Variant report

Variant	nsv537669
Chromosome Location	chr5:12520949-12778382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1176)
CpG islands
(count:611)
Chromatin interactive
region (count:93)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:12645737-12645937	K562	blood:	n/a	n/a
2	ARID3A	chr5:12629284-12629314	K562	blood:	n/a	n/a
3	ARID3A	chr5:12573954-12574062	K562	blood:	n/a	n/a
4	ARID3A	chr5:12615141-12616053	K562	blood:	n/a	n/a
5	ARID3A	chr5:12611278-12611564	K562	blood:	n/a	n/a
6	ARID3A	chr5:12772446-12772684	K562	blood:	n/a	n/a
7	ARID3A	chr5:12587530-12587610	K562	blood:	n/a	n/a
8	ARID3A	chr5:12605684-12605760	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:12625817-12626175	K562	blood:	n/a	n/a
10	ATF1	chr5:12772433-12772741	K562	blood:	n/a	n/a
11	ATF1	chr5:12611394-12611564	K562	blood:	n/a	n/a
12	ATF1	chr5:12625855-12626127	K562	blood:	n/a	n/a
13	ATF1	chr5:12599710-12599720	K562	blood:	n/a	n/a
14	ATF1	chr5:12615012-12615715	K562	blood:	n/a	n/a
15	ATF1	chr5:12636538-12636665	K562	blood:	n/a	n/a
16	ATF1	chr5:12777500-12777758	K562	blood:	n/a	n/a
17	ATF1	chr5:12612014-12612205	K562	blood:	n/a	n/a
18	ATF2	chr5:12668042-12668298	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr5:12657998-12658420	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr5:12623287-12624095	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr5:12667909-12668201	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr5:12658521-12660660	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr5:12648499-12649011	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr5:12660692-12662536	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr5:12662712-12663504	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr5:12662664-12663813	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF3	chr5:12772414-12772810	K562	blood:	n/a	n/a
28	ATF3	chr5:12772509-12772655	K562	blood:	n/a	n/a
29	BACH1	chr5:12772460-12772773	K562	blood:	n/a	n/a
30	BACH1	chr5:12615423-12615929	K562	blood:	n/a	n/a
31	BACH1	chr5:12627924-12628106	K562	blood:	n/a	n/a
32	BACH1	chr5:12627636-12627648	K562	blood:	n/a	n/a
33	BCLAF1	chr5:12615205-12615584	K562	blood:	n/a	n/a
34	BHLHE40	chr5:12614798-12616107	K562	blood:	n/a	n/a
35	BHLHE40	chr5:12772578-12772678	K562	blood:	n/a	n/a
36	BHLHE40	chr5:12616429-12616837	K562	blood:	n/a	n/a
37	BHLHE40	chr5:12574678-12575143	K562	blood:	n/a	n/a
38	CBX3	chr5:12615155-12615822	K562	blood:	n/a	n/a
39	CBX3	chr5:12574582-12575256	K562	blood:	n/a	n/a
40	CBX3	chr5:12578931-12579331	K562	blood:	n/a	n/a
41	CBX3	chr5:12662769-12663016	K562	blood:	n/a	n/a
42	CBX3	chr5:12772417-12772891	K562	blood:	n/a	n/a
43	CCNT2	chr5:12574035-12574280	K562	blood:	n/a	n/a
44	CCNT2	chr5:12615096-12615905	K562	blood:	n/a	n/a
45	CCNT2	chr5:12678478-12678604	K562	blood:	n/a	n/a
46	CCNT2	chr5:12759535-12759728	K562	blood:	n/a	n/a
47	CCNT2	chr5:12574667-12575084	K562	blood:	n/a	n/a
48	CEBPB	chr5:12596972-12597269	K562	blood:	n/a	chr5:12597048-12597061 chr5:12597048-12597061
49	CEBPB	chr5:12566709-12566868	A549	lung:	n/a	chr5:12566765-12566776
50	CEBPB	chr5:12766940-12767161	HepG2	liver:	n/a	chr5:12767063-12767074

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:12660863-12660913	HL-60	blood:	n/a
2	chr5:12660863-12660913	HL-60	blood:	n/a
3	chr5:12669584-12669634	GM06990	blood:	n/a
4	chr5:12636281-12636331	BJ	skin:	n/a
5	chr5:12669584-12669634	ECC-1	luminal epithelium:	n/a
6	chr5:12661875-12661925	BJ	skin:	n/a
7	chr5:12623177-12623227	ovcar-3	ovarian:	n/a
8	chr5:12661875-12661925	AG09319	gingival:	n/a
9	chr5:12636281-12636331	BE2_C	brain:	n/a
10	chr5:12661875-12661925	AoSMC	blood vessel:	n/a
11	chr5:12636281-12636331	PFSK-1	brain:	n/a
