Variant report

Variant	nsv876857
Chromosome Location	chr3:60472815-60558331
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:122)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:60490547-60490897	GM12878	blood:	n/a	n/a
2	ATF3	chr3:60541358-60541754	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:60506210-60506414	K562	blood:	n/a	n/a
4	BACH1	chr3:60477738-60477770	K562	blood:	n/a	n/a
5	BATF	chr3:60490607-60490758	GM12878	blood:	n/a	n/a
6	BATF	chr3:60538939-60539154	GM12878	blood:	n/a	n/a
7	BATF	chr3:60541502-60541804	GM12878	blood:	n/a	chr3:60541671-60541682
8	BATF	chr3:60541461-60541885	GM12878	blood:	n/a	chr3:60541671-60541682
9	BATF	chr3:60522246-60522459	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:60514439-60514714	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:60541504-60541905	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:60490569-60490827	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:60541461-60541764	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:60490610-60490852	GM12878	blood:	n/a	n/a
15	BCL3	chr3:60541457-60541820	GM12878	blood:	n/a	n/a
16	BCLAF1	chr3:60541470-60541822	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:60500477-60500907	K562	blood:	n/a	n/a
18	BHLHE40	chr3:60500213-60500224	K562	blood:	n/a	n/a
19	BHLHE40	chr3:60541385-60541970	GM12878	blood:	n/a	n/a
20	CEBPB	chr3:60556976-60557552	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr3:60492999-60493149	K562	blood:	n/a	n/a
22	CEBPB	chr3:60473036-60473256	K562	blood:	n/a	chr3:60473083-60473094 chr3:60473083-60473092
23	CEBPB	chr3:60502891-60503236	HepG2	liver:	n/a	chr3:60503042-60503059 chr3:60503044-60503055
24	CEBPB	chr3:60528680-60529009	K562	blood:	n/a	n/a
25	CEBPB	chr3:60502858-60503358	K562	blood:	n/a	chr3:60503042-60503059 chr3:60503044-60503055
26	CEBPB	chr3:60502880-60503221	IMR90	lung:	n/a	chr3:60503042-60503059 chr3:60503044-60503055
27	CEBPB	chr3:60541559-60541835	GM12878	blood:	n/a	n/a
28	CEBPB	chr3:60515719-60515918	K562	blood:	n/a	n/a
29	CEBPB	chr3:60502935-60503162	H1-hESC	embryonic stem cell:	n/a	chr3:60503042-60503059 chr3:60503044-60503055
30	CHD1	chr3:60541274-60541431	GM12878	blood:	n/a	n/a
31	CHD2	chr3:60490587-60490880	GM12878	blood:	n/a	n/a
32	CREB1	chr3:60490511-60490992	GM12878	blood:	n/a	n/a
33	CREB1	chr3:60538902-60539194	GM12878	blood:	n/a	n/a
34	CREB1	chr3:60490627-60490860	GM12878	blood:	n/a	n/a
35	CTBP2	chr3:60541259-60542058	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr3:60522216-60522593	GM12878	blood:	n/a	n/a
37	CTCF	chr3:60513280-60513430	AG10803	skin:	n/a	n/a
38	CTCF	chr3:60513140-60513290	RPTEC	kidney:	n/a	n/a
39	CTCF	chr3:60478338-60478356	Fibrobl	skin:	n/a	n/a
40	CTCF	chr3:60538760-60538803	ProgFib	skin:	n/a	n/a
41	CTCF	chr3:60478295-60478332	MCF-7	breast:	n/a	n/a
42	CTCF	chr3:60513277-60513325	LNCaP	prostate:	n/a	n/a
43	CTCF	chr3:60522294-60522513	LNCaP	prostate:	n/a	n/a
44	CTCF	chr3:60513240-60513390	AG10803	skin:	n/a	n/a
45	CTCF	chr3:60529465-60529510	GM10266	blood:	n/a	n/a
46	CTCF	chr3:60522322-60522498	LNCaP	prostate:	n/a	n/a
47	CTCF	chr3:60513180-60513330	HMEC	breast:	n/a	n/a
48	CTCF	chr3:60513220-60513370	AG09309	skin:	n/a	n/a
49	CTCF	chr3:60512440-60512590	GM12867	blood:	n/a	chr3:60512516-60512524
50	CTCF	chr3:60513200-60513350	AG04449	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:60534659-60534709	NB4	blood:	n/a
2	chr3:60534659-60534709	PrEC	prostate:	n/a
3	chr3:60541935-60541985	NT2-D1	testis:	n/a
4	chr3:60541935-60541985	AG09319	gingival:	n/a
5	chr3:60541935-60541985	Hela-S3	cervix:	n/a
6	chr3:60534659-60534709	HUVEC	blood vessel:	n/a
7	chr3:60541935-60541985	HAEpiC	amniotic membrane:	n/a
8	chr3:60534659-60534709	SK-N-SH_RA	brain:	n/a
9	chr3:60541935-60541985	HCM	heart:	n/a
10	chr3:60534659-60534709	HEK293	kidney:	embryo
11	chr3:60534659-60534709	HNPCEpiC	eye:	n/a
12	chr3:60541935-60541985	GM12891	blood:	n/a
13	chr3:60541935-60541985	SK-N-SH	brain:	n/a
14	chr3:60534659-60534709	HCF	heart:	n/a
15	chr3:60534659-60534709	A549	lung:	n/a
16	chr3:60541935-60541985	IMR90	lung:	fetal
