Variant report

Variant	esv1851181
Chromosome Location	chr5:79953567-79962367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:62 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr5:79957926-79958360	HCT-116	colon:	n/a	n/a
2	CEBPB	chr5:79958002-79958274	HepG2	liver:	n/a	chr5:79958130-79958141
3	CEBPB	chr5:79957338-79957530	HepG2	liver:	n/a	chr5:79957471-79957482
4	CEBPB	chr5:79954969-79955261	A549	lung:	n/a	chr5:79955136-79955147
5	CEBPB	chr5:79957951-79958340	HCT-116	colon:	n/a	chr5:79958130-79958141
6	CEBPB	chr5:79955004-79955236	MCF-7	breast:	n/a	chr5:79955136-79955147
7	CEBPB	chr5:79958004-79958309	IMR90	lung:	n/a	chr5:79958130-79958141
8	CEBPB	chr5:79954908-79955339	IMR90	lung:	n/a	chr5:79955136-79955147
9	CEBPB	chr5:79958006-79958301	A549	lung:	n/a	chr5:79958130-79958141
10	CEBPB	chr5:79958098-79958272	K562	blood:	n/a	chr5:79958130-79958141
11	CEBPB	chr5:79954976-79955264	HepG2	liver:	n/a	chr5:79955136-79955147
12	CEBPB	chr5:79954944-79955314	Hela-S3	cervix:	n/a	chr5:79955136-79955147
13	CEBPB	chr5:79955089-79955146	K562	blood:	n/a	n/a
14	CEBPB	chr5:79957984-79958369	Hela-S3	cervix:	n/a	chr5:79958130-79958141
15	CEBPB	chr5:79958027-79958387	HCT-116	colon:	n/a	chr5:79958130-79958141
16	CTCF	chr5:79955660-79955810	HepG2	liver:	n/a	n/a
17	E2F4	chr5:79955075-79955150	MCF10A-Er-Src	breast:	n/a	n/a
18	E2F4	chr5:79957966-79958243	MCF10A-Er-Src	breast:	n/a	n/a
19	EP300	chr5:79960828-79961468	SK-N-SH	brain:	n/a	n/a
20	EP300	chr5:79959117-79959160	K562	blood:	n/a	n/a
21	EP300	chr5:79958024-79958330	Hela-S3	cervix:	n/a	chr5:79958277-79958291
22	FOS	chr5:79957954-79958368	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr5:79954953-79955262	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr5:79957963-79958358	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr5:79954921-79955329	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr5:79954951-79955290	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr5:79954936-79955322	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr5:79957954-79958369	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr5:79957954-79958345	MCF10A-Er-Src	breast:	n/a	n/a
30	GATA3	chr5:79960719-79961583	SK-N-SH	brain:	n/a	n/a
31	GATA3	chr5:79960721-79961533	SK-N-SH	brain:	n/a	n/a
32	JUN	chr5:79958089-79958230	HepG2	liver:	n/a	n/a
33	JUND	chr5:79957998-79958230	HepG2	liver:	n/a	n/a
34	JUND	chr5:79960860-79961370	SK-N-SH	brain:	n/a	n/a
35	MYC	chr5:79955062-79955185	MCF10A-Er-Src	breast:	n/a	n/a
36	MYC	chr5:79954540-79954588	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr5:79955062-79955272	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr5:79958028-79958309	MCF10A-Er-Src	breast:	n/a	n/a
39	NFIC	chr5:79960669-79961468	SK-N-SH	brain:	n/a	n/a
40	PBX3	chr5:79960749-79961377	SK-N-SH	brain:	n/a	n/a
41	PBX3	chr5:79960823-79961395	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr5:79956829-79956845	K562	blood:	n/a	n/a
43	POLR2A	chr5:79960867-79961349	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr5:79956822-79956995	ProgFib	skin:	n/a	n/a
45	POLR2A	chr5:79957750-79958196	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr5:79956670-79956683	MCF-7	breast:	n/a	n/a
47	POLR2A	chr5:79961333-79961503	MCF10A-Er-Src	breast:	n/a	n/a
48	SETDB1	chr5:79959033-79959371	U2OS	brain:	n/a	n/a
49	SMC3	chr5:79959756-79959844	HepG2	liver:	n/a	n/a
50	STAT3	chr5:79955065-79955276	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:79953697-79953747	SKMC	muscle:	n/a
2	chr5:79953697-79953747	HRPEpiC	eye:	n/a
3	chr5:79953697-79953747	AG04450	lung:	fetal
4	chr5:79953697-79953747	T-47D	breast:	n/a
5	chr5:79953697-79953747	HIPEpiC	eye:	n/a
6	chr5:79953697-79953747	HNPCEpiC	eye:	n/a
7	chr5:79953697-79953747	NB4	blood:	n/a
8	chr5:79953697-79953747	ovcar-3	ovarian:	n/a
9	chr5:79953697-79953747	HepG2	liver:	n/a
10	chr5:79953697-79953747	H1-hESC	embryonic stem cell:	embryo
11	chr5:79953697-79953747	Hepatocyte	liver:	n/a
12	chr5:79953697-79953747	AG09319	gingival:	n/a
13	chr5:79953697-79953747	A549	lung:	n/a
14	chr5:79953697-79953747	ProgFib	skin:	n/a
15	chr5:79953697-79953747	GM06990	blood:	n/a
16	chr5:79953697-79953747	ECC-1	luminal epithelium:	n/a
17	chr5:79953697-79953747	K562	blood:	n/a
18	chr5:79953697-79953747	AoSMC	blood vessel:	n/a
19	chr5:79953697-79953747	Hela-S3	cervix:	n/a
20	chr5:79953697-79953747	BJ	skin:	n/a
21	chr5:79953697-79953747	AG04449	skin:	fetal
22	chr5:79953697-79953747	GM19239	blood:	n/a
23	chr5:79953697-79953747	HEK293	kidney:	embryo
24	chr5:79953697-79953747	GM12878	blood:	n/a
25	chr5:79953697-79953747	HUVEC	blood vessel:	n/a
26	chr5:79953697-79953747	GM12892	blood:	n/a
27	chr5:79953697-79953747	SK-N-SH_RA	brain:	n/a
28	chr5:79953697-79953747	HCM	heart:	n/a
29	chr5:79953697-79953747	PFSK-1	brain:	n/a
30	chr5:79953697-79953747	BE2_C	brain:	n/a
31	chr5:79953697-79953747	NHDF-neo	bronchial:	n/a
32	chr5:79953697-79953747	MCF10A-Er-Src	breast:	n/a
33	chr5:79953697-79953747	HRE	kidney:	n/a
