Variant report

Variant	nsv1030223
Chromosome Location	chr5:37463746-37514800
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	BACH1	chr5:37512136-37512171	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	chr5:37488479-37488841	K562	blood:	n/a	n/a
6	CBX3	chr5:37471796-37472190	K562	blood:	n/a	n/a
7	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
8	CEBPB	chr5:37481844-37481981	K562	blood:	n/a	chr5:37481876-37481887
9	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
10	CEBPB	chr5:37474447-37474554	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:37481844-37481867	HepG2	liver:	n/a	n/a
12	CEBPB	chr5:37494846-37495179	Hela-S3	cervix:	n/a	n/a
13	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
14	CEBPB	chr5:37480989-37481283	K562	blood:	n/a	n/a
15	CEBPB	chr5:37480974-37481250	K562	blood:	n/a	n/a
16	CEBPB	chr5:37493291-37493471	A549	lung:	n/a	n/a
17	CEBPB	chr5:37503418-37503494	A549	lung:	n/a	n/a
18	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
19	CEBPD	chr5:37480945-37481331	K562	blood:	n/a	n/a
20	CHD2	chr5:37489676-37489723	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr5:37495100-37495250	AG10803	skin:	n/a	n/a
22	CTCF	chr5:37495420-37495570	HVMF	connective:	n/a	chr5:37495448-37495469
23	CTCF	chr5:37495120-37495270	GM12874	blood:	n/a	n/a
24	CTCF	chr5:37495240-37495390	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr5:37495340-37495490	BJ	skin:	n/a	chr5:37495448-37495469
26	CTCF	chr5:37495320-37495470	HCT-116	colon:	n/a	chr5:37495448-37495469
27	CTCF	chr5:37495340-37495490	AG04450	lung:	n/a	chr5:37495448-37495469
28	CTCF	chr5:37495320-37495470	SK-N-SH_RA	brain:	n/a	chr5:37495448-37495469
29	CTCF	chr5:37495358-37495552	MCF-7	breast:	n/a	chr5:37495448-37495469
30	CTCF	chr5:37495374-37495487	ProgFib	skin:	n/a	chr5:37495448-37495469
31	CTCF	chr5:37495420-37495570	AG09319	gingival:	n/a	chr5:37495448-37495469
32	CTCF	chr5:37495300-37495450	NHLF	lung:	n/a	n/a
33	CTCF	chr5:37490044-37490162	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr5:37495294-37495623	GM12878	blood:	n/a	chr5:37495448-37495469
35	CTCF	chr5:37495320-37495470	HA-sp	spinal cord:	n/a	chr5:37495448-37495469
36	CTCF	chr5:37464854-37464911	Fibrobl	skin:	n/a	n/a
37	CTCF	chr5:37464740-37464890	HVMF	connective:	n/a	n/a
38	CTCF	chr5:37464860-37464981	MCF-7	breast:	n/a	n/a
39	CTCF	chr5:37495380-37495530	AG04450	lung:	n/a	chr5:37495448-37495469
40	CTCF	chr5:37495380-37495530	BJ	skin:	n/a	chr5:37495448-37495469
41	CTCF	chr5:37495295-37495631	IMR90	lung:	n/a	chr5:37495448-37495469
42	CTCF	chr5:37495380-37495530	HPAF	blood vessel:	n/a	chr5:37495448-37495469
43	CTCF	chr5:37506888-37507075	H1-hESC	embryonic stem cell:	n/a	chr5:37506968-37506977 chr5:37506964-37506977
44	CTCF	chr5:37495480-37495630	A549	lung:	n/a	n/a
45	CTCF	chr5:37495340-37495490	SAEC	small airway:	n/a	chr5:37495448-37495469
46	CTCF	chr5:37495320-37495470	BE2_C	brain:	n/a	chr5:37495448-37495469
47	CTCF	chr5:37506900-37507050	HBMEC	blood vessel:	n/a	chr5:37506968-37506977 chr5:37506964-37506977
48	CTCF	chr5:37464760-37464910	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr5:37512956-37512983	GM13976	blood:	n/a	n/a
50	CTCF	chr5:37495300-37495450	NHDF-neo	bronchial:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:37484025-37484075	PrEC	prostate:	n/a
2	chr5:37484025-37484075	NHBE	bronchial:	n/a
3	chr5:37484025-37484075	PANC-1	pancreas:	n/a
4	chr5:37484025-37484075	AG10803	skin:	n/a
5	chr5:37484025-37484075	H1-hESC	embryonic stem cell:	embryo
6	chr5:37484025-37484075	NH-A	brain:	n/a
7	chr5:37484025-37484075	HIPEpiC	eye:	n/a
8	chr5:37484025-37484075	SK-N-SH	brain:	n/a
9	chr5:37484025-37484075	HMEC	breast:	n/a
10	chr5:37484025-37484075	BE2_C	brain:	n/a
11	chr5:37484025-37484075	IMR90	lung:	fetal
12	chr5:37484025-37484075	SK-N-SH_RA	brain:	n/a
13	chr5:37484025-37484075	HCM	heart:	n/a
14	chr5:37484025-37484075	K562	blood:	n/a
15	chr5:37484025-37484075	HEK293	kidney:	embryo
16	chr5:37484025-37484075	HPAEpiC	pulmonary alveolar:	n/a
17	chr5:37484025-37484075	GM19239	blood:	n/a
18	chr5:37484025-37484075	CMK	blood:	n/a
19	chr5:37484025-37484075	HAEpiC	amniotic membrane:	n/a
20	chr5:37484025-37484075	GM06990	blood:	n/a
21	chr5:37484025-37484075	NT2-D1	testis:	n/a
22	chr5:37484025-37484075	PFSK-1	brain:	n/a
23	chr5:37484025-37484075	GM12891	blood:	n/a
24	chr5:37484025-37484075	ProgFib	skin:	n/a
25	chr5:37484025-37484075	Caco-2	colon:	n/a
26	chr5:37484025-37484075	BJ	skin:	n/a
27	chr5:37484025-37484075	A549	lung:	n/a
28	chr5:37484025-37484075	HL-60	blood:	n/a
29	chr5:37484025-37484075	T-47D	breast:	n/a
30	chr5:37484025-37484075	LNCaP	prostate:	n/a
31	chr5:37484025-37484075	AG04450	lung:	fetal
32	chr5:37484025-37484075	GM12892	blood:	n/a
33	chr5:37484025-37484075	HRE	kidney:	n/a
