Variant report

Variant	nsv432417
Chromosome Location	chr3:43045796-43098296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:223)
CpG islands
(count:183)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:223 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:43069542-43069785	K562	blood:	n/a	n/a
2	ATF1	chr3:43059368-43059658	K562	blood:	n/a	n/a
3	ATF1	chr3:43045843-43046033	K562	blood:	n/a	n/a
4	BACH1	chr3:43053436-43053460	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:43079532-43079812	GM12878	blood:	n/a	chr3:43079638-43079646
6	BATF	chr3:43079514-43079787	GM12878	blood:	n/a	chr3:43079638-43079646
7	BHLHE40	chr3:43066108-43066320	K562	blood:	n/a	n/a
8	BHLHE40	chr3:43078382-43078582	GM12878	blood:	n/a	n/a
9	CBX3	chr3:43086210-43086527	K562	blood:	n/a	n/a
10	CEBPB	chr3:43061955-43062234	HepG2	liver:	n/a	chr3:43062103-43062114 chr3:43062103-43062116
11	CEBPB	chr3:43078428-43078749	Hela-S3	cervix:	n/a	chr3:43078583-43078594
12	CEBPB	chr3:43080206-43080461	K562	blood:	n/a	chr3:43080209-43080221 chr3:43080382-43080393 chr3:43080381-43080394 chr3:43080381-43080392
13	CEBPB	chr3:43078482-43078638	K562	blood:	n/a	chr3:43078583-43078594
14	CEBPB	chr3:43078423-43078666	MCF-7	breast:	n/a	chr3:43078583-43078594
15	CEBPB	chr3:43078407-43078780	K562	blood:	n/a	chr3:43078583-43078594
16	CEBPB	chr3:43078406-43078774	HepG2	liver:	n/a	chr3:43078583-43078594
17	CEBPB	chr3:43078415-43078763	IMR90	lung:	n/a	chr3:43078583-43078594
18	CEBPB	chr3:43080307-43080549	K562	blood:	n/a	chr3:43080382-43080393 chr3:43080381-43080394 chr3:43080381-43080392
19	CEBPB	chr3:43080288-43080570	HepG2	liver:	n/a	chr3:43080382-43080393 chr3:43080381-43080394 chr3:43080381-43080392
20	CEBPB	chr3:43078410-43078698	K562	blood:	n/a	chr3:43078583-43078594
21	CEBPB	chr3:43078413-43078733	A549	lung:	n/a	chr3:43078583-43078594
22	CEBPB	chr3:43078430-43078742	H1-hESC	embryonic stem cell:	n/a	chr3:43078583-43078594
23	CEBPB	chr3:43070205-43070371	HepG2	liver:	n/a	n/a
24	CHD2	chr3:43078405-43078594	GM12878	blood:	n/a	n/a
25	CREB1	chr3:43058443-43059700	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr3:43059204-43059788	K562	blood:	n/a	n/a
27	CREB1	chr3:43058979-43059739	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr3:43059289-43059745	K562	blood:	n/a	n/a
29	CREB1	chr3:43056474-43056845	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr3:43051240-43051390	HMEC	breast:	n/a	n/a
31	CTCF	chr3:43051120-43051270	HepG2	liver:	n/a	n/a
32	CTCF	chr3:43051260-43051410	NB4	blood:	n/a	n/a
33	CTCF	chr3:43073100-43073250	HMEC	breast:	n/a	n/a
34	CTCF	chr3:43076303-43076324	K562	blood:	n/a	n/a
35	CTCF	chr3:43051200-43051350	BJ	skin:	n/a	n/a
36	CTCF	chr3:43051120-43051270	HEK293	kidney:	n/a	n/a
37	CTCF	chr3:43051152-43051315	K562	blood:	n/a	n/a
38	CTCF	chr3:43051160-43051310	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr3:43051200-43051350	AG09319	gingival:	n/a	n/a
40	CTCF	chr3:43051085-43051342	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr3:43083700-43083850	GM12864	blood:	n/a	n/a
42	CTCF	chr3:43051140-43051290	GM12869	blood:	n/a	n/a
43	CTCF	chr3:43051120-43051270	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr3:43051160-43051310	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr3:43051120-43051270	K562	blood:	n/a	n/a
46	CTCF	chr3:43051240-43051390	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:43051100-43051250	GM12873	blood:	n/a	n/a
48	CTCF	chr3:43051196-43051307	MCF-7	breast:	n/a	n/a
49	CTCF	chr3:43056040-43056330	GM12868	blood:	n/a	n/a
50	CTCF	chr3:43073000-43073150	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:43073152-43073202	HRPEpiC	eye:	n/a
2	chr3:43073152-43073202	GM19239	blood:	n/a
3	chr3:43073058-43073108	PrEC	prostate:	n/a
4	chr3:43073152-43073202	MCF10A-Er-Src	breast:	n/a
5	chr3:43073152-43073202	MCF-7	breast:	n/a
6	chr3:43097994-43098044	GM12891	blood:	n/a
7	chr3:43073152-43073202	CMK	blood:	n/a
8	chr3:43097994-43098044	MCF10A-Er-Src	breast:	n/a
9	chr3:43097994-43098044	AG04450	lung:	fetal
10	chr3:43073152-43073202	NHBE	bronchial:	n/a
11	chr3:43097994-43098044	AG04449	skin:	fetal
12	chr3:43073058-43073108	AG04449	skin:	fetal
13	chr3:43073058-43073108	PANC-1	pancreas:	n/a
14	chr3:43097994-43098044	HL-60	blood:	n/a
15	chr3:43073058-43073108	HCT-116	colon:	n/a
16	chr3:43073152-43073202	ovcar-3	ovarian:	n/a
17	chr3:43073058-43073108	HMEC	breast:	n/a
18	chr3:43097994-43098044	HCF	heart:	n/a
19	chr3:43073058-43073108	GM12878	blood:	n/a
20	chr3:43073152-43073202	ProgFib	skin:	n/a
21	chr3:43073152-43073202	K562	blood:	n/a
22	chr3:43073058-43073108	GM12892	blood:	n/a
23	chr3:43073058-43073108	HRPEpiC	eye:	n/a
24	chr3:43073058-43073108	MCF-7	breast:	n/a
25	chr3:43073152-43073202	ECC-1	luminal epithelium:	n/a
26	chr3:43097994-43098044	GM06990	blood:	n/a
27	chr3:43097994-43098044	HepG2	liver:	n/a
28	chr3:43073152-43073202	NHDF-neo	bronchial:	n/a
29	chr3:43097994-43098044	HIPEpiC	eye:	n/a
30	chr3:43073058-43073108	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:43073152-43073202	HRE	kidney:	n/a
32	chr3:43097994-43098044	NHBE	bronchial:	n/a
33	chr3:43073058-43073108	LNCaP	prostate:	n/a
