Variant report

Variant	nsv901502
Chromosome Location	chr14:25074711-25101706
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	CEBPB	chr14:25100063-25100442	ECC-1	luminal epithelium:	n/a	n/a
2	CEBPB	chr14:25101078-25101218	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:25085847-25085933	HepG2	liver:	n/a	n/a
4	CEBPB	chr14:25077240-25077399	K562	blood:	n/a	n/a
5	CEBPB	chr14:25077145-25077424	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:25077149-25077457	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr14:25100082-25100392	IMR90	lung:	n/a	n/a
8	CEBPB	chr14:25099857-25100463	MCF-7	breast:	n/a	n/a
9	CEBPB	chr14:25077150-25077379	K562	blood:	n/a	n/a
10	CEBPB	chr14:25085712-25086021	MCF-7	breast:	n/a	n/a
11	CTCF	chr14:25074700-25074850	A549	lung:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
12	CTCF	chr14:25074700-25074850	BE2_C	brain:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
13	CTCF	chr14:25074560-25074830	NHEK	skin:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
14	CTCF	chr14:25074631-25074974	GM19238	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
15	CTCF	chr14:25074740-25074890	HA-sp	spinal cord:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
16	CTCF	chr14:25074700-25074850	HVMF	connective:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
17	CTCF	chr14:25075080-25075230	GM12871	blood:	n/a	n/a
18	CTCF	chr14:25085820-25085970	GM12864	blood:	n/a	n/a
19	CTCF	chr14:25074720-25074870	RPTEC	kidney:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
20	CTCF	chr14:25074639-25074933	A549	lung:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
21	CTCF	chr14:25074628-25074909	Medullo	brain:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
22	CTCF	chr14:25074700-25074850	GM12871	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
23	CTCF	chr14:25074652-25074935	MCF-7	breast:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
24	CTCF	chr14:25074660-25074810	AG10803	skin:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
25	CTCF	chr14:25074680-25074830	GM12870	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
26	CTCF	chr14:25074655-25074908	MCF-7	breast:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
27	CTCF	chr14:25081100-25081250	GM06990	blood:	n/a	n/a
28	CTCF	chr14:25074639-25074965	GM19240	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
29	CTCF	chr14:25074657-25074907	SK-N-SH_RA	brain:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
30	CTCF	chr14:25074700-25074850	HUVEC	blood vessel:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
31	CTCF	chr14:25074700-25074850	Caco-2	colon:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
32	CTCF	chr14:25074740-25074890	HPF	lung:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
33	CTCF	chr14:25074720-25074870	GM12875	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
34	CTCF	chr14:25074478-25075142	A549	lung:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
35	CTCF	chr14:25074638-25074973	GM12891	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
36	CTCF	chr14:25074595-25074888	K562	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
37	CTCF	chr14:25074680-25074830	K562	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
38	CTCF	chr14:25074720-25074870	MCF-7	breast:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
39	CTCF	chr14:25074504-25074990	HepG2	liver:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
40	CTCF	chr14:25074502-25074994	HCT-116	colon:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
41	CTCF	chr14:25074609-25074925	HepG2	liver:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
42	CTCF	chr14:25074700-25074850	AG09319	gingival:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
43	CTCF	chr14:25074663-25074911	K562	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
44	CTCF	chr14:25074740-25074890	GM12878	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
45	CTCF	chr14:25074653-25074905	Lung_OC	lung:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
46	CTCF	chr14:25074700-25074850	HEEpiC	esophagus:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
47	CTCF	chr14:25074680-25074830	RPTEC	kidney:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
48	CTCF	chr14:25074599-25074969	K562	blood:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
49	CTCF	chr14:25074740-25074890	HBMEC	blood vessel:	n/a	chr14:25074744-25074757 chr14:25074742-25074760
50	CTCF	chr14:25074588-25075031	MCF-7	breast:	n/a	chr14:25074744-25074757 chr14:25074742-25074760

