Variant report

Variant	nsv566154
Chromosome Location	chr14:105590884-105633499
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:2689)
Chromatin interactive
region (count:76)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
2	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
3	CBX3	chr14:105597533-105598007	HCT-116	colon:	n/a	n/a
4	CBX3	chr14:105607430-105607762	K562	blood:	n/a	n/a
5	CBX3	chr14:105597490-105598063	HCT-116	colon:	n/a	n/a
6	CBX3	chr14:105606324-105606692	K562	blood:	n/a	n/a
7	CBX3	chr14:105606276-105606713	K562	blood:	n/a	n/a
8	CEBPB	chr14:105602051-105602404	K562	blood:	n/a	chr14:105602218-105602229
9	CEBPB	chr14:105602082-105602324	Hela-S3	cervix:	n/a	chr14:105602218-105602229
10	CEBPB	chr14:105602053-105602402	A549	lung:	n/a	chr14:105602218-105602229
11	CEBPB	chr14:105602145-105602475	MCF-7	breast:	n/a	chr14:105602218-105602229
12	CEBPB	chr14:105602202-105602233	H1-hESC	embryonic stem cell:	n/a	chr14:105602218-105602229
13	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr14:105602020-105602475	A549	lung:	n/a	chr14:105602218-105602229
15	CEBPB	chr14:105602070-105602404	HepG2	liver:	n/a	chr14:105602218-105602229
16	CEBPB	chr14:105602049-105602403	IMR90	lung:	n/a	chr14:105602218-105602229
17	CHD2	chr14:105632638-105632642	K562	blood:	n/a	n/a
18	CHD2	chr14:105628806-105628928	HepG2	liver:	n/a	n/a
19	CREB1	chr14:105603330-105603686	K562	blood:	n/a	n/a
20	CTCF	chr14:105631489-105631643	Hela-S3	cervix:	n/a	chr14:105631554-105631562
21	CTCF	chr14:105611526-105611711	MCF-7	breast:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
22	CTCF	chr14:105611550-105611694	Hela-S3	cervix:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
23	CTCF	chr14:105611498-105611721	H1-hESC	embryonic stem cell:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
24	CTCF	chr14:105611540-105611690	GM12875	blood:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
25	CTCF	chr14:105613160-105613310	HepG2	liver:	n/a	n/a
26	CTCF	chr14:105629100-105629250	NHEK	skin:	n/a	n/a
27	CTCF	chr14:105631700-105631850	MCF-7	breast:	n/a	n/a
28	CTCF	chr14:105617724-105617869	MCF-7	breast:	n/a	n/a
29	CTCF	chr14:105633040-105633190	WERI-Rb-1	eye:	n/a	chr14:105633102-105633120 chr14:105633104-105633117
30	CTCF	chr14:105631540-105631690	HMEC	breast:	n/a	chr14:105631554-105631562
31	CTCF	chr14:105603849-105604026	HepG2	liver:	n/a	n/a
32	CTCF	chr14:105611549-105611693	MCF-7	breast:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
33	CTCF	chr14:105611547-105611705	GM12892	blood:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
34	CTCF	chr14:105628840-105628990	AG04449	skin:	n/a	n/a
35	CTCF	chr14:105611480-105611630	AG04449	skin:	n/a	chr14:105611569-105611579
36	CTCF	chr14:105613155-105613312	GM12878	blood:	n/a	n/a
37	CTCF	chr14:105631477-105631669	MCF-7	breast:	n/a	chr14:105631554-105631562
38	CTCF	chr14:105632440-105632590	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr14:105633058-105633173	Hela-S3	cervix:	n/a	chr14:105633102-105633120 chr14:105633104-105633117
40	CTCF	chr14:105611620-105611770	HBMEC	blood vessel:	n/a	chr14:105611626-105611634
41	CTCF	chr14:105592700-105592850	NHEK	skin:	n/a	chr14:105592711-105592724
42	CTCF	chr14:105603945-105603982	HepG2	liver:	n/a	n/a
43	CTCF	chr14:105611560-105611710	HMEC	breast:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
44	CTCF	chr14:105631500-105631650	Hela-S3	cervix:	n/a	chr14:105631554-105631562
45	CTCF	chr14:105631480-105631630	WERI-Rb-1	eye:	n/a	chr14:105631554-105631562
46	CTCF	chr14:105628909-105628967	GM13976	blood:	n/a	n/a
47	CTCF	chr14:105611560-105611699	HepG2	liver:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
48	CTCF	chr14:105628780-105628930	AG04449	skin:	n/a	n/a
49	CTCF	chr14:105613180-105613330	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr14:105631470-105631685	MCF-7	breast:	n/a	chr14:105631554-105631562

(count:2689 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105600994-105601044	AG10803	skin:	n/a
2	chr14:105609831-105609881	GM12892	blood:	n/a
3	chr14:105609831-105609881	NT2-D1	testis:	n/a
4	chr14:105617308-105617358	NHDF-neo	bronchial:	n/a
5	chr14:105612753-105612803	AG04450	lung:	fetal
6	chr14:105600994-105601044	AG10803	skin:	n/a
7	chr14:105609831-105609881	GM12892	blood:	n/a
8	chr14:105609831-105609881	NT2-D1	testis:	n/a
9	chr14:105617308-105617358	NHDF-neo	bronchial:	n/a
10	chr14:105612753-105612803	AG04450	lung:	fetal
11	chr14:105603389-105603439	RPTEC	kidney:	n/a
12	chr14:105609411-105609461	A549	lung:	n/a
13	chr14:105612753-105612803	ProgFib	skin:	n/a
14	chr14:105619511-105619561	SKMC	muscle:	n/a
15	chr14:105608973-105609023	NHDF-neo	bronchial:	n/a
