Variant report

Variant	nsv1037260
Chromosome Location	chr12:123956749-124023069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1389)
CpG islands
(count:795)
Chromatin interactive
region (count:109)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1389 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:124018494-124018555	K562	blood:	n/a	n/a
2	ARID3A	chr12:124017367-124017624	K562	blood:	n/a	n/a
3	ARID3A	chr12:124003707-124004059	HepG2	liver:	n/a	n/a
4	BACH1	chr12:124019171-124019340	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:124018798-124018914	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:123968146-123968423	GM12878	blood:	n/a	chr12:123968294-123968305
7	BCL11A	chr12:124016656-124016943	GM12878	blood:	n/a	chr12:124016835-124016844
8	BCL3	chr12:124015207-124015490	GM12878	blood:	n/a	n/a
9	BCL3	chr12:124017686-124018120	A549	lung:	n/a	chr12:124018049-124018058 chr12:124017704-124017717
10	BCLAF1	chr12:124016596-124017027	GM12878	blood:	n/a	chr12:124016835-124016844
11	BHLHE40	chr12:124017508-124017986	HepG2	liver:	n/a	chr12:124017636-124017652
12	BHLHE40	chr12:123956962-123957454	HepG2	liver:	n/a	n/a
13	BHLHE40	chr12:124003729-124004077	HepG2	liver:	n/a	n/a
14	BHLHE40	chr12:124018484-124018487	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:123956931-123957373	HepG2	liver:	n/a	n/a
16	BHLHE40	chr12:124018423-124019050	HepG2	liver:	n/a	n/a
17	BHLHE40	chr12:124017420-124018105	K562	blood:	n/a	chr12:124017636-124017652
18	BHLHE40	chr12:123956984-123957446	HepG2	liver:	n/a	n/a
19	BHLHE40	chr12:124016448-124016532	K562	blood:	n/a	n/a
20	BHLHE40	chr12:124017548-124018031	GM12878	blood:	n/a	chr12:124017636-124017652
21	BRCA1	chr12:124017817-124017913	HepG2	liver:	n/a	n/a
22	BRCA1	chr12:124017418-124017970	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr12:123982463-123982739	K562	blood:	n/a	n/a
24	CBX3	chr12:124017259-124018108	K562	blood:	n/a	n/a
25	CCNT2	chr12:124017594-124018993	K562	blood:	n/a	chr12:124018745-124018754
26	CEBPB	chr12:124018984-124018993	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:123982687-123982999	A549	lung:	n/a	chr12:123982818-123982829
28	CEBPB	chr12:124000573-124000766	HepG2	liver:	n/a	n/a
29	CEBPB	chr12:123978629-123978929	HepG2	liver:	n/a	n/a
30	CEBPB	chr12:123982641-123983273	HepG2	liver:	n/a	chr12:123982818-123982829
31	CEBPB	chr12:124000511-124000754	IMR90	lung:	n/a	n/a
32	CEBPB	chr12:124000476-124000758	K562	blood:	n/a	n/a
33	CEBPB	chr12:123982769-123982948	IMR90	lung:	n/a	chr12:123982818-123982829
34	CEBPB	chr12:123956974-123957221	HepG2	liver:	n/a	n/a
35	CEBPB	chr12:123982698-123983328	HepG2	liver:	n/a	chr12:123982818-123982829
36	CEBPB	chr12:124019007-124019041	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:124017334-124018091	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr12:123982741-123982944	K562	blood:	n/a	chr12:123982818-123982829
39	CEBPB	chr12:124000502-124000812	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr12:123982610-123982991	MCF-7	breast:	n/a	chr12:123982818-123982829
