Variant report

Variant	nsv564177
Chromosome Location	chr14:31381351-31425437
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:164)
CpG islands
(count:184)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:164 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:31390506-31390821	K562	blood:	n/a	chr14:31390697-31390708
2	CEBPB	chr14:31407843-31408215	IMR90	lung:	n/a	chr14:31408020-31408031
3	CEBPB	chr14:31390567-31390856	HepG2	liver:	n/a	chr14:31390697-31390708
4	CEBPB	chr14:31390531-31390873	Hela-S3	cervix:	n/a	chr14:31390697-31390708
5	CEBPB	chr14:31390541-31390863	IMR90	lung:	n/a	chr14:31390697-31390708
6	CEBPB	chr14:31407849-31408190	H1-hESC	embryonic stem cell:	n/a	chr14:31408020-31408031
7	CEBPB	chr14:31397272-31397408	HepG2	liver:	n/a	chr14:31397379-31397390
8	CEBPB	chr14:31407861-31408215	A549	lung:	n/a	chr14:31408020-31408031
9	CEBPB	chr14:31390557-31390875	K562	blood:	n/a	chr14:31390697-31390708
10	CEBPB	chr14:31407859-31408202	Hela-S3	cervix:	n/a	chr14:31408020-31408031
11	CEBPB	chr14:31407822-31408276	MCF-7	breast:	n/a	chr14:31408020-31408031
12	CEBPB	chr14:31407827-31408269	A549	lung:	n/a	chr14:31408020-31408031
13	CEBPB	chr14:31407840-31408130	MCF-7	breast:	n/a	chr14:31408020-31408031
14	CEBPB	chr14:31407864-31408203	K562	blood:	n/a	chr14:31408020-31408031
15	CEBPB	chr14:31407850-31408210	HepG2	liver:	n/a	chr14:31408020-31408031
16	CTCF	chr14:31393940-31393994	GM10248	blood:	n/a	n/a
17	CTCF	chr14:31391640-31391790	HepG2	liver:	n/a	n/a
18	CTCF	chr14:31391080-31391230	HepG2	liver:	n/a	n/a
19	CTCF	chr14:31412000-31412150	MCF-7	breast:	n/a	n/a
20	CTCF	chr14:31418360-31418510	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr14:31412500-31412650	HepG2	liver:	n/a	n/a
22	CUX1	chr14:31384783-31384787	K562	blood:	n/a	n/a
23	E2F4	chr14:31390564-31390847	MCF10A-Er-Src	breast:	n/a	chr14:31390731-31390748 chr14:31390734-31390745
24	ELK1	chr14:31399850-31399858	GM12878	blood:	n/a	n/a
25	EP300	chr14:31390259-31390420	K562	blood:	n/a	n/a
26	EP300	chr14:31390561-31390807	Hela-S3	cervix:	n/a	chr14:31390694-31390708
27	FAM48A	chr14:31407910-31408034	GM12878	blood:	n/a	n/a
28	FAM48A	chr14:31412676-31412850	GM12878	blood:	n/a	n/a
29	FOS	chr14:31390577-31390853	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr14:31404712-31404893	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr14:31390543-31390860	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr14:31390531-31390856	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr14:31404773-31404973	HUVEC	blood vessel:	n/a	n/a
34	FOS	chr14:31404730-31404846	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr14:31390563-31390854	MCF10A-Er-Src	breast:	n/a	n/a
36	GATA2	chr14:31404630-31404983	HUVEC	blood vessel:	n/a	n/a
37	GATA3	chr14:31400694-31401259	SK-N-SH	brain:	n/a	chr14:31400832-31400845
38	GATA3	chr14:31404486-31405143	SK-N-SH	brain:	n/a	n/a
39	GATA3	chr14:31404506-31405144	SK-N-SH	brain:	n/a	n/a
40	GATA3	chr14:31404600-31405041	MCF-7	breast:	n/a	n/a
41	GATA3	chr14:31389636-31390347	SH-SY5Y	brain:	n/a	chr14:31390316-31390323 chr14:31390315-31390325
42	IRF1	chr14:31390340-31390428	K562	blood:	n/a	n/a
43	IRF1	chr14:31395264-31395370	K562	blood:	n/a	n/a
44	JUN	chr14:31393268-31393333	HepG2	liver:	n/a	n/a
45	JUN	chr14:31390557-31390879	HUVEC	blood vessel:	n/a	n/a
46	JUN	chr14:31409000-31409285	HUVEC	blood vessel:	n/a	n/a
47	JUND	chr14:31390613-31390839	K562	blood:	n/a	n/a
48	JUND	chr14:31393200-31393327	HepG2	liver:	n/a	n/a
49	MAFF	chr14:31399888-31400095	HepG2	liver:	n/a	chr14:31399959-31399977
50	MAFF	chr14:31384144-31384291	HepG2	liver:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31389792-31389842	NB4	blood:	n/a
2	chr14:31389792-31389842	NB4	blood:	n/a
3	chr14:31408344-31408394	ECC-1	luminal epithelium:	n/a
4	chr14:31389792-31389842	MCF-7	breast:	n/a
5	chr14:31408344-31408394	HCPEpiC	choroid plexus:	n/a
6	chr14:31398430-31398480	AG04450	lung:	fetal
7	chr14:31389792-31389842	AG04450	lung:	fetal
8	chr14:31408344-31408394	Jurkat	blood:	n/a
9	chr14:31408344-31408394	Caco-2	colon:	n/a
10	chr14:31389792-31389842	Hepatocyte	liver:	n/a
11	chr14:31389792-31389842	K562	blood:	n/a
