Variant report

Variant	nsv980968
Chromosome Location	chr5:37348697-37363379
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	ARID3A	chr5:37349046-37349675	HepG2	liver:	n/a	n/a
2	CEBPB	chr5:37357913-37358113	K562	blood:	n/a	n/a
3	CEBPB	chr5:37349333-37349648	HepG2	liver:	n/a	n/a
4	CTCF	chr5:37352902-37352915	K562	blood:	n/a	n/a
5	CTCF	chr5:37353557-37353588	GM20000	blood:	n/a	n/a
6	CTCF	chr5:37358703-37358754	Pancreas_OC	pancreas:	n/a	n/a
7	EP300	chr5:37349139-37349717	HepG2	liver:	n/a	chr5:37349399-37349409 chr5:37349362-37349376 chr5:37349364-37349378
8	EP300	chr5:37349298-37349585	HepG2	liver:	n/a	chr5:37349399-37349409 chr5:37349362-37349376 chr5:37349364-37349378
9	EP300	chr5:37349203-37349626	HepG2	liver:	n/a	chr5:37349399-37349409 chr5:37349362-37349376 chr5:37349364-37349378
10	FOXA1	chr5:37349047-37349815	HepG2	liver:	n/a	n/a
11	FOXA1	chr5:37349156-37349741	HepG2	liver:	n/a	n/a
12	FOXA1	chr5:37349047-37349772	HepG2	liver:	n/a	n/a
13	FOXA1	chr5:37349248-37349636	HepG2	liver:	n/a	n/a
14	FOXA2	chr5:37348786-37350114	HepG2	liver:	n/a	chr5:37349942-37349954
15	FOXA2	chr5:37348973-37349644	HepG2	liver:	n/a	n/a
16	HDAC2	chr5:37349236-37349601	HepG2	liver:	n/a	chr5:37349365-37349379 chr5:37349364-37349378 chr5:37349363-37349377 chr5:37349367-37349381 chr5:37349400-37349409 chr5:37349366-37349380 chr5:37349371-37349385 chr5:37349361-37349375 chr5:37349372-37349386
17	HDAC2	chr5:37349196-37349625	HepG2	liver:	n/a	chr5:37349365-37349379 chr5:37349364-37349378 chr5:37349363-37349377 chr5:37349367-37349381 chr5:37349400-37349409 chr5:37349366-37349380 chr5:37349371-37349385 chr5:37349361-37349375 chr5:37349372-37349386
18	HEY1	chr5:37349442-37349609	HepG2	liver:	n/a	n/a
19	HNF4A	chr5:37349300-37349573	HepG2	liver:	n/a	n/a
20	HNF4A	chr5:37349220-37349622	HepG2	liver:	n/a	n/a
21	HNF4G	chr5:37349294-37349607	HepG2	liver:	n/a	chr5:37349439-37349454
22	HNF4G	chr5:37349318-37349600	HepG2	liver:	n/a	chr5:37349439-37349454
23	IRF1	chr5:37354085-37354113	K562	blood:	n/a	n/a
24	JUND	chr5:37349314-37349596	HepG2	liver:	n/a	n/a
25	JUND	chr5:37361600-37361656	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAFF	chr5:37349287-37349570	HepG2	liver:	n/a	n/a
27	MAFK	chr5:37349307-37349608	HepG2	liver:	n/a	n/a
28	MBD4	chr5:37349154-37349643	HepG2	liver:	n/a	n/a
29	MYBL2	chr5:37349108-37349777	HepG2	liver:	n/a	n/a
30	MYC	chr5:37354620-37354681	MCF-7	breast:	n/a	n/a
31	NFIC	chr5:37349271-37349607	HepG2	liver:	n/a	n/a
32	NFIC	chr5:37349079-37349833	HepG2	liver:	n/a	n/a
33	POLR2A	chr5:37361496-37362263	K562	blood:	n/a	n/a
34	POLR2A	chr5:37357337-37357354	HepG2	liver:	n/a	n/a
35	POLR2A	chr5:37354693-37354794	Hela-S3	cervix:	n/a	n/a
36	POLR2A	chr5:37352389-37352701	HepG2	liver:	n/a	n/a
37	POLR2A	chr5:37349948-37350665	K562	blood:	n/a	n/a
38	POLR2A	chr5:37356055-37356199	HepG2	liver:	n/a	n/a
39	POLR2A	chr5:37359466-37359478	HepG2	liver:	n/a	n/a
40	POLR2A	chr5:37353402-37353449	HepG2	liver:	n/a	n/a
41	POLR2A	chr5:37352964-37352996	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr5:37348991-37349018	HepG2	liver:	n/a	n/a
43	POLR2A	chr5:37361929-37362275	Hela-S3	cervix:	n/a	n/a
44	POLR2A	chr5:37354590-37354765	K562	blood:	n/a	n/a
45	POLR2A	chr5:37354824-37354914	K562	blood:	n/a	n/a
46	POLR2A	chr5:37356547-37356696	HepG2	liver:	n/a	n/a
47	POLR2A	chr5:37361406-37362151	K562	blood:	n/a	n/a
48	POLR2A	chr5:37354700-37354731	K562	blood:	n/a	n/a
49	POLR2A	chr5:37362157-37362319	H1-hESC	embryonic stem cell:	n/a	n/a
50	POLR2A	chr5:37354659-37354842	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
2	chr5:37349723..37351295-chr5:37369578..37371440,2	K562	blood:
3	chr15:94515130..94515844-chr5:37350902..37351467,2	MCF-7	breast:
4	chr5:37358150..37361413-chr5:37362395..37366227,3	K562	blood:
5	chr5:37351031..37353005-chr5:37354563..37356913,2	K562	blood:
6	chr5:37341337..37344195-chr5:37360002..37362809,2	K562	blood:
7	chr5:37361813..37365556-chr5:37369411..37373994,6	K562	blood:
8	chr5:37363225..37366000-chr5:37368563..37371283,3	K562	blood:
9	chr5:37326722..37329430-chr5:37348015..37351389,3	K562	blood:
10	chr5:37362418..37364207-chr5:37369498..37371536,2	MCF-7	breast:
11	chr5:37353747..37356748-chr5:37369994..37371965,3	K562	blood:
12	chr5:37351031..37353005-chr5:37354563..37356913,2	K562	blood:
13	chr5:37348597..37351209-chr5:37351351..37353763,2	K562	blood:

Variant related genes	Relation type
NUP155	TF binding region
ENSG00000113569	chromatin interactions
ENSG00000251880	chromatin interactions

Extended variants
information (count: 632 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371568956	chr5:37348727-37348728	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs546698508	chr5:37348744-37348745	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs376582812	chr5:37348748-37348749	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570978134	chr5:37348761-37348762	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538457771	chr5:37348799-37348800	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188070062	chr5:37348805-37348806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575190350	chr5:37348821-37348822	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536530396	chr5:37348822-37348823	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs549208381	chr5:37348870-37348871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs75113488	chr5:37348875-37348876	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192727751	chr5:37348880-37348881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540227509	chr5:37348881-37348882	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs28541312	chr5:37348940-37348941	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537963232	chr5:37348943-37348944	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs370791046	chr5:37348946-37348947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557498635	chr5:37348978-37348979	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577363723	chr5:37348982-37348983	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs184304620	chr5:37349008-37349009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs563063738	chr5:37349023-37349024	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530362763	chr5:37349042-37349043	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548842731	chr5:37349055-37349056	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs560597205	chr5:37349069-37349070	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186876713	chr5:37349117-37349118	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs191537544	chr5:37349118-37349119	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113010070	chr5:37349140-37349141	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs35729800	chr5:37349160-37349161	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs78296629	chr5:37349162-37349163	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs397997407	chr5:37349173-37349174	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538334736	chr5:37349204-37349205	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550392853	chr5:37349207-37349208	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568686481	chr5:37349219-37349220	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs536030248	chr5:37349223-37349224	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369390221	chr5:37349253-37349254	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs201036380	chr5:37349296-37349297	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs71619852	chr5:37349359-37349360	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75411551	chr5:37349360-37349361	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550342158	chr5:37349361-37349362	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77983250	chr5:37349372-37349373	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs80162589	chr5:37349373-37349374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114486369	chr5:37349408-37349409	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375285736	chr5:37349439-37349440	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs71619853	chr5:37349452-37349453	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558988712	chr5:37349521-37349522	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs577454724	chr5:37349554-37349555	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs184879411	chr5:37349566-37349567	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs34277073	chr5:37349597-37349598	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs556826267	chr5:37349599-37349600	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs575001088	chr5:37349655-37349656	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs566239087	chr5:37349695-37349696	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs375581599	chr5:37349708-37349709	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Autism	22549408	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37289000-37369200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr5:37296400-37365400	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr5:37296400-37369000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr5:37296800-37353200	Strong transcription	Fetal Thymus	thymus
5	chr5:37296800-37358400	Strong transcription	Placenta	Placenta
6	chr5:37296800-37358600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr5:37296800-37358600	Strong transcription	Liver	Liver
8	chr5:37296800-37359000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:37296800-37359800	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr5:37296800-37359800	Strong transcription	Fetal Intestine Large	intestine
11	chr5:37296800-37360000	Strong transcription	Adipose Nuclei	Adipose
12	chr5:37296800-37364600	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr5:37296800-37364600	Strong transcription	Dnd41	blood
14	chr5:37296800-37365600	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr5:37297000-37364200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr5:37297000-37365400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:37297200-37358800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr5:37297400-37364600	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr5:37297800-37359800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr5:37307800-37368600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr5:37308800-37353200	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr5:37308800-37365400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr5:37311600-37351400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr5:37311600-37365400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:37311600-37365400	Strong transcription	Fetal Muscle Leg	muscle
26	chr5:37318400-37359000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr5:37319000-37358400	Strong transcription	Duodenum Mucosa	Duodenum
28	chr5:37319200-37364600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:37319400-37365400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr5:37319800-37349200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:37321600-37359600	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr5:37322200-37360000	Strong transcription	Hela-S3	cervix
33	chr5:37323200-37358800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
34	chr5:37323400-37363600	Weak transcription	Stomach Mucosa	stomach
35	chr5:37324400-37365400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr5:37328600-37350600	Weak transcription	Fetal Heart	heart
37	chr5:37330000-37364200	Strong transcription	Fetal Muscle Trunk	muscle
38	chr5:37330400-37349600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr5:37330800-37349200	Strong transcription	Fetal Intestine Small	intestine
40	chr5:37330800-37349200	Strong transcription	Fetal Stomach	stomach
41	chr5:37331000-37349200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr5:37331200-37349000	Strong transcription	Thymus	Thymus
43	chr5:37332800-37349200	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr5:37334000-37349800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr5:37334800-37369600	Weak transcription	HSMMtube	muscle
46	chr5:37335200-37360000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
47	chr5:37335400-37360000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr5:37335800-37349200	Strong transcription	Lung	lung
49	chr5:37335800-37358400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr5:37335800-37358400	Strong transcription	Duodenum Smooth Muscle	Duodenum

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