Variant report

Variant	nsv1018722
Chromosome Location	chr5:37438609-37507131
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	chr5:37488479-37488841	K562	blood:	n/a	n/a
2	CBX3	chr5:37471796-37472190	K562	blood:	n/a	n/a
3	CBX3	chr5:37453412-37453631	K562	blood:	n/a	n/a
4	CBX3	chr5:37480974-37481326	K562	blood:	n/a	n/a
5	CBX3	chr5:37481486-37481876	K562	blood:	n/a	n/a
6	CBX3	chr5:37481023-37481289	K562	blood:	n/a	n/a
7	CEBPB	chr5:37444992-37445006	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:37503418-37503494	A549	lung:	n/a	n/a
9	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
10	CEBPB	chr5:37444828-37445104	IMR90	lung:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
11	CEBPB	chr5:37474447-37474554	HepG2	liver:	n/a	n/a
12	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
13	CEBPB	chr5:37444819-37445115	HepG2	liver:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
14	CEBPB	chr5:37481844-37481981	K562	blood:	n/a	chr5:37481876-37481887
15	CEBPB	chr5:37494846-37495179	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr5:37444823-37445171	A549	lung:	n/a	chr5:37444971-37444982 chr5:37445001-37445012
17	CEBPB	chr5:37480989-37481283	K562	blood:	n/a	n/a
18	CEBPB	chr5:37481844-37481867	HepG2	liver:	n/a	n/a
19	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
20	CEBPB	chr5:37493291-37493471	A549	lung:	n/a	n/a
21	CEBPB	chr5:37480974-37481250	K562	blood:	n/a	n/a
22	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
23	CEBPD	chr5:37480945-37481331	K562	blood:	n/a	n/a
24	CHD2	chr5:37489676-37489723	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr5:37495340-37495490	HA-sp	spinal cord:	n/a	chr5:37495448-37495469
26	CTCF	chr5:37495420-37495570	HVMF	connective:	n/a	chr5:37495448-37495469
27	CTCF	chr5:37464780-37464930	AG04450	lung:	n/a	n/a
28	CTCF	chr5:37495335-37495573	MCF-7	breast:	n/a	chr5:37495448-37495469
29	CTCF	chr5:37464780-37464930	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:37506920-37507070	GM12872	blood:	n/a	chr5:37506968-37506977 chr5:37506964-37506977
31	CTCF	chr5:37495380-37495530	AoAF	blood vessel:	n/a	chr5:37495448-37495469
32	CTCF	chr5:37495360-37495510	HBMEC	blood vessel:	n/a	chr5:37495448-37495469
33	CTCF	chr5:37495380-37495530	SAEC	small airway:	n/a	chr5:37495448-37495469
34	CTCF	chr5:37481065-37481291	K562	blood:	n/a	n/a
35	CTCF	chr5:37495120-37495270	GM12874	blood:	n/a	n/a
36	CTCF	chr5:37495420-37495570	AG09319	gingival:	n/a	chr5:37495448-37495469
37	CTCF	chr5:37464760-37464910	HepG2	liver:	n/a	n/a
38	CTCF	chr5:37495340-37495490	HPF	lung:	n/a	chr5:37495448-37495469
39	CTCF	chr5:37495300-37495450	HL-60	blood:	n/a	n/a
40	CTCF	chr5:37495380-37495530	AG04450	lung:	n/a	chr5:37495448-37495469
41	CTCF	chr5:37495560-37495710	AG09309	skin:	n/a	n/a
42	CTCF	chr5:37495295-37495631	IMR90	lung:	n/a	chr5:37495448-37495469
43	CTCF	chr5:37464760-37464910	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:37506920-37507070	K562	blood:	n/a	chr5:37506968-37506977 chr5:37506964-37506977
45	CTCF	chr5:37464746-37464952	K562	blood:	n/a	n/a
46	CTCF	chr5:37464860-37465010	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr5:37495360-37495510	HCT-116	colon:	n/a	chr5:37495448-37495469
48	CTCF	chr5:37495300-37495450	AG09309	skin:	n/a	n/a
49	CTCF	chr5:37495460-37495610	NHEK	skin:	n/a	n/a
50	CTCF	chr5:37464760-37464910	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37484025-37484075	HRE	kidney:	n/a
2	chr5:37484025-37484075	HNPCEpiC	eye:	n/a
3	chr5:37484025-37484075	Hela-S3	cervix:	n/a
4	chr5:37484025-37484075	LNCaP	prostate:	n/a
5	chr5:37484025-37484075	AG10803	skin:	n/a
6	chr5:37484025-37484075	H1-hESC	embryonic stem cell:	embryo
7	chr5:37484025-37484075	IMR90	lung:	fetal
8	chr5:37484025-37484075	RPTEC	kidney:	n/a
9	chr5:37484025-37484075	AG09309	skin:	n/a
10	chr5:37484025-37484075	HAEpiC	amniotic membrane:	n/a
11	chr5:37484025-37484075	NHBE	bronchial:	n/a
12	chr5:37484025-37484075	GM12878	blood:	n/a
13	chr5:37484025-37484075	HUVEC	blood vessel:	n/a
14	chr5:37484025-37484075	SK-N-SH_RA	brain:	n/a
15	chr5:37484025-37484075	GM19239	blood:	n/a
16	chr5:37484025-37484075	NH-A	brain:	n/a
17	chr5:37484025-37484075	CMK	blood:	n/a
18	chr5:37484025-37484075	HIPEpiC	eye:	n/a
19	chr5:37484025-37484075	HCPEpiC	choroid plexus:	n/a
20	chr5:37484025-37484075	K562	blood:	n/a
21	chr5:37484025-37484075	PANC-1	pancreas:	n/a
22	chr5:37484025-37484075	NB4	blood:	n/a
23	chr5:37484025-37484075	AG04449	skin:	fetal
24	chr5:37484025-37484075	NHDF-neo	bronchial:	n/a
25	chr5:37484025-37484075	SK-N-MC	brain:	n/a
26	chr5:37484025-37484075	HEEpiC	esophagus:	n/a
27	chr5:37484025-37484075	BJ	skin:	n/a
28	chr5:37484025-37484075	A549	lung:	n/a
29	chr5:37484025-37484075	SAEC	small airway:	n/a
30	chr5:37484025-37484075	GM12891	blood:	n/a
31	chr5:37484025-37484075	HRCEpiC	kidney:	n/a
32	chr5:37484025-37484075	PFSK-1	brain:	n/a
33	chr5:37484025-37484075	Jurkat	blood:	n/a
34	chr5:37484025-37484075	SKMC	muscle:	n/a
35	chr5:37484025-37484075	ECC-1	luminal epithelium:	n/a
36	chr5:37484025-37484075	MCF-7	breast:	n/a
37	chr5:37484025-37484075	HPAEpiC	pulmonary alveolar:	n/a
38	chr5:37484025-37484075	U87	brain:	n/a
39	chr5:37484025-37484075	Hepatocyte	liver:	n/a
40	chr5:37484025-37484075	HepG2	liver:	n/a
41	chr5:37484025-37484075	ProgFib	skin:	n/a
42	chr5:37484025-37484075	HMEC	breast:	n/a
43	chr5:37484025-37484075	BE2_C	brain:	n/a
44	chr5:37484025-37484075	HRPEpiC	eye:	n/a
45	chr5:37484025-37484075	T-47D	breast:	n/a
46	chr5:37484025-37484075	HCF	heart:	n/a
47	chr5:37484025-37484075	NT2-D1	testis:	n/a
48	chr5:37484025-37484075	GM12892	blood:	n/a
49	chr5:37484025-37484075	ovcar-3	ovarian:	n/a
50	chr5:37484025-37484075	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
2	chr5:37438128..37441611-chr5:37451601..37454118,3	K562	blood:
3	chr5:37488881..37490858-chr5:37567347..37569058,2	K562	blood:
4	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
5	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
6	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
7	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
8	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
9	chr5:37495049..37495731-chr5:37758036..37758591,2	MCF-7	breast:
10	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
11	chr5:37495029..37495917-chr5:37837475..37838072,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP155-5	chr5:37505790-37506959	NONHSAT101066

