Variant report

Variant	esv1797113
Chromosome Location	chr3:160217483-160245980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:123)
CpG islands
(count:183)
Chromatin interactive
region (count:20)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:123 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:160224665-160225118	HepG2	liver:	n/a	n/a
2	BHLHE40	chr3:160224849-160225136	HepG2	liver:	n/a	n/a
3	BHLHE40	chr3:160224885-160225144	HepG2	liver:	n/a	n/a
4	BHLHE40	chr3:160224835-160225211	HepG2	liver:	n/a	n/a
5	CEBPB	chr3:160224843-160225101	MCF-7	breast:	n/a	n/a
6	CEBPB	chr3:160238089-160238114	K562	blood:	n/a	n/a
7	CEBPB	chr3:160226526-160226871	HepG2	liver:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
8	CEBPB	chr3:160224803-160225096	IMR90	lung:	n/a	n/a
9	CEBPB	chr3:160224684-160225085	A549	lung:	n/a	n/a
10	CEBPB	chr3:160224769-160225125	HepG2	liver:	n/a	n/a
11	CEBPB	chr3:160226540-160226885	A549	lung:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
12	CEBPB	chr3:160224786-160225205	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:160224772-160225172	HepG2	liver:	n/a	n/a
14	CEBPB	chr3:160224810-160225059	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:160226570-160226847	IMR90	lung:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
16	CEBPB	chr3:160243718-160243984	HepG2	liver:	n/a	chr3:160243843-160243854
17	CEBPB	chr3:160226549-160226835	K562	blood:	n/a	chr3:160226699-160226710 chr3:160226699-160226712
18	CEBPB	chr3:160224807-160225078	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr3:160231084-160231157	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr3:160236650-160236695	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr3:160227060-160227210	NB4	blood:	n/a	n/a
22	CUX1	chr3:160237895-160237951	K562	blood:	n/a	n/a
23	E2F4	chr3:160230096-160230102	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr3:160224702-160225119	HepG2	liver:	n/a	chr3:160224902-160224912
25	EP300	chr3:160224681-160225173	HepG2	liver:	n/a	chr3:160224902-160224912
26	FAM48A	chr3:160244863-160244947	GM12878	blood:	n/a	n/a
27	FOS	chr3:160224251-160224520	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr3:160235224-160235418	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr3:160224320-160224413	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr3:160224273-160224466	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr3:160224635-160224783	MCF10A-Er-Src	breast:	n/a	chr3:160224641-160224650 chr3:160224640-160224650 chr3:160224640-160224650
32	FOXA1	chr3:160224631-160225130	HepG2	liver:	n/a	n/a
33	FOXA1	chr3:160224609-160225139	HepG2	liver:	n/a	n/a
34	FOXA1	chr3:160224697-160225175	HepG2	liver:	n/a	n/a
35	FOXA1	chr3:160224794-160225140	HepG2	liver:	n/a	n/a
36	FOXA2	chr3:160224707-160225146	HepG2	liver:	n/a	n/a
37	HDAC2	chr3:160224798-160225155	HepG2	liver:	n/a	n/a
38	HDAC2	chr3:160224748-160225134	HepG2	liver:	n/a	n/a
39	HNF4G	chr3:160224911-160225150	HepG2	liver:	n/a	n/a
40	IRF1	chr3:160222067-160222114	K562	blood:	n/a	n/a
41	JUN	chr3:160223213-160223388	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUN	chr3:160224447-160224538	K562	blood:	n/a	n/a
43	MAFF	chr3:160245846-160245970	HepG2	liver:	n/a	chr3:160245891-160245909
44	MAFF	chr3:160245842-160245941	K562	blood:	n/a	chr3:160245891-160245909
45	MAFK	chr3:160245741-160246055	IMR90	lung:	n/a	chr3:160245893-160245904 chr3:160245893-160245908
46	MAFK	chr3:160243890-160244033	HepG2	liver:	n/a	chr3:160243939-160243950 chr3:160243938-160243952 chr3:160243939-160243950
47	MAFK	chr3:160228174-160228407	HepG2	liver:	n/a	n/a
48	MAFK	chr3:160245770-160246055	HepG2	liver:	n/a	chr3:160245893-160245904 chr3:160245893-160245908
49	MAFK	chr3:160245802-160245928	Hela-S3	cervix:	n/a	chr3:160245893-160245904 chr3:160245893-160245908
50	MAFK	chr3:160222460-160222536	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:160233797-160233847	GM06990	blood:	n/a
