Variant report

Variant	nsv902453
Chromosome Location	chr14:105625743-105660766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1322)
CpG islands
(count:1831)
Chromatin interactive
region (count:92)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1322 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105635551-105635751	K562	blood:	n/a	n/a
2	ARID3A	chr14:105646970-105647099	K562	blood:	n/a	n/a
3	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
4	ATF3	chr14:105647527-105647695	GM12878	blood:	n/a	n/a
5	ATF3	chr14:105647476-105647754	K562	blood:	n/a	n/a
6	ATF3	chr14:105647408-105647698	GM12878	blood:	n/a	n/a
7	BACH1	chr14:105635446-105635818	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:105650175-105650256	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:105647431-105647661	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
12	BHLHE40	chr14:105635049-105635625	K562	blood:	n/a	n/a
13	BHLHE40	chr14:105647471-105647910	GM12878	blood:	n/a	chr14:105647556-105647572
14	BHLHE40	chr14:105647446-105647893	K562	blood:	n/a	chr14:105647556-105647572
15	BHLHE40	chr14:105641106-105641239	GM12878	blood:	n/a	n/a
16	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
17	CBX3	chr14:105635458-105635833	K562	blood:	n/a	n/a
18	CBX3	chr14:105654397-105654814	K562	blood:	n/a	n/a
19	CBX3	chr14:105654534-105654767	K562	blood:	n/a	n/a
20	CCNT2	chr14:105647484-105647639	K562	blood:	n/a	n/a
21	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
22	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
23	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr14:105646836-105646884	K562	blood:	n/a	n/a
25	CHD2	chr14:105634239-105634449	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr14:105628806-105628928	HepG2	liver:	n/a	n/a
27	CHD2	chr14:105647556-105647857	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr14:105635003-105635186	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr14:105632638-105632642	K562	blood:	n/a	n/a
30	CHD2	chr14:105633690-105633737	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr14:105635604-105635860	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr14:105635288-105635741	K562	blood:	n/a	n/a
33	CREB1	chr14:105647357-105647807	A549	lung:	n/a	n/a
34	CREB1	chr14:105633974-105634413	A549	lung:	n/a	n/a
35	CREB1	chr14:105634956-105635290	A549	lung:	n/a	n/a
36	CTCF	chr14:105635561-105635764	A549	lung:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
37	CTCF	chr14:105635640-105635790	HEK293	kidney:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
38	CTCF	chr14:105635546-105635733	SK-N-SH_RA	brain:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
39	CTCF	chr14:105635602-105635722	MCF-7	breast:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
40	CTCF	chr14:105644460-105644610	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr14:105635580-105635730	MCF-7	breast:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
42	CTCF	chr14:105647482-105647578	MCF-7	breast:	n/a	n/a
43	CTCF	chr14:105633860-105634010	HCT-116	colon:	n/a	n/a
44	CTCF	chr14:105654360-105654510	GM12872	blood:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654465-105654481
45	CTCF	chr14:105647709-105647724	GM19239	blood:	n/a	n/a
46	CTCF	chr14:105653613-105653722	GM20000	blood:	n/a	n/a
47	CTCF	chr14:105659164-105659258	GM10248	blood:	n/a	n/a
48	CTCF	chr14:105654420-105654570	GM12874	blood:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654465-105654481
49	CTCF	chr14:105647584-105647594	MCF-7	breast:	n/a	n/a
50	CTCF	chr14:105635600-105635750	HMEC	breast:	n/a	chr14:105635654-105635667 chr14:105635651-105635669

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105635081-105635131	GM12891	blood:	n/a
2	chr14:105635081-105635131	GM12891	blood:	n/a
3	chr14:105634387-105634437	HCPEpiC	choroid plexus:	n/a
4	chr14:105635236-105635286	T-47D	breast:	n/a
5	chr14:105657710-105657760	HNPCEpiC	eye:	n/a
6	chr14:105659807-105659857	GM12892	blood:	n/a
7	chr14:105658949-105658999	AG04450	lung:	fetal
8	chr14:105635081-105635131	HEK293	kidney:	embryo
9	chr14:105649747-105649797	RPTEC	kidney:	n/a
10	chr14:105635239-105635289	HEK293	kidney:	embryo
11	chr14:105657710-105657760	Hepatocyte	liver:	n/a
12	chr14:105635236-105635286	Hela-S3	cervix:	n/a
13	chr14:105649097-105649147	HPAEpiC	pulmonary alveolar:	n/a
14	chr14:105647407-105647457	ECC-1	luminal epithelium:	n/a
15	chr14:105647734-105647784	HCT-116	colon:	n/a
16	chr14:105648024-105648074	AoSMC	blood vessel:	n/a
17	chr14:105658685-105658735	AoSMC	blood vessel:	n/a
18	chr14:105648224-105648274	SK-N-MC	brain:	n/a
19	chr14:105648697-105648747	SK-N-MC	brain:	n/a
