Variant report

Variant	nsv470013
Chromosome Location	chr4:8315938-8377058
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:893)
CpG islands
(count:2441)
Chromatin interactive
region (count:37)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:8322318-8322343	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:8337663-8338676	K562	blood:	n/a	n/a
3	ATF1	chr4:8338113-8338723	K562	blood:	n/a	n/a
4	ATF2	chr4:8359490-8359857	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:8338259-8338488	K562	blood:	n/a	n/a
6	ATF3	chr4:8338200-8338505	K562	blood:	n/a	n/a
7	BACH1	chr4:8359436-8359516	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:8317763-8317973	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:8319138-8319178	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr4:8374852-8375403	GM12878	blood:	n/a	n/a
11	BCL3	chr4:8374921-8375373	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:8376765-8376915	K562	blood:	n/a	n/a
13	BHLHE40	chr4:8349894-8350191	HepG2	liver:	n/a	chr4:8350024-8350033
14	BHLHE40	chr4:8347666-8347969	HepG2	liver:	n/a	chr4:8347718-8347734
15	BHLHE40	chr4:8354399-8354611	K562	blood:	n/a	chr4:8354498-8354507 chr4:8354496-8354512
16	BHLHE40	chr4:8349911-8350172	GM12878	blood:	n/a	chr4:8350024-8350033
17	BHLHE40	chr4:8373374-8373615	K562	blood:	n/a	n/a
18	BHLHE40	chr4:8372628-8373087	K562	blood:	n/a	chr4:8372836-8372845 chr4:8372836-8372845
19	BHLHE40	chr4:8317386-8317761	A549	lung:	n/a	n/a
20	BHLHE40	chr4:8369879-8369917	K562	blood:	n/a	n/a
21	BHLHE40	chr4:8349739-8350219	K562	blood:	n/a	chr4:8350024-8350033
22	BHLHE40	chr4:8338352-8338392	HepG2	liver:	n/a	n/a
23	BHLHE40	chr4:8317142-8317955	HepG2	liver:	n/a	n/a
24	BHLHE40	chr4:8338007-8338840	K562	blood:	n/a	n/a
25	BHLHE40	chr4:8340380-8340596	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:8322202-8322402	K562	blood:	n/a	n/a
27	BHLHE40	chr4:8351624-8351692	K562	blood:	n/a	n/a
28	BHLHE40	chr4:8317095-8317954	K562	blood:	n/a	n/a
29	CBX3	chr4:8337628-8338021	K562	blood:	n/a	n/a
30	CBX3	chr4:8338094-8338489	K562	blood:	n/a	n/a
31	CCNT2	chr4:8337718-8338616	K562	blood:	n/a	n/a
32	CCNT2	chr4:8344651-8344753	K562	blood:	n/a	n/a
33	CEBPB	chr4:8338104-8338538	K562	blood:	n/a	n/a
34	CEBPB	chr4:8317516-8317907	ECC-1	luminal epithelium:	n/a	chr4:8317759-8317771
35	CEBPB	chr4:8317618-8317916	HepG2	liver:	n/a	chr4:8317759-8317771
36	CEBPB	chr4:8338264-8338475	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:8317438-8317961	MCF-7	breast:	n/a	chr4:8317759-8317771
38	CEBPB	chr4:8353775-8353986	HepG2	liver:	n/a	n/a
39	CEBPB	chr4:8317238-8318062	ECC-1	luminal epithelium:	n/a	chr4:8317759-8317771 chr4:8317373-8317385
40	CEBPB	chr4:8348129-8348326	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:8338135-8338513	K562	blood:	n/a	n/a
42	CEBPB	chr4:8338216-8338398	K562	blood:	n/a	n/a
43	CEBPB	chr4:8317224-8317986	Hela-S3	cervix:	n/a	chr4:8317759-8317771 chr4:8317373-8317385
44	CEBPB	chr4:8348143-8348389	A549	lung:	n/a	n/a
45	CEBPB	chr4:8317556-8317946	IMR90	lung:	n/a	chr4:8317759-8317771
46	CEBPB	chr4:8336727-8337075	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:8348127-8348308	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr4:8324156-8324379	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr4:8348205-8348405	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:8317679-8317795	H1-hESC	embryonic stem cell:	n/a	chr4:8317759-8317771

(count:2441 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:8374561-8374611	HIPEpiC	eye:	n/a
2	chr4:8374561-8374611	HIPEpiC	eye:	n/a
3	chr4:8355043-8355093	AG09319	gingival:	n/a
4	chr4:8348121-8348171	NB4	blood:	n/a
5	chr4:8374697-8374747	AG04449	skin:	fetal
6	chr4:8359458-8359508	HCF	heart:	n/a
7	chr4:8346218-8346268	PANC-1	pancreas:	n/a
8	chr4:8374561-8374611	ProgFib	skin:	n/a
9	chr4:8345588-8345638	BJ	skin:	n/a
10	chr4:8376764-8376814	ECC-1	luminal epithelium:	n/a
11	chr4:8368486-8368536	HL-60	blood:	n/a
12	chr4:8373516-8373566	AG09309	skin:	n/a
13	chr4:8355043-8355093	GM12891	blood:	n/a
14	chr4:8373438-8373488	Hela-S3	cervix:	n/a
15	chr4:8359247-8359297	LNCaP	prostate:	n/a
16	chr4:8374182-8374232	LNCaP	prostate:	n/a
17	chr4:8345211-8345261	AG09319	gingival:	n/a
18	chr4:8347266-8347316	LNCaP	prostate:	n/a
19	chr4:8359499-8359549	HIPEpiC	eye:	n/a