12	chr14:31389792-31389842	MCF10A-Er-Src	breast:	n/a
13	chr14:31408344-31408394	K562	blood:	n/a
14	chr14:31389792-31389842	HUVEC	blood vessel:	n/a
15	chr14:31398430-31398480	SK-N-SH	brain:	n/a
16	chr14:31389792-31389842	Caco-2	colon:	n/a
17	chr14:31389792-31389842	PANC-1	pancreas:	n/a
18	chr14:31389792-31389842	ProgFib	skin:	n/a
19	chr14:31398430-31398480	HepG2	liver:	n/a
20	chr14:31389792-31389842	H1-hESC	embryonic stem cell:	embryo
21	chr14:31398430-31398480	U87	brain:	n/a
22	chr14:31398430-31398480	HAEpiC	amniotic membrane:	n/a
23	chr14:31398430-31398480	GM12891	blood:	n/a
24	chr14:31408344-31408394	HIPEpiC	eye:	n/a
25	chr14:31389792-31389842	HPAEpiC	pulmonary alveolar:	n/a
26	chr14:31398430-31398480	A549	lung:	n/a
27	chr14:31408344-31408394	PFSK-1	brain:	n/a
28	chr14:31408344-31408394	AG04449	skin:	fetal
29	chr14:31398430-31398480	HRE	kidney:	n/a
30	chr14:31389792-31389842	AG09309	skin:	n/a
31	chr14:31408344-31408394	SK-N-SH_RA	brain:	n/a
32	chr14:31408344-31408394	HUVEC	blood vessel:	n/a
33	chr14:31389792-31389842	NH-A	brain:	n/a
34	chr14:31408344-31408394	NHDF-neo	bronchial:	n/a
35	chr14:31389792-31389842	SK-N-MC	brain:	n/a
36	chr14:31398430-31398480	CMK	blood:	n/a
37	chr14:31398430-31398480	AG10803	skin:	n/a
38	chr14:31389792-31389842	LNCaP	prostate:	n/a
39	chr14:31398430-31398480	HCM	heart:	n/a
40	chr14:31389792-31389842	NHBE	bronchial:	n/a
41	chr14:31408344-31408394	SK-N-MC	brain:	n/a
42	chr14:31389792-31389842	HRPEpiC	eye:	n/a
43	chr14:31389792-31389842	ECC-1	luminal epithelium:	n/a
44	chr14:31398430-31398480	HEEpiC	esophagus:	n/a
45	chr14:31398430-31398480	NHBE	bronchial:	n/a
46	chr14:31389792-31389842	IMR90	lung:	fetal
47	chr14:31408344-31408394	HRCEpiC	kidney:	n/a
48	chr14:31398430-31398480	SAEC	small airway:	n/a
49	chr14:31389792-31389842	BJ	skin:	n/a
50	chr14:31398430-31398480	AG09319	gingival:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:31376657..31378769-chr14:31384602..31386523,2	MCF-7	breast:
2	chr14:31385237..31388114-chr14:31390780..31394488,3	MCF-7	breast:
3	chr14:31420168..31423130-chr14:31493763..31496178,2	MCF-7	breast:
4	chr14:31387011..31389077-chr14:31394255..31396560,2	K562	blood:
5	chr14:31385492..31389361-chr14:31390065..31392327,4	K562	blood:
6	chr14:31398507..31401730-chr14:31402844..31406226,4	K562	blood:
7	chr14:31400245..31402113-chr14:31403843..31406707,2	MCF-7	breast:
8	chr14:31406134..31408433-chr14:31516211..31518078,2	K562	blood:
9	chr14:31412377..31414525-chr14:31418622..31420542,2	MCF-7	breast:
10	chr14:31390350..31392275-chr14:31395263..31396767,2	K562	blood:
11	chr14:31397468..31399701-chr14:31410285..31412729,2	MCF-7	breast:
12	chr14:31387011..31389077-chr14:31394255..31396560,2	K562	blood:
13	chr14:31412013..31413799-chr14:31413815..31415852,2	MCF-7	breast:
14	chr14:31390350..31392275-chr14:31395263..31396767,2	K562	blood:
15	chr14:31400245..31402113-chr14:31403843..31406707,2	MCF-7	breast:
16	chr14:31412377..31414525-chr14:31418622..31420542,2	MCF-7	breast:
17	chr14:31385237..31388114-chr14:31390780..31394488,3	MCF-7	breast:
18	chr14:31398507..31401730-chr14:31402844..31406226,4	K562	blood:
19	chr14:31425052..31427072-chr14:31430189..31431943,2	K562	blood:
20	chr14:31417991..31420027-chr14:31423345..31424852,2	K562	blood:
21	chr14:31402683..31406428-chr14:31407313..31410233,6	K562	blood:
22	chr14:31385492..31389361-chr14:31390065..31392327,4	K562	blood:
23	chr14:31404383..31406657-chr14:31409869..31411808,3	MCF-7	breast:
24	chr14:31397468..31399701-chr14:31410285..31412729,2	MCF-7	breast:
25	chr14:31412013..31413799-chr14:31413815..31415852,2	MCF-7	breast:
26	chr14:31417991..31420027-chr14:31423345..31424852,2	K562	blood:
27	chr14:31422050..31424018-chr14:31493292..31496577,3	K562	blood:

No data

Variant related genes	Relation type
STRN3	TF binding region
STRN3	CpG island
ENSG00000196792	chromatin interactions
ENSG00000100478	chromatin interactions

Extended variants
