Variant report

Variant	esv1827255
Chromosome Location	chr5:145484386-145505556
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:157)
CpG islands
(count:184)
Chromatin interactive
region (count:15)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:157 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:145491007-145491405	K562	blood:	n/a	n/a
2	ARID3A	chr5:145492144-145492554	K562	blood:	n/a	n/a
3	ATF1	chr5:145491068-145491344	K562	blood:	n/a	n/a
4	BHLHE40	chr5:145491060-145491363	K562	blood:	n/a	n/a
5	CBX3	chr5:145490964-145491389	K562	blood:	n/a	n/a
6	CCNT2	chr5:145491028-145491331	K562	blood:	n/a	n/a
7	CCNT2	chr5:145492071-145492366	K562	blood:	n/a	n/a
8	CEBPB	chr5:145490778-145491379	K562	blood:	n/a	n/a
9	CEBPB	chr5:145487491-145487785	K562	blood:	n/a	chr5:145487655-145487666
10	CEBPB	chr5:145487479-145487845	IMR90	lung:	n/a	chr5:145487655-145487666
11	CEBPB	chr5:145487545-145487740	Hela-S3	cervix:	n/a	chr5:145487655-145487666
12	CEBPB	chr5:145487541-145487752	HepG2	liver:	n/a	chr5:145487655-145487666
13	CEBPB	chr5:145487512-145487712	H1-hESC	embryonic stem cell:	n/a	chr5:145487655-145487666
14	CEBPB	chr5:145487582-145487705	HepG2	liver:	n/a	chr5:145487655-145487666
15	CEBPB	chr5:145487474-145487781	K562	blood:	n/a	chr5:145487655-145487666
16	CEBPB	chr5:145487507-145487783	MCF-7	breast:	n/a	chr5:145487655-145487666
17	CEBPD	chr5:145490985-145491421	K562	blood:	n/a	n/a
18	CTCF	chr5:145505300-145505570	Caco-2	colon:	n/a	n/a
19	CTCF	chr5:145492257-145492274	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr5:145492848-145492864	GM10266	blood:	n/a	n/a
21	CUX1	chr5:145491793-145492656	K562	blood:	n/a	n/a
22	CUX1	chr5:145489480-145489804	K562	blood:	n/a	n/a
23	E2F4	chr5:145485488-145485673	MCF10A-Er-Src	breast:	n/a	n/a
24	EBF1	chr5:145496074-145496372	GM12878	blood:	n/a	chr5:145496218-145496229
25	EBF1	chr5:145496013-145496431	GM12878	blood:	n/a	chr5:145496218-145496229
26	EP300	chr5:145490943-145491413	K562	blood:	n/a	n/a
27	EP300	chr5:145492181-145492450	K562	blood:	n/a	n/a
28	EP300	chr5:145489190-145489659	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr5:145490990-145491458	K562	blood:	n/a	n/a
30	EP300	chr5:145489244-145489604	SK-N-SH_RA	brain:	n/a	n/a
31	GABPA	chr5:145491016-145491322	K562	blood:	n/a	n/a
32	GATA1	chr5:145490881-145491532	PBDE	blood:	n/a	n/a
33	GATA2	chr5:145491062-145491353	SH-SY5Y	brain:	n/a	n/a
34	GATA2	chr5:145490945-145491393	K562	blood:	n/a	n/a
35	GATA3	chr5:145499190-145499564	MCF-7	breast:	n/a	n/a
36	GATA3	chr5:145498970-145499661	MCF-7	breast:	n/a	chr5:145499169-145499177 chr5:145499089-145499100
37	GATA3	chr5:145498930-145499836	MCF-7	breast:	n/a	chr5:145499169-145499177 chr5:145499089-145499100
38	GATA3	chr5:145503907-145503931	SH-SY5Y	brain:	n/a	n/a
39	GTF2F1	chr5:145499759-145499798	H1-hESC	embryonic stem cell:	n/a	n/a
40	HMGN3	chr5:145491106-145491323	K562	blood:	n/a	n/a
41	IRF1	chr5:145490923-145491483	K562	blood:	n/a	n/a
42	IRF1	chr5:145491012-145491530	K562	blood:	n/a	n/a
43	IRF1	chr5:145491784-145492052	K562	blood:	n/a	n/a
44	IRF1	chr5:145493778-145493792	K562	blood:	n/a	n/a
45	JUN	chr5:145485395-145485486	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUN	chr5:145489263-145489399	H1-hESC	embryonic stem cell:	n/a	n/a
47	JUND	chr5:145499117-145499511	MCF-7	breast:	n/a	n/a
48	JUND	chr5:145491016-145491368	K562	blood:	n/a	n/a
49	KAP1	chr5:145491013-145491705	K562	blood:	n/a	n/a
50	MAFF	chr5:145504202-145504502	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:145484364-145484414	PFSK-1	brain:	n/a