12	chr5:12574688-12574738	GM19239	blood:	n/a
13	chr5:12636281-12636331	MCF-7	breast:	n/a
14	chr5:12661875-12661925	AG04449	skin:	fetal
15	chr5:12660863-12660913	GM19239	blood:	n/a
16	chr5:12669584-12669634	U87	brain:	n/a
17	chr5:12574688-12574738	AG04449	skin:	fetal
18	chr5:12636281-12636331	SK-N-SH_RA	brain:	n/a
19	chr5:12574872-12574922	GM06990	blood:	n/a
20	chr5:12623177-12623227	AG10803	skin:	n/a
21	chr5:12665869-12665919	ovcar-3	ovarian:	n/a
22	chr5:12615428-12615478	Hepatocyte	liver:	n/a
23	chr5:12574872-12574922	H1-hESC	embryonic stem cell:	embryo
24	chr5:12623177-12623227	GM19239	blood:	n/a
25	chr5:12574872-12574922	AG10803	skin:	n/a
26	chr5:12660863-12660913	NHDF-neo	bronchial:	n/a
27	chr5:12636281-12636331	HRE	kidney:	n/a
28	chr5:12665869-12665919	HRCEpiC	kidney:	n/a
29	chr5:12669584-12669634	A549	lung:	n/a
30	chr5:12623177-12623227	HRE	kidney:	n/a
31	chr5:12661875-12661925	SK-N-SH_RA	brain:	n/a
32	chr5:12623177-12623227	K562	blood:	n/a
33	chr5:12615428-12615478	GM12892	blood:	n/a
34	chr5:12663018-12663068	NB4	blood:	n/a
35	chr5:12623177-12623227	BJ	skin:	n/a
36	chr5:12660863-12660913	HCPEpiC	choroid plexus:	n/a
37	chr5:12660863-12660913	Caco-2	colon:	n/a
38	chr5:12669584-12669634	SK-N-MC	brain:	n/a
39	chr5:12665869-12665919	HCPEpiC	choroid plexus:	n/a
40	chr5:12669584-12669634	HRE	kidney:	n/a
41	chr5:12574688-12574738	T-47D	breast:	n/a
42	chr5:12661875-12661925	SK-N-MC	brain:	n/a
43	chr5:12636281-12636331	NH-A	brain:	n/a
44	chr5:12636281-12636331	GM12892	blood:	n/a
45	chr5:12665869-12665919	T-47D	breast:	n/a
46	chr5:12669584-12669634	AG04449	skin:	fetal
47	chr5:12665869-12665919	HCT-116	colon:	n/a
48	chr5:12663018-12663068	AG04450	lung:	fetal
49	chr5:12574688-12574738	SK-N-SH_RA	brain:	n/a
50	chr5:12660863-12660913	HRPEpiC	eye:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:12557146..12558747-chr5:12560771..12562482,2	K562	blood:
2	chr5:12679944..12681930-chr5:12685116..12688736,4	K562	blood:
3	chr5:12647069..12649041-chr5:12653810..12656965,3	K562	blood:
4	chr5:12652370..12654399-chr5:12657778..12661483,4	K562	blood:
5	chr5:12653349..12655490-chr5:12663314..12666064,2	K562	blood:
6	chr5:12757621..12760058-chr5:12760754..12763671,2	K562	blood:
7	chr5:12768829..12771225-chr5:12773503..12776685,3	K562	blood:
8	chr5:12554220..12555829-chr5:12556078..12558191,2	MCF-7	breast:
9	chr5:12637154..12639145-chr5:12647301..12649033,2	K562	blood:
10	chr5:12576312..12579149-chr5:12776108..12778231,2	K562	blood:
11	chr5:12608674..12611130-chr5:12636501..12638880,2	K562	blood:
12	chr5:12579389..12581538-chr5:12592252..12594102,2	K562	blood:
13	chr5:12569399..12571855-chr5:12571987..12574855,2	K562	blood:
14	chr5:12702448..12704226-chr5:12718051..12720709,2	K562	blood:
15	chr5:12583560..12586029-chr5:12586598..12589035,2	K562	blood:
16	chr5:12292464..12293235-chr5:12598697..12599332,3	MCF-7	breast:
17	chr5:12562087..12563881-chr5:12566086..12568996,3	K562	blood:
18	chr5:12576814..12579689-chr5:12594654..12596559,2	K562	blood:
19	chr5:12718842..12720474-chr5:12721962..12723532,2	K562	blood:
20	chr5:12760900..12763053-chr5:12763056..12765696,2	K562	blood:
21	chr5:12679944..12681930-chr5:12685116..12688736,4	K562	blood:
22	chr5:12546310..12548435-chr5:12549138..12551097,2	K562	blood:
23	chr5:12653349..12655490-chr5:12663314..12666064,2	K562	blood:
24	chr5:12562087..12563726-chr5:12565679..12568553,2	K562	blood:
25	chr5:12696352..12698473-chr5:12701723..12704711,2	MCF-7	breast:
26	chr5:12546310..12548435-chr5:12549138..12551097,2	K562	blood:
27	chr5:12743681..12745562-chr5:12760278..12762840,2	K562	blood:
28	chr5:12757621..12760058-chr5:12760754..12763671,2	K562	blood:
29	chr5:12572185..12574233-chr5:12590584..12592577,2	K562	blood:
30	chr5:12554220..12555829-chr5:12556078..12558191,2	MCF-7	breast:
31	chr5:12696352..12698473-chr5:12701723..12704711,2	MCF-7	breast:
32	chr5:12760900..12763053-chr5:12763056..12765696,2	K562	blood:
33	chr5:12579389..12581538-chr5:12592252..12594102,2	K562	blood:
34	chr5:12637154..12639145-chr5:12647301..12649033,2	K562	blood:
35	chr5:12566855..12569678-chr5:12570834..12573967,4	MCF-7	breast:
36	chr5:12614374..12617488-chr5:12617619..12619777,3	K562	blood:
37	chr10:102105957..102107814-chr5:12679811..12681638,2	MCF-7	breast:
38	chr1:153295251..153295999-chr5:12761269..12762010,2	MCF-7	breast:
39	chr5:12710496..12712610-chr5:12713708..12716321,2	MCF-7	breast:
40	chr5:12589520..12591629-chr5:12614668..12616853,2	K562	blood:
41	chr5:12571887..12574871-chr5:12612831..12615771,3	K562	blood:
42	chr5:12581974..12583485-chr5:12585485..12587761,2	K562	blood:
43	chr5:12588618..12591381-chr5:12596169..12597807,2	K562	blood:
44	chr5:12580769..12583015-chr5:13118744..13121010,2	K562	blood:
45	chr5:12579463..12582015-chr5:12766907..12769227,3	K562	blood:
46	chr5:12537002..12539656-chr5:12586201..12588814,2	K562	blood:
47	chr5:12577735..12580318-chr5:12581576..12583762,3	K562	blood:
48	chr5:12576312..12579149-chr5:12776108..12778231,2	K562	blood:
49	chr5:12579405..12581985-chr5:12616959..12619800,2	K562	blood:
50	chr5:12710496..12712610-chr5:12713708..12716321,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIO-9	chr5:12708650-12708792	l_2878_chr5:12648870-12708792_testes
2	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
3	lnc-TRIO-4	chr5:12759471-12759760	ENSG00000248131
4	lnc-TRIO-9	chr5:12707759-12708641	l_2878_chr5:12648870-12708792_testes
5	lnc-CTNND2-3	chr5:12663441-12664022	NONHSAT100517
6	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
7	lnc-TRIO-4	chr5:12711310-12711411	ENSG00000248131
8	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
9	lnc-CTNND2-3	chr5:12659546-12660157	NONHSAT100517
10	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
11	lnc-CTNND2-3	chr5:12653170-12654688	NONHSAT100517
12	lnc-TRIO-4	chr5:12711310-12711411	NONHSAT100511
13	lnc-TRIO-9	chr5:12648871-12648890	l_2878_chr5:12648870-12708792_testes
14	lnc-CTNND2-3	chr5:12657511-12658227	NONHSAT100517
15	lnc-CTNND2-3	chr5:12737810-12737969	NONHSAT100517
16	lnc-TRIO-4	chr5:12574969-12575164	NONHSAT100511
17	lnc-CTNND2-3	chr5:12723669-12723939	NONHSAT100517
18	lnc-TRIO-4	chr5:12574969-12575164	ENSG00000248131
19	lnc-TRIO-4	chr5:12595809-12595890	ENSG00000248131
20	lnc-TRIO-4	chr5:12711310-12711411	ENSG00000248131
21	lnc-TRIO-4	chr5:12574969-12575164	NONHSAT100514
22	lnc-TRIO-4	chr5:12654759-12655799	ENSG00000248131
23	lnc-TRIO-4	chr5:12595809-12595890	NONHSAT100514
24	lnc-TRIO-4	chr5:12711310-12711411	NONHSAT100514

No data

Variant related genes	Relation type
ENSG00000248783	TF binding region
CT49	TF binding region
ENSG00000264921	TF binding region
ENSG00000248783	CpG island
CT49	CpG island
ENSG00000264921	CpG island
ENSG00000099194	chromatin interactions
ENSG00000248783	chromatin interactions
ENSG00000248131	chromatin interactions
ENSG00000231188	chromatin interactions
ARHGEF7	miRNA target sites
FAM171A1	miRNA target sites
ABL2	miRNA target sites
PURA	miRNA target sites
PSMD7	miRNA target sites
BMPR2	miRNA target sites
CITED2	miRNA target sites
TRIM44	miRNA target sites
MLL2	miRNA target sites
NIN	miRNA target sites

Extended variants
