Variant report

Variant	nsv561613
Chromosome Location	chr13:50013622-50086266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1589)
CpG islands
(count:2384)
Chromatin interactive
region (count:79)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:50022201-50022473	K562	blood:	n/a	n/a
2	ARID3A	chr13:50038795-50039574	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:50017884-50018589	HepG2	liver:	n/a	n/a
4	ARID3A	chr13:50040074-50041075	HepG2	liver:	n/a	n/a
5	ARID3A	chr13:50018043-50018342	K562	blood:	n/a	n/a
6	ARID3A	chr13:50018824-50019531	K562	blood:	n/a	n/a
7	ATF2	chr13:50028627-50029260	GM12878	blood:	n/a	n/a
8	ATF2	chr13:50017722-50018650	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr13:50028547-50029303	GM12878	blood:	n/a	n/a
10	ATF2	chr13:50017524-50018660	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr13:50069823-50070213	GM12878	blood:	n/a	n/a
12	ATF2	chr13:50069871-50070277	GM12878	blood:	n/a	n/a
13	ATF2	chr13:50017921-50018315	GM12878	blood:	n/a	n/a
14	ATF2	chr13:50017799-50018696	GM12878	blood:	n/a	n/a
15	BACH1	chr13:50070386-50070773	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr13:50033735-50034011	GM12878	blood:	n/a	n/a
17	BATF	chr13:50069835-50070194	GM12878	blood:	n/a	n/a
18	BATF	chr13:50028595-50029091	GM12878	blood:	n/a	n/a
19	BATF	chr13:50028580-50029122	GM12878	blood:	n/a	n/a
20	BATF	chr13:50033761-50033980	GM12878	blood:	n/a	n/a
21	BATF	chr13:50069852-50070221	GM12878	blood:	n/a	n/a
22	BCL11A	chr13:50069845-50070179	GM12878	blood:	n/a	n/a
23	BCL11A	chr13:50069906-50070213	GM12878	blood:	n/a	n/a
24	BCLAF1	chr13:50017479-50018901	GM12878	blood:	n/a	chr13:50018730-50018743
25	BCLAF1	chr13:50017854-50018762	GM12878	blood:	n/a	chr13:50018730-50018743
26	BCLAF1	chr13:50069804-50070564	GM12878	blood:	n/a	n/a
27	BHLHE40	chr13:50019167-50019537	HepG2	liver:	n/a	n/a
28	BHLHE40	chr13:50040050-50040053	HepG2	liver:	n/a	n/a
29	BHLHE40	chr13:50019165-50019509	A549	lung:	n/a	n/a
30	BHLHE40	chr13:50070011-50070578	K562	blood:	n/a	n/a
31	BHLHE40	chr13:50017907-50019581	K562	blood:	n/a	n/a
32	BHLHE40	chr13:50017572-50017700	HepG2	liver:	n/a	n/a
33	BHLHE40	chr13:50017924-50019861	GM12878	blood:	n/a	n/a
34	BHLHE40	chr13:50069894-50070748	GM12878	blood:	n/a	n/a
35	BHLHE40	chr13:50070022-50070675	HepG2	liver:	n/a	n/a
36	BHLHE40	chr13:50028754-50029257	GM12878	blood:	n/a	n/a
37	BRCA1	chr13:50017808-50018576	GM12878	blood:	n/a	n/a
38	BRCA1	chr13:50017752-50018443	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr13:50017797-50019617	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr13:50017958-50018595	HepG2	liver:	n/a	n/a
41	CBX3	chr13:50017976-50018310	K562	blood:	n/a	n/a
42	CBX3	chr13:50017739-50018627	K562	blood:	n/a	n/a
43	CBX3	chr13:50037420-50037685	K562	blood:	n/a	n/a
44	CBX3	chr13:50037375-50037753	HCT-116	colon:	n/a	n/a
45	CBX3	chr13:50037345-50037712	K562	blood:	n/a	n/a
46	CCNT2	chr13:50069986-50070520	K562	blood:	n/a	n/a
47	CCNT2	chr13:50018091-50019133	K562	blood:	n/a	chr13:50018752-50018761
48	CEBPB	chr13:50056604-50056893	IMR90	lung:	n/a	n/a
49	CEBPB	chr13:50039217-50039524	IMR90	lung:	n/a	n/a
50	CEBPB	chr13:50017986-50018199	HepG2	liver:	n/a	n/a

