Variant report

Variant	nsv510631
Chromosome Location	chr14:25045183-25172311
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1301)
CpG islands
(count:794)
Chromatin interactive
region (count:24)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1301 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:25157027-25157552	K562	blood:	n/a	n/a
2	ARID3A	chr14:25148156-25148558	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:25148251-25148451	K562	blood:	n/a	n/a
4	ATF1	chr14:25157264-25157573	K562	blood:	n/a	n/a
5	ATF1	chr14:25154135-25154423	K562	blood:	n/a	n/a
6	ATF2	chr14:25134748-25135214	GM12878	blood:	n/a	n/a
7	ATF2	chr14:25148111-25148508	GM12878	blood:	n/a	n/a
8	ATF2	chr14:25134617-25135272	GM12878	blood:	n/a	n/a
9	ATF2	chr14:25142064-25144158	GM12878	blood:	n/a	n/a
10	ATF2	chr14:25142711-25143277	GM12878	blood:	n/a	n/a
11	ATF3	chr14:25165483-25166765	K562	blood:	n/a	n/a
12	ATF3	chr14:25166331-25166543	K562	blood:	n/a	n/a
13	ATF3	chr14:25148105-25148528	GM12878	blood:	n/a	n/a
14	ATF3	chr14:25165518-25166012	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr14:25143853-25144084	GM12878	blood:	n/a	n/a
16	BATF	chr14:25142763-25143083	GM12878	blood:	n/a	n/a
17	BATF	chr14:25148148-25148389	GM12878	blood:	n/a	n/a
18	BATF	chr14:25143774-25144136	GM12878	blood:	n/a	n/a
19	BATF	chr14:25134646-25135176	GM12878	blood:	n/a	n/a
20	BATF	chr14:25142586-25143163	GM12878	blood:	n/a	n/a
21	BATF	chr14:25134700-25135144	GM12878	blood:	n/a	n/a
22	BATF	chr14:25164342-25164705	GM12878	blood:	n/a	chr14:25164501-25164512
23	BCL11A	chr14:25134669-25135147	GM12878	blood:	n/a	n/a
24	BCL11A	chr14:25166344-25166691	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:25142700-25143130	GM12878	blood:	n/a	n/a
26	BCL11A	chr14:25142791-25143079	GM12878	blood:	n/a	n/a
27	BCL11A	chr14:25142193-25142638	GM12878	blood:	n/a	chr14:25142442-25142451
28	BCL11A	chr14:25142225-25142572	GM12878	blood:	n/a	chr14:25142442-25142451
29	BCL11A	chr14:25162269-25162532	GM12878	blood:	n/a	n/a
30	BCL3	chr14:25142720-25143143	GM12878	blood:	n/a	n/a
31	BCL3	chr14:25165780-25166204	GM12878	blood:	n/a	n/a
32	BCL3	chr14:25142759-25143085	GM12878	blood:	n/a	n/a
33	BCL3	chr14:25161896-25162173	GM12878	blood:	n/a	n/a
34	BCL3	chr14:25166290-25167098	GM12878	blood:	n/a	n/a
35	BCL3	chr14:25165622-25166228	GM12878	blood:	n/a	n/a
36	BCL3	chr14:25166296-25166860	GM12878	blood:	n/a	n/a
37	BCLAF1	chr14:25134538-25135216	GM12878	blood:	n/a	n/a
38	BCLAF1	chr14:25148089-25148442	GM12878	blood:	n/a	chr14:25148263-25148272
39	BCLAF1	chr14:25143494-25144216	GM12878	blood:	n/a	n/a
40	BCLAF1	chr14:25142481-25143120	GM12878	blood:	n/a	n/a
41	BCLAF1	chr14:25148025-25148603	GM12878	blood:	n/a	chr14:25148263-25148272
42	BCLAF1	chr14:25141997-25143221	GM12878	blood:	n/a	chr14:25142442-25142451
43	BHLHE40	chr14:25164481-25164861	GM12878	blood:	n/a	n/a
44	BHLHE40	chr14:25162249-25162831	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:25142219-25143199	GM12878	blood:	n/a	n/a
46	BHLHE40	chr14:25148107-25148493	GM12878	blood:	n/a	n/a
47	BHLHE40	chr14:25157281-25158076	K562	blood:	n/a	n/a
48	BHLHE40	chr14:25148155-25148512	K562	blood:	n/a	n/a
49	BHLHE40	chr14:25148107-25148488	HepG2	liver:	n/a	n/a
50	BRCA1	chr14:25148203-25148403	GM12878	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:25104483-25104533	CMK	blood:	n/a
2	chr14:25104483-25104533	CMK	blood:	n/a
3	chr14:25100740-25100790	GM06990	blood:	n/a
4	chr14:25045625-25045675	HPAEpiC	pulmonary alveolar:	n/a
5	chr14:25046117-25046167	HCT-116	colon:	n/a
6	chr14:25103730-25103780	CMK	blood:	n/a
7	chr14:25103301-25103351	GM12878	blood:	n/a
8	chr14:25079357-25079407	MCF-7	breast:	n/a
9	chr14:25100740-25100790	PrEC	prostate:	n/a
10	chr14:25103730-25103780	SAEC	small airway:	n/a
11	chr14:25103730-25103780	HCT-116	colon:	n/a
12	chr14:25159330-25159380	HNPCEpiC	eye:	n/a
13	chr14:25103730-25103780	ECC-1	luminal epithelium:	n/a
14	chr14:25078609-25078659	LNCaP	prostate:	n/a
15	chr14:25103301-25103351	HCF	heart:	n/a
16	chr14:25075816-25075866	HCPEpiC	choroid plexus:	n/a
17	chr14:25103546-25103596	GM12878	blood:	n/a
