Variant report

Variant	nsv997330
Chromosome Location	chr1:147185938-147313966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:976)
CpG islands
(count:1221)
Chromatin interactive
region (count:102)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:147280155-147280630	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:147191236-147191467	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:147189082-147189480	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:147287788-147287850	K562	blood:	n/a	n/a
5	ATF1	chr1:147283979-147283988	K562	blood:	n/a	n/a
6	ATF1	chr1:147293156-147293271	K562	blood:	n/a	n/a
7	ATF3	chr1:147280132-147280418	HepG2	liver:	n/a	n/a
8	BACH1	chr1:147309256-147309748	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:147191189-147191402	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr1:147305765-147305846	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL3	chr1:147311445-147311805	GM12878	blood:	n/a	n/a
12	BHLHE40	chr1:147280178-147280382	HepG2	liver:	n/a	n/a
13	BHLHE40	chr1:147280127-147280501	HepG2	liver:	n/a	n/a
14	BRCA1	chr1:147273148-147273197	Hela-S3	cervix:	n/a	chr1:147273166-147273173
15	CEBPB	chr1:147280153-147280499	K562	blood:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
16	CEBPB	chr1:147229432-147229831	ECC-1	luminal epithelium:	n/a	chr1:147229607-147229618
17	CEBPB	chr1:147229334-147229924	MCF-7	breast:	n/a	chr1:147229607-147229618
18	CEBPB	chr1:147280100-147280410	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
19	CEBPB	chr1:147280093-147280519	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
20	CEBPB	chr1:147259741-147259892	K562	blood:	n/a	n/a
21	CEBPB	chr1:147216542-147216757	HepG2	liver:	n/a	chr1:147216614-147216625
22	CEBPB	chr1:147280084-147280789	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
23	CEBPB	chr1:147189291-147189452	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:147229401-147229823	ECC-1	luminal epithelium:	n/a	chr1:147229607-147229618
25	CEBPB	chr1:147280103-147280524	Hela-S3	cervix:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
26	CEBPB	chr1:147259655-147259937	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:147193797-147194355	MCF-7	breast:	n/a	n/a
28	CEBPB	chr1:147193738-147194358	MCF-7	breast:	n/a	n/a
29	CEBPB	chr1:147269626-147269645	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr1:147229299-147229827	MCF-7	breast:	n/a	chr1:147229607-147229618
31	CEBPB	chr1:147193787-147194298	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:147259715-147259949	A549	lung:	n/a	n/a
33	CEBPB	chr1:147193911-147194150	HepG2	liver:	n/a	n/a
34	CEBPB	chr1:147253715-147253880	HepG2	liver:	n/a	chr1:147253804-147253815 chr1:147253805-147253816
35	CEBPB	chr1:147280132-147280751	A549	lung:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
36	CEBPB	chr1:147279582-147279829	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr1:147280141-147280538	HepG2	liver:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
38	CEBPB	chr1:147193887-147194133	A549	lung:	n/a	n/a
39	CEBPB	chr1:147229457-147229747	HepG2	liver:	n/a	chr1:147229607-147229618
40	CEBPB	chr1:147216573-147216767	Hela-S3	cervix:	n/a	chr1:147216614-147216625
41	CEBPB	chr1:147278481-147278496	HepG2	liver:	n/a	n/a
42	CEBPB	chr1:147277448-147277776	HepG2	liver:	n/a	n/a
43	CEBPB	chr1:147280136-147280454	K562	blood:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
44	CEBPB	chr1:147247214-147247439	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr1:147189238-147189669	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr1:147188952-147189765	MCF-7	breast:	n/a	n/a
47	CEBPB	chr1:147193938-147194130	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr1:147280158-147280664	IMR90	lung:	n/a	chr1:147280320-147280331 chr1:147280273-147280284
49	CEBPB	chr1:147259680-147259951	IMR90	lung:	n/a	n/a
50	CEBPB	chr1:147259630-147259998	MCF-7	breast:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:147245485-147245535	SK-N-SH_RA	brain:	n/a
2	chr1:147245485-147245535	SK-N-SH_RA	brain:	n/a
