Variant report

Variant	nsv590300
Chromosome Location	chr3:52090597-52096432
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:543)
CpG islands
(count:549)
Chromatin interactive
region (count:17)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:52091171-52091620	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:52091304-52091460	K562	blood:	n/a	n/a
3	ATF3	chr3:52091223-52091370	GM12878	blood:	n/a	n/a
4	ATF3	chr3:52091179-52091464	K562	blood:	n/a	n/a
5	BACH1	chr3:52090669-52092031	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr3:52091071-52091368	A549	lung:	n/a	n/a
7	BHLHE40	chr3:52091031-52091599	HepG2	liver:	n/a	chr3:52091498-52091514
8	BHLHE40	chr3:52091060-52091780	GM12878	blood:	n/a	chr3:52091498-52091514
9	BHLHE40	chr3:52090492-52090850	GM12878	blood:	n/a	chr3:52090590-52090606
10	BHLHE40	chr3:52090568-52091738	K562	blood:	n/a	chr3:52091498-52091514 chr3:52090590-52090606
11	BRCA1	chr3:52091711-52091722	HepG2	liver:	n/a	n/a
12	BRCA1	chr3:52091286-52091629	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr3:52090881-52091344	K562	blood:	n/a	n/a
14	CCNT2	chr3:52090536-52091099	K562	blood:	n/a	chr3:52090909-52090918
15	CCNT2	chr3:52091319-52091762	K562	blood:	n/a	n/a
16	CEBPB	chr3:52091057-52091843	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:52091112-52091711	HepG2	liver:	n/a	n/a
18	CEBPD	chr3:52091363-52091723	HepG2	liver:	n/a	n/a
19	CEBPD	chr3:52090478-52090797	HepG2	liver:	n/a	n/a
20	CHD2	chr3:52090566-52091794	Hela-S3	cervix:	n/a	chr3:52090988-52090998 chr3:52090658-52090665
21	CHD2	chr3:52090664-52090890	K562	blood:	n/a	n/a
22	CHD2	chr3:52091241-52091652	K562	blood:	n/a	n/a
23	CHD2	chr3:52090621-52091791	GM12878	blood:	n/a	chr3:52090988-52090998 chr3:52090658-52090665
24	CHD2	chr3:52090894-52091692	H1-hESC	embryonic stem cell:	n/a	chr3:52090988-52090998
25	CHD2	chr3:52091286-52091446	HepG2	liver:	n/a	n/a
26	CREB1	chr3:52091101-52091718	A549	lung:	n/a	n/a
27	CREB1	chr3:52090810-52091839	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr3:52090713-52091930	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr3:52091014-52091831	GM12878	blood:	n/a	n/a
30	CREB1	chr3:52090526-52090768	A549	lung:	n/a	n/a
31	CTCF	chr3:52091140-52091290	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr3:52091208-52091776	GM12878	blood:	n/a	chr3:52091657-52091665
33	CTCF	chr3:52090840-52090990	GM12873	blood:	n/a	n/a
34	CTCF	chr3:52091281-52091756	K562	blood:	n/a	chr3:52091657-52091665
35	CTCF	chr3:52091500-52091650	HEK293	kidney:	n/a	n/a
36	CTCF	chr3:52091540-52091690	SK-N-SH_RA	brain:	n/a	chr3:52091657-52091665
37	CTCF	chr3:52091520-52091670	GM06990	blood:	n/a	chr3:52091657-52091665
38	CTCF	chr3:52091520-52091670	WERI-Rb-1	eye:	n/a	chr3:52091657-52091665
39	CTCF	chr3:52091880-52092110	NHLF	lung:	n/a	n/a
40	CTCF	chr3:52091560-52091710	AG04449	skin:	n/a	chr3:52091657-52091665
41	CTCF	chr3:52091520-52091670	GM12870	blood:	n/a	chr3:52091657-52091665
42	CTCF	chr3:52090569-52090666	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr3:52091700-52091850	HRE	kidney:	n/a	n/a
44	CTCF	chr3:52091540-52091690	HMEC	breast:	n/a	chr3:52091657-52091665
45	CTCF	chr3:52091580-52091730	HCT-116	colon:	n/a	chr3:52091657-52091665
46	CTCF	chr3:52090678-52090728	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr3:52091562-52091695	GM10248	blood:	n/a	chr3:52091657-52091665
48	CTCF	chr3:52091510-52091741	NHEK	skin:	n/a	chr3:52091657-52091665
49	CTCF	chr3:52091547-52091711	MCF-7	breast:	n/a	chr3:52091657-52091665
50	CTCF	chr3:52091559-52091669	LNCaP	prostate:	n/a	chr3:52091657-52091665

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52091651-52091701	HMEC	breast:	n/a
2	chr3:52093899-52093949	HNPCEpiC	eye:	n/a
3	chr3:52091604-52091654	HEEpiC	esophagus:	n/a
4	chr3:52091651-52091701	ECC-1	luminal epithelium:	n/a
5	chr3:52091063-52091113	PrEC	prostate:	n/a
6	chr3:52091604-52091654	SK-N-SH_RA	brain:	n/a
