Variant report

Variant	nsv1032464
Chromosome Location	chr5:112076061-112192380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:925)
CpG islands
(count:183)
Chromatin interactive
region (count:90)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:112130972-112131342	K562	blood:	n/a	n/a
2	ARID3A	chr5:112093343-112093652	K562	blood:	n/a	n/a
3	ARID3A	chr5:112078257-112078771	K562	blood:	n/a	n/a
4	ARID3A	chr5:112190980-112191136	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:112183987-112184179	K562	blood:	n/a	n/a
6	ATF1	chr5:112078087-112078543	K562	blood:	n/a	n/a
7	ATF2	chr5:112184002-112184276	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr5:112078181-112078413	K562	blood:	n/a	n/a
9	BACH1	chr5:112078317-112078667	K562	blood:	n/a	n/a
10	BACH1	chr5:112133552-112133730	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:112174332-112174337	K562	blood:	n/a	n/a
12	BACH1	chr5:112177582-112177905	K562	blood:	n/a	n/a
13	BACH1	chr5:112175678-112176318	K562	blood:	n/a	n/a
14	BACH1	chr5:112098083-112098175	K562	blood:	n/a	n/a
15	BACH1	chr5:112178733-112178940	K562	blood:	n/a	n/a
16	BACH1	chr5:112184062-112184354	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr5:112175099-112175345	K562	blood:	n/a	n/a
18	BACH1	chr5:112133692-112133888	K562	blood:	n/a	n/a
19	BATF	chr5:112184000-112184275	GM12878	blood:	n/a	n/a
20	BCL3	chr5:112146817-112147132	GM12878	blood:	n/a	n/a
21	BCLAF1	chr5:112183907-112184300	GM12878	blood:	n/a	chr5:112184052-112184061
22	BHLHE40	chr5:112078050-112078722	K562	blood:	n/a	n/a
23	BHLHE40	chr5:112183826-112184181	K562	blood:	n/a	n/a
24	BRCA1	chr5:112183982-112184350	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:112093416-112093570	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr5:112190403-112190716	K562	blood:	n/a	n/a
27	CBX3	chr5:112175360-112175786	K562	blood:	n/a	n/a
28	CBX3	chr5:112078032-112078532	K562	blood:	n/a	n/a
29	CBX3	chr5:112190417-112190712	K562	blood:	n/a	n/a
30	CCNT2	chr5:112131109-112131323	K562	blood:	n/a	n/a
31	CCNT2	chr5:112111899-112112038	K562	blood:	n/a	n/a
32	CEBPB	chr5:112159680-112160033	K562	blood:	n/a	chr5:112159859-112159870
33	CEBPB	chr5:112122991-112123292	IMR90	lung:	n/a	n/a
34	CEBPB	chr5:112129799-112129926	K562	blood:	n/a	n/a
35	CEBPB	chr5:112159702-112159992	IMR90	lung:	n/a	chr5:112159859-112159870
36	CEBPB	chr5:112159758-112160081	MCF-7	breast:	n/a	chr5:112159859-112159870
37	CEBPB	chr5:112163762-112163793	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:112183095-112183355	A549	lung:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
39	CEBPB	chr5:112131102-112131423	K562	blood:	n/a	n/a
40	CEBPB	chr5:112146183-112146433	HepG2	liver:	n/a	n/a
41	CEBPB	chr5:112106567-112106720	IMR90	lung:	n/a	chr5:112106636-112106647
42	CEBPB	chr5:112183069-112183373	K562	blood:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
43	CEBPB	chr5:112122376-112122699	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:112115159-112115510	A549	lung:	n/a	chr5:112115337-112115348
45	CEBPB	chr5:112146166-112146418	A549	lung:	n/a	n/a
46	CEBPB	chr5:112115167-112115502	HepG2	liver:	n/a	chr5:112115337-112115348
47	CEBPB	chr5:112159744-112160018	A549	lung:	n/a	chr5:112159859-112159870
48	CEBPB	chr5:112183059-112183386	IMR90	lung:	n/a	chr5:112183214-112183225 chr5:112183214-112183223 chr5:112183212-112183223
49	CEBPB	chr5:112159730-112159991	H1-hESC	embryonic stem cell:	n/a	chr5:112159859-112159870
50	CEBPB	chr5:112120449-112120736	IMR90	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:112130390-112130440	Jurkat	blood:	n/a
2	chr5:112160748-112160798	SK-N-SH_RA	brain:	n/a
3	chr5:112160748-112160798	GM12878	blood:	n/a
4	chr5:112182657-112182707	GM06990	blood:	n/a
5	chr5:112160748-112160798	PFSK-1	brain:	n/a
6	chr5:112160748-112160798	HUVEC	blood vessel:	n/a
7	chr5:112160748-112160798	NH-A	brain:	n/a
8	chr5:112182657-112182707	RPTEC	kidney:	n/a
9	chr5:112160748-112160798	K562	blood:	n/a
10	chr5:112160748-112160798	BE2_C	brain:	n/a
11	chr5:112160748-112160798	SK-N-SH	brain:	n/a
12	chr5:112182657-112182707	IMR90	lung:	fetal
13	chr5:112130390-112130440	NHDF-neo	bronchial:	n/a
14	chr5:112130390-112130440	PANC-1	pancreas:	n/a
15	chr5:112160748-112160798	U87	brain:	n/a
16	chr5:112182657-112182707	Hela-S3	cervix:	n/a
17	chr5:112130390-112130440	AoSMC	blood vessel:	n/a
18	chr5:112130390-112130440	H1-hESC	embryonic stem cell:	embryo
19	chr5:112160748-112160798	MCF-7	breast:	n/a
20	chr5:112160748-112160798	ECC-1	luminal epithelium:	n/a
21	chr5:112160748-112160798	Hela-S3	cervix:	n/a
22	chr5:112182657-112182707	NT2-D1	testis:	n/a
23	chr5:112182657-112182707	BE2_C	brain:	n/a
24	chr5:112182657-112182707	BJ	skin:	n/a
