Variant report

Variant	nsv614962
Chromosome Location	chr9:104204614-104240708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1209)
CpG islands
(count:244)
Chromatin interactive
region (count:40)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1209 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104224778-104225327	K562	blood:	n/a	n/a
2	ARID3A	chr9:104211633-104211832	K562	blood:	n/a	n/a
3	ARID3A	chr9:104207280-104208125	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:104227683-104227970	K562	blood:	n/a	n/a
5	ARID3A	chr9:104204696-104205484	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:104221326-104221658	HepG2	liver:	n/a	n/a
7	ATF1	chr9:104227631-104227968	K562	blood:	n/a	n/a
8	ATF1	chr9:104224865-104225348	K562	blood:	n/a	n/a
9	ATF2	chr9:104211545-104211916	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr9:104221166-104221629	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr9:104224811-104225151	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr9:104227629-104227994	K562	blood:	n/a	n/a
13	ATF3	chr9:104224849-104225153	K562	blood:	n/a	n/a
14	BACH1	chr9:104224831-104225167	K562	blood:	n/a	n/a
15	BACH1	chr9:104211500-104211895	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr9:104224409-104225425	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr9:104225732-104225964	GM12878	blood:	n/a	n/a
18	BCL3	chr9:104228458-104228698	GM12878	blood:	n/a	n/a
19	BCL3	chr9:104211493-104212025	A549	lung:	n/a	chr9:104211667-104211675
20	BHLHE40	chr9:104211362-104211952	K562	blood:	n/a	chr9:104211458-104211474 chr9:104211497-104211513 chr9:104211492-104211508
21	BHLHE40	chr9:104211319-104211633	GM12878	blood:	n/a	chr9:104211458-104211474 chr9:104211497-104211513 chr9:104211492-104211508
22	BHLHE40	chr9:104227748-104227900	K562	blood:	n/a	n/a
23	BRCA1	chr9:104221279-104221637	HepG2	liver:	n/a	n/a
24	BRCA1	chr9:104211448-104211877	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr9:104211443-104211894	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr9:104224825-104225402	K562	blood:	n/a	n/a
27	CBX3	chr9:104221124-104221722	HCT-116	colon:	n/a	n/a
28	CBX3	chr9:104227580-104227966	K562	blood:	n/a	n/a
29	CBX3	chr9:104211351-104211946	K562	blood:	n/a	n/a
30	CCNT2	chr9:104211372-104211783	K562	blood:	n/a	n/a
31	CCNT2	chr9:104223265-104223610	K562	blood:	n/a	n/a
32	CEBPB	chr9:104209516-104209580	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr9:104227658-104228038	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:104207479-104208395	HepG2	liver:	n/a	chr9:104207840-104207851
35	CEBPB	chr9:104227690-104228077	A549	lung:	n/a	n/a
36	CEBPB	chr9:104207649-104208371	HepG2	liver:	n/a	chr9:104207840-104207851
37	CEBPB	chr9:104207653-104207969	HepG2	liver:	n/a	chr9:104207840-104207851
38	CEBPB	chr9:104227623-104228435	A549	lung:	n/a	n/a
39	CEBPB	chr9:104227658-104227965	K562	blood:	n/a	n/a
40	CEBPB	chr9:104227659-104228400	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:104207579-104208113	A549	lung:	n/a	chr9:104207840-104207851
42	CEBPB	chr9:104227506-104228215	HCT-116	colon:	n/a	n/a
43	CEBPB	chr9:104207628-104207992	K562	blood:	n/a	chr9:104207840-104207851
44	CEBPB	chr9:104207655-104208363	IMR90	lung:	n/a	chr9:104207840-104207851
45	CEBPB	chr9:104227534-104228068	A549	lung:	n/a	n/a
46	CEBPB	chr9:104227636-104228081	MCF-7	breast:	n/a	n/a
47	CEBPB	chr9:104227581-104227984	MCF-7	breast:	n/a	n/a
48	CEBPB	chr9:104227566-104228028	K562	blood:	n/a	n/a
49	CEBPB	chr9:104207706-104207942	K562	blood:	n/a	chr9:104207840-104207851
50	CEBPB	chr9:104227718-104227937	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104238593-104238643	PFSK-1	brain:	n/a
2	chr9:104214581-104214631	AG09309	skin:	n/a
3	chr9:104237697-104237747	U87	brain:	n/a
4	chr9:104211410-104211460	HEEpiC	esophagus:	n/a
5	chr9:104237697-104237747	ovcar-3	ovarian:	n/a
6	chr9:104238593-104238643	HRE	kidney:	n/a
7	chr9:104238593-104238643	ProgFib	skin:	n/a
8	chr9:104211410-104211460	HIPEpiC	eye:	n/a
9	chr9:104237697-104237747	Caco-2	colon:	n/a
10	chr9:104211410-104211460	SK-N-SH_RA	brain:	n/a
11	chr9:104214581-104214631	NHDF-neo	bronchial:	n/a
12	chr9:104211410-104211460	HAEpiC	amniotic membrane:	n/a
13	chr9:104214581-104214631	HNPCEpiC	eye:	n/a
14	chr9:104238593-104238643	GM12892	blood:	n/a
15	chr9:104237697-104237747	GM12878	blood:	n/a
16	chr9:104238593-104238643	HCPEpiC	choroid plexus:	n/a
17	chr9:104211410-104211460	HRPEpiC	eye:	n/a
18	chr9:104211410-104211460	Caco-2	colon:	n/a
19	chr9:104214581-104214631	HRCEpiC	kidney:	n/a