41	CEBPB	chr12:124003729-124004082	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:124003707-124004158	MCF-7	breast:	n/a	n/a
43	CEBPB	chr12:123982727-123982889	HepG2	liver:	n/a	chr12:123982818-123982829
44	CEBPB	chr12:123978630-123978882	A549	lung:	n/a	n/a
45	CEBPB	chr12:124003796-124003973	HepG2	liver:	n/a	n/a
46	CEBPB	chr12:124004971-124005076	HepG2	liver:	n/a	n/a
47	CEBPB	chr12:124000488-124000809	K562	blood:	n/a	n/a
48	CEBPD	chr12:124018426-124018877	HepG2	liver:	n/a	n/a
49	CEBPD	chr12:124018621-124018818	HepG2	liver:	n/a	n/a
50	CEBPD	chr12:123956907-123957216	HepG2	liver:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124018993-124019043	Hela-S3	cervix:	n/a
2	chr12:124021914-124021964	GM12892	blood:	n/a
3	chr12:124018993-124019043	Hela-S3	cervix:	n/a
4	chr12:124021914-124021964	GM12892	blood:	n/a
5	chr12:123957442-123957492	SKMC	muscle:	n/a
6	chr12:124018993-124019043	HCT-116	colon:	n/a
7	chr12:123998085-123998135	HRPEpiC	eye:	n/a
8	chr12:124021914-124021964	HL-60	blood:	n/a
9	chr12:123957029-123957079	PANC-1	pancreas:	n/a
10	chr12:124016861-124016911	Hepatocyte	liver:	n/a
11	chr12:124014409-124014459	HEK293	kidney:	embryo
12	chr12:124019284-124019334	HL-60	blood:	n/a
13	chr12:124017975-124018025	NHBE	bronchial:	n/a
14	chr12:123957442-123957492	HRCEpiC	kidney:	n/a
15	chr12:124018993-124019043	NT2-D1	testis:	n/a
16	chr12:124016861-124016911	HRCEpiC	kidney:	n/a
17	chr12:124017975-124018025	Hepatocyte	liver:	n/a
18	chr12:123998085-123998135	AG04449	skin:	fetal
19	chr12:123957410-123957460	BE2_C	brain:	n/a
20	chr12:123998115-123998165	U87	brain:	n/a
21	chr12:124016861-124016911	SKMC	muscle:	n/a
22	chr12:124021914-124021964	GM06990	blood:	n/a
23	chr12:124018993-124019043	SKMC	muscle:	n/a
24	chr12:123957029-123957079	GM12878	blood:	n/a
25	chr12:123957029-123957079	HEK293	kidney:	embryo
26	chr12:124018492-124018542	NT2-D1	testis:	n/a
27	chr12:124018993-124019043	PrEC	prostate:	n/a
28	chr12:124019284-124019334	CMK	blood:	n/a
29	chr12:124014409-124014459	GM19239	blood:	n/a
30	chr12:124014409-124014459	ECC-1	luminal epithelium:	n/a
31	chr12:124019284-124019334	GM12892	blood:	n/a
32	chr12:124014409-124014459	HAEpiC	amniotic membrane:	n/a
33	chr12:123998115-123998165	HPAEpiC	pulmonary alveolar:	n/a
34	chr12:123957442-123957492	HCT-116	colon:	n/a
35	chr12:124014409-124014459	Caco-2	colon:	n/a
36	chr12:124019284-124019334	PFSK-1	brain:	n/a
37	chr12:124018993-124019043	RPTEC	kidney:	n/a
38	chr12:123998085-123998135	GM12878	blood:	n/a
39	chr12:123998115-123998165	NH-A	brain:	n/a
40	chr12:123998085-123998135	NT2-D1	testis:	n/a
41	chr12:124019284-124019334	NB4	blood:	n/a
42	chr12:124016861-124016911	HCT-116	colon:	n/a
43	chr12:124018492-124018542	HCF	heart:	n/a
44	chr12:123957029-123957079	K562	blood:	n/a
45	chr12:124014409-124014459	HCPEpiC	choroid plexus:	n/a
46	chr12:124019284-124019334	ECC-1	luminal epithelium:	n/a
47	chr12:123957029-123957079	MCF-7	breast:	n/a
48	chr12:124018492-124018542	Jurkat	blood:	n/a
49	chr12:124021914-124021964	HNPCEpiC	eye:	n/a
50	chr12:123957029-123957079	NT2-D1	testis:	n/a

