Variant report

Variant	nsv834745
Chromosome Location	chr3:79055426-79227937
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	chr3:79068039-79068132	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:79135583-79136111	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:79068380-79069105	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:79081822-79082269	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:79065781-79066770	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:79067726-79067740	HepG2	liver:	n/a	n/a
7	ATF2	chr3:79068411-79069110	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr3:79067837-79069031	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL3	chr3:79068372-79068876	A549	lung:	n/a	chr3:79068616-79068625 chr3:79068529-79068542 chr3:79068528-79068537
10	BCLAF1	chr3:79135672-79135892	GM12878	blood:	n/a	chr3:79135864-79135877
11	BHLHE40	chr3:79067819-79068316	GM12878	blood:	n/a	chr3:79068219-79068235 chr3:79067995-79068011 chr3:79068093-79068109
12	BHLHE40	chr3:79068558-79068991	A549	lung:	n/a	n/a
13	BHLHE40	chr3:79071195-79071428	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:79057371-79057372	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:79078243-79078303	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:79081928-79082157	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:79067881-79069379	HepG2	liver:	n/a	chr3:79068219-79068235 chr3:79067995-79068011 chr3:79068093-79068109 chr3:79068460-79068476
18	BHLHE40	chr3:79130911-79130915	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:79068546-79069073	GM12878	blood:	n/a	n/a
20	BRCA1	chr3:79068672-79069075	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr3:79065785-79066651	Hela-S3	cervix:	n/a	chr3:79065967-79065974
22	BRCA1	chr3:79067813-79069047	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr3:79135663-79135898	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr3:79068843-79068890	GM12878	blood:	n/a	n/a
25	CEBPB	chr3:79135660-79136161	IMR90	lung:	n/a	chr3:79135964-79135975 chr3:79135964-79135977 chr3:79135964-79135977 chr3:79135965-79135976
26	CEBPB	chr3:79223915-79223981	IMR90	lung:	n/a	n/a
27	CEBPB	chr3:79140977-79141172	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:79088365-79088601	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr3:79164617-79164987	HepG2	liver:	n/a	chr3:79164801-79164814 chr3:79164772-79164785 chr3:79164642-79164655 chr3:79164801-79164814 chr3:79164802-79164813
30	CEBPB	chr3:79096736-79097091	IMR90	lung:	n/a	chr3:79096882-79096893
31	CEBPB	chr3:79089835-79090204	Hela-S3	cervix:	n/a	chr3:79089969-79089980 chr3:79089970-79089979 chr3:79089968-79089981
32	CEBPB	chr3:79068430-79069041	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr3:79217176-79217559	IMR90	lung:	n/a	n/a
34	CEBPB	chr3:79135661-79136089	A549	lung:	n/a	chr3:79135964-79135975 chr3:79135964-79135977 chr3:79135964-79135977 chr3:79135965-79135976
35	CEBPB	chr3:79189825-79190353	IMR90	lung:	n/a	chr3:79190235-79190248
36	CEBPB	chr3:79135610-79136110	Hela-S3	cervix:	n/a	chr3:79135964-79135975 chr3:79135964-79135977 chr3:79135964-79135977 chr3:79135965-79135976
37	CEBPB	chr3:79067088-79067113	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:79170300-79170573	A549	lung:	n/a	chr3:79170424-79170435
39	CEBPB	chr3:79088367-79088668	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:79066312-79068101	Hela-S3	cervix:	n/a	chr3:79066510-79066521 chr3:79066510-79066521 chr3:79066510-79066523
41	CEBPB	chr3:79089783-79090285	IMR90	lung:	n/a	chr3:79089969-79089980 chr3:79089970-79089979 chr3:79089968-79089981
42	CEBPB	chr3:79089825-79090113	HepG2	liver:	n/a	chr3:79089969-79089980 chr3:79089970-79089979 chr3:79089968-79089981
43	CEBPB	chr3:79164680-79164859	H1-hESC	embryonic stem cell:	n/a	chr3:79164801-79164814 chr3:79164772-79164785 chr3:79164801-79164814 chr3:79164802-79164813
44	CEBPB	chr3:79066460-79066657	H1-hESC	embryonic stem cell:	n/a	chr3:79066510-79066521 chr3:79066510-79066521 chr3:79066510-79066523
45	CEBPB	chr3:79078124-79078400	IMR90	lung:	n/a	n/a
46	CEBPB	chr3:79170365-79170565	HepG2	liver:	n/a	chr3:79170424-79170435
47	CEBPB	chr3:79135790-79136129	HepG2	liver:	n/a	chr3:79135964-79135975 chr3:79135964-79135977 chr3:79135964-79135977 chr3:79135965-79135976
48	CEBPB	chr3:79161543-79161562	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr3:79190003-79190252	A549	lung:	n/a	chr3:79190235-79190248
50	CEBPB	chr3:79135750-79136123	K562	blood:	n/a	chr3:79135964-79135975 chr3:79135964-79135977 chr3:79135964-79135977 chr3:79135965-79135976

