Variant report

Variant	nsv832613
Chromosome Location	chr13:53524319-53687188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:856)
Chromatin interactive
region (count:40)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 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	ATF2	chr13:53542153-53542575	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr13:53542095-53542571	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr13:53529544-53530133	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr13:53542094-53542532	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr13:53542290-53542490	K562	blood:	n/a	n/a
6	BACH1	chr13:53594969-53595371	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr13:53529764-53530098	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr13:53603089-53603236	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr13:53542231-53542661	GM12878	blood:	n/a	chr13:53542371-53542379 chr13:53542490-53542499
10	BHLHE40	chr13:53542299-53542584	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:53542283-53542517	K562	blood:	n/a	n/a
12	BRCA1	chr13:53635359-53635364	GM12878	blood:	n/a	n/a
13	BRCA1	chr13:53542239-53542439	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:53528907-53529080	H1-hESC	embryonic stem cell:	n/a	n/a
15	CCNT2	chr13:53581180-53581496	K562	blood:	n/a	n/a
16	CCNT2	chr13:53565834-53566223	K562	blood:	n/a	n/a
17	CEBPB	chr13:53584874-53585129	HepG2	liver:	n/a	chr13:53585006-53585017
18	CEBPB	chr13:53542236-53542516	K562	blood:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
19	CEBPB	chr13:53542320-53542537	K562	blood:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
20	CEBPB	chr13:53529721-53530131	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr13:53529188-53529231	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr13:53553508-53553733	HepG2	liver:	n/a	chr13:53553564-53553575 chr13:53553574-53553583 chr13:53553564-53553577
23	CEBPB	chr13:53542288-53542638	A549	lung:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
24	CEBPB	chr13:53621139-53621397	HepG2	liver:	n/a	chr13:53621277-53621288 chr13:53621278-53621289
25	CEBPB	chr13:53636947-53637143	HepG2	liver:	n/a	chr13:53637095-53637106 chr13:53637094-53637105 chr13:53637094-53637107 chr13:53637094-53637107 chr13:53637096-53637105
26	CEBPB	chr13:53541997-53542641	IMR90	lung:	n/a	chr13:53542103-53542116 chr13:53542450-53542463 chr13:53542450-53542461 chr13:53542103-53542114 chr13:53542103-53542116
27	CEBPB	chr13:53572495-53572974	A549	lung:	n/a	chr13:53572808-53572819
28	CEBPB	chr13:53542231-53542612	HepG2	liver:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
29	CEBPB	chr13:53542210-53542611	MCF-7	breast:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
30	CEBPB	chr13:53572678-53572974	K562	blood:	n/a	chr13:53572808-53572819
31	CEBPB	chr13:53542317-53542534	HepG2	liver:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
32	CEBPB	chr13:53572645-53572962	Hela-S3	cervix:	n/a	chr13:53572808-53572819
33	CEBPB	chr13:53572507-53572983	IMR90	lung:	n/a	chr13:53572808-53572819
34	CEBPB	chr13:53542258-53542638	K562	blood:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
35	CEBPB	chr13:53542210-53542637	A549	lung:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
36	CEBPB	chr13:53554955-53555276	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr13:53572444-53572981	HepG2	liver:	n/a	chr13:53572808-53572819
38	CEBPB	chr13:53654819-53655007	A549	lung:	n/a	n/a
39	CEBPB	chr13:53542335-53542487	HepG2	liver:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
40	CEBPB	chr13:53542067-53542619	A549	lung:	n/a	chr13:53542103-53542116 chr13:53542450-53542463 chr13:53542450-53542461 chr13:53542103-53542114 chr13:53542103-53542116
41	CEBPB	chr13:53572688-53572970	H1-hESC	embryonic stem cell:	n/a	chr13:53572808-53572819
42	CEBPB	chr13:53649698-53649989	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr13:53542197-53542622	ECC-1	luminal epithelium:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
44	CEBPB	chr13:53542235-53542629	Hela-S3	cervix:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
45	CEBPB	chr13:53542096-53543026	H1-hESC	embryonic stem cell:	n/a	chr13:53542103-53542116 chr13:53542450-53542463 chr13:53542450-53542461 chr13:53542103-53542114 chr13:53542103-53542116
46	CEBPB	chr13:53542234-53542545	ECC-1	luminal epithelium:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
47	CEBPB	chr13:53542082-53542614	HepG2	liver:	n/a	chr13:53542103-53542116 chr13:53542450-53542463 chr13:53542450-53542461 chr13:53542103-53542114 chr13:53542103-53542116
48	CEBPB	chr13:53542190-53542558	MCF-7	breast:	n/a	chr13:53542450-53542463 chr13:53542450-53542461
49	CEBPD	chr13:53542297-53542492	HepG2	liver:	n/a	n/a
50	CHD1	chr13:53542131-53542604	IMR90	lung:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:53618826-53618876	Caco-2	colon:	n/a
2	chr13:53536706-53536756	HCPEpiC	choroid plexus:	n/a