20	chr4:8368486-8368536	PrEC	prostate:	n/a
21	chr4:8359247-8359297	PFSK-1	brain:	n/a
22	chr4:8351738-8351788	MCF10A-Er-Src	breast:	n/a
23	chr4:8351738-8351788	SAEC	small airway:	n/a
24	chr4:8351738-8351788	HepG2	liver:	n/a
25	chr4:8372758-8372808	GM12892	blood:	n/a
26	chr4:8376254-8376304	Hepatocyte	liver:	n/a
27	chr4:8375240-8375290	H1-hESC	embryonic stem cell:	embryo
28	chr4:8347674-8347724	U87	brain:	n/a
29	chr4:8374429-8374479	HAEpiC	amniotic membrane:	n/a
30	chr4:8376254-8376304	Caco-2	colon:	n/a
31	chr4:8368486-8368536	HUVEC	blood vessel:	n/a
32	chr4:8372840-8372890	HUVEC	blood vessel:	n/a
33	chr4:8359499-8359549	HEEpiC	esophagus:	n/a
34	chr4:8359499-8359549	HAEpiC	amniotic membrane:	n/a
35	chr4:8374561-8374611	PrEC	prostate:	n/a
36	chr4:8372758-8372808	T-47D	breast:	n/a
37	chr4:8351738-8351788	AG04449	skin:	fetal
38	chr4:8372691-8372741	MCF-7	breast:	n/a
39	chr4:8374182-8374232	HRPEpiC	eye:	n/a
40	chr4:8347266-8347316	Jurkat	blood:	n/a
41	chr4:8368575-8368625	IMR90	lung:	fetal
42	chr4:8374429-8374479	NH-A	brain:	n/a
43	chr4:8346218-8346268	ProgFib	skin:	n/a
44	chr4:8372691-8372741	ProgFib	skin:	n/a
45	chr4:8373553-8373603	HL-60	blood:	n/a
46	chr4:8346138-8346188	GM12878	blood:	n/a
47	chr4:8374561-8374611	HCM	heart:	n/a
48	chr4:8376764-8376814	NT2-D1	testis:	n/a
49	chr4:8345588-8345638	AG04450	lung:	fetal
50	chr4:8347832-8347882	SK-N-SH	brain:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
2	chr4:8315694..8318647-chr4:8336893..8339393,2	K562	blood:
3	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
4	chr4:8315694..8318647-chr4:8336893..8339393,2	K562	blood:
5	chr4:8338499..8340014-chr4:8350078..8351770,2	K562	blood:
6	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
7	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
8	chr4:8312041..8314245-chr4:8317234..8319161,2	K562	blood:
9	chr4:8322827..8325228-chr4:8329737..8331737,2	K562	blood:
10	chr4:8337029..8339751-chr4:8340402..8342759,2	K562	blood:
11	chr4:8346988..8348504-chr4:8352358..8355226,2	K562	blood:
12	chr4:8348558..8350885-chr4:8366825..8368402,2	MCF-7	breast:
13	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
14	chr4:8338499..8340014-chr4:8350078..8351770,2	K562	blood:
15	chr4:8326199..8328705-chr4:8337836..8339581,2	K562	blood:
16	chr4:8327689..8329411-chr4:8330180..8333204,3	MCF-7	breast:
17	chr4:8347622..8350029-chr4:8351308..8354631,3	MCF-7	breast:
18	chr4:8356734..8359057-chr4:8360589..8363448,2	K562	blood:
19	chr4:8370118..8372500-chr4:8374648..8377546,2	K562	blood:
20	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
21	chr4:8322827..8325228-chr4:8329737..8331737,2	K562	blood:
22	chr4:8327689..8329411-chr4:8330180..8333204,3	MCF-7	breast:
23	chr4:8311363..8313807-chr4:8315101..8317109,2	K562	blood:
24	chr4:8366720..8368366-chr4:8370008..8372883,2	K562	blood:
25	chr4:8183603..8185806-chr4:8316475..8318494,2	MCF-7	breast:
26	chr4:8306129..8312354-chr4:8314662..8318399,6	MCF-7	breast:
27	chr4:8372807..8374828-chr4:8375470..8377502,2	K562	blood:
28	chr4:8368733..8370902-chr4:8378657..8380163,2	MCF-7	breast:
29	chr4:8358055..8360875-chr4:8366726..8369353,3	K562	blood:
30	chr4:8362353..8364168-chr4:8365634..8367261,2	K562	blood:
31	chr4:8356411..8359057-chr4:8360589..8362711,2	K562	blood:
32	chr4:8337029..8339751-chr4:8340402..8342759,2	K562	blood:
33	chr4:8326199..8328705-chr4:8337836..8339581,2	K562	blood:
34	chr4:8321399..8323453-chr4:8336725..8338364,2	K562	blood:
35	chr4:8308134..8310233-chr4:8366379..8367956,2	K562	blood:
36	chr4:8346988..8348504-chr4:8352358..8355226,2	K562	blood:
37	chr4:8372002..8373720-chr4:8374604..8376742,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOX3-1	chr4:8356817-8360065	ENSG00000251615.3
2	lnc-HTRA3-1	chr4:8322008-8322249	NONHSAT095084
3	lnc-METTL19-5	chr4:8376346-8376594	l_2595_chr4:8372786-8374779_heart
4	lnc-HTRA3-1	chr4:8321863-8321895	NONHSAT095084
5	lnc-HTRA3-1	chr4:8323853-8323970	XLOC_003444
6	lnc-HTRA3-1	chr4:8322006-8322249	XLOC_003444
7	lnc-HTRA3-4	chr4:8358805-8360149	NONHSAT095089
8	lnc-METTL19-5	chr4:8374584-8374779	l_2595_chr4:8372786-8374779_heart
9	lnc-ACOX3-1	chr4:8357038-8359103	ENSG00000251615
10	lnc-HTRA3-1	chr4:8323923-8323970	XLOC_003444
11	lnc-HTRA3-1	chr4:8325446-8325692	XLOC_003444