2	chr3:160233563-160233613	HMEC	breast:	n/a
3	chr3:160219522-160219572	CMK	blood:	n/a
4	chr3:160219522-160219572	PANC-1	pancreas:	n/a
5	chr3:160233563-160233613	HRPEpiC	eye:	n/a
6	chr3:160233563-160233613	NH-A	brain:	n/a
7	chr3:160233563-160233613	HL-60	blood:	n/a
8	chr3:160233797-160233847	HepG2	liver:	n/a
9	chr3:160233797-160233847	A549	lung:	n/a
10	chr3:160233563-160233613	SK-N-MC	brain:	n/a
11	chr3:160233563-160233613	HCF	heart:	n/a
12	chr3:160219522-160219572	HRPEpiC	eye:	n/a
13	chr3:160233797-160233847	Hela-S3	cervix:	n/a
14	chr3:160219522-160219572	HepG2	liver:	n/a
15	chr3:160233563-160233613	LNCaP	prostate:	n/a
16	chr3:160233563-160233613	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:160219522-160219572	HCT-116	colon:	n/a
18	chr3:160233563-160233613	CMK	blood:	n/a
19	chr3:160233797-160233847	HUVEC	blood vessel:	n/a
20	chr3:160219522-160219572	SKMC	muscle:	n/a
21	chr3:160233797-160233847	ProgFib	skin:	n/a
22	chr3:160233797-160233847	U87	brain:	n/a
23	chr3:160233563-160233613	GM12891	blood:	n/a
24	chr3:160233797-160233847	PANC-1	pancreas:	n/a
25	chr3:160233797-160233847	RPTEC	kidney:	n/a
26	chr3:160219522-160219572	H1-hESC	embryonic stem cell:	embryo
27	chr3:160233797-160233847	ECC-1	luminal epithelium:	n/a
28	chr3:160233563-160233613	K562	blood:	n/a
29	chr3:160219522-160219572	HEEpiC	esophagus:	n/a
30	chr3:160233563-160233613	PANC-1	pancreas:	n/a
31	chr3:160233797-160233847	BJ	skin:	n/a
32	chr3:160219522-160219572	K562	blood:	n/a
33	chr3:160233797-160233847	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:160219522-160219572	AG04450	lung:	fetal
35	chr3:160233797-160233847	HCPEpiC	choroid plexus:	n/a
36	chr3:160233563-160233613	U87	brain:	n/a
37	chr3:160233563-160233613	AG10803	skin:	n/a
38	chr3:160233797-160233847	HCT-116	colon:	n/a
39	chr3:160219522-160219572	BE2_C	brain:	n/a
40	chr3:160233797-160233847	AG10803	skin:	n/a
41	chr3:160219522-160219572	PFSK-1	brain:	n/a
42	chr3:160233797-160233847	T-47D	breast:	n/a
43	chr3:160233797-160233847	MCF10A-Er-Src	breast:	n/a
44	chr3:160233563-160233613	HIPEpiC	eye:	n/a
45	chr3:160233797-160233847	IMR90	lung:	fetal
46	chr3:160219522-160219572	SAEC	small airway:	n/a
47	chr3:160233797-160233847	HAEpiC	amniotic membrane:	n/a
48	chr3:160233563-160233613	ECC-1	luminal epithelium:	n/a
49	chr3:160233563-160233613	SKMC	muscle:	n/a
50	chr3:160233563-160233613	PFSK-1	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:160167035..160169821-chr3:160232708..160234646,2	K562	blood:
2	chr3:160214963..160217572-chr3:160217602..160219755,2	MCF-7	breast:
3	chr3:160223761..160225418-chr3:160235399..160237999,2	K562	blood:
4	chr3:160214963..160217572-chr3:160217602..160219755,2	MCF-7	breast:
5	chr3:160204576..160208180-chr3:160214688..160218928,3	MCF-7	breast:
6	chr3:160229725..160231499-chr3:160231673..160233379,2	MCF-7	breast:
7	chr3:160209082..160210967-chr3:160217809..160219865,2	K562	blood:
8	chr3:160243184..160245065-chr3:160260331..160263083,2	K562	blood:
9	chr3:160242999..160245781-chr3:160282351..160283886,2	MCF-7	breast:
10	chr3:160220685..160224773-chr3:160234023..160237053,3	MCF-7	breast:
11	chr3:160221864..160223670-chr3:160224243..160226921,2	MCF-7	breast:
12	chr3:160167490..160169764-chr3:160223909..160225875,2	K562	blood:
13	chr3:160220685..160224773-chr3:160234023..160237053,3	MCF-7	breast:
14	chr3:160245830..160248208-chr3:160254358..160256155,2	K562	blood:
15	chr3:160216490..160219028-chr3:160268486..160271353,2	K562	blood:
16	chr3:160221864..160223670-chr3:160224243..160226921,2	MCF-7	breast:
17	chr3:160230934..160232886-chr3:160280729..160283145,2	K562	blood:
18	chr3:160209467..160214464-chr3:160215473..160219309,5	K562	blood:
19	chr3:160243874..160245789-chr3:160246088..160248768,2	K562	blood:
20	chr3:160223761..160225418-chr3:160235399..160237999,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM59-1	chr3:160216454-160217772	NONHSAT092996
2	lnc-TRIM59-2	chr3:160232695-160233024	NONHSAT092997

