Variant report

Variant	nsv1004470
Chromosome Location	chr3:69597148-69728231
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	ATF1	chr3:69714150-69714472	K562	blood:	n/a	n/a
2	ATF1	chr3:69701784-69702178	K562	blood:	n/a	n/a
3	BHLHE40	chr3:69714188-69714370	K562	blood:	n/a	n/a
4	BHLHE40	chr3:69597722-69597761	K562	blood:	n/a	n/a
5	CEBPB	chr3:69696959-69697231	K562	blood:	n/a	n/a
6	CEBPB	chr3:69696932-69697239	IMR90	lung:	n/a	n/a
7	CEBPB	chr3:69714508-69714733	A549	lung:	n/a	chr3:69714650-69714663
8	CEBPB	chr3:69717462-69717716	H1-hESC	embryonic stem cell:	n/a	chr3:69717583-69717592 chr3:69717581-69717592 chr3:69717582-69717593 chr3:69717581-69717594
9	CEBPB	chr3:69696927-69697264	HepG2	liver:	n/a	n/a
10	CEBPB	chr3:69614678-69614941	K562	blood:	n/a	chr3:69614794-69614805
11	CEBPB	chr3:69614727-69614865	IMR90	lung:	n/a	chr3:69614794-69614805
12	CEBPB	chr3:69637696-69637896	H1-hESC	embryonic stem cell:	n/a	chr3:69637794-69637805 chr3:69637795-69637806
13	CEBPB	chr3:69717444-69717760	HepG2	liver:	n/a	chr3:69717583-69717592 chr3:69717581-69717592 chr3:69717582-69717593 chr3:69717581-69717594
14	CEBPB	chr3:69634716-69634958	H1-hESC	embryonic stem cell:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
15	CEBPB	chr3:69659531-69659560	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:69614637-69614892	HepG2	liver:	n/a	chr3:69614794-69614805
17	CEBPB	chr3:69634645-69634992	A549	lung:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
18	CEBPB	chr3:69646344-69646636	IMR90	lung:	n/a	chr3:69646473-69646484
19	CEBPB	chr3:69696982-69697192	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr3:69614689-69614925	H1-hESC	embryonic stem cell:	n/a	chr3:69614794-69614805
21	CEBPB	chr3:69637396-69637922	HepG2	liver:	n/a	chr3:69637794-69637805 chr3:69637795-69637806
22	CEBPB	chr3:69608030-69608399	Hela-S3	cervix:	n/a	chr3:69608212-69608223
23	CEBPB	chr3:69666554-69666767	HepG2	liver:	n/a	chr3:69666717-69666728
24	CEBPB	chr3:69714584-69714686	Hela-S3	cervix:	n/a	chr3:69714650-69714663
25	CEBPB	chr3:69608148-69608310	HepG2	liver:	n/a	chr3:69608212-69608223
26	CEBPB	chr3:69634649-69634993	IMR90	lung:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
27	CEBPB	chr3:69634651-69634994	HepG2	liver:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
28	CEBPB	chr3:69717439-69717693	MCF-7	breast:	n/a	chr3:69717583-69717592 chr3:69717581-69717592 chr3:69717582-69717593 chr3:69717581-69717594
29	CEBPB	chr3:69717434-69717744	K562	blood:	n/a	chr3:69717583-69717592 chr3:69717581-69717592 chr3:69717582-69717593 chr3:69717581-69717594
30	CEBPB	chr3:69674162-69674362	HepG2	liver:	n/a	chr3:69674222-69674233
31	CEBPB	chr3:69697065-69697102	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr3:69646319-69646614	A549	lung:	n/a	chr3:69646473-69646484
33	CEBPB	chr3:69646327-69646649	HepG2	liver:	n/a	chr3:69646473-69646484
34	CEBPB	chr3:69634687-69634976	K562	blood:	n/a	chr3:69634815-69634824 chr3:69634815-69634824 chr3:69634813-69634826 chr3:69634815-69634824
35	CEBPB	chr3:69696938-69697234	A549	lung:	n/a	n/a
36	CEBPB	chr3:69684168-69684321	A549	lung:	n/a	n/a
37	CEBPB	chr3:69666612-69666872	A549	lung:	n/a	chr3:69666717-69666728
38	CEBPB	chr3:69674148-69674348	A549	lung:	n/a	chr3:69674222-69674233
39	CEBPB	chr3:69666599-69666853	IMR90	lung:	n/a	chr3:69666717-69666728
40	CEBPB	chr3:69696997-69697271	MCF-7	breast:	n/a	n/a
41	CEBPB	chr3:69717330-69717754	MCF-7	breast:	n/a	chr3:69717583-69717592 chr3:69717581-69717592 chr3:69717582-69717593 chr3:69717581-69717594
42	CTCF	chr3:69720320-69720470	NHDF-neo	bronchial:	n/a	chr3:69720424-69720445 chr3:69720429-69720447 chr3:69720430-69720446
43	CTCF	chr3:69720760-69720910	AG04450	lung:	n/a	n/a
44	CTCF	chr3:69720380-69720530	BJ	skin:	n/a	chr3:69720424-69720445 chr3:69720429-69720447 chr3:69720430-69720446
45	CTCF	chr3:69720360-69720510	AG09309	skin:	n/a	chr3:69720424-69720445 chr3:69720429-69720447 chr3:69720430-69720446