17	chr3:60534659-60534709	ovcar-3	ovarian:	n/a
18	chr3:60534659-60534709	PANC-1	pancreas:	n/a
19	chr3:60534659-60534709	K562	blood:	n/a
20	chr3:60541935-60541985	H1-hESC	embryonic stem cell:	embryo
21	chr3:60534659-60534709	HPAEpiC	pulmonary alveolar:	n/a
22	chr3:60534659-60534709	H1-hESC	embryonic stem cell:	embryo
23	chr3:60541935-60541985	AG09309	skin:	n/a
24	chr3:60541935-60541985	LNCaP	prostate:	n/a
25	chr3:60534659-60534709	AoSMC	blood vessel:	n/a
26	chr3:60534659-60534709	AG09309	skin:	n/a
27	chr3:60534659-60534709	NHDF-neo	bronchial:	n/a
28	chr3:60534659-60534709	HRE	kidney:	n/a
29	chr3:60534659-60534709	HL-60	blood:	n/a
30	chr3:60541935-60541985	HNPCEpiC	eye:	n/a
31	chr3:60534659-60534709	HCT-116	colon:	n/a
32	chr3:60534659-60534709	AG10803	skin:	n/a
33	chr3:60541935-60541985	MCF10A-Er-Src	breast:	n/a
34	chr3:60534659-60534709	HRCEpiC	kidney:	n/a
35	chr3:60541935-60541985	HRPEpiC	eye:	n/a
36	chr3:60534659-60534709	SK-N-MC	brain:	n/a
37	chr3:60541935-60541985	HMEC	breast:	n/a
38	chr3:60541935-60541985	HUVEC	blood vessel:	n/a
39	chr3:60534659-60534709	HRPEpiC	eye:	n/a
40	chr3:60534659-60534709	GM19239	blood:	n/a
41	chr3:60534659-60534709	BE2_C	brain:	n/a
42	chr3:60541935-60541985	HRCEpiC	kidney:	n/a
43	chr3:60541935-60541985	BE2_C	brain:	n/a
44	chr3:60541935-60541985	BJ	skin:	n/a
45	chr3:60534659-60534709	HCM	heart:	n/a
46	chr3:60534659-60534709	NH-A	brain:	n/a
47	chr3:60541935-60541985	A549	lung:	n/a
48	chr3:60541935-60541985	HL-60	blood:	n/a
49	chr3:60534659-60534709	SKMC	muscle:	n/a
50	chr3:60534659-60534709	GM06990	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:60488135..60490633-chr3:60491194..60494068,2	K562	blood:
2	chr3:60509060..60510930-chr3:60511428..60512938,2	K562	blood:
3	chr3:60503536..60506034-chr3:60508761..60510926,2	K562	blood:
4	chr3:60483853..60486464-chr3:60489187..60492049,2	K562	blood:
5	chr3:60532780..60534867-chr3:60539940..60541452,2	K562	blood:
6	chr3:60532780..60534867-chr3:60539940..60541452,2	K562	blood:
7	chr3:60502053..60505036-chr3:60509426..60512103,2	K562	blood:
8	chr3:60492215..60494697-chr3:60503496..60505338,2	K562	blood:
9	chr3:60500352..60502884-chr3:60536251..60537952,2	K562	blood:
10	chr3:60506754..60508368-chr3:60516500..60519417,2	K562	blood:
11	chr3:60500352..60502884-chr3:60536251..60537952,2	K562	blood:
12	chr3:60263321..60265309-chr3:60503721..60505576,2	K562	blood:
13	chr3:60503536..60506034-chr3:60508761..60510926,2	K562	blood:
14	chr3:60492215..60494697-chr3:60503496..60505338,2	K562	blood:
15	chr3:60486499..60489215-chr3:60499142..60502130,2	K562	blood:
16	chr3:60540686..60542357-chr3:60544396..60547360,2	MCF-7	breast:
17	chr3:60486499..60489215-chr3:60499142..60502130,2	K562	blood:
18	chr3:60488135..60490633-chr3:60491194..60494068,2	K562	blood:
19	chr3:60475674..60478079-chr3:60479619..60482202,2	K562	blood:
20	chr3:60506754..60508368-chr3:60516500..60519417,2	K562	blood:
21	chr3:60476221..60479058-chr3:60482642..60484706,2	K562	blood:
22	chr3:60483853..60486464-chr3:60489187..60492049,2	K562	blood:
23	chr3:60476221..60479058-chr3:60482642..60484706,2	K562	blood:
24	chr3:60540686..60542357-chr3:60544396..60547360,2	MCF-7	breast:
25	chr3:60509060..60510930-chr3:60511428..60512938,2	K562	blood:
26	chr3:60502053..60505036-chr3:60509426..60512103,2	K562	blood:
27	chr3:60467604..60470651-chr3:60470930..60473335,3	K562	blood:
28	chr3:60468425..60470651-chr3:60470930..60473335,2	K562	blood:
29	chr3:60475674..60478079-chr3:60479619..60482202,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FEZF2-9	chr3:60521543-60522712	NONHSAT090160

No data

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

Extended variants
