Variant report

Variant	nsv883013
Chromosome Location	chr5:145595837-145651979
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:201)
CpG islands
(count:0)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:145620815-145620864	K562	blood:	n/a	n/a
2	BATF	chr5:145618600-145618803	GM12878	blood:	n/a	chr5:145618713-145618724
3	BHLHE40	chr5:145597993-145598128	K562	blood:	n/a	n/a
4	BHLHE40	chr5:145646919-145646923	K562	blood:	n/a	n/a
5	CCNT2	chr5:145645217-145645417	K562	blood:	n/a	n/a
6	CEBPB	chr5:145647342-145647592	IMR90	lung:	n/a	n/a
7	CEBPB	chr5:145602761-145603093	A549	lung:	n/a	n/a
8	CEBPB	chr5:145602736-145603055	K562	blood:	n/a	n/a
9	CEBPB	chr5:145602739-145603127	K562	blood:	n/a	n/a
10	CEBPB	chr5:145602752-145603193	A549	lung:	n/a	n/a
11	CEBPB	chr5:145602786-145603066	A549	lung:	n/a	n/a
12	CEBPB	chr5:145602778-145603060	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr5:145602753-145603097	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:145602753-145603105	IMR90	lung:	n/a	n/a
15	CEBPB	chr5:145602766-145603103	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr5:145621131-145621164	Fibrobl	skin:	n/a	n/a
17	CTCF	chr5:145643220-145643370	HCT-116	colon:	n/a	n/a
18	CTCF	chr5:145599602-145599655	GM20000	blood:	n/a	n/a
19	CTCF	chr5:145596283-145596334	LNCaP	prostate:	n/a	n/a
20	CUX1	chr5:145597745-145598207	K562	blood:	n/a	chr5:145598161-145598177
21	EBF1	chr5:145629456-145629710	GM12878	blood:	n/a	n/a
22	EP300	chr5:145597719-145597996	K562	blood:	n/a	chr5:145597927-145597941
23	FOS	chr5:145620619-145620946	HUVEC	blood vessel:	n/a	chr5:145620777-145620788
24	FOS	chr5:145620777-145620830	MCF10A-Er-Src	breast:	n/a	chr5:145620777-145620788
25	FOS	chr5:145620630-145620823	MCF10A-Er-Src	breast:	n/a	chr5:145620777-145620788
26	FOS	chr5:145644265-145644349	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr5:145620579-145620869	MCF10A-Er-Src	breast:	n/a	chr5:145620777-145620788
28	FOS	chr5:145620590-145620820	MCF10A-Er-Src	breast:	n/a	chr5:145620777-145620788
29	FOSL2	chr5:145620524-145620900	SK-N-SH	brain:	n/a	n/a
30	FOXA1	chr5:145623205-145623546	HepG2	liver:	n/a	n/a
31	GATA1	chr5:145597764-145598231	PBDE	blood:	n/a	chr5:145597929-145597939
32	GATA3	chr5:145645116-145645655	MCF-7	breast:	n/a	chr5:145645412-145645420 chr5:145645413-145645420 chr5:145645413-145645420 chr5:145645413-145645420 chr5:145645408-145645424
33	GATA3	chr5:145600859-145601016	SH-SY5Y	brain:	n/a	n/a
34	GATA3	chr5:145636965-145637331	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr5:145647221-145647606	SK-N-SH	brain:	n/a	n/a
36	GATA3	chr5:145644768-145644928	SH-SY5Y	brain:	n/a	n/a
37	IKZF1	chr5:145618590-145618928	GM12878	blood:	n/a	n/a
38	IRF1	chr5:145623241-145623362	K562	blood:	n/a	n/a
39	IRF1	chr5:145597727-145598324	K562	blood:	n/a	chr5:145597739-145597751 chr5:145597932-145597946 chr5:145597739-145597751 chr5:145597748-145597755 chr5:145597936-145597946
40	IRF1	chr5:145597705-145598143	K562	blood:	n/a	chr5:145597739-145597751 chr5:145597932-145597946 chr5:145597739-145597751 chr5:145597748-145597755 chr5:145597936-145597946
41	JUN	chr5:145601596-145601627	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUN	chr5:145620685-145620691	HepG2	liver:	n/a	n/a
43	JUND	chr5:145620674-145620713	HepG2	liver:	n/a	chr5:145620689-145620700
44	JUND	chr5:145620550-145621082	SK-N-SH	brain:	n/a	chr5:145620689-145620700
45	KAP1	chr5:145604749-145604943	K562	blood:	n/a	n/a
46	MAFF	chr5:145598915-145599163	K562	blood:	n/a	n/a
47	MAFF	chr5:145598846-145599168	HepG2	liver:	n/a	n/a
48	MAFF	chr5:145651106-145651414	HepG2	liver:	n/a	n/a
49	MAFF	chr5:145601637-145601891	K562	blood:	n/a	chr5:145601751-145601769
50	MAFF	chr5:145651231-145651292	K562	blood:	n/a	n/a

