Variant report

Variant	nsv430570
Chromosome Location	chr13:49961137-50089844
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2015)
CpG islands
(count:2748)
Chromatin interactive
region (count:102)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50040074-50041075	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:50018824-50019531	K562	blood:	n/a	n/a
3	ARID3A	chr13:50018043-50018342	K562	blood:	n/a	n/a
4	ARID3A	chr13:49995639-49995842	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:50017884-50018589	HepG2	liver:	n/a	n/a
6	ARID3A	chr13:50038795-50039574	HepG2	liver:	n/a	n/a
7	ARID3A	chr13:50022201-50022473	K562	blood:	n/a	n/a
8	ATF2	chr13:50028547-50029303	GM12878	blood:	n/a	n/a
9	ATF2	chr13:50017722-50018650	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr13:50017921-50018315	GM12878	blood:	n/a	n/a
11	ATF2	chr13:50069871-50070277	GM12878	blood:	n/a	n/a
12	ATF2	chr13:50069823-50070213	GM12878	blood:	n/a	n/a
13	ATF2	chr13:50017799-50018696	GM12878	blood:	n/a	n/a
14	ATF2	chr13:50028627-50029260	GM12878	blood:	n/a	n/a
15	ATF2	chr13:50017524-50018660	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:50070386-50070773	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:49974206-49974216	K562	blood:	n/a	n/a
18	BATF	chr13:50033761-50033980	GM12878	blood:	n/a	n/a
19	BATF	chr13:50069852-50070221	GM12878	blood:	n/a	n/a
20	BATF	chr13:50033735-50034011	GM12878	blood:	n/a	n/a
21	BATF	chr13:50028595-50029091	GM12878	blood:	n/a	n/a
22	BATF	chr13:50069835-50070194	GM12878	blood:	n/a	n/a
23	BATF	chr13:50028580-50029122	GM12878	blood:	n/a	n/a
24	BCL11A	chr13:50069906-50070213	GM12878	blood:	n/a	n/a
25	BCL11A	chr13:50069845-50070179	GM12878	blood:	n/a	n/a
26	BCLAF1	chr13:50017854-50018762	GM12878	blood:	n/a	chr13:50018730-50018743
27	BCLAF1	chr13:50069804-50070564	GM12878	blood:	n/a	n/a
28	BCLAF1	chr13:50017479-50018901	GM12878	blood:	n/a	chr13:50018730-50018743
29	BHLHE40	chr13:49995589-49995906	HepG2	liver:	n/a	n/a
30	BHLHE40	chr13:50028754-50029257	GM12878	blood:	n/a	n/a
31	BHLHE40	chr13:50017907-50019581	K562	blood:	n/a	n/a
32	BHLHE40	chr13:50040050-50040053	HepG2	liver:	n/a	n/a
33	BHLHE40	chr13:50069894-50070748	GM12878	blood:	n/a	n/a
34	BHLHE40	chr13:50017572-50017700	HepG2	liver:	n/a	n/a
35	BHLHE40	chr13:50070022-50070675	HepG2	liver:	n/a	n/a
36	BHLHE40	chr13:49984789-49984955	GM12878	blood:	n/a	n/a
37	BHLHE40	chr13:50017924-50019861	GM12878	blood:	n/a	n/a
38	BHLHE40	chr13:50019165-50019509	A549	lung:	n/a	n/a
39	BHLHE40	chr13:50070011-50070578	K562	blood:	n/a	n/a
40	BHLHE40	chr13:50019167-50019537	HepG2	liver:	n/a	n/a
41	BRCA1	chr13:50017808-50018576	GM12878	blood:	n/a	n/a
42	BRCA1	chr13:50017958-50018595	HepG2	liver:	n/a	n/a
43	BRCA1	chr13:50017797-50019617	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr13:50017752-50018443	H1-hESC	embryonic stem cell:	n/a	n/a
45	CBX3	chr13:49978763-49979094	K562	blood:	n/a	n/a
46	CBX3	chr13:50017739-50018627	K562	blood:	n/a	n/a
47	CBX3	chr13:49978764-49979124	K562	blood:	n/a	n/a
48	CBX3	chr13:50017976-50018310	K562	blood:	n/a	n/a
49	CBX3	chr13:50037420-50037685	K562	blood:	n/a	n/a
50	CBX3	chr13:50037345-50037712	K562	blood:	n/a	n/a

(count:2748 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50070499-50070549	SK-N-SH_RA	brain:	n/a
2	chr13:50030794-50030844	AG04450	lung:	fetal
3	chr13:50070482-50070532	HepG2	liver:	n/a
4	chr13:50070499-50070549	SK-N-SH_RA	brain:	n/a
5	chr13:50030794-50030844	AG04450	lung:	fetal
6	chr13:50070482-50070532	HepG2	liver:	n/a
7	chr13:50018157-50018207	GM12878	blood:	n/a
8	chr13:50024293-50024343	BE2_C	brain:	n/a
9	chr13:50018406-50018456	K562	blood:	n/a
10	chr13:50024703-50024753	Caco-2	colon:	n/a
11	chr13:49977110-49977160	BJ	skin:	n/a
12	chr13:50070504-50070554	RPTEC	kidney:	n/a
13	chr13:50069489-50069539	GM12892	blood:	n/a
14	chr13:50070482-50070532	SK-N-SH	brain:	n/a
15	chr13:50024703-50024753	HCT-116	colon:	n/a
16	chr13:50019081-50019131	BJ	skin:	n/a
17	chr13:50070550-50070600	HIPEpiC	eye:	n/a
18	chr13:50024293-50024343	AG04450	lung:	fetal