7	chr3:52091484-52091534	HCF	heart:	n/a
8	chr3:52090732-52090782	Caco-2	colon:	n/a
9	chr3:52091829-52091879	LNCaP	prostate:	n/a
10	chr3:52091282-52091332	HEEpiC	esophagus:	n/a
11	chr3:52091604-52091654	HRPEpiC	eye:	n/a
12	chr3:52091651-52091701	AG04449	skin:	fetal
13	chr3:52091282-52091332	PANC-1	pancreas:	n/a
14	chr3:52093899-52093949	HL-60	blood:	n/a
15	chr3:52091604-52091654	GM06990	blood:	n/a
16	chr3:52091829-52091879	NH-A	brain:	n/a
17	chr3:52091484-52091534	ECC-1	luminal epithelium:	n/a
18	chr3:52091063-52091113	HAEpiC	amniotic membrane:	n/a
19	chr3:52091063-52091113	HL-60	blood:	n/a
20	chr3:52090647-52090697	PrEC	prostate:	n/a
21	chr3:52091604-52091654	BE2_C	brain:	n/a
22	chr3:52090732-52090782	Hela-S3	cervix:	n/a
23	chr3:52093899-52093949	A549	lung:	n/a
24	chr3:52093899-52093949	HRPEpiC	eye:	n/a
25	chr3:52091282-52091332	GM19239	blood:	n/a
26	chr3:52091829-52091879	K562	blood:	n/a
27	chr3:52091063-52091113	Caco-2	colon:	n/a
28	chr3:52093899-52093949	NB4	blood:	n/a
29	chr3:52090647-52090697	SK-N-SH	brain:	n/a
30	chr3:52090647-52090697	NHDF-neo	bronchial:	n/a
31	chr3:52091484-52091534	HAEpiC	amniotic membrane:	n/a
32	chr3:52091604-52091654	SK-N-MC	brain:	n/a
33	chr3:52091063-52091113	SK-N-SH_RA	brain:	n/a
34	chr3:52093899-52093949	RPTEC	kidney:	n/a
35	chr3:52093899-52093949	SAEC	small airway:	n/a
36	chr3:52090647-52090697	Hepatocyte	liver:	n/a
37	chr3:52091829-52091879	AG04450	lung:	fetal
38	chr3:52090732-52090782	HIPEpiC	eye:	n/a
39	chr3:52091063-52091113	HEEpiC	esophagus:	n/a
40	chr3:52091829-52091879	GM12891	blood:	n/a
41	chr3:52091604-52091654	Jurkat	blood:	n/a
42	chr3:52091651-52091701	U87	brain:	n/a
43	chr3:52091829-52091879	HepG2	liver:	n/a
44	chr3:52091484-52091534	LNCaP	prostate:	n/a
45	chr3:52091829-52091879	U87	brain:	n/a
46	chr3:52090732-52090782	SK-N-MC	brain:	n/a
47	chr3:52091282-52091332	HRCEpiC	kidney:	n/a
48	chr3:52091282-52091332	AoSMC	blood vessel:	n/a
49	chr3:52091484-52091534	A549	lung:	n/a
50	chr3:52090732-52090782	GM12892	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:52015921..52019600-chr3:52088214..52092499,4	K562	blood:
2	chr1:149222699..149225112-chr3:52088904..52091700,2	MCF-7	breast:
3	chr3:52089814..52091351-chr3:52187528..52189873,2	K562	blood:
4	chr3:52089468..52092661-chr3:52093229..52096649,5	K562	blood:
5	chr3:51974263..51977386-chr3:52088681..52091436,3	K562	blood:
6	chr3:52028052..52030007-chr3:52093333..52094846,2	K562	blood:
7	chr3:52088485..52093169-chr3:52093699..52100396,11	MCF-7	breast:
8	chr3:52088485..52093169-chr3:52093699..52100396,11	MCF-7	breast:
9	chr3:52093207..52095585-chr3:52103069..52105025,2	K562	blood:
10	chr3:52091359..52093112-chr3:52104568..52106950,2	K562	blood:
11	chr3:52026823..52031380-chr3:52087204..52091486,4	K562	blood:
12	chr3:51975919..51976628-chr3:52090698..52091583,2	K562	blood:
13	chr19:12901888..12902868-chr3:52090426..52090997,2	Hela-S3	cervix:
14	chr3:52016320..52018909-chr3:52089400..52091632,2	MCF-7	breast:
15	chr3:52028061..52031321-chr3:52088873..52092735,5	MCF-7	breast:
16	chr3:52093528..52096299-chr3:52098821..52100652,4	K562	blood:
17	chr3:52094254..52096500-chr3:52125955..52128876,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf74-1	chr3:52096110-52099128	NONHSAT089896

No data

Variant related genes	Relation type
DUSP7	TF binding region
DUSP7	CpG island
ENSG00000243989	chromatin interactions
ENSG00000256097	chromatin interactions
ENSG00000171223	chromatin interactions
ENSG00000114767	chromatin interactions
ENSG00000164087	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000041880	chromatin interactions
ENSG00000162244	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000164086	chromatin interactions

Extended variants