No data

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:145596366..145598063-chr5:145648958..145650482,2	K562	blood:
2	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
3	chr5:145625814..145628687-chr5:145636719..145638380,2	K562	blood:
4	chr5:145596117..145598265-chr5:145605012..145606909,2	K562	blood:
5	chr5:145643342..145645989-chr5:145650081..145652639,2	K562	blood:
6	chr5:145601632..145604303-chr5:145605562..145607960,2	MCF-7	breast:
7	chr5:145601632..145604303-chr5:145605562..145607960,2	MCF-7	breast:
8	chr5:145596366..145598063-chr5:145648958..145650482,2	K562	blood:
9	chr5:145615949..145618767-chr5:145647272..145650054,2	K562	blood:
10	chr5:145588075..145590940-chr5:145591754..145595862,4	K562	blood:
11	chr5:145607480..145610119-chr5:145611867..145613573,2	MCF-7	breast:
12	chr5:145594426..145596514-chr5:145599170..145601456,2	K562	blood:
13	chr5:145587290..145589374-chr5:145604476..145606867,3	K562	blood:
14	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
15	chr5:145591065..145593762-chr5:145596165..145598951,2	K562	blood:
16	chr5:145560154..145562997-chr5:145607826..145610384,3	K562	blood:
17	chr5:145595165..145597126-chr5:145598903..145601685,2	K562	blood:
18	chr5:145594426..145596514-chr5:145599170..145601456,2	K562	blood:
19	chr5:145625443..145628007-chr5:145629715..145633107,5	K562	blood:
20	chr5:145558240..145560527-chr5:145600863..145603054,2	K562	blood:
21	chr5:145625443..145628007-chr5:145629715..145633107,5	K562	blood:
22	chr5:145581405..145584024-chr5:145596123..145597883,2	K562	blood:
23	chr5:145607480..145610119-chr5:145611867..145613573,2	MCF-7	breast:
24	chr5:145612339..145614307-chr5:145615895..145618813,2	MCF-7	breast:
25	chr5:145625869..145628007-chr5:145631607..145633546,2	K562	blood:
26	chr5:145615949..145618767-chr5:145647272..145650054,2	K562	blood:
27	chr5:145647167..145649031-chr5:145653206..145654859,2	K562	blood:
28	chr5:145596117..145598265-chr5:145605012..145606909,2	K562	blood:
29	chr5:145643342..145645989-chr5:145650081..145652639,2	K562	blood:
30	chr5:145625814..145628687-chr5:145636719..145638380,2	K562	blood:
31	chr5:145582359..145584728-chr5:145597576..145599110,2	MCF-7	breast:
32	chr5:145595165..145597126-chr5:145598903..145601685,2	K562	blood:

No data

Variant related genes	Relation type
RBM27	TF binding region
RNU7-180P	TF binding region
ENSG00000133706	chromatin interactions
ENSG00000091009	chromatin interactions