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:25100740-25100790	HL-60	blood:	n/a
2	chr14:25100740-25100790	HNPCEpiC	eye:	n/a
3	chr14:25078609-25078659	AG09319	gingival:	n/a
4	chr14:25078609-25078659	BE2_C	brain:	n/a
5	chr14:25100740-25100790	SK-N-SH	brain:	n/a
6	chr14:25078609-25078659	HUVEC	blood vessel:	n/a
7	chr14:25079357-25079407	HEK293	kidney:	embryo
8	chr14:25075816-25075866	A549	lung:	n/a
9	chr14:25078609-25078659	CMK	blood:	n/a
10	chr14:25079357-25079407	NHDF-neo	bronchial:	n/a
11	chr14:25079357-25079407	GM12892	blood:	n/a
12	chr14:25100740-25100790	RPTEC	kidney:	n/a
13	chr14:25079357-25079407	ECC-1	luminal epithelium:	n/a
14	chr14:25078609-25078659	GM12891	blood:	n/a
15	chr14:25075816-25075866	HRE	kidney:	n/a
16	chr14:25078609-25078659	NHDF-neo	bronchial:	n/a
17	chr14:25100740-25100790	HRCEpiC	kidney:	n/a
18	chr14:25079357-25079407	BE2_C	brain:	n/a
19	chr14:25078609-25078659	Jurkat	blood:	n/a
20	chr14:25078609-25078659	HCT-116	colon:	n/a
21	chr14:25075816-25075866	ProgFib	skin:	n/a
22	chr14:25079357-25079407	HCPEpiC	choroid plexus:	n/a
23	chr14:25100740-25100790	AG10803	skin:	n/a
24	chr14:25100740-25100790	CMK	blood:	n/a
25	chr14:25100740-25100790	Jurkat	blood:	n/a
26	chr14:25078609-25078659	GM06990	blood:	n/a
27	chr14:25075816-25075866	PANC-1	pancreas:	n/a
28	chr14:25075816-25075866	ECC-1	luminal epithelium:	n/a
29	chr14:25100740-25100790	HIPEpiC	eye:	n/a
30	chr14:25078609-25078659	AG10803	skin:	n/a
31	chr14:25079357-25079407	MCF10A-Er-Src	breast:	n/a
32	chr14:25079357-25079407	Jurkat	blood:	n/a
33	chr14:25075816-25075866	HMEC	breast:	n/a
34	chr14:25075816-25075866	Hela-S3	cervix:	n/a
35	chr14:25078609-25078659	HCM	heart:	n/a
36	chr14:25075816-25075866	HNPCEpiC	eye:	n/a
37	chr14:25079357-25079407	HUVEC	blood vessel:	n/a
38	chr14:25078609-25078659	AoSMC	blood vessel:	n/a
39	chr14:25075816-25075866	HCM	heart:	n/a
40	chr14:25078609-25078659	LNCaP	prostate:	n/a
41	chr14:25079357-25079407	GM06990	blood:	n/a
42	chr14:25078609-25078659	IMR90	lung:	fetal
43	chr14:25075816-25075866	HPAEpiC	pulmonary alveolar:	n/a
44	chr14:25078609-25078659	AG09309	skin:	n/a
45	chr14:25100740-25100790	AoSMC	blood vessel:	n/a
46	chr14:25100740-25100790	K562	blood:	n/a
47	chr14:25079357-25079407	ovcar-3	ovarian:	n/a
48	chr14:25078609-25078659	ProgFib	skin:	n/a
49	chr14:25075816-25075866	HRCEpiC	kidney:	n/a
50	chr14:25079357-25079407	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:25094138..25097137-chr14:25102005..25104386,2	K562	blood:
2	chr14:25074327..25075453-chr14:25147858..25148813,10	MCF-7	breast:
3	chr14:25071276..25072810-chr14:25080337..25081851,2	MCF-7	breast:
4	chr14:25074565..25075282-chr14:25147884..25148791,4	K562	blood:
5	chr14:25073839..25075708-chr14:25147848..25148766,18	MCF-7	breast:
6	chr14:25098847..25101531-chr14:25147119..25149675,2	MCF-7	breast:
7	chr14:24950851..24951362-chr14:25074499..25075225,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-80A15.1.1-2	chr14:25092174-25092332	ENSG00000258657.1

Variant related genes	Relation type
GZMH	TF binding region
GZMH	CpG island
ENSG00000100453	chromatin interactions

