Variant report

Variant	esv2752577
Chromosome Location	chr14:36768276-36805529
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:36787931-36788470	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:36769601-36770046	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:36784635-36784815	K562	blood:	n/a	n/a
4	ARID3A	chr14:36789827-36789998	K562	blood:	n/a	n/a
5	ARID3A	chr14:36785526-36785702	K562	blood:	n/a	n/a
6	ARID3A	chr14:36789353-36790203	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:36786874-36787050	HepG2	liver:	n/a	n/a
8	ATF1	chr14:36789684-36790159	K562	blood:	n/a	n/a
9	ATF2	chr14:36789612-36790132	GM12878	blood:	n/a	n/a
10	ATF2	chr14:36789693-36790117	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr14:36769592-36769971	GM12878	blood:	n/a	n/a
12	ATF2	chr14:36789725-36790108	GM12878	blood:	n/a	n/a
13	ATF2	chr14:36769598-36769998	GM12878	blood:	n/a	n/a
14	ATF3	chr14:36789354-36790107	HepG2	liver:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
15	ATF3	chr14:36789765-36789985	GM12878	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
16	ATF3	chr14:36789736-36790012	K562	blood:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
17	ATF3	chr14:36789635-36790064	H1-hESC	embryonic stem cell:	n/a	chr14:36789882-36789890 chr14:36789880-36789890 chr14:36789879-36789892 chr14:36789880-36789893 chr14:36789846-36789855 chr14:36789871-36789891
18	BATF	chr14:36769541-36769888	GM12878	blood:	n/a	chr14:36769803-36769813
19	BATF	chr14:36784705-36785059	GM12878	blood:	n/a	chr14:36784842-36784853
20	BATF	chr14:36784726-36785054	GM12878	blood:	n/a	chr14:36784842-36784853
21	BCL11A	chr14:36769496-36769723	GM12878	blood:	n/a	n/a
22	BCL3	chr14:36789549-36790347	A549	lung:	n/a	n/a
23	BCL3	chr14:36784682-36784987	GM12878	blood:	n/a	chr14:36784811-36784820
24	BHLHE40	chr14:36789595-36790169	K562	blood:	n/a	n/a
25	BHLHE40	chr14:36784748-36785137	GM12878	blood:	n/a	n/a
26	BRCA1	chr14:36789668-36790245	HepG2	liver:	n/a	n/a
27	BRCA1	chr14:36788746-36788783	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr14:36789033-36790188	Hela-S3	cervix:	n/a	n/a
29	CBX3	chr14:36789680-36790403	K562	blood:	n/a	n/a
30	CCNT2	chr14:36789394-36790044	K562	blood:	n/a	chr14:36789846-36789855
31	CEBPB	chr14:36789602-36790208	MCF-7	breast:	n/a	n/a
32	CEBPB	chr14:36798107-36798380	HepG2	liver:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
33	CEBPB	chr14:36789584-36790156	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:36789455-36790200	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:36791061-36791224	K562	blood:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
36	CEBPB	chr14:36790993-36791264	HepG2	liver:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
37	CEBPB	chr14:36796560-36796920	HepG2	liver:	n/a	n/a
38	CEBPB	chr14:36791032-36791270	A549	lung:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
39	CEBPB	chr14:36798124-36798432	Hela-S3	cervix:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
40	CEBPB	chr14:36796572-36796924	A549	lung:	n/a	n/a
41	CEBPB	chr14:36789653-36790109	HepG2	liver:	n/a	n/a
42	CEBPB	chr14:36798093-36798434	A549	lung:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
43	CEBPB	chr14:36798092-36798403	K562	blood:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
44	CEBPB	chr14:36789686-36790191	IMR90	lung:	n/a	n/a
45	CEBPB	chr14:36769071-36769262	K562	blood:	n/a	chr14:36769203-36769214
46	CEBPB	chr14:36789718-36790083	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr14:36769079-36769350	HepG2	liver:	n/a	chr14:36769203-36769214
48	CEBPB	chr14:36785526-36785655	K562	blood:	n/a	n/a
49	CEBPB	chr14:36789746-36790117	K562	blood:	n/a	n/a
50	CEBPB	chr14:36778595-36778871	HepG2	liver:	n/a	chr14:36778710-36778718 chr14:36778717-36778728 chr14:36778716-36778729 chr14:36778716-36778727