34	chr5:37484025-37484075	HRPEpiC	eye:	n/a
35	chr5:37484025-37484075	MCF-7	breast:	n/a
36	chr5:37484025-37484075	Hepatocyte	liver:	n/a
37	chr5:37484025-37484075	SK-N-MC	brain:	n/a
38	chr5:37484025-37484075	U87	brain:	n/a
39	chr5:37484025-37484075	AoSMC	blood vessel:	n/a
40	chr5:37484025-37484075	AG09309	skin:	n/a
41	chr5:37484025-37484075	HEEpiC	esophagus:	n/a
42	chr5:37484025-37484075	HNPCEpiC	eye:	n/a
43	chr5:37484025-37484075	HepG2	liver:	n/a
44	chr5:37484025-37484075	NB4	blood:	n/a
45	chr5:37484025-37484075	HCPEpiC	choroid plexus:	n/a
46	chr5:37484025-37484075	SAEC	small airway:	n/a
47	chr5:37484025-37484075	GM12878	blood:	n/a
48	chr5:37484025-37484075	HCT-116	colon:	n/a
49	chr5:37484025-37484075	SKMC	muscle:	n/a
50	chr5:37484025-37484075	ECC-1	luminal epithelium:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:37440538..37443537-chr5:37502324..37504824,2	K562	blood:
2	chr5:37509914..37511896-chr5:37518755..37521412,2	K562	blood:
3	chr5:37477675..37480288-chr5:37486843..37489829,2	K562	blood:
4	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
5	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
6	chr5:37495029..37495917-chr5:37837475..37838072,2	MCF-7	breast:
7	chr5:37495049..37495731-chr5:37758036..37758591,2	MCF-7	breast:
8	chr5:37503334..37505446-chr5:37509179..37510910,2	K562	blood:
9	chr5:37496762..37498368-chr5:37500019..37501730,2	MCF-7	breast:
10	chr5:37488881..37490858-chr5:37567347..37569058,2	K562	blood:

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: 1957 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11750212	chr5:37463746-37463747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374073186	chr5:37463769-37463770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs56008521	chr5:37463809-37463810	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs572468537	chr5:37463810-37463811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187880665	chr5:37463874-37463875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs149747728	chr5:37463914-37463915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs78769631	chr5:37463915-37463916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373153669	chr5:37463922-37463923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35852975	chr5:37463926-37463927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs544063021	chr5:37463946-37463947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192876001	chr5:37463961-37463962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529943269	chr5:37464022-37464023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542099362	chr5:37464030-37464031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs560492719	chr5:37464047-37464048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs527651800	chr5:37464062-37464063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184919938	chr5:37464067-37464068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188126164	chr5:37464082-37464083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113595237	chr5:37464133-37464134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570151229	chr5:37464211-37464212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7725018	chr5:37464231-37464232	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs568779345	chr5:37464232-37464233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113610786	chr5:37464239-37464240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs180840968	chr5:37464321-37464322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs111392129	chr5:37464334-37464335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146947996	chr5:37464358-37464359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533524940	chr5:37464393-37464394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111552809	chr5:37464403-37464404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576857107	chr5:37464409-37464410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184545809	chr5:37464501-37464502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556088486	chr5:37464507-37464508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs553027800	chr5:37464568-37464569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574141657	chr5:37464571-37464572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189374069	chr5:37464666-37464667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572681206	chr5:37464672-37464673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560458457	chr5:37464677-37464678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376261608	chr5:37464710-37464711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141940912	chr5:37464850-37464851	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546202598	