19	chr13:50070766-50070816	AG09319	gingival:	n/a
20	chr13:50070718-50070768	HEK293	kidney:	embryo
21	chr13:49990767-49990817	SK-N-SH_RA	brain:	n/a
22	chr13:50070102-50070152	HL-60	blood:	n/a
23	chr13:50070102-50070152	HCF	heart:	n/a
24	chr13:50074189-50074239	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:50024293-50024343	Caco-2	colon:	n/a
26	chr13:49976473-49976523	HUVEC	blood vessel:	n/a
27	chr13:49990767-49990817	K562	blood:	n/a
28	chr13:50024281-50024331	SKMC	muscle:	n/a
29	chr13:50074189-50074239	AG10803	skin:	n/a
30	chr13:50018514-50018564	LNCaP	prostate:	n/a
31	chr13:50018514-50018564	MCF10A-Er-Src	breast:	n/a
32	chr13:50070499-50070549	SAEC	small airway:	n/a
33	chr13:50070045-50070095	HEEpiC	esophagus:	n/a
34	chr13:49977110-49977160	NB4	blood:	n/a
35	chr13:49990767-49990817	CMK	blood:	n/a
36	chr13:50070436-50070486	A549	lung:	n/a
37	chr13:50070504-50070554	SAEC	small airway:	n/a
38	chr13:50070045-50070095	HepG2	liver:	n/a
39	chr13:50056284-50056334	HUVEC	blood vessel:	n/a
40	chr13:49975643-49975693	HRPEpiC	eye:	n/a
41	chr13:50056284-50056334	BE2_C	brain:	n/a
42	chr13:50070436-50070486	Jurkat	blood:	n/a
43	chr13:50069509-50069559	NHBE	bronchial:	n/a
44	chr13:50070766-50070816	NB4	blood:	n/a
45	chr13:50070550-50070600	ovcar-3	ovarian:	n/a
46	chr13:49977110-49977160	ovcar-3	ovarian:	n/a
47	chr13:50014904-50014954	HCF	heart:	n/a
48	chr13:50070102-50070152	NHBE	bronchial:	n/a
49	chr13:50070520-50070570	HepG2	liver:	n/a
50	chr13:50025780-50025830	HEK293	kidney:	embryo

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr13:49875049..49876153-chr13:50010754..50011724,7	MCF-7	breast:
2	chr13:50011471..50014414-chr13:50018159..50020318,3	K562	blood:
3	chr13:50017298..50020087-chr13:50026645..50030235,3	MCF-7	breast:
4	chr13:50068585..50069355-chr13:50091395..50092213,3	MCF-7	breast:
5	chr10:75173616..75174305-chr13:50017762..50018728,2	HCT-116	colon:
6	chr13:49885803..49888221-chr13:49971631..49973979,2	MCF-7	breast:
7	chr13:49971896..49974860-chr13:49997349..49999388,2	MCF-7	breast:
8	chr13:50068457..50070652-chr13:50081260..50083175,3	MCF-7	breast:
9	chr13:49820441..49822930-chr13:50018500..50020473,2	K562	blood:
10	chr13:49961570..49963263-chr13:49972646..49974956,2	MCF-7	breast:
11	chr13:50064832..50068654-chr13:50068754..50072882,4	K562	blood:
12	chr13:50007011..50008886-chr13:50012564..50014839,2	MCF-7	breast:
13	chr13:50038863..50040866-chr13:50041548..50043299,2	K562	blood:
14	chr13:49948746..49951030-chr13:49963060..49965178,2	K562	blood:
15	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
16	chr13:50072641..50077099-chr13:50079863..50082927,4	MCF-7	breast:
17	chr13:50061212..50063170-chr13:50068743..50071652,2	MCF-7	breast:
18	chr13:50027049..50030534-chr13:50032779..50035441,4	K562	blood:
19	chr13:49978042..49980061-chr13:49981033..49983689,2	K562	blood:
20	chr13:50068795..50071791-chr13:50072712..50074851,3	K562	blood:
21	chr1:36554087..36554720-chr13:50018951..50019561,2	NB4	blood:
22	chr13:50010568..50013780-chr13:50016581..50020506,3	MCF-7	breast:
23	chr13:50071647..50073472-chr13:50180377..50183221,3	MCF-7	breast:
24	chr13:49874978..49875489-chr13:50010786..50011661,2	MCF-7	breast:
25	chr13:50019424..50021164-chr13:50065782..50068488,2	MCF-7	breast:
26	chr13:50071814..50073656-chr13:50077738..50079536,2	MCF-7	breast:
27	chr13:50045650..50047733-chr13:50190939..50192914,2	MCF-7	breast:
28	chr13:50060291..50062533-chr13:50067429..50069545,2	K562	blood:
29	chr13:50027025..50029589-chr13:50038716..50040663,2	MCF-7	breast:
30	chr13:50016992..50019784-chr13:50159235..50161344,2	K562	blood:
31	chr13:50016481..50018378-chr13:50070335..50072171,3	K562	blood:
32	chr13:49961570..49963263-chr13:49972646..49974956,2	MCF-7	breast:
33	chr13:50061212..50063170-chr13:50068743..50071652,2	MCF-7	breast:
34	chr13:50027049..50030534-chr13:50032779..50035441,4	K562	blood:
35	chr13:50020031..50021593-chr13:50030911..50032935,2	MCF-7	breast:
36	chr13:50016715..50020360-chr13:50068508..50074036,7	MCF-7	breast:
37	chr13:49874986..49875912-chr13:49995476..49996152,3	MCF-7	breast:
38	chr13:50087217..50089138-chr13:50160277..50162233,2	MCF-7	breast:
39	chr13:50029751..50032528-chr13:50034704..50037567,2	MCF-7	breast:
40	chr13:50016638..50018754-chr19:46028466..46031236,2	MCF-7	breast:
41	chr13:50086453..50086953-chr6:134694834..134695454,2	MCF-7	breast:
42	chr13:49971896..49974860-chr13:49997349..49999388,2	MCF-7	breast:
43	chr13:49875221..49876253-chr13:50010820..50011928,3	K562	blood:
44	chr13:50007202..50009372-chr13:50016314..50018307,2	K562	blood:
45	chr13:50061049..50067624-chr13:50068104..50073631,8	MCF-7	breast:
46	chr13:50086064..50088335-chr13:50090580..50092913,2	K562	blood:
47	chr13:50017253..50018810-chr16:3331703..3334184,2	MCF-7	breast:
48	chr13:50017920..50018425-chr3:127317278..127318186,2	NB4	blood:
49	chr13:50072605..50075983-chr13:50085931..50088388,3	MCF-7	breast:
50	chr13:50017638..50018206-chr6:35436122..35436718,2	NB4	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SETDB2-1	chr13:50080771-50080892	NONHSAT033746
2	lnc-AL136218.1-2	chr13:50008222-50008359	NONHSAT033741
3	lnc-AL136218.1-1	chr13:49998089-49998144	NONHSAT033742
4	lnc-SETDB2-1	chr13:50070372-50070584	NONHSAT033747
5	lnc-AL136218.1-1	chr13:49999416-49999586	NONHSAT033742
6	lnc-AL136218.1-2	chr13:50007454-50007529	NONHSAT033741
7	lnc-AL136218.1-2	chr13:49988140-49988335	NONHSAT033741
8	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033746
9	lnc-PHF11-2	chr13:50019689-50020088	NONHSAT033744
10	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033747
11	lnc-AL136218.1-1	chr13:49999345-49999351	NONHSAT033743
12	lnc-AL136218.1-2	chr13:49975269-49975406	NONHSAT033740
13	lnc-SETDB2-1	chr13:50070120-50070231	NONHSAT033746
14	lnc-SETDB2-1	chr13:50087195-50087302	NONHSAT033747
15	lnc-AL136218.1-2	chr13:49975531-49975723	NONHSAT033740
16	lnc-PHF11-1	chr13:50063383-50063500	NONHSAT033745
17	lnc-AL136218.1-2	chr13:50018122-50018200	NONHSAT033741
18	lnc-SETDB2-1	chr13:50087195-50087302	NONHSAT033746
19	lnc-AL136218.1-2	chr13:49987048-49987176	NONHSAT033740
20	lnc-AL136218.1-1	chr13:49999396-49999977	NONHSAT033743
21	lnc-AL136218.1-2	chr13:49975632-49975723	NONHSAT033741
22	lnc-PHF11-1	chr13:50063106-50063206	NONHSAT033745
23	lnc-AL136218.1-1	chr13:49993070-49993573	NONHSAT033742
24	lnc-PHF11-2	chr13:50018820-50018993	NONHSAT033744

No data

Variant related genes	Relation type
PHF11	TF binding region
CAB39L	TF binding region
SETDB2	TF binding region
SNRPGP14	TF binding region
ENSG00000215462	TF binding region
PHF11	CpG island
CAB39L	CpG island
SETDB2	CpG island
SNRPGP14	CpG island
ENSG00000215462	CpG island
ENSG00000073111	chromatin interactions
ENSG00000136147	chromatin interactions
ENSG00000116863	chromatin interactions
ENSG00000125753	chromatin interactions
ENSG00000136169	chromatin interactions
ENSG00000215462	chromatin interactions
ENSG00000138279	chromatin interactions
ENSG00000236577	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000198755	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000199788	chromatin interactions
ENSG00000136144	chromatin interactions
ENSG00000102543	chromatin interactions
ENSG00000017797	chromatin interactions
ENSG00000006194	chromatin interactions
ENSG00000102547	chromatin interactions

Extended variants
information (count: 4456 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:4456 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13378690	chr13:49961137-49961138	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545431943	chr13:49961176-49961177	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs13378689	chr13:49961252-49961253	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs79479699	chr13:49961257-49961258	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs74072556	chr13:49961299-49961300	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs563234949	chr13:49961326-49961327	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568385274	chr13:49961349-49961350	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs530673761	