Variant report

Variant	nsv832840
Chromosome Location	chr14:81270033-81423583
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1460)
CpG islands
(count:1346)
Chromatin interactive
region (count:41)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1460 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81421092-81421441	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:81407660-81407725	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:81316579-81316945	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:81408038-81408468	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:81421155-81421357	K562	blood:	n/a	n/a
6	ARID3A	chr14:81316628-81317009	K562	blood:	n/a	n/a
7	ARID3A	chr14:81408108-81408383	K562	blood:	n/a	n/a
8	ATF1	chr14:81397207-81397512	K562	blood:	n/a	n/a
9	ATF2	chr14:81397008-81397875	GM12878	blood:	n/a	n/a
10	ATF2	chr14:81397108-81397920	GM12878	blood:	n/a	n/a
11	ATF3	chr14:81397162-81397461	K562	blood:	n/a	n/a
12	BACH1	chr14:81421988-81422007	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:81421226-81421524	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr14:81311278-81311558	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr14:81422602-81422695	K562	blood:	n/a	n/a
16	BACH1	chr14:81316611-81316731	K562	blood:	n/a	n/a
17	BACH1	chr14:81407866-81408111	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr14:81407987-81408051	K562	blood:	n/a	n/a
19	BACH1	chr14:81311347-81311451	K562	blood:	n/a	n/a
20	BATF	chr14:81396399-81396771	GM12878	blood:	n/a	chr14:81396581-81396592
21	BATF	chr14:81396449-81396747	GM12878	blood:	n/a	chr14:81396581-81396592
22	BATF	chr14:81397314-81397799	GM12878	blood:	n/a	n/a
23	BATF	chr14:81406533-81406767	GM12878	blood:	n/a	chr14:81406669-81406679 chr14:81406668-81406679
24	BATF	chr14:81397048-81397838	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:81396984-81397264	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:81396986-81397858	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:81397382-81397717	GM12878	blood:	n/a	n/a
28	BCL3	chr14:81397207-81397791	GM12878	blood:	n/a	n/a
29	BCL3	chr14:81397382-81397705	GM12878	blood:	n/a	n/a
30	BCLAF1	chr14:81421043-81421453	GM12878	blood:	n/a	chr14:81421296-81421309
31	BCLAF1	chr14:81397335-81397813	GM12878	blood:	n/a	n/a
32	BCLAF1	chr14:81397245-81397849	GM12878	blood:	n/a	n/a
33	BCLAF1	chr14:81407837-81408461	GM12878	blood:	n/a	n/a
34	BCLAF1	chr14:81407906-81408368	GM12878	blood:	n/a	n/a
35	BHLHE40	chr14:81421148-81421499	K562	blood:	n/a	chr14:81421348-81421364
36	BHLHE40	chr14:81397131-81397461	K562	blood:	n/a	n/a
37	BHLHE40	chr14:81407612-81408380	K562	blood:	n/a	n/a
38	BHLHE40	chr14:81397115-81397778	GM12878	blood:	n/a	n/a
39	BHLHE40	chr14:81407974-81408354	GM12878	blood:	n/a	n/a
40	BHLHE40	chr14:81408033-81408295	HepG2	liver:	n/a	n/a
41	BRCA1	chr14:81421111-81421414	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr14:81407957-81408768	GM12878	blood:	n/a	n/a
43	BRCA1	chr14:81407519-81408600	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr14:81408192-81408491	HepG2	liver:	n/a	n/a
45	CBX3	chr14:81334100-81334485	HCT-116	colon:	n/a	n/a
46	CBX3	chr14:81397142-81397629	HCT-116	colon:	n/a	n/a
47	CCNT2	chr14:81421175-81421533	K562	blood:	n/a	n/a
48	CEBPB	chr14:81411632-81411788	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr14:81411592-81411951	A549	lung:	n/a	n/a
50	CEBPB	chr14:81284289-81284332	H1-hESC	embryonic stem cell:	n/a	chr14:81284311-81284322

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81408086-81408136	Hepatocyte	liver:	n/a
2	chr14:81422160-81422210	AoSMC	blood vessel:	n/a
3	chr14:81405846-81405896	SK-N-MC	brain:	n/a
4	chr14:81407087-81407137	RPTEC	kidney:	n/a
5	chr14:81408086-81408136	Hepatocyte	liver:	n/a
6	chr14:81422160-81422210	AoSMC	blood vessel:	n/a
7	chr14:81405846-81405896	SK-N-MC	brain:	n/a
8	chr14:81407087-81407137	RPTEC	kidney:	n/a
9	chr14:81421763-81421813	HCPEpiC	choroid plexus:	n/a
10	chr14:81421600-81421650	HCT-116	colon:	n/a
11	chr14:81408124-81408174	HIPEpiC	eye:	n/a
12	chr14:81421508-81421558	HCT-116	colon:	n/a
13	chr14:81286861-81286911	HEK293	kidney:	embryo
14	chr14:81421600-81421650	AG04449	skin:	fetal
15	chr14:81421770-81421820	NT2-D1	testis:	n/a
16	chr14:81408086-81408136	U87	brain:	n/a
17	chr14:81421322-81421372	HCPEpiC	choroid plexus:	n/a
