Variant report

Variant	esv3404444
Chromosome Location	chr5:41701527-41744979
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:419)
CpG islands
(count:122)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:41738826-41739323	K562	blood:	n/a	n/a
2	ATF1	chr5:41738859-41739346	K562	blood:	n/a	n/a
3	ATF2	chr5:41740330-41741106	GM12878	blood:	n/a	n/a
4	ATF3	chr5:41738846-41739115	K562	blood:	n/a	n/a
5	CEBPB	chr5:41705734-41705783	A549	lung:	n/a	n/a
6	CEBPB	chr5:41710228-41710516	IMR90	lung:	n/a	chr5:41710374-41710385
7	CEBPB	chr5:41736747-41737124	IMR90	lung:	n/a	n/a
8	CEBPB	chr5:41741341-41741660	HepG2	liver:	n/a	chr5:41741505-41741516 chr5:41741504-41741517
9	CEBPB	chr5:41710311-41710399	HepG2	liver:	n/a	chr5:41710374-41710385
10	CEBPB	chr5:41710285-41710407	H1-hESC	embryonic stem cell:	n/a	chr5:41710374-41710385
11	CEBPB	chr5:41708053-41708406	IMR90	lung:	n/a	n/a
12	CEBPD	chr5:41738758-41739171	K562	blood:	n/a	n/a
13	CREB1	chr5:41738703-41739240	K562	blood:	n/a	n/a
14	CTCF	chr5:41722576-41722692	GM13976	blood:	n/a	n/a
15	CTCF	chr5:41722600-41722750	AG09309	skin:	n/a	n/a
16	CTCF	chr5:41708032-41708760	SK-N-SH	brain:	n/a	n/a
17	CTCF	chr5:41708340-41708490	AG09309	skin:	n/a	n/a
18	CTCF	chr5:41722620-41722770	GM12875	blood:	n/a	n/a
19	CTCF	chr5:41708300-41708450	GM12875	blood:	n/a	n/a
20	CTCF	chr5:41722500-41722650	GM12864	blood:	n/a	n/a
21	CTCF	chr5:41722580-41722730	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr5:41708360-41708442	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr5:41722543-41722720	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr5:41708300-41708450	HFF-Myc	foreskin:	n/a	n/a
25	CTCF	chr5:41708260-41708410	HCT-116	colon:	n/a	n/a
26	CTCF	chr5:41708260-41708410	WI-38	lung:	n/a	n/a
27	CTCF	chr5:41708320-41708470	A549	lung:	n/a	n/a
28	CTCF	chr5:41708600-41708750	HMEC	breast:	n/a	n/a
29	CTCF	chr5:41708360-41708510	HEK293	kidney:	n/a	n/a
30	CTCF	chr5:41708359-41708514	GM19240	blood:	n/a	n/a
31	CTCF	chr5:41722560-41722710	BE2_C	brain:	n/a	n/a
32	CTCF	chr5:41722620-41722770	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr5:41722540-41722690	HMEC	breast:	n/a	n/a
34	CTCF	chr5:41722580-41722730	GM12869	blood:	n/a	n/a
35	CTCF	chr5:41708300-41708450	HCFaa	heart:	n/a	n/a
36	CTCF	chr5:41708220-41708370	WI-38	lung:	n/a	n/a
37	CTCF	chr5:41708320-41708470	HMEC	breast:	n/a	n/a
38	CTCF	chr5:41722540-41722690	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr5:41708300-41708450	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr5:41722580-41722730	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr5:41722540-41722690	AG09319	gingival:	n/a	n/a
42	CTCF	chr5:41708320-41708470	GM12870	blood:	n/a	n/a
43	CTCF	chr5:41708600-41708750	GM12871	blood:	n/a	n/a
44	CTCF	chr5:41708328-41708485	HepG2	liver:	n/a	n/a
45	CTCF	chr5:41708300-41708450	HPF	lung:	n/a	n/a
46	CTCF	chr5:41719667-41719677	GM12878	blood:	n/a	n/a
47	CTCF	chr5:41722560-41722710	GM06990	blood:	n/a	n/a
48	CTCF	chr5:41708320-41708470	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr5:41708380-41708530	RPTEC	kidney:	n/a	n/a
50	CTCF	chr5:41722560-41722710	AG09319	gingival:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:41708556-41708606	SKMC	muscle:	n/a
2	chr5:41708556-41708606	HUVEC	blood vessel:	n/a
3	chr5:41708556-41708606	HCM	heart:	n/a
4	chr5:41708556-41708606	GM12878	blood:	n/a
5	chr5:41708556-41708606	RPTEC	kidney:	n/a
6	chr5:41730687-41730737	BJ	skin:	n/a
7	chr5:41708556-41708606	NHDF-neo	bronchial:	n/a
8	chr5:41708556-41708606	SK-N-SH_RA	brain:	n/a
9	chr5:41730687-41730737	Hela-S3	cervix:	n/a
10	chr5:41708556-41708606	K562	blood:	n/a
11	chr5:41730687-41730737	ovcar-3	ovarian:	n/a
12	chr5:41708556-41708606	PrEC	prostate:	n/a
13	chr5:41730687-41730737	NHDF-neo	bronchial:	n/a
14	chr5:41730687-41730737	HCF	heart:	n/a
15	chr5:41708556-41708606	HAEpiC	amniotic membrane:	n/a
16	chr5:41730687-41730737	MCF-7	breast:	n/a
17	chr5:41708556-41708606	PANC-1	pancreas:	n/a
18	chr5:41708556-41708606	HCF	heart:	n/a
19	chr5:41708556-41708606	HMEC	breast:	n/a
20	chr5:41708556-41708606	SK-N-SH	brain:	n/a
21	chr5:41730687-41730737	A549	lung:	n/a
22	chr5:41730687-41730737	SAEC	small airway:	n/a
23	chr5:41708556-41708606	HRE	kidney:	n/a
24	chr5:41730687-41730737	NHBE	bronchial:	n/a
25	chr5:41708556-41708606	CMK	blood:	n/a
26	chr5:41708556-41708606	BJ	skin:	n/a
27	chr5:41708556-41708606	Hepatocyte	liver:	n/a
28	chr5:41730687-41730737	AG09319	gingival:	n/a
29	chr5:41730687-41730737	AG10803	skin:	n/a
30	chr5:41708556-41708606	AoSMC	blood vessel:	n/a
31	chr5:41730687-41730737	SK-N-MC	brain:	n/a
32	chr5:41708556-41708606	T-47D	breast:	n/a
33	chr5:41730687-41730737	HCT-116	colon:	n/a
34	chr5:41730687-41730737	SK-N-SH_RA	brain:	n/a
35	chr5:41730687-41730737	HEEpiC	esophagus:	n/a
36	chr5:41708556-41708606	AG04449	skin:	fetal
37	chr5:41730687-41730737	Caco-2	colon:	n/a
38	chr5:41708556-41708606	NH-A	brain:	n/a
39	chr5:41730687-41730737	CMK	blood:	n/a
40	chr5:41708556-41708606	HNPCEpiC	eye:	n/a
