Variant report

Variant	nsv1054427
Chromosome Location	chr14:36780743-36819931
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	chr14:36785526-36785702	K562	blood:	n/a	n/a
2	ARID3A	chr14:36787931-36788470	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:36789353-36790203	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:36784635-36784815	K562	blood:	n/a	n/a
5	ARID3A	chr14:36786874-36787050	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:36789827-36789998	K562	blood:	n/a	n/a
7	ATF1	chr14:36789684-36790159	K562	blood:	n/a	n/a
8	ATF2	chr14:36789693-36790117	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr14:36789725-36790108	GM12878	blood:	n/a	n/a
10	ATF2	chr14:36789612-36790132	GM12878	blood:	n/a	n/a
11	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
12	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
13	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
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	BATF	chr14:36784705-36785059	GM12878	blood:	n/a	chr14:36784842-36784853
16	BATF	chr14:36784726-36785054	GM12878	blood:	n/a	chr14:36784842-36784853
17	BCL3	chr14:36789549-36790347	A549	lung:	n/a	n/a
18	BCL3	chr14:36784682-36784987	GM12878	blood:	n/a	chr14:36784811-36784820
19	BHLHE40	chr14:36784748-36785137	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:36789595-36790169	K562	blood:	n/a	n/a
21	BRCA1	chr14:36788746-36788783	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr14:36789033-36790188	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr14:36789668-36790245	HepG2	liver:	n/a	n/a
24	CBX3	chr14:36789680-36790403	K562	blood:	n/a	n/a
25	CCNT2	chr14:36789394-36790044	K562	blood:	n/a	chr14:36789846-36789855
26	CEBPB	chr14:36798092-36798403	K562	blood:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
27	CEBPB	chr14:36789718-36790083	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr14:36789699-36790108	A549	lung:	n/a	n/a
29	CEBPB	chr14:36798118-36798425	IMR90	lung:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
30	CEBPB	chr14:36798076-36798444	HepG2	liver:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
31	CEBPB	chr14:36816351-36816680	HepG2	liver:	n/a	chr14:36816493-36816506 chr14:36816494-36816505 chr14:36816493-36816504
32	CEBPB	chr14:36796555-36796909	IMR90	lung:	n/a	n/a
33	CEBPB	chr14:36796560-36796920	HepG2	liver:	n/a	n/a
34	CEBPB	chr14:36789746-36790117	K562	blood:	n/a	n/a
35	CEBPB	chr14:36789602-36790208	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:36791061-36791224	K562	blood:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
37	CEBPB	chr14:36798107-36798380	HepG2	liver:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
38	CEBPB	chr14:36790993-36791264	HepG2	liver:	n/a	chr14:36791141-36791154 chr14:36791142-36791153 chr14:36791141-36791152
39	CEBPB	chr14:36785526-36785655	K562	blood:	n/a	n/a
40	CEBPB	chr14:36796572-36796924	A549	lung:	n/a	n/a
41	CEBPB	chr14:36816355-36816631	A549	lung:	n/a	chr14:36816493-36816506 chr14:36816494-36816505 chr14:36816493-36816504
42	CEBPB	chr14:36805980-36806101	HepG2	liver:	n/a	chr14:36806038-36806049
43	CEBPB	chr14:36789563-36790259	GM12878	blood:	n/a	n/a
44	CEBPB	chr14:36789686-36790191	IMR90	lung:	n/a	n/a
45	CEBPB	chr14:36798124-36798432	Hela-S3	cervix:	n/a	chr14:36798250-36798261 chr14:36798249-36798260
46	CEBPB	chr14:36789455-36790200	HepG2	liver:	n/a	n/a
47	CEBPB	chr14:36789331-36790233	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr14:36789730-36790173	K562	blood:	n/a	n/a
49	CEBPB	chr14:36789653-36790109	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:36796651-36796792	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:36789488-36789538	GM06990	blood:	n/a
2	chr14:36789488-36789538	GM06990	blood:	n/a
3	chr14:36789886-36789936	Jurkat	blood:	n/a
4	chr14:36789810-36789860	HMEC	breast:	n/a
5	chr14:36789488-36789538	HRPEpiC	eye:	n/a
6	chr14:36789810-36789860	HRPEpiC	eye:	n/a
7	chr14:36789488-36789538	BJ	skin:	n/a
8	chr14:36789691-36789741	HRE	kidney:	n/a
9	chr14:36790242-36790292	GM19239	blood:	n/a
10	chr14:36789691-36789741	HL-60	blood:	n/a
11	chr14:36789810-36789860	NHBE	bronchial:	n/a
12	chr14:36790242-36790292	CMK	blood:	n/a
13	chr14:36790242-36790292	PrEC	prostate:	n/a
14	chr14:36789691-36789741	PANC-1	pancreas:	n/a
15	chr14:36783435-36783485	AG09319	gingival:	n/a
16	chr14:36783435-36783485	SK-N-MC	brain:	n/a
17	chr14:36789810-36789860	RPTEC	kidney:	n/a
18	chr14:36783435-36783485	BE2_C	brain:	n/a
19	chr14:36789985-36790035	Hepatocyte	liver:	n/a
20	chr14:36789810-36789860	A549	lung:	n/a
21	chr14:36789488-36789538	HEK293	kidney:	embryo
22	chr14:36783435-36783485	PANC-1	pancreas:	n/a
23	chr14:36783435-36783485	NHBE	bronchial:	n/a
24	chr14:36783435-36783485	K562	blood:	n/a
25	chr14:36789810-36789860	AG09319	gingival:	n/a
26	chr14:36789488-36789538	AG09319	gingival:	n/a
27	chr14:36789488-36789538	Hela-S3	cervix:	n/a
28	chr14:36789691-36789741	SKMC	muscle:	n/a
29	chr14:36789985-36790035	HepG2	liver:	n/a
30	chr14:36789985-36790035	U87	brain:	n/a
31	chr14:36783435-36783485	BJ	skin:	n/a
32	chr14:36789886-36789936	HEEpiC	esophagus:	n/a
33	chr14:36789985-36790035	H1-hESC	embryonic stem cell:	embryo
34	chr14:36783435-36783485	PrEC	prostate:	n/a
35	chr14:36789886-36789936	NB4	blood:	n/a