34	chr5:79953697-79953747	SK-N-SH	brain:	n/a
35	chr5:79953697-79953747	SAEC	small airway:	n/a
36	chr5:79953697-79953747	HPAEpiC	pulmonary alveolar:	n/a
37	chr5:79953697-79953747	PrEC	prostate:	n/a
38	chr5:79953697-79953747	NT2-D1	testis:	n/a
39	chr5:79953697-79953747	U87	brain:	n/a
40	chr5:79953697-79953747	SK-N-MC	brain:	n/a
41	chr5:79953697-79953747	GM12891	blood:	n/a
42	chr5:79953697-79953747	HEEpiC	esophagus:	n/a
43	chr5:79953697-79953747	LNCaP	prostate:	n/a
44	chr5:79953697-79953747	AG10803	skin:	n/a
45	chr5:79953697-79953747	HMEC	breast:	n/a
46	chr5:79953697-79953747	HCF	heart:	n/a
47	chr5:79953697-79953747	HAEpiC	amniotic membrane:	n/a
48	chr5:79953697-79953747	NHBE	bronchial:	n/a
49	chr5:79953697-79953747	RPTEC	kidney:	n/a
50	chr5:79953697-79953747	CMK	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:79958590..79961048-chr5:80005503..80007376,2	K562	blood:
2	chr5:79702114..79706204-chr5:79947823..79953616,8	MCF-7	breast:
3	chr5:79950633..79952503-chr5:79956783..79958628,2	MCF-7	breast:
4	chr5:79949469..79952058-chr5:79960023..79961648,2	MCF-7	breast:
5	chr5:79959827..79961745-chr5:79962101..79964799,2	K562	blood:
6	chr5:79949138..79951235-chr5:79952143..79954933,3	K562	blood:
7	chr5:79949138..79951235-chr5:79952143..79954241,3	K562	blood:
8	chr5:79948482..79951173-chr5:79961260..79964699,4	MCF-7	breast:
9	chr5:79959818..79962346-chr5:79962374..79963921,2	MCF-7	breast:
10	chr5:79955227..79957557-chr5:79958269..79961071,2	K562	blood:
11	chr5:79959827..79961745-chr5:79962101..79964799,2	K562	blood:
12	chr5:79950067..79952417-chr5:79958282..79961440,3	K562	blood:
13	chr5:79781713..79786255-chr5:79948613..79954295,12	MCF-7	breast:
14	chr5:79956607..79959193-chr5:79962502..79964568,2	MCF-7	breast:
15	chr5:79956480..79958255-chr5:79962360..79963991,2	MCF-7	breast:
16	chr5:79955227..79957557-chr5:79958269..79961071,2	K562	blood:
17	chr5:79950476..79953342-chr5:79955489..79957771,3	K562	blood:
18	chr5:79956480..79958255-chr5:79962360..79963991,2	MCF-7	breast:
19	chr5:79948428..79952825-chr5:79952965..79955776,5	MCF-7	breast:

No data

Variant related genes	Relation type
DHFR	TF binding region
DHFR	CpG island
ENSG00000228716	chromatin interactions
ENSG00000113318	chromatin interactions
ENSG00000152380	chromatin interactions
ENSG00000249042	chromatin interactions
ENSG00000039319	chromatin interactions

Extended variants
information (count: 417 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:417 , 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	rs575936728	chr5:79953571-79953572	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs1382542	chr5:79953581-79953582	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs555340838	chr5:79953593-79953594	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs200346550	chr5:79953681-79953682	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs201317884	chr5:79953682-79953683	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs575217375	chr5:79953708-79953709	Weak transcription Strong transcription Genic enhancers	CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs1643655	chr5:79953776-79953777	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs560560125	chr5:79953786-79953787	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs115800801	chr5:79953788-79953789	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs2405880	chr5:79953793-79953794	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs369384745	chr5:79953854-79953855	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs375162431	chr5:79953855-79953856	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs369965673	chr5:79953856-79953857	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs374785204	chr5:79953857-79953858	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs397942439	chr5:79953869-79953870	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs562623016	chr5:79953884-79953885	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs369098636	chr5:79953910-79953911	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs72765566	chr5:79953948-79953949	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs567874207	chr5:79953966-79953967	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs187236465	chr5:79954024-79954025	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs150421619	chr5:79954064-79954065	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs35086803	chr5:79954076-79954077	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs191897606	chr5:79954087-79954088	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs386689492	chr5:79954097-79954098	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs1677676	chr5:79954098-79954099	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs377730227	chr5:79954125-79954126	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs535501257	chr5:79954126-79954127	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs373886669	chr5:79954174-79954175	