Variant report

Variant	nsv541520
Chromosome Location	chr12:67056831-67189837
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:954)
CpG islands
(count:549)
Chromatin interactive
region (count:54)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:954 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:67170642-67171041	GM12878	blood:	n/a	n/a
2	BACH1	chr12:67076780-67076853	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr12:67170708-67171069	GM12878	blood:	n/a	n/a
4	BATF	chr12:67170761-67171074	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:67170790-67171069	GM12878	blood:	n/a	n/a
6	BCL11A	chr12:67170768-67171000	GM12878	blood:	n/a	n/a
7	BCLAF1	chr12:67082643-67082952	GM12878	blood:	n/a	n/a
8	BRCA1	chr12:67087970-67087977	GM12878	blood:	n/a	n/a
9	CEBPB	chr12:67178069-67178104	HepG2	liver:	n/a	n/a
10	CEBPB	chr12:67073473-67073797	A549	lung:	n/a	n/a
11	CEBPB	chr12:67073534-67073750	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:67073446-67073794	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:67170935-67171105	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr12:67131490-67131690	K562	blood:	n/a	n/a
15	CEBPB	chr12:67073528-67073838	MCF-7	breast:	n/a	n/a
16	CEBPB	chr12:67113492-67113613	K562	blood:	n/a	n/a
17	CEBPB	chr12:67131609-67131785	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr12:67138611-67139048	MCF-7	breast:	n/a	n/a
19	CEBPB	chr12:67073457-67073808	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:67073468-67073795	IMR90	lung:	n/a	n/a
21	CEBPB	chr12:67082643-67082935	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr12:67138715-67138996	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:67130864-67131019	HepG2	liver:	n/a	n/a
24	CEBPB	chr12:67138648-67139144	MCF-7	breast:	n/a	n/a
25	CEBPB	chr12:67138687-67139031	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr12:67138695-67138991	K562	blood:	n/a	n/a
27	CEBPB	chr12:67084108-67084286	HepG2	liver:	n/a	chr12:67084134-67084145
28	CEBPB	chr12:67095950-67096156	HepG2	liver:	n/a	chr12:67096084-67096095
29	CEBPB	chr12:67073474-67073755	K562	blood:	n/a	n/a
30	CHD1	chr12:67127652-67127842	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr12:67127788-67127973	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr12:67082701-67082981	HepG2	liver:	n/a	n/a
33	CTCF	chr12:67087792-67087976	Pancreas_OC	pancreas:	n/a	n/a
34	CTCF	chr12:67092468-67092608	MCF-7	breast:	n/a	chr12:67092537-67092558 chr12:67092535-67092553
35	CTCF	chr12:67082740-67082890	AoAF	blood vessel:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
36	CTCF	chr12:67087820-67087970	K562	blood:	n/a	n/a
37	CTCF	chr12:67082740-67082890	AG09319	gingival:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
38	CTCF	chr12:67087740-67087890	GM12864	blood:	n/a	n/a
39	CTCF	chr12:67082727-67082894	SK-N-SH_RA	brain:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
40	CTCF	chr12:67082740-67082890	RPTEC	kidney:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
41	CTCF	chr12:67082760-67082910	NHLF	lung:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
42	CTCF	chr12:67087780-67087930	WI-38	lung:	n/a	n/a
43	CTCF	chr12:67102540-67102690	GM12874	blood:	n/a	chr12:67102633-67102654 chr12:67102638-67102656 chr12:67102639-67102655
44	CTCF	chr12:67087820-67087970	AG09309	skin:	n/a	n/a
45	CTCF	chr12:67138840-67138990	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr12:67082560-67082710	HVMF	connective:	n/a	n/a
47	CTCF	chr12:67082690-67083009	K562	blood:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
48	CTCF	chr12:67102500-67102650	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr12:67082720-67082870	GM12873	blood:	n/a	chr12:67082822-67082830 chr12:67082817-67082835
50	CTCF	chr12:67087800-67087950	GM12865	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:67127781-67127831	U87	brain:	n/a
2	chr12:67127781-67127831	T-47D	breast:	n/a
3	chr12:67072769-67072819	SKMC	muscle:	n/a
4	chr12:67072769-67072819	Hepatocyte	liver:	n/a
5	chr12:67073266-67073316	HCM	heart:	n/a
6	chr12:67073022-67073072	NH-A	brain:	n/a
7	chr12:67127781-67127831	HEEpiC	esophagus:	n/a
8	chr12:67072951-67073001	U87	brain:	n/a
9	chr12:67160208-67160258	A549	lung:	n/a
10	chr12:67072988-67073038	AG04449	skin:	fetal
11	chr12:67160208-67160258	MCF-7	breast:	n/a
12	chr12:67072769-67072819	AG04449	skin:	fetal
13	chr12:67073760-67073810	PANC-1	pancreas:	n/a
14	chr12:67073022-67073072	HRCEpiC	kidney:	n/a
15	chr12:67072769-67072819	PANC-1	pancreas:	n/a
16	chr12:67072769-67072819	HMEC	breast:	n/a
17	chr12:67072769-67072819	NB4	blood:	n/a
18	chr12:67127781-67127831	HL-60	blood:	n/a
19	chr12:67073062-67073112	HL-60	blood:	n/a
20	chr12:67073022-67073072	ovcar-3	ovarian:	n/a
21	chr12:67073266-67073316	HCF	heart:	n/a