46	CTCF	chr3:69720164-69720633	A549	lung:	n/a	chr3:69720424-69720445 chr3:69720429-69720447 chr3:69720430-69720446
47	CTCF	chr3:69610060-69610210	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr3:69720340-69720490	GM12866	blood:	n/a	chr3:69720424-69720445 chr3:69720429-69720447 chr3:69720430-69720446
49	CTCF	chr3:69720380-69720530	Caco-2	colon:	n/a	chr3:69720424-69720445 chr3:69720429-69720447 chr3:69720430-69720446
50	CTCF	chr3:69714580-69714730	HBMEC	blood vessel:	n/a	chr3:69714700-69714709

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:69710144-69710194	HRPEpiC	eye:	n/a
2	chr3:69726759-69726809	HEK293	kidney:	embryo
3	chr3:69710586-69710636	H1-hESC	embryonic stem cell:	embryo
4	chr3:69726908-69726958	HL-60	blood:	n/a
5	chr3:69710586-69710636	HL-60	blood:	n/a
6	chr3:69710586-69710636	AoSMC	blood vessel:	n/a
7	chr3:69710144-69710194	HAEpiC	amniotic membrane:	n/a
8	chr3:69726759-69726809	HRCEpiC	kidney:	n/a
9	chr3:69710144-69710194	U87	brain:	n/a
10	chr3:69710710-69710760	HRCEpiC	kidney:	n/a
11	chr3:69726908-69726958	NB4	blood:	n/a
12	chr3:69710710-69710760	GM12878	blood:	n/a
13	chr3:69710586-69710636	AG09309	skin:	n/a
14	chr3:69710144-69710194	ProgFib	skin:	n/a
15	chr3:69710144-69710194	NHBE	bronchial:	n/a
16	chr3:69710586-69710636	HIPEpiC	eye:	n/a
17	chr3:69726759-69726809	H1-hESC	embryonic stem cell:	embryo
18	chr3:69710710-69710760	H1-hESC	embryonic stem cell:	embryo
19	chr3:69710586-69710636	PFSK-1	brain:	n/a
20	chr3:69710710-69710760	Caco-2	colon:	n/a
21	chr3:69710710-69710760	SK-N-SH_RA	brain:	n/a
22	chr3:69726908-69726958	HUVEC	blood vessel:	n/a
23	chr3:69710586-69710636	HRCEpiC	kidney:	n/a
24	chr3:69726908-69726958	HRE	kidney:	n/a
25	chr3:69710710-69710760	HAEpiC	amniotic membrane:	n/a
26	chr3:69726908-69726958	NT2-D1	testis:	n/a
27	chr3:69726759-69726809	HPAEpiC	pulmonary alveolar:	n/a
28	chr3:69710586-69710636	AG04450	lung:	fetal
29	chr3:69726908-69726958	IMR90	lung:	fetal
30	chr3:69710710-69710760	K562	blood:	n/a
31	chr3:69726759-69726809	RPTEC	kidney:	n/a
32	chr3:69710144-69710194	AG09309	skin:	n/a
33	chr3:69710586-69710636	SK-N-SH	brain:	n/a
34	chr3:69710710-69710760	LNCaP	prostate:	n/a
35	chr3:69726759-69726809	AG09309	skin:	n/a
36	chr3:69726759-69726809	A549	lung:	n/a
37	chr3:69726759-69726809	GM12891	blood:	n/a
38	chr3:69726908-69726958	ovcar-3	ovarian:	n/a
39	chr3:69726908-69726958	ProgFib	skin:	n/a
40	chr3:69710710-69710760	HEEpiC	esophagus:	n/a
41	chr3:69710144-69710194	A549	lung:	n/a
42	chr3:69726759-69726809	HCM	heart:	n/a
43	chr3:69710144-69710194	CMK	blood:	n/a
44	chr3:69710710-69710760	AoSMC	blood vessel:	n/a
45	chr3:69726908-69726958	BJ	skin:	n/a
46	chr3:69726759-69726809	Jurkat	blood:	n/a
47	chr3:69710586-69710636	AG10803	skin:	n/a
48	chr3:69710710-69710760	Hepatocyte	liver:	n/a
49	chr3:69710586-69710636	NB4	blood:	n/a
50	chr3:69710144-69710194	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:69488505..69489608-chr3:69719988..69721323,5	MCF-7	breast:
2	chr3:69694033..69698273-chr3:69701406..69703258,4	K562	blood:
3	chr3:69501416..69502491-chr3:69720194..69720929,3	MCF-7	breast:
4	chr3:69660815..69663559-chr3:69665701..69667253,2	K562	blood:
5	chr3:69608607..69610932-chr3:69614152..69616466,2	K562	blood:
6	chr3:69704610..69707455-chr3:69833061..69835848,2	K562	blood:
7	chr3:69694033..69698273-chr3:69701406..69703258,4	K562	blood:
8	chr3:69169765..69171080-chr3:69719979..69720844,3	K562	blood:
9	chr3:69358701..69359571-chr3:69719880..69720869,3	MCF-7	breast:
10	chr3:69608607..69610932-chr3:69614152..69616466,2	K562	blood:
11	chr3:69660815..69663559-chr3:69665701..69667253,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MITF-2	chr3:69640492-69640563	XLOC_002695
2	lnc-MITF-2	chr3:69641596-69642272	XLOC_002695

Variant related genes	Relation type
ENSG00000241667	TF binding region
ENSG00000240842	TF binding region
ENSG00000241667	CpG island
ENSG00000240842	CpG island
SMAD4	miRNA target sites
