Variant report

Variant	nsv541926
Chromosome Location	chr13:111378180-111516489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1115)
CpG islands
(count:1470)
Chromatin interactive
region (count:85)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1115 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr13:111447284-111447297	K562	blood:	n/a	n/a
2	BACH1	chr13:111449903-111450220	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:111464436-111464574	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:111465481-111465697	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr13:111469521-111469785	GM12878	blood:	n/a	n/a
6	BCL3	chr13:111469504-111469868	GM12878	blood:	n/a	n/a
7	BCLAF1	chr13:111471682-111472178	GM12878	blood:	n/a	chr13:111471711-111471725 chr13:111471772-111471780
8	BHLHE40	chr13:111379072-111379390	GM12878	blood:	n/a	n/a
9	BHLHE40	chr13:111471788-111472088	K562	blood:	n/a	n/a
10	BHLHE40	chr13:111453663-111453686	HepG2	liver:	n/a	n/a
11	BHLHE40	chr13:111471837-111472159	GM12878	blood:	n/a	n/a
12	BRCA1	chr13:111410659-111411006	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr13:111471787-111472089	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr13:111408514-111409201	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr13:111465073-111465094	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr13:111509582-111509925	K562	blood:	n/a	n/a
17	CBX3	chr13:111445887-111446174	K562	blood:	n/a	n/a
18	CBX3	chr13:111395804-111396162	K562	blood:	n/a	n/a
19	CBX3	chr13:111405013-111405268	K562	blood:	n/a	n/a
20	CBX3	chr13:111405001-111405202	K562	blood:	n/a	n/a
21	CBX3	chr13:111480950-111481337	K562	blood:	n/a	n/a
22	CEBPB	chr13:111495200-111495319	Hela-S3	cervix:	n/a	chr13:111495242-111495253
23	CEBPB	chr13:111451934-111452653	IMR90	lung:	n/a	chr13:111452466-111452477
24	CEBPB	chr13:111466449-111466655	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr13:111497918-111498191	H1-hESC	embryonic stem cell:	n/a	chr13:111498041-111498054 chr13:111498040-111498057 chr13:111498042-111498053
26	CEBPB	chr13:111497925-111498192	Hela-S3	cervix:	n/a	chr13:111498041-111498054 chr13:111498040-111498057 chr13:111498042-111498053
27	CEBPB	chr13:111412030-111412397	IMR90	lung:	n/a	n/a
28	CEBPB	chr13:111412149-111412318	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr13:111497896-111498209	IMR90	lung:	n/a	chr13:111498041-111498054 chr13:111498040-111498057 chr13:111498042-111498053
30	CEBPB	chr13:111428160-111428285	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:111408501-111409085	Hela-S3	cervix:	n/a	chr13:111408690-111408703
32	CEBPB	chr13:111497911-111498198	HepG2	liver:	n/a	chr13:111498041-111498054 chr13:111498040-111498057 chr13:111498042-111498053
33	CEBPB	chr13:111418405-111418422	HepG2	liver:	n/a	n/a
34	CEBPB	chr13:111495121-111495374	HepG2	liver:	n/a	chr13:111495242-111495253
35	CEBPB	chr13:111386992-111387181	HepG2	liver:	n/a	n/a
36	CEBPB	chr13:111497931-111498236	K562	blood:	n/a	chr13:111498041-111498054 chr13:111498040-111498057 chr13:111498042-111498053
37	CEBPB	chr13:111495166-111495378	A549	lung:	n/a	chr13:111495242-111495253
38	CEBPB	chr13:111410576-111411108	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr13:111378282-111378402	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr13:111489101-111489260	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr13:111441434-111441578	K562	blood:	n/a	n/a
42	CEBPB	chr13:111452464-111452542	K562	blood:	n/a	chr13:111452466-111452477
43	CEBPB	chr13:111386959-111387236	HepG2	liver:	n/a	n/a
44	CEBPB	chr13:111495119-111495372	IMR90	lung:	n/a	chr13:111495242-111495253
45	CEBPB	chr13:111468390-111468549	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr13:111412157-111412355	HepG2	liver:	n/a	n/a
47	CEBPB	chr13:111497999-111498127	A549	lung:	n/a	chr13:111498041-111498054 chr13:111498040-111498057 chr13:111498042-111498053
48	CEBPB	chr13:111452397-111452624	HepG2	liver:	n/a	chr13:111452466-111452477
49	CEBPB	chr13:111408536-111408834	IMR90	lung:	n/a	chr13:111408690-111408703
