Variant report

Variant	nsv969967
Chromosome Location	chr5:97744486-97756918
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	BATF	chr5:97746502-97746660	GM12878	blood:	n/a	n/a
2	BCL11A	chr5:97746518-97746652	GM12878	blood:	n/a	n/a
3	BCL11A	chr5:97746451-97746723	GM12878	blood:	n/a	n/a
4	BHLHE40	chr5:97746497-97746672	HepG2	liver:	n/a	n/a
5	CEBPB	chr5:97752620-97752745	HepG2	liver:	n/a	n/a
6	CEBPB	chr5:97749852-97751208	IMR90	lung:	n/a	chr5:97750380-97750391
7	CEBPB	chr5:97750006-97750503	HepG2	liver:	n/a	chr5:97750380-97750391
8	E2F4	chr5:97752096-97752367	MCF10A-Er-Src	breast:	n/a	n/a
9	EP300	chr5:97755805-97755860	GM12878	blood:	n/a	chr5:97755823-97755832
10	EP300	chr5:97755819-97755860	GM12878	blood:	n/a	chr5:97755823-97755832
11	EP300	chr5:97750465-97751168	SK-N-SH	brain:	n/a	n/a
12	EP300	chr5:97750407-97751250	SK-N-SH	brain:	n/a	n/a
13	FOS	chr5:97750627-97751267	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr5:97750655-97751350	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr5:97752250-97752771	MCF10A-Er-Src	breast:	n/a	chr5:97752414-97752421 chr5:97752414-97752423 chr5:97752415-97752426
16	FOS	chr5:97750679-97751378	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr5:97752258-97752763	MCF10A-Er-Src	breast:	n/a	chr5:97752414-97752421 chr5:97752414-97752423 chr5:97752415-97752426
18	FOS	chr5:97752252-97752639	MCF10A-Er-Src	breast:	n/a	chr5:97752414-97752421 chr5:97752414-97752423 chr5:97752415-97752426
19	FOSL2	chr5:97746467-97746666	HepG2	liver:	n/a	n/a
20	FOSL2	chr5:97746453-97746777	HepG2	liver:	n/a	n/a
21	FOSL2	chr5:97752145-97752703	SK-N-SH	brain:	n/a	chr5:97752414-97752421 chr5:97752414-97752423 chr5:97752415-97752426
22	FOSL2	chr5:97750668-97751095	SK-N-SH	brain:	n/a	n/a
23	FOSL2	chr5:97750448-97751209	SK-N-SH	brain:	n/a	n/a
24	GABPA	chr5:97746534-97746630	Hela-S3	cervix:	n/a	n/a
25	GATA3	chr5:97751978-97752928	SK-N-SH	brain:	n/a	chr5:97752264-97752280 chr5:97752264-97752280 chr5:97752261-97752282 chr5:97752268-97752277
26	GATA3	chr5:97750383-97751245	SK-N-SH	brain:	n/a	n/a
27	GATA3	chr5:97750356-97751211	SK-N-SH	brain:	n/a	n/a
28	GATA3	chr5:97751997-97752800	SK-N-SH	brain:	n/a	chr5:97752264-97752280 chr5:97752264-97752280 chr5:97752261-97752282 chr5:97752268-97752277
29	HEY1	chr5:97746499-97746638	HepG2	liver:	n/a	n/a
30	HEY1	chr5:97746495-97746674	HepG2	liver:	n/a	n/a
31	JUN	chr5:97748905-97749132	HepG2	liver:	n/a	n/a
32	JUND	chr5:97756259-97756412	HepG2	liver:	n/a	n/a
33	JUND	chr5:97746535-97746633	HepG2	liver:	n/a	n/a
34	JUND	chr5:97750516-97751164	SK-N-SH	brain:	n/a	n/a
35	JUND	chr5:97748787-97749137	HepG2	liver:	n/a	n/a
36	JUND	chr5:97746513-97746650	HepG2	liver:	n/a	n/a
37	MAFF	chr5:97752128-97752186	HepG2	liver:	n/a	n/a
38	MAFK	chr5:97752088-97752256	HepG2	liver:	n/a	chr5:97752144-97752164
39	MAFK	chr5:97752029-97752581	IMR90	lung:	n/a	chr5:97752497-97752511 chr5:97752498-97752509 chr5:97752144-97752164
40	MAFK	chr5:97750524-97751271	IMR90	lung:	n/a	n/a
41	MAFK	chr5:97752066-97752208	HepG2	liver:	n/a	chr5:97752144-97752164
42	MAFK	chr5:97753127-97753314	HepG2	liver:	n/a	chr5:97753194-97753209
43	MAFK	chr5:97753191-97753302	HepG2	liver:	n/a	chr5:97753194-97753209
44	MYC	chr5:97750872-97751059	MCF10A-Er-Src	breast:	n/a	n/a
45	NFIC	chr5:97750401-97751200	SK-N-SH	brain:	n/a	n/a
46	PAX5	chr5:97746515-97746646	GM12878	blood:	n/a	n/a
47	PBX3	chr5:97750510-97751434	SK-N-SH	brain:	n/a	n/a
48	PBX3	chr5:97750481-97751540	SK-N-SH	brain:	n/a	n/a
49	PBX3	chr5:97746531-97746638	GM12878	blood:	n/a	n/a
50	POLR2A	chr5:97749426-97749528	ProgFib	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97745972-97746022	A549	lung:	n/a
2	chr5:97745972-97746022	CMK	blood:	n/a
3	chr5:97746735-97746785	CMK	blood:	n/a
4	chr5:97745972-97746022	HAEpiC	amniotic membrane:	n/a
5	chr5:97746735-97746785	HCF	heart:	n/a
6	chr5:97746735-97746785	HAEpiC	amniotic membrane:	n/a
7	chr5:97745972-97746022	NB4	blood:	n/a
8	chr5:97746735-97746785	MCF10A-Er-Src	breast:	n/a
9	chr5:97746735-97746785	Hela-S3	cervix:	n/a
10	chr5:97746735-97746785	AG04450	lung:	fetal
11	chr5:97746735-97746785	AG09319	gingival:	n/a
12	chr5:97745972-97746022	HUVEC	blood vessel:	n/a
13	chr5:97746735-97746785	SKMC	muscle:	n/a
14	chr5:97745972-97746022	GM12892	blood:	n/a
15	chr5:97745972-97746022	Hela-S3	cervix:	n/a
16	chr5:97745972-97746022	HRPEpiC	eye:	n/a
17	chr5:97746735-97746785	HMEC	breast:	n/a
18	chr5:97745972-97746022	HCPEpiC	choroid plexus:	n/a
19	chr5:97746735-97746785	RPTEC	kidney:	n/a
20	chr5:97746735-97746785	SK-N-SH_RA	brain:	n/a
21	chr5:97745972-97746022	Caco-2	colon:	n/a
22	chr5:97746735-97746785	HCT-116	colon:	n/a
23	chr5:97746735-97746785	T-47D	breast:	n/a
