Variant report

Variant	esv3383044
Chromosome Location	chr3:56466497-56483664
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:56481200-56481491	K562	blood:	n/a	n/a
2	ARID3A	chr3:56481167-56481484	HepG2	liver:	n/a	n/a
3	CEBPB	chr3:56478248-56478620	HepG2	liver:	n/a	chr3:56478429-56478438 chr3:56478429-56478438 chr3:56478427-56478440 chr3:56478429-56478438 chr3:56478428-56478439 chr3:56478429-56478438
4	CEBPB	chr3:56477651-56477909	HepG2	liver:	n/a	chr3:56477785-56477796 chr3:56477786-56477797
5	CEBPB	chr3:56478253-56478614	A549	lung:	n/a	chr3:56478429-56478438 chr3:56478429-56478438 chr3:56478427-56478440 chr3:56478429-56478438 chr3:56478428-56478439 chr3:56478429-56478438
6	CEBPB	chr3:56478285-56478577	K562	blood:	n/a	chr3:56478429-56478438 chr3:56478429-56478438 chr3:56478427-56478440 chr3:56478429-56478438 chr3:56478428-56478439 chr3:56478429-56478438
7	CEBPB	chr3:56478242-56478632	K562	blood:	n/a	chr3:56478429-56478438 chr3:56478429-56478438 chr3:56478427-56478440 chr3:56478429-56478438 chr3:56478428-56478439 chr3:56478429-56478438
8	CEBPB	chr3:56478251-56478626	H1-hESC	embryonic stem cell:	n/a	chr3:56478429-56478438 chr3:56478429-56478438 chr3:56478427-56478440 chr3:56478429-56478438 chr3:56478428-56478439 chr3:56478429-56478438
9	CEBPB	chr3:56478267-56478690	A549	lung:	n/a	chr3:56478429-56478438 chr3:56478429-56478438 chr3:56478427-56478440 chr3:56478429-56478438 chr3:56478428-56478439 chr3:56478429-56478438
10	CEBPB	chr3:56477691-56477932	A549	lung:	n/a	chr3:56477785-56477796 chr3:56477786-56477797
11	CEBPB	chr3:56478248-56478617	IMR90	lung:	n/a	chr3:56478429-56478438 chr3:56478429-56478438 chr3:56478427-56478440 chr3:56478429-56478438 chr3:56478428-56478439 chr3:56478429-56478438
12	CEBPB	chr3:56481148-56481362	H1-hESC	embryonic stem cell:	n/a	chr3:56481347-56481355
13	CHD2	chr3:56481198-56481396	HepG2	liver:	n/a	n/a
14	CHD2	chr3:56481153-56481331	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr3:56480710-56480767	Gliobla	brain:	n/a	n/a
16	CTCF	chr3:56481240-56481390	HEEpiC	esophagus:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
17	CTCF	chr3:56480460-56480610	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr3:56480580-56480669	LNCaP	prostate:	n/a	n/a
19	CTCF	chr3:56481200-56481350	GM12874	blood:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
20	CTCF	chr3:56480552-56480641	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr3:56480540-56480690	GM12878	blood:	n/a	n/a
22	CTCF	chr3:56481240-56481390	HA-sp	spinal cord:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
23	CTCF	chr3:56481260-56481410	GM12878	blood:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
24	CTCF	chr3:56480340-56480490	GM12878	blood:	n/a	n/a
25	CTCF	chr3:56480856-56481630	SK-N-SH	brain:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
26	CTCF	chr3:56481260-56481410	AG04449	skin:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
27	CTCF	chr3:56480580-56480730	HepG2	liver:	n/a	n/a
28	CTCF	chr3:56480480-56480630	GM06990	blood:	n/a	n/a
29	CTCF	chr3:56480504-56480722	IMR90	lung:	n/a	n/a
30	CTCF	chr3:56480580-56480730	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr3:56481260-56481410	GM12872	blood:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
32	CTCF	chr3:56481280-56481430	GM06990	blood:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
33	CTCF	chr3:56481044-56481503	HepG2	liver:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
34	CTCF	chr3:56480500-56480650	AG10803	skin:	n/a	n/a
35	CTCF	chr3:56481194-56481465	K562	blood:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
36	CTCF	chr3:56481460-56481610	GM12867	blood:	n/a	n/a
37	CTCF	chr3:56481174-56481459	SK-N-SH_RA	brain:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
38	CTCF	chr3:56480480-56480630	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:56481214-56481465	GM20000	blood:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
40	CTCF	chr3:56481260-56481410	GM12865	blood:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
41	CTCF	chr3:56480520-56480670	GM12870	blood:	n/a	n/a
42	CTCF	chr3:56481260-56481410	HAc	cerebellar:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
43	CTCF	chr3:56481181-56481472	Hela-S3	cervix:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
44	CTCF	chr3:56480551-56480589	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:56480520-56480670	HCM	heart:	n/a	n/a
46	CTCF	chr3:56481260-56481410	HepG2	liver:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
47	CTCF	chr3:56481220-56481370	HVMF	connective:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
48	CTCF	chr3:56481123-56481472	Fibrobl	skin:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331
49	CTCF	chr3:56480540-56480690	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr3:56481240-56481390	HPAF	blood vessel:	n/a	chr3:56481308-56481329 chr3:56481314-56481330 chr3:56481313-56481331

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:56475339-56475389	PANC-1	pancreas:	n/a
2	chr3:56475339-56475389	MCF10A-Er-Src	breast:	n/a
3	chr3:56475339-56475389	HCT-116	colon:	n/a
4	chr3:56475339-56475389	ovcar-3	ovarian:	n/a
5	chr3:56475339-56475389	CMK	blood:	n/a
6	chr3:56475339-56475389	HIPEpiC	eye:	n/a
7	chr3:56475339-56475389	AG04450	lung:	fetal
8	chr3:56475339-56475389	GM12878	blood:	n/a
9	chr3:56475339-56475389	AG09319	gingival:	n/a
10	chr3:56475339-56475389	HCM	heart:	n/a