3	chr1:147197536-147197586	NB4	blood:	n/a
4	chr1:147233887-147233937	HCPEpiC	choroid plexus:	n/a
5	chr1:147246154-147246204	ovcar-3	ovarian:	n/a
6	chr1:147245494-147245544	AG10803	skin:	n/a
7	chr1:147253401-147253451	GM12892	blood:	n/a
8	chr1:147245168-147245218	NHDF-neo	bronchial:	n/a
9	chr1:147233743-147233793	AoSMC	blood vessel:	n/a
10	chr1:147246839-147246889	Hela-S3	cervix:	n/a
11	chr1:147245168-147245218	NT2-D1	testis:	n/a
12	chr1:147233738-147233788	AG04449	skin:	fetal
13	chr1:147231862-147231912	NHBE	bronchial:	n/a
14	chr1:147233887-147233937	Hepatocyte	liver:	n/a
15	chr1:147245626-147245676	IMR90	lung:	fetal
16	chr1:147246154-147246204	T-47D	breast:	n/a
17	chr1:147231862-147231912	GM12878	blood:	n/a
18	chr1:147230209-147230259	H1-hESC	embryonic stem cell:	embryo
19	chr1:147245626-147245676	HAEpiC	amniotic membrane:	n/a
20	chr1:147233743-147233793	SKMC	muscle:	n/a
21	chr1:147231862-147231912	Hela-S3	cervix:	n/a
22	chr1:147245626-147245676	SK-N-MC	brain:	n/a
23	chr1:147231524-147231574	HEEpiC	esophagus:	n/a
24	chr1:147230209-147230259	HEEpiC	esophagus:	n/a
25	chr1:147231524-147231574	PANC-1	pancreas:	n/a
26	chr1:147231061-147231111	HRPEpiC	eye:	n/a
27	chr1:147245494-147245544	IMR90	lung:	fetal
28	chr1:147230452-147230502	SK-N-SH	brain:	n/a
29	chr1:147232608-147232658	HIPEpiC	eye:	n/a
30	chr1:147230209-147230259	HCT-116	colon:	n/a
31	chr1:147245485-147245535	BJ	skin:	n/a
32	chr1:147245168-147245218	HCM	heart:	n/a
33	chr1:147233738-147233788	HL-60	blood:	n/a
34	chr1:147245168-147245218	IMR90	lung:	fetal
35	chr1:147246839-147246889	ECC-1	luminal epithelium:	n/a
36	chr1:147233743-147233793	HCT-116	colon:	n/a
37	chr1:147246329-147246379	BJ	skin:	n/a
38	chr1:147309347-147309397	Jurkat	blood:	n/a
39	chr1:147233887-147233937	AG09319	gingival:	n/a
40	chr1:147245168-147245218	HUVEC	blood vessel:	n/a
41	chr1:147246839-147246889	AG04450	lung:	fetal
42	chr1:147246839-147246889	NH-A	brain:	n/a
43	chr1:147233110-147233160	HRE	kidney:	n/a
44	chr1:147253401-147253451	AG09309	skin:	n/a
45	chr1:147245626-147245676	Caco-2	colon:	n/a
46	chr1:147233743-147233793	HCPEpiC	choroid plexus:	n/a
47	chr1:147230209-147230259	HMEC	breast:	n/a
48	chr1:147231061-147231111	K562	blood:	n/a
49	chr1:147253401-147253451	NT2-D1	testis:	n/a
50	chr1:147245626-147245676	SK-N-SH	brain:	n/a

(count:102 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:147274506..147277076-chr1:147285425..147287009,2	K562	blood:
2	chr1:147234187..147237058-chr1:147240099..147241730,2	MCF-7	breast:
3	chr1:147216774..147217411-chr1:147362235..147362885,2	K562	blood:
4	chr1:147194857..147197261-chr1:147362926..147365705,2	MCF-7	breast:
5	chr1:147247003..147248756-chr1:147253569..147255678,2	K562	blood:
6	chr1:147141882..147144286-chr1:147193380..147195326,2	MCF-7	breast:
7	chr1:147208419..147212694-chr1:147216367..147220265,3	MCF-7	breast:
8	chr1:147280614..147282894-chr1:147286254..147288918,3	K562	blood:
9	chr1:147189146..147191909-chr1:147192462..147194196,3	MCF-7	breast:
10	chr1:147195370..147197758-chr1:147352674..147354271,2	MCF-7	breast:
11	chr1:147313489..147315540-chr1:147360218..147362457,2	K562	blood:
12	chr1:147187841..147191070-chr1:147191880..147194262,4	MCF-7	breast:
13	chr1:147195860..147197594-chr1:147201052..147203782,2	K562	blood:
14	chr1:147213977..147216109-chr1:147228245..147230874,2	K562	blood:
15	chr1:147232773..147235381-chr1:147235921..147238475,2	K562	blood:
16	chr1:147190469..147193203-chr1:147339308..147341475,2	MCF-7	breast:
17	chr1:147212472..147214713-chr1:147214718..147216268,2	MCF-7	breast:
18	chr1:147229847..147231847-chr1:147237550..147240548,2	MCF-7	breast:
19	chr1:147194515..147197013-chr1:147361402..147365473,61	MCF-7	breast:
20	chr1:147194479..147196491-chr1:147360773..147362653,2	MCF-7	breast:
21	chr1:147232773..147235381-chr1:147235921..147238475,2	K562	blood:
22	chr1:147130729..147132251-chr1:147185783..147188406,2	MCF-7	breast:
23	chr1:147195873..147196793-chr1:147312843..147313525,2	MCF-7	breast:
24	chr1:147218454..147220532-chr1:147233214..147234923,2	MCF-7	breast:
25	chr1:147253982..147256046-chr1:147260183..147262374,2	K562	blood:
26	chr1:147208419..147212694-chr1:147216367..147220265,3	MCF-7	breast:
27	chr1:147186761..147189030-chr1:147190650..147192653,2	K562	blood:
28	chr1:147195860..147197594-chr1:147201052..147203782,2	K562	blood:
29	chr1:147222918..147226453-chr1:147226545..147230518,7	MCF-7	breast:
30	chr1:147266191..147267912-chr1:147271628..147273288,2	MCF-7	breast:
31	chr1:147240071..147242067-chr1:147245350..147247970,2	MCF-7	breast:
32	chr1:147218316..147222428-chr1:147225799..147230204,6	MCF-7	breast:
33	chr1:147306497..147308637-chr1:147308840..147310925,2	MCF-7	breast:
34	chr1:147189146..147191909-chr1:147192462..147194196,3	MCF-7	breast:
35	chr1:147272185..147274968-chr1:147288763..147290507,2	K562	blood:
36	chr1:147276129..147278611-chr1:147279190..147281299,2	MCF-7	breast:
37	chr1:147268842..147272094-chr1:147272923..147275545,3	K562	blood:
38	chr1:147252565..147254194-chr1:147257728..147259512,2	MCF-7	breast:
39	chr1:147195260..147198617-chr1:147199229..147201930,3	MCF-7	breast:
40	chr1:147194962..147196746-chr1:147362023..147363000,13	MCF-7	breast:
41	chr1:147214667..147217419-chr1:147235402..147238099,2	MCF-7	breast:
42	chr1:147268842..147272094-chr1:147272923..147275545,3	K562	blood:
43	chr1:147229847..147231847-chr1:147237550..147240548,2	MCF-7	breast:
44	chr1:147218454..147220532-chr1:147233214..147234923,2	MCF-7	breast:
45	chr1:147209469..147211828-chr1:147222916..147225569,2	MCF-7	breast:
46	chr1:147225486..147227195-chr1:147227978..147229551,2	MCF-7	breast:
47	chr1:147243719..147246413-chr1:147246599..147248961,2	MCF-7	breast:
48	chr1:147189303..147191696-chr1:147194595..147196173,2	MCF-7	breast:
49	chr1:147195512..147196780-chr1:147364142..147365569,12	MCF-7	breast:
50	chr1:147290796..147294633-chr1:147295711..147299117,4	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BCL9-4	chr1:147199410-147199544	NONHSAT006041
2	lnc-BCL9-4	chr1:147197029-147197201	ucscGeneNc_uc009wkw_1
3	lnc-GJA8-1	chr1:147260720-147261065	XLOC_000387
4	lnc-GJA5-1	chr1:147209596-147209751	XLOC_001006
5	lnc-BCL9-4	chr1:147199915-147199992	ucscGeneNc_uc009wkw_1
6	lnc-GJA8-1	chr1:147249700-147249833	XLOC_000387
7	lnc-BCL9-4	chr1:147199410-147199544	ucscGeneNc_uc009wkw_1
8	lnc-BCL9-4	chr1:147199915-147200203	NONHSAT006044
9	lnc-BCL9-4	chr1:147217869-147218218	NONHSAT006041
10	lnc-GJA8-1	chr1:147249689-147249833	XLOC_000387
11	lnc-GJA8-1	chr1:147264755-147267415	XLOC_000387
12	lnc-GJA5-1	chr1:147210816-147210939	XLOC_001006
13	lnc-GJA5-2	chr1:147281915-147282433	XLOC_001007
14	lnc-BCL9-4	chr1:147199410-147199544	NONHSAT006043
15	lnc-BCL9-4	chr1:147199915-147199992	NONHSAT006043
16	lnc-GJA5-2	chr1:147283214-147283468	XLOC_001007
17	lnc-BCL9-2	chr1:147230462-147230517	ENSG00000234482.1
18	lnc-BCL9-4	chr1:147194955-147195009	NONHSAT006043
19	lnc-BCL9-4	chr1:147194946-147195009	NONHSAT006041
20	lnc-BCL9-4	chr1:147199409-147199544	NONHSAT006044
21	lnc-BCL9-4	chr1:147218961-147219678	ucscGeneNc_uc009wkw_1
22	lnc-BCL9-2	chr1:147229426-147229879	ENSG00000234482.1

No data

Variant related genes	Relation type
GJA5	TF binding region
ENSG00000234482	TF binding region
ENSG00000223728	TF binding region
ENSG00000234190	TF binding region
GJA5	CpG island
ENSG00000234482	CpG island
ENSG00000223728	CpG island
ENSG00000234190	CpG island
ENSG00000234482	chromatin interactions
ENSG00000234190	chromatin interactions
ENSG00000143140	chromatin interactions
ENSG00000121634	chromatin interactions
ENSG00000162836	chromatin interactions
ENSG00000223728	chromatin interactions
SOCS4	miRNA target sites
ARHGAP1	miRNA target sites

Extended variants
information (count: 4320 )
Associated
traits (count: 152 )

