Variant report

Variant	nsv1037350
Chromosome Location	chr13:51272518-51447354
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:919)
CpG islands
(count:1345)
Chromatin interactive
region (count:25)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51375519-51375780	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:51274196-51274450	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:51404184-51404321	HepG2	liver:	n/a	n/a
4	ATF1	chr13:51313105-51313545	K562	blood:	n/a	n/a
5	ATF2	chr13:51384920-51385573	GM12878	blood:	n/a	n/a
6	ATF3	chr13:51370719-51370856	K562	blood:	n/a	chr13:51370772-51370781
7	BACH1	chr13:51417128-51417648	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr13:51405645-51405949	GM12878	blood:	n/a	chr13:51405822-51405833
9	BCLAF1	chr13:51385013-51385619	GM12878	blood:	n/a	chr13:51385395-51385404
10	BCLAF1	chr13:51375218-51375887	GM12878	blood:	n/a	n/a
11	BCLAF1	chr13:51385061-51385558	GM12878	blood:	n/a	chr13:51385395-51385404
12	BHLHE40	chr13:51385120-51385486	GM12878	blood:	n/a	n/a
13	BHLHE40	chr13:51375054-51375061	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:51375493-51375693	HepG2	liver:	n/a	n/a
15	CEBPB	chr13:51404081-51404357	IMR90	lung:	n/a	chr13:51404248-51404261 chr13:51404249-51404260
16	CEBPB	chr13:51283223-51283473	K562	blood:	n/a	chr13:51283352-51283363
17	CEBPB	chr13:51383389-51383649	HepG2	liver:	n/a	chr13:51383531-51383544 chr13:51383531-51383544 chr13:51383533-51383544 chr13:51383533-51383544 chr13:51383531-51383542
18	CEBPB	chr13:51288169-51288243	A549	lung:	n/a	chr13:51288178-51288189
19	CEBPB	chr13:51288049-51288417	IMR90	lung:	n/a	chr13:51288178-51288189
20	CEBPB	chr13:51381665-51381802	A549	lung:	n/a	chr13:51381700-51381713 chr13:51381700-51381711
21	CEBPB	chr13:51418588-51418589	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr13:51375457-51375775	HepG2	liver:	n/a	n/a
23	CEBPB	chr13:51404057-51404453	Hela-S3	cervix:	n/a	chr13:51404248-51404261 chr13:51404249-51404260
24	CEBPB	chr13:51404118-51404381	A549	lung:	n/a	chr13:51404248-51404261 chr13:51404249-51404260
25	CEBPB	chr13:51370602-51370661	A549	lung:	n/a	n/a
26	CEBPB	chr13:51288176-51288420	K562	blood:	n/a	chr13:51288178-51288189
27	CEBPB	chr13:51283298-51283495	HepG2	liver:	n/a	chr13:51283352-51283363
28	CEBPB	chr13:51404082-51404431	HepG2	liver:	n/a	chr13:51404248-51404261 chr13:51404249-51404260
29	CEBPB	chr13:51288094-51288355	HepG2	liver:	n/a	chr13:51288178-51288189
30	CEBPB	chr13:51283160-51283482	HCT-116	colon:	n/a	chr13:51283352-51283363
31	CEBPB	chr13:51416806-51416947	HepG2	liver:	n/a	chr13:51416887-51416898
32	CHD1	chr13:51385193-51385446	GM12878	blood:	n/a	n/a
33	CHD1	chr13:51305579-51305897	GM12878	blood:	n/a	n/a
34	CHD2	chr13:51417715-51418316	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr13:51385115-51385647	GM12878	blood:	n/a	n/a
36	CTBP2	chr13:51417099-51418470	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr13:51380160-51380310	BJ	skin:	n/a	n/a
38	CTCF	chr13:51397501-51397574	GM13976	blood:	n/a	n/a
39	CTCF	chr13:51375432-51375874	H1-hESC	embryonic stem cell:	n/a	chr13:51375643-51375664
