Variant report

Variant	nsv525920
Chromosome Location	chr12:50285061-50304949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:354)
CpG islands
(count:733)
Chromatin interactive
region (count:32)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:50303605-50303834	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr12:50285200-50285400	K562	blood:	n/a	n/a
3	BHLHE40	chr12:50303727-50303965	K562	blood:	n/a	n/a
4	BHLHE40	chr12:50286245-50286475	K562	blood:	n/a	n/a
5	CBX3	chr12:50303693-50304041	K562	blood:	n/a	n/a
6	CBX3	chr12:50293290-50293580	K562	blood:	n/a	n/a
7	CEBPB	chr12:50297929-50298298	IMR90	lung:	n/a	chr12:50298117-50298128 chr12:50298117-50298130
8	CEBPB	chr12:50298062-50298235	HepG2	liver:	n/a	chr12:50298117-50298128 chr12:50298117-50298130
9	CEBPB	chr12:50298015-50298295	H1-hESC	embryonic stem cell:	n/a	chr12:50298117-50298128 chr12:50298117-50298130
10	CEBPB	chr12:50303627-50304049	Hela-S3	cervix:	n/a	n/a
11	CEBPD	chr12:50286093-50286491	K562	blood:	n/a	n/a
12	CHD2	chr12:50288102-50288482	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr12:50303591-50303951	Hela-S3	cervix:	n/a	n/a
14	CTCF	chr12:50289769-50289898	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr12:50296300-50296450	AG04450	lung:	n/a	n/a
16	CTCF	chr12:50296300-50296450	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr12:50297620-50297770	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr12:50296320-50296470	GM12872	blood:	n/a	n/a
19	CTCF	chr12:50296280-50296430	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr12:50296278-50296480	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr12:50296180-50296330	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr12:50289760-50289910	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr12:50289782-50289909	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:50296280-50296430	HEK293	kidney:	n/a	n/a
25	CTCF	chr12:50289795-50289821	Fibrobl	skin:	n/a	n/a
26	CTCF	chr12:50296116-50296545	K562	blood:	n/a	n/a
27	CTCF	chr12:50296176-50296431	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr12:50296204-50296510	K562	blood:	n/a	n/a
29	CTCF	chr12:50296240-50296390	GM12868	blood:	n/a	n/a
30	CTCF	chr12:50296280-50296430	GM12875	blood:	n/a	n/a
31	CTCF	chr12:50301651-50301738	GM10248	blood:	n/a	n/a
32	CTCF	chr12:50289739-50290009	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr12:50296080-50296230	GM12872	blood:	n/a	n/a
34	CTCF	chr12:50296300-50296450	GM12875	blood:	n/a	n/a
35	CTCF	chr12:50296240-50296390	GM12873	blood:	n/a	n/a
36	CTCF	chr12:50296356-50296429	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr12:50296320-50296470	GM12866	blood:	n/a	n/a
38	CTCF	chr12:50289767-50289935	NHEK	skin:	n/a	n/a
39	CTCF	chr12:50296280-50296430	Caco-2	colon:	n/a	n/a
40	CTCF	chr12:50296362-50296407	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:50292900-50293050	GM12864	blood:	n/a	n/a
42	CTCF	chr12:50289793-50289920	K562	blood:	n/a	n/a
43	CTCF	chr12:50297340-50297490	BE2_C	brain:	n/a	n/a
44	CTCF	chr12:50296280-50296430	GM12871	blood:	n/a	n/a
45	CTCF	chr12:50296280-50296430	HepG2	liver:	n/a	n/a
46	CTCF	chr12:50296320-50296470	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr12:50296320-50296470	GM12865	blood:	n/a	n/a
48	CTCF	chr12:50296300-50296450	GM12864	blood:	n/a	n/a
49	CTCF	chr12:50296355-50296393	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:50297480-50297630	NHDF-neo	bronchial:	n/a	chr12:50297519-50297532

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:50297936-50297986	SK-N-MC	brain:	n/a
2	chr12:50297936-50297986	SK-N-MC	brain:	n/a
3	chr12:50297581-50297631	A549	lung:	n/a
4	chr12:50297936-50297986	NHBE	bronchial:	n/a
5	chr12:50293815-50293865	GM12891	blood:	n/a
6	chr12:50297777-50297827	H1-hESC	embryonic stem cell:	embryo
7	chr12:50293815-50293865	HIPEpiC	eye:	n/a
8	chr12:50297581-50297631	K562	blood:	n/a
9	chr12:50297936-50297986	HEK293	kidney:	embryo
10	chr12:50288819-50288869	SK-N-MC	brain:	n/a
11	chr12:50293815-50293865	HMEC	breast:	n/a
12	chr12:50297936-50297986	LNCaP	prostate:	n/a
13	chr12:50303785-50303835	MCF-7	breast:	n/a
14	chr12:50297588-50297638	CMK	blood:	n/a
15	chr12:50297793-50297843	HRPEpiC	eye:	n/a
16	chr12:50300243-50300293	HRE	kidney:	n/a
17	chr12:50297581-50297631	U87	brain:	n/a
18	chr12:50298731-50298781	HRPEpiC	eye:	n/a
19	chr12:50297581-50297631	Hepatocyte	liver:	n/a
