Variant report

Variant	nsv1025364
Chromosome Location	chr4:189402309-189710397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1094)
CpG islands
(count:1896)
Chromatin interactive
region (count:12)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1094 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:189455499-189455789	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:189456095-189456482	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:189659351-189659620	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:189527693-189528168	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:189499935-189500273	HepG2	liver:	n/a	n/a
6	BACH1	chr4:189649632-189649850	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:189580313-189580512	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr4:189456176-189456442	HepG2	liver:	n/a	n/a
9	BHLHE40	chr4:189527879-189528027	HepG2	liver:	n/a	n/a
10	BHLHE40	chr4:189539576-189539609	K562	blood:	n/a	n/a
11	BRCA1	chr4:189404735-189404847	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:189618403-189618710	Hela-S3	cervix:	n/a	chr4:189618559-189618570
13	CEBPB	chr4:189560699-189560954	A549	lung:	n/a	n/a
14	CEBPB	chr4:189612960-189613423	IMR90	lung:	n/a	n/a
15	CEBPB	chr4:189549105-189549301	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:189527875-189528128	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:189618409-189618665	H1-hESC	embryonic stem cell:	n/a	chr4:189618559-189618570
18	CEBPB	chr4:189560714-189560941	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:189433899-189434105	HepG2	liver:	n/a	chr4:189433976-189433987
20	CEBPB	chr4:189663658-189663821	IMR90	lung:	n/a	n/a
21	CEBPB	chr4:189517237-189517434	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:189549147-189549347	A549	lung:	n/a	n/a
23	CEBPB	chr4:189591136-189591163	HepG2	liver:	n/a	chr4:189591147-189591158
24	CEBPB	chr4:189618280-189618777	HCT-116	colon:	n/a	chr4:189618559-189618570
25	CEBPB	chr4:189560668-189561000	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:189628220-189628566	IMR90	lung:	n/a	chr4:189628489-189628497
27	CEBPB	chr4:189584550-189585245	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:189581873-189582175	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:189549174-189549466	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:189628311-189628484	A549	lung:	n/a	n/a
31	CEBPB	chr4:189516061-189516240	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:189495393-189495495	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:189456046-189456370	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:189493605-189493919	HepG2	liver:	n/a	chr4:189493776-189493787
35	CEBPB	chr4:189493638-189493884	IMR90	lung:	n/a	chr4:189493776-189493787
36	CEBPB	chr4:189514350-189514601	A549	lung:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
37	CEBPB	chr4:189690675-189690948	IMR90	lung:	n/a	chr4:189690814-189690827 chr4:189690816-189690827
38	CEBPB	chr4:189636117-189636455	IMR90	lung:	n/a	n/a
39	CEBPB	chr4:189551807-189551980	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:189618399-189618727	A549	lung:	n/a	chr4:189618559-189618570
41	CEBPB	chr4:189584573-189585174	A549	lung:	n/a	n/a
42	CEBPB	chr4:189584536-189584848	A549	lung:	n/a	n/a
43	CEBPB	chr4:189560668-189560998	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:189618382-189618748	IMR90	lung:	n/a	chr4:189618559-189618570
45	CEBPB	chr4:189514320-189514661	IMR90	lung:	n/a	chr4:189514490-189514501 chr4:189514359-189514372 chr4:189514489-189514500
46	CEBPB	chr4:189618245-189618777	HCT-116	colon:	n/a	chr4:189618559-189618570
47	CEBPB	chr4:189424052-189424344	IMR90	lung:	n/a	chr4:189424170-189424181
48	CEBPB	chr4:189424045-189424347	HepG2	liver:	n/a	chr4:189424047-189424059 chr4:189424170-189424181
49	CEBPB	chr4:189584550-189585193	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:189493631-189493895	A549	lung:	n/a	chr4:189493776-189493787

(count:1896 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:189580633-189580683	HUVEC	blood vessel:	n/a
2	chr4:189552386-189552436	RPTEC	kidney:	n/a
3	chr4:189485260-189485310	SK-N-SH	brain:	n/a
4	chr4:189659536-189659586	SK-N-SH	brain:	n/a
5	chr4:189476613-189476663	HNPCEpiC	eye:	n/a
6	chr4:189580633-189580683	HUVEC	blood vessel:	n/a
7	chr4:189552386-189552436	RPTEC	kidney:	n/a
8	chr4:189485260-189485310	SK-N-SH	brain:	n/a
9	chr4:189659536-189659586	SK-N-SH	brain:	n/a
10	chr4:189476613-189476663	HNPCEpiC	eye:	n/a
11	chr4:189580633-189580683	HRE	kidney:	n/a
12	chr4:189580596-189580646	K562	blood:	n/a
13	chr4:189655175-189655225	Hela-S3	cervix:	n/a
14	chr4:189578842-189578892	HMEC	breast:	n/a
