Variant report

Variant	nsv822091
Chromosome Location	chr3:52582073-52587321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:48)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:48 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr3:52586794-52586844	Kidney_OC	kidney:	n/a	n/a
2	FOS	chr3:52586317-52586456	MCF10A-Er-Src	breast:	n/a	chr3:52586358-52586366 chr3:52586357-52586367 chr3:52586357-52586367 chr3:52586357-52586367
3	FOXA2	chr3:52586181-52586456	A549	lung:	n/a	n/a
4	FOXA2	chr3:52586121-52586495	A549	lung:	n/a	n/a
5	PAX5	chr3:52582438-52582579	GM12892	blood:	n/a	n/a
6	POLR2A	chr3:52586645-52586863	HepG2	liver:	n/a	n/a
7	POLR2A	chr3:52583170-52583215	HepG2	liver:	n/a	n/a
8	POLR2A	chr3:52583659-52583838	HepG2	liver:	n/a	n/a
9	POLR2A	chr3:52586245-52586249	MCF-7	breast:	n/a	n/a
10	POLR2A	chr3:52587023-52587098	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr3:52585304-52585319	MCF-7	breast:	n/a	n/a
12	POLR2A	chr3:52586573-52586949	U87	brain:	n/a	n/a
13	POLR2A	chr3:52584340-52584793	HepG2	liver:	n/a	n/a
14	POLR2A	chr3:52586266-52586302	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr3:52585295-52585296	MCF-7	breast:	n/a	n/a
16	POLR2A	chr3:52586150-52586224	MCF-7	breast:	n/a	n/a
17	POLR2A	chr3:52585775-52585791	HepG2	liver:	n/a	n/a
18	POLR2A	chr3:52584153-52584156	HepG2	liver:	n/a	n/a
19	POLR2A	chr3:52584393-52584404	MCF-7	breast:	n/a	n/a
20	POLR2A	chr3:52584962-52585122	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr3:52582935-52582963	HepG2	liver:	n/a	n/a
22	POLR2A	chr3:52586164-52586364	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr3:52586594-52586631	HepG2	liver:	n/a	n/a
24	POLR2A	chr3:52582128-52582188	MCF-7	breast:	n/a	n/a
25	POLR2A	chr3:52585383-52585629	SK-N-SH	brain:	n/a	n/a
26	POLR2A	chr3:52582576-52582893	HepG2	liver:	n/a	n/a
27	POLR2A	chr3:52585153-52585576	U87	brain:	n/a	n/a
28	POLR2A	chr3:52584406-52584914	MCF-7	breast:	n/a	n/a
29	POLR2A	chr3:52583234-52583441	HepG2	liver:	n/a	n/a
30	POLR2A	chr3:52587139-52587234	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr3:52583860-52584095	HepG2	liver:	n/a	n/a
32	POLR2A	chr3:52582111-52582168	K562	blood:	n/a	n/a
33	POLR2A	chr3:52583663-52583721	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr3:52584671-52584754	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr3:52586573-52587005	U87	brain:	n/a	n/a
36	POLR2A	chr3:52585153-52585661	U87	brain:	n/a	n/a
37	POLR2A	chr3:52584452-52584630	K562	blood:	n/a	n/a
38	POLR2A	chr3:52582195-52582222	GM12878	blood:	n/a	n/a
39	POLR2A	chr3:52585272-52585277	MCF-7	breast:	n/a	n/a
40	POLR2A	chr3:52586653-52587110	K562	blood:	n/a	n/a
41	POLR2A	chr3:52586660-52587119	MCF-7	breast:	n/a	n/a
42	POLR2A	chr3:52585841-52585842	HepG2	liver:	n/a	n/a
43	POLR2A	chr3:52586348-52586455	K562	blood:	n/a	n/a
44	POLR2A	chr3:52585195-52585636	HepG2	liver:	n/a	n/a
45	POLR2A	chr3:52584572-52584596	K562	blood:	n/a	n/a
46	RFX5	chr3:52582059-52582154	Hela-S3	cervix:	n/a	n/a
47	STAT3	chr3:52585253-52585322	MCF10A-Er-Src	breast:	n/a	n/a
48	YY1	chr3:52582059-52582255	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52583646-52583696	U87	brain:	n/a
2	chr3:52583646-52583696	HIPEpiC	eye:	n/a
3	chr3:52583646-52583696	PANC-1	pancreas:	n/a
4	chr3:52583646-52583696	T-47D	breast:	n/a
5	chr3:52583646-52583696	HEEpiC	esophagus:	n/a
6	chr3:52583646-52583696	NH-A	brain:	n/a
7	chr3:52583646-52583696	AG10803	skin:	n/a
8	chr3:52583646-52583696	LNCaP	prostate:	n/a
9	chr3:52583646-52583696	GM12892	blood:	n/a
10	chr3:52583646-52583696	Caco-2	colon:	n/a
11	chr3:52583646-52583696	IMR90	lung:	fetal
12	chr3:52583646-52583696	K562	blood:	n/a
13	chr3:52583646-52583696	Jurkat	blood:	n/a
14	chr3:52583646-52583696	ovcar-3	ovarian:	n/a
15	chr3:52583646-52583696	Hela-S3	cervix:	n/a
16	chr3:52583646-52583696	AG09319	gingival:	n/a
17	chr3:52583646-52583696	AG04450	lung:	fetal
18	chr3:52583646-52583696	HCF	heart:	n/a
19	chr3:52583646-52583696	HL-60	blood:	n/a
20	chr3:52583646-52583696	MCF-7	breast:	n/a
21	chr3:52583646-52583696	HRPEpiC	eye:	n/a
22	chr3:52583646-52583696	A549	lung:	n/a
23	chr3:52583646-52583696	AG04449	skin:	fetal
24	chr3:52583646-52583696	BJ	skin:	n/a
25	chr3:52583646-52583696	NT2-D1	testis:	n/a
26	chr3:52583646-52583696	HAEpiC	amniotic membrane:	n/a
27	chr3:52583646-52583696	AoSMC	blood vessel:	n/a
28	chr3:52583646-52583696	NHDF-neo	bronchial:	n/a
29	chr3:52583646-52583696	AG09309	skin:	n/a
30	chr3:52583646-52583696	SK-N-SH_RA	brain:	n/a
31	chr3:52583646-52583696	HNPCEpiC	eye:	n/a
32	chr3:52583646-52583696	HCPEpiC	choroid plexus:	n/a
33	chr3:52583646-52583696	HCT-116	colon:	n/a
34	chr3:52583646-52583696	HUVEC	blood vessel:	n/a
35	chr3:52583646-52583696	CMK	blood:	n/a
36	chr3:52583646-52583696	SAEC	small airway:	n/a
37	chr3:52583646-52583696	GM12891	blood:	n/a
38	chr3:52583646-52583696	GM06990	blood:	n/a
39	chr3:52583646-52583696	SKMC	muscle:	n/a