20	chr12:50297477-50297527	HepG2	liver:	n/a
21	chr12:50298731-50298781	K562	blood:	n/a
22	chr12:50298731-50298781	HEK293	kidney:	embryo
23	chr12:50297936-50297986	HIPEpiC	eye:	n/a
24	chr12:50298731-50298781	HAEpiC	amniotic membrane:	n/a
25	chr12:50297581-50297631	HRE	kidney:	n/a
26	chr12:50293815-50293865	HRPEpiC	eye:	n/a
27	chr12:50298731-50298781	SK-N-SH_RA	brain:	n/a
28	chr12:50297581-50297631	ovcar-3	ovarian:	n/a
29	chr12:50300243-50300293	SKMC	muscle:	n/a
30	chr12:50303785-50303835	HCPEpiC	choroid plexus:	n/a
31	chr12:50298731-50298781	GM12891	blood:	n/a
32	chr12:50297581-50297631	BJ	skin:	n/a
33	chr12:50288819-50288869	H1-hESC	embryonic stem cell:	embryo
34	chr12:50303785-50303835	PFSK-1	brain:	n/a
35	chr12:50297793-50297843	SKMC	muscle:	n/a
36	chr12:50288819-50288869	HNPCEpiC	eye:	n/a
37	chr12:50297477-50297527	HAEpiC	amniotic membrane:	n/a
38	chr12:50303785-50303835	GM19239	blood:	n/a
39	chr12:50297777-50297827	NHDF-neo	bronchial:	n/a
40	chr12:50288819-50288869	AG09309	skin:	n/a
41	chr12:50297777-50297827	ovcar-3	ovarian:	n/a
42	chr12:50297936-50297986	SKMC	muscle:	n/a
43	chr12:50300243-50300293	HMEC	breast:	n/a
44	chr12:50297945-50297995	ECC-1	luminal epithelium:	n/a
45	chr12:50297588-50297638	HRE	kidney:	n/a
46	chr12:50297777-50297827	A549	lung:	n/a
47	chr12:50300243-50300293	Hela-S3	cervix:	n/a
48	chr12:50297477-50297527	HUVEC	blood vessel:	n/a
49	chr12:50288819-50288869	Hela-S3	cervix:	n/a
50	chr12:50303785-50303835	U87	brain:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:50286408..50287924-chr12:50296514..50298335,2	MCF-7	breast:
2	chr12:50283500..50287015-chr12:50298892..50302094,3	MCF-7	breast:
3	chr12:50289663..50291836-chr12:50301537..50303310,2	MCF-7	breast:
4	chr12:50266064..50268660-chr12:50284486..50286265,2	K562	blood:
5	chr12:50133876..50136071-chr12:50286990..50288779,2	MCF-7	breast:
6	chr12:50280227..50282176-chr12:50287942..50290577,2	K562	blood:
7	chr12:50285473..50288081-chr12:50312540..50314584,2	K562	blood:
8	chr12:50285846..50287432-chr12:50291861..50294460,2	K562	blood:
9	chr12:50281662..50285882-chr12:50286690..50289422,5	MCF-7	breast:
10	chr12:50280749..50283185-chr12:50302000..50304856,3	MCF-7	breast:
11	chr12:50286993..50289592-chr12:50396016..50398113,2	MCF-7	breast:
12	chr12:50290402..50293463-chr12:50294998..50297478,3	MCF-7	breast:
13	chr12:50302479..50304923-chr12:50336805..50339549,2	MCF-7	breast:
14	chr12:50287732..50289351-chr12:50337980..50339700,2	MCF-7	breast:
15	chr12:50285846..50288716-chr12:50291928..50294510,3	K562	blood:
16	chr12:50303280..50304785-chr12:50307920..50310046,2	K562	blood:
17	chr12:50262446..50266372-chr12:50284381..50286469,3	MCF-7	breast:
18	chr12:50301650..50304024-chr12:50450316..50452712,2	MCF-7	breast:
19	chr12:50221331..50224259-chr12:50293444..50296232,2	K562	blood:
20	chr12:50295593..50300153-chr12:50302401..50306371,6	MCF-7	breast:
21	chr12:50290402..50293463-chr12:50294998..50297478,3	MCF-7	breast:
22	chr12:50302143..50304526-chr12:50326820..50329441,2	K562	blood:
23	chr12:50257354..50258880-chr12:50284102..50286835,2	K562	blood:
24	chr12:50259475..50261235-chr12:50302095..50303974,2	MCF-7	breast:
25	chr12:50283616..50286348-chr12:50323415..50325001,2	MCF-7	breast:
26	chr12:50283500..50287015-chr12:50298892..50302094,3	MCF-7	breast:
27	chr12:50280144..50282226-chr12:50283386..50285640,2	K562	blood:
28	chr12:50293107..50297008-chr12:50298407..50301335,3	MCF-7	breast:
29	chr12:50281662..50285882-chr12:50286690..50289422,5	MCF-7	breast:
30	chr12:50278311..50281286-chr12:50298604..50300536,3	MCF-7	breast:
31	chr12:50287995..50291255-chr12:50301230..50303586,3	MCF-7	breast:
32	chr12:50295593..50300153-chr12:50302401..50306371,6	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAIM2-1	chr12:50302665-50302896	ENSG00000258135
2	lnc-FAIM2-1	chr12:50304228-50305073	ENSG00000258135
3	lnc-FAIM2-1	chr12:50304692-50304837	ENSG00000258135
4	lnc-FAIM2-1	chr12:50302665-50302896	ENSG00000258135
5	lnc-FAIM2-1	chr12:50302666-50304837	NONHSAT028150
6	lnc-FAIM2-1	chr12:50302665-50302896	ENSG00000258135
7	lnc-FAIM2-1	chr12:50302676-50304837	ENSG00000258135
8	lnc-FAIM2-1	chr12:50302667-50302896	XLOC_010072
9	lnc-FAIM2-1	chr12:50302668-50304837	XLOC_010072

No data

Variant related genes	Relation type
ENSG00000257771	TF binding region
FAIM2	TF binding region