20	chr9:104238593-104238643	BJ	skin:	n/a
21	chr9:104238593-104238643	HNPCEpiC	eye:	n/a
22	chr9:104238593-104238643	GM19239	blood:	n/a
23	chr9:104211410-104211460	NT2-D1	testis:	n/a
24	chr9:104214581-104214631	HCT-116	colon:	n/a
25	chr9:104214581-104214631	HAEpiC	amniotic membrane:	n/a
26	chr9:104238593-104238643	NHDF-neo	bronchial:	n/a
27	chr9:104237697-104237747	PFSK-1	brain:	n/a
28	chr9:104214581-104214631	Caco-2	colon:	n/a
29	chr9:104214581-104214631	HEEpiC	esophagus:	n/a
30	chr9:104237697-104237747	K562	blood:	n/a
31	chr9:104211410-104211460	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:104211410-104211460	ProgFib	skin:	n/a
33	chr9:104238593-104238643	H1-hESC	embryonic stem cell:	embryo
34	chr9:104238593-104238643	MCF10A-Er-Src	breast:	n/a
35	chr9:104238593-104238643	HCT-116	colon:	n/a
36	chr9:104214581-104214631	Hepatocyte	liver:	n/a
37	chr9:104237697-104237747	AG10803	skin:	n/a
38	chr9:104237697-104237747	GM19239	blood:	n/a
39	chr9:104237697-104237747	HL-60	blood:	n/a
40	chr9:104211410-104211460	SK-N-SH	brain:	n/a
41	chr9:104214581-104214631	HIPEpiC	eye:	n/a
42	chr9:104238593-104238643	NH-A	brain:	n/a
43	chr9:104211410-104211460	AG09319	gingival:	n/a
44	chr9:104211410-104211460	HEK293	kidney:	embryo
45	chr9:104238593-104238643	PrEC	prostate:	n/a
46	chr9:104237697-104237747	H1-hESC	embryonic stem cell:	embryo
47	chr9:104237697-104237747	AG04450	lung:	fetal
48	chr9:104214581-104214631	HCPEpiC	choroid plexus:	n/a
49	chr9:104211410-104211460	HNPCEpiC	eye:	n/a
50	chr9:104237697-104237747	AG04449	skin:	fetal

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:104224910..104226777-chr9:104240738..104243531,2	K562	blood:
2	chr9:104221066..104221882-chr9:107505389..107506114,2	K562	blood:
3	chr9:104230694..104236463-chr9:104246967..104249431,5	K562	blood:
4	chr9:104234812..104237553-chr9:104247151..104249445,2	MCF-7	breast:
5	chr9:104236917..104238965-chr9:104238999..104241326,2	K562	blood:
6	chr9:104232654..104234512-chr9:104236570..104239757,3	K562	blood:
7	chr9:104232654..104234512-chr9:104236570..104239757,3	K562	blood:
8	chr9:104220056..104222734-chr9:104292272..104293989,2	K562	blood:
9	chr9:104231072..104233238-chr9:104234059..104235841,2	MCF-7	breast:
10	chr9:104221425..104221969-chr9:104295249..104296028,2	MCF-7	breast:
11	chr9:104239622..104242586-chr9:104248313..104251248,3	K562	blood:
12	chr9:104211411..104211984-chr9:104329284..104330026,2	MCF-7	breast:
13	chr9:104190295..104194061-chr9:104205470..104208320,4	K562	blood:
14	chr9:104212462..104214116-chr9:104215702..104218126,2	MCF-7	breast:
15	chr9:104226892..104228195-chr9:104292114..104293047,7	MCF-7	breast:
16	chr9:104221051..104221944-chr9:104292075..104293445,6	MCF-7	breast:
17	chr9:104223612..104225291-chr9:104247459..104250202,2	K562	blood:
18	chr9:104211455..104212266-chr9:104227296..104227829,2	K562	blood:
19	chr9:104237414..104239742-chr9:104246128..104247680,2	K562	blood:
20	chr9:104197118..104199793-chr9:104230175..104232444,2	K562	blood:
21	chr9:104232214..104234343-chr9:104235852..104238668,2	K562	blood:
22	chr9:104208004..104209865-chr9:104292464..104295242,2	K562	blood:
23	chr9:104159548..104162633-chr9:104207516..104209377,3	MCF-7	breast:
24	chr9:104212462..104214116-chr9:104215702..104218126,2	MCF-7	breast:
25	chr9:104160996..104162683-chr9:104210087..104212007,2	K562	blood:
26	chr9:104228846..104231278-chr9:104239828..104242361,2	K562	blood:
27	chr9:104221464..104223281-chr9:104260800..104263635,2	K562	blood:
28	chr2:170838366..170838866-chr9:104211065..104211816,2	MCF-7	breast:
29	chr9:104236917..104238965-chr9:104238999..104241326,2	K562	blood:
30	chr9:104160683..104161236-chr9:104211196..104212187,2	MCF-7	breast:
31	chr9:104221027..104221969-chr9:104291863..104293035,11	MCF-7	breast:
32	chr9:104219436..104220096-chr9:104292310..104293060,2	MCF-7	breast:
33	chr9:104220969..104222009-chr9:104292098..104293000,3	K562	blood:
34	chr9:104232214..104234343-chr9:104235852..104238668,2	K562	blood:
35	chr9:104171015..104173390-chr9:104201738..104204667,2	K562	blood:
36	chr9:104227401..104228428-chr9:104292031..104293031,5	K562	blood:
37	chr9:104221002..104221801-chr9:104329610..104330484,3	MCF-7	breast:
38	chr9:104221036..104221738-chr9:104355766..104356658,2	MCF-7	breast:
39	chr9:104211110..104212494-chr9:104220920..104222010,4	MCF-7	breast:
40	chr9:104221444..104221955-chr9:104329285..104330133,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF20-1	chr9:104231661-104231902	ENSG00000225376.1
