Variant report

Variant	nsv1048064
Chromosome Location	chr14:68991041-69012766
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:265)
CpG islands
(count:122)
Chromatin interactive
region (count:24)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr14:68993152-68994426	Hela-S3	cervix:	n/a	n/a
2	CBX3	chr14:69001937-69002975	HCT-116	colon:	n/a	n/a
3	CEBPB	chr14:68996561-68996761	HepG2	liver:	n/a	chr14:68996605-68996616 chr14:68996604-68996617
4	CEBPB	chr14:69010894-69011277	IMR90	lung:	n/a	n/a
5	CEBPB	chr14:68996595-68996691	K562	blood:	n/a	chr14:68996605-68996616 chr14:68996604-68996617
6	CEBPB	chr14:68993207-68993489	IMR90	lung:	n/a	chr14:68993333-68993344
7	CEBPB	chr14:68993322-68993354	HepG2	liver:	n/a	chr14:68993333-68993344
8	CEBPB	chr14:68993222-68993440	A549	lung:	n/a	chr14:68993333-68993344
9	CEBPB	chr14:68993081-68994521	Hela-S3	cervix:	n/a	chr14:68993333-68993344
10	CHD2	chr14:69002174-69002500	Hela-S3	cervix:	n/a	n/a
11	CHD2	chr14:68993074-68994466	Hela-S3	cervix:	n/a	n/a
12	CTCF	chr14:69001780-69001930	RPTEC	kidney:	n/a	n/a
13	CTCF	chr14:68992320-68992470	HEEpiC	esophagus:	n/a	n/a
14	CTCF	chr14:69002500-69002650	GM12873	blood:	n/a	n/a
15	CTCF	chr14:69002240-69002390	HMEC	breast:	n/a	n/a
16	CTCF	chr14:68990900-68991050	HCM	heart:	n/a	n/a
17	CTCF	chr14:68990792-68991092	K562	blood:	n/a	n/a
18	CTCF	chr14:69002340-69002490	HMEC	breast:	n/a	n/a
19	CTCF	chr14:68990790-68991072	K562	blood:	n/a	n/a
20	CTCF	chr14:69002260-69002410	HCFaa	heart:	n/a	n/a
21	CTCF	chr14:68991220-68991370	AG10803	skin:	n/a	n/a
22	CTCF	chr14:69002292-69002366	NHEK	skin:	n/a	n/a
23	CTCF	chr14:69002340-69002490	AG10803	skin:	n/a	n/a
24	CTCF	chr14:69002220-69002370	AG04449	skin:	n/a	n/a
25	CTCF	chr14:69002260-69002410	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr14:69002280-69002430	BJ	skin:	n/a	n/a
27	CTCF	chr14:68990900-68991050	NHEK	skin:	n/a	n/a
28	CTCF	chr14:69002320-69002550	AG09319	gingival:	n/a	n/a
29	CTCF	chr14:69001920-69002070	HMEC	breast:	n/a	n/a
30	CTCF	chr14:68990687-68991126	MCF-7	breast:	n/a	n/a
31	CTCF	chr14:69002260-69002410	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr14:69002260-69002410	AG09319	gingival:	n/a	n/a
33	CTCF	chr14:69002220-69002370	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr14:69001918-69001942	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr14:69002338-69002357	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr14:69002260-69002410	HMF	breast:	n/a	n/a
37	CTCF	chr14:69001880-69002030	BJ	skin:	n/a	n/a
38	CTCF	chr14:69002280-69002430	HMF	breast:	n/a	n/a
39	CTCF	chr14:69001840-69001990	AG10803	skin:	n/a	n/a
40	CTCF	chr14:69002260-69002410	AG04449	skin:	n/a	n/a
41	CTCF	chr14:69002240-69002390	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr14:69002300-69002450	AG10803	skin:	n/a	n/a
43	CTCF	chr14:69001840-69001990	NHEK	skin:	n/a	n/a
44	CTCF	chr14:69002260-69002410	HPAF	blood vessel:	n/a	n/a
45	E2F4	chr14:69002193-69002509	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr14:69010299-69010510	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr14:68992946-68993446	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr14:69009103-69009437	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr14:69009791-69009883	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr14:69010891-69011336	MCF10A-Er-Src	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:69012387-69012437	SK-N-SH	brain:	n/a
2	chr14:69006140-69006190	HCM	heart:	n/a
3	chr14:69006140-69006190	Caco-2	colon:	n/a
4	chr14:69006140-69006190	HMEC	breast:	n/a
5	chr14:69012387-69012437	Caco-2	colon:	n/a
6	chr14:69006140-69006190	K562	blood:	n/a
7	chr14:69006140-69006190	PANC-1	pancreas:	n/a
8	chr14:69006140-69006190	PFSK-1	brain:	n/a
9	chr14:69006140-69006190	ECC-1	luminal epithelium:	n/a
10	chr14:69012387-69012437	NH-A	brain:	n/a
11	chr14:69012387-69012437	U87	brain:	n/a