ENSG00000257771	CpG island
FAIM2	CpG island
ENSG00000258057	chromatin interactions
ENSG00000110881	chromatin interactions
ENSG00000258135	chromatin interactions
ENSG00000161800	chromatin interactions
ENSG00000167566	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000135472	chromatin interactions
ENSG00000257771	chromatin interactions

Extended variants
information (count: 851 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs297924	chr12:50285061-50285062	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs538488366	chr12:50285071-50285072	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75366467	chr12:50285102-50285103	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs539121881	chr12:50285122-50285123	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370393562	chr12:50285135-50285136	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs61926090	chr12:50285195-50285196	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552509093	chr12:50285219-50285220	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76680945	chr12:50285246-50285247	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553952626	chr12:50285306-50285307	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11169200	chr12:50285329-50285330	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372291929	chr12:50285334-50285335	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577011433	chr12:50285336-50285337	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147202166	chr12:50285358-50285359	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556355158	chr12:50285375-50285376	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs389911	chr12:50285407-50285408	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148281797	chr12:50285408-50285409	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367596291	chr12:50285409-50285410	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397832846	chr12:50285417-50285418	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576275164	chr12:50285436-50285437	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145142172	chr12:50285440-50285441	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1574598	chr12:50285475-50285476	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs191471688	chr12:50285497-50285498	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376023962	chr12:50285515-50285516	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs530142345	chr12:50285536-50285537	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs17201502	chr12:50285562-50285563	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs560258533	chr12:50285590-50285591	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373845453	chr12:50285706-50285707	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532422930	chr12:50285726-50285727	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182844966	chr12:50285752-50285753	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73116335	chr12:50285780-50285781	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs371123668	chr12:50285792-50285793	Weak transcription Strong transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569396077	chr12:50285826-50285827	Weak transcription Strong transcription Bivalent Enhancer Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs535886699	chr12:50285892-50285893	Weak transcription Strong transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs531931928	chr12:50285902-50285903	Weak transcription Strong transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs553086464	chr12:50285931-50285932	Weak transcription Strong transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374187615	chr12:50285994-50285995	Weak transcription Strong transcription Bivalent Enhancer Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs11169202	chr12:50286054-50286055	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs905619	chr12:50286055-50286056	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs142374810	chr12:50286073-50286074	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547372458	chr12:50286121-50286122	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs297925	chr12:50286122-50286123	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs536163015	chr12:50286129-50286130	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188706228	