22	chr12:67073022-67073072	Jurkat	blood:	n/a
23	chr12:67073062-67073112	HMEC	breast:	n/a
24	chr12:67073022-67073072	GM12891	blood:	n/a
25	chr12:67072951-67073001	NB4	blood:	n/a
26	chr12:67127781-67127831	LNCaP	prostate:	n/a
27	chr12:67072951-67073001	BJ	skin:	n/a
28	chr12:67127781-67127831	ovcar-3	ovarian:	n/a
29	chr12:67072951-67073001	ECC-1	luminal epithelium:	n/a
30	chr12:67073062-67073112	A549	lung:	n/a
31	chr12:67073266-67073316	HRE	kidney:	n/a
32	chr12:67160208-67160258	Hela-S3	cervix:	n/a
33	chr12:67073266-67073316	NHBE	bronchial:	n/a
34	chr12:67073760-67073810	MCF10A-Er-Src	breast:	n/a
35	chr12:67160208-67160258	SK-N-SH_RA	brain:	n/a
36	chr12:67072951-67073001	HCPEpiC	choroid plexus:	n/a
37	chr12:67073266-67073316	SK-N-SH_RA	brain:	n/a
38	chr12:67073022-67073072	HMEC	breast:	n/a
39	chr12:67072769-67072819	SAEC	small airway:	n/a
40	chr12:67072951-67073001	HL-60	blood:	n/a
41	chr12:67127781-67127831	PANC-1	pancreas:	n/a
42	chr12:67072951-67073001	LNCaP	prostate:	n/a
43	chr12:67073062-67073112	PrEC	prostate:	n/a
44	chr12:67127781-67127831	GM06990	blood:	n/a
45	chr12:67073062-67073112	SKMC	muscle:	n/a
46	chr12:67127781-67127831	AG09309	skin:	n/a
47	chr12:67160208-67160258	GM06990	blood:	n/a
48	chr12:67073760-67073810	HAEpiC	amniotic membrane:	n/a
49	chr12:67073022-67073072	MCF10A-Er-Src	breast:	n/a
50	chr12:67127781-67127831	HepG2	liver:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:67102904..67104726-chr12:67105810..67107426,2	MCF-7	breast:
2	chr12:67082410..67083294-chr12:67254648..67255604,5	MCF-7	breast:
3	chr12:67079528..67081954-chr12:67090312..67092253,2	K562	blood:
4	chr12:67092025..67093817-chr12:67096340..67098697,2	MCF-7	breast:
5	chr12:67103027..67105591-chr12:67109305..67111957,2	K562	blood:
6	chr12:66745697..66746293-chr12:67082336..67083172,2	MCF-7	breast:
7	chr12:67083332..67087175-chr12:67091989..67094050,4	K562	blood:
8	chr12:67054441..67056343-chr12:67057026..67059042,3	MCF-7	breast:
9	chr12:67103027..67105591-chr12:67109305..67111957,2	K562	blood:
10	chr12:67132372..67134745-chr12:67135516..67139525,4	MCF-7	breast:
11	chr12:67155440..67157393-chr12:67158810..67161653,2	MCF-7	breast:
12	chr12:66924711..66926666-chr12:67101075..67103092,2	MCF-7	breast:
13	chr12:67105154..67107956-chr12:67110716..67113455,2	MCF-7	breast:
14	chr12:67092981..67095022-chr12:67095390..67096975,2	MCF-7	breast:
15	chr12:67091996..67092975-chr12:67101719..67102723,3	MCF-7	breast:
16	chr12:67083332..67087175-chr12:67091989..67094050,4	K562	blood:
17	chr12:67076449..67078895-chr12:67089539..67091893,2	MCF-7	breast:
18	chr12:66942264..66943151-chr12:67082787..67083333,2	MCF-7	breast:
19	chr12:67109144..67111332-chr12:67122763..67125755,2	K562	blood:
20	chr12:67071707..67074499-chr12:67077173..67078844,2	K562	blood:
21	chr12:67092019..67092945-chr12:67254522..67255578,9	MCF-7	breast:
22	chr12:67092025..67093817-chr12:67096340..67098697,2	MCF-7	breast:
23	chr12:67073537..67076031-chr12:67078174..67080837,2	K562	blood:
24	chr12:67092981..67095022-chr12:67095390..67096975,2	MCF-7	breast:
25	chr12:67110006..67111455-chr12:67254721..67255586,6	MCF-7	breast:
26	chr12:67174375..67176870-chr12:67178960..67180503,2	K562	blood:
27	chr12:67173926..67176766-chr12:67210508..67212832,2	MCF-7	breast:
28	chr12:67053423..67055434-chr12:67055731..67058319,2	K562	blood:
29	chr12:67109764..67110463-chr12:67254735..67255402,2	MCF-7	breast:
30	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
31	chr12:67082373..67083323-chr12:67255078..67255633,2	MCF-7	breast:
32	chr12:67184228..67185827-chr12:67187513..67190445,3	MCF-7	breast:
33	chr12:67105154..67107956-chr12:67110716..67113455,2	MCF-7	breast:
34	chr12:67075881..67076642-chr12:67254630..67255196,2	MCF-7	breast:
35	chr12:67076449..67078895-chr12:67089539..67091893,2	MCF-7	breast:
36	chr12:67067995..67069958-chr12:67071524..67073123,2	MCF-7	breast:
37	chr12:67071707..67073529-chr12:67076657..67078844,2	K562	blood:
38	chr12:67073537..67076031-chr12:67078174..67080837,2	K562	blood:
39	chr12:67102904..67104726-chr12:67105810..67107426,2	MCF-7	breast:
40	chr12:67133078..67135278-chr12:67140129..67142008,2	MCF-7	breast:
41	chr12:67135712..67138658-chr12:67140137..67142202,2	K562	blood:
42	chr12:67155440..67157393-chr12:67158810..67161653,2	MCF-7	breast:
43	chr12:67079528..67081954-chr12:67090312..67092253,2	K562	blood:
44	chr12:67181348..67184002-chr12:67184358..67185894,2	K562	blood:
45	chr12:66745711..66746634-chr12:67087184..67088269,6	MCF-7	breast:
46	chr12:67091996..67092975-chr12:67101719..67102723,3	MCF-7	breast:
47	chr12:67133078..67135278-chr12:67140129..67142008,2	MCF-7	breast:
48	chr12:67169597..67171791-chr2:190019336..190021927,2	MCF-7	breast:
49	chr12:67110471..67111538-chr12:67254403..67256131,14	MCF-7	breast:
50	chr12:67132372..67134745-chr12:67135516..67139525,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMBIM4-4	chr12:67111894-67112178	l_672_chr12:67111893-67114021_adrenal
2	lnc-TMBIM4-4	chr12:67113331-67113418	l_672_chr12:67111893-67114021_adrenal
3	lnc-TMBIM4-4	chr12:67113856-67114021	l_672_chr12:67111893-67114021_adrenal
4	lnc-TMBIM4-4	chr12:67115010-67115062	l_672_chr12:67111893-67114021_adrenal
5	lnc-TMBIM4-4	chr12:67112662-67112726	l_672_chr12:67111893-67114021_adrenal
6	lnc-TMBIM4-4	chr12:67122111-67122188	l_672_chr12:67111893-67114021_adrenal
7	lnc-TMBIM4-4	chr12:67131414-67131624	l_672_chr12:67111893-67114021_adrenal

No data

Variant related genes	Relation type
GRIP1	TF binding region
GRIP1	CpG island
ENSG00000155974	chromatin interactions

Extended variants
information (count: 4528 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4528 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11176366	chr12:67056831-67056832	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190671900	chr12:67056833-67056834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559818859	chr12:67056838-67056839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139271383	chr12:67056866-67056867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537662370	chr12:67056900-67056901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556178542	chr12:67056913-67056914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs142588883	chr12:67056933-67056934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs528629897	chr12:67056937-67056938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369641855	chr12:67056940-67056941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528545360	chr12:67056958-67056959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376829773	chr12:67057001-67057002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs548180508	chr12:67057036-67057037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74098225	chr12:67057044-67057045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs183246471	chr12:67057083-67057084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554164066	chr12:67057190-67057191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572370403	chr12:67057193-67057194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568164870	chr12:67057208-67057209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35031382	chr12:67057236-67057237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558622671	chr12:67057248-67057249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368792306	chr12:67057249-67057250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546284569	chr12:67057274-67057275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564580435	chr12:67057287-67057288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576663788	chr12:67057328-67057329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544076995	chr12:67057338-67057339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146661036	chr12:67057370-67057371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368474522	chr12:67057395-67057396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146009159	chr12:67057405-67057406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529628228	chr12:67057453-67057454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371488163	chr12:67057472-67057473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7977214	chr12:67057498-67057499	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs560067832	chr12:67057500-67057501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7977223	chr12:67057533-67057534	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs7977133	chr12:67057551-67057552	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs570255744	chr12:67057592-67057593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187726137	chr12:67057610-67057611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549979717	chr12:67057631-67057632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568240723	chr12:67057648-67057649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78564134	chr12:67057744-67057745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190682572	chr12:67057765-67057766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139299656	chr12:67057799-67057800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs150020647	chr12:67057812-67057813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs145193656	chr12:67057837-67057838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576651101	chr12:67057897-67057898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551923623	chr12:67057921-67057922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543639309	chr12:67057965-67057966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562336230	chr12:67058022-67058023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574175513	chr12:67058124-67058125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541678770	chr12:67058136-67058137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs17181903	chr12:67058160-67058161	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs112211708	chr12:67058188-67058189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Fibroblasts	20926602	CNVD