34	chr3:43073152-43073202	AG04450	lung:	fetal
35	chr3:43073058-43073108	AG04450	lung:	fetal
36	chr3:43073058-43073108	SK-N-MC	brain:	n/a
37	chr3:43073058-43073108	HCM	heart:	n/a
38	chr3:43073152-43073202	HEK293	kidney:	embryo
39	chr3:43097994-43098044	AoSMC	blood vessel:	n/a
40	chr3:43073152-43073202	HAEpiC	amniotic membrane:	n/a
41	chr3:43073058-43073108	HCF	heart:	n/a
42	chr3:43097994-43098044	RPTEC	kidney:	n/a
43	chr3:43073152-43073202	Jurkat	blood:	n/a
44	chr3:43073058-43073108	RPTEC	kidney:	n/a
45	chr3:43073058-43073108	SAEC	small airway:	n/a
46	chr3:43073152-43073202	HNPCEpiC	eye:	n/a
47	chr3:43097994-43098044	NHDF-neo	bronchial:	n/a
48	chr3:43073152-43073202	Caco-2	colon:	n/a
49	chr3:43073058-43073108	T-47D	breast:	n/a
50	chr3:43073152-43073202	AG10803	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:43044130..43046332-chr3:43052045..43054420,2	K562	blood:
2	chr3:43044130..43046332-chr3:43052045..43054420,2	K562	blood:
3	chr3:43062963..43065859-chr3:43071110..43073966,2	K562	blood:
4	chr3:43059886..43061659-chr3:43065331..43067767,2	MCF-7	breast:
5	chr3:43059886..43061659-chr3:43065331..43067767,2	MCF-7	breast:
6	chr3:43092511..43095463-chr3:43096998..43098764,2	K562	blood:
7	chr3:43068747..43070408-chr3:43073620..43075322,2	MCF-7	breast:
8	chr3:43092511..43095463-chr3:43096998..43098764,2	K562	blood:
9	chr3:43060384..43063031-chr3:43093535..43095957,2	K562	blood:
10	chr3:43060384..43063031-chr3:43093535..43095957,2	K562	blood:
11	chr3:43068747..43070408-chr3:43073620..43075322,2	MCF-7	breast:
12	chr3:43047918..43050087-chr3:43062104..43064961,2	K562	blood:
13	chr3:43047918..43050087-chr3:43062104..43064961,2	K562	blood:
14	chr3:43062963..43065859-chr3:43071110..43073966,2	K562	blood:
15	chr3:43034015..43036894-chr3:43051666..43054452,2	K562	blood:
16	chr3:43042013..43044443-chr3:43044465..43047233,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF662-1	chr3:43095013-43095766	NONHSAT089276

No data

Variant related genes	Relation type
ENSG00000232375	TF binding region
ENSG00000232375	CpG island

Extended variants
information (count: 1936 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1936 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7624799	chr3:43045803-43045804	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs571245722	chr3:43045836-43045837	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537081832	chr3:43045843-43045844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs6442134	chr3:43045875-43045876	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs565117967	chr3:43045977-43045978	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs146362095	chr3:43046000-43046001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs542026262	chr3:43046025-43046026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs186332890	chr3:43046034-43046035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148597628	chr3:43046048-43046049	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541696358	chr3:43046121-43046122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564481468	chr3:43046158-43046159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9821320	chr3:43046269-43046270	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs544743890	chr3:43046282-43046283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543415609	chr3:43046288-43046289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72869053	chr3:43046298-43046299	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs529403265	chr3:43046299-43046300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548875786	chr3:43046333-43046334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141973446	chr3:43046384-43046385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528307488	chr3:43046389-43046390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563046266	chr3:43046447-43046448	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs200019643	chr3:43046469-43046470	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs183976295	chr3:43046483-43046484	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs186094185	chr3:43046506-43046507	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs35759250	chr3:43046549-43046550	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs200885965	chr3:43046552-43046553	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs370920181	chr3:43046610-43046611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548961341	chr3:43046661-43046662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs150511987	chr3:43046692-43046693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529045015	chr3:43046693-43046694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113013869	chr3:43046699-43046700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs59565527	chr3:43046702-43046703	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs191012552	chr3:43046719-43046720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552827575	chr3:43046760-43046761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528378610	chr3:43046883-43046884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572591806	