(count:2384 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:50019081-50019131	HL-60	blood:	n/a
2	chr13:50069705-50069755	A549	lung:	n/a
3	chr13:50018636-50018686	Jurkat	blood:	n/a
4	chr13:50070499-50070549	GM06990	blood:	n/a
5	chr13:50069705-50069755	HRE	kidney:	n/a
6	chr13:50019081-50019131	HL-60	blood:	n/a
7	chr13:50069705-50069755	A549	lung:	n/a
8	chr13:50018636-50018686	Jurkat	blood:	n/a
9	chr13:50070499-50070549	GM06990	blood:	n/a
10	chr13:50069705-50069755	HRE	kidney:	n/a
11	chr13:50070436-50070486	AG04450	lung:	fetal
12	chr13:50018636-50018686	GM19239	blood:	n/a
13	chr13:50018171-50018221	HCM	heart:	n/a
14	chr13:50070102-50070152	PFSK-1	brain:	n/a
15	chr13:50018359-50018409	HCF	heart:	n/a
16	chr13:50070482-50070532	HRPEpiC	eye:	n/a
17	chr13:50070550-50070600	T-47D	breast:	n/a
18	chr13:50021335-50021385	PFSK-1	brain:	n/a
19	chr13:50018409-50018459	HCF	heart:	n/a
20	chr13:50069705-50069755	HAEpiC	amniotic membrane:	n/a
21	chr13:50024703-50024753	MCF-7	breast:	n/a
22	chr13:50069509-50069559	Caco-2	colon:	n/a
23	chr13:50070499-50070549	PANC-1	pancreas:	n/a
24	chr13:50018044-50018094	HEK293	kidney:	embryo
25	chr13:50070766-50070816	H1-hESC	embryonic stem cell:	embryo
26	chr13:50074189-50074239	HCM	heart:	n/a
27	chr13:50018355-50018405	HNPCEpiC	eye:	n/a
28	chr13:50074189-50074239	Caco-2	colon:	n/a
29	chr13:50018359-50018409	HMEC	breast:	n/a
30	chr13:50018531-50018581	K562	blood:	n/a
31	chr13:50070436-50070486	BJ	skin:	n/a
32	chr13:50069722-50069772	A549	lung:	n/a
33	chr13:50018171-50018221	U87	brain:	n/a
34	chr13:50069509-50069559	AG04450	lung:	fetal
35	chr13:50070499-50070549	AG09319	gingival:	n/a
36	chr13:50070504-50070554	HepG2	liver:	n/a
37	chr13:50024293-50024343	SAEC	small airway:	n/a
38	chr13:50070436-50070486	NT2-D1	testis:	n/a
39	chr13:50018355-50018405	SAEC	small airway:	n/a
40	chr13:50018171-50018221	A549	lung:	n/a
41	chr13:50070550-50070600	AG04449	skin:	fetal
42	chr13:50070499-50070549	HRE	kidney:	n/a
43	chr13:50069722-50069772	MCF-7	breast:	n/a
44	chr13:50070504-50070554	U87	brain:	n/a
45	chr13:50018359-50018409	K562	blood:	n/a
46	chr13:50070718-50070768	Jurkat	blood:	n/a
47	chr13:50018355-50018405	Hela-S3	cervix:	n/a
48	chr13:50019081-50019131	HMEC	breast:	n/a
49	chr13:50018359-50018409	AG04449	skin:	fetal
50	chr13:50025780-50025830	HCM	heart:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:50027049..50030534-chr13:50032779..50035441,4	K562	blood:
2	chr13:50045650..50047733-chr13:50190939..50192914,2	MCF-7	breast:
3	chr13:50071814..50073656-chr13:50077738..50079536,2	MCF-7	breast:
4	chr13:50022863..50025187-chr13:50116857..50119478,2	K562	blood:
5	chr13:50061049..50067624-chr13:50068104..50073631,8	MCF-7	breast:
6	chr13:50038641..50040451-chr13:50143314..50145864,2	MCF-7	breast:
7	chr13:50017298..50020087-chr13:50026645..50030235,3	MCF-7	breast:
8	chr13:50068064..50069672-chr13:50174689..50176260,2	MCF-7	breast:
9	chr13:50029751..50032528-chr13:50034704..50037567,2	MCF-7	breast:
10	chr13:50085860..50087945-chr13:50089850..50091816,2	MCF-7	breast:
11	chr13:50016715..50020360-chr13:50068508..50074036,7	MCF-7	breast:
12	chr13:49820441..49822930-chr13:50018500..50020473,2	K562	blood:
13	chr13:50068457..50070652-chr13:50081260..50083175,3	MCF-7	breast:
14	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
15	chr13:50022438..50024030-chr13:50027384..50029296,2	MCF-7	breast:
16	chr13:49820702..49823407-chr13:50017509..50020339,3	MCF-7	breast:
17	chr10:75173616..75174305-chr13:50017762..50018728,2	HCT-116	colon:
18	chr13:50072641..50077099-chr13:50079863..50082927,4	MCF-7	breast:
19	chr13:50016440..50019751-chr13:50141127..50144444,4	MCF-7	breast:
20	chr13:50070028..50071869-chr13:50072608..50075376,5	MCF-7	breast:
21	chr13:50019424..50021164-chr13:50065782..50068488,2	MCF-7	breast:
22	chr13:50016481..50018378-chr13:50070335..50072171,3	K562	blood:
23	chr13:50016508..50019619-chr13:50158297..50162493,5	MCF-7	breast:
24	chr13:50017253..50018810-chr16:3331703..3334184,2	MCF-7	breast:
25	chr13:50020071..50022197-chr13:50067941..50070115,2	K562	blood:
26	chr13:50016483..50020444-chr13:50068529..50072853,4	MCF-7	breast:
27	chr13:50060291..50062533-chr13:50067429..50069545,2	K562	blood:
28	chr13:50016715..50020360-chr13:50068508..50074036,7	MCF-7	breast:
29	chr13:50064832..50068654-chr13:50068754..50072882,4	K562	blood:
30	chr13:50071845..50075663-chr13:50092471..50095842,3	K562	blood:
31	chr13:50020464..50022245-chr13:50034255..50036825,2	K562	blood:
32	chr13:50063834..50065648-chr13:50067086..50070077,2	MCF-7	breast:
33	chr13:50068585..50069355-chr13:50091395..50092213,3	MCF-7	breast:
34	chr13:50086064..50088335-chr13:50090580..50092913,2	K562	blood:
35	chr13:50016483..50020444-chr13:50068529..50072853,4	MCF-7	breast:
36	chr13:50072641..50077099-chr13:50079863..50082927,4	MCF-7	breast:
37	chr13:50033311..50035354-chr13:50074002..50076664,2	MCF-7	breast:
38	chr13:50017920..50018425-chr3:127317278..127318186,2	NB4	blood:
39	chr13:50069004..50071273-chr13:50075738..50077658,2	MCF-7	breast:
40	chr13:50071647..50073472-chr13:50180377..50183221,3	MCF-7	breast:
41	chr13:50016895..50018613-chr13:50024420..50026981,2	MCF-7	breast:
42	chr13:50038863..50040866-chr13:50041548..50043299,2	K562	blood:
43	chr13:49993633..49996417-chr13:50068251..50070383,2	K562	blood:
44	chr13:50061212..50063170-chr13:50068743..50071652,2	MCF-7	breast:
45	chr13:50018375..50018943-chr9:33025160..33025792,2	NB4	blood:
46	chr13:50071814..50073656-chr13:50077738..50079536,2	MCF-7	breast:
47	chr13:50018060..50018635-chr18:9475189..9475739,2	NB4	blood:
48	chr13:50027025..50029589-chr13:50038716..50040663,2	MCF-7	breast:
49	chr13:50016638..50018754-chr19:46028466..46031236,2	MCF-7	breast:
50	chr13:50068906..50071236-chr13:50159028..50161203,3	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SETDB2-1	chr13:50070120-50070231	NONHSAT033746
2	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033747
3	lnc-PHF11-2	chr13:50019689-50020088	NONHSAT033744
4	lnc-PHF11-2	chr13:50018820-50018993	NONHSAT033744
5	lnc-PHF11-1	chr13:50063106-50063206	NONHSAT033745
6	lnc-PHF11-1	chr13:50063383-50063500	NONHSAT033745
7	lnc-SETDB2-1	chr13:50080771-50080892	NONHSAT033746
8	lnc-AL136218.1-2	chr13:50018122-50018200	NONHSAT033741
9	lnc-SETDB2-1	chr13:50070372-50070584	NONHSAT033747
10	lnc-SETDB2-1	chr13:50071192-50071353	NONHSAT033746