15	chr4:189580507-189580557	GM12878	blood:	n/a
16	chr4:189433040-189433090	K562	blood:	n/a
17	chr4:189476745-189476795	HCT-116	colon:	n/a
18	chr4:189548707-189548757	MCF-7	breast:	n/a
19	chr4:189548707-189548757	BE2_C	brain:	n/a
20	chr4:189572647-189572697	AG10803	skin:	n/a
21	chr4:189485260-189485310	T-47D	breast:	n/a
22	chr4:189580798-189580848	IMR90	lung:	fetal
23	chr4:189552677-189552727	HL-60	blood:	n/a
24	chr4:189659523-189659573	SK-N-MC	brain:	n/a
25	chr4:189433040-189433090	SAEC	small airway:	n/a
26	chr4:189655242-189655292	GM06990	blood:	n/a
27	chr4:189580331-189580381	SK-N-SH_RA	brain:	n/a
28	chr4:189577711-189577761	H1-hESC	embryonic stem cell:	embryo
29	chr4:189580507-189580557	HCPEpiC	choroid plexus:	n/a
30	chr4:189612833-189612883	AG09309	skin:	n/a
31	chr4:189580633-189580683	HL-60	blood:	n/a
32	chr4:189541174-189541224	HEK293	kidney:	embryo
33	chr4:189583617-189583667	HNPCEpiC	eye:	n/a
34	chr4:189572647-189572697	IMR90	lung:	fetal
35	chr4:189659536-189659586	HUVEC	blood vessel:	n/a
36	chr4:189659536-189659586	HRE	kidney:	n/a
37	chr4:189552339-189552389	Caco-2	colon:	n/a
38	chr4:189659523-189659573	T-47D	breast:	n/a
39	chr4:189552339-189552389	AG09309	skin:	n/a
40	chr4:189655175-189655225	HUVEC	blood vessel:	n/a
41	chr4:189612833-189612883	BJ	skin:	n/a
42	chr4:189552677-189552727	HEK293	kidney:	embryo
43	chr4:189655175-189655225	U87	brain:	n/a
44	chr4:189553390-189553440	ProgFib	skin:	n/a
45	chr4:189659523-189659573	Hepatocyte	liver:	n/a
46	chr4:189578842-189578892	AG09309	skin:	n/a
47	chr4:189553390-189553440	HCF	heart:	n/a
48	chr4:189552339-189552389	AG04449	skin:	fetal
49	chr4:189476613-189476663	HCT-116	colon:	n/a
50	chr4:189552386-189552436	K562	blood:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
2	chr4:189510385..189513322-chr4:189513349..189516296,2	MCF-7	breast:
3	chr4:189617734..189620588-chr4:189620667..189622688,2	K562	blood:
4	chr4:189702571..189703442-chr4:190123148..190123787,2	MCF-7	breast:
5	chr4:189659633..189661135-chr6:153323368..153324975,2	MCF-7	breast:
6	chr4:189704602..189705331-chr9:126840912..126841898,2	MCF-7	breast:
7	chr4:189427438..189430236-chr6:107435359..107438052,2	MCF-7	breast:
8	chr4:189617734..189620588-chr4:189620667..189622688,2	K562	blood:
9	chr4:189658248..189662329-chr6:153321108..153324955,4	K562	blood:
10	chr4:189659109..189659751-chr6:153323423..153323945,2	NB4	blood:
11	chr4:189659615..189661129-chr6:153313575..153315096,2	K562	blood:
12	chr4:189658110..189659728-chr6:153322361..153324298,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML1-5	chr4:189697811-189697921	XLOC_003836
2	lnc-TRIML1-5	chr4:189706415-189706559	XLOC_003836
3	lnc-TRIML1-4	chr4:189678833-189678898	ENSG00000249269
4	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099745
5	lnc-TRIML1-4	chr4:189699838-189700133	ENSG00000249269
6	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
7	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
8	lnc-TRIML1-4	chr4:189689945-189690019	ENSG00000249269
9	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
10	lnc-TRIML1-10	chr4:189635786-189636060	ucscGeneNc_uc003izp_1
11	lnc-TRIML1-3	chr4:189406933-189407019	NONHSAT099749
12	lnc-TRIML1-10	chr4:189694883-189696700	ucscGeneNc_uc003izp_1
13	lnc-TRIML1-3	chr4:189522922-189523062	ENSG00000249378
14	lnc-TRIML1-5	chr4:189706450-189706665	XLOC_003836
15	lnc-TRIML1-3	chr4:189406933-189407076	NONHSAT099746
16	lnc-TRIML1-10	chr4:189634846-189634904	ucscGeneNc_uc003izp_1
17	lnc-TRIML2-6	chr4:189698770-189699205	XLOC_004227
18	lnc-TRIML1-3	chr4:189522922-189523025	NONHSAT099749
19	lnc-TRIML1-3	chr4:189406933-189407028	XLOC_003834
20	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
21	lnc-TRIML1-3	chr4:189601875-189602205	ENSG00000249378
22	lnc-TRIML1-9	chr4:189661661-189662435	NONHSAT099754
23	lnc-TRIML1-10	chr4:189643927-189644013	ucscGeneNc_uc003izp_1
24	lnc-TRIML2-6	chr4:189699739-189700052	NONHSAT099763
25	lnc-TRIML2-6	chr4:189698862-189699205	XLOC_004227
26	lnc-TRIML1-3	chr4:189522922-189523062	NONHSAT099745
27	lnc-TRIML1-10	chr4:189614812-189614910	ucscGeneNc_uc003izp_1
28	lnc-TRIML1-3	chr4:189406933-189407019	XLOC_003834
29	lnc-TRIML2-6	chr4:189698833-189699205	ENSG00000250626
30	lnc-TRIML1-5	chr4:189705067-189705165	XLOC_003836
31	lnc-TRIML1-3	chr4:189522922-189523060	XLOC_003834
32	lnc-TRIML1-10	chr4:189613729-189613822	ucscGeneNc_uc003izp_1
33	lnc-TRIML2-6	chr4:189698833-189699205	XLOC_004227
34	lnc-TRIML1-3	chr4:189406933-189407011	XLOC_003834
35	lnc-TRIML1-3	chr4:189406933-189407019	ENSG00000249378
36	lnc-TRIML1-5	chr4:189706916-189707064	XLOC_003836
37	lnc-TRIML1-3	chr4:189457889-189459706	XLOC_003834

No data

Variant related genes	Relation type
