Variant report

Variant	nsv883267
Chromosome Location	chr5:178925558-178951106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:245)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:245 , 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	ARID3A	chr5:178931255-178932227	HepG2	liver:	n/a	n/a
2	BATF	chr5:178945312-178945640	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:178945316-178945685	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:178932135-178932152	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:178931662-178931840	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:178931609-178932069	HepG2	liver:	n/a	n/a
7	CTCF	chr5:178946506-178946661	GM10266	blood:	n/a	chr5:178946578-178946587
8	CTCF	chr5:178946600-178946750	HPF	lung:	n/a	n/a
9	CTCF	chr5:178936259-178936313	GM20000	blood:	n/a	n/a
10	CTCF	chr5:178946455-178946688	LNCaP	prostate:	n/a	chr5:178946578-178946587
11	CTCF	chr5:178946580-178946730	AG09309	skin:	n/a	n/a
12	CTCF	chr5:178946488-178946623	A549	lung:	n/a	chr5:178946578-178946587
13	CTCF	chr5:178946539-178946565	GM19240	blood:	n/a	n/a
14	CTCF	chr5:178931820-178931970	HRE	kidney:	n/a	n/a
15	CTCF	chr5:178946540-178946690	HVMF	connective:	n/a	chr5:178946578-178946587
16	CTCF	chr5:178946532-178946610	GM20000	blood:	n/a	chr5:178946578-178946587
17	CTCF	chr5:178946486-178946654	Medullo	brain:	n/a	chr5:178946578-178946587
18	CTCF	chr5:178946600-178946750	BJ	skin:	n/a	n/a
19	CTCF	chr5:178946620-178946770	HepG2	liver:	n/a	n/a
20	CTCF	chr5:178931912-178932089	HepG2	liver:	n/a	n/a
21	CTCF	chr5:178946494-178946650	GM10248	blood:	n/a	chr5:178946578-178946587
22	CTCF	chr5:178946450-178946675	K562	blood:	n/a	chr5:178946578-178946587
23	CTCF	chr5:178946548-178946671	HepG2	liver:	n/a	chr5:178946578-178946587
24	CTCF	chr5:178946525-178946613	Fibrobl	skin:	n/a	chr5:178946578-178946587
25	CTCF	chr5:178931920-178932070	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr5:178946463-178946708	LNCaP	prostate:	n/a	chr5:178946578-178946587
27	CTCF	chr5:178945564-178945568	GM12891	blood:	n/a	n/a
28	CTCF	chr5:178944880-178945030	HCT-116	colon:	n/a	n/a
29	CTCF	chr5:178945296-178945336	GM12878	blood:	n/a	n/a
30	CTCF	chr5:178946600-178946750	GM12872	blood:	n/a	n/a
31	CTCF	chr5:178946640-178946790	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr5:178946580-178946730	GM12870	blood:	n/a	n/a
33	CTCF	chr5:178946426-178946757	K562	blood:	n/a	chr5:178946578-178946587
34	CTCF	chr5:178946476-178946677	Pancreas_OC	pancreas:	n/a	chr5:178946578-178946587
35	CTCF	chr5:178946680-178946830	HVMF	connective:	n/a	n/a
36	CTCF	chr5:178946424-178946705	MCF-7	breast:	n/a	chr5:178946578-178946587
37	CTCF	chr5:178946471-178946693	Spleen_OC	spleen:	n/a	chr5:178946578-178946587
38	CTCF	chr5:178946471-178946606	MCF-7	breast:	n/a	chr5:178946578-178946587
39	CTCF	chr5:178946493-178946639	GM19239	blood:	n/a	chr5:178946578-178946587
40	CTCF	chr5:178946620-178946770	GM12878	blood:	n/a	n/a
41	CTCF	chr5:178946436-178946679	K562	blood:	n/a	chr5:178946578-178946587
42	CTCF	chr5:178945553-178945559	GM12891	blood:	n/a	n/a
43	CTCF	chr5:178944900-178945050	HepG2	liver:	n/a	n/a
44	CTCF	chr5:178946640-178946790	A549	lung:	n/a	n/a
45	CTCF	chr5:178944869-178944959	MCF-7	breast:	n/a	n/a
46	CTCF	chr5:178946560-178946710	BJ	skin:	n/a	chr5:178946578-178946587