18	chr14:25100740-25100790	ProgFib	skin:	n/a
19	chr14:25045607-25045657	A549	lung:	n/a
20	chr14:25104483-25104533	ProgFib	skin:	n/a
21	chr14:25046121-25046171	CMK	blood:	n/a
22	chr14:25103730-25103780	HIPEpiC	eye:	n/a
23	chr14:25104483-25104533	HEK293	kidney:	embryo
24	chr14:25045607-25045657	HEEpiC	esophagus:	n/a
25	chr14:25159330-25159380	CMK	blood:	n/a
26	chr14:25078609-25078659	ProgFib	skin:	n/a
27	chr14:25159330-25159380	HCF	heart:	n/a
28	chr14:25103546-25103596	HRE	kidney:	n/a
29	chr14:25079357-25079407	NHBE	bronchial:	n/a
30	chr14:25079357-25079407	SK-N-SH	brain:	n/a
31	chr14:25075816-25075866	PFSK-1	brain:	n/a
32	chr14:25079357-25079407	SK-N-SH_RA	brain:	n/a
33	chr14:25045607-25045657	HepG2	liver:	n/a
34	chr14:25159330-25159380	HRPEpiC	eye:	n/a
35	chr14:25103730-25103780	HPAEpiC	pulmonary alveolar:	n/a
36	chr14:25079357-25079407	Jurkat	blood:	n/a
37	chr14:25079357-25079407	T-47D	breast:	n/a
38	chr14:25103730-25103780	AoSMC	blood vessel:	n/a
39	chr14:25103546-25103596	AG09309	skin:	n/a
40	chr14:25103730-25103780	ovcar-3	ovarian:	n/a
41	chr14:25045625-25045675	A549	lung:	n/a
42	chr14:25103730-25103780	Hepatocyte	liver:	n/a
43	chr14:25159330-25159380	GM06990	blood:	n/a
44	chr14:25079357-25079407	PrEC	prostate:	n/a
45	chr14:25103301-25103351	SKMC	muscle:	n/a
46	chr14:25079357-25079407	HCM	heart:	n/a
47	chr14:25079357-25079407	IMR90	lung:	fetal
48	chr14:25046121-25046171	PrEC	prostate:	n/a
49	chr14:25079357-25079407	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:25100740-25100790	AG04449	skin:	fetal

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:25160085..25162899-chr14:25176597..25178827,2	K562	blood:
2	chr14:25074565..25075282-chr14:25147884..25148791,4	K562	blood:
3	chr14:24905848..24906564-chr14:25147935..25148721,2	MCF-7	breast:
4	chr14:25098847..25101531-chr14:25147119..25149675,2	MCF-7	breast:
5	chr14:24950478..24951496-chr14:25147845..25148826,8	MCF-7	breast:
6	chr14:25145702..25148414-chr14:25151278..25153378,2	MCF-7	breast:
7	chr14:24950851..24951362-chr14:25074499..25075225,3	MCF-7	breast:
8	chr14:25074327..25075453-chr14:25147858..25148813,10	MCF-7	breast:
9	chr14:25071276..25072810-chr14:25080337..25081851,2	MCF-7	breast:
10	chr14:25071276..25072810-chr14:25080337..25081851,2	MCF-7	breast:
11	chr14:25145702..25148414-chr14:25151278..25153378,2	MCF-7	breast:
12	chr14:25098847..25101531-chr14:25147119..25149675,2	MCF-7	breast:
13	chr14:25073839..25075708-chr14:25147848..25148766,18	MCF-7	breast:
14	chr14:25074327..25075453-chr14:25147858..25148813,10	MCF-7	breast:
15	chr14:25148275..25148836-chr14:25875689..25876564,2	MCF-7	breast:
16	chr14:25147349..25148317-chr15:49914642..49915614,2	MCF-7	breast:
17	chr14:24950901..24951428-chr14:25147948..25148704,2	K562	blood:
18	chr14:24950446..24951536-chr14:25147799..25148973,31	MCF-7	breast:
19	chr14:25159291..25161247-chr14:25162465..25165191,2	K562	blood:
20	chr14:25073839..25075708-chr14:25147848..25148766,18	MCF-7	breast:
21	chr14:25159291..25161247-chr14:25162465..25165191,2	K562	blood:
22	chr14:25074565..25075282-chr14:25147884..25148791,4	K562	blood:
23	chr14:25140264..25140953-chr2:153574247..153575204,2	MCF-7	breast:
24	chr14:25094138..25097137-chr14:25102005..25104386,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-80A15.1.1-6	chr14:25108336-25110411	FPKM1_group_8576_transcript_3
2	lnc-RP11-80A15.1.1-6	chr14:25108305-25108468	FPKM1_group_8576_transcript_3
3	lnc-RP11-80A15.1.1-2	chr14:25092174-25092332	ENSG00000258657.1
4	lnc-RP11-80A15.1.1-2	chr14:25126731-25126980	ENSG00000258657.1
5	lnc-RP11-80A15.1.1-6	chr14:25108615-25110690	NONHSAT036068
6	lnc-RP11-80A15.1.1-6	chr14:25108305-25108468	NONHSAT036068
7	lnc-RP11-80A15.1.1-2	chr14:25123853-25123913	ENSG00000258657.1
8	lnc-RP11-80A15.1.1-2	chr14:25065191-25065208	ENSG00000258657.1

No data

Variant related genes	Relation type
GZMB	TF binding region
ENSG00000258657	TF binding region
GZMH	TF binding region
CTSG	TF binding region
GZMB	CpG island
ENSG00000258657	CpG island
GZMH	CpG island
CTSG	CpG island
ENSG00000100453	chromatin interactions