ENSG00000249269	TF binding region
RNU7-192P	TF binding region
LINC01060	TF binding region
ENSG00000251619	TF binding region
ENSG00000250523	TF binding region
ENSG00000180015	TF binding region
ENSG00000249269	CpG island
RNU7-192P	CpG island
LINC01060	CpG island
ENSG00000251619	CpG island
ENSG00000250523	CpG island
ENSG00000180015	CpG island
ENSG00000112031	chromatin interactions
ENSG00000178409	chromatin interactions
MAP2K4	miRNA target sites
TAPBP	miRNA target sites
UBFD1	miRNA target sites
PRNP	miRNA target sites
DIP2C	miRNA target sites
PTGFRN	miRNA target sites
MPP5	miRNA target sites
RASSF2	miRNA target sites
FAM104A	miRNA target sites
PFN2	miRNA target sites
KCNK1	miRNA target sites
USP1	miRNA target sites

Extended variants
information (count: 12377 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:12377 , 50 per page) page: 1 2 3 4 5 6 7 ... 248

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11734123	chr4:189402309-189402310	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546550359	chr4:189402322-189402323	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs376248139	chr4:189402327-189402328	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs184430324	chr4:189402337-189402338	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576780255	chr4:189402354-189402355	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs11734128	chr4:189402363-189402364	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs561892349	chr4:189402368-189402369	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs572400058	chr4:189402417-189402418	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs574685497	chr4:189402428-189402429	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs542001478	chr4:189402431-189402432	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs550070791	chr4:189402437-189402438	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs2102359	chr4:189402454-189402455	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs561353539	chr4:189402486-189402487	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs367680776	chr4:189402494-189402495	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs113199193	chr4:189402498-189402499	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs142537753	chr4:189402507-189402508	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs146010178	chr4:189402518-189402519	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs371937223	chr4:189402574-189402575	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs535318563	chr4:189402630-189402631	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs548579793	chr4:189402657-189402658	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs552569563	chr4:189402676-189402677	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs534764111	chr4:189402679-189402680	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs557548051	chr4:189402713-189402714	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs2089408	chr4:189402769-189402770	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs540056823	chr4:189402786-189402787	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs562590715	chr4:189402818-189402819	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs78062585	chr4:189402827-189402828	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs143238278	chr4:189402852-189402853	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs112284990	chr4:189402853-189402854	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs115205362	chr4:189402858-189402859	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs75111403	chr4:189402885-189402886	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs188991676	chr4:189402937-189402938	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs564439066	chr4:189402949-189402950	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs533225435	chr4:189402984-189402985	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs144496637	chr4:189403021-189403022	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563103668	chr4:189403052-189403053	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs375885973	chr4:189403059-189403060	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs529191702	chr4:189403060-189403061	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs148391664	chr4:189403066-189403067	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs558244647	chr4:189403081-189403082	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs565699513	chr4:189403117-189403118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181484193	chr4:189403183-189403184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551550518	