Variant report

Variant	esv3441182
Chromosome Location	chr3:101042062-101045060
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:46)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:46 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:101044254-101045060	K562	blood:	n/a	n/a
2	BHLHE40	chr3:101044311-101044888	K562	blood:	n/a	n/a
3	CCNT2	chr3:101044635-101044946	K562	blood:	n/a	n/a
4	CEBPB	chr3:101044285-101044958	K562	blood:	n/a	n/a
5	CEBPB	chr3:101042075-101042087	A549	lung:	n/a	n/a
6	CEBPB	chr3:101044289-101044881	K562	blood:	n/a	n/a
7	CEBPD	chr3:101044605-101044946	K562	blood:	n/a	n/a
8	CEBPD	chr3:101044551-101045002	K562	blood:	n/a	n/a
9	E2F4	chr3:101043093-101043372	MCF10A-Er-Src	breast:	n/a	n/a
10	EP300	chr3:101044387-101044960	K562	blood:	n/a	n/a
11	EP300	chr3:101044341-101045007	K562	blood:	n/a	n/a
12	EP300	chr3:101043325-101043524	K562	blood:	n/a	n/a
13	GATA1	chr3:101044687-101044892	PBDEFetal	blood:	n/a	n/a
14	GATA1	chr3:101044251-101045033	K562	blood:	n/a	n/a
15	GATA1	chr3:101044241-101045366	PBDE	blood:	n/a	chr3:101045177-101045188
16	GATA2	chr3:101044506-101044951	K562	blood:	n/a	n/a
17	IRF1	chr3:101044198-101045023	K562	blood:	n/a	chr3:101044976-101044996 chr3:101044978-101044992 chr3:101044978-101044995 chr3:101044980-101044994 chr3:101044984-101044994
18	IRF1	chr3:101043434-101043532	K562	blood:	n/a	n/a
19	MAFF	chr3:101044249-101044481	HepG2	liver:	n/a	chr3:101044374-101044392
20	MAFF	chr3:101044218-101044838	K562	blood:	n/a	chr3:101044374-101044392
21	MAFK	chr3:101044222-101044534	K562	blood:	n/a	chr3:101044375-101044390
22	MAFK	chr3:101044085-101044479	HepG2	liver:	n/a	chr3:101044375-101044390
23	MAFK	chr3:101044064-101044526	HepG2	liver:	n/a	chr3:101044375-101044390
24	MAX	chr3:101044296-101044518	K562	blood:	n/a	n/a
25	MAX	chr3:101044334-101044899	K562	blood:	n/a	n/a
26	MYC	chr3:101044298-101044853	K562	blood:	n/a	n/a
27	MYC	chr3:101044344-101044950	K562	blood:	n/a	n/a
28	NR2F2	chr3:101044583-101044914	K562	blood:	n/a	n/a
29	NR2F2	chr3:101044490-101044966	K562	blood:	n/a	n/a
30	PML	chr3:101044555-101044964	K562	blood:	n/a	n/a
31	PML	chr3:101044556-101044927	K562	blood:	n/a	n/a
32	POLR2A	chr3:101044522-101044957	K562	blood:	n/a	n/a
33	POLR2A	chr3:101044644-101044952	K562	blood:	n/a	n/a
34	POLR2A	chr3:101044688-101044894	K562	blood:	n/a	n/a
35	RCOR1	chr3:101044320-101044950	K562	blood:	n/a	n/a
36	SPI1	chr3:101044763-101044957	K562	blood:	n/a	n/a
37	STAT3	chr3:101043996-101044111	MCF10A-Er-Src	breast:	n/a	n/a
38	STAT5A	chr3:101044532-101045012	K562	blood:	n/a	n/a
39	TAL1	chr3:101044303-101045069	K562	blood:	n/a	n/a
40	TBL1XR1	chr3:101043140-101043203	K562	blood:	n/a	n/a
41	TEAD4	chr3:101044530-101044961	K562	blood:	n/a	n/a
42	TEAD4	chr3:101044246-101045011	K562	blood:	n/a	n/a
43	TRIM28	chr3:101044564-101045004	K562	blood:	n/a	n/a
44	USF1	chr3:101044278-101044556	K562	blood:	n/a	n/a
45	USF1	chr3:101044233-101044555	K562	blood:	n/a	n/a
46	ZMIZ1	chr3:101044651-101044931	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:101044447-101044497	MCF10A-Er-Src	breast:	n/a