chr13:49961393-49961394	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs115328669	chr13:49961408-49961409	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565433686	chr13:49961451-49961452	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs71216546	chr13:49961536-49961537	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs112966388	chr13:49961537-49961538	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12716689	chr13:49961538-49961539	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs141944174	chr13:49961550-49961551	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs536222773	chr13:49961564-49961565	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs12716690	chr13:49961568-49961569	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs570042326	chr13:49961615-49961616	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs13378702	chr13:49961625-49961626	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs181851726	chr13:49961644-49961645	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs558786456	chr13:49961712-49961713	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs187269876	chr13:49961789-49961790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs57278686	chr13:49961802-49961803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542513708	chr13:49961871-49961872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs199873931	chr13:49961898-49961899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61399188	chr13:49961906-49961907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9535220	chr13:49961960-49961961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs553283450	chr13:49962002-49962003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574832728	chr13:49962032-49962033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs541452531	chr13:49962045-49962046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs139993786	chr13:49962078-49962079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575136247	chr13:49962079-49962080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190452038	chr13:49962156-49962157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546015956	chr13:49962165-49962166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371617706	chr13:49962166-49962167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs375814452	chr13:49962203-49962204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369241634	chr13:49962204-49962205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs180714992	chr13:49962215-49962216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532549328	chr13:49962242-49962243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185598120	chr13:49962294-49962295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9535221	chr13:49962316-49962317	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs559613017	chr13:49962390-49962391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs11839534	chr13:49962393-49962394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185970544	chr13:49962405-49962406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548610444	chr13:49962407-49962408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9526551	chr13:49962409-49962410	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs9526552	chr13:49962416-49962417	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs9535222	chr13:49962452-49962453	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs149841903	chr13:49962584-49962585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534810305	chr13:49962709-49962710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553246723	chr13:49962717-49962718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

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
Breast cancer	17899364	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
Alveolar rhabdomyosarcoma	16790082	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