ENSG00000177917	chromatin interactions
ENSG00000196504	chromatin interactions

Extended variants
information (count: 4135 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4135 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543580425	chr14:25045194-25045195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563785902	chr14:25045205-25045206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529371088	chr14:25045226-25045227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549619107	chr14:25045312-25045313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs114229747	chr14:25045323-25045324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs367789722	chr14:25045330-25045331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs528802049	chr14:25045341-25045342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201130652	chr14:25045342-25045343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372142154	chr14:25045350-25045351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201059100	chr14:25045362-25045363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs61737123	chr14:25045386-25045387	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374688403	chr14:25045434-25045435	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs376980998	chr14:25045458-25045459	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537031403	chr14:25045573-25045574	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs12878578	chr14:25045589-25045590	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs17105315	chr14:25045608-25045609	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs536471320	chr14:25045637-25045638	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs367916783	chr14:25045647-25045648	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs12878759	chr14:25045684-25045685	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs572660946	chr14:25045719-25045720	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs147440029	chr14:25045735-25045736	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs558793620	chr14:25045743-25045744	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs3759639	chr14:25045744-25045745	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs543750537	chr14:25045830-25045831	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs74039133	chr14:25045833-25045834	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs148028351	chr14:25045842-25045843	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs192272037	chr14:25045852-25045853	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs560026265	chr14:25045871-25045872	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs528691621	chr14:25045885-25045886	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs114889683	chr14:25045902-25045903	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs565559610	chr14:25045981-25045982	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs112232237	chr14:25045990-25045991	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs531079531	chr14:25046015-25046016	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs550574824	chr14:25046024-25046025	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs185867624	chr14:25046047-25046048	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs535952636	chr14:25046089-25046090	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs141758550	chr14:25046090-25046091	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538760325	chr14:25046096-25046097	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs546279994	chr14:25046100-25046101	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs566357529	chr14:25046117-25046118	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs577150113	chr14:25046255-25046256	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs115464526	chr14:25046267-25046268	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs558432349	chr14:25046290-25046291	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575515825	chr14:25046301-25046302	