Variant report

Variant	esv17051
Chromosome Location	chr3:46794424-46851520
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:368)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
2	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
3	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
4	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
5	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
6	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
7	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
9	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
10	CTCF	chr3:46794460-46794610	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr3:46798359-46798450	LNCaP	prostate:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
12	CTCF	chr3:46798336-46798412	H1-hESC	embryonic stem cell:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
13	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr3:46798280-46798430	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
15	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
16	CTCF	chr3:46794360-46794510	GM12873	blood:	n/a	n/a
17	CTCF	chr3:46798400-46798550	HVMF	connective:	n/a	n/a
18	CTCF	chr3:46798300-46798450	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
19	CTCF	chr3:46850100-46850250	GM12864	blood:	n/a	chr3:46850217-46850226
20	CTCF	chr3:46794520-46794670	GM12864	blood:	n/a	n/a
21	CTCF	chr3:46850080-46850230	GM12873	blood:	n/a	chr3:46850217-46850226
22	CTCF	chr3:46794560-46794710	HCT-116	colon:	n/a	n/a
23	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr3:46798034-46798529	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
25	CTCF	chr3:46798354-46798408	Gliobla	brain:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
26	CTCF	chr3:46846140-46846290	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
28	CTCF	chr3:46794460-46794610	GM06990	blood:	n/a	n/a
29	CTCF	chr3:46798136-46798509	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
30	CTCF	chr3:46798300-46798450	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
31	CTCF	chr3:46794500-46794650	GM12866	blood:	n/a	n/a
32	CTCF	chr3:46798134-46798571	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
33	CTCF	chr3:46850200-46850350	GM12864	blood:	n/a	chr3:46850217-46850226
34	CTCF	chr3:46794500-46794650	GM12873	blood:	n/a	n/a
35	CTCF	chr3:46797989-46798564	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
36	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
37	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr3:46798156-46798539	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
39	CTCF	chr3:46794500-46794650	GM12872	blood:	n/a	n/a
40	CTCF	chr3:46850120-46850270	GM12873	blood:	n/a	chr3:46850217-46850226
41	CTCF	chr3:46794600-46794750	GM12875	blood:	n/a	n/a
42	CTCF	chr3:46794616-46794658	GM19240	blood:	n/a	n/a
43	CTCF	chr3:46798280-46798435	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
44	CTCFL	chr3:46798258-46798497	K562	blood:	n/a	n/a
45	CTCFL	chr3:46798305-46798476	K562	blood:	n/a	n/a
46	E2F4	chr3:46799519-46799724	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F6	chr3:46798300-46798501	K562	blood:	n/a	n/a
48	E2F6	chr3:46798276-46798526	K562	blood:	n/a	n/a
49	EBF1	chr3:46821837-46822068	GM12878	blood:	n/a	chr3:46821936-46821947 chr3:46821916-46821927
50	FAM48A	chr3:46839688-46839827	GM12878	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46796026-46796076	SK-N-SH	brain:	n/a
2	chr3:46850588-46850638	NHDF-neo	bronchial:	n/a
3	chr3:46796026-46796076	SK-N-SH	brain:	n/a
4	chr3:46850588-46850638	NHDF-neo	bronchial:	n/a
5	chr3:46796026-46796076	BJ	skin:	n/a
6	chr3:46798240-46798290	ECC-1	luminal epithelium:	n/a
7	chr3:46798240-46798290	AG04450	lung:	fetal
8	chr3:46796026-46796076	HRCEpiC	kidney:	n/a
9	chr3:46797928-46797978	HEK293	kidney:	embryo
10	chr3:46850588-46850638	GM06990	blood:	n/a
11	chr3:46799010-46799060	IMR90	lung:	fetal
12	chr3:46797928-46797978	GM12892	blood:	n/a
13	chr3:46796026-46796076	HCF	heart:	n/a
14	chr3:46799010-46799060	A549	lung:	n/a
15	chr3:46801208-46801258	AG09309	skin:	n/a
16	chr3:46798240-46798290	Jurkat	blood:	n/a
17	chr3:46797928-46797978	A549	lung:	n/a
18	chr3:46799010-46799060	HUVEC	blood vessel:	n/a
19	chr3:46799010-46799060	SAEC	small airway:	n/a
20	chr3:46798240-46798290	AoSMC	blood vessel:	n/a
21	chr3:46798240-46798290	HIPEpiC	eye:	n/a
22	chr3:46796026-46796076	HEEpiC	esophagus:	n/a
23	chr3:46801208-46801258	HepG2	liver:	n/a
24	chr3:46797928-46797978	GM19239	blood:	n/a
25	chr3:46850588-46850638	HAEpiC	amniotic membrane:	n/a
26	chr3:46798240-46798290	AG10803	skin:	n/a
27	chr3:46796026-46796076	HRPEpiC	eye:	n/a
28	chr3:46801208-46801258	LNCaP	prostate:	n/a
29	chr3:46797928-46797978	Jurkat	blood:	n/a
30	chr3:46799010-46799060	HCPEpiC	choroid plexus:	n/a
31	chr3:46798240-46798290	H1-hESC	embryonic stem cell:	embryo
32	chr3:46850588-46850638	HEK293	kidney:	embryo
33	chr3:46850588-46850638	A549	lung:	n/a
34	chr3:46799010-46799060	LNCaP	prostate:	n/a
35	chr3:46797928-46797978	SK-N-SH	brain:	n/a
36	chr3:46801208-46801258	MCF-7	breast:	n/a
37	chr3:46799010-46799060	ECC-1	luminal epithelium:	n/a
38	chr3:46799010-46799060	Hela-S3	cervix:	n/a
39	chr3:46797928-46797978	HepG2	liver:	n/a
40	chr3:46801208-46801258	PrEC	prostate:	n/a
41	chr3:46850588-46850638	HCM	heart:	n/a
42	chr3:46796026-46796076	NHDF-neo	bronchial:	n/a
43	chr3:46801208-46801258	HAEpiC	amniotic membrane:	n/a
44	chr3:46850588-46850638	NHBE	bronchial:	n/a
45	chr3:46797928-46797978	NH-A	brain:	n/a
46	chr3:46797928-46797978	AG04450	lung:	fetal
47	chr3:46799010-46799060	GM12892	blood:	n/a
48	chr3:46798240-46798290	SK-N-MC	brain:	n/a
49	chr3:46799010-46799060	NB4	blood:	n/a
50	chr3:46799010-46799060	HL-60	blood:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
2	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
3	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
4	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
5	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
6	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
7	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
8	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
9	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
10	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
11	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
12	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
13	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
14	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
15	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
16	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
17	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457
2	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458
3	lnc-PRSS50-1	chr3:46797532-46798119	NONHSAT089457

