Variant report

Variant	nsv4928
Chromosome Location	chr5:97689980-97734899
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:91)
CpG islands
(count:306)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:91 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:97697601-97697741	H1-hESC	embryonic stem cell:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
2	CEBPB	chr5:97712721-97712774	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr5:97697598-97697834	A549	lung:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
4	CEBPB	chr5:97697542-97697873	IMR90	lung:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
5	CEBPB	chr5:97697523-97697868	HepG2	liver:	n/a	chr5:97697695-97697706 chr5:97697727-97697739
6	CHD2	chr5:97725871-97725896	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr5:97734424-97734458	Fibrobl	skin:	n/a	chr5:97734431-97734449
8	CTCF	chr5:97717524-97717592	LNCaP	prostate:	n/a	n/a
9	CTCF	chr5:97696115-97696254	Fibrobl	skin:	n/a	n/a
10	CTCF	chr5:97705660-97705810	GM06990	blood:	n/a	n/a
11	CTCF	chr5:97727929-97728182	A549	lung:	n/a	n/a
12	E2F4	chr5:97715254-97715454	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr5:97703823-97704173	HUVEC	blood vessel:	n/a	chr5:97704010-97704017 chr5:97704008-97704018 chr5:97704009-97704017 chr5:97704007-97704018 chr5:97704009-97704017 chr5:97704007-97704018
14	FOXA1	chr5:97704968-97705237	T-47D	breast:	n/a	n/a
15	GATA2	chr5:97715291-97715697	HUVEC	blood vessel:	n/a	n/a
16	GATA2	chr5:97703798-97704131	HUVEC	blood vessel:	n/a	n/a
17	GATA2	chr5:97700866-97701207	SH-SY5Y	brain:	n/a	chr5:97701006-97701017
18	GATA3	chr5:97715111-97715405	SH-SY5Y	brain:	n/a	chr5:97715125-97715132
19	GATA3	chr5:97715230-97715588	SK-N-SH	brain:	n/a	n/a
20	GATA3	chr5:97700624-97700824	SH-SY5Y	brain:	n/a	n/a
21	JUND	chr5:97697670-97697781	HepG2	liver:	n/a	n/a
22	KAP1	chr5:97706759-97707127	K562	blood:	n/a	n/a
23	MAFF	chr5:97732810-97732991	HepG2	liver:	n/a	chr5:97732902-97732920
24	MAFF	chr5:97732879-97732907	K562	blood:	n/a	n/a
25	MAFF	chr5:97707611-97707685	K562	blood:	n/a	n/a
26	MAFK	chr5:97731308-97731546	HepG2	liver:	n/a	chr5:97731450-97731465
27	MAFK	chr5:97694657-97694718	HepG2	liver:	n/a	n/a
28	MAFK	chr5:97731389-97731525	IMR90	lung:	n/a	chr5:97731450-97731465
29	MAFK	chr5:97732768-97733008	HepG2	liver:	n/a	chr5:97732903-97732918
30	MAFK	chr5:97707545-97707796	HepG2	liver:	n/a	n/a
31	MAFK	chr5:97732732-97733089	IMR90	lung:	n/a	chr5:97732903-97732918
32	MAFK	chr5:97711745-97712018	HepG2	liver:	n/a	n/a
33	MAFK	chr5:97731373-97731506	HepG2	liver:	n/a	chr5:97731450-97731465
34	MAFK	chr5:97707617-97707774	IMR90	lung:	n/a	n/a
35	MAFK	chr5:97694599-97694738	HepG2	liver:	n/a	n/a
36	MAFK	chr5:97732782-97733037	HepG2	liver:	n/a	chr5:97732903-97732918
37	MAZ	chr5:97707870-97707987	HepG2	liver:	n/a	n/a
38	MYC	chr5:97705870-97705945	MCF10A-Er-Src	breast:	n/a	n/a
39	MYC	chr5:97696156-97696171	MCF-7	breast:	n/a	n/a
40	MYC	chr5:97696144-97696155	MCF-7	breast:	n/a	n/a
41	MYC	chr5:97696173-97696248	MCF-7	breast:	n/a	n/a
42	MYC	chr5:97696086-97696161	MCF-7	breast:	n/a	n/a
43	MYC	chr5:97696135-97696139	MCF-7	breast:	n/a	n/a