20	chr14:105639304-105639354	CMK	blood:	n/a
21	chr14:105639304-105639354	HMEC	breast:	n/a
22	chr14:105635081-105635131	NT2-D1	testis:	n/a
23	chr14:105658949-105658999	HL-60	blood:	n/a
24	chr14:105635763-105635813	ovcar-3	ovarian:	n/a
25	chr14:105635706-105635756	HUVEC	blood vessel:	n/a
26	chr14:105634387-105634437	PFSK-1	brain:	n/a
27	chr14:105634387-105634437	NHBE	bronchial:	n/a
28	chr14:105655178-105655228	SK-N-SH	brain:	n/a
29	chr14:105647194-105647244	T-47D	breast:	n/a
30	chr14:105647194-105647244	CMK	blood:	n/a
31	chr14:105648697-105648747	LNCaP	prostate:	n/a
32	chr14:105649747-105649797	HepG2	liver:	n/a
33	chr14:105635763-105635813	HCM	heart:	n/a
34	chr14:105655178-105655228	HRE	kidney:	n/a
35	chr14:105634387-105634437	CMK	blood:	n/a
36	chr14:105634387-105634437	ovcar-3	ovarian:	n/a
37	chr14:105639304-105639354	AG09319	gingival:	n/a
38	chr14:105651786-105651836	GM12892	blood:	n/a
39	chr14:105635706-105635756	HCM	heart:	n/a
40	chr14:105647507-105647557	AG09319	gingival:	n/a
41	chr14:105634387-105634437	T-47D	breast:	n/a
42	chr14:105635769-105635819	BE2_C	brain:	n/a
43	chr14:105655178-105655228	Caco-2	colon:	n/a
44	chr14:105635708-105635758	GM12891	blood:	n/a
45	chr14:105648697-105648747	ProgFib	skin:	n/a
46	chr14:105647510-105647560	NHDF-neo	bronchial:	n/a
47	chr14:105634387-105634437	H1-hESC	embryonic stem cell:	embryo
48	chr14:105647407-105647457	AG09319	gingival:	n/a
49	chr14:105634387-105634437	NHDF-neo	bronchial:	n/a
50	chr14:105649097-105649147	HRE	kidney:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:105647532..105649524-chr14:105654465..105656702,2	MCF-7	breast:
2	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
3	chr14:105642956..105644640-chr14:105647161..105649743,2	MCF-7	breast:
4	chr14:105486956..105489375-chr14:105652100..105655755,4	MCF-7	breast:
5	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
6	chr14:105638805..105642866-chr14:105643000..105645474,4	K562	blood:
7	chr14:105647877..105649605-chr14:105663025..105665566,2	MCF-7	breast:
8	chr14:105660449..105662714-chr14:105737778..105740475,2	MCF-7	breast:
9	chr14:105635510..105639334-chr14:105658974..105662269,3	K562	blood:
10	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
11	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
12	chr14:105556806..105557482-chr14:105648408..105649374,2	K562	blood:
13	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
14	chr14:105631482..105635033-chr14:105765939..105767661,3	K562	blood:
15	chr14:105512170..105512763-chr14:105653793..105654556,2	MCF-7	breast:
16	chr14:105636616..105638377-chr14:105781844..105784159,2	K562	blood:
17	chr14:105635593..105636402-chr14:105818301..105819224,3	K562	blood:
18	chr14:105646294..105648744-chr14:105860219..105862499,2	MCF-7	breast:
19	chr14:105635244..105636129-chr14:105665708..105667054,3	K562	blood:
20	chr14:105655523..105657045-chr14:105657884..105660647,2	MCF-7	breast:
21	chr14:105649676..105651978-chr14:105660260..105663010,3	K562	blood:
22	chr14:105556861..105558363-chr14:105628903..105631842,2	K562	blood:
23	chr14:105620616..105622856-chr14:105624629..105627730,3	MCF-7	breast:
24	chr14:105645461..105647244-chr14:105649629..105652172,2	MCF-7	breast:
25	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
26	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
27	chr14:105611629..105615687-chr14:105625576..105630230,4	K562	blood:
28	chr14:105511711..105512332-chr14:105633666..105634346,2	MCF-7	breast:
29	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
30	chr14:105550862..105553369-chr14:105650448..105653112,3	MCF-7	breast:
31	chr14:105450462..105452951-chr14:105633617..105637647,3	MCF-7	breast:
32	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
33	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
34	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:
35	chr14:105637173..105640162-chr14:105646187..105648550,3	MCF-7	breast:
36	chr14:105640130..105641650-chr6:31587480..31589137,3	K562	blood:
37	chr14:105559890..105560867-chr14:105633779..105634301,2	MCF-7	breast:
38	chr14:105611401..105614212-chr14:105625101..105627298,2	MCF-7	breast:
39	chr14:105634303..105636398-chr14:105650780..105653428,2	MCF-7	breast:
40	chr14:105647774..105650762-chr14:105651625..105655733,5	MCF-7	breast:
41	chr14:105636897..105638962-chr14:105660422..105663007,2	MCF-7	breast:
42	chr14:105644378..105646118-chr14:105647825..105650297,2	MCF-7	breast:
43	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
44	chr14:105433467..105435387-chr14:105640925..105642715,2	MCF-7	breast:
45	chr14:105644378..105646118-chr14:105647825..105650297,2	MCF-7	breast:
46	chr14:105502174..105504922-chr14:105632204..105633983,2	MCF-7	breast:
47	chr14:105633713..105635633-chr7:75987137..75988852,2	K562	blood:
48	chr14:105555328..105560254-chr14:105631379..105635555,5	MCF-7	breast:
49	chr14:105557317..105562216-chr14:105628986..105634761,7	MCF-7	breast:
50	chr14:105629335..105630135-chr14:105669031..105669954,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-1	chr14:105639541-105639584	ENSG00000257816.1
2	lnc-BTBD6-1	chr14:105639787-105640155	ENSG00000257816.1

No data

Variant related genes	Relation type
NUDT14	TF binding region
JAG2	TF binding region
ENSG00000257622	TF binding region
NUDT14	CpG island
JAG2	CpG island
ENSG00000257622	CpG island
ENSG00000226174	chromatin interactions
ENSG00000256498	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000140104	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000170027	chromatin interactions
ENSG00000183828	chromatin interactions

Extended variants
information (count: 1293 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10138486	chr14:105625743-105625744	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587620457	chr14:105625758-105625759	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs144441797	chr14:105625791-105625792	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587757562	chr14:105625877-105625878	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs113157791	chr14:105625960-105625961	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs587630748	chr14:105625963-105625964	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587685885	chr14:105625987-105625988	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377100577	chr14:105625988-105625989	Weak transcription Enhancers Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs369357217	chr14:105626065-105626066	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs191084968	chr14:105626087-105626088	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs148384669	chr14:105626107-105626108	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182105934	chr14:105626138-105626139	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141569398	chr14:105626149-105626150	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587652440	chr14:105626189-105626190	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs148761217	chr14:105626191-105626192	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs71129280	chr14:105626239-105626240	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587765342	chr14:105626323-105626324	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147528298	chr14:105626327-105626328	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs140083307	chr14:105626330-105626331	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587718811	chr14:105626344-105626345	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs199688919	chr14:105626345-105626346	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187103355	chr14:105626346-105626347	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191604826	chr14:105626348-105626349	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74460504	chr14:105626350-105626351	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs11848499	chr14:105626594-105626595	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs587670688	chr14:105626756-105626757	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs373548278	chr14:105626778-105626779	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs370872824	chr14:105626863-105626864	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183025262	chr14:105626874-105626875	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587709609	chr14:105626896-105626897	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs587610798	chr14:105626923-105626924	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587661575	chr14:105626924-105626925	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587745314	chr14:105626938-105626939	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs587620128	chr14:105626939-105626940	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587677497	chr14:105626963-105626964	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188645620	chr14:105626974-105626975	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs145508143	chr14:105627017-105627018	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113849868	chr14:105627018-105627019	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587684060	chr14:105627121-105627122	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs192807518	chr14:105627172-105627173	