Variant overlapped rSNPs/rCNVs (count:4320 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187402858	chr1:147185988-147185989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs587709667	chr1:147186021-147186022	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587612258	chr1:147186071-147186072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587657863	chr1:147186084-147186085	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587720917	chr1:147186112-147186113	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs192385483	chr1:147186139-147186140	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183672532	chr1:147186159-147186160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116356156	chr1:147186165-147186166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs189015302	chr1:147186171-147186172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140991896	chr1:147186218-147186219	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs7556268	chr1:147186221-147186222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs192506317	chr1:147186236-147186237	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146471480	chr1:147186255-147186256	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587676679	chr1:147186265-147186266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587773846	chr1:147186280-147186281	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs147619925	chr1:147186381-147186382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587721621	chr1:147186383-147186384	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587773374	chr1:147186441-147186442	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs113724534	chr1:147186444-147186445	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183547578	chr1:147186471-147186472	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs587710530	chr1:147186503-147186504	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142143444	chr1:147186540-147186541	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs187141773	chr1:147186579-147186580	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587722756	chr1:147186583-147186584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs12045461	chr1:147186589-147186590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12760985	chr1:147186616-147186617	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs587638861	chr1:147186624-147186625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs79842738	chr1:147186646-147186647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs75409619	chr1:147186722-147186723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587598747	chr1:147186743-147186744	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146219247	chr1:147186809-147186810	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs34841473	chr1:147186856-147186857	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191530655	chr1:147186927-147186928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs79071562	chr1:147186931-147186932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587660615	chr1:147186974-147186975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs587768336	chr1:147186995-147186996	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587641910	chr1:147187014-147187015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138636979	chr1:147187032-147187033	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587758295	chr1:147187038-147187039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184404011	chr1:147187069-147187070	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587681345	chr1:147187110-147187111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587767077	chr1:147187114-147187115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148836065	chr1:147187121-147187122	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587685477	chr1:147187158-147187159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587767529	chr1:147187185-147187186	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs114740037	chr1:147187369-147187370	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs587716436	chr1:147187382-147187383	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189793332	chr1:147187437-147187438	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587648613	chr1:147187553-147187554	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114615912	chr1:147187557-147187558	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:152)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20369283	CNVD