50	CHD2	chr13:111450876-111450887	HepG2	liver:	n/a	n/a

(count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:111466326-111466376	T-47D	breast:	n/a
2	chr13:111505942-111505992	HL-60	blood:	n/a
3	chr13:111474862-111474912	GM12892	blood:	n/a
4	chr13:111452040-111452090	HRE	kidney:	n/a
5	chr13:111505528-111505578	HCT-116	colon:	n/a
6	chr13:111474862-111474912	T-47D	breast:	n/a
7	chr13:111466326-111466376	T-47D	breast:	n/a
8	chr13:111505942-111505992	HL-60	blood:	n/a
9	chr13:111474862-111474912	GM12892	blood:	n/a
10	chr13:111452040-111452090	HRE	kidney:	n/a
11	chr13:111505528-111505578	HCT-116	colon:	n/a
12	chr13:111474862-111474912	T-47D	breast:	n/a
13	chr13:111451902-111451952	HNPCEpiC	eye:	n/a
14	chr13:111474347-111474397	NHDF-neo	bronchial:	n/a
15	chr13:111466326-111466376	ovcar-3	ovarian:	n/a
16	chr13:111483035-111483085	HCF	heart:	n/a
17	chr13:111452040-111452090	U87	brain:	n/a
18	chr13:111464554-111464604	HCPEpiC	choroid plexus:	n/a
19	chr13:111464554-111464604	RPTEC	kidney:	n/a
20	chr13:111462688-111462738	NB4	blood:	n/a
21	chr13:111505942-111505992	SK-N-MC	brain:	n/a
22	chr13:111466326-111466376	HCT-116	colon:	n/a
23	chr13:111451902-111451952	BE2_C	brain:	n/a
24	chr13:111474862-111474912	HMEC	breast:	n/a
25	chr13:111483028-111483078	Jurkat	blood:	n/a
26	chr13:111473128-111473178	BJ	skin:	n/a
27	chr13:111460277-111460327	SAEC	small airway:	n/a
28	chr13:111465028-111465078	H1-hESC	embryonic stem cell:	embryo
29	chr13:111460277-111460327	HRE	kidney:	n/a
30	chr13:111512675-111512725	NH-A	brain:	n/a
31	chr13:111483028-111483078	IMR90	lung:	fetal
32	chr13:111512675-111512725	HIPEpiC	eye:	n/a
33	chr13:111449880-111449930	NH-A	brain:	n/a
34	chr13:111466326-111466376	Caco-2	colon:	n/a
35	chr13:111483035-111483085	Hela-S3	cervix:	n/a
36	chr13:111505761-111505811	BE2_C	brain:	n/a
37	chr13:111462688-111462738	K562	blood:	n/a
38	chr13:111512675-111512725	NB4	blood:	n/a
39	chr13:111468250-111468300	Hepatocyte	liver:	n/a
40	chr13:111466326-111466376	NT2-D1	testis:	n/a
41	chr13:111468250-111468300	NT2-D1	testis:	n/a
42	chr13:111505942-111505992	AG09309	skin:	n/a
43	chr13:111483035-111483085	HNPCEpiC	eye:	n/a
44	chr13:111512675-111512725	HPAEpiC	pulmonary alveolar:	n/a
45	chr13:111451972-111452022	HCT-116	colon:	n/a
46	chr13:111474862-111474912	MCF-7	breast:	n/a
47	chr13:111460277-111460327	RPTEC	kidney:	n/a
48	chr13:111505528-111505578	ovcar-3	ovarian:	n/a
49	chr13:111409394-111409444	HL-60	blood:	n/a
50	chr13:111451972-111452022	GM12892	blood:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:111446514..111449037-chr13:111563387..111565739,2	K562	blood:
2	chr13:111363451..111365084-chr13:111398821..111400939,2	MCF-7	breast:
3	chr13:111245511..111246504-chr13:111471490..111472454,5	K562	blood:
4	chr13:111385516..111387873-chr13:111397501..111399093,2	K562	blood:
5	chr13:111513558..111516412-chr13:111565638..111567321,2	K562	blood:
6	chr13:111378082..111379664-chr13:111380125..111381869,2	MCF-7	breast:
7	chr13:111365574..111367776-chr13:111408041..111410290,2	MCF-7	breast:
8	chr13:111514027..111516534-chr13:111520643..111522636,2	MCF-7	breast:
9	chr13:111364714..111368488-chr13:111470610..111472671,4	MCF-7	breast:
10	chr13:111366177..111368396-chr13:111465118..111467461,3	K562	blood:
11	chr13:111365721..111368310-chr13:111480710..111483286,2	MCF-7	breast:
12	chr13:111482968..111484865-chr13:111489471..111491447,2	K562	blood:
13	chr13:111385516..111387873-chr13:111397501..111399093,2	K562	blood:
14	chr13:111368423..111371345-chr13:111411343..111413791,2	K562	blood:
15	chr13:111505906..111508659-chr13:111518320..111522599,4	K562	blood:
16	chr13:111368245..111369754-chr13:111427344..111430230,2	K562	blood:
17	chr13:111370419..111377483-chr13:111379803..111385146,6	MCF-7	breast:
18	chr13:111366010..111368933-chr13:111455449..111458304,2	K562	blood:
19	chr13:111367943..111368809-chr13:111471498..111472219,2	K562	blood:
20	chr13:111296952..111297606-chr13:111471742..111472464,3	MCF-7	breast:
21	chr13:111481139..111483690-chr13:111483705..111486036,2	K562	blood:
22	chr13:111376558..111379495-chr13:111384909..111386975,2	K562	blood:
23	chr13:111366336..111368907-chr13:111472705..111474418,3	MCF-7	breast:
24	chr13:111454971..111457410-chr13:111461598..111464131,2	MCF-7	breast:
25	chr13:111364727..111367050-chr13:111474479..111476653,2	K562	blood:
26	chr13:111475489..111478479-chr13:111487607..111490371,2	MCF-7	breast:
27	chr13:111508517..111510312-chr13:111519062..111521550,2	K562	blood:
28	chr13:111366039..111368766-chr13:111442537..111445494,2	MCF-7	breast:
29	chr13:111377814..111380233-chr13:111525539..111528111,2	K562	blood:
30	chr13:111364944..111367524-chr13:111462114..111463732,2	MCF-7	breast:
31	chr13:111365698..111367704-chr13:111465190..111467444,3	K562	blood:
32	chr13:111367187..111368970-chr13:111441304..111443834,2	K562	blood:
33	chr13:111363576..111369085-chr13:111458761..111470393,19	MCF-7	breast:
34	chr13:111366010..111369280-chr13:111453160..111458306,4	K562	blood:
35	chr13:111366114..111368858-chr13:111390283..111392801,3	MCF-7	breast:
36	chr13:111513700..111517268-chr13:111518205..111523270,8	K562	blood:
37	chr13:111475489..111478479-chr13:111487607..111490371,2	MCF-7	breast:
38	chr13:111425021..111427046-chr13:111427615..111429619,2	K562	blood:
39	chr1:17231485..17232075-chr13:111393932..111394932,3	Hela-S3	cervix:
40	chr13:111366357..111368867-chr13:111506839..111508404,2	MCF-7	breast:
41	chr13:111479845..111482670-chr13:111567559..111569603,2	K562	blood:
42	chr13:111364610..111367581-chr13:111494571..111498052,3	MCF-7	breast:
43	chr13:111363345..111367659-chr13:111448633..111451265,3	K562	blood:
44	chr13:111425021..111427046-chr13:111427615..111429619,2	K562	blood:
45	chr13:111510544..111513300-chr13:111518911..111522516,3	K562	blood:
46	chr13:111365245..111367807-chr13:111384791..111387198,2	MCF-7	breast:
47	chr13:111454971..111457410-chr13:111461598..111464131,2	MCF-7	breast:
48	chr13:111366091..111368052-chr13:111448002..111451334,4	MCF-7	breast:
49	chr13:111465055..111467713-chr13:111467771..111470419,3	K562	blood:
50	chr13:111368245..111370564-chr13:111427344..111430230,3	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ING1-2	chr13:111430473-111430574	NONHSAT035174
2	lnc-LINC00346-1	chr13:111515843-111521973	XLOC_010723
3	lnc-ING1-1	chr13:111477209-111477944	XLOC_010500
4	lnc-LINC00346-1	chr13:111516334-111522655	NONHSAT035182
5	lnc-CARS2-1	chr13:111415021-111415480	NONHSAT035172
6	lnc-ING1-2	chr13:111428731-111429099	NONHSAT035174
7	lnc-ING1-1	chr13:111490563-111491493	XLOC_010500

No data

Variant related genes	Relation type
RPL21P107	TF binding region
LINC00567	TF binding region
RPL21P107	CpG island
LINC00567	CpG island
ENSG00000259831	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000088448	chromatin interactions
ENSG00000255874	chromatin interactions

Extended variants
information (count: 4941 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4941 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567675229	chr13:111378194-111378195	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs534665646	chr13:111378199-111378200	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72663423	chr13:111378205-111378206	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527324023	chr13:111378261-111378262	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538747573	chr13:111378272-111378273	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs143548872	chr13:111378286-111378287	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371022883	chr13:111378328-111378329	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192699831	chr13:111378356-111378357	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs151279473	chr13:111378417-111378418	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs560167369	chr13:111378484-111378485	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529838501	chr13:111378511-111378512	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376072303	chr13:111378518-111378519	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576666904	chr13:111378521-111378522	