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36789886-36789936	NH-A	brain:	n/a
2	chr14:36789886-36789936	NH-A	brain:	n/a
3	chr14:36789886-36789936	AG09309	skin:	n/a
4	chr14:36789810-36789860	HCM	heart:	n/a
5	chr14:36783435-36783485	RPTEC	kidney:	n/a
6	chr14:36789886-36789936	AG10803	skin:	n/a
7	chr14:36789488-36789538	HEEpiC	esophagus:	n/a
8	chr14:36789810-36789860	BE2_C	brain:	n/a
9	chr14:36789886-36789936	SKMC	muscle:	n/a
10	chr14:36783435-36783485	GM06990	blood:	n/a
11	chr14:36789886-36789936	PrEC	prostate:	n/a
12	chr14:36790242-36790292	HRCEpiC	kidney:	n/a
13	chr14:36789886-36789936	K562	blood:	n/a
14	chr14:36783435-36783485	AG04450	lung:	fetal
15	chr14:36789691-36789741	PANC-1	pancreas:	n/a
16	chr14:36789985-36790035	AG09309	skin:	n/a
17	chr14:36789985-36790035	HEEpiC	esophagus:	n/a
18	chr14:36790242-36790292	NHDF-neo	bronchial:	n/a
19	chr14:36790242-36790292	HCF	heart:	n/a
20	chr14:36789488-36789538	HMEC	breast:	n/a
21	chr14:36783435-36783485	BJ	skin:	n/a
22	chr14:36789488-36789538	Hepatocyte	liver:	n/a
23	chr14:36789691-36789741	IMR90	lung:	fetal
24	chr14:36789488-36789538	PANC-1	pancreas:	n/a
25	chr14:36789488-36789538	Jurkat	blood:	n/a
26	chr14:36790242-36790292	GM12878	blood:	n/a
27	chr14:36783435-36783485	HRCEpiC	kidney:	n/a
28	chr14:36789810-36789860	HNPCEpiC	eye:	n/a
29	chr14:36789691-36789741	MCF10A-Er-Src	breast:	n/a
30	chr14:36789691-36789741	HIPEpiC	eye:	n/a
31	chr14:36789691-36789741	H1-hESC	embryonic stem cell:	embryo
32	chr14:36789691-36789741	HEEpiC	esophagus:	n/a
33	chr14:36790242-36790292	SAEC	small airway:	n/a
34	chr14:36790242-36790292	HEEpiC	esophagus:	n/a
35	chr14:36783435-36783485	AG04449	skin:	fetal
36	chr14:36789691-36789741	Hepatocyte	liver:	n/a
37	chr14:36783435-36783485	AG10803	skin:	n/a
38	chr14:36789488-36789538	BJ	skin:	n/a
39	chr14:36783435-36783485	K562	blood:	n/a
40	chr14:36789985-36790035	H1-hESC	embryonic stem cell:	embryo
41	chr14:36789691-36789741	CMK	blood:	n/a
42	chr14:36789691-36789741	GM06990	blood:	n/a
43	chr14:36789985-36790035	HUVEC	blood vessel:	n/a
44	chr14:36789985-36790035	HMEC	breast:	n/a
45	chr14:36789691-36789741	HNPCEpiC	eye:	n/a
46	chr14:36789488-36789538	HIPEpiC	eye:	n/a
47	chr14:36783435-36783485	HepG2	liver:	n/a
48	chr14:36790242-36790292	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:36789886-36789936	HepG2	liver:	n/a
50	chr14:36789985-36790035	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
2	chr14:36781444..36784031-chr14:36790836..36792756,2	K562	blood:
3	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
4	chr1:53308102..53308983-chr14:36776394..36777212,2	MCF-7	breast:
5	chr14:36760298..36763164-chr14:36770896..36773643,2	K562	blood:
6	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
7	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
8	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
9	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:
10	chr14:36763341..36766160-chr14:36772206..36774961,2	K562	blood:
11	chr14:36774640..36776851-chr14:36779144..36781211,2	K562	blood:
12	chr14:36538483..36541249-chr14:36788541..36791272,2	MCF-7	breast:
13	chr14:36789374..36789875-chr8:119123638..119124514,2	Hela-S3	cervix:
14	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
15	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
16	chr14:36777999..36779910-chr14:36780693..36782263,2	K562	blood:
17	chr14:36778847..36780826-chr14:36784208..36786054,2	MCF-7	breast:
18	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
19	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
20	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
21	chr14:36780477..36782487-chr14:36786743..36788959,2	MCF-7	breast:
22	chr14:36772767..36774449-chr14:36777469..36780447,2	K562	blood:
23	chr14:36757907..36759500-chr14:36766689..36768870,2	MCF-7	breast:
24	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
25	chr14:36787110..36790093-chr14:36792032..36793692,2	K562	blood:
26	chr14:36784989..36787450-chr14:36787865..36790918,4	K562	blood:
27	chr14:36784077..36786059-chr14:36788034..36791140,4	MCF-7	breast:
28	chr14:36777645..36780229-chr14:36786756..36790572,4	MCF-7	breast:
29	chr14:36539398..36539927-chr14:36782854..36783534,2	MCF-7	breast:
30	chr14:36780690..36783423-chr14:36785409..36787697,2	K562	blood:
31	chr14:36774640..36777657-chr14:36778032..36780826,3	K562	blood:
32	chr14:36788593..36791761-chr14:36792192..36795536,3	K562	blood:
33	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFTA3-2	chr14:36785664-36785887	uc_374_-
2	lnc-PAX9-10	chr14:36785664-36785887	uc_374_+

Variant related genes	Relation type
MBIP	TF binding region
MBIP	CpG island
ENSG00000182197	chromatin interactions
ENSG00000203995	chromatin interactions
ENSG00000257585	chromatin interactions
ENSG00000151332	chromatin interactions