SPTY2D1	miRNA target sites

Extended variants
information (count: 3943 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3943 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6549238	chr3:69597148-69597149	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147937609	chr3:69597170-69597171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551053198	chr3:69597175-69597176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572290670	chr3:69597186-69597187	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541190593	chr3:69597209-69597210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs113640314	chr3:69597254-69597255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7623494	chr3:69597285-69597286	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73835890	chr3:69597297-69597298	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs17006109	chr3:69597307-69597308	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs184434844	chr3:69597329-69597330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs58220383	chr3:69597413-69597414	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs7623601	chr3:69597424-69597425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200562683	chr3:69597443-69597444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147120039	chr3:69597444-69597445	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567412218	chr3:69597487-69597488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17006111	chr3:69597496-69597497	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs527888310	chr3:69597549-69597550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547537256	chr3:69597584-69597585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565951914	chr3:69597639-69597640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74670517	chr3:69597679-69597680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528323165	chr3:69597684-69597685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1126301	chr3:69597700-69597701	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs188003072	chr3:69597710-69597711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73835891	chr3:69597717-69597718	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs56000524	chr3:69597733-69597734	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs572533101	chr3:69597868-69597869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs372465118	chr3:69597874-69597875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs72937490	chr3:69597895-69597896	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs12629703	chr3:69597914-69597915	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs577902710	chr3:69597916-69597917	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138247872	chr3:69597917-69597918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536621133	chr3:69597921-69597922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs149141318	chr3:69597922-69597923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540270196	chr3:69597928-69597929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542225372	chr3:69597966-69597967	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143259806	chr3:69597975-69597976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs17006112	chr3:69598109-69598110	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs4488832	chr3:69598133-69598134	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs148324676	chr3:69598137-69598138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533327302	chr3:69598155-69598156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72937492	chr3:69598156-69598157	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs570218249	chr3:69598193-69598194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9818139	chr3:69598341-69598342	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs555429474	chr3:69598392-69598393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs192523715	chr3:69598404-69598405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114938118	chr3:69598413-69598414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558270610	chr3:69598457-69598458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577942918	chr3:69598510-69598511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543227046	chr3:69598512-69598513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184518790	chr3:69598516-69598517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
