Variant report

Variant	nsv968168
Chromosome Location	chr5:37443092-37487412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr5:37471796-37472190	K562	blood:	n/a	n/a
2	CBX3	chr5:37481023-37481289	K562	blood:	n/a	n/a
3	CBX3	chr5:37481486-37481876	K562	blood:	n/a	n/a
4	CBX3	chr5:37480974-37481326	K562	blood:	n/a	n/a
5	CBX3	chr5:37453412-37453631	K562	blood:	n/a	n/a
6	CEBPB	chr5:37480989-37481283	K562	blood:	n/a	n/a
7	CEBPB	chr5:37463551-37463849	K562	blood:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
8	CEBPB	chr5:37444823-37445171	A549	lung:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
9	CEBPB	chr5:37463652-37463834	IMR90	lung:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
10	CEBPB	chr5:37444819-37445115	HepG2	liver:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
11	CEBPB	chr5:37463617-37463777	MCF-7	breast:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
12	CEBPB	chr5:37481844-37481981	K562	blood:	n/a	chr5:37481876-37481887
13	CEBPB	chr5:37444992-37445006	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr5:37444828-37445104	IMR90	lung:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
15	CEBPB	chr5:37480974-37481250	K562	blood:	n/a	n/a
16	CEBPB	chr5:37474447-37474554	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:37463538-37463865	HepG2	liver:	n/a	chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463703 chr5:37463692-37463701 chr5:37463690-37463701 chr5:37463692-37463701 chr5:37463691-37463702 chr5:37463692-37463701
18	CEBPB	chr5:37481844-37481867	HepG2	liver:	n/a	n/a
19	CEBPD	chr5:37480945-37481331	K562	blood:	n/a	n/a
20	CTCF	chr5:37464760-37464910	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr5:37464860-37464981	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:37464760-37464910	A549	lung:	n/a	n/a
23	CTCF	chr5:37464760-37464910	AG09319	gingival:	n/a	n/a
24	CTCF	chr5:37464760-37464910	NHLF	lung:	n/a	n/a
25	CTCF	chr5:37464854-37464911	Fibrobl	skin:	n/a	n/a
26	CTCF	chr5:37464860-37465010	AG10803	skin:	n/a	n/a
27	CTCF	chr5:37464746-37464952	K562	blood:	n/a	n/a
28	CTCF	chr5:37464760-37464910	HCPEpiC	choroid plexus:	n/a	n/a
29	CTCF	chr5:37464800-37464950	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr5:37464760-37464910	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr5:37464760-37464910	HepG2	liver:	n/a	n/a
32	CTCF	chr5:37464980-37465130	NHLF	lung:	n/a	n/a
33	CTCF	chr5:37445131-37445166	GM13976	blood:	n/a	n/a
34	CTCF	chr5:37480910-37481430	K562	blood:	n/a	n/a
35	CTCF	chr5:37464760-37464910	MCF-7	breast:	n/a	n/a
36	CTCF	chr5:37481065-37481291	K562	blood:	n/a	n/a
37	CTCF	chr5:37464760-37464910	HCFaa	heart:	n/a	n/a
38	CTCF	chr5:37464780-37464930	AG04450	lung:	n/a	n/a
39	CTCF	chr5:37464780-37464930	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:37464740-37464890	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr5:37464743-37464950	T-47D	breast:	n/a	n/a
42	CTCF	chr5:37464883-37464948	A549	lung:	n/a	n/a
43	CTCF	chr5:37464740-37464890	HVMF	connective:	n/a	n/a
44	CTCF	chr5:37481057-37481370	K562	blood:	n/a	n/a
45	CTCF	chr5:37448377-37448433	Medullo	brain:	n/a	n/a
46	CTCF	chr5:37464760-37464910	AG09309	skin:	n/a	n/a
47	CTCF	chr5:37468277-37468303	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr5:37464760-37464910	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr5:37468604-37468672	LNCaP	prostate:	n/a	n/a
50	CTCF	chr5:37464760-37464910	HMF	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37484025-37484075	ovcar-3	ovarian:	n/a
2	chr5:37484025-37484075	NHBE	bronchial:	n/a
3	chr5:37484025-37484075	MCF-7	breast:	n/a
4	chr5:37484025-37484075	AG09309	skin:	n/a
5	chr5:37484025-37484075	SKMC	muscle:	n/a
6	chr5:37484025-37484075	HCF	heart:	n/a
7	chr5:37484025-37484075	PANC-1	pancreas:	n/a
8	chr5:37484025-37484075	RPTEC	kidney:	n/a
9	chr5:37484025-37484075	HIPEpiC	eye:	n/a
10	chr5:37484025-37484075	HCT-116	colon:	n/a
11	chr5:37484025-37484075	AG04450	lung:	fetal
12	chr5:37484025-37484075	HEEpiC	esophagus:	n/a
13	chr5:37484025-37484075	HRE	kidney:	n/a
14	chr5:37484025-37484075	HRPEpiC	eye:	n/a
15	chr5:37484025-37484075	ECC-1	luminal epithelium:	n/a
16	chr5:37484025-37484075	HUVEC	blood vessel:	n/a
17	chr5:37484025-37484075	SK-N-SH_RA	brain:	n/a
18	chr5:37484025-37484075	GM12892	blood:	n/a
19	chr5:37484025-37484075	A549	lung:	n/a
20	chr5:37484025-37484075	NT2-D1	testis:	n/a
21	chr5:37484025-37484075	BJ	skin:	n/a
22	chr5:37484025-37484075	Jurkat	blood:	n/a
23	chr5:37484025-37484075	Hela-S3	cervix:	n/a
24	chr5:37484025-37484075	Caco-2	colon:	n/a
25	chr5:37484025-37484075	AoSMC	blood vessel:	n/a
26	chr5:37484025-37484075	NH-A	brain:	n/a
27	chr5:37484025-37484075	ProgFib	skin:	n/a
28	chr5:37484025-37484075	BE2_C	brain:	n/a
