Variant report

Variant	nsv980770
Chromosome Location	chr5:179028114-179030375
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:38)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:38 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:179029260-179029410	GM12871	blood:	n/a	n/a
2	GABPA	chr5:179029253-179029540	K562	blood:	n/a	n/a
3	POLR2A	chr5:179029357-179029514	K562	blood:	n/a	n/a
4	POLR2A	chr5:179028767-179030003	ECC-1	luminal epithelium:	n/a	n/a
5	POLR2A	chr5:179029050-179029910	A549	lung:	n/a	n/a
6	POLR2A	chr5:179029246-179029368	Hela-S3	cervix:	n/a	n/a
7	POLR2A	chr5:179029247-179029521	A549	lung:	n/a	n/a
8	POLR2A	chr5:179028897-179029956	HepG2	liver:	n/a	n/a
9	POLR2A	chr5:179028244-179028356	HepG2	liver:	n/a	n/a
10	POLR2A	chr5:179029195-179029514	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr5:179030336-179030696	A549	lung:	n/a	n/a
12	POLR2A	chr5:179028831-179029509	ECC-1	luminal epithelium:	n/a	n/a
13	POLR2A	chr5:179030336-179030817	A549	lung:	n/a	n/a
14	POLR2A	chr5:179028880-179029074	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr5:179027897-179028114	ECC-1	luminal epithelium:	n/a	n/a
16	POLR2A	chr5:179029236-179029808	GM12878	blood:	n/a	n/a
17	POLR2A	chr5:179029785-179029886	HepG2	liver:	n/a	n/a
18	POLR2A	chr5:179028965-179029042	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr5:179029161-179029566	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr5:179029776-179029959	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr5:179029536-179029546	K562	blood:	n/a	n/a
22	POLR2A	chr5:179029087-179029873	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr5:179030347-179030833	GM12878	blood:	n/a	n/a
24	POLR2A	chr5:179030310-179030823	ECC-1	luminal epithelium:	n/a	n/a
25	POLR2A	chr5:179030243-179030790	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr5:179030284-179030789	PANC-1	pancreas:	n/a	n/a
27	POLR2A	chr5:179027863-179028162	ECC-1	luminal epithelium:	n/a	n/a
28	POLR2A	chr5:179029295-179029557	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr5:179028374-179028398	K562	blood:	n/a	n/a
30	POLR2A	chr5:179029836-179029842	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr5:179029115-179029325	IMR90	lung:	n/a	n/a
32	POLR2A	chr5:179029370-179029496	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr5:179029434-179029585	GM12878	blood:	n/a	n/a
34	POLR2A	chr5:179028202-179028238	HepG2	liver:	n/a	n/a
35	POLR2A	chr5:179030314-179030762	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr5:179028120-179028150	HepG2	liver:	n/a	n/a
37	POLR2A	chr5:179029269-179029679	GM12892	blood:	n/a	n/a
38	POLR2A	chr5:179030153-179030834	ECC-1	luminal epithelium:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179029719-179029769	IMR90	lung:	fetal
2	chr5:179029719-179029769	Jurkat	blood:	n/a
3	chr5:179029719-179029769	HPAEpiC	pulmonary alveolar:	n/a
4	chr5:179029719-179029769	HRE	kidney:	n/a
5	chr5:179029719-179029769	MCF10A-Er-Src	breast:	n/a
6	chr5:179029719-179029769	HRCEpiC	kidney:	n/a
7	chr5:179029719-179029769	HAEpiC	amniotic membrane:	n/a
8	chr5:179029719-179029769	PANC-1	pancreas:	n/a
9	chr5:179029719-179029769	NH-A	brain:	n/a
10	chr5:179029719-179029769	HCPEpiC	choroid plexus:	n/a
11	chr5:179029719-179029769	Caco-2	colon:	n/a
12	chr5:179029719-179029769	NB4	blood:	n/a
13	chr5:179029719-179029769	HIPEpiC	eye:	n/a
14	chr5:179029719-179029769	HepG2	liver:	n/a
15	chr5:179029719-179029769	SKMC	muscle:	n/a
16	chr5:179029719-179029769	A549	lung:	n/a
17	chr5:179029719-179029769	BJ	skin:	n/a
18	chr5:179029719-179029769	GM12892	blood:	n/a
19	chr5:179029719-179029769	CMK	blood:	n/a
20	chr5:179029719-179029769	HUVEC	blood vessel:	n/a
21	chr5:179029719-179029769	MCF-7	breast:	n/a
22	chr5:179029719-179029769	GM19239	blood:	n/a
23	chr5:179029719-179029769	HEK293	kidney:	embryo
24	chr5:179029719-179029769	Hepatocyte	liver:	n/a
25	chr5:179029719-179029769	T-47D	breast:	n/a
26	chr5:179029719-179029769	SK-N-MC	brain:	n/a
27	chr5:179029719-179029769	AG09309	skin:	n/a
28	chr5:179029719-179029769	HRPEpiC	eye:	n/a
29	chr5:179029719-179029769	RPTEC	kidney:	n/a
30	chr5:179029719-179029769	ovcar-3	ovarian:	n/a
31	chr5:179029719-179029769	AG04450	lung:	fetal
32	chr5:179029719-179029769	SK-N-SH_RA	brain:	n/a
33	chr5:179029719-179029769	HNPCEpiC	eye:	n/a
34	chr5:179029719-179029769	U87	brain:	n/a
35	chr5:179029719-179029769	AG04449	skin:	fetal
36	chr5:179029719-179029769	HEEpiC	esophagus:	n/a
37	chr5:179029719-179029769	LNCaP	prostate:	n/a
38	chr5:179029719-179029769	NT2-D1	testis:	n/a
39	chr5:179029719-179029769	AG10803	skin:	n/a
40	chr5:179029719-179029769	HCF	heart:	n/a
41	chr5:179029719-179029769	PFSK-1	brain:	n/a
42	chr5:179029719-179029769	GM06990	blood:	n/a
43	chr5:179029719-179029769	H1-hESC	embryonic stem cell:	embryo