18	chr14:81421770-81421820	NHDF-neo	bronchial:	n/a
19	chr14:81421763-81421813	Jurkat	blood:	n/a
20	chr14:81392851-81392901	HCM	heart:	n/a
21	chr14:81422160-81422210	T-47D	breast:	n/a
22	chr14:81408086-81408136	HepG2	liver:	n/a
23	chr14:81408275-81408325	NH-A	brain:	n/a
24	chr14:81422098-81422148	SKMC	muscle:	n/a
25	chr14:81407988-81408038	GM12878	blood:	n/a
26	chr14:81421403-81421453	IMR90	lung:	fetal
27	chr14:81407087-81407137	HCPEpiC	choroid plexus:	n/a
28	chr14:81421770-81421820	GM12891	blood:	n/a
29	chr14:81421322-81421372	ECC-1	luminal epithelium:	n/a
30	chr14:81408124-81408174	Caco-2	colon:	n/a
31	chr14:81421600-81421650	ovcar-3	ovarian:	n/a
32	chr14:81422160-81422210	GM12891	blood:	n/a
33	chr14:81422098-81422148	HCM	heart:	n/a
34	chr14:81421983-81422033	RPTEC	kidney:	n/a
35	chr14:81286861-81286911	MCF10A-Er-Src	breast:	n/a
36	chr14:81421403-81421453	HCF	heart:	n/a
37	chr14:81405846-81405896	NB4	blood:	n/a
38	chr14:81421989-81422039	BE2_C	brain:	n/a
39	chr14:81421983-81422033	U87	brain:	n/a
40	chr14:81407988-81408038	Jurkat	blood:	n/a
41	chr14:81422160-81422210	MCF10A-Er-Src	breast:	n/a
42	chr14:81407988-81408038	NT2-D1	testis:	n/a
43	chr14:81405846-81405896	MCF10A-Er-Src	breast:	n/a
44	chr14:81286861-81286911	SK-N-SH_RA	brain:	n/a
45	chr14:81421508-81421558	HRE	kidney:	n/a
46	chr14:81405846-81405896	HCT-116	colon:	n/a
47	chr14:81408086-81408136	SKMC	muscle:	n/a
48	chr14:81421989-81422039	AoSMC	blood vessel:	n/a
49	chr14:81421297-81421347	AG09319	gingival:	n/a
50	chr14:81405846-81405896	NHBE	bronchial:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81401530..81405637-chr14:81405681..81409826,5	K562	blood:
2	chr14:81397350..81398918-chr14:81404330..81405953,2	MCF-7	breast:
3	chr14:81369142..81371991-chr14:81374635..81376596,2	K562	blood:
4	chr14:81421283..81423197-chr14:81423259..81426025,2	K562	blood:
5	chr14:81381982..81384021-chr14:81385728..81388999,4	MCF-7	breast:
6	chr14:80522390..80523095-chr14:81316377..81317031,2	MCF-7	breast:
7	chr14:81396675..81399080-chr14:81400094..81402837,4	K562	blood:
8	chr14:81400340..81402827-chr14:81422342..81424603,2	K562	blood:
9	chr14:79808988..79811235-chr14:81320946..81323442,2	MCF-7	breast:
10	chr14:81397911..81402411-chr14:81683829..81688491,5	K562	blood:
11	chr14:80522343..80523122-chr14:81329349..81329875,2	MCF-7	breast:
12	chr14:81405070..81407655-chr14:81893214..81894963,2	K562	blood:
13	chr14:81420793..81423189-chr14:81424553..81427836,4	MCF-7	breast:
14	chr14:81381982..81384021-chr14:81385728..81388999,4	MCF-7	breast:
15	chr14:81396675..81399080-chr14:81400094..81402837,4	K562	blood:
16	chr14:81300294..81302523-chr14:81306225..81308137,2	K562	blood:
17	chr14:81300294..81302523-chr14:81306225..81308137,2	K562	blood:
18	chr14:81413969..81417033-chr14:81418099..81421076,3	K562	blood:
19	chr14:81400340..81402827-chr14:81422342..81424603,2	K562	blood:
20	chr14:81388857..81391378-chr14:81393034..81394576,2	K562	blood:
21	chr14:81389769..81391378-chr14:81393076..81395517,2	K562	blood:
22	chr14:81413969..81417033-chr14:81418099..81421076,3	K562	blood:
23	chr14:81401790..81404001-chr14:81408260..81409826,2	K562	blood:
24	chr14:81406001..81408090-chr14:81684696..81687286,2	MCF-7	breast:
25	chr14:79425453..79426658-chr14:81316149..81316920,3	MCF-7	breast:
26	chr14:81405781..81407858-chr14:81414654..81417606,2	K562	blood:
27	chr14:81401790..81404001-chr14:81408260..81409826,2	K562	blood:
28	chr14:81276542..81279336-chr14:81283354..81285060,2	K562	blood:
29	chr14:81389769..81391378-chr14:81393076..81395517,2	K562	blood:
30	chr14:81388857..81391378-chr14:81393034..81394576,2	K562	blood:
31	chr14:81383115..81385804-chr14:81388822..81391574,2	K562	blood:
32	chr14:81421307..81423560-chr14:81685821..81687772,2	MCF-7	breast:
33	chr14:81105972..81108126-chr14:81297370..81299564,2	K562	blood:
34	chr14:81367649..81369753-chr14:81370909..81372936,2	MCF-7	breast:
35	chr14:81316288..81318355-chr14:81684357..81686706,2	K562	blood:
36	chr14:81396050..81399080-chr14:81399956..81402754,3	K562	blood:
37	chr14:81383115..81385804-chr14:81388822..81391574,2	K562	blood:
38	chr14:81421283..81423197-chr14:81423259..81426025,2	K562	blood:
39	chr14:81409086..81412079-chr14:81684654..81686943,2	K562	blood:
40	chr14:81276542..81279336-chr14:81283354..81285060,2	K562	blood:
41	chr14:81396050..81399080-chr14:81399956..81402754,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP128-1	chr14:81411900-81412111	NONHSAT038042

No data

Variant related genes	Relation type
ENSG00000258452	TF binding region
TSHR	TF binding region
CEP128	TF binding region
ENSG00000258452	CpG island
TSHR	CpG island
CEP128	CpG island
ENSG00000100629	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000165409	chromatin interactions
ENSG00000140022	chromatin interactions

Extended variants
information (count: 5635 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5635 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs328213	chr14:81270157-81270158	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs530603007	chr14:81270207-81270208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181003915	chr14:81270212-81270213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564375672	chr14:81270248-81270249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528479909	chr14:81270268-81270269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546934277	chr14:81270270-81270271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs118001556	chr14:81270286-81270287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs328212	chr14:81270314-81270315	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs71456221	chr14:81270453-81270454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71416850	chr14:81270477-81270478	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs199603008	chr14:81270481-81270482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185128680	chr14:81270485-81270486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370300391	chr14:81270531-81270532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535005689	chr14:81270543-81270544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs565753998	chr14:81270553-81270554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs567110857	chr14:81270566-81270567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530831901	chr14:81270567-81270568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114973903	chr14:81270668-81270669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140840492	chr14:81270677-81270678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552593436	chr14:81270773-81270774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150127742	chr14:81270802-81270803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557823963	chr14:81270847-81270848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535207871	chr14:81270859-81270860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550409783	chr14:81270958-81270959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs556604342	chr14:81270976-81270977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575368833	chr14:81271000-81271001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs10150034	chr14:81271029-81271030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs327434	chr14:81271071-81271072	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs529813403	chr14:81271088-81271089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575788408	chr14:81271140-81271141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573132113	chr14:81271158-81271159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138763692	chr14:81271179-81271180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61979449	chr14:81271236-81271237	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs529292379	chr14:81271247-81271248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140446627	chr14:81271381-81271382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374269154	chr14:81271386-81271387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189934486	chr14:81271419-81271420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562945099	chr14:81271455-81271456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34529456	chr14:81271463-81271464	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11847393	chr14:81271464-81271465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551989858	chr14:81271480-81271481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558989514	chr14:81271497-81271498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566947096	