(count:109 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr12:123991239..123993026-chr12:124017278..124020244,2	MCF-7	breast:
2	chr12:123948940..123951509-chr12:124017235..124019368,2	MCF-7	breast:
3	chr12:123990733..123992754-chr12:123992876..123995822,2	MCF-7	breast:
4	chr12:124008463..124013124-chr12:124014349..124019990,8	MCF-7	breast:
5	chr12:123988823..123991080-chr12:124013221..124015111,2	K562	blood:
6	chr12:123988823..123991080-chr12:124013221..124015111,2	K562	blood:
7	chr12:123962852..123965430-chr12:123971196..123972717,2	K562	blood:
8	chr12:123960921..123963126-chr12:124005515..124007518,2	K562	blood:
9	chr12:123912338..123913868-chr12:124018894..124020678,2	K562	blood:
10	chr12:123848570..123850665-chr12:124003755..124005978,2	MCF-7	breast:
11	chr12:123971133..123973721-chr12:123974833..123977007,2	K562	blood:
12	chr12:124018963..124020649-chr12:124025084..124027162,2	MCF-7	breast:
13	chr12:124013201..124014769-chr12:124068693..124071334,2	MCF-7	breast:
14	chr12:124015709..124018064-chr12:124066858..124069100,3	MCF-7	breast:
15	chr12:124017823..124018449-chr6:26156256..26156790,2	HCT-116	colon:
16	chr12:123966913..123969860-chr12:123971684..123973718,2	K562	blood:
17	chr12:124006455..124008310-chr12:124016022..124017705,2	K562	blood:
18	chr12:123967112..123969101-chr12:124016900..124018566,2	K562	blood:
19	chr12:123954067..123957606-chr12:124016638..124019089,3	MCF-7	breast:
20	chr12:123981034..123983200-chr12:124016906..124019887,2	MCF-7	breast:
21	chr12:124002890..124005569-chr12:124009063..124010830,3	MCF-7	breast:
22	chr12:123859632..123861218-chr12:123970833..123973407,2	K562	blood:
23	chr12:123996470..123998238-chr12:124004249..124005999,2	K562	blood:
24	chr12:124017444..124019100-chr12:124084646..124086674,2	MCF-7	breast:
25	chr12:123981817..123985054-chr12:123986830..123990425,4	K562	blood:
26	chr12:123942477..123944445-chr12:123961035..123963054,2	K562	blood:
27	chr12:123944753..123946360-chr12:124004239..124006066,2	K562	blood:
28	chr12:123960921..123963126-chr12:124005515..124007518,2	K562	blood:
29	chr12:123871162..123873569-chr12:123956036..123957807,2	MCF-7	breast:
30	chr12:124003899..124005845-chr12:124016075..124018818,3	MCF-7	breast:
31	chr12:124018210..124020140-chr12:124067644..124069375,2	MCF-7	breast:
32	chr12:123872416..123876102-chr12:124017252..124019601,4	MCF-7	breast:
33	chr12:123997284..124000079-chr12:124017073..124019484,2	MCF-7	breast:
34	chr12:123997284..124000079-chr12:124017073..124019484,2	MCF-7	breast:
35	chr12:124009480..124011316-chr12:124016803..124019267,2	K562	blood:
36	chr12:123988703..123991026-chr12:123998047..123999844,2	MCF-7	breast:
37	chr12:123848006..123850199-chr12:123954531..123957237,2	MCF-7	breast:
38	chr12:123873494..123875550-chr12:124015653..124017169,2	MCF-7	breast:
39	chr12:124018289..124019128-chr19:50370267..50370907,2	Hela-S3	cervix:
40	chr12:123865983..123868893-chr12:123989514..123992053,2	K562	blood:
41	chr12:123874611..123876401-chr12:123967217..123969868,2	K562	blood:
42	chr12:123982775..123984633-chr12:124027531..124030099,2	MCF-7	breast:
43	chr12:123942564..123944577-chr12:124016063..124019666,4	MCF-7	breast:
44	chr12:123921093..123923259-chr12:123989085..123991083,2	K562	blood:
45	chr12:124007811..124010230-chr12:124011879..124014265,2	MCF-7	breast:
46	chr12:123998884..124001416-chr12:124016546..124018370,2	K562	blood:
47	chr12:123944467..123946033-chr12:123963161..123965280,2	K562	blood:
48	chr12:123987186..123989370-chr12:124003960..124006021,2	K562	blood:
49	chr12:123998884..124001416-chr12:124016546..124018370,2	K562	blood:
50	chr12:124016749..124018606-chr12:124069216..124071514,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNRNP35-1	chr12:123955639-123956909	NR_104103
2	lnc-SNRNP35-2	chr12:123997031-123997972	NONHSAT031595
3	lnc-SNRNP35-2	chr12:123994929-123996488	NONHSAT031595

