Variant report

Variant	esv3429404
Chromosome Location	chr5:1590952-1594050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:245)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr5:1591739-1592078	GM12878	blood:	n/a	n/a
2	CTCF	chr5:1593360-1593510	HPAF	blood vessel:	n/a	n/a
3	HCFC1	chr5:1593989-1595151	Hela-S3	cervix:	n/a	n/a
4	HEY1	chr5:1593831-1594757	K562	blood:	n/a	n/a
5	HEY1	chr5:1593757-1595375	HepG2	liver:	n/a	n/a
6	MTA3	chr5:1593943-1594999	GM12878	blood:	n/a	n/a
7	MYC	chr5:1591662-1591735	HUVEC	blood vessel:	n/a	n/a
8	NR2F2	chr5:1594014-1595192	MCF-7	breast:	n/a	n/a
9	PBX3	chr5:1591775-1592046	GM12878	blood:	n/a	n/a
10	PBX3	chr5:1592282-1592450	GM12878	blood:	n/a	n/a
11	POLR2A	chr5:1593811-1595004	GM12878	blood:	n/a	n/a
12	POLR2A	chr5:1592115-1592347	GM12878	blood:	n/a	n/a
13	POLR2A	chr5:1593754-1594250	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr5:1593574-1595153	HepG2	liver:	n/a	n/a
15	POLR2A	chr5:1593329-1593398	HepG2	liver:	n/a	n/a
16	POLR2A	chr5:1593687-1595340	GM12878	blood:	n/a	n/a
17	POLR2A	chr5:1593237-1593262	HepG2	liver:	n/a	n/a
18	POLR2A	chr5:1593033-1593607	GM12878	blood:	n/a	n/a
19	POLR2A	chr5:1591814-1591829	HepG2	liver:	n/a	n/a
20	POLR2A	chr5:1592279-1592365	K562	blood:	n/a	n/a
21	POLR2A	chr5:1593842-1594146	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr5:1593215-1593453	GM12878	blood:	n/a	n/a
23	POLR2A	chr5:1593733-1594929	GM12891	blood:	n/a	n/a
24	POLR2A	chr5:1592162-1592392	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr5:1592751-1592932	HepG2	liver:	n/a	n/a
26	POLR2A	chr5:1591593-1591681	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr5:1593846-1595062	GM12878	blood:	n/a	n/a
28	POLR2A	chr5:1592151-1592354	HepG2	liver:	n/a	n/a
29	POLR2A	chr5:1592575-1593577	GM12892	blood:	n/a	n/a
30	POLR2A	chr5:1593627-1595019	GM12892	blood:	n/a	n/a
31	POLR2A	chr5:1591962-1591982	K562	blood:	n/a	n/a
32	POLR2A	chr5:1593752-1594097	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr5:1591770-1592551	GM12878	blood:	n/a	n/a
34	POLR2A	chr5:1592112-1592357	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr5:1593725-1594142	GM12891	blood:	n/a	n/a
36	POLR2A	chr5:1592704-1592947	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr5:1593747-1594051	GM12878	blood:	n/a	n/a
38	POLR2A	chr5:1591882-1592052	HepG2	liver:	n/a	n/a
39	POLR2A	chr5:1591995-1592044	K562	blood:	n/a	n/a
40	POLR2A	chr5:1591858-1592002	GM12878	blood:	n/a	n/a
41	POLR2A	chr5:1592104-1592475	HepG2	liver:	n/a	n/a
42	POLR2A	chr5:1593785-1594169	GM12892	blood:	n/a	n/a
43	POLR2A	chr5:1592739-1592989	GM12878	blood:	n/a	n/a
44	POLR2A	chr5:1591635-1592503	GM12892	blood:	n/a	n/a
45	POLR2A	chr5:1593680-1595156	GM12892	blood:	n/a	n/a