information (count: 3070 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3070 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2362892	chr3:60472815-60472816	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs376575878	chr3:60472876-60472877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs1447972	chr3:60472883-60472884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs535219300	chr3:60472907-60472908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs409769	chr3:60472909-60472910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs553248408	chr3:60472949-60472950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2362894	chr3:60472970-60472971	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs438501	chr3:60473010-60473011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs4485674	chr3:60473029-60473030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2734352	chr3:60473033-60473034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs180745271	chr3:60473055-60473056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542639404	chr3:60473075-60473076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545674366	chr3:60473083-60473084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs373359213	chr3:60473087-60473088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs572961447	chr3:60473168-60473169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145845504	chr3:60473191-60473192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138737010	chr3:60473206-60473207	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs71313774	chr3:60473213-60473214	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577787436	chr3:60473251-60473252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9861820	chr3:60473265-60473266	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs9824052	chr3:60473289-60473290	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs530518196	chr3:60473297-60473298	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs17063274	chr3:60473310-60473311	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs560874986	chr3:60473362-60473363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183670453	chr3:60473363-60473364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs17063275	chr3:60473370-60473371	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs571714944	chr3:60473408-60473409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370483440	chr3:60473413-60473414	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142782289	chr3:60473421-60473422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111462343	chr3:60473422-60473423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs394509	chr3:60473475-60473476	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs147405069	chr3:60473492-60473493	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9882078	chr3:60473498-60473499	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs201356661	chr3:60473511-60473512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9862176	chr3:60473555-60473556	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs184998696	chr3:60473567-60473568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559045845	chr3:60473569-60473570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72882105	chr3:60473597-60473598	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs139171117	chr3:60473599-60473600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149533879	chr3:60473632-60473633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs35511149	chr3:60473636-60473637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144179404	chr3:60473662-60473663	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs440450	chr3:60473672-60473673	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs371583379	chr3:60473685-60473686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9828307	chr3:60473698-60473699	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs79647958	chr3:60473709-60473710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148711456	chr3:60473727-60473728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565017995	chr3:60473766-60473767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568511179	chr3:60473772-60473773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532593129	chr3:60473806-60473807	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21785460	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