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:79137306-79137356	HUVEC	blood vessel:	n/a
2	chr3:79137306-79137356	HIPEpiC	eye:	n/a
3	chr3:79137306-79137356	HUVEC	blood vessel:	n/a
4	chr3:79137306-79137356	HIPEpiC	eye:	n/a
5	chr3:79079292-79079342	HRCEpiC	kidney:	n/a
6	chr3:79223561-79223611	GM06990	blood:	n/a
7	chr3:79067437-79067487	SAEC	small airway:	n/a
8	chr3:79068813-79068863	NT2-D1	testis:	n/a
9	chr3:79068857-79068907	ovcar-3	ovarian:	n/a
10	chr3:79068813-79068863	LNCaP	prostate:	n/a
11	chr3:79068831-79068881	SKMC	muscle:	n/a
12	chr3:79067596-79067646	ovcar-3	ovarian:	n/a
13	chr3:79068831-79068881	GM12892	blood:	n/a
14	chr3:79068857-79068907	HRE	kidney:	n/a
15	chr3:79189311-79189361	GM12891	blood:	n/a
16	chr3:79068292-79068342	BE2_C	brain:	n/a
17	chr3:79068292-79068342	GM12891	blood:	n/a
18	chr3:79068813-79068863	PrEC	prostate:	n/a
19	chr3:79174694-79174744	HCM	heart:	n/a
20	chr3:79079292-79079342	T-47D	breast:	n/a
21	chr3:79071297-79071347	HEEpiC	esophagus:	n/a
22	chr3:79067437-79067487	HEK293	kidney:	embryo
23	chr3:79069897-79069947	CMK	blood:	n/a
24	chr3:79071297-79071347	GM12892	blood:	n/a
25	chr3:79223592-79223642	HMEC	breast:	n/a
26	chr3:79174694-79174744	BJ	skin:	n/a
27	chr3:79210914-79210964	BJ	skin:	n/a
28	chr3:79068857-79068907	Hepatocyte	liver:	n/a
29	chr3:79067437-79067487	BJ	skin:	n/a
30	chr3:79223561-79223611	HRE	kidney:	n/a
31	chr3:79068292-79068342	SK-N-MC	brain:	n/a
32	chr3:79067920-79067970	PANC-1	pancreas:	n/a
33	chr3:79068292-79068342	IMR90	lung:	fetal
34	chr3:79223592-79223642	MCF10A-Er-Src	breast:	n/a
35	chr3:79067920-79067970	HepG2	liver:	n/a
36	chr3:79079292-79079342	SAEC	small airway:	n/a
37	chr3:79067920-79067970	T-47D	breast:	n/a
38	chr3:79067437-79067487	ovcar-3	ovarian:	n/a
39	chr3:79067085-79067135	MCF10A-Er-Src	breast:	n/a
40	chr3:79069897-79069947	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:79071297-79071347	SK-N-SH_RA	brain:	n/a
42	chr3:79065762-79065812	PrEC	prostate:	n/a
43	chr3:79079292-79079342	HEEpiC	esophagus:	n/a
44	chr3:79068441-79068491	NHBE	bronchial:	n/a
45	chr3:79067437-79067487	HCPEpiC	choroid plexus:	n/a
46	chr3:79068857-79068907	HAEpiC	amniotic membrane:	n/a
47	chr3:79223561-79223611	AG10803	skin:	n/a
48	chr3:79067920-79067970	AG04450	lung:	fetal
49	chr3:79067085-79067135	HRCEpiC	kidney:	n/a
50	chr3:79067596-79067646	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:79081752..79082476-chr3:79410956..79411574,2	MCF-7	breast:
2	chr3:79066979..79068727-chr3:79070778..79072579,3	MCF-7	breast:
3	chr3:79059187..79061732-chr3:79063739..79067331,3	MCF-7	breast:
4	chr3:79067397..79070050-chr3:79087652..79089809,3	MCF-7	breast:
5	chr3:79135544..79136046-chr3:79418260..79418912,2	MCF-7	breast:
6	chr3:78708203..78709235-chr3:79081525..79082508,6	MCF-7	breast:
7	chr3:79067926..79070397-chr3:79076118..79078305,2	MCF-7	breast:
8	chr3:79056426..79058913-chr3:79066777..79068329,2	MCF-7	breast:
9	chr3:79135076..79136114-chr3:79410411..79411762,9	MCF-7	breast:
10	chr3:79135269..79136279-chr3:79410679..79411261,3	MCF-7	breast:
11	chr3:79031147..79033864-chr3:79073232..79075055,2	MCF-7	breast:
12	chr3:79061171..79063415-chr3:79068475..79070021,2	MCF-7	breast:
13	chr14:77723065..77723902-chr3:79134805..79135701,2	MCF-7	breast:
14	chr3:79067238..79070008-chr3:79073032..79075853,3	MCF-7	breast:
15	chr3:79135060..79137431-chr3:79411322..79412881,2	MCF-7	breast:
16	chr3:79059187..79061732-chr3:79063739..79067331,3	MCF-7	breast:
17	chr3:78906432..78907240-chr3:79081609..79082489,3	MCF-7	breast:

Variant related genes	Relation type
ROBO1	TF binding region
ROBO1	CpG island
ENSG00000169855	chromatin interactions

Extended variants
information (count: 4024 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:4024 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111284738	chr3:79055428-79055429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574877195	chr3:79055429-79055430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371967888	chr3:79055448-79055449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542812844	chr3:79055473-79055474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541572999	chr3:79055520-79055521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79235293	chr3:79055527-79055528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs202158429	chr3:79055671-79055672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548490600	chr3:79055712-79055713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545372170	chr3:79055725-79055726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs564866917	chr3:79055756-79055757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115548435	chr3:79055760-79055761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541025404	chr3:79055766-79055767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11708079	chr3:79055785-79055786	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs11442702	chr3:79055838-79055839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs397936948	chr3:79055839-79055840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6788693	chr3:79055867-79055868	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549947782	chr3:79055872-79055873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374554749	chr3:79055893-79055894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149038226	chr3:79055907-79055908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11345487	chr3:79055908-79055909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76445331	chr3:79055923-79055924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs57260990	chr3:79055926-79055927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371809705	chr3:79055927-79055928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11127638	chr3:79055931-79055932	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs371461100	chr3:79055938-79055939	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552491183	chr3:79055955-79055956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566369596	chr3:79055986-79055987	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534661853	chr3:79056007-79056008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs548582574	chr3:79056028-79056029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538753656	chr3:79056050-79056051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs537572628	chr3:79056058-79056059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73122655	chr3:79056077-79056078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs17016689	chr3:79056099-79056100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs371839375	chr3:79056112-79056113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560952008	chr3:79056138-79056139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189039207	chr3:79056180-79056181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111649846	chr3:79056242-79056243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540636525	chr3:79056267-79056268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560973874	chr3:79056281-79056282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574427127	chr3:79056282-79056283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543158327	chr3:79056292-79056293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139818512	chr3:79056293-79056294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532527392	chr3:79056380-79056381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs193140147	chr3:79056395-79056396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs201289061	chr3:79056451-79056452	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs143222686	chr3:79056455-79056456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs528795579	chr3:79056457-79056458	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs548270805	chr3:79056494-79056495	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184095140	chr3:79056510-79056511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs199764690	chr3:79056527-79056528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16912164	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:79040800-79062000	Weak transcription	Ovary	ovary
2	chr3:79044600-79061600	Weak transcription	Fetal Kidney	kidney
3	chr3:79044800-79064600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:79052000-79059000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:79052400-79056400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr3:79052400-79057000	Weak transcription	Fetal Brain Male	brain
7	chr3:79052800-79060000	Weak transcription	Fetal Lung	lung
8	chr3:79053000-79057400	Enhancers	HepG2	liver
9	chr3:79053200-79055600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr3:79053200-79057000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr3:79053200-79061200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr3:79053200-79061400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr3:79053800-79056400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:79054200-79055600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr3:79054200-79059200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr3:79054200-79061000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr3:79054400-79058600	Weak transcription	Brain Hippocampus Middle	brain
18	chr3:79054400-79059200	Weak transcription	Fetal Brain Female	brain
19	chr3:79054400-79066600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:79054600-79055600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr3:79054600-79055800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr3:79054600-79056400	Weak transcription	Brain Angular Gyrus	brain
23	chr3:79054600-79058600	Weak transcription	Brain Cingulate Gyrus	brain
24	chr3:79054600-79059000	Weak transcription	Brain Substantia Nigra	brain
25	chr3:79054600-79060200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:79054600-79061000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr3:79054600-79061800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:79054600-79062000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:79054600-79064600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr3:79054800-79056200	Enhancers	Osteobl	bone
31	chr3:79055000-79056000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:79055200-79055600	Weak transcription	A549	lung
33	chr3:79055400-79055600	Enhancers	NHDF-Ad	bronchial
34	chr3:79055400-79055800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr3:79055400-79055800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:79055400-79056400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr3:79055400-79056400	Weak transcription	Brain Anterior Caudate	brain
38	chr3:79055600-79055800	Enhancers	A549	lung
39	chr3:79055600-79056200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:79055600-79061000	Weak transcription	Aorta	Aorta
41	chr3:79055600-79061400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr3:79055600-79061400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:79055600-79062000	Weak transcription	NHDF-Ad	bronchial
44	chr3:79055800-79056600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr3:79055800-79056800	Weak transcription	A549	lung
46	chr3:79055800-79057800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr3:79055800-79061400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr3:79056000-79057000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:79056200-79060200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr3:79056200-79062000	Weak transcription	Osteobl	bone

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