Extended variants
information (count: 2045 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2045 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2963930	chr5:145595837-145595838	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559519182	chr5:145595856-145595857	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs543534594	chr5:145595871-145595872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548435070	chr5:145596028-145596029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568225305	chr5:145596074-145596075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541821440	chr5:145596078-145596079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536805277	chr5:145596115-145596116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192337975	chr5:145596150-145596151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs76953332	chr5:145596152-145596153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539378419	chr5:145596157-145596158	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs60892265	chr5:145596180-145596181	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs112673995	chr5:145596190-145596191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs546209874	chr5:145596214-145596215	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs183224703	chr5:145596216-145596217	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs150286754	chr5:145596220-145596221	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369958562	chr5:145596273-145596274	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575431353	chr5:145596301-145596302	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs544000601	chr5:145596309-145596310	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs563908906	chr5:145596339-145596340	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186840306	chr5:145596351-145596352	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545489878	chr5:145596370-145596371	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546228025	chr5:145596372-145596373	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191358350	chr5:145596379-145596380	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528435408	chr5:145596410-145596411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs182764481	chr5:145596470-145596471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372913335	chr5:145596497-145596498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs144901691	chr5:145596502-145596503	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs550337873	chr5:145596509-145596510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs570600624	chr5:145596579-145596580	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533245947	chr5:145596583-145596584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546534384	chr5:145596589-145596590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375853048	chr5:145596617-145596618	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76173590	chr5:145596629-145596630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188241080	chr5:145596632-145596633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566759647	chr5:145596637-145596638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs529704017	chr5:145596648-145596649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149210917	chr5:145596681-145596682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs555416475	chr5:145596695-145596696	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568959292	chr5:145596727-145596728	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs146898158	chr5:145596732-145596733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs79252485	chr5:145596782-145596783	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs557589110	chr5:145596791-145596792	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139385112	chr5:145596819-145596820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113819330	chr5:145596825-145596826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553344503	chr5:145596831-145596832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573503505	chr5:145596853-145596854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs137857770	chr5:145596923-145596924	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541787900	chr5:145596971-145596972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545963169	chr5:145597027-145597028	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34610071	chr5:145597028-145597029	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	16864856	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	20864512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1564 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145584400-145598800	Weak transcription	NH-A	brain
2	chr5:145584400-145606600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr5:145584600-145606400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr5:145584800-145597200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr5:145584800-145599000	Weak transcription	Fetal Muscle Leg	muscle
6	chr5:145584800-145608000	Weak transcription	Esophagus	oesophagus
7	chr5:145584800-145631200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr5:145585000-145598800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr5:145585000-145599000	Weak transcription	Fetal Brain Female	brain
10	chr5:145585000-145602600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:145585200-145598600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:145585200-145598600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr5:145585200-145598800	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr5:145585200-145598800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr5:145585200-145598800	Weak transcription	HMEC	breast
16	chr5:145585200-145598800	Weak transcription	NHEK	skin
17	chr5:145585200-145609200	Weak transcription	Brain Anterior Caudate	brain
18	chr5:145585400-145597400	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr5:145585400-145598200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr5:145585400-145598200	Weak transcription	HUVEC	blood vessel
21	chr5:145585400-145598400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr5:145585400-145609000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr5:145585600-145597400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr5:145585600-145599000	Weak transcription	Thymus	Thymus
25	chr5:145585600-145599200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:145585600-145601000	Weak transcription	Right Atrium	heart
27	chr5:145585600-145610200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:145585800-145598400	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr5:145585800-145598800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr5:145585800-145601800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr5:145586000-145599000	Weak transcription	HSMM	muscle
32	chr5:145586200-145597000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr5:145586400-145598800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:145586400-145604000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr5:145586400-145616800	Weak transcription	Right Ventricle	heart
36	chr5:145586800-145598600	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr5:145587000-145597400	Weak transcription	Psoas Muscle	Psoas
38	chr5:145588200-145597600	Weak transcription	Dnd41	blood
39	chr5:145588200-145598200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr5:145588200-145599000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr5:145588200-145608000	Weak transcription	Gastric	stomach
42	chr5:145588200-145609200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:145589000-145633200	Weak transcription	Brain Angular Gyrus	brain
44	chr5:145589200-145599000	Weak transcription	Aorta	Aorta
45	chr5:145589200-145615400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr5:145589400-145599000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr5:145589400-145610200	Weak transcription	Fetal Kidney	kidney
48	chr5:145589600-145597800	Weak transcription	Colon Smooth Muscle	Colon
49	chr5:145589600-145597800	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr5:145589600-145598800	Weak transcription	Rectal Smooth Muscle	rectum

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