44	chr5:179029719-179029769	HMEC	breast:	n/a
45	chr5:179029719-179029769	GM12891	blood:	n/a
46	chr5:179029719-179029769	Hela-S3	cervix:	n/a
47	chr5:179029719-179029769	ECC-1	luminal epithelium:	n/a
48	chr5:179029719-179029769	GM12878	blood:	n/a
49	chr5:179029719-179029769	BE2_C	brain:	n/a
50	chr5:179029719-179029769	SK-N-SH	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:178975690..178977861-chr5:179029775..179032308,2	K562	blood:
2	chr5:179023716..179025532-chr5:179027753..179029789,2	K562	blood:
3	chr5:179026297..179028558-chr5:179033139..179034878,3	MCF-7	breast:
4	chr5:178999030..179001028-chr5:179028298..179031172,2	MCF-7	breast:
5	chr5:179015557..179018325-chr5:179025854..179028795,2	K562	blood:
6	chr5:179022085..179025563-chr5:179027402..179030728,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRNPH1-1	chr5:179029065-179029267	ENSG00000244945.1
2	lnc-HNRNPH1-1	chr5:179029378-179029773	ENSG00000244945.1

No data

Variant related genes	Relation type
RUFY1	TF binding region
RUFY1	CpG island
ENSG00000176783	chromatin interactions
ENSG00000249140	chromatin interactions

Extended variants
information (count: 117 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:117 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571892760	chr5:179028115-179028116	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs146328821	chr5:179028164-179028165	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs111814142	chr5:179028173-179028174	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs112557024	chr5:179028174-179028175	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538990234	chr5:179028175-179028176	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs56864882	chr5:179028178-179028179	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs575789688	chr5:179028211-179028212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147404218	chr5:179028233-179028234	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555104048	chr5:179028236-179028237	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138431996	chr5:179028238-179028239	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555602511	chr5:179028255-179028256	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs80110417	chr5:179028262-179028263	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs143893801	chr5:179028274-179028275	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12516518	chr5:179028296-179028297	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs577047325	chr5:179028323-179028324	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs76489189	chr5:179028370-179028371	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs541351402	chr5:179028406-179028407	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs544219370	chr5:179028410-179028411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148710431	chr5:179028454-179028455	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs141583131	chr5:179028469-179028470	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs150913454	chr5:179028495-179028496	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs115146337	chr5:179028519-179028520	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs376386722	chr5:179028545-179028546	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs184159458	chr5:179028616-179028617	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs551733178	chr5:179028618-179028619	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs570400954	chr5:179028637-179028638	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539310590	chr5:179028699-179028700	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs374498458	chr5:179028752-179028753	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569387683	chr5:179028771-179028772	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536862114	chr5:179028780-179028781	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555069154	chr5:179028794-179028795	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs573360057	chr5:179028811-179028812	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534318835	chr5:179028813-179028814	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537148767	chr5:179028819-179028820	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs75814169	chr5:179028820-179028821	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs79549521	chr5:179028841-179028842	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs56169514	chr5:179028844-179028845	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs558900377	chr5:179028850-179028851	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577176030	chr5:179028868-179028869	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200571428	