40	CTCF	chr13:51375640-51375790	HAc	cerebellar:	n/a	chr13:51375643-51375664
41	CTCF	chr13:51441220-51441370	HEK293	kidney:	n/a	n/a
42	CTCF	chr13:51288340-51288490	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr13:51337020-51337170	GM06990	blood:	n/a	chr13:51337079-51337097
44	CTCF	chr13:51375580-51375730	GM12872	blood:	n/a	chr13:51375643-51375664
45	CTCF	chr13:51380004-51380247	GM12878	blood:	n/a	n/a
46	CTCF	chr13:51319800-51319950	BE2_C	brain:	n/a	chr13:51319905-51319914
47	CTCF	chr13:51375600-51375750	GM12868	blood:	n/a	chr13:51375643-51375664
48	CTCF	chr13:51375565-51375772	Hela-S3	cervix:	n/a	chr13:51375643-51375664
49	CTCF	chr13:51275738-51275752	ProgFib	skin:	n/a	n/a
50	CTCF	chr13:51379980-51380130	WI-38	lung:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51353941-51353991	HIPEpiC	eye:	n/a
2	chr13:51375420-51375470	SK-N-SH_RA	brain:	n/a
3	chr13:51417469-51417519	GM12892	blood:	n/a
4	chr13:51353941-51353991	HIPEpiC	eye:	n/a
5	chr13:51375420-51375470	SK-N-SH_RA	brain:	n/a
6	chr13:51417469-51417519	GM12892	blood:	n/a
7	chr13:51418020-51418070	HL-60	blood:	n/a
8	chr13:51326803-51326853	ovcar-3	ovarian:	n/a
9	chr13:51418092-51418142	HIPEpiC	eye:	n/a
10	chr13:51418221-51418271	SKMC	muscle:	n/a
11	chr13:51417686-51417736	SKMC	muscle:	n/a
12	chr13:51418221-51418271	GM19239	blood:	n/a
13	chr13:51417846-51417896	NHBE	bronchial:	n/a
14	chr13:51326803-51326853	AG09319	gingival:	n/a
15	chr13:51381934-51381984	Jurkat	blood:	n/a
16	chr13:51417929-51417979	BE2_C	brain:	n/a
17	chr13:51326803-51326853	LNCaP	prostate:	n/a
18	chr13:51417929-51417979	NHBE	bronchial:	n/a
19	chr13:51353941-51353991	CMK	blood:	n/a
20	chr13:51418053-51418103	HUVEC	blood vessel:	n/a
21	chr13:51375420-51375470	AG09319	gingival:	n/a
22	chr13:51418221-51418271	HMEC	breast:	n/a
23	chr13:51418092-51418142	LNCaP	prostate:	n/a
24	chr13:51381839-51381889	NHBE	bronchial:	n/a
25	chr13:51414275-51414325	HCF	heart:	n/a
26	chr13:51381934-51381984	HepG2	liver:	n/a
27	chr13:51353941-51353991	HEK293	kidney:	embryo
28	chr13:51417977-51418027	Caco-2	colon:	n/a
29	chr13:51416749-51416799	LNCaP	prostate:	n/a
30	chr13:51416639-51416689	K562	blood:	n/a
31	chr13:51326803-51326853	NHDF-neo	bronchial:	n/a
32	chr13:51421269-51421319	K562	blood:	n/a
33	chr13:51417977-51418027	Hepatocyte	liver:	n/a
34	chr13:51418614-51418664	HCPEpiC	choroid plexus:	n/a
35	chr13:51375420-51375470	SKMC	muscle:	n/a
36	chr13:51418041-51418091	HL-60	blood:	n/a
37	chr13:51381839-51381889	AG10803	skin:	n/a
38	chr13:51417686-51417736	NT2-D1	testis:	n/a
39	chr13:51414275-51414325	HIPEpiC	eye:	n/a
40	chr13:51417846-51417896	ovcar-3	ovarian:	n/a
41	chr13:51416749-51416799	NHBE	bronchial:	n/a
42	chr13:51417977-51418027	HMEC	breast:	n/a
43	chr13:51418041-51418091	HEK293	kidney:	embryo
44	chr13:51417977-51418027	HNPCEpiC	eye:	n/a
45	chr13:51418092-51418142	SK-N-MC	brain:	n/a
46	chr13:51414275-51414325	GM12878	blood:	n/a
47	chr13:51417923-51417973	GM12891	blood:	n/a
48	chr13:51361994-51362044	LNCaP	prostate:	n/a
49	chr13:51416639-51416689	MCF10A-Er-Src	breast:	n/a
50	chr13:51326803-51326853	BJ	skin:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:51330144..51332927-chr13:51336662..51340363,3	MCF-7	breast:
2	chr13:51276998..51279149-chr13:51301224..51304150,2	K562	blood:
3	chr13:51298771..51301176-chr13:51301369..51304366,2	K562	blood:
4	chr13:51309482..51311809-chr13:51312574..51314678,2	MCF-7	breast:
5	chr13:50509886..50512507-chr13:51369827..51372761,2	MCF-7	breast:
6	chr13:51271422..51272928-chr13:51274925..51277429,2	K562	blood:
7	chr13:51411222..51413606-chr13:51414748..51417656,3	K562	blood:
8	chr13:51401520..51403421-chr13:51482404..51485271,2	MCF-7	breast:
9	chr13:50549935..50550921-chr13:51375357..51376443,3	K562	blood:
10	chr13:51330144..51332927-chr13:51336662..51340363,3	MCF-7	breast:
11	chr13:51411222..51413606-chr13:51414748..51417656,3	K562	blood:
12	chr13:50744261..50745564-chr13:51379576..51380194,3	MCF-7	breast:
13	chr12:82971566..82972433-chr13:51277425..51278166,2	MCF-7	breast:
14	chr13:51353458..51355441-chr13:51357181..51360029,2	MCF-7	breast:
15	chr13:50509009..50510772-chr13:51377519..51380149,2	MCF-7	breast:
16	chr13:51353458..51355441-chr13:51357181..51360029,2	MCF-7	breast:
17	chr13:51271422..51272928-chr13:51274925..51277429,2	K562	blood:
18	chr13:51288784..51290859-chr13:51363482..51364986,2	MCF-7	breast:
19	chr13:51309482..51311809-chr13:51312574..51314678,2	MCF-7	breast:
20	chr13:51444050..51446783-chr13:51482621..51484438,2	K562	blood:
21	chr13:50699832..50701606-chr13:51373165..51375472,2	MCF-7	breast:
22	chr13:51370732..51372602-chr13:51373640..51375696,2	MCF-7	breast:
23	chr13:51276998..51279149-chr13:51301224..51304150,2	K562	blood:
24	chr13:51298771..51301176-chr13:51301369..51304366,2	K562	blood:
25	chr13:51370732..51372602-chr13:51373640..51375696,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNASEH2B-1	chr13:51414164-51414230	ENSG00000237152.2
2	lnc-RNASEH2B-1	chr13:51381992-51382122	ENSG00000237152.1
3	lnc-DLEU7-4	chr13:51289562-51289619	NONHSAT033864
4	lnc-RNASEH2B-1	chr13:51392657-51392728	ENSG00000237152.2
5	lnc-RNASEH2B-1	chr13:51422673-51424041	NONHSAT033866
6	lnc-RNASEH2B-1	chr13:51382676-51382843	ENSG00000237152.1
7	lnc-DLEU7-4	chr13:51285144-51287376	NONHSAT033864
8	lnc-RNASEH2B-1	chr13:51422673-51423190	ENSG00000237152.2
9	lnc-RNASEH2B-5	chr13:51280047-51280235	l_845_chr13:51276687-51285368_prostate
10	lnc-RNASEH2B-1	chr13:51422673-51423145	ENSG00000237152.1
11	lnc-RNASEH2B-5	chr13:51278974-51279337	l_845_chr13:51276687-51285368_prostate
12	lnc-RNASEH2B-3	chr13:51297275-51297372	NONHSAT033843
13	lnc-RNASEH2B-5	chr13:51276688-51276938	l_845_chr13:51276687-51285368_prostate
14	lnc-RNASEH2B-1	chr13:51382676-51382842	NONHSAT033866
15	lnc-RNASEH2B-1	chr13:51392657-51392728	NONHSAT033866
16	lnc-RNASEH2B-5	chr13:51285294-51285955	l_845_chr13:51276687-51285368_prostate
17	lnc-RNASEH2B-1	chr13:51382676-51382842	ENSG00000237152.2
18	lnc-RNASEH2B-1	chr13:51381992-51382122	ENSG00000237152.2
19	lnc-RNASEH2B-3	chr13:51293783-51293846	NONHSAT033843
20	lnc-RNASEH2B-1	chr13:51414164-51414230	NONHSAT033866
21	lnc-RNASEH2B-1	chr13:51414093-51414230	ENSG00000237152.1
22	lnc-RNASEH2B-1	chr13:51381991-51382122	NONHSAT033866
23	lnc-RNASEH2B-4	chr13:51287754-51289476	NONHSAT033865