information (count: 1689 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1689 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2273171	chr14:31381351-31381352	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370862787	chr14:31381358-31381359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567061192	chr14:31381368-31381369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374998447	chr14:31381412-31381413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200377860	chr14:31381437-31381438	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555096883	chr14:31381440-31381441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375675562	chr14:31381456-31381457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537906843	chr14:31381457-31381458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs556318414	chr14:31381474-31381475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115310492	chr14:31381484-31381485	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139808154	chr14:31381485-31381486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560389556	chr14:31381535-31381536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371780098	chr14:31381574-31381575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560273343	chr14:31381613-31381614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143126442	chr14:31381639-31381640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527811014	chr14:31381724-31381725	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549060539	chr14:31381741-31381742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs17097503	chr14:31381744-31381745	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs146667285	chr14:31381749-31381750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75552334	chr14:31381812-31381813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17097507	chr14:31381913-31381914	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs371749955	chr14:31381932-31381933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189038741	chr14:31381942-31381943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74040942	chr14:31381957-31381958	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531795936	chr14:31381996-31381997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533309315	chr14:31381998-31381999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139172446	chr14:31382021-31382022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567131455	chr14:31382029-31382030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147856130	chr14:31382051-31382052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374988149	chr14:31382052-31382053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528011178	chr14:31382062-31382063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116027882	chr14:31382079-31382080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144988291	chr14:31382089-31382090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537845274	chr14:31382097-31382098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556257008	chr14:31382116-31382117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571408943	chr14:31382118-31382119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs538820945	chr14:31382145-31382146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74040944	chr14:31382152-31382153	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs572287664	chr14:31382156-31382157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149097336	chr14:31382159-31382160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542521288	chr14:31382161-31382162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184510479	chr14:31382180-31382181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79904953	chr14:31382239-31382240	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573650915	chr14:31382262-31382263	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544208797	chr14:31382346-31382347	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143179659	chr14:31382375-31382376	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533294453	chr14:31382397-31382398	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560484891	chr14:31382406-31382407	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545568936	chr14:31382542-31382543	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560448285	chr14:31382554-31382555	Weak transcription Strong transcription Enhancers	TF binding region	1 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