2	chr3:101044447-101044497	NT2-D1	testis:	n/a
3	chr3:101044447-101044497	A549	lung:	n/a
4	chr3:101044447-101044497	AG04450	lung:	fetal
5	chr3:101044447-101044497	Caco-2	colon:	n/a
6	chr3:101044447-101044497	GM12891	blood:	n/a
7	chr3:101044447-101044497	NHDF-neo	bronchial:	n/a
8	chr3:101044447-101044497	CMK	blood:	n/a
9	chr3:101044447-101044497	RPTEC	kidney:	n/a
10	chr3:101044447-101044497	HIPEpiC	eye:	n/a
11	chr3:101044447-101044497	HepG2	liver:	n/a
12	chr3:101044447-101044497	AG09309	skin:	n/a
13	chr3:101044447-101044497	HCPEpiC	choroid plexus:	n/a
14	chr3:101044447-101044497	LNCaP	prostate:	n/a
15	chr3:101044447-101044497	HAEpiC	amniotic membrane:	n/a
16	chr3:101044447-101044497	K562	blood:	n/a
17	chr3:101044447-101044497	AG04449	skin:	fetal
18	chr3:101044447-101044497	NB4	blood:	n/a
19	chr3:101044447-101044497	GM12892	blood:	n/a
20	chr3:101044447-101044497	SKMC	muscle:	n/a
21	chr3:101044447-101044497	U87	brain:	n/a
22	chr3:101044447-101044497	ovcar-3	ovarian:	n/a
23	chr3:101044447-101044497	HCT-116	colon:	n/a
24	chr3:101044447-101044497	HEK293	kidney:	embryo
25	chr3:101044447-101044497	GM06990	blood:	n/a
26	chr3:101044447-101044497	HCM	heart:	n/a
27	chr3:101044447-101044497	HRCEpiC	kidney:	n/a
28	chr3:101044447-101044497	AG09319	gingival:	n/a
29	chr3:101044447-101044497	PrEC	prostate:	n/a
30	chr3:101044447-101044497	BJ	skin:	n/a
31	chr3:101044447-101044497	MCF-7	breast:	n/a
32	chr3:101044447-101044497	PANC-1	pancreas:	n/a
33	chr3:101044447-101044497	ECC-1	luminal epithelium:	n/a
34	chr3:101044447-101044497	NH-A	brain:	n/a
35	chr3:101044447-101044497	HUVEC	blood vessel:	n/a
36	chr3:101044447-101044497	NHBE	bronchial:	n/a
37	chr3:101044447-101044497	HMEC	breast:	n/a
38	chr3:101044447-101044497	SAEC	small airway:	n/a
39	chr3:101044447-101044497	BE2_C	brain:	n/a
40	chr3:101044447-101044497	PFSK-1	brain:	n/a
41	chr3:101044447-101044497	GM19239	blood:	n/a
42	chr3:101044447-101044497	Jurkat	blood:	n/a
43	chr3:101044447-101044497	SK-N-SH	brain:	n/a
44	chr3:101044447-101044497	HEEpiC	esophagus:	n/a
45	chr3:101044447-101044497	GM12878	blood:	n/a
46	chr3:101044447-101044497	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:101044447-101044497	SK-N-SH_RA	brain:	n/a
48	chr3:101044447-101044497	SK-N-MC	brain:	n/a
49	chr3:101044447-101044497	HRE	kidney:	n/a
50	chr3:101044447-101044497	T-47D	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:101034562..101037047-chr3:101040318..101043205,2	K562	blood:
2	chr3:101040613..101042326-chr3:101043316..101046300,2	MCF-7	breast:
3	chr3:101040613..101042326-chr3:101043316..101046300,2	MCF-7	breast:
4	chr3:101040780..101043358-chr3:101279256..101281040,2	MCF-7	breast:
5	chr3:101037115..101040053-chr3:101040832..101043761,2	K562	blood:
6	chr3:101040010..101042925-chr3:101044427..101046951,2	K562	blood:
7	chr3:101043939..101046244-chr3:101049634..101052193,2	K562	blood:
8	chr3:101044050..101046352-chr3:101047857..101049368,2	K562	blood:
9	chr3:101042282..101045217-chr3:101046433..101048205,2	MCF-7	breast:
10	chr3:101040010..101042925-chr3:101044427..101046951,2	K562	blood:

No data

Variant related genes	Relation type
IMPG2	TF binding region
IMPG2	CpG island
ENSG00000174173	chromatin interactions
ENSG00000138468	chromatin interactions
ENSG00000081148	chromatin interactions

Extended variants
information (count: 103 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:103 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574349943	chr3:101042068-101042069	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs541150980	chr3:101042073-101042074	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs563196749	chr3:101042085-101042086	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs377062444	chr3:101042139-101042140	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs77376128	chr3:101042160-101042161	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs1520656	chr3:101042179-101042180	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs117616160	chr3:101042184-101042185	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4305402	chr3:101042232-101042233	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs78077634	chr3:101042265-101042266	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs147180499	chr3:101042346-101042347	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs190453864	chr3:101042354-101042355	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs529229090	chr3:101042360-101042361	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs550954444	chr3:101042363-101042364	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs569221452	chr3:101042414-101042415	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs114396287	chr3:101042440-101042441	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs144525356	chr3:101042483-101042484	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570293061	chr3:101042499-101042500	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs534555057	chr3:101042520-101042521	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs552984836	chr3:101042536-101042537	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs568353751	chr3:101042570-101042571	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7431086	chr3:101042594-101042595	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs75968504	chr3:101042620-101042621	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575377632	chr3:101042631-101042632	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs181955663	chr3:101042633-101042634	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs115649447	chr3:101042704-101042705	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs112443404	chr3:101042749-101042750	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs375834529	chr3:101042750-101042751	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs71132567	chr3:101042786-101042787	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs56320903	chr3:101042788-101042789	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs60557191	chr3:101042793-101042794	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs73863047	chr3:101042794-101042795	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs557932503	chr3:101042808-101042809	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs375295861	chr3:101042849-101042850	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs369535081	chr3:101042860-101042861	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs573464594	chr3:101042867-101042868	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540829301	chr3:101042874-101042875	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs562195886	chr3:101042915-101042916	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs531514999	chr3:101042932-101042933	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550032624	chr3:101043008-101043009	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs529611594	chr3:101043018-101043019	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs148928762	chr3:101043085-101043086	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs74873407	chr3:101043132-101043133	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs538707331	chr3:101043153-101043154	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs533186016	chr3:101043168-101043169	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs551461066	chr3:101043208-101043209	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs142824380	chr3:101043282-101043283	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs186049157	chr3:101043482-101043483	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs13440	chr3:101043488-101043489	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs497953	chr3:101043565-101043566	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs568238471	chr3:101043569-101043570	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101028000-101044200	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr3:101029400-101044400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:101029800-101044600	Weak transcription	Primary T cells from cord blood	blood
4	chr3:101030200-101044200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr3:101030200-101044600	Weak transcription	Fetal Lung	lung
6	chr3:101030200-101045800	Weak transcription	HUVEC	blood vessel
7	chr3:101030200-101052800	Weak transcription	Fetal Stomach	stomach
8	chr3:101030400-101062400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr3:101030800-101065400	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr3:101030800-101096400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr3:101031000-101044200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr3:101031800-101044000	Weak transcription	Primary B cells from cord blood	blood
13	chr3:101032200-101044000	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr3:101032200-101055600	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr3:101037000-101043800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:101037200-101044800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr3:101037200-101046000	Weak transcription	Left Ventricle	heart
18	chr3:101037600-101045400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr3:101038600-101101800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr3:101038800-101045400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr3:101038800-101048000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr3:101038800-101089800	Weak transcription	Pancreas	Pancrea
23	chr3:101039400-101048000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr3:101039600-101046400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:101039800-101106600	Weak transcription	Thymus	Thymus
26	chr3:101040200-101044400	Weak transcription	Adipose Nuclei	Adipose
27	chr3:101040400-101042400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr3:101040400-101044400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr3:101040400-101044400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:101040400-101045800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:101040400-101046000	Weak transcription	HSMM	muscle
32	chr3:101040400-101048200	Weak transcription	Fetal Muscle Leg	muscle
33	chr3:101040400-101070800	Weak transcription	NHDF-Ad	bronchial
34	chr3:101040600-101044200	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr3:101040600-101045800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr3:101040600-101046000	Weak transcription	Fetal Intestine Large	intestine
37	chr3:101040600-101086800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr3:101040800-101043400	Weak transcription	Liver	Liver
39	chr3:101040800-101043800	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr3:101040800-101044000	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr3:101040800-101044400	Weak transcription	Fetal Thymus	thymus
42	chr3:101040800-101044600	Weak transcription	Dnd41	blood
43	chr3:101040800-101045400	Weak transcription	Fetal Brain Female	brain
44	chr3:101040800-101046000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr3:101040800-101056000	Weak transcription	Lung	lung
46	chr3:101040800-101076000	Weak transcription	Esophagus	oesophagus
47	chr3:101040800-101090000	Weak transcription	Brain Angular Gyrus	brain
48	chr3:101041000-101044800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr3:101041400-101044200	Weak transcription	Primary B cells from peripheral blood	blood
50	chr3:101042000-101045200	Weak transcription	Placenta Amnion	Placenta Amnion

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