2	lnc-C9orf125-2	chr9:104235442-104237132	NONHSAT133739
3	lnc-RNF20-1	chr9:104237158-104237324	ENSG00000225376.1
4	lnc-RNF20-1	chr9:104231492-104231902	NONHSAT133735
5	lnc-RNF20-1	chr9:104231604-104231902	ENSG00000225376.1
6	lnc-RNF20-1	chr9:104231632-104231727	NONHSAT133738
7	lnc-RNF20-1	chr9:104231492-104231902	NONHSAT133734
8	lnc-RNF20-1	chr9:104231631-104231902	NONHSAT133737
9	lnc-RNF20-1	chr9:104230744-104230890	ENSG00000225376.1
10	lnc-RNF20-1	chr9:104235485-104236343	NONHSAT133737

No data

Variant related genes	Relation type
ENSG00000270982	TF binding region
ENSG00000225376	TF binding region
ENSG00000270982	CpG island
ENSG00000225376	CpG island
ENSG00000225376	chromatin interactions
ENSG00000136897	chromatin interactions
ENSG00000136872	chromatin interactions
ENSG00000136870	chromatin interactions
ENSG00000165152	chromatin interactions
ENSG00000270982	chromatin interactions

Extended variants
information (count: 1424 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573816	chr9:104204614-104204615	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569129530	chr9:104204707-104204708	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147730827	chr9:104204752-104204753	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551170126	chr9:104204764-104204765	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571072165	chr9:104204793-104204794	Enhancers Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533660666	chr9:104204829-104204830	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs142628284	chr9:104204857-104204858	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567182834	chr9:104204861-104204862	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs536243016	chr9:104204913-104204914	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs77528658	chr9:104204920-104204921	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs547125895	chr9:104204928-104204929	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs576686799	chr9:104204945-104204946	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs545685120	chr9:104204948-104204949	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs559217053	chr9:104205017-104205018	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570071	chr9:104205038-104205039	Enhancers Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs188224003	chr9:104205049-104205050	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374324493	chr9:104205062-104205063	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561424241	chr9:104205069-104205070	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191911739	chr9:104205070-104205071	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201848719	chr9:104205081-104205082	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543802567	chr9:104205085-104205086	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536469791	chr9:104205131-104205132	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531515371	chr9:104205146-104205147	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372171827	chr9:104205162-104205163	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551230200	chr9:104205175-104205176	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73501217	chr9:104205270-104205271	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs527465867	chr9:104205272-104205273	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146906361	chr9:104205291-104205292	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184153848	chr9:104205298-104205299	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148180958	chr9:104205306-104205307	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs66662619	chr9:104205335-104205336	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs569523538	chr9:104205360-104205361	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113448389	chr9:104205370-104205371	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375624503	chr9:104205393-104205394	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189379678	chr9:104205405-104205406	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35126768	chr9:104205467-104205468	Enhancers Flanking Active TSS Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572719893	chr9:104205473-104205474	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs541640408	chr9:104205534-104205535	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141161637	chr9:104205587-104205588	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs182046565	