Variant report

Variant	nsv1041996
Chromosome Location	chr13:52544805-52581501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:835)
CpG islands
(count:61)
Chromatin interactive
region (count:49)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:52563190-52563561	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:52570833-52570979	K562	blood:	n/a	n/a
3	ARID3A	chr13:52552612-52552790	K562	blood:	n/a	n/a
4	ARID3A	chr13:52573430-52573694	K562	blood:	n/a	n/a
5	ARID3A	chr13:52572282-52572284	K562	blood:	n/a	n/a
6	ARID3A	chr13:52545711-52546101	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:52548554-52548896	K562	blood:	n/a	n/a
8	ARID3A	chr13:52572112-52572486	HepG2	liver:	n/a	n/a
9	ARID3A	chr13:52551248-52551261	HepG2	liver:	n/a	n/a
10	ARID3A	chr13:52575376-52575602	K562	blood:	n/a	n/a
11	ARID3A	chr13:52553095-52553479	HepG2	liver:	n/a	n/a
12	ARID3A	chr13:52553083-52553442	K562	blood:	n/a	n/a
13	ATF1	chr13:52550582-52550871	K562	blood:	n/a	n/a
14	ATF1	chr13:52552888-52553465	K562	blood:	n/a	n/a
15	ATF1	chr13:52548576-52549016	K562	blood:	n/a	n/a
16	ATF3	chr13:52553156-52553449	K562	blood:	n/a	n/a
17	ATF3	chr13:52553234-52553408	HepG2	liver:	n/a	n/a
18	ATF3	chr13:52553085-52553510	HepG2	liver:	n/a	n/a
19	ATF3	chr13:52553100-52553433	K562	blood:	n/a	n/a
20	BACH1	chr13:52565558-52565707	K562	blood:	n/a	n/a
21	BACH1	chr13:52552836-52552992	K562	blood:	n/a	n/a
22	BHLHE40	chr13:52552947-52553274	K562	blood:	n/a	n/a
23	BHLHE40	chr13:52569873-52571048	K562	blood:	n/a	n/a
24	BHLHE40	chr13:52571930-52572392	K562	blood:	n/a	n/a
25	BHLHE40	chr13:52575263-52575546	K562	blood:	n/a	n/a
26	BHLHE40	chr13:52573093-52573293	K562	blood:	n/a	n/a
27	BHLHE40	chr13:52548631-52548941	K562	blood:	n/a	n/a
28	BHLHE40	chr13:52572183-52572510	HepG2	liver:	n/a	n/a
29	CBX3	chr13:52548596-52548966	K562	blood:	n/a	n/a
30	CBX3	chr13:52552933-52553521	K562	blood:	n/a	n/a
31	CCNT2	chr13:52567682-52567742	K562	blood:	n/a	n/a
32	CCNT2	chr13:52553111-52553442	K562	blood:	n/a	n/a
33	CCNT2	chr13:52572006-52572390	K562	blood:	n/a	n/a
34	CEBPB	chr13:52552906-52553547	K562	blood:	n/a	chr13:52553277-52553288
35	CEBPB	chr13:52545666-52545916	HepG2	liver:	n/a	n/a
36	CEBPB	chr13:52553016-52553490	HepG2	liver:	n/a	chr13:52553277-52553288
37	CEBPB	chr13:52552982-52553509	HepG2	liver:	n/a	chr13:52553277-52553288
38	CEBPB	chr13:52553182-52553416	H1-hESC	embryonic stem cell:	n/a	chr13:52553277-52553288
39	CEBPB	chr13:52572226-52572289	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr13:52553148-52553409	Hela-S3	cervix:	n/a	chr13:52553277-52553288
41	CEBPB	chr13:52572168-52572414	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr13:52551103-52551345	HepG2	liver:	n/a	chr13:52551249-52551260
43	CEBPB	chr13:52553126-52553428	HepG2	liver:	n/a	chr13:52553277-52553288
44	CEBPB	chr13:52563239-52563557	HepG2	liver:	n/a	chr13:52563389-52563400
45	CEBPB	chr13:52566899-52567191	K562	blood:	n/a	n/a
46	CEBPB	chr13:52553016-52553495	HepG2	liver:	n/a	chr13:52553277-52553288
47	CEBPB	chr13:52567794-52568037	K562	blood:	n/a	n/a
48	CEBPB	chr13:52570834-52571110	K562	blood:	n/a	n/a
49	CEBPB	chr13:52552875-52553551	K562	blood:	n/a	chr13:52553277-52553288
50	CEBPB	chr13:52553064-52553389	K562	blood:	n/a	chr13:52553277-52553288

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52572769-52572819	AG09309	skin:	n/a
2	chr13:52572769-52572819	HUVEC	blood vessel:	n/a
3	chr13:52572769-52572819	ECC-1	luminal epithelium:	n/a
4	chr13:52572769-52572819	HL-60	blood:	n/a
5	chr13:52572769-52572819	HepG2	liver:	n/a
6	chr13:52572769-52572819	SKMC	muscle:	n/a
7	chr13:52572769-52572819	MCF-7	breast:	n/a
8	chr13:52572769-52572819	H1-hESC	embryonic stem cell:	embryo
9	chr13:52572769-52572819	BJ	skin:	n/a
10	chr13:52572769-52572819	HAEpiC	amniotic membrane:	n/a
11	chr13:52572769-52572819	SK-N-SH	brain:	n/a
12	chr13:52572769-52572819	GM06990	blood:	n/a
13	chr13:52572769-52572819	NT2-D1	testis:	n/a
14	chr13:52572769-52572819	HEK293	kidney:	embryo
15	chr13:52572769-52572819	HIPEpiC	eye:	n/a
16	chr13:52572769-52572819	IMR90	lung:	fetal
17	chr13:52572769-52572819	SAEC	small airway:	n/a
18	chr13:52572769-52572819	SK-N-MC	brain:	n/a
19	chr13:52572769-52572819	BE2_C	brain:	n/a
20	chr13:52572769-52572819	HCM	heart:	n/a
21	chr13:52572769-52572819	HNPCEpiC	eye:	n/a
22	chr13:52572769-52572819	NB4	blood:	n/a
23	chr13:52572769-52572819	MCF10A-Er-Src	breast:	n/a
24	chr13:52572769-52572819	PFSK-1	brain:	n/a