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs587615520	chr14:105627195-105627196	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs147282825	chr14:105627300-105627301	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs117847921	chr14:105627312-105627313	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs78133416	chr14:105627327-105627328	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs587723623	chr14:105627333-105627334	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs185719226	chr14:105627418-105627419	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs587677015	chr14:105627436-105627437	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs587712868	chr14:105627437-105627438	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs587605478	chr14:105627455-105627456	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs587644290	chr14:105627490-105627491	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1678 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105602800-105629800	Weak transcription	K562	blood
2	chr14:105606800-105631600	Weak transcription	Hela-S3	cervix
3	chr14:105607600-105632000	Weak transcription	Brain Angular Gyrus	brain
4	chr14:105609400-105631400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr14:105610000-105631400	Weak transcription	HUVEC	blood vessel
6	chr14:105613400-105631400	Weak transcription	Brain Anterior Caudate	brain
7	chr14:105613600-105631400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr14:105613800-105631400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr14:105615800-105633200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr14:105618200-105627400	Weak transcription	Brain Germinal Matrix	brain
11	chr14:105619200-105628600	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr14:105619800-105626800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:105620200-105630800	Weak transcription	Fetal Thymus	thymus
14	chr14:105622000-105627600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr14:105622200-105627600	Weak transcription	Adipose Nuclei	Adipose
16	chr14:105622200-105628800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr14:105622200-105628800	Weak transcription	Left Ventricle	heart
18	chr14:105622200-105631200	Weak transcription	Lung	lung
19	chr14:105622800-105628600	Weak transcription	Gastric	stomach
20	chr14:105622800-105632000	Weak transcription	Fetal Brain Female	brain
21	chr14:105622800-105632200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr14:105622800-105632800	Weak transcription	Fetal Intestine Small	intestine
23	chr14:105623000-105629400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr14:105623200-105627600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr14:105624200-105627800	Weak transcription	HMEC	breast
26	chr14:105624400-105628600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:105624600-105625800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:105624600-105626800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr14:105624600-105627200	Weak transcription	NHEK	skin
30	chr14:105624800-105625800	Enhancers	Fetal Muscle Leg	muscle
31	chr14:105624800-105626000	Bivalent Enhancer	Placenta	Placenta
32	chr14:105625200-105625800	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr14:105625200-105626800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:105625200-105626800	Weak transcription	Right Ventricle	heart
35	chr14:105625400-105625800	Enhancers	Fetal Muscle Trunk	muscle
36	chr14:105625400-105626600	Weak transcription	Pancreas	Pancrea
37	chr14:105625400-105627600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr14:105625600-105625800	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr14:105625600-105626000	Enhancers	A549	lung
40	chr14:105625800-105626600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr14:105625800-105626800	Weak transcription	Fetal Muscle Trunk	muscle
42	chr14:105625800-105626800	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr14:105625800-105627200	Weak transcription	Fetal Muscle Leg	muscle
44	chr14:105626000-105631200	Weak transcription	A549	lung
45	chr14:105626200-105627600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr14:105626600-105628800	Enhancers	Pancreas	Pancrea
47	chr14:105626600-105628800	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr14:105626800-105627400	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr14:105626800-105627400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:105626800-105627600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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