information (count: 172 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:172 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574001754	chr3:52090625-52090626	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs370131035	chr3:52090654-52090655	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
3	rs544491726	chr3:52090766-52090767	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
4	rs562786354	chr3:52090848-52090849	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
5	rs373346098	chr3:52090959-52090960	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
6	rs545208868	chr3:52090960-52090961	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
7	rs144010185	chr3:52090987-52090988	Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
8	rs527758216	chr3:52091078-52091079	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs549362399	chr3:52091110-52091111	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs561228020	chr3:52091111-52091112	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs531677641	chr3:52091184-52091185	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs550097479	chr3:52091197-52091198	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs375377016	chr3:52091226-52091227	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs192588423	chr3:52091240-52091241	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs9851576	chr3:52091254-52091255	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547246223	chr3:52091287-52091288	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs565768074	chr3:52091322-52091323	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs115180250	chr3:52091336-52091337	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs554181875	chr3:52091397-52091398	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs76212097	chr3:52091400-52091401	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs373219908	chr3:52091460-52091461	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs556029619	chr3:52091484-52091485	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs182145727	chr3:52091490-52091491	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs556427494	chr3:52091495-52091496	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs376274853	chr3:52091554-52091555	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs577883337	chr3:52091600-52091601	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs545607772	chr3:52091628-52091629	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs186738850	chr3:52091659-52091660	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs572512298	chr3:52091673-52091674	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs542746615	chr3:52091690-52091691	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs561313509	chr3:52091742-52091743	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs75746592	chr3:52091759-52091760	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs57236484	chr3:52091770-52091771	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs565199503	chr3:52091836-52091837	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs532259043	chr3:52091864-52091865	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs369174073	chr3:52091921-52091922	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs118129097	chr3:52091959-52091960	Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs536390050	chr3:52092049-52092050	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs372568855	chr3:52092052-52092053	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs547856864	chr3:52092083-52092084	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs569349269	chr3:52092139-52092140	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs536666902	chr3:52092285-52092286	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs534080605	chr3:52092317-52092318	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs535265224	chr3:52092323-52092324	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs558103567	chr3:52092335-52092336	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs578201164	chr3:52092404-52092405	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs538924471	chr3:52092405-52092406	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs554386976	chr3:52092418-52092419	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs145964321	chr3:52092439-52092440	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs139880658	chr3:52092468-52092469	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52086800-52090800	Active TSS	Rectal Smooth Muscle	rectum
