Variant report

Variant	nsv901495
Chromosome Location	chr14:24429249-24489235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1064)
CpG islands
(count:1467)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1064 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24483172-24483507	K562	blood:	n/a	n/a
2	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:24443416-24443612	HepG2	liver:	n/a	n/a
4	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
5	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr14:24439122-24439137	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
9	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
10	BCL11A	chr14:24435772-24436067	GM12878	blood:	n/a	chr14:24435972-24435981
11	BHLHE40	chr14:24438814-24439115	HepG2	liver:	n/a	n/a
12	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
13	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
14	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
16	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
17	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
18	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
19	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
20	CEBPB	chr14:24454165-24454464	MCF-7	breast:	n/a	n/a
21	CEBPB	chr14:24454491-24454833	Hela-S3	cervix:	n/a	chr14:24454690-24454701
22	CEBPB	chr14:24454506-24454789	A549	lung:	n/a	chr14:24454690-24454701
23	CEBPB	chr14:24454350-24454830	A549	lung:	n/a	chr14:24454690-24454701
24	CEBPB	chr14:24454143-24454908	A549	lung:	n/a	chr14:24454690-24454701
25	CEBPB	chr14:24454306-24454822	HepG2	liver:	n/a	chr14:24454690-24454701
26	CEBPB	chr14:24454542-24454918	MCF-7	breast:	n/a	chr14:24454690-24454701
27	CEBPB	chr14:24454359-24454892	IMR90	lung:	n/a	chr14:24454690-24454701
28	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:24454237-24454396	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:24454258-24454790	MCF-7	breast:	n/a	chr14:24454690-24454701
31	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
32	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
33	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
34	CEBPD	chr14:24439025-24439361	HepG2	liver:	n/a	n/a
35	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
36	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
37	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
38	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
39	CHD2	chr14:24439126-24439200	GM12878	blood:	n/a	chr14:24439140-24439150
40	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
41	CTCF	chr14:24483200-24483477	HepG2	liver:	n/a	n/a
42	CTCF	chr14:24483260-24483410	AG09309	skin:	n/a	n/a
43	CTCF	chr14:24483280-24483430	K562	blood:	n/a	n/a
44	CTCF	chr14:24458460-24458610	HRE	kidney:	n/a	n/a
45	CTCF	chr14:24483300-24483450	GM12866	blood:	n/a	n/a
46	CTCF	chr14:24483240-24483390	HFF	foreskin:	n/a	n/a
47	CTCF	chr14:24446580-24446730	AG09309	skin:	n/a	n/a
48	CTCF	chr14:24446480-24446630	SAEC	small airway:	n/a	n/a
49	CTCF	chr14:24446500-24446650	AG09319	gingival:	n/a	n/a
50	CTCF	chr14:24483240-24483390	GM06990	blood:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24458208-24458258	IMR90	lung:	fetal
2	chr14:24475053-24475103	AG04450	lung:	fetal
3	chr14:24435159-24435209	CMK	blood:	n/a
4	chr14:24458208-24458258	IMR90	lung:	fetal
5	chr14:24475053-24475103	AG04450	lung:	fetal
6	chr14:24435159-24435209	CMK	blood:	n/a
7	chr14:24439430-24439480	HCF	heart:	n/a
8	chr14:24458004-24458054	GM06990	blood:	n/a
9	chr14:24439157-24439207	ECC-1	luminal epithelium:	n/a
10	chr14:24476478-24476528	HCF	heart:	n/a
11	chr14:24435159-24435209	AG09309	skin:	n/a
12	chr14:24454443-24454493	NHDF-neo	bronchial:	n/a
13	chr14:24457915-24457965	SKMC	muscle:	n/a
14	chr14:24438909-24438959	HEK293	kidney:	embryo
15	chr14:24457509-24457559	HRCEpiC	kidney:	n/a
16	chr14:24473832-24473882	HEEpiC	esophagus:	n/a
17	chr14:24439157-24439207	SKMC	muscle:	n/a
18	chr14:24475906-24475956	HEEpiC	esophagus:	n/a
19	chr14:24457915-24457965	AG10803	skin:	n/a
20	chr14:24478620-24478670	H1-hESC	embryonic stem cell:	embryo
21	chr14:24457915-24457965	PrEC	prostate:	n/a
22	chr14:24458345-24458395	HCF	heart:	n/a
23	chr14:24458004-24458054	HEK293	kidney:	embryo
24	chr14:24457993-24458043	HIPEpiC	eye:	n/a
25	chr14:24458000-24458050	NHBE	bronchial:	n/a
26	chr14:24457893-24457943	SK-N-SH	brain:	n/a
27	chr14:24457993-24458043	NH-A	brain:	n/a
28	chr14:24439430-24439480	HRCEpiC	kidney:	n/a
29	chr14:24476478-24476528	HRPEpiC	eye:	n/a
30	chr14:24458000-24458050	HNPCEpiC	eye:	n/a
31	chr14:24458345-24458395	AoSMC	blood vessel:	n/a
32	chr14:24476559-24476609	MCF-7	breast:	n/a
33	chr14:24475053-24475103	ovcar-3	ovarian:	n/a
34	chr14:24458004-24458054	SAEC	small airway:	n/a
35	chr14:24476559-24476609	HCPEpiC	choroid plexus:	n/a
36	chr14:24458299-24458349	MCF-7	breast:	n/a
37	chr14:24457915-24457965	HMEC	breast:	n/a
