Variant report

Variant	esv3444499
Chromosome Location	chr3:51449727-51469614
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:45)
CpG islands
(count:122)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:45 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:51468228-51468337	K562	blood:	n/a	n/a
2	CEBPB	chr3:51454254-51454570	A549	lung:	n/a	chr3:51454412-51454423 chr3:51454410-51454421
3	CEBPB	chr3:51454236-51454587	IMR90	lung:	n/a	chr3:51454412-51454423 chr3:51454410-51454421
4	CEBPB	chr3:51466688-51467011	HepG2	liver:	n/a	chr3:51466859-51466870
5	CEBPB	chr3:51466670-51466980	A549	lung:	n/a	chr3:51466859-51466870
6	CEBPB	chr3:51454239-51454596	HepG2	liver:	n/a	chr3:51454412-51454423 chr3:51454410-51454421
7	IRF1	chr3:51460148-51460158	K562	blood:	n/a	n/a
8	JUND	chr3:51452492-51452731	HepG2	liver:	n/a	n/a
9	MAFF	chr3:51459182-51459476	HepG2	liver:	n/a	chr3:51459313-51459331
10	MAFF	chr3:51459167-51459429	K562	blood:	n/a	chr3:51459313-51459331
11	MAFK	chr3:51459244-51459463	HepG2	liver:	n/a	chr3:51459314-51459328 chr3:51459315-51459330 chr3:51459316-51459327
12	MAFK	chr3:51459259-51459459	Hela-S3	cervix:	n/a	chr3:51459314-51459328 chr3:51459315-51459330 chr3:51459316-51459327
13	MAFK	chr3:51459179-51459445	IMR90	lung:	n/a	chr3:51459314-51459328 chr3:51459315-51459330 chr3:51459316-51459327
14	MAFK	chr3:51459166-51459490	HepG2	liver:	n/a	chr3:51459314-51459328 chr3:51459315-51459330 chr3:51459316-51459327
15	POLR2A	chr3:51467347-51467420	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr3:51459776-51459866	K562	blood:	n/a	n/a
17	POLR2A	chr3:51462016-51462073	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr3:51457923-51458180	HL-60	blood:	n/a	n/a
19	POLR2A	chr3:51457609-51457809	K562	blood:	n/a	n/a
20	POLR2A	chr3:51457523-51457918	K562	blood:	n/a	n/a
21	POLR2A	chr3:51452419-51452454	HepG2	liver:	n/a	n/a
22	POLR2A	chr3:51454585-51454773	HepG2	liver:	n/a	n/a
23	POLR2A	chr3:51468826-51468946	GM12878	blood:	n/a	n/a
24	POLR2A	chr3:51452145-51452149	HepG2	liver:	n/a	n/a
25	POLR2A	chr3:51453462-51453606	K562	blood:	n/a	n/a
26	POLR2A	chr3:51452075-51452092	HUVEC	blood vessel:	n/a	n/a
27	POLR2A	chr3:51457684-51458201	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr3:51457569-51457768	MCF-7	breast:	n/a	n/a
29	POLR2A	chr3:51457197-51457327	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr3:51463257-51463309	Gliobla	brain:	n/a	n/a
31	POLR2A	chr3:51457152-51457202	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr3:51452785-51453104	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr3:51452650-51452832	HepG2	liver:	n/a	n/a
34	POLR2A	chr3:51458056-51458158	MCF-7	breast:	n/a	n/a
35	POLR2A	chr3:51453260-51453447	HepG2	liver:	n/a	n/a
36	POLR2A	chr3:51457049-51457128	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr3:51451952-51452055	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr3:51452353-51452397	HepG2	liver:	n/a	n/a
39	POLR2A	chr3:51456050-51456222	Hela-S3	cervix:	n/a	n/a
40	RFX5	chr3:51465481-51465664	K562	blood:	n/a	n/a
41	STAT3	chr3:51451888-51451890	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr3:51450852-51450891	MCF10A-Er-Src	breast:	n/a	n/a
43	TCF7L2	chr3:51458009-51458209	Hela-S3	cervix:	n/a	n/a
44	USF2	chr3:51454304-51454338	Hela-S3	cervix:	n/a	n/a
45	WRNIP1	chr3:51455540-51455647	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51456307-51456357	PFSK-1	brain:	n/a