11	chr3:56475339-56475389	HCPEpiC	choroid plexus:	n/a
12	chr3:56475339-56475389	GM19239	blood:	n/a
13	chr3:56475339-56475389	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:56475339-56475389	SK-N-SH	brain:	n/a
15	chr3:56475339-56475389	T-47D	breast:	n/a
16	chr3:56475339-56475389	Hela-S3	cervix:	n/a
17	chr3:56475339-56475389	BE2_C	brain:	n/a
18	chr3:56475339-56475389	PrEC	prostate:	n/a
19	chr3:56475339-56475389	AoSMC	blood vessel:	n/a
20	chr3:56475339-56475389	HAEpiC	amniotic membrane:	n/a
21	chr3:56475339-56475389	NHBE	bronchial:	n/a
22	chr3:56475339-56475389	NB4	blood:	n/a
23	chr3:56475339-56475389	HRE	kidney:	n/a
24	chr3:56475339-56475389	HEEpiC	esophagus:	n/a
25	chr3:56475339-56475389	SK-N-MC	brain:	n/a
26	chr3:56475339-56475389	K562	blood:	n/a
27	chr3:56475339-56475389	BJ	skin:	n/a
28	chr3:56475339-56475389	AG04449	skin:	fetal
29	chr3:56475339-56475389	Caco-2	colon:	n/a
30	chr3:56475339-56475389	ProgFib	skin:	n/a
31	chr3:56475339-56475389	GM06990	blood:	n/a
32	chr3:56475339-56475389	MCF-7	breast:	n/a
33	chr3:56475339-56475389	GM12891	blood:	n/a
34	chr3:56475339-56475389	AG09309	skin:	n/a
35	chr3:56475339-56475389	A549	lung:	n/a
36	chr3:56475339-56475389	SAEC	small airway:	n/a
37	chr3:56475339-56475389	AG10803	skin:	n/a
38	chr3:56475339-56475389	SKMC	muscle:	n/a
39	chr3:56475339-56475389	HL-60	blood:	n/a
40	chr3:56475339-56475389	HMEC	breast:	n/a
41	chr3:56475339-56475389	ECC-1	luminal epithelium:	n/a
42	chr3:56475339-56475389	LNCaP	prostate:	n/a
43	chr3:56475339-56475389	NHDF-neo	bronchial:	n/a
44	chr3:56475339-56475389	U87	brain:	n/a
45	chr3:56475339-56475389	RPTEC	kidney:	n/a
46	chr3:56475339-56475389	NT2-D1	testis:	n/a
47	chr3:56475339-56475389	Jurkat	blood:	n/a
48	chr3:56475339-56475389	HNPCEpiC	eye:	n/a
49	chr3:56475339-56475389	HEK293	kidney:	embryo
50	chr3:56475339-56475389	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:56374174..56375293-chr3:56480529..56481653,5	MCF-7	breast:
2	chr3:56374176..56374999-chr3:56478634..56479183,2	MCF-7	breast:
3	chr3:56481629..56483491-chr3:56506642..56508323,2	MCF-7	breast:
4	chr3:56480877..56481665-chr3:56581433..56582100,2	MCF-7	breast:
5	chr3:56475922..56478879-chr3:56492161..56494889,2	K562	blood:
6	chr3:56381327..56381925-chr3:56480879..56481641,3	MCF-7	breast:
7	chr3:56480674..56481598-chr3:56528399..56529268,2	MCF-7	breast:

Variant related genes	Relation type
ERC2	TF binding region
ERC2	CpG island

Extended variants
information (count: 638 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:638 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553773656	chr3:56466497-56466498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs80217008	chr3:56466526-56466527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72875337	chr3:56466530-56466531	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs185584813	chr3:56466537-56466538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9857355	chr3:56466542-56466543	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs545585706	chr3:56466547-56466548	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564786839	chr3:56466548-56466549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573036264	chr3:56466561-56466562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs141083195	chr3:56466575-56466576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547386457	chr3:56466641-56466642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144897372	chr3:56466679-56466680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138775986	chr3:56466692-56466693	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs149291297	chr3:56466738-56466739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs563244341	chr3:56466771-56466772	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569936207	chr3:56466820-56466821	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191637874	chr3:56466824-56466825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs552366981	chr3:56466873-56466874	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181762054	chr3:56466883-56466884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144574426	chr3:56466925-56466926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553881908	chr3:56466937-56466938	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578043485	chr3:56466955-56466956	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573686056	chr3:56467006-56467007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536695407	chr3:56467012-56467013	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556530851	chr3:56467064-56467065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs187319125	chr3:56467073-56467074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545237376	chr3:56467082-56467083	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559672184	chr3:56467083-56467084	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565494767	chr3:56467084-56467085	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532219590	chr3:56467110-56467111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs572706017	chr3:56467196-56467197	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs541118864	chr3:56467197-56467198	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112309768	chr3:56467199-56467200	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143863427	chr3:56467220-56467221	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536498559	