44	POLR2A	chr5:97729159-97729222	A549	lung:	n/a	n/a
45	POLR2A	chr5:97728011-97728189	A549	lung:	n/a	n/a
46	POLR2A	chr5:97728396-97728541	Gliobla	brain:	n/a	n/a
47	POLR2A	chr5:97728642-97729101	A549	lung:	n/a	n/a
48	POLR2A	chr5:97726856-97726914	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr5:97725498-97725523	ProgFib	skin:	n/a	n/a
50	POLR2A	chr5:97725410-97725497	ProgFib	skin:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97703334-97703384	HRCEpiC	kidney:	n/a
2	chr5:97703334-97703384	HRCEpiC	kidney:	n/a
3	chr5:97703334-97703384	MCF-7	breast:	n/a
4	chr5:97703334-97703384	IMR90	lung:	fetal
5	chr5:97725789-97725839	K562	blood:	n/a
6	chr5:97725789-97725839	HRCEpiC	kidney:	n/a
7	chr5:97728181-97728231	HEK293	kidney:	embryo
8	chr5:97703334-97703384	HMEC	breast:	n/a
9	chr5:97728181-97728231	Jurkat	blood:	n/a
10	chr5:97725789-97725839	CMK	blood:	n/a
11	chr5:97728038-97728088	AG10803	skin:	n/a
12	chr5:97727913-97727963	GM12891	blood:	n/a
13	chr5:97728038-97728088	NHDF-neo	bronchial:	n/a
14	chr5:97703334-97703384	Jurkat	blood:	n/a
15	chr5:97728038-97728088	RPTEC	kidney:	n/a
16	chr5:97703334-97703384	Hela-S3	cervix:	n/a
17	chr5:97725789-97725839	ovcar-3	ovarian:	n/a
18	chr5:97725789-97725839	ProgFib	skin:	n/a
19	chr5:97728181-97728231	AG04449	skin:	fetal
20	chr5:97728038-97728088	HRE	kidney:	n/a
21	chr5:97728181-97728231	PrEC	prostate:	n/a
22	chr5:97703334-97703384	NHDF-neo	bronchial:	n/a
23	chr5:97725789-97725839	SAEC	small airway:	n/a
24	chr5:97728038-97728088	CMK	blood:	n/a
25	chr5:97703334-97703384	NH-A	brain:	n/a
26	chr5:97728181-97728231	Hela-S3	cervix:	n/a
27	chr5:97727913-97727963	HRE	kidney:	n/a
28	chr5:97703334-97703384	HRE	kidney:	n/a
29	chr5:97727913-97727963	ECC-1	luminal epithelium:	n/a
30	chr5:97725789-97725839	T-47D	breast:	n/a
31	chr5:97728038-97728088	HRPEpiC	eye:	n/a
32	chr5:97728038-97728088	SKMC	muscle:	n/a
33	chr5:97728038-97728088	U87	brain:	n/a
34	chr5:97703334-97703384	AG04449	skin:	fetal
35	chr5:97728181-97728231	HCPEpiC	choroid plexus:	n/a
36	chr5:97703334-97703384	AoSMC	blood vessel:	n/a
37	chr5:97703334-97703384	HRPEpiC	eye:	n/a
38	chr5:97725789-97725839	HCF	heart:	n/a
39	chr5:97727913-97727963	HepG2	liver:	n/a
40	chr5:97728038-97728088	SK-N-MC	brain:	n/a
41	chr5:97728181-97728231	RPTEC	kidney:	n/a
42	chr5:97727913-97727963	AG09309	skin:	n/a
43	chr5:97728038-97728088	AG04450	lung:	fetal
44	chr5:97725789-97725839	AG09309	skin:	n/a
45	chr5:97703334-97703384	SAEC	small airway:	n/a
46	chr5:97703334-97703384	HCT-116	colon:	n/a
47	chr5:97703334-97703384	PFSK-1	brain:	n/a
48	chr5:97727913-97727963	SKMC	muscle:	n/a
49	chr5:97728181-97728231	ECC-1	luminal epithelium:	n/a
50	chr5:97727913-97727963	HRCEpiC	kidney:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:97701258..97703130-chr5:97705966..97708009,2	K562	blood:
2	chr5:97689861..97692016-chr5:97695118..97697823,2	K562	blood:
3	chr5:97701474..97704049-chr5:97723105..97724886,2	K562	blood:
4	chr5:97701258..97703130-chr5:97705966..97708009,2	K562	blood:
5	chr5:97689861..97692016-chr5:97695118..97697823,2	K562	blood:
6	chr5:97701474..97704049-chr5:97723105..97724886,2	K562	blood:

No data

Variant related genes	Relation type
KRT8P32	TF binding region
KRT8P32	CpG island

Extended variants
information (count: 1573 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1573 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540885569	chr5:97690022-97690023	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs192916488	chr5:97690114-97690115	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs532515756	chr5:97690259-97690260	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs550980436	chr5:97690270-97690271	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs185087390	chr5:97690300-97690301	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs530133692	chr5:97690306-97690307	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs559791164	chr5:97690313-97690314	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs549200683	chr5:97690355-97690356	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs79620166	chr5:97690403-97690404	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs534604919	chr5:97690406-97690407	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs146715678	chr5:97690426-97690427	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs570924806	chr5:97690460-97690461	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs538279732	chr5:97690473-97690474	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs556681767	chr5:97690486-97690487	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs10054643	chr5:97690531-97690532	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs575339672	chr5:97690537-97690538	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs542319398	chr5:97690572-97690573	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs555150548	chr5:97690609-97690610	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs187834550	chr5:97690649-97690650	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs147913640	chr5:97690653-97690654	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs116373125	chr5:97690658-97690659	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs192365217	chr5:97690678-97690679	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs571294652	chr5:97690693-97690694	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs184655017	chr5:97690701-97690702	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs10036788	chr5:97690794-97690795	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs73159206	chr5:97690818-97690819	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs115832023	chr5:97690828-97690829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548346732	chr5:97690853-97690854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550845518	chr5:97690888-97690889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537067849	chr5:97690955-97690956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1455424	chr5:97690959-97690960	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs536441519	chr5:97691004-97691005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546371858	chr5:97691007-97691008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188273460	chr5:97691038-97691039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1455425	chr5:97691101-97691102	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs550562429	chr5:97691147-97691148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371587933	chr5:97691192-97691193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568715402	chr5:97691195-97691196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542158560	chr5:97693553-97693554	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs561219214	chr5:97693579-97693580	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs77677377	chr5:97693639-97693640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182005308	chr5:97693770-97693771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545860507	chr5:97693771-97693772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34517148	chr5:97693943-97693944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60740293	chr5:97693951-97693952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564099277	chr5:97693962-97693963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200789358	chr5:97694024-97694025	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201344796	chr5:97694029-97694030	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531311696	chr5:97694038-97694039	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113025733	chr5:97694039-97694040	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97690000-97690400	Active TSS	NHDF-Ad	bronchial
2	chr5:97690400-97690800	Flanking Active TSS	NHDF-Ad	bronchial
3	chr5:97690400-97691200	Enhancers	Dnd41	blood
4	chr5:97690800-97691000	Enhancers	NHDF-Ad	bronchial
5	chr5:97693400-97693600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:97693600-97696800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:97694000-97696600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:97695800-97696000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:97696000-97696200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:97696000-97696200	ZNF genes & repeats	Gastric	stomach
11	chr5:97696200-97696600	ZNF genes & repeats	Spleen	Spleen
12	chr5:97696200-97700800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:97696200-97700800	Weak transcription	Gastric	stomach
14	chr5:97696600-97697600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:97697600-97702000	Weak transcription	Pancreas	Pancrea
16	chr5:97697600-97705200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:97700200-97700800	Enhancers	Fetal Intestine Large	intestine
18	chr5:97700200-97700800	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr5:97700200-97701600	Enhancers	Brain Germinal Matrix	brain
20	chr5:97700400-97700800	Enhancers	Fetal Stomach	stomach
21	chr5:97700800-97701000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr5:97700800-97701200	Enhancers	Fetal Muscle Leg	muscle
23	chr5:97702000-97702200	Enhancers	Pancreas	Pancrea
24	chr5:97703400-97704000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr5:97703800-97704000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr5:97703800-97704600	Enhancers	HUVEC	blood vessel
27	chr5:97704000-97704200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr5:97705000-97705400	Enhancers	Stomach Mucosa	stomach
29	chr5:97705200-97707200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:97707200-97719200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:97709600-97710400	Enhancers	Brain Germinal Matrix	brain
32	chr5:97709600-97710800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr5:97710000-97710600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr5:97710000-97711200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:97710400-97710600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr5:97710600-97712200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr5:97710800-97712400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr5:97710800-97712400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr5:97711200-97711600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr5:97711600-97714600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr5:97712000-97713800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr5:97712200-97714200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr5:97712400-97712800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr5:97712400-97714000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:97712400-97714600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:97712400-97714600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr5:97712600-97714200	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr5:97712800-97713800	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr5:97713400-97714000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:97713600-97713800	Enhancers	H1 Cell Line	embryonic stem cell

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