3	chr13:53618826-53618876	Caco-2	colon:	n/a
4	chr13:53536706-53536756	HCPEpiC	choroid plexus:	n/a
5	chr13:53536706-53536756	BE2_C	brain:	n/a
6	chr13:53541996-53542046	NB4	blood:	n/a
7	chr13:53601944-53601994	HEK293	kidney:	embryo
8	chr13:53603286-53603336	T-47D	breast:	n/a
9	chr13:53601944-53601994	SK-N-SH	brain:	n/a
10	chr13:53602856-53602906	NB4	blood:	n/a
11	chr13:53618826-53618876	NB4	blood:	n/a
12	chr13:53643428-53643478	HMEC	breast:	n/a
13	chr13:53536706-53536756	SK-N-MC	brain:	n/a
14	chr13:53618826-53618876	HMEC	breast:	n/a
15	chr13:53602266-53602316	H1-hESC	embryonic stem cell:	embryo
16	chr13:53568518-53568568	SK-N-MC	brain:	n/a
17	chr13:53625240-53625290	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:53568518-53568568	HCT-116	colon:	n/a
19	chr13:53603286-53603336	Hela-S3	cervix:	n/a
20	chr13:53603286-53603336	HL-60	blood:	n/a
21	chr13:53595003-53595053	HepG2	liver:	n/a
22	chr13:53625240-53625290	HL-60	blood:	n/a
23	chr13:53568518-53568568	T-47D	breast:	n/a
24	chr13:53602856-53602906	NHDF-neo	bronchial:	n/a
25	chr13:53649596-53649646	HCF	heart:	n/a
26	chr13:53603286-53603336	HCT-116	colon:	n/a
27	chr13:53595003-53595053	GM12878	blood:	n/a
28	chr13:53603157-53603207	NH-A	brain:	n/a
29	chr13:53536706-53536756	GM12892	blood:	n/a
30	chr13:53602856-53602906	LNCaP	prostate:	n/a
31	chr13:53602385-53602435	PFSK-1	brain:	n/a
32	chr13:53649596-53649646	ProgFib	skin:	n/a
33	chr13:53541996-53542046	SK-N-SH_RA	brain:	n/a
34	chr13:53602266-53602316	PrEC	prostate:	n/a
35	chr13:53602266-53602316	HCT-116	colon:	n/a
36	chr13:53643428-53643478	Jurkat	blood:	n/a
37	chr13:53601944-53601994	A549	lung:	n/a
38	chr13:53568518-53568568	HNPCEpiC	eye:	n/a
39	chr13:53602856-53602906	GM19239	blood:	n/a
40	chr13:53568518-53568568	HRE	kidney:	n/a
41	chr13:53618826-53618876	NH-A	brain:	n/a
42	chr13:53603286-53603336	GM12892	blood:	n/a
43	chr13:53603157-53603207	AG09319	gingival:	n/a
44	chr13:53618826-53618876	NHBE	bronchial:	n/a
45	chr13:53649596-53649646	HCM	heart:	n/a
46	chr13:53541996-53542046	CMK	blood:	n/a
47	chr13:53568518-53568568	PANC-1	pancreas:	n/a
48	chr13:53602385-53602435	BJ	skin:	n/a
49	chr13:53603157-53603207	T-47D	breast:	n/a
50	chr13:53625240-53625290	NHBE	bronchial:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:53568172..53569756-chr13:53571238..53574203,2	K562	blood:
2	chr13:53423819..53426475-chr13:53542000..53544855,3	MCF-7	breast:
3	chr13:53542220..53542850-chr13:53763028..53763897,2	MCF-7	breast:
4	chr13:53424499..53425128-chr13:53541822..53542463,2	MCF-7	breast:
5	chr13:53225241..53227656-chr13:53534118..53536424,2	MCF-7	breast:
6	chr13:53559011..53561266-chr13:53563541..53566437,2	K562	blood:
7	chr13:53541952..53542484-chr13:53774972..53775830,2	MCF-7	breast:
8	chr13:53541944..53542859-chr13:53725655..53726169,3	K562	blood:
9	chr13:53426133..53429015-chr13:53553120..53555019,2	MCF-7	breast:
10	chr13:53572841..53574377-chr13:53577403..53579187,2	MCF-7	breast:
11	chr13:53559011..53561266-chr13:53563541..53566437,2	K562	blood:
12	chr13:53542013..53542636-chr13:53643135..53643785,2	MCF-7	breast:
13	chr13:53419539..53420191-chr13:53542097..53542726,2	MCF-7	breast:
14	chr13:53565024..53567097-chr13:53569738..53571480,2	K562	blood:
15	chr13:53433491..53436451-chr13:53545366..53547312,2	MCF-7	breast:
16	chr13:53578412..53579423-chr13:53725671..53726625,4	MCF-7	breast:
17	chr13:53183231..53184124-chr13:53542318..53542852,2	MCF-7	breast:
18	chr13:53606592..53607433-chr17:59786738..59787471,2	MCF-7	breast:
19	chr13:53239569..53240100-chr13:53542246..53542777,2	MCF-7	breast:
20	chr13:53685373..53687823-chr13:53688675..53690825,2	K562	blood:
21	chr13:53470858..53471661-chr13:53542403..53542998,2	MCF-7	breast:
22	chr13:53565024..53567097-chr13:53569738..53571480,2	K562	blood:
23	chr13:53542013..53542636-chr13:53643135..53643785,2	MCF-7	breast:
24	chr13:53436198..53437192-chr13:53541905..53542851,4	MCF-7	breast:
25	chr13:53449518..53452433-chr13:53575693..53577870,2	K562	blood:
26	chr13:53425233..53426207-chr13:53541827..53542911,3	MCF-7	breast:
27	chr13:53578448..53579351-chr13:53763194..53763965,2	MCF-7	breast:
28	chr13:53318284..53318806-chr13:53541913..53542479,2	K562	blood:
29	chr13:53541918..53542704-chr13:53775013..53775632,3	MCF-7	breast:
30	chr13:53471668..53472284-chr13:53541753..53542848,5	MCF-7	breast:
31	chr13:53542162..53542897-chr13:53725656..53726553,4	MCF-7	breast:
32	chr13:53553077..53555596-chr13:53555632..53558421,4	MCF-7	breast:
33	chr13:53436203..53437284-chr13:53541893..53542828,3	MCF-7	breast:
34	chr13:53568172..53569756-chr13:53571238..53574203,2	K562	blood:
35	chr13:53572841..53574377-chr13:53577403..53579187,2	MCF-7	breast:
36	chr13:53436242..53436760-chr13:53542342..53542902,2	K562	blood:
37	chr13:53243897..53244672-chr13:53542148..53542746,2	MCF-7	breast:
38	chr13:53424748..53427468-chr13:53541401..53543631,2	MCF-7	breast:
39	chr13:53553077..53555596-chr13:53555632..53558421,4	MCF-7	breast:
40	chr13:53593128..53594726-chr13:53763262..53764959,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH8-6	chr13:53604749-53605002	NONHSAT034005
2	lnc-PCDH8-2	chr13:53676441-53676607	NONHSAT034007
3	lnc-PCDH8-6	chr13:53598998-53599565	NONHSAT034005
4	lnc-PCDH8-2	chr13:53673539-53673826	NONHSAT034007
5	lnc-PCDH8-2	chr13:53676441-53676607	NONHSAT034008
6	lnc-PCDH8-2	chr13:53684996-53685075	NONHSAT034008
7	lnc-PCDH8-2	chr13:53684996-53685106	XLOC_010624
8	lnc-PCDH8-2	chr13:53673539-53673826	NONHSAT034008
9	lnc-PCDH8-6	chr13:53593072-53593180	NONHSAT034003
10	lnc-PCDH8-6	chr13:53604498-53604749	NONHSAT034004
11	lnc-PCDH8-6	chr13:53603010-53603207	NONHSAT034005
12	lnc-PCDH8-6	chr13:53599416-53599565	NONHSAT034003
13	lnc-PCDH8-6	chr13:53597285-53597408	NONHSAT034003
14	lnc-PCDH8-2	chr13:53673550-53673826	XLOC_010624
15	lnc-OLFM4-1	chr13:53650459-53650848	XLOC_010397
16	lnc-OLFM4-1	chr13:53631291-53631321	XLOC_010397
17	lnc-PCDH8-6	chr13:53604749-53605002	NONHSAT034003
18	lnc-PCDH8-6	chr13:53599416-53599565	NONHSAT034004
19	lnc-PCDH8-2	chr13:53676441-53676607	XLOC_010624
20	lnc-PCDH8-2	chr13:53684996-53685075	XLOC_010624
21	lnc-PCDH8-6	chr13:53603010-53603207	NONHSAT034004
22	lnc-PCDH8-2	chr13:53673540-53673826	XLOC_010624
23	lnc-PCDH8-6	chr13:53587925-53588345	NONHSAT034003
24	lnc-PCDH8-2	chr13:53676441-53676607	XLOC_010624
25	lnc-PCDH8-6	chr13:53596460-53596891	NONHSAT034004

No data

Variant related genes	Relation type
OLFM4	TF binding region
OLFM4	CpG island
ENSG00000237092	chromatin interactions
ENSG00000165416	chromatin interactions
PAPD5	miRNA target sites
MLL3	miRNA target sites
CBX3	miRNA target sites

Extended variants
information (count: 5958 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:5958 , 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	rs148673133	chr13:53524342-53524343	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs191883895	chr13:53524343-53524344	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs545184090	chr13:53524348-53524349	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs369907484	chr13:53524373-53524374	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs564260867	chr13:53524407-53524408	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs533027965	chr13:53524441-53524442	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs373154518	chr13:53524460-53524461	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs564384714	chr13:53524472-53524473	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs546864946	chr13:53524498-53524499	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs10564781	chr13:53524539-53524540	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs201272662	chr13:53524543-53524544	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs112257482	chr13:53524562-53524563	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs374853348	chr13:53524613-53524614	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs115854609	chr13:53524617-53524618	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs568878541	chr13:53524664-53524665	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs184771861	chr13:53524695-53524696	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs75250976	chr13:53524699-53524700	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs80135858	chr13:53524711-53524712	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs1323104	chr13:53524749-53524750	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs375778346	chr13:53524846-53524847	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs573969324	chr13:53524870-53524871	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs371040403	chr13:53524879-53524880	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs556101076	chr13:53524894-53524895	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs370511346	chr13:53524913-53524914	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs142793470	chr13:53524949-53524950	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs528848529	chr13:53524954-53524955	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs545481125	chr13:53524958-53524959	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs147495582	chr13:53524959-53524960	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs139968416	chr13:53524996-53524997	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs540024724	chr13:53525006-53525007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560403065	chr13:53525026-53525027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529161422	chr13:53525039-53525040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190248338	chr13:53525041-53525042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182319450	chr13:53525045-53525046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562461975	chr13:53525046-53525047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145355087	