47	CTCF	chr5:178946468-178946645	HepG2	liver:	n/a	chr5:178946578-178946587
48	CTCF	chr5:178946480-178946641	GM13976	blood:	n/a	chr5:178946578-178946587
49	CTCF	chr5:178946560-178946710	Hela-S3	cervix:	n/a	chr5:178946578-178946587
50	CTCF	chr5:178946600-178946750	HBMEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178950795-178950845	HPAEpiC	pulmonary alveolar:	n/a
2	chr5:178950795-178950845	HPAEpiC	pulmonary alveolar:	n/a
3	chr5:178945540-178945590	BJ	skin:	n/a
4	chr5:178945540-178945590	MCF10A-Er-Src	breast:	n/a
5	chr5:178950795-178950845	HUVEC	blood vessel:	n/a
6	chr5:178945540-178945590	HRCEpiC	kidney:	n/a
7	chr5:178945540-178945590	GM12878	blood:	n/a
8	chr5:178950855-178950905	LNCaP	prostate:	n/a
9	chr5:178945540-178945590	GM06990	blood:	n/a
10	chr5:178950795-178950845	ovcar-3	ovarian:	n/a
11	chr5:178945540-178945590	H1-hESC	embryonic stem cell:	embryo
12	chr5:178945540-178945590	AG04449	skin:	fetal
13	chr5:178950855-178950905	AG10803	skin:	n/a
14	chr5:178950795-178950845	CMK	blood:	n/a
15	chr5:178950795-178950845	HIPEpiC	eye:	n/a
16	chr5:178950855-178950905	SK-N-SH	brain:	n/a
17	chr5:178950855-178950905	PANC-1	pancreas:	n/a
18	chr5:178950855-178950905	MCF-7	breast:	n/a
19	chr5:178950795-178950845	SK-N-MC	brain:	n/a
20	chr5:178945540-178945590	HPAEpiC	pulmonary alveolar:	n/a
21	chr5:178950855-178950905	HCT-116	colon:	n/a
22	chr5:178945540-178945590	IMR90	lung:	fetal
23	chr5:178945540-178945590	T-47D	breast:	n/a
24	chr5:178950795-178950845	GM06990	blood:	n/a
25	chr5:178945540-178945590	HRE	kidney:	n/a
26	chr5:178950855-178950905	A549	lung:	n/a
27	chr5:178945540-178945590	PrEC	prostate:	n/a
28	chr5:178950795-178950845	SKMC	muscle:	n/a
29	chr5:178945540-178945590	ovcar-3	ovarian:	n/a
30	chr5:178950855-178950905	NH-A	brain:	n/a
31	chr5:178950855-178950905	HNPCEpiC	eye:	n/a
32	chr5:178950855-178950905	HRPEpiC	eye:	n/a
33	chr5:178950795-178950845	ECC-1	luminal epithelium:	n/a
34	chr5:178950795-178950845	AG04450	lung:	fetal
35	chr5:178950795-178950845	AG04449	skin:	fetal
36	chr5:178950795-178950845	HMEC	breast:	n/a
37	chr5:178950795-178950845	HCM	heart:	n/a
38	chr5:178945540-178945590	HNPCEpiC	eye:	n/a
39	chr5:178950855-178950905	GM12892	blood:	n/a
40	chr5:178945540-178945590	HCF	heart:	n/a
41	chr5:178950855-178950905	SAEC	small airway:	n/a
42	chr5:178945540-178945590	AG09309	skin:	n/a
43	chr5:178950855-178950905	BJ	skin:	n/a
44	chr5:178950855-178950905	T-47D	breast:	n/a
45	chr5:178945540-178945590	SK-N-SH	brain:	n/a
46	chr5:178950855-178950905	GM06990	blood:	n/a
47	chr5:178950795-178950845	MCF10A-Er-Src	breast:	n/a
48	chr5:178950855-178950905	HMEC	breast:	n/a
49	chr5:178950795-178950845	RPTEC	kidney:	n/a
50	chr5:178950855-178950905	BE2_C	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:178946216..178946980-chr5:179095346..179096018,3	MCF-7	breast:
2	chr5:178923732..178926017-chr5:178977562..178979960,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPH1-2	chr5:178949497-178950926	ENSG00000251657
2	lnc-HNRNPH1-3	chr5:178942465-178942580	ENSG00000253652
3	lnc-RUFY1-4	chr5:178951021-178952136	NONHSAT105587
4	lnc-RUFY1-4	chr5:178949401-178949705	NONHSAT105586
5	lnc-RUFY1-4	chr5:178950418-178950475	NONHSAT105586
6	lnc-RUFY1-4	chr5:178951021-178952136	NONHSAT105586
7	lnc-RUFY1-4	chr5:178950374-178950475	NONHSAT105587
8	lnc-HNRNPH1-3	chr5:178930323-178930741	ENSG00000253652