25	chr13:52572769-52572819	GM19239	blood:	n/a
26	chr13:52572769-52572819	CMK	blood:	n/a
27	chr13:52572769-52572819	HRCEpiC	kidney:	n/a
28	chr13:52572769-52572819	NHDF-neo	bronchial:	n/a
29	chr13:52572769-52572819	GM12891	blood:	n/a
30	chr13:52572769-52572819	Hela-S3	cervix:	n/a
31	chr13:52572769-52572819	AG10803	skin:	n/a
32	chr13:52572769-52572819	HCF	heart:	n/a
33	chr13:52572769-52572819	PrEC	prostate:	n/a
34	chr13:52572769-52572819	AG09319	gingival:	n/a
35	chr13:52572769-52572819	ovcar-3	ovarian:	n/a
36	chr13:52572769-52572819	GM12878	blood:	n/a
37	chr13:52572769-52572819	K562	blood:	n/a
38	chr13:52572769-52572819	Hepatocyte	liver:	n/a
39	chr13:52572769-52572819	HCPEpiC	choroid plexus:	n/a
40	chr13:52572769-52572819	HEEpiC	esophagus:	n/a
41	chr13:52572769-52572819	AG04450	lung:	fetal
42	chr13:52572769-52572819	Jurkat	blood:	n/a
43	chr13:52572769-52572819	SK-N-SH_RA	brain:	n/a
44	chr13:52572769-52572819	HMEC	breast:	n/a
45	chr13:52572769-52572819	GM12892	blood:	n/a
46	chr13:52572769-52572819	HCT-116	colon:	n/a
47	chr13:52572769-52572819	PANC-1	pancreas:	n/a
48	chr13:52572769-52572819	U87	brain:	n/a
49	chr13:52572769-52572819	NH-A	brain:	n/a
50	chr13:52572769-52572819	A549	lung:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:52576391..52578184-chr13:52580333..52583322,2	K562	blood:
2	chr13:52571069..52573595-chr13:52575661..52577767,2	K562	blood:
3	chr13:52565945..52573624-chr13:52584322..52588378,8	K562	blood:
4	chr13:52547935..52549465-chr13:52552409..52555264,2	K562	blood:
5	chr13:52564916..52570042-chr13:52571727..52575592,5	MCF-7	breast:
6	chr13:52576391..52578184-chr13:52580333..52583322,2	K562	blood:
7	chr13:52566849..52570695-chr13:52572398..52574312,4	K562	blood:
8	chr13:52578707..52580280-chr13:52581287..52584072,2	MCF-7	breast:
9	chr13:52571069..52573595-chr13:52575661..52577767,2	K562	blood:
10	chr13:52496511..52499468-chr13:52568718..52570837,2	MCF-7	breast:
11	chr13:52571352..52573505-chr13:52585420..52587212,2	MCF-7	breast:
12	chr13:52537621..52539429-chr13:52564535..52567211,2	K562	blood:
13	chr13:52549808..52551859-chr13:52553072..52555669,2	K562	blood:
14	chr13:52555699..52557383-chr13:52562997..52565551,2	MCF-7	breast:
15	chr13:52573978..52576897-chr13:52584867..52586656,2	MCF-7	breast:
16	chr13:52549808..52551859-chr13:52553072..52555669,2	K562	blood:
17	chr13:52494195..52496775-chr13:52571479..52573811,2	MCF-7	breast:
18	chr13:52562562..52567113-chr13:52569338..52572980,4	MCF-7	breast:
19	chr12:112278104..112280783-chr13:52545598..52548127,2	MCF-7	breast:
20	chr13:52578352..52579378-chr13:52701728..52702446,3	MCF-7	breast:
21	chr13:52575013..52575922-chr13:52701577..52702244,3	MCF-7	breast:
22	chr13:52580573..52584111-chr13:52584996..52587718,3	MCF-7	breast:
23	chr13:52543974..52546024-chr13:52586365..52587928,2	MCF-7	breast:
24	chr13:52561953..52567975-chr13:52568159..52572243,8	K562	blood:
25	chr13:52566849..52570695-chr13:52572398..52574312,4	K562	blood:
26	chr13:52538366..52539879-chr13:52542214..52544813,2	K562	blood:
27	chr13:52532889..52534545-chr13:52566217..52568860,2	MCF-7	breast:
28	chr13:52555699..52557383-chr13:52562997..52565551,2	MCF-7	breast:
29	chr13:52573284..52575867-chr13:52579600..52581887,2	K562	blood:
30	chr13:52561953..52567975-chr13:52568159..52572243,8	K562	blood:
31	chr13:52546299..52549465-chr13:52553764..52557298,3	K562	blood:
32	chr13:52538417..52541078-chr13:52553924..52556751,2	K562	blood:
33	chr13:52538063..52541078-chr13:52554449..52557060,3	K562	blood:
34	chr13:52547595..52550530-chr13:52570344..52571885,2	K562	blood:
35	chr13:52570761..52572532-chr13:52599540..52601096,2	K562	blood:
36	chr13:52567202..52571172-chr13:52583807..52586943,6	K562	blood:
37	chr13:52562562..52567113-chr13:52569338..52572980,4	MCF-7	breast:
38	chr13:52550522..52553056-chr13:52572837..52575567,2	MCF-7	breast:
39	chr13:52550522..52553056-chr13:52572837..52575567,2	MCF-7	breast:
40	chr13:52572621..52575296-chr13:52579187..52581060,2	K562	blood:
41	chr13:52564916..52570042-chr13:52571727..52575592,5	MCF-7	breast:
42	chr13:52572621..52575296-chr13:52579187..52581060,2	K562	blood:
43	chr13:52575215..52575920-chr13:52599748..52600741,2	MCF-7	breast:
44	chr13:52578707..52580280-chr13:52581287..52584072,2	MCF-7	breast:
45	chr13:52388590..52390745-chr13:52574163..52575780,2	MCF-7	breast:
46	chr13:52574870..52575940-chr13:52702794..52703691,3	K562	blood:
47	chr13:52568982..52573456-chr13:52591589..52596221,4	K562	blood:
48	chr13:52573284..52575867-chr13:52579600..52581887,2	K562	blood:
49	chr13:52025684..52028500-chr13:52574540..52576324,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NEK5-2	chr13:52574442-52574608	l_851_chr13:52571540-52583296_testes
2	lnc-NEK5-2	chr13:52571541-52571827	l_851_chr13:52571540-52583296_testes

No data

Variant related genes	Relation type
ATP7B	TF binding region
ATP7B	CpG island
ENSG00000236044	chromatin interactions
ENSG00000253710	chromatin interactions
ENSG00000089022	chromatin interactions
ENSG00000248594	chromatin interactions
ENSG00000234608	chromatin interactions
ENSG00000224892	chromatin interactions
ENSG00000123191	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000197168	chromatin interactions
ENSG00000102786	chromatin interactions

Extended variants
information (count: 1365 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:1365 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1801244	chr13:52544805-52544806	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150018860	chr13:52544809-52544810	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs551602841	chr13:52544811-52544812	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186300062	chr13:52544820-52544821	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs377234918	chr13:52544857-52544858	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532864884	chr13:52544874-52544875	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs145173864	chr13:52544880-52544881	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs74087029	chr13:52544977-52544978	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs3742288	chr13:52544978-52544979	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs377550856	chr13:52544983-52544984	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs539058476	chr13:52544994-52544995	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74087030	chr13:52545038-52545039	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569208880	chr13:52545054-52545055	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538028865	chr13:52545064-52545065	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182167184	chr13:52545138-52545139	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs3825527	chr13:52545141-52545142	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs540737195	chr13:52545168-52545169	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs376732897	chr13:52545169-52545170	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145157941	chr13:52545210-52545211	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186904273	chr13:52545217-52545218	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs28368815	chr13:52545226-52545227	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs573957788	chr13:52545257-52545258	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192657928	chr13:52545326-52545327	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563189921	chr13:52545359-52545360	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183437767	chr13:52545366-52545367	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545148441	chr13:52545381-52545382	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188374327	chr13:52545402-52545403	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs76365773	chr13:52545417-52545418	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs115621455	chr13:52545420-52545421	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184375933	chr13:52545423-52545424	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs77611236	chr13:52545445-52545446	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536623270	chr13:52545469-52545470	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs7999812	chr13:52545495-52545496	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs569170678	chr13:52545503-52545504	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs189211328	chr13:52545542-52545543	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558791248	chr13:52545573-52545574	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557949245	chr13:52545671-52545672	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs377046362	chr13:52545679-52545680	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs192610154	chr13:52545684-52545685	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs183569974	chr13:52545685-52545686	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs554221463	