46	TAF1	chr5:1593820-1595043	HepG2	liver:	n/a	n/a
47	TCF12	chr5:1593801-1593992	GM12878	blood:	n/a	n/a
48	TCF3	chr5:1592131-1592452	GM12878	blood:	n/a	chr5:1592139-1592148
49	TCF3	chr5:1593846-1594079	GM12878	blood:	n/a	n/a
50	TCF3	chr5:1591747-1592110	GM12878	blood:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:1591904-1591954	CMK	blood:	n/a
2	chr5:1591904-1591954	CMK	blood:	n/a
3	chr5:1591904-1591954	BJ	skin:	n/a
4	chr5:1594021-1594071	SKMC	muscle:	n/a
5	chr5:1591904-1591954	LNCaP	prostate:	n/a
6	chr5:1591977-1592027	SK-N-SH_RA	brain:	n/a
7	chr5:1594021-1594071	SK-N-SH_RA	brain:	n/a
8	chr5:1594021-1594071	GM06990	blood:	n/a
9	chr5:1591929-1591979	BJ	skin:	n/a
10	chr5:1591929-1591979	RPTEC	kidney:	n/a
11	chr5:1594021-1594071	Caco-2	colon:	n/a
12	chr5:1591929-1591979	GM12891	blood:	n/a
13	chr5:1591977-1592027	HIPEpiC	eye:	n/a
14	chr5:1594021-1594071	LNCaP	prostate:	n/a
15	chr5:1594021-1594071	HUVEC	blood vessel:	n/a
16	chr5:1591977-1592027	HepG2	liver:	n/a
17	chr5:1591904-1591954	SK-N-SH	brain:	n/a
18	chr5:1591977-1592027	ovcar-3	ovarian:	n/a
19	chr5:1594021-1594071	HEK293	kidney:	embryo
20	chr5:1594021-1594071	SK-N-SH	brain:	n/a
21	chr5:1591977-1592027	HPAEpiC	pulmonary alveolar:	n/a
22	chr5:1594021-1594071	Hepatocyte	liver:	n/a
23	chr5:1594021-1594071	U87	brain:	n/a
24	chr5:1591929-1591979	HMEC	breast:	n/a
25	chr5:1591977-1592027	NB4	blood:	n/a
26	chr5:1591904-1591954	Jurkat	blood:	n/a
27	chr5:1591904-1591954	GM12891	blood:	n/a
28	chr5:1591977-1592027	LNCaP	prostate:	n/a
29	chr5:1594021-1594071	CMK	blood:	n/a
30	chr5:1591929-1591979	AG04449	skin:	fetal
31	chr5:1594021-1594071	MCF-7	breast:	n/a
32	chr5:1591977-1592027	GM19239	blood:	n/a
33	chr5:1591929-1591979	T-47D	breast:	n/a
34	chr5:1591929-1591979	SK-N-SH_RA	brain:	n/a
35	chr5:1591904-1591954	HCPEpiC	choroid plexus:	n/a
36	chr5:1594021-1594071	NHBE	bronchial:	n/a
37	chr5:1591977-1592027	HMEC	breast:	n/a
38	chr5:1594021-1594071	Jurkat	blood:	n/a
39	chr5:1591904-1591954	SAEC	small airway:	n/a
40	chr5:1594021-1594071	GM12878	blood:	n/a
41	chr5:1591977-1592027	H1-hESC	embryonic stem cell:	embryo
42	chr5:1591977-1592027	SK-N-MC	brain:	n/a
43	chr5:1594021-1594071	AoSMC	blood vessel:	n/a
44	chr5:1591977-1592027	HCT-116	colon:	n/a
45	chr5:1591904-1591954	BE2_C	brain:	n/a
46	chr5:1591977-1592027	HRPEpiC	eye:	n/a
47	chr5:1591977-1592027	AG09309	skin:	n/a
48	chr5:1591904-1591954	K562	blood:	n/a
49	chr5:1591929-1591979	NHDF-neo	bronchial:	n/a
50	chr5:1591904-1591954	NT2-D1	testis:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:1523398..1525514-chr5:1593049..1596124,4	MCF-7	breast:
2	chr5:1521816..1527528-chr5:1592860..1598605,11	MCF-7	breast:

No data

Variant related genes	Relation type
SDHAP3	TF binding region
ENSG00000271119	TF binding region
ENSG00000248126	TF binding region
SDHAP3	CpG island
ENSG00000271119	CpG island
ENSG00000248126	CpG island
ENSG00000153395	chromatin interactions

Extended variants
information (count: 194 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:194 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551807979	chr5:1591009-1591010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs567019261	chr5:1591039-1591040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191068329	chr5:1591040-1591041	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549435906	chr5:1591052-1591053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567701596	chr5:1591062-1591063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs28581205	chr5:1591068-1591069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs544895850	chr5:1591071-1591072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs28756288	chr5:1591092-1591093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75963593	chr5:1591099-1591100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs28696155	chr5:1591100-1591101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556101213	chr5:1591102-1591103	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs577620051	chr5:1591103-1591104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539321763	chr5:1591105-1591106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182359693	chr5:1591116-1591117	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147324735	chr5:1591141-1591142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs28550517	chr5:1591157-1591158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs540098045	chr5:1591172-1591173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561810086	chr5:1591181-1591182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143376293	chr5:1591182-1591183	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544327293	chr5:1591192-1591193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs560502853	chr5:1591218-1591219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531215831	chr5:1591220-1591221	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549815795	chr5:1591241-1591242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560651600	chr5:1591247-1591248	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527883504	chr5:1591269-1591270	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549351746	chr5:1591310-1591311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187859118	chr5:1591323-1591324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs193142802	chr5:1591347-1591348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550127572	chr5:1591359-1591360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs28393207	chr5:1591363-1591364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28475422	chr5:1591365-1591366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538756826	chr5:1591367-1591368	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549886667	chr5:1591377-1591378	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371082831	chr5:1591378-1591379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs70957379	chr5:1591387-1591388	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs60637192	chr5:1591392-1591393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571275812	chr5:1591394-1591395	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56223420	chr5:1591397-1591398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71595061	chr5:1591399-1591400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12054898	chr5:1591404-1591405	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551301294	chr5:1591423-1591424	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35447962	chr5:1591424-1591425	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs55727355	chr5:1591440-1591441	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs12054673	chr5:1591472-1591473	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12054861	chr5:1591498-1591499	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148629952	chr5:1591518-1591519	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183325354	chr5:1591538-1591539	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569069139	chr5:1591588-1591589	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373688788	chr5:1591589-1591590	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555223652	chr5:1591602-1591603	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16608533	CNVD
Cervical cancer	16585170	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	17925434	CNVD
Ovarian cancer	20844748	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	21829676	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	19181860	CNVD
prenatal diagnosis	20453657	CNVD
Developmental delay	19490664	CNVD
Human papillomavirus	17975027	CNVD
Acute monocytic leukemia	16498392	CNVD
Gastric cancer	16891809	CNVD
Intracranial aneurysm	16715129	CNVD
Emphysema	19352772	CNVD
Chordoma	18071362	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	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
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21509527	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Oral cancer	22144094	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Developmental delay	21147756	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
Melanoma	22183965	CNVD
Lung adenocarcinoma	17982442	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1565800-1594200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr5:1566200-1594200	Weak transcription	Brain Substantia Nigra	brain
3	chr5:1568000-1594000	Weak transcription	K562	blood
4	chr5:1568400-1594000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr5:1568400-1594000	Weak transcription	Right Ventricle	heart
6	chr5:1568800-1594200	Weak transcription	Brain Hippocampus Middle	brain
7	chr5:1568800-1594200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr5:1569000-1591600	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:1569000-1594000	Weak transcription	HSMM	muscle
10	chr5:1569000-1594200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:1569000-1594200	Weak transcription	Psoas Muscle	Psoas
12	chr5:1569400-1594000	Weak transcription	HSMMtube	muscle
13	chr5:1569400-1594000	Weak transcription	HUVEC	blood vessel
14	chr5:1569400-1594200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:1569600-1594000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
16	chr5:1569600-1594400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr5:1569800-1594000	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr5:1570600-1594000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr5:1571200-1594400	Weak transcription	Stomach Mucosa	stomach
20	chr5:1571400-1594000	Weak transcription	A549	lung
21	chr5:1571800-1594000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:1571800-1594000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr5:1571800-1594000	Weak transcription	Small Intestine	intestine
24	chr5:1572600-1594000	Weak transcription	Placenta	Placenta
25	chr5:1573200-1594200	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr5:1578600-1594000	Weak transcription	Esophagus	oesophagus
27	chr5:1579600-1594000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr5:1579800-1594000	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr5:1582400-1595000	Weak transcription	Fetal Heart	heart
30	chr5:1584400-1594000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr5:1585200-1593400	Weak transcription	Fetal Thymus	thymus
32	chr5:1585200-1593800	Weak transcription	Fetal Brain Male	brain
33	chr5:1585200-1594000	Weak transcription	Fetal Kidney	kidney
34	chr5:1585200-1594000	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr5:1585400-1594000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr5:1585600-1593600	Strong transcription	Fetal Stomach	stomach
37	chr5:1586000-1593800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr5:1586400-1594000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr5:1587200-1592400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:1587400-1591400	Strong transcription	Fetal Muscle Trunk	muscle
41	chr5:1587400-1591800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr5:1587400-1592600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr5:1587400-1593200	Strong transcription	Dnd41	blood
44	chr5:1587400-1593400	Strong transcription	Fetal Intestine Small	intestine
45	chr5:1587600-1592600	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr5:1587800-1592600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:1588000-1591200	Weak transcription	Brain Germinal Matrix	brain
48	chr5:1588000-1592200	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr5:1588000-1593400	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr5:1588000-1594000	Weak transcription	Colon Smooth Muscle	Colon

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