2	chr5:145484364-145484414	PFSK-1	brain:	n/a
3	chr5:145484536-145484586	AG04449	skin:	fetal
4	chr5:145484536-145484586	HEEpiC	esophagus:	n/a
5	chr5:145484536-145484586	CMK	blood:	n/a
6	chr5:145484705-145484755	ovcar-3	ovarian:	n/a
7	chr5:145484536-145484586	PFSK-1	brain:	n/a
8	chr5:145484364-145484414	SKMC	muscle:	n/a
9	chr5:145484536-145484586	HCF	heart:	n/a
10	chr5:145484364-145484414	HEEpiC	esophagus:	n/a
11	chr5:145484364-145484414	GM19239	blood:	n/a
12	chr5:145484705-145484755	HRCEpiC	kidney:	n/a
13	chr5:145484705-145484755	SK-N-SH_RA	brain:	n/a
14	chr5:145484536-145484586	NHDF-neo	bronchial:	n/a
15	chr5:145484364-145484414	Hepatocyte	liver:	n/a
16	chr5:145484705-145484755	ECC-1	luminal epithelium:	n/a
17	chr5:145484364-145484414	GM12892	blood:	n/a
18	chr5:145484705-145484755	HL-60	blood:	n/a
19	chr5:145484536-145484586	HPAEpiC	pulmonary alveolar:	n/a
20	chr5:145484364-145484414	AG04449	skin:	fetal
21	chr5:145484705-145484755	NT2-D1	testis:	n/a
22	chr5:145484705-145484755	H1-hESC	embryonic stem cell:	embryo
23	chr5:145484536-145484586	HL-60	blood:	n/a
24	chr5:145484705-145484755	AG04450	lung:	fetal
25	chr5:145484364-145484414	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:145484536-145484586	IMR90	lung:	fetal
27	chr5:145484364-145484414	AG04450	lung:	fetal
28	chr5:145484705-145484755	MCF10A-Er-Src	breast:	n/a
29	chr5:145484705-145484755	AG04449	skin:	fetal
30	chr5:145484536-145484586	HAEpiC	amniotic membrane:	n/a
31	chr5:145484364-145484414	ECC-1	luminal epithelium:	n/a
32	chr5:145484364-145484414	T-47D	breast:	n/a
33	chr5:145484536-145484586	BJ	skin:	n/a
34	chr5:145484364-145484414	HNPCEpiC	eye:	n/a
35	chr5:145484536-145484586	GM06990	blood:	n/a
36	chr5:145484705-145484755	HCT-116	colon:	n/a
37	chr5:145484705-145484755	MCF-7	breast:	n/a
38	chr5:145484705-145484755	SK-N-MC	brain:	n/a
39	chr5:145484364-145484414	NHBE	bronchial:	n/a
40	chr5:145484705-145484755	Jurkat	blood:	n/a
41	chr5:145484364-145484414	K562	blood:	n/a
42	chr5:145484536-145484586	NHBE	bronchial:	n/a
43	chr5:145484705-145484755	HRPEpiC	eye:	n/a
44	chr5:145484705-145484755	CMK	blood:	n/a
45	chr5:145484705-145484755	GM06990	blood:	n/a
46	chr5:145484705-145484755	HMEC	breast:	n/a
47	chr5:145484364-145484414	NHDF-neo	bronchial:	n/a
48	chr5:145484536-145484586	Hela-S3	cervix:	n/a
49	chr5:145484364-145484414	RPTEC	kidney:	n/a
50	chr5:145484536-145484586	HRPEpiC	eye:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:145505030..145506633-chr5:145530746..145532367,2	K562	blood:
2	chr5:145493604..145496584-chr6:32937107..32938718,2	MCF-7	breast:
3	chr5:145495840..145497455-chr5:145497723..145500099,2	MCF-7	breast:
4	chr5:145494583..145495584-chr6:32939701..32940736,3	MCF-7	breast:
5	chr5:145493604..145496604-chr6:32938745..32942030,4	MCF-7	breast:
6	chr5:145493583..145495104-chr6:32939099..32942485,4	K562	blood:
7	chr5:145467931..145470149-chr5:145485691..145487881,2	K562	blood:
8	chr5:145495840..145497455-chr5:145497723..145500099,2	MCF-7	breast:
9	chr5:145500906..145503400-chr5:145526760..145528273,2	K562	blood:
10	chr5:145494583..145495103-chr6:32939502..32940568,7	Hela-S3	cervix:
11	chr5:145494896..145498767-chr5:145501979..145504223,3	K562	blood:
12	chr5:145494584..145495104-chr6:32939517..32940451,5	HCT-116	colon:
13	chr5:145502833..145504880-chr8:144679405..144681801,2	MCF-7	breast:
14	chr5:145494896..145498767-chr5:145501979..145504223,3	K562	blood:
15	chr5:145493583..145495104-chr6:32936625..32942485,6	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH3RF2-1	chr5:145499880-145499975	ENSG00000251556.1

