Variant report

Variant	esv3401381
Chromosome Location	chr5:14402002-14404800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:92)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:92 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:14403862-14403864	GM19239	blood:	n/a	n/a
2	CTCF	chr5:14404111-14404115	GM19239	blood:	n/a	n/a
3	CTCF	chr5:14404038-14404041	GM19239	blood:	n/a	n/a
4	CTCF	chr5:14403850-14403861	GM19239	blood:	n/a	n/a
5	CTCF	chr5:14404119-14404161	GM19239	blood:	n/a	n/a
6	CTCF	chr5:14403867-14404024	GM19239	blood:	n/a	n/a
7	CTCF	chr5:14403720-14403870	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr5:14403522-14403627	GM19239	blood:	n/a	n/a
9	EBF1	chr5:14403659-14404106	GM12878	blood:	n/a	n/a
10	EBF1	chr5:14403666-14404256	GM12878	blood:	n/a	n/a
11	EP300	chr5:14401422-14402214	SK-N-SH_RA	brain:	n/a	n/a
12	EP300	chr5:14401448-14402148	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr5:14401339-14402263	SK-N-SH	brain:	n/a	n/a
14	EP300	chr5:14398890-14402705	SK-N-SH	brain:	n/a	chr5:14400674-14400681
15	GATA2	chr5:14401499-14402120	SH-SY5Y	brain:	n/a	n/a
16	GATA3	chr5:14401366-14402323	SK-N-SH	brain:	n/a	n/a
17	GATA3	chr5:14401751-14402082	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr5:14401375-14402357	SK-N-SH	brain:	n/a	n/a
19	IRF4	chr5:14403513-14404152	GM12878	blood:	n/a	n/a
20	JUND	chr5:14397332-14402457	SK-N-SH	brain:	n/a	chr5:14398493-14398507 chr5:14400452-14400461 chr5:14398516-14398530 chr5:14399615-14399622
21	MXI1	chr5:14398320-14402661	SK-N-SH	brain:	n/a	n/a
22	MYC	chr5:14403988-14404218	MCF-7	breast:	n/a	n/a
23	MYC	chr5:14402603-14402760	H1-hESC	embryonic stem cell:	n/a	n/a
24	MYC	chr5:14404237-14404258	GM12878	blood:	n/a	n/a
25	MYC	chr5:14403309-14403586	MCF-7	breast:	n/a	n/a
26	MYC	chr5:14403589-14403961	MCF-7	breast:	n/a	n/a
27	NFIC	chr5:14401493-14402327	SK-N-SH	brain:	n/a	n/a
28	PAX5	chr5:14403633-14404114	GM12878	blood:	n/a	n/a
29	PAX5	chr5:14403166-14404310	GM12878	blood:	n/a	n/a
30	PAX5	chr5:14403150-14403602	GM12878	blood:	n/a	n/a
31	PAX5	chr5:14403663-14404022	GM12878	blood:	n/a	n/a
32	PBX3	chr5:14401404-14402257	SK-N-SH	brain:	n/a	n/a