chr3:56467221-56467222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs199904696	chr3:56467222-56467223	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113300685	chr3:56467223-56467224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113815335	chr3:56467224-56467225	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs62255935	chr3:56467226-56467227	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143266529	chr3:56467232-56467233	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs60440857	chr3:56467239-56467240	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561013965	chr3:56467260-56467261	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs74283987	chr3:56467324-56467325	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549759008	chr3:56467328-56467329	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs57784387	chr3:56467388-56467389	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs532460673	chr3:56467448-56467449	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs148005960	chr3:56467525-56467526	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs115265390	chr3:56467561-56467562	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs192275232	chr3:56467630-56467631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11719646	chr3:56467691-56467692	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs567422837	chr3:56467757-56467758	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	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
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	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 mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Renal cell carcinoma	18765545	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:56447400-56469200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr3:56450000-56467800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:56450000-56469800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:56456400-56479600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr3:56456600-56467400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr3:56456800-56467000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr3:56456800-56467400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr3:56456800-56467400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr3:56456800-56467400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr3:56456800-56467600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr3:56456800-56468000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr3:56456800-56468400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:56457600-56473400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr3:56458000-56474800	Weak transcription	Fetal Heart	heart
15	chr3:56458600-56468400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr3:56460000-56466600	Weak transcription	Brain Germinal Matrix	brain
17	chr3:56460800-56467400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:56462400-56467400	Weak transcription	Fetal Brain Female	brain
19	chr3:56463600-56467600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:56464000-56467000	Weak transcription	Pancreas	Pancrea
21	chr3:56465000-56468800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr3:56465600-56468000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:56465600-56468400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr3:56466200-56468200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr3:56466400-56469000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:56466400-56471600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr3:56466600-56468800	Strong transcription	Brain Germinal Matrix	brain
28	chr3:56467000-56467600	Enhancers	Pancreas	Pancrea
29	chr3:56467000-56469000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr3:56467200-56467400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr3:56467200-56473000	Weak transcription	HUVEC	blood vessel
32	chr3:56467400-56467600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr3:56467400-56467600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:56467400-56469000	Strong transcription	H1 Cell Line	embryonic stem cell
35	chr3:56467400-56469000	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr3:56467400-56469000	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr3:56467400-56469000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
38	chr3:56467400-56469000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr3:56467400-56469000	Strong transcription	Fetal Brain Female	brain
40	chr3:56467600-56468800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:56467600-56469200	Strong transcription	HUES48 Cell Line	embryonic stem cell
42	chr3:56467600-56469600	Weak transcription	Pancreas	Pancrea
43	chr3:56467600-56470400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:56467600-56470600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:56468000-56469000	Strong transcription	H9 Cell Line	embryonic stem cell
46	chr3:56468000-56469000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:56468200-56469000	Strong transcription	Brain Cingulate Gyrus	brain
48	chr3:56468400-56469000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:56468400-56469000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:56468400-56469000	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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