40	chr3:52583646-52583696	HEK293	kidney:	embryo
41	chr3:52583646-52583696	PFSK-1	brain:	n/a
42	chr3:52583646-52583696	HepG2	liver:	n/a
43	chr3:52583646-52583696	PrEC	prostate:	n/a
44	chr3:52583646-52583696	RPTEC	kidney:	n/a
45	chr3:52583646-52583696	ProgFib	skin:	n/a
46	chr3:52583646-52583696	HCM	heart:	n/a
47	chr3:52583646-52583696	HRE	kidney:	n/a
48	chr3:52583646-52583696	HRCEpiC	kidney:	n/a
49	chr3:52583646-52583696	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:52583646-52583696	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:52582290..52585059-chr3:52585315..52587211,2	MCF-7	breast:
2	chr3:52569665..52571812-chr3:52580710..52583139,2	K562	blood:
3	chr3:52579491..52583913-chr3:52584069..52587223,6	K562	blood:
4	chr3:52569842..52571498-chr3:52584728..52587706,2	MCF-7	breast:
5	chr3:52570313..52572775-chr3:52580397..52583533,3	MCF-7	breast:
6	chr3:52583735..52585349-chr3:52718060..52720039,2	K562	blood:
7	chr3:52574434..52577960-chr3:52578839..52582098,4	MCF-7	breast:
8	chr3:52578493..52580735-chr3:52582072..52584660,3	K562	blood:
9	chr3:52567466..52569592-chr3:52583401..52584922,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-856P	TF binding region
RNU6-856P	CpG island
ENSG00000252768	chromatin interactions
ENSG00000168268	chromatin interactions
ENSG00000163939	chromatin interactions
ENSG00000163938	chromatin interactions
ENSG00000168273	chromatin interactions

Extended variants
information (count: 165 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:165 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577666469	chr3:52582076-52582077	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs371624499	chr3:52582107-52582108	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs539871380	chr3:52582112-52582113	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200304933	chr3:52582125-52582126	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376146705	chr3:52582209-52582210	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs200020801	chr3:52582210-52582211	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138449080	chr3:52582226-52582227	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527392994	chr3:52582238-52582239	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs201397730	chr3:52582240-52582241	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs375268569	chr3:52582248-52582249	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs200335538	chr3:52582269-52582270	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374097140	chr3:52582307-52582308	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs377400872	chr3:52582326-52582327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs181169016	chr3:52582349-52582350	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs533903873	chr3:52582405-52582406	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs185624077	chr3:52582409-52582410	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs62256904	chr3:52582443-52582444	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs372814552	chr3:52582445-52582446	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs78797142	chr3:52582459-52582460	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs190385536	chr3:52582474-52582475	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs181574755	chr3:52582481-52582482	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556707554	chr3:52582488-52582489	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs576670047	chr3:52582503-52582504	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs187161131	chr3:52582515-52582516	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs570485330	chr3:52582546-52582547	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141161690	chr3:52582627-52582628	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs540210890	chr3:52582662-52582663	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147369106	chr3:52582695-52582696	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs371267260	chr3:52582737-52582738	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573680225	chr3:52582738-52582739	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542394991	chr3:52582830-52582831	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs562249423	chr3:52582945-52582946	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs552453144	chr3:52582946-52582947	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs531354857	chr3:52582983-52582984	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs530711822	chr3:52583040-52583041	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs551182777	chr3:52583060-52583061	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs537829376	chr3:52583099-52583100	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs191823388	chr3:52583118-52583119	