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Cancer	18162546	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Urothelial cell carcinoma	18451213	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Mental retardation	17847001	CNVD
Neuroticism	17667963	CNVD
Squamous cell cancer	19047905	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Autism	22102821	CNVD
Prostate cancer	19363497	CNVD
Malaria	21533027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21518781	CNVD
Esophageal cancer	21518781	CNVD
Cancer	20164919	CNVD
Schizophrenia	20967226	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Gastric cancer	22315472	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60472400-60473200	Weak transcription	Fetal Intestine Large	intestine
2	chr3:60472800-60473800	Weak transcription	Fetal Intestine Small	intestine
3	chr3:60473200-60473800	Enhancers	Duodenum Mucosa	Duodenum
4	chr3:60473200-60474400	Enhancers	Fetal Intestine Large	intestine
5	chr3:60473400-60473800	Enhancers	Fetal Heart	heart
6	chr3:60473800-60474200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:60473800-60474400	Enhancers	Gastric	stomach
8	chr3:60474000-60474200	Enhancers	Fetal Intestine Small	intestine
9	chr3:60483200-60484000	Enhancers	Brain Germinal Matrix	brain
10	chr3:60483400-60483800	Enhancers	Fetal Lung	lung
11	chr3:60483400-60485000	Enhancers	Fetal Heart	heart
12	chr3:60483600-60484000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:60483600-60484000	Enhancers	Duodenum Smooth Muscle	Duodenum
14	chr3:60483600-60484000	Enhancers	Fetal Brain Female	brain
15	chr3:60490200-60491000	Enhancers	Primary B cells from peripheral blood	blood
16	chr3:60499600-60500200	ZNF genes & repeats	Adipose Nuclei	Adipose
17	chr3:60499800-60500200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr3:60499800-60501000	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr3:60500000-60501000	Enhancers	Fetal Muscle Trunk	muscle
20	chr3:60500200-60500600	Weak transcription	Adipose Nuclei	Adipose
21	chr3:60500600-60500800	Enhancers	Adipose Nuclei	Adipose
22	chr3:60500600-60500800	Enhancers	Right Atrium	heart
23	chr3:60500600-60501000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr3:60500600-60501000	Enhancers	Right Ventricle	heart
25	chr3:60500600-60501200	Enhancers	Fetal Heart	heart
26	chr3:60500600-60501200	Enhancers	K562	blood
27	chr3:60500800-60501200	Enhancers	Fetal Kidney	kidney
28	chr3:60500800-60501200	Enhancers	Left Ventricle	heart
29	chr3:60500800-60501600	Weak transcription	Right Atrium	heart
30	chr3:60507600-60508200	Enhancers	Fetal Brain Male	brain
31	chr3:60509400-60523400	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr3:60514800-60519000	Weak transcription	Fetal Kidney	kidney
33	chr3:60516200-60516400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr3:60518200-60519000	Enhancers	Fetal Brain Female	brain
35	chr3:60519000-60519200	Enhancers	Fetal Kidney	kidney
36	chr3:60519200-60522200	Weak transcription	Fetal Kidney	kidney
37	chr3:60521600-60522200	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr3:60521800-60522800	Enhancers	GM12878-XiMat	blood
39	chr3:60522000-60523400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr3:60522200-60522600	Active TSS	Pancreatic Islets	Pancreatic Islet
41	chr3:60522200-60522800	Enhancers	Fetal Kidney	kidney
42	chr3:60522200-60523800	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr3:60523400-60523600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr3:60523400-60528600	Weak transcription	HUES64 Cell Line	embryonic stem cell
45	chr3:60525800-60526400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:60526400-60529400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr3:60528600-60529000	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr3:60528800-60529200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr3:60528800-60529200	Enhancers	Rectal Smooth Muscle	rectum
50	chr3:60528800-60529600	Enhancers	Fetal Stomach	stomach

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