Extended variants
information (count: 865 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4900833	chr14:36768276-36768277	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs79341640	chr14:36768277-36768278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370304446	chr14:36768281-36768282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs17849936	chr14:36768295-36768296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537837993	chr14:36768302-36768303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374762601	chr14:36768312-36768313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147919885	chr14:36768319-36768320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571382371	chr14:36768389-36768390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs17175248	chr14:36768407-36768408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539282636	chr14:36768454-36768455	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553147316	chr14:36768505-36768506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183129783	chr14:36768506-36768507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187668311	chr14:36768520-36768521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs369423113	chr14:36768541-36768542	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115960393	chr14:36768609-36768610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34724648	chr14:36768667-36768668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs570347122	chr14:36768668-36768669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397809887	chr14:36768681-36768682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575359205	chr14:36768695-36768696	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544206205	chr14:36768702-36768703	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559215377	chr14:36768716-36768717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558697692	chr14:36768718-36768719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577831062	chr14:36768719-36768720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112390515	chr14:36768752-36768753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539923799	chr14:36768754-36768755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560743063	chr14:36768807-36768808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529425412	chr14:36768888-36768889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549689269	chr14:36768897-36768898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs562837144	chr14:36768910-36768911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531621283	chr14:36768915-36768916	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551346361	chr14:36768929-36768930	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571271567	chr14:36768935-36768936	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534048528	chr14:36769065-36769066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs577054632	chr14:36769111-36769112	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs58529268	chr14:36769112-36769113	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566700552	chr14:36769164-36769165	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs535288991	chr14:36769206-36769207	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs555662827	chr14:36769209-36769210	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs374948828	chr14:36769285-36769286	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575594133	chr14:36769288-36769289	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538106443	chr14:36769295-36769296	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140613194	chr14:36769306-36769307	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs61535449	chr14:36769318-36769319	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs540334397	chr14:36769331-36769332	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539111182	chr14:36769355-36769356	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs541124925	chr14:36769440-36769441	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560552589	chr14:36769450-36769451	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559980895	chr14:36769522-36769523	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs35630157	chr14:36769576-36769577	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs550323789	chr14:36769602-36769603	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Acute lymphoblastic leukemia	20067559	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Lung cancer	20031968	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1083 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36761000-36785000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:36762000-36770400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr14:36762000-36778800	Weak transcription	Fetal Intestine Small	intestine
4	chr14:36762600-36769800	Weak transcription	NHLF	lung
5	chr14:36763400-36769600	Weak transcription	Colon Smooth Muscle	Colon
6	chr14:36763800-36777800	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr14:36764400-36784000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr14:36764800-36768400	Strong transcription	Fetal Muscle Leg	muscle
9	chr14:36764800-36769000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr14:36764800-36769000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr14:36764800-36769600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr14:36764800-36770800	Strong transcription	Fetal Muscle Trunk	muscle
13	chr14:36765000-36769200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:36765000-36769400	Strong transcription	HepG2	liver
15	chr14:36765000-36779400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr14:36765000-36781200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr14:36765200-36768400	Strong transcription	Primary T cells from cord blood	blood
18	chr14:36765200-36769000	Strong transcription	HSMM	muscle
19	chr14:36765200-36781400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr14:36765400-36768400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr14:36765400-36768400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr14:36765400-36768400	Strong transcription	Ovary	ovary
23	chr14:36765400-36769000	Strong transcription	Primary hematopoietic stem cells	blood
24	chr14:36765400-36769000	Strong transcription	Brain Hippocampus Middle	brain
25	chr14:36765400-36771000	Strong transcription	Duodenum Smooth Muscle	Duodenum
26	chr14:36765400-36773000	Strong transcription	Fetal Brain Female	brain
27	chr14:36765400-36775200	Strong transcription	Adipose Nuclei	Adipose
28	chr14:36765400-36781400	Strong transcription	Placenta	Placenta
29	chr14:36765400-36788800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:36765600-36768400	Strong transcription	Brain Germinal Matrix	brain
31	chr14:36765600-36768800	Strong transcription	HMEC	breast
32	chr14:36765600-36769200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr14:36765600-36770800	Strong transcription	Fetal Lung	lung
34	chr14:36765600-36781000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr14:36765800-36769000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr14:36765800-36769000	Strong transcription	HUVEC	blood vessel
37	chr14:36765800-36769600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr14:36765800-36769600	Strong transcription	Osteobl	bone
39	chr14:36765800-36770000	Strong transcription	Liver	Liver
40	chr14:36765800-36770400	Strong transcription	Brain Anterior Caudate	brain
41	chr14:36765800-36771000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr14:36765800-36771000	Strong transcription	Fetal Intestine Large	intestine
43	chr14:36765800-36771200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr14:36765800-36772000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:36765800-36775600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr14:36765800-36776400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr14:36765800-36780000	Weak transcription	K562	blood
48	chr14:36765800-36781000	Strong transcription	Duodenum Mucosa	Duodenum
49	chr14:36765800-36781200	Strong transcription	HUES6 Cell Line	embryonic stem cell
50	chr14:36765800-36782200	Strong transcription	HUES64 Cell Line	embryonic stem cell

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