33	PBX3	chr5:14401438-14402263	SK-N-SH	brain:	n/a	n/a
34	PBX3	chr5:14403701-14403880	GM12878	blood:	n/a	n/a
35	POLR2A	chr5:14403152-14404202	GM12891	blood:	n/a	n/a
36	POLR2A	chr5:14403626-14403671	MCF-7	breast:	n/a	n/a
37	POLR2A	chr5:14403051-14403144	GM12878	blood:	n/a	n/a
38	POLR2A	chr5:14401635-14402112	SK-N-SH	brain:	n/a	n/a
39	POLR2A	chr5:14402597-14404326	GM12892	blood:	n/a	n/a
40	POLR2A	chr5:14403162-14403232	GM12878	blood:	n/a	n/a
41	POLR2A	chr5:14403438-14404311	HepG2	liver:	n/a	n/a
42	POLR2A	chr5:14403102-14403153	ProgFib	skin:	n/a	n/a
43	POLR2A	chr5:14403629-14403993	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr5:14401471-14402253	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr5:14403052-14404213	GM12878	blood:	n/a	n/a
46	POLR2A	chr5:14403059-14403281	HepG2	liver:	n/a	n/a
47	POLR2A	chr5:14403166-14403231	ProgFib	skin:	n/a	n/a
48	POLR2A	chr5:14403677-14403709	MCF-7	breast:	n/a	n/a
49	POLR2A	chr5:14403091-14403100	ProgFib	skin:	n/a	n/a
50	POLR2A	chr5:14403806-14403827	MCF-7	breast:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:14400585..14402209-chr5:14407795..14410766,2	MCF-7	breast:
2	chr5:13976900..13977474-chr5:14404551..14405480,2	MCF-7	breast:
3	chr5:14399431..14402316-chr5:14403363..14405249,2	K562	blood:
4	chr5:14399431..14402316-chr5:14403363..14405249,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM105A-8	chr5:14402511-14403249	NONHSAT100538
2	lnc-FAM105A-8	chr5:14402511-14403249	NONHSAT100537
3	lnc-FAM105A-8	chr5:14404136-14404156	NONHSAT100537
4	lnc-FAM105A-8	chr5:14404211-14404315	NONHSAT100537
5	lnc-FAM105A-8	chr5:14404211-14404315	NONHSAT100538
6	lnc-FAM105A-8	chr5:14403419-14403439	NONHSAT100535
7	lnc-FAM105A-8	chr5:14402511-14403249	NONHSAT100535
8	lnc-FAM105A-8	chr5:14403671-14403691	NONHSAT100538
9	lnc-FAM105A-8	chr5:14402511-14403249	NONHSAT100536
10	lnc-FAM105A-8	chr5:14404118-14404434	NONHSAT100534
11	lnc-FAM105A-8	chr5:14402179-14403231	NONHSAT100534
12	lnc-FAM105A-8	chr5:14403290-14403418	NONHSAT100534
13	lnc-FAM105A-8	chr5:14404211-14404315	NONHSAT100536
14	lnc-FAM105A-8	chr5:14404211-14404315	NONHSAT100535
15	lnc-FAM105A-8	chr5:14403398-14403418	NONHSAT100536