chr12:50286154-50286155	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546278490	chr12:50286166-50286167	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs297926	chr12:50286182-50286183	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs115658395	chr12:50286183-50286184	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs555673324	chr12:50286201-50286202	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116062195	chr12:50286241-50286242	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540234745	chr12:50286248-50286249	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547891319	chr12:50286266-50286267	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD

Chromatin state (count:616 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:50267000-50297000	Weak transcription	Right Atrium	heart
2	chr12:50275000-50294800	Weak transcription	Fetal Brain Male	brain
3	chr12:50277800-50288000	Strong transcription	Brain Hippocampus Middle	brain
4	chr12:50278800-50286200	Strong transcription	Brain Inferior Temporal Lobe	brain
5	chr12:50278800-50286200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr12:50279000-50286000	Strong transcription	Brain Anterior Caudate	brain
7	chr12:50279200-50288000	Strong transcription	Brain Cingulate Gyrus	brain
8	chr12:50279400-50286600	Strong transcription	Brain Angular Gyrus	brain
9	chr12:50279600-50285400	Strong transcription	Fetal Brain Female	brain
10	chr12:50281200-50285200	Strong transcription	Fetal Stomach	stomach
11	chr12:50281200-50288000	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr12:50281400-50286200	Enhancers	Stomach Mucosa	stomach
13	chr12:50282000-50285200	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr12:50282400-50287800	Weak transcription	A549	lung
15	chr12:50282600-50288200	Strong transcription	Brain Substantia Nigra	brain
16	chr12:50282800-50287200	Weak transcription	Hela-S3	cervix
17	chr12:50283000-50288000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr12:50283400-50287800	Weak transcription	Esophagus	oesophagus
19	chr12:50283400-50288000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr12:50283600-50286000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:50283600-50290600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr12:50284000-50288000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:50284400-50285800	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr12:50284400-50288400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:50285000-50285200	Enhancers	Sigmoid Colon	Sigmoid Colon
26	chr12:50285000-50285400	Weak transcription	Gastric	stomach
27	chr12:50285000-50286000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr12:50285000-50287000	Weak transcription	Brain Germinal Matrix	brain
29	chr12:50285000-50287000	Enhancers	K562	blood
30	chr12:50285200-50285800	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr12:50285400-50286000	Enhancers	Gastric	stomach
32	chr12:50285400-50289800	Weak transcription	Fetal Brain Female	brain
33	chr12:50285800-50286400	Active TSS	Spleen	Spleen
34	chr12:50285800-50286800	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr12:50286000-50286400	Genic enhancers	Brain Anterior Caudate	brain
36	chr12:50286000-50287200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:50286200-50286400	Bivalent Enhancer	Fetal Lung	lung
38	chr12:50286200-50286600	Genic enhancers	Brain Inferior Temporal Lobe	brain
39	chr12:50286200-50286600	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr12:50286200-50287800	Weak transcription	Stomach Mucosa	stomach
41	chr12:50286400-50287800	Weak transcription	Spleen	Spleen
42	chr12:50286400-50288000	Strong transcription	Brain Anterior Caudate	brain
43	chr12:50286600-50287600	Weak transcription	Fetal Stomach	stomach
44	chr12:50286600-50288000	Strong transcription	Brain Inferior Temporal Lobe	brain
45	chr12:50286600-50288000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr12:50286600-50288400	Weak transcription	Brain Angular Gyrus	brain
47	chr12:50287000-50292000	Weak transcription	K562	blood
48	chr12:50287000-50295000	Strong transcription	Brain Germinal Matrix	brain
49	chr12:50287200-50287600	Enhancers	Hela-S3	cervix
50	chr12:50287600-50288000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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