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573582666	chr13:111378544-111378545	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540626295	chr13:111378572-111378573	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559378810	chr13:111378576-111378577	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs2038952	chr13:111378652-111378653	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs184319552	chr13:111378724-111378725	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563507914	chr13:111378788-111378789	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563175918	chr13:111378873-111378874	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs189602268	chr13:111378999-111379000	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs181209279	chr13:111379042-111379043	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs139280929	chr13:111379078-111379079	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs2033947	chr13:111379089-111379090	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs184971953	chr13:111379106-111379107	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs115168878	chr13:111379110-111379111	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs547890005	chr13:111379127-111379128	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs76616334	chr13:111379131-111379132	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs188938152	chr13:111379209-111379210	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs557003175	chr13:111379228-111379229	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs569128656	chr13:111379260-111379261	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs146898350	chr13:111379263-111379264	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs555250546	chr13:111379270-111379271	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs368446961	chr13:111379273-111379274	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs117447571	chr13:111379274-111379275	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs540918791	chr13:111379303-111379304	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs181631343	chr13:111379314-111379315	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs577695256	chr13:111379326-111379327	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs527268711	chr13:111379327-111379328	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs534476074	chr13:111379352-111379353	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs2165418	chr13:111379365-111379366	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs147780604	chr13:111379375-111379376	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs530743842	chr13:111379424-111379425	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs368061624	chr13:111379444-111379445	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs35427744	chr13:111379480-111379481	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs570276462	chr13:111379631-111379632	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs561133718	chr13:111379642-111379643	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs528406651	chr13:111379652-111379653	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs570781589	chr13:111379710-111379711	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs539246200	chr13:111379736-111379737	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Cancer	20164919	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
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	17908304	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
Acute myeloid leukemia	21251322	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Burkitt''s lymphoma	20823134	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Burkitt''s lymphoma	19759907	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Medulloblastoma	19270706	CNVD
Mental retardation	17124404	CNVD
Leukemia	18688285	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21858162	CNVD
Melanoma	17363583	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
abnormal development	18461090	CNVD