41	chr5:41730687-41730737	HAEpiC	amniotic membrane:	n/a
42	chr5:41730687-41730737	H1-hESC	embryonic stem cell:	embryo
43	chr5:41730687-41730737	HCM	heart:	n/a
44	chr5:41730687-41730737	GM06990	blood:	n/a
45	chr5:41708556-41708606	ProgFib	skin:	n/a
46	chr5:41730687-41730737	IMR90	lung:	fetal
47	chr5:41708556-41708606	PFSK-1	brain:	n/a
48	chr5:41708556-41708606	LNCaP	prostate:	n/a
49	chr5:41730687-41730737	HRE	kidney:	n/a
50	chr5:41730687-41730737	AoSMC	blood vessel:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:41723873..41725703-chr5:41731043..41733042,2	K562	blood:
2	chr5:41723873..41725703-chr5:41731043..41733042,2	K562	blood:
3	chr5:41736012..41737687-chr5:41741619..41743667,2	K562	blood:
4	chr5:41726795..41729567-chr5:41730109..41732618,2	K562	blood:
5	chr5:41726795..41729567-chr5:41730109..41732618,2	K562	blood:
6	chr5:41707948..41708855-chr5:41843327..41844349,3	MCF-7	breast:
7	chr5:41707271..41710047-chr5:41712912..41714812,2	MCF-7	breast:
8	chr5:41736012..41737687-chr5:41741619..41743667,2	K562	blood:
9	chr5:41713901..41715819-chr5:41720276..41722337,2	K562	blood:
10	chr5:41708161..41708687-chr5:41843376..41844127,2	K562	blood:
11	chr5:41713901..41715819-chr5:41720276..41722337,2	K562	blood:
12	chr5:41725766..41729567-chr5:41730109..41733963,3	K562	blood:
13	chr5:41696534..41699336-chr5:41700309..41702314,2	K562	blood:
14	chr5:41715717..41717936-chr5:41762141..41764322,2	K562	blood:
15	chr5:41707271..41710047-chr5:41712912..41714812,2	MCF-7	breast:
16	chr5:41707935..41709217-chr5:41842894..41844288,11	MCF-7	breast:
17	chr5:41725766..41729567-chr5:41730109..41733963,3	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	OXCT1	hsa-miR-1	chr5:41730284-41730308

Variant related genes	Relation type
OXCT1	TF binding region
OXCT1	CpG island
ENSG00000083720	chromatin interactions

Extended variants
information (count: 940 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139851069	chr5:41707434-41707435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545303762	chr5:41707439-41707440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563294973	chr5:41707440-41707441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371472584	chr5:41707441-41707442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543097847	chr5:41707458-41707459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540731286	chr5:41707483-41707484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561259419	chr5:41707521-41707522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142122391	chr5:41707558-41707559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535368738	chr5:41707560-41707561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79420030	chr5:41707607-41707608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532401883	chr5:41707648-41707649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs590716	chr5:41707685-41707686	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs114352476	chr5:41707707-41707708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372890674	chr5:41707711-41707712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181472533	chr5:41707712-41707713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34412181	chr5:41707715-41707716	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs533905097	chr5:41707742-41707743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140301201	chr5:41707749-41707750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577817704	chr5:41707778-41707779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545289823	chr5:41707783-41707784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs557269150	chr5:41707790-41707791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575579025	chr5:41707805-41707806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs1423241	chr5:41707827-41707828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561354935	chr5:41707831-41707832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528542192	chr5:41707842-41707843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540724887	chr5:41707893-41707894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549676954	chr5:41707901-41707902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565072389	chr5:41707921-41707922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186101693	chr5:41707958-41707959	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369740072	chr5:41707960-41707961	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs1582539	chr5:41707974-41707975	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145132889	chr5:41707977-41707978	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs35387279	chr5:41707981-41707982	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs374574845	chr5:41707990-41707991	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs553896179	chr5:41707993-41707994	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs142334049	chr5:41708057-41708058	