25	chr5:112130390-112130440	Hepatocyte	liver:	n/a
26	chr5:112160748-112160798	HAEpiC	amniotic membrane:	n/a
27	chr5:112130390-112130440	GM12892	blood:	n/a
28	chr5:112160748-112160798	HEEpiC	esophagus:	n/a
29	chr5:112160748-112160798	HIPEpiC	eye:	n/a
30	chr5:112160748-112160798	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:112130390-112130440	NHBE	bronchial:	n/a
32	chr5:112160748-112160798	H1-hESC	embryonic stem cell:	embryo
33	chr5:112182657-112182707	GM12891	blood:	n/a
34	chr5:112160748-112160798	BJ	skin:	n/a
35	chr5:112182657-112182707	NHDF-neo	bronchial:	n/a
36	chr5:112160748-112160798	HCM	heart:	n/a
37	chr5:112182657-112182707	ovcar-3	ovarian:	n/a
38	chr5:112182657-112182707	HCF	heart:	n/a
39	chr5:112160748-112160798	T-47D	breast:	n/a
40	chr5:112130390-112130440	MCF-7	breast:	n/a
41	chr5:112130390-112130440	PrEC	prostate:	n/a
42	chr5:112160748-112160798	A549	lung:	n/a
43	chr5:112160748-112160798	HEK293	kidney:	embryo
44	chr5:112130390-112130440	HL-60	blood:	n/a
45	chr5:112160748-112160798	HRCEpiC	kidney:	n/a
46	chr5:112130390-112130440	AG04450	lung:	fetal
47	chr5:112182657-112182707	A549	lung:	n/a
48	chr5:112160748-112160798	HMEC	breast:	n/a
49	chr5:112160748-112160798	AG04450	lung:	fetal
50	chr5:112130390-112130440	GM12878	blood:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:112103979..112106564-chr5:112195241..112197726,2	K562	blood:
2	chr5:112064316..112067247-chr5:112074858..112077502,2	K562	blood:
3	chr5:112077462..112079150-chr5:112174470..112176548,2	K562	blood:
4	chr5:112077462..112079150-chr5:112174470..112176548,2	K562	blood:
5	chr5:112071994..112074935-chr5:112084057..112088000,3	K562	blood:
6	chr5:112157931..112160849-chr5:112162546..112165691,3	MCF-7	breast:
7	chr5:112027068..112028032-chr5:112092853..112093558,4	MCF-7	breast:
8	chr5:112065589..112068321-chr5:112080133..112082832,2	MCF-7	breast:
9	chr5:112186187..112188435-chr5:112189268..112191839,2	K562	blood:
10	chr5:112137172..112140072-chr5:112143234..112145432,3	K562	blood:
11	chr5:111881640..111883991-chr5:112093471..112095416,2	K562	blood:
12	chr5:112188139..112189765-chr5:112194415..112196734,2	K562	blood:
13	chr5:112026916..112029331-chr5:112092996..112093925,9	K562	blood:
14	chr5:112036075..112039383-chr5:112077944..112080401,3	K562	blood:
15	chr5:112152202..112156283-chr5:112195630..112198484,4	MCF-7	breast:
16	chr5:112159983..112161663-chr5:112163922..112165564,2	K562	blood:
17	chr5:112180772..112183270-chr5:112188278..112191041,2	K562	blood:
18	chr5:112026203..112028934-chr5:112090617..112094558,3	K562	blood:
19	chr5:112129867..112132143-chr5:112136582..112139044,2	K562	blood:
20	chr5:112185924..112187591-chr5:112256473..112259234,2	K562	blood:
21	chr5:112123613..112127041-chr5:112129146..112132302,3	K562	blood:
22	chr5:112154161..112155749-chr5:112161168..112163115,2	K562	blood:
23	chr5:112176263..112181367-chr5:112181688..112184725,5	K562	blood:
24	chr5:112132025..112134986-chr5:112254619..112257174,2	K562	blood:
25	chr5:112079996..112082107-chr5:112090951..112092973,3	K562	blood:
26	chr5:112181480..112186029-chr5:112194933..112197058,4	MCF-7	breast:
27	chr5:112121618..112123708-chr5:112137434..112139348,2	K562	blood:
28	chr5:112129867..112132143-chr5:112136582..112139044,2	K562	blood:
29	chr5:112070188..112073138-chr5:112174884..112177444,2	K562	blood:
30	chr5:112182395..112185166-chr5:112196158..112198172,2	K562	blood:
31	chr5:112180694..112183270-chr5:112188278..112192219,3	K562	blood:
32	chr5:112187455..112190392-chr5:112195264..112197441,4	MCF-7	breast:
33	chr5:112079996..112081734-chr5:112090951..112092973,2	K562	blood:
34	chr5:112191204..112194360-chr5:112195263..112198616,8	MCF-7	breast:
35	chr5:111990789..111993618-chr5:112182329..112184626,2	K562	blood:
36	chr5:112183666..112186404-chr5:112196672..112198293,2	K562	blood:
37	chr5:112070801..112074184-chr5:112077517..112081527,4	K562	blood:
38	chr5:112183702..112184406-chr5:112257678..112258474,2	MCF-7	breast:
39	chr5:112123801..112127041-chr5:112128309..112132302,4	K562	blood:
40	chr5:112132327..112135284-chr5:112197116..112198935,2	K562	blood:
41	chr5:112070264..112074990-chr5:112075213..112080518,8	K562	blood:
42	chr5:111886846..111887851-chr5:112092877..112093891,4	MCF-7	breast:
43	chr5:112121866..112123891-chr5:112136309..112139852,3	K562	blood:
44	chr5:112089718..112092112-chr5:112180535..112183405,2	K562	blood:
45	chr5:112133420..112135351-chr5:112144014..112145746,2	K562	blood:
46	chr5:112163610..112167333-chr5:112168382..112170842,3	K562	blood:
47	chr5:112126744..112130086-chr5:112131543..112134649,3	MCF-7	breast:
48	chr5:112080239..112082396-chr5:112082414..112084260,2	K562	blood:
49	chr5:112058057..112061004-chr5:112174922..112177064,2	K562	blood:
50	chr5:112121618..112123708-chr5:112137434..112139348,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000258864	TF binding region
RNU6-482P	TF binding region
ENSG00000272869	TF binding region
APC	TF binding region
SRP19	TF binding region
CBX3P3	TF binding region
ENSG00000258864	CpG island
RNU6-482P	CpG island
ENSG00000272869	CpG island
APC	CpG island
SRP19	CpG island
CBX3P3	CpG island
ENSG00000258864	chromatin interactions
ENSG00000272869	chromatin interactions
ENSG00000134982	chromatin interactions
ENSG00000251014	chromatin interactions
ENSG00000153037	chromatin interactions
ENSG00000238363	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000129625	chromatin interactions
ENSG00000172795	chromatin interactions

Extended variants
information (count: 5726 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5726 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567037024	chr5:112076066-112076067	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs555807011	chr5:112076088-112076089	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs182028279	chr5:112076118-112076119	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186631763	chr5:112076136-112076137	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75791687	chr5:112076188-112076189	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557241733	chr5:112076200-112076201	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575411458	chr5:112076212-112076213	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142963263	chr5:112076221-112076222	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs545226243	chr5:112076222-112076223	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs537089770	chr5:112076223-112076224	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11286305	chr5:112076240-112076241	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs558527497	chr5:112076244-112076245	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs375117466	chr5:112076277-112076278	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs11950732	chr5:112076291-112076292	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs559554752	chr5:112076304-112076305	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs574999185	chr5:112076317-112076318	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574241448	chr5:112076335-112076336	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542011835	chr5:112076342-112076343	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs564018208	chr5:112076401-112076402	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190247441	chr5:112076442-112076443	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs9326864	chr5:112076449-112076450	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs77714918	chr5:112076490-112076491	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76705974	chr5:112076493-112076494	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75496952	chr5:112076502-112076503	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73791446	chr5:112076553-112076554	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs372022178	chr5:112076576-112076577	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528228741	chr5:112076604-112076605	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs182537230	chr5:112076621-112076622	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs568032203	chr5:112076629-112076630	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs6859799	chr5:112076633-112076634	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs529086564	chr5:112076660-112076661	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185484398	chr5:112076670-112076671	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569182367	chr5:112076800-112076801	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs189842127	chr5:112076822-112076823	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs539327998	chr5:112076823-112076824	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs183509480	chr5:112076870-112076871	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543874883	chr5:112076872-112076873	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs9686520	chr5:112076879-112076880	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs114140821	chr5:112076894-112076895	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553435534	chr5:112076901-112076902	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs188996022	chr5:112076961-112076962	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562458532	chr5:112077058-112077059	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574799757	chr5:112077074-112077075	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542449394	chr5:112077076-112077077	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369624674	chr5:112077107-112077108	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs193036404	chr5:112077118-112077119	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372243659	chr5:112077209-112077210	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs77678513	chr5:112077215-112077216	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs377743883	chr5:112077224-112077225	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560276325	chr5:112077238-112077239	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	21518781	CNVD