Oral cancer	21386901	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Obesity	21131291	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD
Melanoma	21430779	CNVD
Cancer	21272361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Neuroblastoma	19536264	CNVD
Pancreatic cancer	21811587	CNVD

Chromatin state (count:1071 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:147183600-147187800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:147184800-147187200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:147186400-147187600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr1:147186800-147187400	Enhancers	Left Ventricle	heart
5	chr1:147187200-147187600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr1:147187200-147187600	Enhancers	Fetal Muscle Leg	muscle
7	chr1:147187400-147189400	Weak transcription	Left Ventricle	heart
8	chr1:147187600-147188800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr1:147187600-147189600	Weak transcription	Fetal Muscle Leg	muscle
10	chr1:147187800-147192000	Enhancers	HepG2	liver
11	chr1:147188200-147188800	Enhancers	Sigmoid Colon	Sigmoid Colon
12	chr1:147188200-147189000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:147188200-147190200	Enhancers	Hela-S3	cervix
14	chr1:147188200-147190400	Enhancers	NHEK	skin
15	chr1:147188400-147189600	Enhancers	Stomach Mucosa	stomach
16	chr1:147188400-147191000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr1:147188600-147189800	Enhancers	Fetal Thymus	thymus
18	chr1:147188600-147190200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:147188600-147190600	Enhancers	Rectal Mucosa Donor 31	rectum
20	chr1:147188600-147190800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr1:147188600-147191800	Enhancers	HMEC	breast
22	chr1:147188800-147189000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:147188800-147189400	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr1:147188800-147190200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr1:147188800-147190600	Enhancers	Primary B cells from peripheral blood	blood
26	chr1:147188800-147191800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:147189000-147190000	Enhancers	Duodenum Mucosa	Duodenum
28	chr1:147189000-147190600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:147189000-147191000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:147189000-147192400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr1:147189200-147189600	Enhancers	A549	lung
32	chr1:147189200-147190200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
33	chr1:147189400-147190000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr1:147189400-147190000	Enhancers	Placenta	Placenta
35	chr1:147189400-147190200	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr1:147189400-147190200	Enhancers	Fetal Muscle Trunk	muscle
37	chr1:147189400-147190200	Enhancers	Gastric	stomach
38	chr1:147189400-147190200	Enhancers	Right Atrium	heart
39	chr1:147189400-147190200	Enhancers	Spleen	Spleen
40	chr1:147189400-147190400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
41	chr1:147189400-147190400	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr1:147189400-147190600	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:147189400-147190800	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr1:147189400-147191800	Enhancers	Left Ventricle	heart
45	chr1:147189400-147191800	Enhancers	Pancreas	Pancrea
46	chr1:147189400-147193000	Enhancers	Esophagus	oesophagus
47	chr1:147189600-147190000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:147189600-147190000	Flanking Active TSS	Stomach Mucosa	stomach
49	chr1:147189600-147190800	Enhancers	Lung	lung
50	chr1:147189600-147191200	Enhancers	Fetal Muscle Leg	muscle

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