chr4:189403239-189403240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551325482	chr4:189403250-189403251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566622034	chr4:189403251-189403252	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199790010	chr4:189403254-189403255	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369955042	chr4:189403255-189403256	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368175217	chr4:189403259-189403260	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142530657	chr4:189403275-189403276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556834707	chr4:189403293-189403294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Cognitive impairment	21505072	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD
Epilepsy	21635232	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Sinonasal adenocarcinoma	21360264	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:189366000-189415600	Weak transcription	Osteobl	bone
2	chr4:189376800-189416200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr4:189385400-189415800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:189397600-189407400	Weak transcription	HMEC	breast
5	chr4:189401000-189402400	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr4:189401600-189402400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:189401600-189402600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr4:189402000-189416200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:189402200-189403200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr4:189402200-189403400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:189402400-189405200	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr4:189402400-189405200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr4:189402400-189409000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:189402600-189414800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:189403200-189404000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:189404000-189404800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:189404800-189405400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:189405200-189406200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr4:189405200-189406600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:189405400-189405800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr4:189405400-189411000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr4:189406200-189407200	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr4:189406600-189407800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:189407200-189408800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr4:189408000-189408200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:189409000-189409200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:189411000-189413000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:189413000-189413800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:189413800-189416200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:189414800-189415000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr4:189415000-189415200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr4:189415000-189415600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr4:189415200-189415400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:189415600-189416800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
35	chr4:189415600-189416800	Strong transcription	Osteobl	bone
36	chr4:189416200-189416600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:189416200-189416600	ZNF genes & repeats	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr4:189416200-189416800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr4:189416200-189416800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr4:189416600-189421600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:189416800-189417800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr4:189416800-189418800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:189416800-189423600	Weak transcription	Osteobl	bone
44	chr4:189417800-189419000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr4:189418800-189458200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr4:189419000-189420000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:189420000-189421600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr4:189421600-189422600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
49	chr4:189421600-189423800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr4:189422400-189424200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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