Extended variants
information (count: 1131 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17257083	chr14:25074711-25074712	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs139098616	chr14:25074723-25074724	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533585533	chr14:25074750-25074751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34032659	chr14:25074774-25074775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537210690	chr14:25074801-25074802	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs12893348	chr14:25074805-25074806	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs12891536	chr14:25074839-25074840	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs554627108	chr14:25074859-25074860	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs536261189	chr14:25074885-25074886	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs76219263	chr14:25074968-25074969	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs149870482	chr14:25075006-25075007	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs17200187	chr14:25075057-25075058	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs558826723	chr14:25075076-25075077	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs575518998	chr14:25075118-25075119	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs544373168	chr14:25075129-25075130	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs554922460	chr14:25075146-25075147	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs574608715	chr14:25075174-25075175	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs543040693	chr14:25075181-25075182	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs12896130	chr14:25075182-25075183	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528628840	chr14:25075199-25075200	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs545184109	chr14:25075230-25075231	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564995072	chr14:25075241-25075242	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531031286	chr14:25075259-25075260	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7144488	chr14:25075260-25075261	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs567653691	chr14:25075261-25075262	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550610702	chr14:25075356-25075357	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs79914603	chr14:25075368-25075369	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139830722	chr14:25075376-25075377	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs566334879	chr14:25075390-25075391	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538588200	chr14:25075393-25075394	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558689398	chr14:25075419-25075420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs568942225	chr14:25075420-25075421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200416293	chr14:25075434-25075435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569125328	chr14:25075435-25075436	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs538051412	chr14:25075453-25075454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs367895948	chr14:25075522-25075523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7140465	chr14:25075531-25075532	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs574724645	chr14:25075561-25075562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540149334	chr14:25075583-25075584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs545602694	chr14:25075593-25075594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs17105894	chr14:25075726-25075727	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2236336	chr14:25075729-25075730	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs376491023	chr14:25075766-25075767	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199648043	chr14:25075771-25075772	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372416422	chr14:25075779-25075780	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376967753	chr14:25075780-25075781	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369721879	chr14:25075789-25075790	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115493987	chr14:25075810-25075811	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140139906	chr14:25075816-25075817	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201578280	chr14:25075817-25075818	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Cancer	20164920	CNVD
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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	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
Breast cancer	21364760	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25067600-25074800	Weak transcription	GM12878-XiMat	blood
2	chr14:25069800-25074800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr14:25074600-25074800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr14:25074600-25075600	Enhancers	Primary T cells fromperipheralblood	blood
5	chr14:25074600-25076600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:25074800-25075000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr14:25074800-25075400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
8	chr14:25074800-25076200	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr14:25074800-25076200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr14:25074800-25076600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr14:25074800-25076600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr14:25074800-25077000	Enhancers	GM12878-XiMat	blood
13	chr14:25074800-25077200	Enhancers	Spleen	Spleen
14	chr14:25074800-25077400	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr14:25074800-25077400	Enhancers	Primary B cells from peripheral blood	blood
16	chr14:25074800-25077400	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr14:25074800-25078000	Enhancers	Fetal Thymus	thymus
18	chr14:25074800-25079200	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr14:25075000-25075200	Enhancers	Duodenum Mucosa	Duodenum
20	chr14:25075000-25077000	Enhancers	Primary B cells from cord blood	blood
21	chr14:25075000-25077400	Enhancers	Primary T cells from cord blood	blood
22	chr14:25075200-25076600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr14:25075200-25076600	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr14:25075200-25076600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr14:25075200-25077200	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr14:25075200-25077200	Weak transcription	Duodenum Mucosa	Duodenum
27	chr14:25075200-25077400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr14:25075400-25076000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr14:25075400-25077200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:25075600-25076800	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr14:25075600-25077400	Enhancers	Primary hematopoietic stem cells	blood
32	chr14:25075600-25078400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
33	chr14:25075800-25076600	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr14:25076000-25077400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr14:25076000-25079000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
36	chr14:25076200-25076400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr14:25076200-25076600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr14:25076200-25081600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:25076400-25076800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr14:25076600-25077200	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr14:25076600-25077400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr14:25076600-25077600	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr14:25076600-25077600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:25076600-25078000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr14:25076800-25077600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr14:25076800-25078600	Enhancers	Fetal Intestine Large	intestine
47	chr14:25077000-25078200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr14:25077000-25078200	Weak transcription	GM12878-XiMat	blood
49	chr14:25077000-25078800	Enhancers	Fetal Intestine Small	intestine
50	chr14:25077200-25077400	Enhancers	Rectal Mucosa Donor 29	rectum

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