Malignant glioma	17146433	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Glioma	17123091	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	20409316	CNVD
Central neurocytomas	17123091	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Neurocytoma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1049 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111369200-111381400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr13:111370200-111379000	Weak transcription	HUVEC	blood vessel
3	chr13:111370200-111383400	Weak transcription	Right Atrium	heart
4	chr13:111370400-111379400	Weak transcription	Fetal Kidney	kidney
5	chr13:111370800-111379200	Weak transcription	Psoas Muscle	Psoas
6	chr13:111370800-111380200	Weak transcription	HSMM	muscle
7	chr13:111370800-111380800	Weak transcription	Hela-S3	cervix
8	chr13:111372200-111378200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr13:111372200-111379000	Weak transcription	Small Intestine	intestine
10	chr13:111372200-111379600	Weak transcription	NHLF	lung
11	chr13:111372200-111380000	Weak transcription	Gastric	stomach
12	chr13:111372200-111381600	Weak transcription	A549	lung
13	chr13:111372200-111383400	Weak transcription	Esophagus	oesophagus
14	chr13:111372200-111383600	Weak transcription	Aorta	Aorta
15	chr13:111372200-111384200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr13:111372400-111379200	Weak transcription	Lung	lung
17	chr13:111372400-111379200	Weak transcription	Pancreas	Pancrea
18	chr13:111372400-111379200	Weak transcription	Rectal Smooth Muscle	rectum
19	chr13:111372400-111379600	Weak transcription	Brain Substantia Nigra	brain
20	chr13:111372400-111380000	Weak transcription	Colonic Mucosa	Colon
21	chr13:111372400-111381400	Weak transcription	Right Ventricle	heart
22	chr13:111372400-111381600	Weak transcription	Fetal Intestine Small	intestine
23	chr13:111372400-111382000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr13:111372400-111382400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr13:111372400-111383200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr13:111372400-111383400	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr13:111372400-111384200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr13:111372600-111378800	Weak transcription	Primary T cells from cord blood	blood
29	chr13:111372600-111379800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr13:111372600-111380000	Weak transcription	Fetal Muscle Leg	muscle
31	chr13:111372600-111381200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr13:111373000-111379800	Weak transcription	Liver	Liver
33	chr13:111373400-111378200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr13:111373400-111379800	Weak transcription	Brain Germinal Matrix	brain
35	chr13:111373600-111378400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr13:111373600-111378600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr13:111373600-111378800	Weak transcription	GM12878-XiMat	blood
38	chr13:111373600-111379000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr13:111373600-111379200	Weak transcription	Fetal Thymus	thymus
40	chr13:111373600-111379800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr13:111373600-111380000	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr13:111373600-111380400	Weak transcription	Primary B cells from cord blood	blood
43	chr13:111373600-111380400	Weak transcription	Fetal Intestine Large	intestine
44	chr13:111373600-111381000	Weak transcription	Fetal Brain Female	brain
45	chr13:111373600-111382600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr13:111373600-111383200	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr13:111373800-111379600	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr13:111373800-111379600	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr13:111373800-111380400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr13:111374200-111382600	Weak transcription	Primary neutrophils fromperipheralblood	blood

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