12	lnc-HTRA3-1	chr4:8323684-8323794	XLOC_003444
13	lnc-HTRA3-1	chr4:8321887-8322249	XLOC_003444
14	lnc-HTRA3-1	chr4:8325446-8325694	XLOC_003444
15	lnc-HTRA3-1	chr4:8323684-8323759	XLOC_003444
16	lnc-ACOX3-5	chr4:8365860-8366475	NONHSAT095091
17	lnc-ACOX3-5	chr4:8367183-8367485	NONHSAT095091
18	lnc-ACOX3-1	chr4:8356817-8359103	NONHSAT095088
19	lnc-METTL19-5	chr4:8372787-8373149	l_2595_chr4:8372786-8374779_heart
20	lnc-HTRA3-1	chr4:8323684-8323780	NONHSAT095084
21	lnc-HTRA3-4	chr4:8358049-8358702	NONHSAT095089

No data

Variant related genes	Relation type
ENSG00000251615	TF binding region
ACOX3	TF binding region
ENSG00000248986	TF binding region
ENSG00000249145	TF binding region
ENSG00000251615	CpG island
ACOX3	CpG island
ENSG00000248986	CpG island
ENSG00000249145	CpG island
ENSG00000251615	chromatin interactions
ENSG00000087008	chromatin interactions
ENSG00000249145	chromatin interactions
ENSG00000248986	chromatin interactions
ENSG00000125089	chromatin interactions
TP53INP1	miRNA target sites

Extended variants
information (count: 3213 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3213 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6823378	chr4:8315938-8315939	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573695753	chr4:8315942-8315943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74824513	chr4:8315964-8315965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375557682	chr4:8315983-8315984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562893241	chr4:8315984-8315985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181675889	chr4:8315989-8315990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114536582	chr4:8316023-8316024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111762968	chr4:8316042-8316043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143499293	chr4:8316061-8316062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527682500	chr4:8316102-8316103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549437555	chr4:8316111-8316112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4696679	chr4:8316128-8316129	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs531658313	chr4:8316142-8316143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372950395	chr4:8316143-8316144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs151187602	chr4:8316156-8316157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568926595	chr4:8316187-8316188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4696680	chr4:8316215-8316216	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs7667031	chr4:8316225-8316226	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs140325116	chr4:8316250-8316251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533536437	chr4:8316255-8316256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs555022713	chr4:8316261-8316262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567257746	chr4:8316285-8316286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537509895	chr4:8316291-8316292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556257680	chr4:8316323-8316324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13110948	chr4:8316338-8316339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530070328	chr4:8316350-8316351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4696681	chr4:8316436-8316437	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs28664747	chr4:8316494-8316495	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs377630434	chr4:8316513-8316514	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4696682	chr4:8316529-8316530	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs4696683	chr4:8316535-8316536	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs150214715	chr4:8316603-8316604	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs4235263	chr4:8316621-8316622	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4463054	chr4:8316699-8316700	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs367769387	chr4:8316727-8316728	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575515581	chr4:8316728-8316729	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185384384	chr4:8316780-8316781	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188426317	