No data

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

Extended variants
information (count: 2512 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:2512 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9316453	chr13:50013622-50013623	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545485795	chr13:50013646-50013647	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs34255142	chr13:50013658-50013659	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs57318076	chr13:50013680-50013681	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs114374533	chr13:50013684-50013685	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs386770866	chr13:50013693-50013694	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs541610506	chr13:50013762-50013763	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs34976750	chr13:50013818-50013819	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs562586737	chr13:50013829-50013830	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs530404327	chr13:50013839-50013840	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs542551849	chr13:50013891-50013892	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs115046858	chr13:50013920-50013921	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs138940777	chr13:50013921-50013922	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs552296150	chr13:50013937-50013938	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs192447971	chr13:50013974-50013975	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs530692170	chr13:50013993-50013994	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs528582683	chr13:50014009-50014010	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs138219386	chr13:50014013-50014014	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs527559021	chr13:50014018-50014019	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs113526776	chr13:50014057-50014058	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs574222358	chr13:50014065-50014066	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs59965720	chr13:50014077-50014078	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs183849251	chr13:50014081-50014082	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs9535245	chr13:50014083-50014084	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs184815704	chr13:50014095-50014096	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs188055168	chr13:50014150-50014151	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs192754129	chr13:50014257-50014258	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569067126	chr13:50014285-50014286	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs555731639	chr13:50014414-50014415	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs539386100	chr13:50014449-50014450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557490751	chr13:50014474-50014475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs78564308	chr13:50014492-50014493	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs540367418	chr13:50014498-50014499	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140733613	chr13:50014519-50014520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs575135447	chr13:50014521-50014522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542058974	chr13:50014523-50014524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs78029351	chr13:50014549-50014550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs575861077	chr13:50014587-50014588	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs184607603	chr13:50014593-50014594	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564167738	chr13:50014640-50014641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189876582	chr13:50014684-50014685	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181476680	chr13:50014695-50014696	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548570675	chr13:50014718-50014719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547586432	chr13:50014737-50014738	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs145887427	chr13:50014811-50014812	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs377071425	chr13:50014852-50014853	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs56314282	chr13:50014888-50014889	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs3036356	chr13:50014895-50014896	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs542343456	chr13:50014902-50014903	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs550518744	chr13:50014905-50014906	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:122)

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

Chromatin state (count:2678 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49978400-50016800	Weak transcription	Fetal Brain Male	brain
2	chr13:49983400-50017000	Weak transcription	Brain Anterior Caudate	brain
3	chr13:49983400-50017400	Weak transcription	Lung	lung
4	chr13:49983600-50017000	Weak transcription	Brain Angular Gyrus	brain
5	chr13:49993800-50017400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr13:49994000-50016200	Weak transcription	NHLF	lung
7	chr13:49994000-50017000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr13:49994000-50017200	Weak transcription	HSMM	muscle
9	chr13:49994200-50017200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr13:49994600-50016000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:49994800-50017200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr13:49995400-50017000	Weak transcription	Liver	Liver
13	chr13:49995600-50017000	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr13:49995800-50017000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr13:49997000-50017000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr13:49997000-50017200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr13:49997400-50017200	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr13:49998600-50017000	Weak transcription	Adipose Nuclei	Adipose
19	chr13:49999000-50017400	Weak transcription	Small Intestine	intestine
20	chr13:50000200-50017200	Weak transcription	Fetal Intestine Small	intestine
21	chr13:50000400-50017000	Weak transcription	Fetal Lung	lung
22	chr13:50000600-50017400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr13:50002600-50017000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:50002600-50017000	Weak transcription	HSMMtube	muscle
25	chr13:50002800-50017000	Weak transcription	Primary T cells from cord blood	blood
26	chr13:50002800-50017000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr13:50002800-50017200	Weak transcription	Fetal Muscle Leg	muscle
28	chr13:50003000-50017000	Weak transcription	Primary neutrophils fromperipheralblood	blood
29	chr13:50003000-50017200	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr13:50003400-50017000	Weak transcription	Brain Germinal Matrix	brain
31	chr13:50003400-50017200	Weak transcription	Fetal Stomach	stomach
32	chr13:50003400-50017200	Weak transcription	Ovary	ovary
33	chr13:50005200-50017000	Weak transcription	Duodenum Mucosa	Duodenum
34	chr13:50005200-50017200	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr13:50006600-50016200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr13:50006800-50016200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr13:50006800-50017000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr13:50007200-50017200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:50007200-50017200	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr13:50007400-50017000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
41	chr13:50007400-50017200	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr13:50007400-50017200	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr13:50007600-50016800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr13:50007600-50017200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr13:50008000-50016200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr13:50008200-50017000	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr13:50008200-50017200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr13:50008400-50017000	Weak transcription	Fetal Brain Female	brain
49	chr13:50008400-50017400	Weak transcription	Left Ventricle	heart
50	chr13:50008600-50016000	Weak transcription	NHDF-Ad	bronchial

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