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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	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
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1007 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31345000-31435400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr14:31345400-31382600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr14:31346600-31382600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr14:31347000-31384600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr14:31347000-31394800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr14:31355800-31414400	Weak transcription	Spleen	Spleen
7	chr14:31356200-31412800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr14:31358000-31428200	Weak transcription	Small Intestine	intestine
9	chr14:31360200-31435600	Weak transcription	Gastric	stomach
10	chr14:31360400-31381800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:31361600-31384400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr14:31361800-31394200	Weak transcription	Fetal Brain Male	brain
13	chr14:31362000-31381400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:31362200-31414400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr14:31362400-31435400	Weak transcription	Colonic Mucosa	Colon
16	chr14:31362600-31382400	Strong transcription	Liver	Liver
17	chr14:31363000-31394400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr14:31363000-31430600	Weak transcription	Brain Angular Gyrus	brain
19	chr14:31363000-31435200	Weak transcription	Esophagus	oesophagus
20	chr14:31363400-31383000	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr14:31363800-31381400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr14:31364400-31415400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr14:31364800-31393200	Weak transcription	Brain Substantia Nigra	brain
24	chr14:31365800-31402200	Weak transcription	Thymus	Thymus
25	chr14:31365800-31414200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr14:31365800-31435600	Weak transcription	Right Ventricle	heart
27	chr14:31367000-31381600	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr14:31367600-31381600	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr14:31369800-31381800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr14:31370000-31381400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
31	chr14:31370000-31381600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:31370000-31381800	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chr14:31370000-31393600	Weak transcription	Lung	lung
34	chr14:31370000-31414400	Weak transcription	Pancreas	Pancrea
35	chr14:31370400-31381600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr14:31370400-31381800	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr14:31370600-31381400	Strong transcription	Dnd41	blood
38	chr14:31370600-31381600	Strong transcription	HSMM	muscle
39	chr14:31370600-31382000	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr14:31370800-31381800	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr14:31371000-31383000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr14:31372400-31381400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:31372400-31414400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:31372600-31381400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr14:31372600-31381400	Strong transcription	Fetal Intestine Large	intestine
46	chr14:31372600-31381400	Strong transcription	Osteobl	bone
47	chr14:31372600-31381800	Strong transcription	Primary B cells from cord blood	blood
48	chr14:31372800-31381800	Strong transcription	Primary B cells from peripheral blood	blood
49	chr14:31373200-31381400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr14:31373200-31381600	Strong transcription	Skeletal Muscle Female	skeletal muscle

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