36	chr14:36789691-36789741	HAEpiC	amniotic membrane:	n/a
37	chr14:36789810-36789860	HepG2	liver:	n/a
38	chr14:36789488-36789538	HCF	heart:	n/a
39	chr14:36789691-36789741	HCT-116	colon:	n/a
40	chr14:36789985-36790035	SK-N-SH_RA	brain:	n/a
41	chr14:36789985-36790035	HRE	kidney:	n/a
42	chr14:36789488-36789538	HCT-116	colon:	n/a
43	chr14:36789488-36789538	SK-N-SH_RA	brain:	n/a
44	chr14:36783435-36783485	T-47D	breast:	n/a
45	chr14:36790242-36790292	NB4	blood:	n/a
46	chr14:36790242-36790292	AG10803	skin:	n/a
47	chr14:36790242-36790292	AG09319	gingival:	n/a
48	chr14:36789886-36789936	AoSMC	blood vessel:	n/a
49	chr14:36789886-36789936	GM12892	blood:	n/a
50	chr14:36789488-36789538	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:36789374..36789875-chr8:119123638..119124514,2	Hela-S3	cervix:
2	chr14:36538483..36541249-chr14:36788541..36791272,2	MCF-7	breast:
3	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
4	chr14:36781444..36784031-chr14:36790836..36792756,2	K562	blood:
5	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
6	chr14:36797776..36799754-chr14:36805074..36807804,2	MCF-7	breast:
7	chr14:36784989..36787450-chr14:36787865..36790918,4	K562	blood:
8	chr14:36788593..36791761-chr14:36792192..36795536,3	K562	blood:
9	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
10	chr14:36787110..36790093-chr14:36792032..36793692,2	K562	blood:
11	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
12	chr14:36779773..36781769-chr14:36782151..36784795,2	K562	blood:
13	chr14:36784077..36786059-chr14:36788034..36791140,4	MCF-7	breast:
14	chr14:36539398..36539927-chr14:36782854..36783534,2	MCF-7	breast:
15	chr14:36768912..36770474-chr14:36787292..36789766,2	MCF-7	breast:
16	chr14:36778847..36780826-chr14:36784208..36786054,2	MCF-7	breast:
17	chr14:36783190..36784933-chr14:36788355..36791806,3	MCF-7	breast:
18	chr14:36780477..36782487-chr14:36786743..36788959,2	MCF-7	breast:
19	chr14:36793727..36795435-chr14:36796192..36797833,2	MCF-7	breast:
20	chr14:36780690..36783423-chr14:36785409..36787697,2	K562	blood:
21	chr14:36778592..36784393-chr14:36785409..36790832,9	K562	blood:
22	chr14:36797776..36799754-chr14:36805074..36807804,2	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
ENSG00000151332	chromatin interactions
ENSG00000257585	chromatin interactions

Extended variants
information (count: 585 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17104349	chr14:36780773-36780774	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569718432	chr14:36780775-36780776	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs375156352	chr14:36780797-36780798	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs140089260	chr14:36780847-36780848	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs532077440	chr14:36780863-36780864	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs191425477	chr14:36780878-36780879	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs367962633	chr14:36780887-36780888	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371414445	chr14:36780896-36780897	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531674663	chr14:36780909-36780910	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs17849937	chr14:36780917-36780918	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374740028	chr14:36780950-36780951	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs369973788	chr14:36780968-36780969	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535350124	chr14:36780989-36780990	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs7154340	chr14:36781037-36781038	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568511342	chr14:36781050-36781051	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs537417341	chr14:36781054-36781055	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs181111689	chr14:36781130-36781131	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs188483	chr14:36781142-36781143	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577280994	chr14:36781186-36781187	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs75941455	chr14:36781205-36781206	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs375176822	chr14:36781238-36781239	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs367769706	chr14:36781241-36781242	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200289229	chr14:36781252-36781253	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs201874269	chr14:36781301-36781302	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs149220752	chr14:36781331-36781332	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536048762	chr14:36781374-36781375	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs140544678	chr14:36781375-36781376	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs58992019	chr14:36781379-36781380	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs540974964	chr14:36781441-36781442	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185405489	chr14:36781449-36781450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs189768354	chr14:36781455-36781456	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12436515	chr14:36781473-36781474	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543031809	chr14:36781525-36781526	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs550217556	