Prostate cancer	22341455	CNVD
Lung cancer	20668451	CNVD
adenomatous polyposis	20649969	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	22014273	CNVD
Colorectal cancer	23471846	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Sezary syndrome	18413736	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2943 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:112072800-112076400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
2	chr5:112073000-112076200	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr5:112073000-112076200	Active TSS	NHLF	lung
4	chr5:112073200-112076600	Active TSS	Brain Cingulate Gyrus	brain
5	chr5:112073800-112086800	Weak transcription	Gastric	stomach
6	chr5:112074000-112095000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr5:112074200-112077600	Weak transcription	Primary T cells from cord blood	blood
8	chr5:112074200-112078800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr5:112074200-112079600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr5:112074200-112081400	Weak transcription	Esophagus	oesophagus
11	chr5:112074200-112083800	Weak transcription	Ovary	ovary
12	chr5:112074200-112084400	Weak transcription	Pancreas	Pancrea
13	chr5:112074200-112093200	Weak transcription	Aorta	Aorta
14	chr5:112074400-112076600	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr5:112074400-112077000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:112074400-112077800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr5:112074400-112078200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:112074400-112078400	Weak transcription	Colon Smooth Muscle	Colon
19	chr5:112074400-112079000	Weak transcription	Small Intestine	intestine
20	chr5:112074400-112079600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr5:112074400-112079600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr5:112074400-112079600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr5:112074400-112081400	Weak transcription	Right Atrium	heart
24	chr5:112074400-112083800	Weak transcription	Psoas Muscle	Psoas
25	chr5:112074400-112083800	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr5:112074400-112090400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr5:112074400-112090400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr5:112074400-112091000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:112074400-112093200	Weak transcription	Right Ventricle	heart
30	chr5:112074400-112094000	Weak transcription	Fetal Intestine Small	intestine
31	chr5:112074400-112095200	Weak transcription	Fetal Muscle Leg	muscle
32	chr5:112074400-112095600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr5:112074400-112095600	Weak transcription	Fetal Thymus	thymus
34	chr5:112074400-112095800	Weak transcription	Fetal Muscle Trunk	muscle
35	chr5:112074400-112102800	Weak transcription	Fetal Stomach	stomach
36	chr5:112074400-112103400	Weak transcription	Left Ventricle	heart
37	chr5:112074400-112119800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:112074400-112125600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr5:112074400-112128600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr5:112074600-112090400	Weak transcription	Primary B cells from cord blood	blood
41	chr5:112074600-112103000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:112074800-112097600	Weak transcription	HMEC	breast
43	chr5:112075000-112078200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr5:112075000-112078600	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr5:112075000-112093000	Weak transcription	Liver	Liver
46	chr5:112075000-112095200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:112075200-112078000	Weak transcription	Fetal Heart	heart
48	chr5:112075200-112092600	Weak transcription	HSMM	muscle
49	chr5:112075200-112094400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr5:112075200-112103000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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