chr13:53525051-53525052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184538909	chr13:53525069-53525070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571279799	chr13:53525100-53525101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs527404790	chr13:53525104-53525105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs151023814	chr13:53525105-53525106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs547642888	chr13:53525119-53525120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs189418698	chr13:53525159-53525160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536504378	chr13:53525178-53525179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs556487048	chr13:53525181-53525182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376728854	chr13:53525188-53525189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181310590	chr13:53525251-53525252	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs539532189	chr13:53525258-53525259	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs538692937	chr13:53525273-53525274	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs371003942	chr13:53525277-53525278	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs572413500	chr13:53525335-53525336	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:53510400-53524400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:53516600-53525600	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr13:53521600-53524800	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr13:53521600-53525200	Enhancers	Fetal Stomach	stomach
5	chr13:53521800-53524800	Enhancers	Fetal Muscle Leg	muscle
6	chr13:53521800-53526000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr13:53522000-53525400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr13:53522600-53525600	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr13:53522800-53527000	Weak transcription	Dnd41	blood
10	chr13:53522800-53529000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:53523200-53527600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr13:53523400-53524800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr13:53523600-53524600	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr13:53523600-53525000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
15	chr13:53523600-53526400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr13:53523800-53524400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr13:53523800-53524400	Enhancers	Brain Hippocampus Middle	brain
18	chr13:53523800-53524400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr13:53523800-53524400	Enhancers	Right Atrium	heart
20	chr13:53523800-53524600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr13:53523800-53524600	Enhancers	Brain Anterior Caudate	brain
22	chr13:53523800-53525200	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr13:53523800-53525400	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr13:53524000-53524400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr13:53524200-53524400	Enhancers	Brain Germinal Matrix	brain
26	chr13:53524200-53525200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr13:53524200-53525200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr13:53524200-53525400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr13:53524200-53525800	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr13:53524200-53526000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr13:53524200-53526000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr13:53524200-53526200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr13:53524200-53528400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:53524200-53528600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr13:53524400-53524800	Enhancers	Fetal Muscle Trunk	muscle
36	chr13:53524400-53525000	Enhancers	Brain Angular Gyrus	brain
37	chr13:53524400-53525000	Enhancers	Brain Cingulate Gyrus	brain
38	chr13:53524400-53526400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:53524400-53527000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:53524600-53529800	Weak transcription	Brain Anterior Caudate	brain
41	chr13:53524800-53526800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr13:53525000-53526200	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr13:53525200-53525400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr13:53525200-53525400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr13:53525200-53527400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr13:53525400-53525800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr13:53525400-53526200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr13:53525400-53529600	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr13:53525600-53526800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr13:53525600-53529600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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