Metanephric adenoma	20802469	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Mental retardation	17220210	CNVD
Osteopoikilosis	17220210	CNVD
short stature	17220210	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Ovarian neoplasms	16753589	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16620391	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21364760	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	22048815	CNVD
Congenital anomalies of the kidney and urinary tract	21113617	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Myxofibrosarcoma	16751306	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Lung cancer	17925434	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Disease	21505450	CNVD
craniofacial dysmorphism	21918468	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	21569311	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67053000-67062200	Weak transcription	Right Atrium	heart
2	chr12:67054600-67059600	Enhancers	Primary B cells from cord blood	blood
3	chr12:67054800-67057800	Enhancers	Primary B cells from peripheral blood	blood
4	chr12:67055000-67057200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr12:67055200-67058200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:67055600-67057000	Enhancers	Fetal Lung	lung
7	chr12:67055600-67057800	Enhancers	HMEC	breast
8	chr12:67055800-67058200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:67056000-67057000	Enhancers	Fetal Brain Male	brain
10	chr12:67056000-67057000	Enhancers	HSMM	muscle
11	chr12:67056000-67057400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr12:67056000-67057400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:67056000-67057400	Enhancers	HUVEC	blood vessel
14	chr12:67056000-67061600	Weak transcription	HSMMtube	muscle
15	chr12:67056200-67057000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:67056400-67057200	Weak transcription	Colon Smooth Muscle	Colon
17	chr12:67056400-67057400	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr12:67056400-67057600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr12:67056400-67057600	Enhancers	Fetal Heart	heart
20	chr12:67056400-67059400	Enhancers	Brain Germinal Matrix	brain
21	chr12:67056800-67058600	Enhancers	NHEK	skin
22	chr12:67056800-67058800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr12:67056800-67061400	Weak transcription	NH-A	brain
24	chr12:67057000-67057400	Weak transcription	Fetal Brain Male	brain
25	chr12:67057000-67058000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:67057000-67061800	Weak transcription	HSMM	muscle
27	chr12:67057200-67058000	Enhancers	Colon Smooth Muscle	Colon
28	chr12:67057200-67059200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:67057400-67057600	Enhancers	Fetal Brain Male	brain
30	chr12:67057400-67057600	Enhancers	Stomach Smooth Muscle	stomach
31	chr12:67057400-67058800	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr12:67057400-67061400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr12:67057600-67057800	Enhancers	Pancreas	Pancrea
34	chr12:67057600-67058600	Weak transcription	Fetal Brain Male	brain
35	chr12:67057600-67060400	Weak transcription	Fetal Heart	heart
36	chr12:67057600-67062000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:67057800-67058800	Weak transcription	Primary B cells from peripheral blood	blood
38	chr12:67057800-67061600	Weak transcription	HMEC	breast
39	chr12:67057800-67062200	Weak transcription	Pancreas	Pancrea
40	chr12:67058000-67059200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr12:67058000-67059400	Weak transcription	Colon Smooth Muscle	Colon
42	chr12:67058200-67059000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr12:67058200-67063400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr12:67058600-67059000	Weak transcription	NHEK	skin
45	chr12:67058600-67059200	Enhancers	Fetal Brain Male	brain
46	chr12:67058800-67059000	Enhancers	Primary B cells from peripheral blood	blood
47	chr12:67058800-67059600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr12:67058800-67059800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr12:67059000-67059600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr12:67059000-67059600	Enhancers	NHEK	skin

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