blood:	n/a
8	chr15:45740677-45740727	NB4	blood:	n/a
9	chr15:45740677-45740727	NH-A	brain:	n/a
10	chr15:45740677-45740727	AG04449	skin:	fetal
11	chr15:45740677-45740727	HRCEpiC	kidney:	n/a
12	chr15:45740677-45740727	PrEC	prostate:	n/a
13	chr15:45740677-45740727	AoSMC	blood vessel:	n/a
14	chr15:45740677-45740727	SK-N-MC	brain:	n/a
15	chr15:45740677-45740727	Hela-S3	cervix:	n/a
16	chr15:45740677-45740727	CMK	blood:	n/a
17	chr15:45740677-45740727	Caco-2	colon:	n/a
18	chr15:45740677-45740727	A549	lung:	n/a
19	chr15:45740677-45740727	RPTEC	kidney:	n/a
20	chr15:45740677-45740727	K562	blood:	n/a
21	chr15:45740677-45740727	GM12878	blood:	n/a
22	chr15:45740677-45740727	HIPEpiC	eye:	n/a
23	chr15:45740677-45740727	NT2-D1	testis:	n/a
24	chr15:45740677-45740727	BE2_C	brain:	n/a
25	chr15:45740677-45740727	HNPCEpiC	eye:	n/a
26	chr15:45740677-45740727	HRPEpiC	eye:	n/a
27	chr15:45740677-45740727	H1-hESC	embryonic stem cell:	embryo
28	chr15:45740677-45740727	LNCaP	prostate:	n/a
29	chr15:45740677-45740727	HCM	heart:	n/a
30	chr15:45740677-45740727	BJ	skin:	n/a
31	chr15:45740677-45740727	HMEC	breast:	n/a
32	chr15:45740677-45740727	HAEpiC	amniotic membrane:	n/a
33	chr15:45740677-45740727	AG10803	skin:	n/a
34	chr15:45740677-45740727	NHDF-neo	bronchial:	n/a
35	chr15:45740677-45740727	GM12891	blood:	n/a
36	chr15:45740677-45740727	AG04450	lung:	fetal
37	chr15:45740677-45740727	Jurkat	blood:	n/a
38	chr15:45740677-45740727	HepG2	liver:	n/a
39	chr15:45740677-45740727	GM06990	blood:	n/a
40	chr15:45740677-45740727	HEEpiC	esophagus:	n/a
41	chr15:45740677-45740727	AG09309	skin:	n/a
42	chr15:45740677-45740727	MCF10A-Er-Src	breast:	n/a
43	chr15:45740677-45740727	ProgFib	skin:	n/a
44	chr15:45740677-45740727	Hepatocyte	liver:	n/a
45	chr15:45740677-45740727	HCF	heart:	n/a
46	chr15:45740677-45740727	ovcar-3	ovarian:	n/a
47	chr15:45740677-45740727	SAEC	small airway:	n/a
48	chr15:45740677-45740727	NHBE	bronchial:	n/a
49	chr15:45740677-45740727	U87	brain:	n/a
50	chr15:45740677-45740727	SKMC	muscle:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:45692773..45694505-chr15:45738421..45740123,2	MCF-7	breast:
2	chr15:45457588..45459238-chr15:45747257..45749159,2	K562	blood:
3	chr15:45722040..45723226-chr15:45748321..45751272,60	MCF-7	breast:
4	chr15:45745258..45747507-chr15:45747517..45749111,2	MCF-7	breast:
5	chr15:45745258..45747507-chr15:45747517..45749111,2	MCF-7	breast:
6	chr15:45740795..45743926-chr15:45878461..45880935,3	MCF-7	breast:
7	chr15:45693986..45696362-chr15:45736299..45740535,4	MCF-7	breast:
8	chr15:45722489..45723181-chr15:45742653..45743318,2	MCF-7	breast:
9	chr15:45693029..45695760-chr15:45741637..45746369,4	MCF-7	breast:
10	chr15:45497493..45498035-chr15:45748602..45749386,2	K562	blood:
11	chr15:45737247..45739664-chr15:45747415..45750054,2	K562	blood:
12	chr15:45693234..45695210-chr15:45748321..45750226,2	MCF-7	breast:
13	chr15:45736069..45742318-chr15:45926037..45929619,6	MCF-7	breast:
14	chr15:45459360..45460864-chr15:45748404..45750669,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C15orf48-1	chr15:45742463-45742488	XLOC_011237
2	lnc-C15orf48-1	chr15:45740960-45740999	ENSG00000259354.1
3	lnc-C15orf48-1	chr15:45740625-45740999	ENSG00000259354.1
4	lnc-C15orf48-1	chr15:45742316-45742488	ENSG00000259354.1
5	lnc-C15orf48-1	chr15:45742448-45742488	ENSG00000259354.1

No data

Variant related genes	Relation type
RNU7-5P	TF binding region
ENSG00000259354	TF binding region
ENSG00000259342	TF binding region
RNU7-5P	CpG island
ENSG00000259354	CpG island
ENSG00000259342	CpG island
ENSG00000259539	chromatin interactions
ENSG00000104164	chromatin interactions
ENSG00000137767	chromatin interactions
ENSG00000171763	chromatin interactions
ENSG00000260170	chromatin interactions
ENSG00000171766	chromatin interactions
ENSG00000166920	chromatin interactions
ENSG00000252285	chromatin interactions