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189349189	chr5:41708145-41708146	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs146421955	chr5:41708148-41708149	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200662920	chr5:41708152-41708153	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs566906830	chr5:41708156-41708157	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs551898385	chr5:41708213-41708214	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116674391	chr5:41708220-41708221	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs59194359	chr5:41708233-41708234	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs549487347	chr5:41708282-41708283	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73752219	chr5:41708287-41708288	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs575818384	chr5:41708334-41708335	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536966532	chr5:41708354-41708355	Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554621092	chr5:41708448-41708449	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531825812	chr5:41708509-41708510	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572127848	chr5:41708556-41708557	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
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
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	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
Melanoma	18172304	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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Hepatocellular carcinoma	18929564	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41707400-41708000	Enhancers	HSMMtube	muscle
2	chr5:41707400-41708800	Enhancers	Osteobl	bone
3	chr5:41707600-41708800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:41708000-41708400	Active TSS	HSMMtube	muscle
5	chr5:41708000-41708800	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:41708200-41708600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:41708400-41708800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr5:41708400-41708800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:41708400-41708800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr5:41708400-41708800	Flanking Active TSS	HSMMtube	muscle
11	chr5:41708400-41709000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr5:41708400-41709000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:41708600-41709000	Enhancers	HSMM	muscle
14	chr5:41708800-41709000	Enhancers	HSMMtube	muscle
15	chr5:41718200-41718400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:41718400-41718800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:41721000-41722000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:41721200-41722200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr5:41721800-41722000	Enhancers	HSMMtube	muscle
20	chr5:41722000-41736800	Weak transcription	HSMMtube	muscle
21	chr5:41722600-41722800	Enhancers	Right Atrium	heart
22	chr5:41722600-41723000	Enhancers	Fetal Muscle Leg	muscle
23	chr5:41722600-41723000	Enhancers	Ovary	ovary
24	chr5:41722800-41723000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr5:41722800-41723000	ZNF genes & repeats	Aorta	Aorta
26	chr5:41722800-41723000	Enhancers	GM12878-XiMat	blood
27	chr5:41723000-41724800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:41723000-41735800	Weak transcription	GM12878-XiMat	blood
29	chr5:41723000-41739200	Weak transcription	Aorta	Aorta
30	chr5:41725200-41725400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr5:41725200-41725400	Enhancers	Right Ventricle	heart
32	chr5:41725400-41725600	Enhancers	Fetal Kidney	kidney
33	chr5:41725400-41728400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:41725400-41739200	Weak transcription	Right Ventricle	heart
35	chr5:41725600-41747400	Weak transcription	Fetal Kidney	kidney
36	chr5:41726000-41726600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr5:41726600-41736000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr5:41726600-41736000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:41726800-41728400	Weak transcription	Primary T cells from cord blood	blood
40	chr5:41727000-41730600	Weak transcription	Left Ventricle	heart
41	chr5:41727200-41727400	Enhancers	Fetal Brain Female	brain
42	chr5:41727200-41728800	Weak transcription	Fetal Thymus	thymus
43	chr5:41727200-41730600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:41727200-41735200	Weak transcription	Stomach Smooth Muscle	stomach
45	chr5:41727200-41735800	Weak transcription	Lung	lung
46	chr5:41727200-41738400	Weak transcription	Thymus	Thymus
47	chr5:41727400-41729000	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr5:41727400-41729000	Weak transcription	Dnd41	blood
49	chr5:41727400-41730400	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr5:41727400-41730400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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