24	chr5:97745972-97746022	HEK293	kidney:	embryo
25	chr5:97745972-97746022	HNPCEpiC	eye:	n/a
26	chr5:97746735-97746785	HL-60	blood:	n/a
27	chr5:97745972-97746022	HCF	heart:	n/a
28	chr5:97745972-97746022	HIPEpiC	eye:	n/a
29	chr5:97746735-97746785	AoSMC	blood vessel:	n/a
30	chr5:97746735-97746785	BE2_C	brain:	n/a
31	chr5:97746735-97746785	AG04449	skin:	fetal
32	chr5:97746735-97746785	SK-N-SH	brain:	n/a
33	chr5:97746735-97746785	GM12892	blood:	n/a
34	chr5:97745972-97746022	MCF10A-Er-Src	breast:	n/a
35	chr5:97746735-97746785	NHDF-neo	bronchial:	n/a
36	chr5:97745972-97746022	SKMC	muscle:	n/a
37	chr5:97746735-97746785	Hepatocyte	liver:	n/a
38	chr5:97746735-97746785	HUVEC	blood vessel:	n/a
39	chr5:97746735-97746785	ProgFib	skin:	n/a
40	chr5:97745972-97746022	LNCaP	prostate:	n/a
41	chr5:97746735-97746785	BJ	skin:	n/a
42	chr5:97746735-97746785	H1-hESC	embryonic stem cell:	embryo
43	chr5:97746735-97746785	SK-N-MC	brain:	n/a
44	chr5:97745972-97746022	GM19239	blood:	n/a
45	chr5:97745972-97746022	BJ	skin:	n/a
46	chr5:97745972-97746022	NH-A	brain:	n/a
47	chr5:97746735-97746785	AG10803	skin:	n/a
48	chr5:97745972-97746022	ProgFib	skin:	n/a
49	chr5:97746735-97746785	GM19239	blood:	n/a
50	chr5:97746735-97746785	GM12878	blood:	n/a

Variant related genes	Relation type
ENSG00000249448	TF binding region
ENSG00000249990	TF binding region
ENSG00000249448	CpG island
ENSG00000249990	CpG island

Extended variants
information (count: 410 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141904425	chr5:97744581-97744582	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543350848	chr5:97744616-97744617	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75697539	chr5:97744652-97744653	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs4702968	chr5:97744742-97744743	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs113291989	chr5:97744775-97744776	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185467729	chr5:97744808-97744809	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs565057218	chr5:97744813-97744814	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565929213	chr5:97744822-97744823	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532665152	chr5:97744916-97744917	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs550779260	chr5:97744952-97744953	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563537016	chr5:97744961-97744962	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139980956	chr5:97744972-97744973	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141835533	chr5:97745017-97745018	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562424141	chr5:97745038-97745039	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs534627989	chr5:97745054-97745055	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546648097	chr5:97745071-97745072	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs56308227	chr5:97745099-97745100	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs372912536	chr5:97745140-97745141	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538767423	chr5:97745161-97745162	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556775957	chr5:97745265-97745266	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77391103	chr5:97745298-97745299	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557920266	chr5:97745359-97745360	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190669735	chr5:97745362-97745363	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554858527	chr5:97745403-97745404	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs560320611	chr5:97745431-97745432	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs76100679	chr5:97745442-97745443	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181506359	chr5:97745450-97745451	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549135921	chr5:97745496-97745497	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10079842	chr5:97745517-97745518	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577157916	chr5:97745518-97745519	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544697410	chr5:97745551-97745552	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370218746	chr5:97745558-97745559	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536717343	chr5:97745560-97745561	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374845914	chr5:97745565-97745566	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556916023	chr5:97745597-97745598	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530750841	chr5:97745625-97745626	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs573549985	chr5:97745630-97745631	