information (count: 7496 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:7496 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553089841	chr5:12520982-12520983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577750329	chr5:12521037-12521038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs207465598	chr5:12521111-12521112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs555947250	chr5:12521123-12521124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563218835	chr5:12521161-12521162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575190099	chr5:12521178-12521179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145714534	chr5:12521229-12521230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547785750	chr5:12521273-12521274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372474471	chr5:12521274-12521275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560575078	chr5:12521286-12521287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs371291425	chr5:12521295-12521296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373813415	chr5:12521310-12521311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183442479	chr5:12521334-12521335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556932956	chr5:12521419-12521420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566095469	chr5:12521420-12521421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188503514	chr5:12521427-12521428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533506000	chr5:12521434-12521435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147743579	chr5:12521482-12521483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571217278	chr5:12521500-12521501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532595406	chr5:12521510-12521511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369536526	chr5:12521533-12521534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199898719	chr5:12521534-12521535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79687135	chr5:12521549-12521550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551226163	chr5:12521609-12521610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142367155	chr5:12521618-12521619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536966819	chr5:12521626-12521627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13187874	chr5:12521653-12521654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs372322340	chr5:12521705-12521706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs13170382	chr5:12521714-12521715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs142262428	chr5:12521724-12521725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558778298	chr5:12521725-12521726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs551587115	chr5:12521742-12521743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577294850	chr5:12521756-12521757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371689852	chr5:12521776-12521777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs151280359	chr5:12521801-12521802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs116150671	chr5:12521802-12521803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7736112	chr5:12521866-12521867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200385304	chr5:12521888-12521889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554509570	chr5:12521978-12521979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572741200	chr5:12521993-12521994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540271013	chr5:12522000-12522001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560746778	chr5:12522037-12522038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575638754	chr5:12522083-12522084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs192788243	chr5:12522099-12522100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369661085	