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
ENSG00000238013	CpG island

Extended variants
information (count: 702 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:702 , 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	rs573192640	chr3:46794436-46794437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184350789	chr3:46794441-46794442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561893627	chr3:46794480-46794481	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189198259	chr3:46794483-46794484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs72893366	chr3:46794496-46794497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563356779	chr3:46794552-46794553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530808323	chr3:46794624-46794625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181760188	chr3:46794628-46794629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573989212	chr3:46794629-46794630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs59356397	chr3:46794643-46794644	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs144230911	chr3:46794645-46794646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs546619674	chr3:46794668-46794669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs377033303	chr3:46794712-46794713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs57268847	chr3:46794745-46794746	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs148704364	chr3:46794798-46794799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533290091	chr3:46794808-46794809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569378156	chr3:46794815-46794816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545452856	chr3:46794871-46794872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540108576	chr3:46794880-46794881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs186436598	chr3:46794887-46794888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143007122	chr3:46794898-46794899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs572899834	chr3:46794899-46794900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563618430	chr3:46794910-46794911	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533886819	chr3:46794925-46794926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188841376	chr3:46794958-46794959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542909653	chr3:46795034-46795035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554524956	chr3:46795035-46795036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61153905	chr3:46795062-46795063	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs544323992	chr3:46795063-46795064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34238793	chr3:46795078-46795079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35880732	chr3:46795084-46795085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs56836203	chr3:46795085-46795086	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs181643407	chr3:46795150-46795151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113388975	chr3:46795180-46795181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs546582866	chr3:46795194-46795195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376581103	chr3:46795236-46795237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374055116	chr3:46795237-46795238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528974901	chr3:46795301-46795302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375805203	chr3:46795304-46795305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550436922	chr3:46795326-46795327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377626764	chr3:46795339-46795340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs151101330	chr3:46795340-46795341	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs551955013	chr3:46795341-46795342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs566782866	chr3:46795564-46795565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534241062	chr3:46795631-46795632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35649252	chr3:46795651-46795652	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186806769	chr3:46795657-46795658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538323586	chr3:46795710-46795711	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556427741	chr3:46795716-46795717	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs34260667	chr3:46795720-46795721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
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
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
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
2	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
3	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
4	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr3:46792400-46797800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:46792800-46795000	Enhancers	Thymus	Thymus
7	chr3:46793400-46795200	Enhancers	Fetal Thymus	thymus
8	chr3:46793400-46800000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr3:46794200-46795000	Enhancers	GM12878-XiMat	blood
10	chr3:46795000-46796000	Weak transcription	Thymus	Thymus
11	chr3:46795200-46796200	Weak transcription	Fetal Thymus	thymus
12	chr3:46795600-46798000	Strong transcription	Skeletal Muscle Male	skeletal muscle
13	chr3:46796000-46796800	Enhancers	Thymus	Thymus
14	chr3:46796400-46796600	Enhancers	Fetal Thymus	thymus
15	chr3:46797600-46797800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr3:46797600-46797800	Bivalent Enhancer	K562	blood
17	chr3:46797600-46798400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:46797800-46798400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:46798000-46798600	Enhancers	Placenta	Placenta
20	chr3:46798000-46798600	Active TSS	K562	blood
21	chr3:46798000-46801400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr3:46798400-46801200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:46800600-46801400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr3:46801000-46801200	Enhancers	Fetal Stomach	stomach
25	chr3:46801000-46801400	Enhancers	Fetal Kidney	kidney
26	chr3:46801000-46801800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr3:46801000-46801800	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:46801000-46802000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr3:46801000-46802000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:46801000-46802000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr3:46801200-46801400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr3:46801200-46801400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:46801200-46801600	Enhancers	H1 Cell Line	embryonic stem cell
34	chr3:46801200-46801600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr3:46801200-46801600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr3:46801200-46801600	Enhancers	Fetal Lung	lung
37	chr3:46801200-46801600	Enhancers	Psoas Muscle	Psoas
38	chr3:46801200-46802000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr3:46801400-46802000	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr3:46801600-46803400	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr3:46802000-46804400	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr3:46804600-46805200	Enhancers	HMEC	breast
43	chr3:46804600-46805400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr3:46804800-46805000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr3:46804800-46805200	Enhancers	NHEK	skin
46	chr3:46805000-46809200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr3:46806000-46806200	Weak transcription	Pancreas	Pancrea
48	chr3:46806200-46806400	ZNF genes & repeats	Pancreas	Pancrea
49	chr3:46809600-46810000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr3:46819200-46820200	Enhancers	Primary B cells from cord blood	blood

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