38	chr14:24457893-24457943	NHBE	bronchial:	n/a
39	chr14:24438909-24438959	GM12892	blood:	n/a
40	chr14:24435159-24435209	LNCaP	prostate:	n/a
41	chr14:24435159-24435209	Caco-2	colon:	n/a
42	chr14:24457993-24458043	SK-N-SH	brain:	n/a
43	chr14:24476478-24476528	SK-N-MC	brain:	n/a
44	chr14:24458099-24458149	AG09309	skin:	n/a
45	chr14:24476478-24476528	MCF-7	breast:	n/a
46	chr14:24458004-24458054	Hepatocyte	liver:	n/a
47	chr14:24458014-24458064	ECC-1	luminal epithelium:	n/a
48	chr14:24458099-24458149	HL-60	blood:	n/a
49	chr14:24475053-24475103	HepG2	liver:	n/a
50	chr14:24458299-24458349	GM06990	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
2	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:
3	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
4	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
5	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:
6	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
7	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
8	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:
9	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
10	chr14:24452194..24454763-chr14:24457643..24460471,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3

No data

Variant related genes	Relation type
DHRS4	TF binding region
DHRS4L2	TF binding region
DHRS4-AS1	TF binding region
DHRS4	CpG island
DHRS4L2	CpG island
DHRS4-AS1	CpG island
ENSG00000100889	chromatin interactions
ENSG00000187630	chromatin interactions
ENSG00000129535	chromatin interactions
ENSG00000215256	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000225766	chromatin interactions

Extended variants
information (count: 2945 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2945 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3742491	chr14:24429249-24429250	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs367976575	chr14:24429253-24429254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs3742492	chr14:24429298-24429299	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs564714166	chr14:24429331-24429332	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs3742493	chr14:24429334-24429335	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs550225110	chr14:24429367-24429368	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567028599	chr14:24429382-24429383	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535993499	chr14:24429384-24429385	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546384144	chr14:24429387-24429388	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566698436	chr14:24429401-24429402	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs193118367	chr14:24429403-24429404	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs3742494	chr14:24429412-24429413	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs577929747	chr14:24429453-24429454	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550261013	chr14:24429464-24429465	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs3742495	chr14:24429477-24429478	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532956613	chr14:24429493-24429494	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543191888	chr14:24429515-24429516	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559685262	chr14:24429532-24429533	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573420224	chr14:24429576-24429577	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs551671737	chr14:24429600-24429601	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28477540	chr14:24429609-24429610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1957687	chr14:24429610-24429611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs550161788	chr14:24429617-24429618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150275135	chr14:24429635-24429636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs138862127	chr14:24429636-24429637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189793625	chr14:24429660-24429661	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs566525923	chr14:24429694-24429695	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538849372	chr14:24429705-24429706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10141263	chr14:24429720-24429721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192393493	chr14:24429725-24429726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537397460	chr14:24429726-24429727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557390241	chr14:24429735-24429736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574125688	chr14:24429736-24429737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183530088	chr14:24429754-24429755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376939766	chr14:24429790-24429791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs149403190	chr14:24429827-24429828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34506026	