2	chr3:51459868-51459918	HIPEpiC	eye:	n/a
3	chr3:51456307-51456357	SK-N-SH_RA	brain:	n/a
4	chr3:51456307-51456357	SAEC	small airway:	n/a
5	chr3:51459868-51459918	HCF	heart:	n/a
6	chr3:51459868-51459918	AG10803	skin:	n/a
7	chr3:51456307-51456357	GM06990	blood:	n/a
8	chr3:51459868-51459918	MCF-7	breast:	n/a
9	chr3:51459868-51459918	GM19239	blood:	n/a
10	chr3:51456307-51456357	BJ	skin:	n/a
11	chr3:51459868-51459918	LNCaP	prostate:	n/a
12	chr3:51459868-51459918	SK-N-SH	brain:	n/a
13	chr3:51456307-51456357	NT2-D1	testis:	n/a
14	chr3:51456307-51456357	ProgFib	skin:	n/a
15	chr3:51456307-51456357	K562	blood:	n/a
16	chr3:51456307-51456357	BE2_C	brain:	n/a
17	chr3:51456307-51456357	ovcar-3	ovarian:	n/a
18	chr3:51456307-51456357	HCM	heart:	n/a
19	chr3:51456307-51456357	T-47D	breast:	n/a
20	chr3:51456307-51456357	HIPEpiC	eye:	n/a
21	chr3:51456307-51456357	Caco-2	colon:	n/a
22	chr3:51459868-51459918	H1-hESC	embryonic stem cell:	embryo
23	chr3:51459868-51459918	U87	brain:	n/a
24	chr3:51456307-51456357	MCF10A-Er-Src	breast:	n/a
25	chr3:51459868-51459918	AoSMC	blood vessel:	n/a
26	chr3:51459868-51459918	Jurkat	blood:	n/a
27	chr3:51456307-51456357	ECC-1	luminal epithelium:	n/a
28	chr3:51459868-51459918	AG04450	lung:	fetal
29	chr3:51456307-51456357	AG04449	skin:	fetal
30	chr3:51456307-51456357	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:51459868-51459918	BE2_C	brain:	n/a
32	chr3:51456307-51456357	CMK	blood:	n/a
33	chr3:51459868-51459918	MCF10A-Er-Src	breast:	n/a
34	chr3:51459868-51459918	HRE	kidney:	n/a
35	chr3:51459868-51459918	HCPEpiC	choroid plexus:	n/a
36	chr3:51456307-51456357	HCT-116	colon:	n/a
37	chr3:51456307-51456357	HCF	heart:	n/a
38	chr3:51456307-51456357	Hela-S3	cervix:	n/a
39	chr3:51456307-51456357	HRCEpiC	kidney:	n/a
40	chr3:51456307-51456357	HEEpiC	esophagus:	n/a
41	chr3:51456307-51456357	HRE	kidney:	n/a
42	chr3:51456307-51456357	HMEC	breast:	n/a
43	chr3:51456307-51456357	LNCaP	prostate:	n/a
44	chr3:51459868-51459918	BJ	skin:	n/a
45	chr3:51459868-51459918	A549	lung:	n/a
46	chr3:51459868-51459918	K562	blood:	n/a
47	chr3:51456307-51456357	MCF-7	breast:	n/a
48	chr3:51459868-51459918	HCT-116	colon:	n/a
49	chr3:51456307-51456357	AG09319	gingival:	n/a
50	chr3:51459868-51459918	SK-N-SH_RA	brain:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51434460..51436629-chr3:51450643..51452423,2	MCF-7	breast:
2	chr3:51431727..51434714-chr3:51452155..51454713,2	K562	blood:
3	chr3:51464596..51467000-chr3:51736520..51738058,2	MCF-7	breast:
4	chr3:51446382..51449018-chr3:51464481..51466257,2	K562	blood:
5	chr3:51430737..51433070-chr3:51447893..51450283,2	K562	blood:
6	chr3:51425602..51427385-chr3:51461999..51464649,2	K562	blood:
7	chr3:51460834..51463432-chr3:51465142..51467609,2	K562	blood:
8	chr3:51429653..51435090-chr3:51454270..51458499,6	MCF-7	breast:
9	chr3:51428405..51432279-chr3:51464614..51468207,4	MCF-7	breast:
10	chr3:51454373..51456954-chr3:51462426..51464818,2	K562	blood:
11	chr3:51454373..51456954-chr3:51462426..51464818,2	K562	blood:
12	chr3:51460834..51463432-chr3:51465142..51467609,2	K562	blood:
13	chr3:51432446..51436234-chr3:51447600..51449947,3	MCF-7	breast:
14	chr3:51426841..51428936-chr3:51461966..51464881,2	MCF-7	breast:
15	chr3:51425475..51427809-chr3:51452594..51455305,2	MCF-7	breast:

No data

Variant related genes	Relation type
VPRBP	TF binding region
ENSG00000270692	TF binding region
VPRBP	CpG island
ENSG00000270692	CpG island
ENSG00000179837	chromatin interactions

Extended variants
information (count: 703 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:703 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540331005	chr3:51449727-51449728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370900217	chr3:51449793-51449794	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561718640	chr3:51449798-51449799	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115019262	chr3:51449914-51449915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544628028	chr3:51449965-51449966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs199661104	chr3:51449992-51449993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562619752	chr3:51450087-51450088	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34027075	chr3:51450112-51450113	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35768235	chr3:51450120-51450121	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs533306620	chr3:51450267-51450268	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114866340	chr3:51450314-51450315	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543501538	chr3:51450366-51450367	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs527336808	chr3:51450369-51450370	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs549123793	chr3:51450403-51450404	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367934393	chr3:51450432-51450433	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs371808687	chr3:51450550-51450551	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529514631	chr3:51450613-51450614	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145725485	chr3:51450627-51450628	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549793390	chr3:51450650-51450651	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs569439756	chr3:51450676-51450677	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374932957	chr3:51450690-51450691	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540134430	chr3:51450692-51450693	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368949993	chr3:51450697-51450698	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372157432	chr3:51450700-51450701	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs76403425	chr3:51450710-51450711	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369580735	chr3:51450791-51450792	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373002372	chr3:51450871-51450872	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376778557	chr3:51450886-51450887	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533995749	chr3:51450887-51450888	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555425850	chr3:51451002-51451003	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188927836	chr3:51451058-51451059	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529201930	chr3:51451096-51451097	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376126468	chr3:51451125-51451126	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs548087448	chr3:51451142-51451143	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544277541	chr3:51451188-51451189	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556562415	chr3:51451199-51451200	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375231657	chr3:51451253-51451254	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs137998310	chr3:51451263-51451264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142608893	chr3:51451273-51451274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575338168	chr3:51451302-51451303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376132539	chr3:51451363-51451364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560363928	chr3:51451424-51451425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527501506	chr3:51451426-51451427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150164231	chr3:51451441-51451442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373181889	chr3:51451459-51451460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs367569254	chr3:51451542-51451543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376129288	chr3:51451552-51451553	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138648367	chr3:51451582-51451583	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181677024	chr3:51451606-51451607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369940346	chr3:51451644-51451645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51430200-51457000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:51431400-51471200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr3:51432000-51455400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
4	chr3:51432200-51450000	Weak transcription	Small Intestine	intestine
5	chr3:51432400-51460000	Strong transcription	Liver	Liver
6	chr3:51432800-51453000	Weak transcription	Psoas Muscle	Psoas
7	chr3:51433400-51477400	Weak transcription	Fetal Heart	heart
8	chr3:51434000-51475600	Strong transcription	Primary T cells fromperipheralblood	blood
9	chr3:51434200-51456000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:51434200-51460200	Strong transcription	Dnd41	blood
11	chr3:51434200-51477600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:51434400-51457200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:51434600-51450000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr3:51434600-51471000	Weak transcription	Stomach Mucosa	stomach
15	chr3:51435200-51478000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:51435600-51460200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:51436600-51451400	Weak transcription	Fetal Brain Male	brain
18	chr3:51436600-51461000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:51436800-51449800	Weak transcription	Right Ventricle	heart
20	chr3:51436800-51461000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:51437800-51460000	Strong transcription	Duodenum Mucosa	Duodenum
22	chr3:51439800-51478000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr3:51440000-51460200	Strong transcription	Monocytes-CD14+_RO01746	blood
24	chr3:51440800-51478200	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr3:51441000-51449800	Weak transcription	A549	lung
26	chr3:51441000-51452200	Weak transcription	Aorta	Aorta
27	chr3:51441000-51453400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr3:51441000-51460200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr3:51441200-51451400	Weak transcription	Fetal Kidney	kidney
30	chr3:51441200-51452000	Weak transcription	NHLF	lung
31	chr3:51441600-51461400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:51441800-51450200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr3:51442200-51450400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr3:51443200-51449800	Weak transcription	Colonic Mucosa	Colon
35	chr3:51444000-51460600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr3:51444000-51461200	Strong transcription	Placenta	Placenta
37	chr3:51444800-51460000	Strong transcription	Primary T cells from cord blood	blood
38	chr3:51444800-51477800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr3:51445400-51450000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr3:51445400-51450000	Strong transcription	HepG2	liver
41	chr3:51445400-51460400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr3:51445400-51478400	Strong transcription	Primary B cells from peripheral blood	blood
43	chr3:51445600-51455400	Strong transcription	HUES48 Cell Line	embryonic stem cell
44	chr3:51445600-51460200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:51445600-51460400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr3:51445800-51456000	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr3:51445800-51460000	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr3:51445800-51460000	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr3:51445800-51460200	Strong transcription	Adipose Nuclei	Adipose
50	chr3:51446000-51450000	Strong transcription	Fetal Intestine Small	intestine

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