29	chr5:37484025-37484075	Hepatocyte	liver:	n/a
30	chr5:37484025-37484075	T-47D	breast:	n/a
31	chr5:37484025-37484075	HRCEpiC	kidney:	n/a
32	chr5:37484025-37484075	HCM	heart:	n/a
33	chr5:37484025-37484075	HNPCEpiC	eye:	n/a
34	chr5:37484025-37484075	HL-60	blood:	n/a
35	chr5:37484025-37484075	AG09319	gingival:	n/a
36	chr5:37484025-37484075	LNCaP	prostate:	n/a
37	chr5:37484025-37484075	SK-N-MC	brain:	n/a
38	chr5:37484025-37484075	NB4	blood:	n/a
39	chr5:37484025-37484075	SK-N-SH	brain:	n/a
40	chr5:37484025-37484075	HAEpiC	amniotic membrane:	n/a
41	chr5:37484025-37484075	NHDF-neo	bronchial:	n/a
42	chr5:37484025-37484075	HepG2	liver:	n/a
43	chr5:37484025-37484075	AG04449	skin:	fetal
44	chr5:37484025-37484075	HEK293	kidney:	embryo
45	chr5:37484025-37484075	IMR90	lung:	fetal
46	chr5:37484025-37484075	CMK	blood:	n/a
47	chr5:37484025-37484075	GM06990	blood:	n/a
48	chr5:37484025-37484075	U87	brain:	n/a
49	chr5:37484025-37484075	HCPEpiC	choroid plexus:	n/a
50	chr5:37484025-37484075	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
2	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
3	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:

Variant related genes	Relation type
WDR70	TF binding region
WDR70	CpG island
ENSG00000082068	chromatin interactions

Extended variants
information (count: 1777 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533844245	chr5:37443146-37443147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558953689	chr5:37443154-37443155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577179872	chr5:37443219-37443220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370394243	chr5:37443243-37443244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190306134	chr5:37443296-37443297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs538194491	chr5:37443297-37443298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs35474582	chr5:37443308-37443309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182909357	chr5:37443310-37443311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs574953219	chr5:37443311-37443312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373300358	chr5:37443315-37443316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186875757	chr5:37443325-37443326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369525003	chr5:37443397-37443398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145897756	chr5:37443401-37443402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs572817415	chr5:37443403-37443404	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373456220	chr5:37443436-37443437	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112033041	chr5:37443453-37443454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200523361	chr5:37443456-37443457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369210929	chr5:37443457-37443458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564753208	chr5:37443469-37443470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376355975	chr5:37443476-37443477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370460677	chr5:37443489-37443490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191778579	chr5:37443494-37443495	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376924895	chr5:37443513-37443514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6451319	chr5:37443518-37443519	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs77042649	chr5:37443561-37443562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183124259	chr5:37443576-37443577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187815028	chr5:37443582-37443583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192498301	chr5:37443592-37443593	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527444006	chr5:37443602-37443603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs552193737	chr5:37443614-37443615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570698178	chr5:37443624-37443625	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563966162	chr5:37443634-37443635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58999463	chr5:37443648-37443649	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556583597	chr5:37443680-37443681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371059152	chr5:37443681-37443682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185676456	chr5:37443712-37443713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554266723	chr5:37443721-37443722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572680679	chr5:37443730-37443731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546349113	chr5:37443745-37443746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs189480578	