No data

Variant related genes	Relation type
TRIO	TF binding region

Extended variants
information (count: 132 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529392624	chr5:14402029-14402030	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs77520462	chr5:14402036-14402037	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs199855241	chr5:14402059-14402060	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs556443605	chr5:14402072-14402073	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs566295879	chr5:14402139-14402140	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs539625947	chr5:14402162-14402163	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs35916035	chr5:14402185-14402186	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs558447781	chr5:14402206-14402207	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs11957060	chr5:14402230-14402231	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs555357518	chr5:14402237-14402238	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs192655836	chr5:14402322-14402323	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs143522898	chr5:14402329-14402330	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs368315135	chr5:14402346-14402347	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs552780120	chr5:14402362-14402363	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs577787665	chr5:14402365-14402366	Weak transcription Strong transcription Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs115182951	chr5:14402414-14402415	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs563606266	chr5:14402434-14402435	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs530667364	chr5:14402435-14402436	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs565134505	chr5:14402438-14402439	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs532625085	chr5:14402480-14402481	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs561786124	chr5:14402550-14402551	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs72748244	chr5:14402553-14402554	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs182674560	chr5:14402599-14402600	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs16899020	chr5:14402621-14402622	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs533589316	chr5:14402660-14402661	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs11957857	chr5:14402681-14402682	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs117148403	chr5:14402687-14402688	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs537791168	chr5:14402714-14402715	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs542322132	chr5:14402739-14402740	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs199710818	chr5:14402805-14402806	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs549690884	chr5:14402830-14402831	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs567306624	chr5:14402858-14402859	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs13356126	chr5:14402871-14402872	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553046919	chr5:14402944-14402945	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs140991538	chr5:14402948-14402949	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs573915008	chr5:14402971-14402972	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs577622525	chr5:14403001-14403002	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs538827153	chr5:14403009-14403010	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs556923011	chr5:14403053-14403054	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs544368692	chr5:14403061-14403062	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs575085641	chr5:14403114-14403115	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs199688684	chr5:14403126-14403127	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs559373706	chr5:14403156-14403157	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs200608558	chr5:14403159-14403160	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs146720545	chr5:14403163-14403164	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs568985942	chr5:14403181-14403182	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs567298862	chr5:14403199-14403200	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs201596730	chr5:14403219-14403220	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs376764284	chr5:14403229-14403230	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs533438586	chr5:14403235-14403236	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Breast cancer	21364760	CNVD
Non-small cell lung cancer	17643093	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	18940311	CNVD
Central neurocytomas	17123091	CNVD
Mental retardation	17847001	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	19546859	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Williams Syndrome	20824207	CNVD
Intracranial aneurysm	16715129	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14354600-14402400	Strong transcription	Liver	Liver
2	chr5:14357600-14422000	Weak transcription	Stomach Mucosa	stomach
3	chr5:14363800-14430600	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr5:14363800-14430600	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr5:14366800-14403200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr5:14380400-14402800	Strong transcription	Primary B cells from peripheral blood	blood
7	chr5:14387200-14405800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:14388000-14402200	Strong transcription	HUES48 Cell Line	embryonic stem cell
9	chr5:14388600-14402600	Strong transcription	Fetal Intestine Large	intestine
10	chr5:14388800-14407200	Weak transcription	Small Intestine	intestine
11	chr5:14392200-14402600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr5:14392200-14406600	Weak transcription	Primary T cells from cord blood	blood
13	chr5:14392400-14406000	Weak transcription	Fetal Heart	heart
14	chr5:14392400-14426800	Weak transcription	Psoas Muscle	Psoas
15	chr5:14392600-14403600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr5:14393200-14402800	Strong transcription	Placenta	Placenta
17	chr5:14393400-14402400	Strong transcription	GM12878-XiMat	blood
18	chr5:14393400-14403200	Strong transcription	Duodenum Smooth Muscle	Duodenum
19	chr5:14393600-14413600	Strong transcription	Primary B cells from cord blood	blood
20	chr5:14393800-14403000	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr5:14394400-14405200	Strong transcription	Fetal Intestine Small	intestine
22	chr5:14394600-14402200	Genic enhancers	NHLF	lung
23	chr5:14395200-14406600	Weak transcription	Fetal Kidney	kidney
24	chr5:14395600-14402200	Genic enhancers	HSMM	muscle
25	chr5:14395800-14406000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr5:14395800-14406000	Weak transcription	Brain Substantia Nigra	brain
27	chr5:14396200-14402200	Genic enhancers	Muscle Satellite Cultured Cells	--
28	chr5:14397400-14402600	Weak transcription	Gastric	stomach
29	chr5:14397400-14402600	Weak transcription	Pancreas	Pancrea
30	chr5:14397400-14405400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr5:14397600-14402400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr5:14397600-14405200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:14397600-14405600	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr5:14397600-14406200	Weak transcription	Brain Hippocampus Middle	brain
35	chr5:14397800-14402600	Weak transcription	Brain Angular Gyrus	brain
36	chr5:14397800-14402800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr5:14398200-14406000	Weak transcription	Thymus	Thymus
38	chr5:14398400-14404800	Weak transcription	Ovary	ovary
39	chr5:14398400-14406000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr5:14398600-14405200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr5:14398600-14405200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr5:14398600-14406000	Weak transcription	Esophagus	oesophagus
43	chr5:14398800-14406200	Weak transcription	Aorta	Aorta
44	chr5:14399000-14419800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr5:14399400-14402200	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr5:14399600-14403200	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr5:14399600-14403200	Strong transcription	Rectal Mucosa Donor 31	rectum
48	chr5:14399600-14416400	Strong transcription	Duodenum Mucosa	Duodenum
49	chr5:14399800-14403000	Strong transcription	Brain Germinal Matrix	brain
50	chr5:14399800-14403200	Strong transcription	HepG2	liver

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