chr14:24429828-24429829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2181423	chr14:24429848-24429849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200365835	chr14:24429849-24429850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552086526	chr14:24429891-24429892	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566881870	chr14:24429935-24429936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537550551	chr14:24429938-24429939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1957688	chr14:24429953-24429954	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs28635008	chr14:24429963-24429964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144808678	chr14:24429989-24429990	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2146573	chr14:24430003-24430004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs181757243	chr14:24430006-24430007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2146574	chr14:24430035-24430036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs529667420	chr14:24430058-24430059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs199531639	chr14:24430148-24430149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1218 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24423400-24431000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:24423600-24430800	Weak transcription	Psoas Muscle	Psoas
3	chr14:24423600-24438800	Weak transcription	Lung	lung
4	chr14:24423600-24438800	Weak transcription	Ovary	ovary
5	chr14:24423800-24430800	Weak transcription	Fetal Thymus	thymus
6	chr14:24423800-24432400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:24423800-24435600	Weak transcription	Primary B cells from cord blood	blood
8	chr14:24423800-24438200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr14:24423800-24438600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr14:24423800-24438600	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr14:24423800-24438800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr14:24423800-24438800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr14:24423800-24438800	Weak transcription	Left Ventricle	heart
14	chr14:24423800-24438800	Weak transcription	Right Ventricle	heart
15	chr14:24423800-24438800	Weak transcription	Osteobl	bone
16	chr14:24424000-24435400	Weak transcription	Primary B cells from peripheral blood	blood
17	chr14:24424000-24437400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr14:24424000-24438200	Weak transcription	Primary T cells fromperipheralblood	blood
19	chr14:24424000-24438200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr14:24424000-24438800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr14:24424000-24438800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr14:24424000-24438800	Weak transcription	HSMM	muscle
23	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
24	chr14:24424200-24435400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr14:24424200-24438200	Weak transcription	Rectal Smooth Muscle	rectum
26	chr14:24424200-24438800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr14:24424200-24438800	Weak transcription	NHEK	skin
28	chr14:24424400-24429800	Weak transcription	Esophagus	oesophagus
29	chr14:24424400-24430000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr14:24424400-24432200	Weak transcription	Dnd41	blood
31	chr14:24424400-24436600	Weak transcription	Gastric	stomach
32	chr14:24424400-24438000	Weak transcription	Stomach Smooth Muscle	stomach
33	chr14:24424400-24438600	Weak transcription	Brain Hippocampus Middle	brain
34	chr14:24424400-24438800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr14:24424400-24438800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr14:24424400-24438800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr14:24424400-24438800	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr14:24424400-24438800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr14:24424400-24438800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr14:24424400-24438800	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr14:24424400-24438800	Weak transcription	Colonic Mucosa	Colon
42	chr14:24424400-24438800	Weak transcription	Fetal Muscle Leg	muscle
43	chr14:24424400-24438800	Weak transcription	Pancreas	Pancrea
44	chr14:24424400-24438800	Weak transcription	Spleen	Spleen
45	chr14:24424400-24438800	Weak transcription	HMEC	breast
46	chr14:24424800-24437600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr14:24424800-24439000	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr14:24425400-24429600	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr14:24425600-24438800	Weak transcription	Fetal Muscle Trunk	muscle
50	chr14:24425800-24429400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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