No data

Variant related genes	Relation type
ENSG00000251545	TF binding region
ENSG00000253652	TF binding region
ENSG00000251545	CpG island
ENSG00000253652	CpG island
ENSG00000176783	chromatin interactions
GAPVD1	miRNA target sites

Extended variants
information (count: 1301 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1301 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10903240	chr5:178925558-178925559	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114026690	chr5:178925561-178925562	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs376576539	chr5:178925586-178925587	Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563617585	chr5:178925615-178925616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530709261	chr5:178925634-178925635	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs370862616	chr5:178925654-178925655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs186533301	chr5:178925720-178925721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368172881	chr5:178925734-178925735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560938463	chr5:178925752-178925753	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs373966731	chr5:178925756-178925757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34054324	chr5:178925805-178925806	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190885685	chr5:178925828-178925829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs183534952	chr5:178925921-178925922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs571150929	chr5:178925925-178925926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566396097	chr5:178925949-178925950	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534675002	chr5:178925950-178925951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs532173307	chr5:178925952-178925953	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551641485	chr5:178925964-178925965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570039019	chr5:178925989-178925990	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188486905	chr5:178926006-178926007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs368448296	chr5:178926016-178926017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs57493603	chr5:178926038-178926039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371918772	chr5:178926084-178926085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112091080	chr5:178926096-178926097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191228547	chr5:178926101-178926102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567380006	chr5:178926161-178926162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374544680	chr5:178926224-178926225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs13173246	chr5:178926360-178926361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577665502	chr5:178926361-178926362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539060826	chr5:178926394-178926395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557271516	chr5:178926450-178926451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187010836	chr5:178926455-178926456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs60261543	chr5:178926484-178926485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs561065231	chr5:178926491-178926492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557070838	chr5:178926505-178926506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371466848	chr5:178926510-178926511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191397363	chr5:178926519-178926520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183578287	chr5:178926555-178926556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565025803	chr5:178926581-178926582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531988199	chr5:178926582-178926583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550180299	chr5:178926588-178926589	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4591737	chr5:178926593-178926594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531117130	chr5:178926600-178926601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4489047	chr5:178926601-178926602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4302571	chr5:178926602-178926603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34902439	chr5:178926604-178926605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs4585433	chr5:178926608-178926609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561801748	chr5:178926609-178926610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571741923	chr5:178926626-178926627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539006829	chr5:178926631-178926632	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

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
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	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
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178913800-178935200	Weak transcription	Right Atrium	heart
2	chr5:178922200-178931400	Weak transcription	Pancreas	Pancrea
3	chr5:178924600-178925600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr5:178924800-178925600	Enhancers	Fetal Brain Female	brain
5	chr5:178924800-178925600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr5:178924800-178925600	Enhancers	NHDF-Ad	bronchial
7	chr5:178925000-178925600	Enhancers	Adipose Nuclei	Adipose
8	chr5:178925200-178925600	Active TSS	Spleen	Spleen
9	chr5:178925400-178925600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:178925400-178925800	Enhancers	Esophagus	oesophagus
11	chr5:178925600-178935000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr5:178926200-178926400	Enhancers	Esophagus	oesophagus
13	chr5:178926200-178926400	Enhancers	Fetal Stomach	stomach
14	chr5:178928600-178931400	Weak transcription	Fetal Stomach	stomach
15	chr5:178931200-178931400	Enhancers	HepG2	liver
16	chr5:178931200-178932400	Enhancers	Liver	Liver
17	chr5:178931200-178932800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:178931400-178931600	Enhancers	Fetal Stomach	stomach
19	chr5:178931400-178931600	Enhancers	Pancreas	Pancrea
20	chr5:178931400-178931800	Enhancers	Fetal Kidney	kidney
21	chr5:178931400-178932800	Flanking Active TSS	HepG2	liver
22	chr5:178931600-178931800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:178931600-178931800	Enhancers	Fetal Lung	lung
24	chr5:178931600-178932000	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr5:178931600-178932200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:178931600-178935200	Weak transcription	Fetal Stomach	stomach
27	chr5:178931800-178933000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:178931800-178936000	Weak transcription	Fetal Kidney	kidney
29	chr5:178931800-178936400	Weak transcription	Fetal Lung	lung
30	chr5:178932800-178933400	Enhancers	HepG2	liver
31	chr5:178933000-178943200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:178933400-178935200	Weak transcription	HepG2	liver
33	chr5:178934600-178936800	Enhancers	Primary B cells from cord blood	blood
34	chr5:178934600-178937000	Enhancers	Primary hematopoietic stem cells short term culture	blood
35	chr5:178934800-178935000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr5:178934800-178935000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:178934800-178935200	Active TSS	Monocytes-CD14+_RO01746	blood
38	chr5:178934800-178936400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr5:178934800-178937000	Enhancers	Primary hematopoietic stem cells	blood
40	chr5:178935000-178935400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
41	chr5:178935000-178935400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:178935000-178937000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr5:178935200-178935400	Enhancers	Fetal Stomach	stomach
44	chr5:178935200-178935400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr5:178935200-178935600	Enhancers	HepG2	liver
46	chr5:178935400-178936000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr5:178935400-178936200	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr5:178935400-178936400	Weak transcription	Fetal Stomach	stomach
49	chr5:178935400-178937200	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr5:178936000-178936800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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