Chronic lymphocytic leukemia	21670202	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
Congenital anomalies of the kidney and urinary tract	20467480	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
Chronic myeloid leukemia	21384125	CNVD
Sezary syndrome	18413736	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21990379	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Alcoholism	21790672	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3318 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49945200-49973000	Weak transcription	Brain Substantia Nigra	brain
2	chr13:49946800-49961400	Weak transcription	Brain Hippocampus Middle	brain
3	chr13:49946800-49961400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr13:49946800-49962600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr13:49946800-49964000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:49948200-49961200	Weak transcription	Brain Angular Gyrus	brain
7	chr13:49948200-49961600	Weak transcription	Ovary	ovary
8	chr13:49949200-49961200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr13:49949200-49971200	Weak transcription	Rectal Smooth Muscle	rectum
10	chr13:49950800-49961600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr13:49951200-49961200	Weak transcription	Brain Anterior Caudate	brain
12	chr13:49960800-49961400	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
13	chr13:49960800-49961600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr13:49960800-49961600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:49961000-49961200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
16	chr13:49961000-49961400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
17	chr13:49961000-49961400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
18	chr13:49961000-49961400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr13:49961000-49961400	Enhancers	Colon Smooth Muscle	Colon
20	chr13:49961000-49961400	Enhancers	K562	blood
21	chr13:49961000-49961600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr13:49961000-49961600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr13:49961000-49961800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:49961000-49962600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr13:49961200-49961400	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr13:49961200-49961600	Enhancers	Brain Anterior Caudate	brain
27	chr13:49961200-49961800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr13:49961200-49961800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr13:49961200-49962200	Enhancers	Brain Angular Gyrus	brain
30	chr13:49961200-49962200	Enhancers	Fetal Heart	heart
31	chr13:49961200-49962400	Enhancers	Hela-S3	cervix
32	chr13:49961400-49962000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr13:49961400-49962200	Enhancers	Brain Hippocampus Middle	brain
34	chr13:49961400-49964400	Weak transcription	Colon Smooth Muscle	Colon
35	chr13:49961600-49961800	Enhancers	Ovary	ovary
36	chr13:49962000-49962400	Enhancers	NHLF	lung
37	chr13:49962000-49962600	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr13:49962400-49962800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr13:49962600-49962800	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr13:49962600-49963200	Enhancers	Stomach Smooth Muscle	stomach
41	chr13:49963200-49969600	Weak transcription	Stomach Smooth Muscle	stomach
42	chr13:49964000-49964200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr13:49964400-49965400	Enhancers	Colon Smooth Muscle	Colon
44	chr13:49965400-49969600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr13:49965400-49969600	Weak transcription	Colon Smooth Muscle	Colon
46	chr13:49967200-49967400	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr13:49967400-49973600	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr13:49969400-49970200	Enhancers	Aorta	Aorta
49	chr13:49969600-49970000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr13:49969600-49970400	Enhancers	Osteobl	bone

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