Variant related genes	Relation type
WDR70	TF binding region
ENSG00000248216	TF binding region
WDR70	CpG island
ENSG00000248216	CpG island
ENSG00000082068	chromatin interactions

Extended variants
information (count: 2599 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2599 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188620254	chr5:37438611-37438612	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs80072962	chr5:37438669-37438670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557713410	chr5:37438712-37438713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371600126	chr5:37438713-37438714	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373458032	chr5:37438730-37438731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192379359	chr5:37438739-37438740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs543493812	chr5:37438744-37438745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184000655	chr5:37438766-37438767	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188594542	chr5:37438800-37438801	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541196503	chr5:37438837-37438838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570186474	chr5:37438886-37438887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559702758	chr5:37438888-37438889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533251524	chr5:37438932-37438933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551515057	chr5:37438971-37438972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs13159282	chr5:37438992-37438993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs5867350	chr5:37439010-37439011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557776743	chr5:37439017-37439018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs397957836	chr5:37439021-37439022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201588768	chr5:37439022-37439023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563699849	chr5:37439168-37439169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530949120	chr5:37439169-37439170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs549466638	chr5:37439183-37439184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148650164	chr5:37439243-37439244	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2366175	chr5:37439263-37439264	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs572222958	chr5:37439266-37439267	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192259376	chr5:37439271-37439272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571634729	chr5:37439281-37439282	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535127711	chr5:37439315-37439316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557507094	chr5:37439352-37439353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201360061	chr5:37439422-37439423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6878120	chr5:37439424-37439425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2366176	chr5:37439428-37439429	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs536594689	chr5:37439469-37439470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555520262	chr5:37439543-37439544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13160250	chr5:37439547-37439548	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs541264177	chr5:37439621-37439622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559567122	chr5:37439685-37439686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543431162	chr5:37439704-37439705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577909071	chr5:37439708-37439709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78794196	chr5:37439725-37439726	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34472295	chr5:37439728-37439729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs75049949	chr5:37439742-37439743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34032020	chr5:37439744-37439745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563397368	chr5:37439824-37439825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530936766	chr5:37439867-37439868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548938257	chr5:37439877-37439878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs561079403	chr5:37439906-37439907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111415299	chr5:37439910-37439911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183969327	chr5:37439939-37439940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187018055	chr5:37439940-37439941	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:1128 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	chr5:37425200-37441600	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr5:37425400-37443400	Weak transcription	Fetal Muscle Trunk	muscle
38	chr5:37425400-37444600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr5:37425400-37445000	Weak transcription	Thymus	Thymus
40	chr5:37425400-37480200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr5:37425600-37443200	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr5:37425600-37446600	Weak transcription	Brain Anterior Caudate	brain
43	chr5:37425600-37446800	Weak transcription	Brain Germinal Matrix	brain
44	chr5:37425600-37451800	Weak transcription	Lung	lung
45	chr5:37425600-37452200	Weak transcription	Spleen	Spleen
46	chr5:37425800-37443400	Weak transcription	Left Ventricle	heart
47	chr5:37425800-37444600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:37425800-37444600	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr5:37425800-37471000	Weak transcription	Fetal Lung	lung
50	chr5:37426000-37443200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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