16	chr14:105619511-105619561	HRCEpiC	kidney:	n/a
17	chr14:105614564-105614614	NH-A	brain:	n/a
18	chr14:105614818-105614868	SAEC	small airway:	n/a
19	chr14:105619634-105619684	PANC-1	pancreas:	n/a
20	chr14:105617308-105617358	HepG2	liver:	n/a
21	chr14:105608260-105608310	HNPCEpiC	eye:	n/a
22	chr14:105617173-105617223	AG09309	skin:	n/a
23	chr14:105614564-105614614	K562	blood:	n/a
24	chr14:105609516-105609566	HRCEpiC	kidney:	n/a
25	chr14:105622992-105623042	GM19239	blood:	n/a
26	chr14:105608474-105608524	RPTEC	kidney:	n/a
27	chr14:105608973-105609023	HAEpiC	amniotic membrane:	n/a
28	chr14:105612130-105612180	HAEpiC	amniotic membrane:	n/a
29	chr14:105622454-105622504	AG09309	skin:	n/a
30	chr14:105615459-105615509	T-47D	breast:	n/a
31	chr14:105618576-105618626	HRE	kidney:	n/a
32	chr14:105613102-105613152	HIPEpiC	eye:	n/a
33	chr14:105617839-105617889	HUVEC	blood vessel:	n/a
34	chr14:105618482-105618532	NH-A	brain:	n/a
35	chr14:105609411-105609461	HMEC	breast:	n/a
36	chr14:105608474-105608524	U87	brain:	n/a
37	chr14:105609472-105609522	ProgFib	skin:	n/a
38	chr14:105622992-105623042	HUVEC	blood vessel:	n/a
39	chr14:105614818-105614868	GM12892	blood:	n/a
40	chr14:105603153-105603203	HepG2	liver:	n/a
41	chr14:105619511-105619561	Caco-2	colon:	n/a
42	chr14:105622454-105622504	Jurkat	blood:	n/a
43	chr14:105622312-105622362	AG04449	skin:	fetal
44	chr14:105618482-105618532	HIPEpiC	eye:	n/a
45	chr14:105612971-105613021	U87	brain:	n/a
46	chr14:105617839-105617889	H1-hESC	embryonic stem cell:	embryo
47	chr14:105618576-105618626	HIPEpiC	eye:	n/a
48	chr14:105612753-105612803	NH-A	brain:	n/a
49	chr14:105609516-105609566	U87	brain:	n/a
50	chr14:105614564-105614614	HIPEpiC	eye:	n/a

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
2	chr14:105445649..105448428-chr14:105631488..105633523,2	MCF-7	breast:
3	chr14:105602588..105606045-chr14:105617930..105622124,4	MCF-7	breast:
4	chr14:105553187..105555561-chr14:105589136..105591325,2	MCF-7	breast:
5	chr14:105606160..105607990-chr14:105612669..105614397,2	MCF-7	breast:
6	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
7	chr14:105584234..105586859-chr14:105605626..105608481,2	MCF-7	breast:
8	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
9	chr14:105617835..105619717-chr14:105620167..105621698,2	MCF-7	breast:
10	chr14:105566584..105569448-chr14:105610028..105612847,2	MCF-7	breast:
11	chr14:105603768..105606019-chr14:105630363..105631971,2	K562	blood:
12	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
13	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
14	chr14:105191017..105193582-chr14:105615897..105618849,2	MCF-7	breast:
15	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:
16	chr14:105610604..105613096-chr14:105619107..105620769,2	K562	blood:
17	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
18	chr14:105613499..105615482-chr14:105618517..105620945,3	MCF-7	breast:
19	chr14:105586207..105587794-chr14:105595383..105596914,2	MCF-7	breast:
20	chr14:105556860..105558487-chr14:105603973..105605818,2	K562	blood:
21	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
22	chr14:105620927..105623497-chr14:105711846..105714187,2	MCF-7	breast:
23	chr14:105632643..105634203-chr14:105776322..105778030,2	K562	blood:
24	chr14:105618326..105620016-chr14:105627831..105630426,2	MCF-7	breast:
25	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
26	chr14:105603827..105606395-chr14:105610368..105612251,2	MCF-7	breast:
27	chr14:105610604..105613096-chr14:105619107..105620769,2	K562	blood:
28	chr14:105441844..105444735-chr14:105632724..105634694,2	MCF-7	breast:
29	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
30	chr14:105605892..105608252-chr14:105621955..105625449,3	K562	blood:
31	chr14:105599383..105601359-chr14:105605338..105607216,2	MCF-7	breast:
32	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
33	chr14:105618156..105621334-chr14:105628329..105630360,3	K562	blood:
34	chr14:105620302..105622152-chr14:105646136..105647731,2	MCF-7	breast:
35	chr14:105632765..105635152-chr14:105864248..105866641,2	K562	blood:
36	chr14:105557317..105562216-chr14:105628986..105634761,7	MCF-7	breast:
37	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
38	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
39	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
40	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
41	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
42	chr14:105620616..105622856-chr14:105624629..105627730,3	MCF-7	breast:
43	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
44	chr14:105556904..105557457-chr14:105630667..105631594,2	MCF-7	breast:
45	chr14:105563166..105566144-chr14:105593732..105596034,2	MCF-7	breast:
46	chr14:105539437..105542411-chr14:105625371..105627547,2	K562	blood:
47	chr14:105597394..105599153-chr14:105603205..105605036,2	K562	blood:
48	chr14:105581813..105588921-chr14:105589522..105595491,7	MCF-7	breast:
49	chr14:105502174..105504922-chr14:105632204..105633983,2	MCF-7	breast:
50	chr14:105601373..105604174-chr14:105610785..105613135,3	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	JAG2	hsa-miR-124-3p	chr14:105608227-105608246
2	JAG2	hsa-miR-124-3p	chr14:105608233-105608227

Variant related genes	Relation type
JAG2	TF binding region
JAG2	CpG island
ENSG00000183828	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000257556	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000185567	chromatin interactions

Extended variants
information (count: 1951 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:1951 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11628893	chr14:105590884-105590885	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587771118	chr14:105590890-105590891	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587669104	chr14:105590897-105590898	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs587725692	chr14:105590898-105590899	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11624283	chr14:105590971-105590972	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs587642056	chr14:105590972-105590973	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587714056	chr14:105590978-105590979	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587598630	chr14:105590980-105590981	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146747749	chr14:105591009-105591010	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
10	rs587724565	chr14:105591038-105591039	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
11	rs373502992	chr14:105591054-105591055	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
12	rs587601419	chr14:105591057-105591058	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
13	rs587677367	chr14:105591159-105591160	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
14	rs74612773	chr14:105591160-105591161	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
15	rs587628911	chr14:105591197-105591198	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
16	rs376360577	chr14:105591256-105591257	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
17	rs140344077	chr14:105591260-105591261	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs143545029	chr14:105591279-105591280	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs4399485	chr14:105591377-105591378	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	mRNA abundance
20	rs187455580	chr14:105591462-105591463	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs587715502	chr14:105591465-105591466	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs587770955	chr14:105591497-105591498	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs587645765	chr14:105591556-105591557	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs117075418	chr14:105591563-105591564	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs4983398	chr14:105591666-105591667	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs376730799	chr14:105591811-105591812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190775447	chr14:105591812-105591813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs587718847	chr14:105591848-105591849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182297433	chr14:105591855-105591856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185028401	chr14:105591887-105591888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs59715822	chr14:105591950-105591951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587724364	chr14:105591971-105591972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs398057475	chr14:105591974-105591975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142889817	chr14:105591975-105591976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs587728194	chr14:105591977-105591978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190276916	chr14:105592020-105592021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587600081	chr14:105592021-105592022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587658972	chr14:105592033-105592034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111631326	chr14:105592102-105592103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386382415	chr14:105592103-105592104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs386382416	chr14:105592112-105592113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs57994662	