chr14:81271511-81271512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145556118	chr14:81271514-81271515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549249036	chr14:81271542-81271543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567733319	chr14:81271576-81271577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs535053332	chr14:81271705-81271706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs376031841	chr14:81271715-81271716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556639626	chr14:81271725-81271726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552160789	chr14:81271793-81271794	Weak transcription Enhancers	n/a	n/a	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
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	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
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:2011 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81192800-81305400	Weak transcription	Primary B cells from cord blood	blood
2	chr14:81246800-81271600	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr14:81251800-81282600	Weak transcription	A549	lung
4	chr14:81256400-81271000	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr14:81259400-81274000	Weak transcription	Aorta	Aorta
6	chr14:81259400-81274000	Weak transcription	Pancreas	Pancrea
7	chr14:81259400-81274200	Weak transcription	Thymus	Thymus
8	chr14:81259400-81278400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr14:81265600-81277200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr14:81265600-81284400	Weak transcription	Fetal Thymus	thymus
11	chr14:81265800-81274600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:81267400-81273800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr14:81267400-81284200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:81267400-81284800	Weak transcription	HSMM	muscle
15	chr14:81269600-81273000	Weak transcription	Fetal Lung	lung
16	chr14:81269600-81284400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:81269800-81270200	ZNF genes & repeats	Dnd41	blood
18	chr14:81270200-81273600	Weak transcription	Dnd41	blood
19	chr14:81271200-81271400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr14:81271200-81271800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr14:81271200-81272200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr14:81271400-81272000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:81271400-81272200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr14:81271400-81272200	Enhancers	NHDF-Ad	bronchial
25	chr14:81271400-81272200	Enhancers	Osteobl	bone
26	chr14:81271600-81272200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr14:81272000-81272200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr14:81272200-81274200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:81272200-81284600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr14:81272600-81275600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr14:81273000-81273200	Enhancers	Fetal Lung	lung
32	chr14:81273400-81284400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr14:81273600-81275000	Genic enhancers	Dnd41	blood
34	chr14:81273800-81274200	Weak transcription	Fetal Stomach	stomach
35	chr14:81273800-81275200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr14:81274000-81274200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr14:81274000-81274800	Strong transcription	Pancreas	Pancrea
38	chr14:81274000-81275000	ZNF genes & repeats	Aorta	Aorta
39	chr14:81274200-81274600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr14:81274200-81274600	ZNF genes & repeats	Fetal Stomach	stomach
41	chr14:81274200-81275200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr14:81274200-81275200	Strong transcription	Thymus	Thymus
43	chr14:81274400-81274600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:81274600-81275200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
45	chr14:81274600-81275200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr14:81274800-81275000	Weak transcription	Fetal Stomach	stomach
47	chr14:81274800-81275000	ZNF genes & repeats	Pancreas	Pancrea
48	chr14:81275000-81277600	Enhancers	Dnd41	blood
49	chr14:81275000-81282600	Weak transcription	Aorta	Aorta
50	chr14:81275200-81282800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links