chr5:12522101-12522102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184879872	chr5:12522110-12522111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186760485	chr5:12522148-12522149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563526849	chr5:12522168-12522169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs530376601	chr5:12522173-12522174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543290902	chr5:12522204-12522205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:12507600-12522400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr5:12532200-12532800	ZNF genes & repeats	Pancreas	Pancrea
3	chr5:12535400-12535600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:12535600-12535800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr5:12562600-12569200	Weak transcription	Placenta	Placenta
6	chr5:12565600-12570400	Weak transcription	K562	blood
7	chr5:12567600-12568200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:12569200-12570800	Strong transcription	Placenta	Placenta
9	chr5:12570400-12572400	Strong transcription	K562	blood
10	chr5:12570800-12573800	Weak transcription	Placenta	Placenta
11	chr5:12572400-12573000	Weak transcription	K562	blood
12	chr5:12573000-12576200	Active TSS	K562	blood
13	chr5:12573800-12575400	Active TSS	Placenta	Placenta
14	chr5:12576200-12577600	Weak transcription	K562	blood
15	chr5:12577800-12578000	ZNF genes & repeats	K562	blood
16	chr5:12578000-12581200	Weak transcription	K562	blood
17	chr5:12579800-12580800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr5:12579800-12581000	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr5:12580200-12580800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr5:12580400-12580800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr5:12581200-12582000	Strong transcription	K562	blood
22	chr5:12582000-12596000	Weak transcription	K562	blood
23	chr5:12596000-12596400	Strong transcription	K562	blood
24	chr5:12596400-12597400	Weak transcription	K562	blood
25	chr5:12597400-12598400	Strong transcription	K562	blood
26	chr5:12598400-12610600	Weak transcription	K562	blood
27	chr5:12599000-12599200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:12602000-12612400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr5:12602400-12602800	Enhancers	Fetal Brain Male	brain
30	chr5:12610600-12610800	Enhancers	K562	blood
31	chr5:12610800-12612000	Active TSS	K562	blood
32	chr5:12612000-12612200	Flanking Active TSS	K562	blood
33	chr5:12612200-12614200	Enhancers	K562	blood
34	chr5:12612400-12612600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
35	chr5:12613400-12613600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:12613600-12617600	Enhancers	Dnd41	blood
37	chr5:12614200-12615000	Flanking Active TSS	K562	blood
38	chr5:12614600-12615200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr5:12614800-12616000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr5:12615000-12615200	Active TSS	K562	blood
41	chr5:12615200-12615400	Flanking Active TSS	K562	blood
42	chr5:12615200-12615600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr5:12615400-12615600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr5:12615400-12615600	Active TSS	K562	blood
45	chr5:12615600-12616200	Flanking Active TSS	K562	blood
46	chr5:12615600-12627200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr5:12616200-12616600	Enhancers	K562	blood
48	chr5:12616200-12622800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:12616600-12616800	Flanking Active TSS	K562	blood
50	chr5:12616800-12617400	Enhancers	K562	blood

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