chr3:43046927-43046928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139444379	chr3:43046979-43046980	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557982888	chr3:43047020-43047021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528359176	chr3:43047028-43047029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs115241769	chr3:43047077-43047078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182685829	chr3:43047099-43047100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144326025	chr3:43047107-43047108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573978482	chr3:43047133-43047134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543089927	chr3:43047190-43047191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559629359	chr3:43047198-43047199	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147804510	chr3:43047207-43047208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187014319	chr3:43047237-43047238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114284359	chr3:43047249-43047250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201580107	chr3:43047278-43047279	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs139540855	chr3:43047287-43047288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539136928	chr3:43047300-43047301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	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
Wilms tumour	17204608	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-small cell lung cancer	21829676	CNVD
Kartagener syndrome	16639409	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Melanoma	21693616	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21364760	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:539 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43043200-43047000	Weak transcription	Fetal Intestine Large	intestine
2	chr3:43043400-43046800	Weak transcription	Brain Substantia Nigra	brain
3	chr3:43043400-43047000	Weak transcription	Brain Anterior Caudate	brain
4	chr3:43043600-43045800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr3:43043600-43046200	Weak transcription	NHLF	lung
6	chr3:43043600-43054400	Weak transcription	Placenta	Placenta
7	chr3:43043800-43054600	Weak transcription	Fetal Kidney	kidney
8	chr3:43044000-43047000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:43044200-43046000	Weak transcription	Osteobl	bone
10	chr3:43044200-43046400	Weak transcription	Fetal Muscle Leg	muscle
11	chr3:43044200-43049800	Weak transcription	Ovary	ovary
12	chr3:43044600-43045800	Weak transcription	Stomach Smooth Muscle	stomach
13	chr3:43044600-43047400	Weak transcription	Liver	Liver
14	chr3:43044600-43052200	Weak transcription	Fetal Stomach	stomach
15	chr3:43044800-43046000	Enhancers	Fetal Thymus	thymus
16	chr3:43044800-43051800	Weak transcription	Brain Hippocampus Middle	brain
17	chr3:43045200-43046600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr3:43045600-43045800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr3:43045600-43045800	Enhancers	HSMMtube	muscle
20	chr3:43045600-43046600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr3:43045600-43046600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr3:43045600-43046600	Enhancers	NHEK	skin
23	chr3:43045600-43047200	Enhancers	HMEC	breast
24	chr3:43045800-43046000	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr3:43045800-43046600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr3:43045800-43046800	Enhancers	Stomach Smooth Muscle	stomach
27	chr3:43045800-43047000	Weak transcription	Thymus	Thymus
28	chr3:43046000-43046400	Weak transcription	Fetal Thymus	thymus
29	chr3:43046000-43046400	Enhancers	Osteobl	bone
30	chr3:43046000-43047400	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr3:43046200-43046400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr3:43046200-43046400	Enhancers	NHDF-Ad	bronchial
33	chr3:43046400-43046600	ZNF genes & repeats	Fetal Muscle Leg	muscle
34	chr3:43046400-43046600	Enhancers	Fetal Thymus	thymus
35	chr3:43046600-43046800	Enhancers	NHLF	lung
36	chr3:43046600-43049000	Weak transcription	Fetal Thymus	thymus
37	chr3:43046600-43053000	Weak transcription	Fetal Muscle Leg	muscle
38	chr3:43046800-43047000	Enhancers	Brain Substantia Nigra	brain
39	chr3:43046800-43047600	Weak transcription	Stomach Smooth Muscle	stomach
40	chr3:43046800-43048000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr3:43046800-43048200	Enhancers	Primary T cells from cord blood	blood
42	chr3:43047000-43047400	Weak transcription	Brain Substantia Nigra	brain
43	chr3:43047000-43047800	Enhancers	Thymus	Thymus
44	chr3:43047000-43048600	Enhancers	Brain Anterior Caudate	brain
45	chr3:43047000-43049600	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr3:43047200-43049400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr3:43047400-43047800	Enhancers	Primary T cells fromperipheralblood	blood
48	chr3:43047400-43048000	Enhancers	Brain Substantia Nigra	brain
49	chr3:43047400-43048400	Enhancers	Liver	Liver
50	chr3:43047600-43047800	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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