chr5:37464893-37464894	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564642281	chr5:37464906-37464907	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543005290	chr5:37464961-37464962	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550199264	chr5:37464977-37464978	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562163183	chr5:37464992-37464993	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529421191	chr5:37465049-37465050	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181532082	chr5:37465054-37465055	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566018974	chr5:37465121-37465122	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10941336	chr5:37465126-37465127	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs551883171	chr5:37465133-37465134	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186876592	chr5:37465146-37465147	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570381296	chr5:37465194-37465195	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537553196	chr5:37465281-37465282	Weak transcription Enhancers	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:825 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37410600-37471000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr5:37420800-37480200	Weak transcription	Brain Hippocampus Middle	brain
3	chr5:37421600-37478400	Weak transcription	Aorta	Aorta
4	chr5:37425400-37480200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:37425800-37471000	Weak transcription	Fetal Lung	lung
6	chr5:37426000-37479800	Weak transcription	HSMM	muscle
7	chr5:37431800-37471000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr5:37435600-37480000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:37441000-37464600	Weak transcription	Psoas Muscle	Psoas
10	chr5:37445200-37467600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:37445200-37471000	Weak transcription	Left Ventricle	heart
12	chr5:37445200-37479800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr5:37445200-37480200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr5:37445200-37480200	Weak transcription	Ovary	ovary
15	chr5:37445200-37480200	Weak transcription	Thymus	Thymus
16	chr5:37445400-37471000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr5:37445400-37480200	Weak transcription	Hela-S3	cervix
18	chr5:37445600-37471000	Weak transcription	Fetal Thymus	thymus
19	chr5:37445600-37480000	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr5:37451800-37477000	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr5:37452000-37470800	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr5:37452000-37471000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:37452000-37471000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr5:37452800-37470600	Weak transcription	Liver	Liver
25	chr5:37452800-37470800	Weak transcription	Primary T cells from cord blood	blood
26	chr5:37452800-37471000	Weak transcription	Fetal Stomach	stomach
27	chr5:37453200-37470600	Weak transcription	Dnd41	blood
28	chr5:37453200-37470800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:37454200-37470600	Weak transcription	Primary B cells from cord blood	blood
30	chr5:37455000-37471000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr5:37455200-37468800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr5:37458000-37480200	Weak transcription	Right Ventricle	heart
33	chr5:37463000-37463800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr5:37463000-37464200	Enhancers	Fetal Muscle Leg	muscle
35	chr5:37463200-37464000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr5:37463200-37464800	Weak transcription	GM12878-XiMat	blood
37	chr5:37463400-37463800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:37463400-37463800	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr5:37463400-37464200	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr5:37463400-37465600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:37463400-37470600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr5:37463600-37463800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr5:37463600-37463800	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr5:37463600-37464200	Enhancers	Muscle Satellite Cultured Cells	--
45	chr5:37463600-37464200	Enhancers	HSMMtube	muscle
46	chr5:37463600-37470800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:37463800-37464400	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr5:37463800-37464800	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr5:37463800-37469000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:37463800-37489600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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