chr5:37443815-37443816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191995829	chr5:37443816-37443817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35743749	chr5:37443831-37443832	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs35326352	chr5:37443872-37443873	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs368204101	chr5:37443895-37443896	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372023094	chr5:37443932-37443933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373363723	chr5:37443960-37443961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568117817	chr5:37444060-37444061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151076876	chr5:37444067-37444068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115619554	chr5:37444084-37444085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71604866	chr5:37444103-37444104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Lung cancer	19153074	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Autism	21701786	CNVD
Cervical cancer	16585170	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:781 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37379800-37444400	Weak transcription	Gastric	stomach
2	chr5:37380000-37443400	Weak transcription	Colonic Mucosa	Colon
3	chr5:37380200-37446800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr5:37380200-37446800	Weak transcription	Fetal Brain Male	brain
5	chr5:37380200-37451200	Weak transcription	Right Ventricle	heart
6	chr5:37393200-37451400	Weak transcription	Pancreas	Pancrea
7	chr5:37395400-37447000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr5:37396800-37454600	Weak transcription	A549	lung
9	chr5:37397200-37446600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr5:37401000-37454000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr5:37401200-37452200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:37406200-37451800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr5:37406400-37446800	Weak transcription	Brain Substantia Nigra	brain
14	chr5:37406600-37451800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr5:37406800-37444600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr5:37406800-37451600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:37410600-37471000	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr5:37413000-37457400	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr5:37418000-37457200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr5:37418200-37444000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:37418200-37444400	Weak transcription	Stomach Smooth Muscle	stomach
22	chr5:37418200-37460000	Weak transcription	Brain Angular Gyrus	brain
23	chr5:37418600-37443200	Weak transcription	Dnd41	blood
24	chr5:37419200-37444800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
25	chr5:37419400-37454000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr5:37420800-37480200	Weak transcription	Brain Hippocampus Middle	brain
27	chr5:37421400-37455800	Weak transcription	Fetal Brain Female	brain
28	chr5:37421600-37454000	Weak transcription	NHDF-Ad	bronchial
29	chr5:37421600-37478400	Weak transcription	Aorta	Aorta
30	chr5:37422000-37443400	Weak transcription	Duodenum Mucosa	Duodenum
31	chr5:37424000-37443200	Weak transcription	Adipose Nuclei	Adipose
32	chr5:37424800-37443200	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr5:37424800-37443200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr5:37424800-37444000	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr5:37424800-37463600	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr5:37425400-37443400	Weak transcription	Fetal Muscle Trunk	muscle
37	chr5:37425400-37444600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr5:37425400-37445000	Weak transcription	Thymus	Thymus
39	chr5:37425400-37480200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr5:37425600-37443200	Weak transcription	Cortex derived primary cultured neurospheres	brain
41	chr5:37425600-37446600	Weak transcription	Brain Anterior Caudate	brain
42	chr5:37425600-37446800	Weak transcription	Brain Germinal Matrix	brain
43	chr5:37425600-37451800	Weak transcription	Lung	lung
44	chr5:37425600-37452200	Weak transcription	Spleen	Spleen
45	chr5:37425800-37443400	Weak transcription	Left Ventricle	heart
46	chr5:37425800-37444600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:37425800-37444600	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr5:37425800-37471000	Weak transcription	Fetal Lung	lung
49	chr5:37426000-37443200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr5:37426000-37479800	Weak transcription	HSMM	muscle

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