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	LARS	hsa-miR-21-5p	chr5:145493041-145493064
2	LARS	hsa-miR-183-5p	chr5:145492683-145492704

Variant related genes	Relation type
PLAC8L1	TF binding region
PLAC8L1	CpG island
ENSG00000204256	chromatin interactions
ENSG00000133706	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000263756	chromatin interactions
ENSG00000104529	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000179886	chromatin interactions

Extended variants
information (count: 760 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs573725652	chr5:145484392-145484393	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
2	rs542697383	chr5:145484398-145484399	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
3	rs562477842	chr5:145484400-145484401	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs531619557	chr5:145484401-145484402	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs544449508	chr5:145484411-145484412	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs564352614	chr5:145484444-145484445	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs181011923	chr5:145484464-145484465	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546894804	chr5:145484504-145484505	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs566527387	chr5:145484584-145484585	Weak transcription Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs529291079	chr5:145484603-145484604	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549443880	chr5:145484647-145484648	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs569281650	chr5:145484660-145484661	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538360316	chr5:145484733-145484734	Weak transcription Strong transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs35652702	chr5:145484741-145484742	Weak transcription Strong transcription	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs145541297	chr5:145484760-145484761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534075943	chr5:145484776-145484777	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs113716122	chr5:145484785-145484786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34170515	chr5:145484896-145484897	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs74982899	chr5:145484991-145484992	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs185909918	chr5:145485078-145485079	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs556507640	chr5:145485085-145485086	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs71581855	chr5:145485166-145485167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs370722598	chr5:145485167-145485168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545094291	chr5:145485183-145485184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564291105	chr5:145485268-145485269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535749090	chr5:145485285-145485286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533396995	chr5:145485381-145485382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540518029	chr5:145485386-145485387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs142634158	chr5:145485467-145485468	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs190863193	chr5:145485500-145485501	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs575071374	chr5:145485505-145485506	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs67350755	chr5:145485547-145485548	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs569251289	chr5:145485556-145485557	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs531671944	chr5:145485595-145485596	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs376637257	chr5:145485634-145485635	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs551908966	chr5:145485664-145485665	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs150951659	chr5:145485888-145485889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555359435	chr5:145485966-145485967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534011452	chr5:145485977-145485978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146394385	chr5:145485979-145485980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567537655	chr5:145485982-145485983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370771724	chr5:145486033-145486034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536561288	chr5:145486072-145486073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145755120	chr5:145486126-145486127	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147773270	chr5:145486132-145486133	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs575989102	chr5:145486151-145486152	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs376826586	chr5:145486215-145486216	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs538355593	chr5:145486231-145486232	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs558274920	chr5:145486239-145486240	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs369250225	chr5:145486288-145486289	Weak transcription	TF binding 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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:535 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145459800-145492000	Weak transcription	HSMMtube	muscle
2	chr5:145469600-145492000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr5:145471800-145492600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:145473600-145491400	Weak transcription	Fetal Brain Female	brain
5	chr5:145474000-145491600	Weak transcription	Primary B cells from cord blood	blood
6	chr5:145474200-145491000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:145474400-145492200	Weak transcription	Brain Angular Gyrus	brain
8	chr5:145474600-145491000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr5:145475000-145495800	Weak transcription	Brain Substantia Nigra	brain
10	chr5:145475200-145491000	Weak transcription	A549	lung
11	chr5:145475200-145491800	Weak transcription	Primary T cells from cord blood	blood
12	chr5:145478000-145487800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:145478000-145492600	Weak transcription	Fetal Stomach	stomach
14	chr5:145478200-145497600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr5:145478400-145491200	Weak transcription	Brain Anterior Caudate	brain
16	chr5:145478400-145492800	Weak transcription	Brain Hippocampus Middle	brain
17	chr5:145478400-145493400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr5:145478400-145497600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr5:145478800-145492600	Weak transcription	Fetal Intestine Small	intestine
20	chr5:145480200-145494000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr5:145481200-145493800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr5:145481200-145560200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr5:145481400-145489200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr5:145481400-145491000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:145481600-145498400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr5:145481800-145491200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:145481800-145492000	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr5:145482000-145491600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr5:145482200-145484400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr5:145482200-145491800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr5:145482200-145497600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr5:145482200-145497800	Weak transcription	Brain Germinal Matrix	brain
33	chr5:145482200-145500800	Weak transcription	Aorta	Aorta
34	chr5:145482400-145491000	Weak transcription	Hela-S3	cervix
35	chr5:145482400-145491400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr5:145482400-145491600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr5:145482400-145497800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr5:145482600-145491400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:145482600-145492200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr5:145482600-145492400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr5:145482600-145501200	Weak transcription	Thymus	Thymus
42	chr5:145482800-145491400	Weak transcription	Adipose Nuclei	Adipose
43	chr5:145482800-145491600	Weak transcription	HUVEC	blood vessel
44	chr5:145482800-145491800	Weak transcription	Primary T cells fromperipheralblood	blood
45	chr5:145482800-145492600	Weak transcription	Pancreas	Pancrea
46	chr5:145482800-145492800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr5:145483000-145491400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:145483000-145491400	Weak transcription	Liver	Liver
49	chr5:145483000-145492000	Weak transcription	Left Ventricle	heart
50	chr5:145483000-145493600	Weak transcription	Stomach Smooth Muscle	stomach

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