chr9:104205592-104205593	Enhancers Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs55785343	chr9:104205604-104205605	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs539855004	chr9:104205609-104205610	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558512764	chr9:104205637-104205638	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs150314401	chr9:104205655-104205656	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs574759343	chr9:104205695-104205696	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34798374	chr9:104205710-104205711	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532347488	chr9:104205714-104205715	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375498504	chr9:104205716-104205717	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs137974142	chr9:104205739-104205740	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527537137	chr9:104205753-104205754	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:981 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104195600-104207200	Enhancers	HepG2	liver
2	chr9:104197000-104211400	Weak transcription	Right Atrium	heart
3	chr9:104197400-104209600	Enhancers	Fetal Intestine Large	intestine
4	chr9:104200800-104206200	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr9:104201600-104205200	Weak transcription	Stomach Mucosa	stomach
6	chr9:104202600-104204800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr9:104202800-104205200	Active TSS	Duodenum Mucosa	Duodenum
8	chr9:104203200-104205200	Active TSS	Liver	Liver
9	chr9:104203200-104206400	Enhancers	Pancreas	Pancrea
10	chr9:104204600-104204800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr9:104204600-104204800	Enhancers	Colon Smooth Muscle	Colon
12	chr9:104204600-104204800	Enhancers	Fetal Brain Male	brain
13	chr9:104204600-104204800	Enhancers	Left Ventricle	heart
14	chr9:104204600-104205000	Flanking Active TSS	Fetal Intestine Small	intestine
15	chr9:104204600-104205800	Enhancers	Fetal Heart	heart
16	chr9:104204800-104205200	Weak transcription	Colon Smooth Muscle	Colon
17	chr9:104204800-104205400	Weak transcription	Fetal Brain Male	brain
18	chr9:104204800-104205600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:104204800-104211400	Weak transcription	Left Ventricle	heart
20	chr9:104205000-104209600	Enhancers	Fetal Intestine Small	intestine
21	chr9:104205200-104205600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr9:104205200-104205600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr9:104205200-104205800	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr9:104205200-104205800	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr9:104205200-104206200	Flanking Active TSS	Liver	Liver
26	chr9:104205200-104206200	Enhancers	Stomach Mucosa	stomach
27	chr9:104205200-104206400	Enhancers	Brain Germinal Matrix	brain
28	chr9:104205200-104208000	Enhancers	Colon Smooth Muscle	Colon
29	chr9:104205400-104206200	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr9:104205400-104206200	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr9:104205400-104206400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr9:104205400-104206600	Enhancers	Fetal Brain Female	brain
33	chr9:104205400-104207000	Enhancers	Fetal Brain Male	brain
34	chr9:104205600-104205800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr9:104205600-104205800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr9:104205600-104206000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr9:104205600-104206000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr9:104205600-104206000	Enhancers	Fetal Muscle Trunk	muscle
39	chr9:104205600-104206000	Enhancers	Psoas Muscle	Psoas
40	chr9:104205600-104206400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr9:104205600-104206400	Enhancers	Brain Cingulate Gyrus	brain
42	chr9:104205600-104207200	Enhancers	Brain Anterior Caudate	brain
43	chr9:104205600-104211400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr9:104205800-104206000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr9:104205800-104206000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:104205800-104206000	Enhancers	Brain Substantia Nigra	brain
47	chr9:104205800-104206000	Enhancers	Rectal Smooth Muscle	rectum
48	chr9:104205800-104206400	Enhancers	Brain Angular Gyrus	brain
49	chr9:104205800-104206400	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr9:104205800-104206400	Enhancers	Fetal Muscle Leg	muscle

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