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	KPNA4	hsa-miR-30a-5p	chr3:160218178-160218199

Variant related genes	Relation type
KPNA4	TF binding region
SCARNA7	TF binding region
KPNA4	CpG island
SCARNA7	CpG island
ENSG00000186432	chromatin interactions
ENSG00000213186	chromatin interactions
ENSG00000229320	chromatin interactions
ENSG00000238741	chromatin interactions

Extended variants
information (count: 1051 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7627756	chr3:160217483-160217484	Weak transcription Strong transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs576556662	chr3:160217513-160217514	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs550255799	chr3:160217542-160217543	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs538836961	chr3:160217547-160217548	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs568561689	chr3:160217616-160217617	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs371863310	chr3:160217689-160217690	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs532795527	chr3:160217715-160217716	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs577853763	chr3:160217739-160217740	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs551317437	chr3:160217752-160217753	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs571079025	chr3:160217757-160217758	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs535302299	chr3:160217828-160217829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144119086	chr3:160217833-160217834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553635585	chr3:160217854-160217855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188932113	chr3:160217855-160217856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536001096	chr3:160217863-160217864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557493755	chr3:160217892-160217893	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144817854	chr3:160217903-160217904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545892465	chr3:160217904-160217905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528501611	chr3:160217913-160217914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs78818334	chr3:160217928-160217929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558106396	chr3:160217936-160217937	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573083950	chr3:160217937-160217938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56389920	chr3:160218009-160218010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558418045	chr3:160218046-160218047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540506046	chr3:160218115-160218116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201233947	chr3:160218153-160218154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561587097	chr3:160218176-160218177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529054373	chr3:160218181-160218182	Weak transcription Strong transcription	miRNA target site	1 gene(s)	Overlapped CNVs	n/a
29	rs367554028	chr3:160218268-160218269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11919332	chr3:160218485-160218486	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs561812249	chr3:160218502-160218503	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528888840	chr3:160218647-160218648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543958485	chr3:160218662-160218663	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562255165	chr3:160218671-160218672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376644547	chr3:160218772-160218773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs11553778	chr3:160218779-160218780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547368213	chr3:160218780-160218781	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551116416	chr3:160218828-160218829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566445066	chr3:160218878-160218879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528821106	chr3:160218959-160218960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190963374	chr3:160218964-160218965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559702994	chr3:160218995-160218996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568723890	chr3:160219018-160219019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533227768	chr3:160219050-160219051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs536064202	chr3:160219052-160219053	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs200652983	chr3:160219066-160219067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372903265	chr3:160219076-160219077	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144391557	chr3:160219083-160219084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200015946	chr3:160219096-160219097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11553776	chr3:160219121-160219122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Effusion lymphoma	18079361	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Cancer	20164919	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160204000-160219000	Weak transcription	Lung	lung
2	chr3:160204000-160219000	Weak transcription	Thymus	Thymus
3	chr3:160204000-160224000	Weak transcription	Gastric	stomach
4	chr3:160204000-160238200	Weak transcription	Small Intestine	intestine
5	chr3:160204200-160217600	Weak transcription	NH-A	brain
6	chr3:160204200-160218800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr3:160204200-160218800	Weak transcription	Fetal Intestine Large	intestine
8	chr3:160204200-160219000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr3:160204200-160219000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:160204200-160219000	Weak transcription	NHEK	skin
11	chr3:160204200-160219200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr3:160204200-160219200	Weak transcription	Aorta	Aorta
13	chr3:160204200-160219200	Weak transcription	Left Ventricle	heart
14	chr3:160204200-160219400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr3:160204200-160224400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr3:160204200-160224800	Weak transcription	GM12878-XiMat	blood
17	chr3:160204200-160225400	Weak transcription	Fetal Kidney	kidney
18	chr3:160209200-160218600	Weak transcription	Stomach Smooth Muscle	stomach
19	chr3:160209200-160219200	Weak transcription	Fetal Stomach	stomach
20	chr3:160209800-160218600	Weak transcription	HSMMtube	muscle
21	chr3:160210200-160218400	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr3:160210200-160219000	Weak transcription	Brain Anterior Caudate	brain
23	chr3:160210600-160219200	Weak transcription	Fetal Lung	lung
24	chr3:160212000-160220400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr3:160212400-160219200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr3:160212600-160218200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr3:160213000-160218800	Weak transcription	Brain Hippocampus Middle	brain
28	chr3:160213000-160219200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr3:160213000-160220200	Weak transcription	Fetal Intestine Small	intestine
30	chr3:160213000-160228600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr3:160213200-160219200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr3:160213200-160219200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr3:160213200-160222800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr3:160213400-160219200	Weak transcription	Fetal Muscle Leg	muscle
35	chr3:160213600-160223800	Weak transcription	Psoas Muscle	Psoas
36	chr3:160214000-160219200	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr3:160214200-160217600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr3:160214400-160217600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr3:160214400-160218200	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr3:160214600-160218800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr3:160214600-160219200	Weak transcription	Fetal Brain Female	brain
42	chr3:160214800-160218200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr3:160214800-160218600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr3:160214800-160219200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr3:160214800-160219200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr3:160215000-160218400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:160215000-160219200	Weak transcription	Ovary	ovary
48	chr3:160215000-160225400	Weak transcription	Fetal Heart	heart
49	chr3:160215200-160218400	Weak transcription	NHLF	lung
50	chr3:160215200-160219000	Weak transcription	K562	blood

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