chr13:52545690-52545691	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs541628194	chr13:52545724-52545725	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs577139446	chr13:52545737-52545738	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs79880428	chr13:52545738-52545739	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs77412455	chr13:52545752-52545753	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs189618017	chr13:52545754-52545755	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs140728501	chr13:52545839-52545840	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs181264736	chr13:52545853-52545854	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs549025077	chr13:52545882-52545883	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs143745341	chr13:52545898-52545899	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52494400-52558000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:52501000-52550400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr13:52509200-52549800	Weak transcription	Brain Substantia Nigra	brain
4	chr13:52509200-52553000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr13:52509400-52548600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr13:52513200-52553000	Weak transcription	Placenta	Placenta
7	chr13:52513400-52555400	Weak transcription	Brain Hippocampus Middle	brain
8	chr13:52516000-52548000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:52516600-52554000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr13:52516800-52555400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr13:52519400-52546000	Weak transcription	Spleen	Spleen
12	chr13:52520600-52553000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr13:52525200-52550200	Weak transcription	Fetal Brain Female	brain
14	chr13:52525400-52553000	Weak transcription	Ovary	ovary
15	chr13:52529600-52553000	Weak transcription	Psoas Muscle	Psoas
16	chr13:52530200-52555400	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr13:52530400-52549000	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr13:52530600-52550400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr13:52530800-52553000	Weak transcription	Fetal Lung	lung
20	chr13:52532800-52548200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr13:52532800-52553000	Weak transcription	Fetal Muscle Trunk	muscle
22	chr13:52534400-52555400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr13:52534600-52546000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr13:52536200-52548400	Weak transcription	Colonic Mucosa	Colon
25	chr13:52536600-52545000	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr13:52537000-52552800	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr13:52539800-52545800	Weak transcription	Right Ventricle	heart
28	chr13:52540000-52554600	Weak transcription	HSMMtube	muscle
29	chr13:52540400-52545200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
30	chr13:52540400-52550400	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr13:52541000-52553000	Weak transcription	Left Ventricle	heart
32	chr13:52541400-52554800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr13:52541600-52545000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr13:52541800-52546000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr13:52541800-52546800	Enhancers	Stomach Mucosa	stomach
36	chr13:52541800-52553000	Weak transcription	Right Atrium	heart
37	chr13:52542400-52545000	Strong transcription	Aorta	Aorta
38	chr13:52542400-52547000	Weak transcription	Esophagus	oesophagus
39	chr13:52542400-52551400	Weak transcription	Lung	lung
40	chr13:52542800-52545000	Strong transcription	Adipose Nuclei	Adipose
41	chr13:52542800-52549600	Weak transcription	Brain Germinal Matrix	brain
42	chr13:52542800-52549600	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr13:52542800-52550200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr13:52542800-52551000	Weak transcription	Fetal Muscle Leg	muscle
45	chr13:52543000-52548200	Weak transcription	Stomach Smooth Muscle	stomach
46	chr13:52543400-52546800	Genic enhancers	Fetal Intestine Small	intestine
47	chr13:52543600-52545200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr13:52543600-52545200	Enhancers	Fetal Heart	heart
49	chr13:52543600-52548000	Weak transcription	Fetal Stomach	stomach
50	chr13:52543800-52545000	Enhancers	Small Intestine	intestine

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