12	chr14:69012387-69012437	NHDF-neo	bronchial:	n/a
13	chr14:69006140-69006190	PrEC	prostate:	n/a
14	chr14:69012387-69012437	HepG2	liver:	n/a
15	chr14:69006140-69006190	T-47D	breast:	n/a
16	chr14:69006140-69006190	CMK	blood:	n/a
17	chr14:69006140-69006190	HPAEpiC	pulmonary alveolar:	n/a
18	chr14:69012387-69012437	NHBE	bronchial:	n/a
19	chr14:69006140-69006190	HRPEpiC	eye:	n/a
20	chr14:69012387-69012437	GM12892	blood:	n/a
21	chr14:69006140-69006190	AG09309	skin:	n/a
22	chr14:69006140-69006190	HCT-116	colon:	n/a
23	chr14:69006140-69006190	AoSMC	blood vessel:	n/a
24	chr14:69006140-69006190	HNPCEpiC	eye:	n/a
25	chr14:69006140-69006190	GM06990	blood:	n/a
26	chr14:69006140-69006190	AG04449	skin:	fetal
27	chr14:69006140-69006190	HCPEpiC	choroid plexus:	n/a
28	chr14:69012387-69012437	HEK293	kidney:	embryo
29	chr14:69012387-69012437	AG10803	skin:	n/a
30	chr14:69012387-69012437	HCPEpiC	choroid plexus:	n/a
31	chr14:69006140-69006190	AG04450	lung:	fetal
32	chr14:69012387-69012437	Hepatocyte	liver:	n/a
33	chr14:69006140-69006190	SK-N-SH_RA	brain:	n/a
34	chr14:69012387-69012437	SK-N-SH_RA	brain:	n/a
35	chr14:69006140-69006190	A549	lung:	n/a
36	chr14:69006140-69006190	Hela-S3	cervix:	n/a
37	chr14:69012387-69012437	AG04450	lung:	fetal
38	chr14:69006140-69006190	GM12878	blood:	n/a
39	chr14:69012387-69012437	SKMC	muscle:	n/a
40	chr14:69006140-69006190	MCF-7	breast:	n/a
41	chr14:69006140-69006190	IMR90	lung:	fetal
42	chr14:69012387-69012437	BJ	skin:	n/a
43	chr14:69006140-69006190	U87	brain:	n/a
44	chr14:69012387-69012437	HCT-116	colon:	n/a
45	chr14:69012387-69012437	MCF-7	breast:	n/a
46	chr14:69012387-69012437	HRCEpiC	kidney:	n/a
47	chr14:69006140-69006190	NT2-D1	testis:	n/a
48	chr14:69006140-69006190	GM19239	blood:	n/a
49	chr14:69012387-69012437	HCF	heart:	n/a
50	chr14:69012387-69012437	ovcar-3	ovarian:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:68995172..68997333-chr14:69028182..69030145,2	MCF-7	breast:
2	chr12:7052631..7053153-chr14:68993272..68993773,2	Hela-S3	cervix:
3	chr14:69003922..69007873-chr14:69256897..69260047,3	MCF-7	breast:
4	chr14:68929507..68933385-chr14:68987583..68991137,3	MCF-7	breast:
5	chr14:68927072..68929537-chr14:68988559..68991128,2	MCF-7	breast:
6	chr14:68987315..68991799-chr14:69260586..69263580,4	MCF-7	breast:
7	chr14:68998490..69000612-chr14:69028274..69029938,2	MCF-7	breast:
8	chr14:69006233..69007064-chr14:69036424..69037353,2	MCF-7	breast:
9	chr14:68990548..68993032-chr14:69095034..69097852,2	MCF-7	breast:
10	chr14:68715321..68716856-chr14:68989735..68992199,2	MCF-7	breast:
11	chr14:69006886..69009005-chr14:69017187..69019247,2	MCF-7	breast:
12	chr14:69001801..69004663-chr14:69006865..69008433,2	MCF-7	breast:
13	chr14:68982120..68984316-chr14:68992913..68995083,2	MCF-7	breast:
14	chr14:68989438..68991863-chr14:69015676..69017457,2	MCF-7	breast:
15	chr14:69000957..69002671-chr14:69010193..69012853,2	MCF-7	breast:
16	chr14:68772101..68775016-chr14:68999200..69001646,2	MCF-7	breast:
17	chr14:68990793..68991332-chr14:69122376..69122983,2	MCF-7	breast:
18	chr14:69001801..69004663-chr14:69006865..69008433,2	MCF-7	breast:
19	chr14:68990794..68994075-chr14:69256455..69260885,5	MCF-7	breast:
20	chr14:68994426..68996258-chr14:69013993..69016421,2	MCF-7	breast:
21	chr14:69009163..69010827-chr14:69260601..69262528,2	MCF-7	breast:
22	chr14:69007812..69009771-chr14:69024457..69026624,2	MCF-7	breast:
23	chr14:68987292..68989067-chr14:68991224..68994887,5	MCF-7	breast:
24	chr14:68990353..68991309-chr14:69036602..69037256,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXD2-6	chr14:69012279-69012341	NONHSAT037485

No data

Variant related genes	Relation type
RAD51B	TF binding region
RAD51B	CpG island
ENSG00000259038	chromatin interactions
ENSG00000182185	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000185650	chromatin interactions

Extended variants