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
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
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69592400-69604200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:69592400-69607600	Weak transcription	Right Ventricle	heart
3	chr3:69592600-69600000	Weak transcription	Fetal Heart	heart
4	chr3:69592800-69597600	Weak transcription	Brain Hippocampus Middle	brain
5	chr3:69595400-69600200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:69596400-69597200	Enhancers	Hela-S3	cervix
7	chr3:69596600-69597200	Enhancers	Fetal Lung	lung
8	chr3:69596600-69597800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr3:69596800-69597400	Enhancers	Brain Substantia Nigra	brain
10	chr3:69596800-69598200	Enhancers	Brain Cingulate Gyrus	brain
11	chr3:69597000-69597800	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr3:69597000-69598000	Weak transcription	Brain Anterior Caudate	brain
13	chr3:69597200-69597600	Weak transcription	Fetal Lung	lung
14	chr3:69597400-69597800	Weak transcription	Brain Substantia Nigra	brain
15	chr3:69597600-69598400	Enhancers	Brain Hippocampus Middle	brain
16	chr3:69597600-69598400	Enhancers	Fetal Lung	lung
17	chr3:69597800-69598800	Enhancers	Brain Substantia Nigra	brain
18	chr3:69597800-69599600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr3:69598000-69598400	Enhancers	Brain Anterior Caudate	brain
20	chr3:69598000-69598600	Enhancers	Fetal Kidney	kidney
21	chr3:69598200-69599400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr3:69598400-69599800	Weak transcription	Brain Hippocampus Middle	brain
23	chr3:69598400-69600000	Weak transcription	Fetal Lung	lung
24	chr3:69598600-69602800	Weak transcription	Fetal Kidney	kidney
25	chr3:69598800-69599200	Weak transcription	Brain Substantia Nigra	brain
26	chr3:69599200-69600000	Enhancers	Brain Substantia Nigra	brain
27	chr3:69599400-69600200	Enhancers	Brain Cingulate Gyrus	brain
28	chr3:69599600-69600200	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr3:69599600-69600200	Enhancers	Ovary	ovary
30	chr3:69599800-69600200	Enhancers	Brain Hippocampus Middle	brain
31	chr3:69600000-69600200	Enhancers	Fetal Heart	heart
32	chr3:69600000-69600800	Enhancers	Brain Angular Gyrus	brain
33	chr3:69600000-69601400	Enhancers	Fetal Lung	lung
34	chr3:69600200-69600600	Weak transcription	Fetal Heart	heart
35	chr3:69600600-69600800	Enhancers	Fetal Heart	heart
36	chr3:69600800-69601400	Enhancers	Adipose Nuclei	Adipose
37	chr3:69600800-69602400	Weak transcription	Fetal Heart	heart
38	chr3:69601000-69601400	Enhancers	Spleen	Spleen
39	chr3:69601400-69602400	Weak transcription	Fetal Lung	lung
40	chr3:69601400-69604000	Weak transcription	Spleen	Spleen
41	chr3:69602400-69603400	Enhancers	Fetal Lung	lung
42	chr3:69602400-69604200	Enhancers	Fetal Heart	heart
43	chr3:69602600-69604800	Enhancers	Liver	Liver
44	chr3:69603000-69603200	Enhancers	Fetal Kidney	kidney
45	chr3:69603000-69603400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr3:69603400-69608200	Weak transcription	Fetal Lung	lung
47	chr3:69603800-69604600	Enhancers	Pancreas	Pancrea
48	chr3:69604000-69604400	Enhancers	Spleen	Spleen
49	chr3:69604200-69604400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr3:69604400-69612400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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