No data

Variant related genes	Relation type
RNA5SP28	TF binding region
DLEU7-AS1	TF binding region
DLEU7	TF binding region
RNA5SP28	CpG island
DLEU7-AS1	CpG island
DLEU7	CpG island
ENSG00000123178	chromatin interactions
ENSG00000186047	chromatin interactions
ENSG00000136104	chromatin interactions
ENSG00000233672	chromatin interactions
ENSG00000231607	chromatin interactions

Extended variants
information (count: 5994 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:5994 , 50 per page) page: 1 2 3 4 5 6 7 ... 120

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2794462	chr13:51272518-51272519	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530640137	chr13:51272557-51272558	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs577603363	chr13:51272581-51272582	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs373102555	chr13:51272584-51272585	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs116340759	chr13:51272631-51272632	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs530278192	chr13:51272678-51272679	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs550325629	chr13:51272690-51272691	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs182935370	chr13:51272704-51272705	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs563755117	chr13:51272717-51272718	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs530854267	chr13:51272729-51272730	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs187572836	chr13:51272749-51272750	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs115633635	chr13:51272775-51272776	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs532840144	chr13:51272777-51272778	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs78913981	chr13:51272796-51272797	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs71744730	chr13:51272892-51272893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532458481	chr13:51272905-51272906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377664134	chr13:51272906-51272907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs797500	chr13:51272907-51272908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202054779	chr13:51272925-51272926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370013719	chr13:51272926-51272927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs797501	chr13:51272927-51272928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148387159	chr13:51272932-51272933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546463711	chr13:51272990-51272991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568181113	chr13:51272992-51272993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12862495	chr13:51273198-51273199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2706236	chr13:51273204-51273205	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370665114	chr13:51273243-51273244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2812232	chr13:51273245-51273246	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs368970580	chr13:51273246-51273247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535758906	chr13:51273249-51273250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs192476181	chr13:51273287-51273288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557771517	chr13:51273310-51273311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573156140	chr13:51273323-51273324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76130578	chr13:51273579-51273580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs706595	chr13:51273586-51273587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183906727	chr13:51273587-51273588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574937184	chr13:51273624-51273625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111333539	chr13:51273670-51273671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542406391	chr13:51273672-51273673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs549674258	chr13:51273743-51273744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144716895	chr13:51273776-51273777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188445980	chr13:51273805-51273806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544225313	chr13:51273856-51273857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs181257413	chr13:51273859-51273860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545819895	chr13:51273918-51273919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs564159776	chr13:51273928-51273929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs56175265	chr13:51274015-51274016	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs55721940	chr13:51274016-51274017	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs568300899	chr13:51274093-51274094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529123196	chr13:51274102-51274103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

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
Trisomy	24170809	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
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	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
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1458 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51265200-51275600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr13:51266000-51274600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr13:51268200-51274800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:51268400-51272600	Weak transcription	Stomach Mucosa	stomach
5	chr13:51268400-51274200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr13:51268400-51277200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr13:51268600-51273600	Weak transcription	HSMM	muscle
8	chr13:51268600-51273800	Weak transcription	HSMMtube	muscle
9	chr13:51268600-51274200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr13:51268600-51274400	Weak transcription	NHDF-Ad	bronchial
11	chr13:51268800-51273800	Weak transcription	Fetal Intestine Large	intestine
12	chr13:51268800-51274600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr13:51269400-51296800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr13:51270600-51272800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr13:51270600-51272800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr13:51270600-51272800	Enhancers	Fetal Muscle Leg	muscle
17	chr13:51270600-51272800	Enhancers	Left Ventricle	heart
18	chr13:51270600-51272800	Enhancers	Psoas Muscle	Psoas
19	chr13:51270600-51276200	Enhancers	Fetal Heart	heart
20	chr13:51270800-51275000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr13:51271000-51274600	Weak transcription	Aorta	Aorta
22	chr13:51271400-51272600	Enhancers	Adipose Nuclei	Adipose
23	chr13:51271600-51272800	Enhancers	Brain Substantia Nigra	brain
24	chr13:51271600-51272800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr13:51271800-51272600	Enhancers	Primary T cells from cord blood	blood
26	chr13:51271800-51272800	Enhancers	Dnd41	blood
27	chr13:51271800-51272800	Enhancers	HMEC	breast
28	chr13:51271800-51273000	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr13:51271800-51281800	Weak transcription	Lung	lung
30	chr13:51272000-51272800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr13:51272000-51272800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr13:51272000-51272800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr13:51272000-51272800	Enhancers	Fetal Intestine Small	intestine
34	chr13:51272000-51272800	Enhancers	Fetal Thymus	thymus
35	chr13:51272000-51272800	Enhancers	NH-A	brain
36	chr13:51272200-51272600	Enhancers	Fetal Brain Female	brain
37	chr13:51272200-51272800	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr13:51272200-51272800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr13:51272200-51272800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr13:51272200-51272800	Enhancers	Brain Anterior Caudate	brain
41	chr13:51272200-51272800	Enhancers	Right Ventricle	heart
42	chr13:51272200-51272800	Flanking Active TSS	HUVEC	blood vessel
43	chr13:51272200-51272800	Enhancers	NHEK	skin
44	chr13:51272400-51272800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr13:51272400-51272800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr13:51272400-51272800	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr13:51272400-51272800	Enhancers	Brain Cingulate Gyrus	brain
48	chr13:51272400-51272800	Enhancers	Brain Hippocampus Middle	brain
49	chr13:51272400-51272800	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr13:51272400-51272800	Enhancers	Fetal Lung	lung

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