2	chr3:52087400-52091800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:52087600-52090800	Enhancers	Fetal Brain Male	brain
4	chr3:52088400-52090800	Active TSS	HSMM	muscle
5	chr3:52088600-52090800	Active TSS	Brain Anterior Caudate	brain
6	chr3:52088600-52091200	Flanking Active TSS	Primary hematopoietic stem cells	blood
7	chr3:52088600-52091600	Active TSS	Psoas Muscle	Psoas
8	chr3:52088600-52091800	Active TSS	Breast Myoepithelial Primary Cells	Breast
9	chr3:52088600-52091800	Active TSS	Aorta	Aorta
10	chr3:52088600-52092000	Active TSS	Fetal Kidney	kidney
11	chr3:52088600-52092000	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr3:52088800-52090800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:52088800-52090800	Active TSS	Primary T helper cells PMA-I stimulated	--
14	chr3:52088800-52090800	Active TSS	Esophagus	oesophagus
15	chr3:52088800-52090800	Active TSS	HMEC	breast
16	chr3:52088800-52090800	Active TSS	NHDF-Ad	bronchial
17	chr3:52088800-52091400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:52088800-52091600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr3:52088800-52091600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr3:52088800-52091600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
21	chr3:52088800-52091600	Active TSS	Brain Substantia Nigra	brain
22	chr3:52088800-52091600	Active TSS	Gastric	stomach
23	chr3:52088800-52091600	Active TSS	Lung	lung
24	chr3:52088800-52091600	Active TSS	Osteobl	bone
25	chr3:52088800-52091800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:52088800-52091800	Active TSS	H9 Cell Line	embryonic stem cell
27	chr3:52088800-52091800	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr3:52088800-52091800	Active TSS	Ovary	ovary
29	chr3:52088800-52091800	Active TSS	Sigmoid Colon	Sigmoid Colon
30	chr3:52088800-52091800	Active TSS	Small Intestine	intestine
31	chr3:52089000-52090600	Active TSS	Fetal Lung	lung
32	chr3:52089000-52090600	Active TSS	Monocytes-CD14+_RO01746	blood
33	chr3:52089000-52090800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr3:52089000-52090800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr3:52089000-52090800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr3:52089000-52090800	Active TSS	Primary monocytes fromperipheralblood	blood
37	chr3:52089000-52090800	Active TSS	Primary T cells from cord blood	blood
38	chr3:52089000-52090800	Active TSS	Primary T cells fromperipheralblood	blood
39	chr3:52089000-52090800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr3:52089000-52090800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
41	chr3:52089000-52090800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr3:52089000-52090800	Active TSS	Muscle Satellite Cultured Cells	--
43	chr3:52089000-52090800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:52089000-52090800	Active TSS	Brain Cingulate Gyrus	brain
45	chr3:52089000-52090800	Active TSS	Brain Hippocampus Middle	brain
46	chr3:52089000-52090800	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr3:52089000-52090800	Active TSS	Colon Smooth Muscle	Colon
48	chr3:52089000-52090800	Active TSS	Fetal Brain Female	brain
49	chr3:52089000-52090800	Active TSS	Rectal Mucosa Donor 31	rectum
50	chr3:52089000-52090800	Active TSS	Right Ventricle	heart

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