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs184108467	chr3:52583124-52583125	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs547747148	chr3:52583155-52583156	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs34764212	chr3:52583162-52583163	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs189623208	chr3:52583224-52583225	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550250956	chr3:52583283-52583284	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570184434	chr3:52583316-52583317	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs138044951	chr3:52583325-52583326	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559227188	chr3:52583335-52583336	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs182306207	chr3:52583337-52583338	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs535050850	chr3:52583418-52583419	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs113782809	chr3:52583424-52583425	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs374728584	chr3:52583426-52583427	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Lung cancer	16618734	CNVD
Neuroblastoma	19686582	CNVD
Renal cell carcinoma	18765545	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52571400-52594200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:52572200-52584400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:52572400-52594200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr3:52572400-52633000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:52573200-52583400	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr3:52573200-52585000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:52573200-52586400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr3:52573200-52589600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr3:52573200-52590400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:52573400-52585200	Weak transcription	Small Intestine	intestine
11	chr3:52573400-52595000	Weak transcription	Stomach Mucosa	stomach
12	chr3:52573600-52583200	Weak transcription	Colonic Mucosa	Colon
13	chr3:52573600-52598400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
14	chr3:52573800-52584600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr3:52574200-52583200	Weak transcription	Spleen	Spleen
16	chr3:52574200-52588400	Strong transcription	Liver	Liver
17	chr3:52574400-52623800	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr3:52574600-52594200	Weak transcription	K562	blood
19	chr3:52574600-52598800	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr3:52574800-52605000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr3:52575600-52585200	Weak transcription	Brain Angular Gyrus	brain
22	chr3:52575800-52584400	Weak transcription	Hela-S3	cervix
23	chr3:52576000-52590400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr3:52576200-52583200	Weak transcription	Lung	lung
25	chr3:52576200-52583600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr3:52576200-52583600	Weak transcription	Gastric	stomach
27	chr3:52576200-52584400	Weak transcription	Right Ventricle	heart
28	chr3:52576800-52625600	Strong transcription	Fetal Thymus	thymus
29	chr3:52577000-52599000	Strong transcription	Fetal Muscle Leg	muscle
30	chr3:52577200-52599000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr3:52577600-52584400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr3:52577600-52595400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:52577600-52598600	Strong transcription	Placenta	Placenta
34	chr3:52577600-52605200	Strong transcription	Dnd41	blood
35	chr3:52578000-52595400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:52578200-52591200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr3:52578200-52625600	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr3:52578400-52582400	Strong transcription	Adipose Nuclei	Adipose
39	chr3:52578400-52582600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
40	chr3:52578400-52588800	Strong transcription	NH-A	brain
41	chr3:52578400-52598600	Strong transcription	HUES64 Cell Line	embryonic stem cell
42	chr3:52578400-52600600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr3:52578600-52582400	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr3:52578600-52587000	Strong transcription	Brain Germinal Matrix	brain
45	chr3:52578800-52582600	Strong transcription	Fetal Brain Female	brain
46	chr3:52578800-52598200	Strong transcription	Primary B cells from cord blood	blood
47	chr3:52578800-52598800	Strong transcription	Primary T cells fromperipheralblood	blood
48	chr3:52578800-52599600	Strong transcription	Fetal Muscle Trunk	muscle
49	chr3:52578800-52601400	Strong transcription	Primary B cells from peripheral blood	blood
50	chr3:52579000-52583000	Strong transcription	Fetal Lung	lung

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