chr4:8316799-8316800	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566339443	chr4:8316836-8316837	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs527536769	chr4:8316844-8316845	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113402569	chr4:8316877-8316878	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs549282325	chr4:8316902-8316903	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs567136232	chr4:8316910-8316911	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181242822	chr4:8316912-8316913	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555982122	chr4:8316916-8316917	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs199990071	chr4:8316927-8316928	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201410351	chr4:8316928-8316929	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112730011	chr4:8316929-8316930	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs112035725	chr4:8316930-8316931	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs76332381	chr4:8316995-8316996	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8279000-8317200	Weak transcription	Gastric	stomach
2	chr4:8311400-8316800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr4:8311600-8317200	Weak transcription	Right Atrium	heart
4	chr4:8311800-8316800	Weak transcription	Left Ventricle	heart
5	chr4:8311800-8320800	Weak transcription	Psoas Muscle	Psoas
6	chr4:8312000-8316600	Weak transcription	Fetal Heart	heart
7	chr4:8312400-8317200	Weak transcription	Right Ventricle	heart
8	chr4:8313000-8316800	Weak transcription	Ovary	ovary
9	chr4:8314000-8316600	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr4:8314600-8316600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:8316400-8318800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:8316600-8317400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
13	chr4:8316600-8317400	Enhancers	Stomach Smooth Muscle	stomach
14	chr4:8316600-8317800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr4:8316600-8318600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:8316600-8318600	Enhancers	Primary hematopoietic stem cells	blood
17	chr4:8316600-8319000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr4:8316600-8319000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr4:8316600-8319200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:8316600-8321000	Enhancers	Fetal Heart	heart
21	chr4:8316800-8317200	Enhancers	Hela-S3	cervix
22	chr4:8316800-8317400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:8316800-8317400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:8316800-8317400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr4:8316800-8317400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:8316800-8317800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr4:8316800-8318000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:8316800-8318200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:8316800-8318200	Enhancers	Fetal Intestine Large	intestine
30	chr4:8316800-8318400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr4:8316800-8318400	Enhancers	Left Ventricle	heart
32	chr4:8316800-8318600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:8316800-8318600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr4:8316800-8318800	Enhancers	Fetal Muscle Leg	muscle
35	chr4:8316800-8318800	Enhancers	Thymus	Thymus
36	chr4:8316800-8319000	Enhancers	Ovary	ovary
37	chr4:8316800-8319200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr4:8316800-8319200	Enhancers	Fetal Thymus	thymus
39	chr4:8316800-8319400	Enhancers	Placenta Amnion	Placenta Amnion
40	chr4:8317000-8317200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr4:8317000-8317200	Enhancers	Duodenum Mucosa	Duodenum
42	chr4:8317000-8317400	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:8317000-8317400	Enhancers	A549	lung
44	chr4:8317000-8317400	Bivalent Enhancer	HepG2	liver
45	chr4:8317000-8317400	Enhancers	HMEC	breast
46	chr4:8317000-8317400	Enhancers	NH-A	brain
47	chr4:8317000-8317400	Enhancers	NHEK	skin
48	chr4:8317000-8317400	Enhancers	Osteobl	bone
49	chr4:8317000-8317600	Enhancers	Fetal Kidney	kidney
50	chr4:8317000-8318000	Enhancers	Fetal Lung	lung

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