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187414088	chr5:97745645-97745646	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75199606	chr5:97745658-97745659	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531386244	chr5:97745723-97745724	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191836726	chr5:97745729-97745730	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139146669	chr5:97745850-97745851	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571268941	chr5:97745895-97745896	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371209214	chr5:97745922-97745923	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72769674	chr5:97745950-97745951	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550660005	chr5:97745966-97745967	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568824715	chr5:97745972-97745973	Strong transcription Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs536872827	chr5:97746000-97746001	Strong transcription Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs186891112	chr5:97746054-97746055	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566705286	chr5:97746076-97746077	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97744200-97755200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:97744400-97749600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr5:97746000-97749800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr5:97748400-97754200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:97748600-97748800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr5:97748600-97754400	Enhancers	NHDF-Ad	bronchial
7	chr5:97748800-97752000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:97748800-97753200	Enhancers	Muscle Satellite Cultured Cells	--
9	chr5:97748800-97753200	Enhancers	HSMM	muscle
10	chr5:97749200-97752800	Enhancers	HSMMtube	muscle
11	chr5:97749200-97752800	Enhancers	NHLF	lung
12	chr5:97749200-97753000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr5:97749200-97753400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr5:97749600-97752000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr5:97749600-97752000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr5:97749600-97753200	Enhancers	Osteobl	bone
17	chr5:97749800-97751200	Enhancers	NHEK	skin
18	chr5:97749800-97752200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr5:97749800-97752800	Enhancers	NH-A	brain
20	chr5:97749800-97753400	Enhancers	HMEC	breast
21	chr5:97750000-97753200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:97750400-97753400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr5:97751200-97751600	Flanking Active TSS	NHEK	skin
24	chr5:97751600-97753400	Enhancers	NHEK	skin
25	chr5:97752000-97752800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:97752000-97760000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:97752000-97760200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr5:97752200-97752600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:97752600-97753200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:97752800-97753000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr5:97753200-97754800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr5:97753200-97755800	Weak transcription	Psoas Muscle	Psoas
33	chr5:97754400-97758800	Weak transcription	NHDF-Ad	bronchial
34	chr5:97754800-97755200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr5:97755000-97755200	Enhancers	Small Intestine	intestine
36	chr5:97755000-97755600	Enhancers	Fetal Intestine Large	intestine
37	chr5:97755000-97755600	Enhancers	Fetal Intestine Small	intestine
38	chr5:97755000-97756600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr5:97755200-97756000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr5:97755200-97758800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr5:97755200-97763800	Weak transcription	Small Intestine	intestine
42	chr5:97755200-97764400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr5:97755400-97756000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr5:97755600-97755800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:97755600-97756000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr5:97755600-97756200	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:97755800-97761800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr5:97756000-97760200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr5:97756600-97758400	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr5:97756800-97757000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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