chr5:179028881-179028882	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs73809492	chr5:179028889-179028890	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs368354140	chr5:179028899-179028900	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs372903598	chr5:179028914-179028915	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs141042003	chr5:179028919-179028920	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs374496321	chr5:179028940-179028941	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs367784503	chr5:179028941-179028942	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs371382038	chr5:179028943-179028944	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs188712175	chr5:179028961-179028962	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs533376423	chr5:179029001-179029002	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs369463562	chr5:179029009-179029010	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178987200-179040800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:178987600-179045600	Strong transcription	Fetal Intestine Small	intestine
3	chr5:178987800-179031000	Strong transcription	Fetal Muscle Leg	muscle
4	chr5:178987800-179045600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr5:178996800-179034000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
6	chr5:178999800-179034800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:179000000-179034200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:179002200-179045600	Strong transcription	Fetal Intestine Large	intestine
9	chr5:179005000-179032400	Strong transcription	Fetal Muscle Trunk	muscle
10	chr5:179007400-179030200	Strong transcription	Primary B cells from peripheral blood	blood
11	chr5:179007400-179033800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr5:179007400-179034800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:179007400-179035200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:179007400-179035200	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr5:179007400-179037400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr5:179007400-179040200	Strong transcription	Placenta	Placenta
17	chr5:179007400-179045000	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr5:179007600-179034400	Strong transcription	Thymus	Thymus
19	chr5:179008200-179032800	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr5:179010000-179034600	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr5:179010800-179034000	Strong transcription	Fetal Thymus	thymus
22	chr5:179011000-179034200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr5:179011000-179045600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr5:179011200-179030400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
25	chr5:179011200-179034000	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr5:179011200-179039000	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:179011200-179043800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr5:179012000-179031600	Strong transcription	Stomach Smooth Muscle	stomach
29	chr5:179012200-179029800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr5:179012200-179034600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr5:179012200-179035000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr5:179012400-179034000	Strong transcription	Fetal Brain Female	brain
33	chr5:179012400-179036400	Strong transcription	Lung	lung
34	chr5:179012600-179032200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr5:179012600-179032200	Strong transcription	Liver	Liver
36	chr5:179012600-179037600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr5:179012600-179047000	Strong transcription	H1 Cell Line	embryonic stem cell
38	chr5:179012800-179031000	Strong transcription	Spleen	Spleen
39	chr5:179012800-179031600	Strong transcription	Adipose Nuclei	Adipose
40	chr5:179012800-179032400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr5:179012800-179034600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr5:179012800-179039000	Strong transcription	Left Ventricle	heart
43	chr5:179012800-179040000	Strong transcription	Duodenum Mucosa	Duodenum
44	chr5:179013000-179034200	Strong transcription	Primary T cells from cord blood	blood
45	chr5:179013600-179037800	Strong transcription	Fetal Stomach	stomach
46	chr5:179013800-179031600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr5:179013800-179035400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:179013800-179044800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr5:179014000-179042000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr5:179014000-179044400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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