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3908	chr12:124020960-124020981	MIMAT0018182

No data

Variant related genes	Relation type
MIR3908	TF binding region
RILPL1	TF binding region
MIR3908	CpG island
RILPL1	CpG island
ENSG00000111358	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000247373	chromatin interactions
ENSG00000139697	chromatin interactions
ENSG00000206897	chromatin interactions
ENSG00000111361	chromatin interactions
ENSG00000086598	chromatin interactions
ENSG00000266655	chromatin interactions
ENSG00000111364	chromatin interactions
ENSG00000256092	chromatin interactions
ENSG00000039650	chromatin interactions
ENSG00000183955	chromatin interactions
ENSG00000188026	chromatin interactions
ENSG00000184209	chromatin interactions
ENSG00000111328	chromatin interactions
ENSG00000150977	chromatin interactions

Extended variants
information (count: 2642 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2642 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3087496	chr12:123956749-123956750	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34523817	chr12:123956762-123956763	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs189339637	chr12:123956868-123956869	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs112742410	chr12:123956875-123956876	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs180921742	chr12:123956884-123956885	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs28613273	chr12:123956904-123956905	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs540807021	chr12:123956918-123956919	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs550750125	chr12:123956930-123956931	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs186338013	chr12:123956948-123956949	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs138712056	chr12:123956956-123956957	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs564091212	chr12:123956970-123956971	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs554637256	chr12:123956991-123956992	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs111439154	chr12:123956995-123956996	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs372948599	chr12:123957030-123957031	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs368948563	chr12:123957049-123957050	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs533696214	chr12:123957081-123957082	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs369661610	chr12:123957133-123957134	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs374451690	chr12:123957135-123957136	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs558610701	chr12:123957164-123957165	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs543677202	chr12:123957165-123957166	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs544426494	chr12:123957171-123957172	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs368368110	chr12:123957201-123957202	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs371036576	chr12:123957277-123957278	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562709136	chr12:123957287-123957288	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs574829269	chr12:123957332-123957333	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs371622049	chr12:123957336-123957337	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs116576935	chr12:123957341-123957342	Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs115998695	chr12:123957411-123957412	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs117739839	chr12:123957425-123957426	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs114746659	chr12:123957446-123957447	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73412254	chr12:123957493-123957494	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564609566	chr12:123957639-123957640	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs11535679	chr12:123957640-123957641	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs550809220	chr12:123957669-123957670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs113135850	chr12:123957718-123957719	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs569054516	chr12:123957733-123957734	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371590740	chr12:123957773-123957774	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548770623	chr12:123957789-123957790	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536575402	chr12:123957859-123957860	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs528712763	chr12:123957860-123957861	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs201067178	chr12:123957867-123957868	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs71088916	chr12:123957868-123957869	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200493792	chr12:123957869-123957870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566384695	chr12:123957878-123957879	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181581460	chr12:123957895-123957896	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558218473	chr12:123957906-123957907	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs186245964	chr12:123957937-123957938	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs9803116	chr12:123957966-123957967	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs190962183	chr12:123957976-123957977	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs574689046	chr12:123957994-123957995	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2761 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123943800-123958800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:123943800-123959600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:123943800-123959600	Weak transcription	Psoas Muscle	Psoas
4	chr12:123943800-123961200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr12:123944600-123995600	Weak transcription	Hela-S3	cervix
6	chr12:123944600-124012200	Strong transcription	Fetal Stomach	stomach
7	chr12:123944800-123964600	Weak transcription	Small Intestine	intestine
8	chr12:123945200-123959200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr12:123945800-123965600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr12:123946000-123965600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr12:123946200-123957600	Strong transcription	Fetal Thymus	thymus
12	chr12:123946200-123957800	Strong transcription	Fetal Muscle Leg	muscle
13	chr12:123946800-123959200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr12:123947200-123958600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr12:123947600-123971800	Strong transcription	Fetal Intestine Small	intestine
16	chr12:123948200-123962800	Strong transcription	Fetal Muscle Trunk	muscle
17	chr12:123949000-123957800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr12:123949000-123966200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:123949000-123984400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr12:123949200-123957600	Strong transcription	Primary T cells from cord blood	blood
21	chr12:123949200-123957600	Strong transcription	Stomach Smooth Muscle	stomach
22	chr12:123950000-123963200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:123950400-123973000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr12:123950600-123958800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr12:123950600-123958800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr12:123950800-123961400	Weak transcription	Right Atrium	heart
27	chr12:123950800-124007600	Weak transcription	Colonic Mucosa	Colon
28	chr12:123952400-123957600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:123953200-123957600	Strong transcription	Placenta Amnion	Placenta Amnion
30	chr12:123953800-123956800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr12:123953800-123968200	Weak transcription	GM12878-XiMat	blood
32	chr12:123954200-123957600	Strong transcription	Brain Substantia Nigra	brain
33	chr12:123954200-123957800	Strong transcription	Brain Hippocampus Middle	brain
34	chr12:123954200-123964600	Strong transcription	Fetal Lung	lung
35	chr12:123954200-123971000	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr12:123954400-123957600	Strong transcription	Adipose Nuclei	Adipose
37	chr12:123954400-123957600	Strong transcription	HSMMtube	muscle
38	chr12:123954400-123957800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr12:123954400-123957800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:123954400-123961200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr12:123954600-123957200	Strong transcription	Colon Smooth Muscle	Colon
42	chr12:123954600-123957400	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr12:123954600-123957600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr12:123954600-123957600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr12:123954600-123957600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr12:123954600-123957600	Strong transcription	Placenta	Placenta
47	chr12:123954600-123957600	Strong transcription	Lung	lung
48	chr12:123954600-123957600	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr12:123954800-123957000	Strong transcription	Spleen	Spleen
50	chr12:123954800-123957600	Strong transcription	Brain Anterior Caudate	brain

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