chr14:36781535-36781536	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563110870	chr14:36781573-36781574	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77376384	chr14:36781621-36781622	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs151324560	chr14:36781638-36781639	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs7155498	chr14:36781650-36781651	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528690005	chr14:36781681-36781682	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs548925244	chr14:36781710-36781711	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs4900924	chr14:36781859-36781860	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs114167267	chr14:36781933-36781934	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs369349881	chr14:36781940-36781941	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs147083648	chr14:36781943-36781944	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs183529441	chr14:36781956-36781957	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539931545	chr14:36781983-36781984	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs144446766	chr14:36781989-36781990	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs553182838	chr14:36782001-36782002	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs371620285	chr14:36782020-36782021	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571937395	chr14:36782023-36782024	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:36761000-36785000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:36764400-36784000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:36765000-36781200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr14:36765200-36781400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
5	chr14:36765400-36781400	Strong transcription	Placenta	Placenta
6	chr14:36765400-36788800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr14:36765600-36781000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr14:36765800-36781000	Strong transcription	Duodenum Mucosa	Duodenum
9	chr14:36765800-36781200	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr14:36765800-36782200	Strong transcription	HUES64 Cell Line	embryonic stem cell
11	chr14:36766000-36781000	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr14:36766000-36781000	Strong transcription	Skeletal Muscle Female	skeletal muscle
13	chr14:36766000-36781400	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr14:36766000-36783400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr14:36766200-36781200	Strong transcription	HUES48 Cell Line	embryonic stem cell
16	chr14:36766200-36781200	Strong transcription	Fetal Thymus	thymus
17	chr14:36766200-36781200	Strong transcription	Rectal Mucosa Donor 29	rectum
18	chr14:36766200-36781400	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr14:36766200-36785400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr14:36766600-36788000	Weak transcription	Fetal Heart	heart
21	chr14:36767000-36781000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr14:36767000-36781400	Strong transcription	Primary T helper cells PMA-I stimulated	--
23	chr14:36767400-36789200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr14:36767400-36789200	Weak transcription	Spleen	Spleen
25	chr14:36769600-36781400	Strong transcription	Primary B cells from cord blood	blood
26	chr14:36770200-36781000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr14:36770400-36781200	Strong transcription	HepG2	liver
28	chr14:36770600-36781200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr14:36770600-36782800	Weak transcription	Hela-S3	cervix
30	chr14:36771600-36781000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr14:36771800-36781000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:36771800-36781000	Strong transcription	Fetal Intestine Large	intestine
33	chr14:36771800-36781200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:36771800-36781200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
35	chr14:36771800-36783200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:36772000-36781000	Strong transcription	Brain Anterior Caudate	brain
37	chr14:36772000-36781000	Strong transcription	Duodenum Smooth Muscle	Duodenum
38	chr14:36772000-36781000	Strong transcription	Left Ventricle	heart
39	chr14:36772000-36781200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr14:36772000-36781400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:36772000-36781400	Strong transcription	Primary B cells from peripheral blood	blood
42	chr14:36772000-36781400	Strong transcription	Liver	Liver
43	chr14:36772200-36780800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr14:36772200-36781000	Strong transcription	Primary hematopoietic stem cells	blood
45	chr14:36772200-36781200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr14:36772200-36781200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr14:36772400-36781000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:36772400-36781200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:36772600-36788800	Weak transcription	Stomach Mucosa	stomach
50	chr14:36772800-36781000	Strong transcription	Osteobl	bone

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