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs537700319	chr14:25046312-25046313	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs557399666	chr14:25046319-25046320	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs574070991	chr14:25046320-25046321	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs543187907	chr14:25046324-25046325	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs150533490	chr14:25046325-25046326	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs573394261	chr14:25046348-25046349	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:868 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:25043200-25047200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:25043200-25047200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr14:25043600-25045600	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr14:25044000-25047400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr14:25044200-25045400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr14:25044600-25045400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:25044600-25045600	Weak transcription	Fetal Thymus	thymus
8	chr14:25044600-25046200	Enhancers	Primary hematopoietic stem cells	blood
9	chr14:25044800-25046400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr14:25044800-25051800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:25045200-25046000	Enhancers	Dnd41	blood
12	chr14:25045400-25045600	Enhancers	Left Ventricle	heart
13	chr14:25045400-25045600	Enhancers	Skeletal Muscle Male	skeletal muscle
14	chr14:25045400-25045800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr14:25045400-25046000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr14:25045600-25046200	Enhancers	Fetal Thymus	thymus
17	chr14:25045600-25046200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr14:25045800-25046400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr14:25046200-25047200	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr14:25047200-25051200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr14:25047200-25051200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr14:25047200-25051200	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr14:25051200-25051600	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr14:25051200-25051800	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr14:25051200-25051800	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr14:25064200-25064400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr14:25064200-25064400	Enhancers	Hela-S3	cervix
28	chr14:25064200-25064800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr14:25064200-25065000	Enhancers	HMEC	breast
30	chr14:25064200-25065600	Enhancers	NHEK	skin
31	chr14:25064400-25064600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:25064400-25064800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr14:25064400-25065000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr14:25064400-25065000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr14:25064400-25065200	Flanking Active TSS	Hela-S3	cervix
36	chr14:25064600-25065200	Enhancers	HepG2	liver
37	chr14:25064800-25065200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:25064800-25065200	Enhancers	A549	lung
39	chr14:25064800-25065600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr14:25065000-25065400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:25065000-25065600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr14:25065000-25065600	Flanking Active TSS	HMEC	breast
43	chr14:25065200-25065600	Active TSS	Hela-S3	cervix
44	chr14:25065200-25066200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:25065600-25066000	Active TSS	HMEC	breast
46	chr14:25065600-25066200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:25066200-25066600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr14:25066200-25069800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr14:25066400-25067200	Enhancers	GM12878-XiMat	blood
50	chr14:25067200-25067600	ZNF genes & repeats	GM12878-XiMat	blood

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