information (count: 715 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10137367	chr14:68991041-68991042	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs2525514	chr14:68991054-68991055	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs564020493	chr14:68991137-68991138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs531186908	chr14:68991162-68991163	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549621217	chr14:68991200-68991201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs528008850	chr14:68991201-68991202	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs184430569	chr14:68991202-68991203	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs36101979	chr14:68991235-68991236	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs570729981	chr14:68991236-68991237	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547448612	chr14:68991268-68991269	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs35619151	chr14:68991276-68991277	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs149687106	chr14:68991278-68991279	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs532950413	chr14:68991279-68991280	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs2842338	chr14:68991286-68991287	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs116681569	chr14:68991287-68991288	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs34866441	chr14:68991303-68991304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs374171797	chr14:68991309-68991310	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs148446429	chr14:68991322-68991323	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs368962308	chr14:68991328-68991329	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs74871166	chr14:68991343-68991344	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs142628704	chr14:68991344-68991345	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs534850912	chr14:68991371-68991372	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189261787	chr14:68991372-68991373	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs192560992	chr14:68991435-68991436	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs545390897	chr14:68991441-68991442	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs536236487	chr14:68991506-68991507	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371476422	chr14:68991511-68991512	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs184200878	chr14:68991524-68991525	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs576023728	chr14:68991539-68991540	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs543328852	chr14:68991550-68991551	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs561495901	chr14:68991551-68991552	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs34702092	chr14:68991747-68991748	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs398038634	chr14:68991753-68991754	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs146503069	chr14:68991761-68991762	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533863748	chr14:68991806-68991807	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540430846	chr14:68991853-68991854	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559401850	chr14:68991860-68991861	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs570511465	chr14:68991861-68991862	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs58315579	chr14:68991873-68991874	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs76346996	chr14:68991901-68991902	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs530739433	chr14:68991911-68991912	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs548860144	chr14:68991914-68991915	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs72727502	chr14:68991941-68991942	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs534829303	chr14:68991971-68991972	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs79729396	chr14:68991999-68992000	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs571737935	chr14:68992028-68992029	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs538724231	chr14:68992048-68992049	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs141127053	chr14:68992054-68992055	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144925803	chr14:68992094-68992095	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs76242603	chr14:68992114-68992115	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	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