chr14:105592114-105592115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369201552	chr14:105592115-105592116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587707908	chr14:105592118-105592119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587612056	chr14:105592122-105592123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs77228776	chr14:105592176-105592177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2735811	chr14:105592191-105592192	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs140764213	chr14:105592222-105592223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587594961	chr14:105592223-105592224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587690840	chr14:105592229-105592230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Non-syndromic sensorineural hearing loss	19587683	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
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:696 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105588000-105592800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr14:105590200-105591200	Enhancers	Colonic Mucosa	Colon
3	chr14:105590400-105591000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
4	chr14:105590400-105602600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr14:105590600-105591800	Enhancers	Primary hematopoietic stem cells	blood
6	chr14:105590800-105591000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr14:105590800-105591000	Enhancers	Duodenum Mucosa	Duodenum
8	chr14:105590800-105591200	Bivalent Enhancer	HepG2	liver
9	chr14:105590800-105591400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr14:105590800-105591400	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr14:105590800-105591400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr14:105590800-105591400	Enhancers	Placenta	Placenta
13	chr14:105590800-105591600	Bivalent Enhancer	Fetal Muscle Leg	muscle
14	chr14:105590800-105593000	Enhancers	Fetal Intestine Large	intestine
15	chr14:105591000-105591200	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr14:105591000-105591200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
17	chr14:105591000-105591200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
18	chr14:105591000-105591400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
19	chr14:105591000-105591400	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr14:105591000-105591600	Enhancers	Primary T cells from cord blood	blood
21	chr14:105591000-105591600	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr14:105591000-105591600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
23	chr14:105591200-105591400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr14:105591200-105591400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
25	chr14:105591200-105591400	Flanking Bivalent TSS/Enh	HepG2	liver
26	chr14:105591200-105591400	Bivalent Enhancer	HSMMtube	muscle
27	chr14:105591200-105591600	Enhancers	Fetal Thymus	thymus
28	chr14:105591200-105592000	Enhancers	Fetal Intestine Small	intestine
29	chr14:105591400-105591600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
30	chr14:105591400-105591600	Bivalent Enhancer	HepG2	liver
31	chr14:105591400-105591800	Enhancers	Duodenum Mucosa	Duodenum
32	chr14:105591800-105592200	Weak transcription	Duodenum Mucosa	Duodenum
33	chr14:105592200-105593400	Enhancers	Duodenum Mucosa	Duodenum
34	chr14:105592400-105593200	Enhancers	Esophagus	oesophagus
35	chr14:105592600-105593600	Enhancers	Fetal Intestine Small	intestine
36	chr14:105592600-105593800	Bivalent Enhancer	HepG2	liver
37	chr14:105592800-105593400	Enhancers	Brain Germinal Matrix	brain
38	chr14:105592800-105593600	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr14:105592800-105593600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr14:105593000-105593200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr14:105593000-105593600	Bivalent Enhancer	Fetal Intestine Large	intestine
42	chr14:105593200-105593400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:105593200-105593400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
44	chr14:105593200-105593400	Bivalent Enhancer	Stomach Mucosa	stomach
45	chr14:105593200-105593400	Bivalent Enhancer	K562	blood
46	chr14:105593400-105593600	Bivalent Enhancer	Fetal Muscle Leg	muscle
47	chr14:105593600-105596200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr14:105596000-105596400	Enhancers	A549	lung
49	chr14:105596200-105596400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr14:105601000-105601400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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