Extended variants
information (count: 464 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:464 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2433621	chr15:45737100-45737101	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188149088	chr15:45737190-45737191	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs544714425	chr15:45737201-45737202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs72711259	chr15:45737253-45737254	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs527797547	chr15:45737254-45737255	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs138883606	chr15:45737272-45737273	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs76191065	chr15:45737273-45737274	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs73412436	chr15:45737299-45737300	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs143241030	chr15:45737315-45737316	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs147105578	chr15:45737350-45737351	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs540607215	chr15:45737356-45737357	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs117572267	chr15:45737357-45737358	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs2467866	chr15:45737394-45737395	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs182017639	chr15:45737410-45737411	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs527266680	chr15:45737428-45737429	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs369996645	chr15:45737466-45737467	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs373573339	chr15:45737467-45737468	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs185628562	chr15:45737472-45737473	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs73412437	chr15:45737491-45737492	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs116360211	chr15:45737606-45737607	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs559034741	chr15:45737640-45737641	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs138550085	chr15:45737649-45737650	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs562069803	chr15:45737651-45737652	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs529386880	chr15:45737656-45737657	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs190104493	chr15:45737693-45737694	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs181700859	chr15:45737713-45737714	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs563713895	chr15:45737716-45737717	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs546028667	chr15:45737727-45737728	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs143786038	chr15:45737783-45737784	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs531366110	chr15:45737787-45737788	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs368035567	chr15:45737807-45737808	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs186403814	chr15:45737815-45737816	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs113754060	chr15:45737823-45737824	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs532736621	chr15:45737824-45737825	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs527366804	chr15:45737830-45737831	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs539219357	chr15:45737833-45737834	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs375965497	chr15:45737834-45737835	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs547219420	chr15:45737835-45737836	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs28460009	chr15:45737836-45737837	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs2486282	chr15:45737905-45737906	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs190083087	chr15:45737906-45737907	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs552864432	chr15:45737911-45737912	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs180888947	chr15:45737920-45737921	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs554422118	chr15:45737934-45737935	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs74733338	chr15:45737994-45737995	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs548782450	chr15:45737995-45737996	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs9972540	chr15:45737998-45737999	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs144232784	chr15:45737999-45738000	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs75790132	chr15:45738004-45738005	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs148728673	chr15:45738051-45738052	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Melanoma	17363583	CNVD
Acute myeloid leukemia	19651601	CNVD
Marfan syndrome	17492313	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45724000-45737200	Weak transcription	Pancreas	Pancrea
2	chr15:45731400-45740400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:45734200-45738000	Enhancers	Stomach Mucosa	stomach
4	chr15:45735200-45737200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:45735200-45737200	Weak transcription	Lung	lung
6	chr15:45735200-45737200	Weak transcription	Osteobl	bone
7	chr15:45735200-45737400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:45735200-45737400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr15:45735200-45737400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:45735200-45737400	Weak transcription	HSMM	muscle
11	chr15:45735200-45737400	Weak transcription	NHDF-Ad	bronchial
12	chr15:45735200-45737600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr15:45735200-45737600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:45735200-45737600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr15:45735200-45740400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr15:45735200-45740400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:45735800-45738600	Enhancers	Esophagus	oesophagus
18	chr15:45736600-45738600	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr15:45736800-45737200	Enhancers	Hela-S3	cervix
20	chr15:45736800-45738200	Enhancers	A549	lung
21	chr15:45736800-45739200	Enhancers	Placenta	Placenta
22	chr15:45736800-45739200	Enhancers	Gastric	stomach
23	chr15:45737000-45737400	Enhancers	Colonic Mucosa	Colon
24	chr15:45737000-45737400	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr15:45737000-45737600	Enhancers	Duodenum Mucosa	Duodenum
26	chr15:45737000-45737800	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr15:45737000-45738400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr15:45737000-45738400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:45737000-45738400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr15:45737000-45738400	Enhancers	Adipose Nuclei	Adipose
31	chr15:45737000-45739000	Enhancers	Fetal Intestine Large	intestine
32	chr15:45737000-45739000	Enhancers	Fetal Intestine Small	intestine
33	chr15:45737200-45737600	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr15:45737200-45738200	Enhancers	Osteobl	bone
35	chr15:45737200-45738400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr15:45737200-45738400	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr15:45737200-45738400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr15:45737200-45738400	Enhancers	Lung	lung
39	chr15:45737200-45738400	Enhancers	Right Atrium	heart
40	chr15:45737200-45738600	Flanking Active TSS	Hela-S3	cervix
41	chr15:45737200-45739000	Enhancers	Liver	Liver
42	chr15:45737200-45739200	Enhancers	Pancreas	Pancrea
43	chr15:45737400-45737600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr15:45737400-45737600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr15:45737400-45737600	Flanking Active TSS	Colonic Mucosa	Colon
46	chr15:45737400-45738000	Enhancers	HSMM	muscle
47	chr15:45737400-45738200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr15:45737400-45738200	Enhancers	HMEC	breast
49	chr15:45737400-45738400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr15:45737400-45738400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell

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