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:68968000-68991200	Enhancers	Fetal Lung	lung
2	chr14:68983600-68991200	Enhancers	NHEK	skin
3	chr14:68983800-68991600	Enhancers	Fetal Muscle Leg	muscle
4	chr14:68983800-68991800	Enhancers	Fetal Stomach	stomach
5	chr14:68984200-68991200	Enhancers	Fetal Heart	heart
6	chr14:68984200-68991800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr14:68984600-68991400	Enhancers	Placenta Amnion	Placenta Amnion
8	chr14:68984600-68991600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:68984600-68991800	Enhancers	Placenta	Placenta
10	chr14:68985800-68994800	Weak transcription	Aorta	Aorta
11	chr14:68986000-68991800	Enhancers	Rectal Smooth Muscle	rectum
12	chr14:68986000-68993400	Weak transcription	Brain Angular Gyrus	brain
13	chr14:68986400-68991600	Enhancers	Colon Smooth Muscle	Colon
14	chr14:68986400-68993000	Weak transcription	NH-A	brain
15	chr14:68987000-68991600	Weak transcription	Thymus	Thymus
16	chr14:68987400-68991800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr14:68987400-68993600	Enhancers	HSMM	muscle
18	chr14:68987400-68996200	Enhancers	Pancreas	Pancrea
19	chr14:68987600-68991200	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr14:68987600-68991400	Enhancers	Esophagus	oesophagus
21	chr14:68987600-68992000	Enhancers	NHLF	lung
22	chr14:68987600-68993400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr14:68987800-68991800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr14:68987800-68991800	Enhancers	Fetal Kidney	kidney
25	chr14:68988000-68991400	Enhancers	Adipose Nuclei	Adipose
26	chr14:68988000-68991800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr14:68988200-68992000	Enhancers	NHDF-Ad	bronchial
28	chr14:68988200-68993600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr14:68988400-68991400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr14:68988400-68991800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr14:68988400-68993400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr14:68988600-68991400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr14:68988600-68993800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr14:68988800-68991800	Weak transcription	Hela-S3	cervix
35	chr14:68988800-68993400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr14:68989000-68993000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr14:68989200-68991600	Weak transcription	Lung	lung
38	chr14:68989200-68993200	Weak transcription	Psoas Muscle	Psoas
39	chr14:68989400-68991200	Enhancers	Brain Hippocampus Middle	brain
40	chr14:68989400-68993000	Weak transcription	A549	lung
41	chr14:68989600-68991400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr14:68989600-68991400	Enhancers	Ovary	ovary
43	chr14:68989600-68993000	Weak transcription	Stomach Mucosa	stomach
44	chr14:68989600-68993000	Weak transcription	HMEC	breast
45	chr14:68989600-68993200	Weak transcription	Gastric	stomach
46	chr14:68989800-68993000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:68989800-68993800	Weak transcription	Primary B cells from cord blood	blood
48	chr14:68990000-68994200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr14:68990000-68995400	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr14:68990000-68995600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links