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs575056630	chr5:79954213-79954214	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs540939429	chr5:79954235-79954236	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs554156968	chr5:79954243-79954244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs570233876	chr5:79954244-79954245	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs114678810	chr5:79954269-79954270	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs144887071	chr5:79954288-79954289	Weak transcription Strong transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs376293229	chr5:79954345-79954346	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs531702628	chr5:79954351-79954352	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs541875456	chr5:79954381-79954382	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs138758045	chr5:79954391-79954392	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs527479608	chr5:79954394-79954395	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs141575303	chr5:79954435-79954436	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570652386	chr5:79954461-79954462	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs532982223	chr5:79954479-79954480	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549518669	chr5:79954505-79954506	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372913725	chr5:79954549-79954550	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs569620506	chr5:79954566-79954567	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs35929737	chr5:79954593-79954594	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370484515	chr5:79954594-79954595	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs145227788	chr5:79954639-79954640	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs184235716	chr5:79954648-79954649	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs568707796	chr5:79954717-79954718	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79951200-79954800	Weak transcription	Ovary	ovary
2	chr5:79951200-79963200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr5:79951400-79956000	Weak transcription	Aorta	Aorta
4	chr5:79951400-79963200	Weak transcription	Right Ventricle	heart
5	chr5:79951600-79953600	Weak transcription	Lung	lung
6	chr5:79951600-79953600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr5:79951600-79953800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr5:79951600-79954200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr5:79951600-79954200	Weak transcription	Colonic Mucosa	Colon
10	chr5:79951600-79954400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr5:79951600-79954400	Weak transcription	Gastric	stomach
12	chr5:79951600-79955000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr5:79951600-79955000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr5:79951600-79955200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:79951600-79959000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:79951600-79962600	Weak transcription	Esophagus	oesophagus
17	chr5:79951600-79963200	Weak transcription	Pancreas	Pancrea
18	chr5:79951600-79963400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr5:79951600-79963400	Weak transcription	Brain Germinal Matrix	brain
20	chr5:79951600-79963600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr5:79951600-79969200	Weak transcription	Stomach Mucosa	stomach
22	chr5:79951600-79972200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
23	chr5:79951600-80015600	Weak transcription	Small Intestine	intestine
24	chr5:79951800-79953600	Weak transcription	Brain Anterior Caudate	brain
25	chr5:79951800-79953600	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr5:79951800-79954000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr5:79951800-79954200	Weak transcription	Brain Cingulate Gyrus	brain
28	chr5:79951800-79954400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr5:79951800-79954400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr5:79951800-79954800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr5:79951800-79955200	Weak transcription	Primary hematopoietic stem cells	blood
32	chr5:79951800-79957600	Weak transcription	Fetal Brain Male	brain
33	chr5:79951800-79960200	Weak transcription	Colon Smooth Muscle	Colon
34	chr5:79951800-79964000	Weak transcription	Brain Substantia Nigra	brain
35	chr5:79951800-79982800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr5:79952000-79953600	Weak transcription	Brain Hippocampus Middle	brain
37	chr5:79952000-79953800	Weak transcription	Thymus	Thymus
38	chr5:79952000-79954000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr5:79952000-79954200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr5:79952000-79955600	Weak transcription	Fetal Lung	lung
41	chr5:79952000-79959800	Weak transcription	HMEC	breast
42	chr5:79952000-79963800	Weak transcription	Fetal Heart	heart
43	chr5:79952200-79953600	Weak transcription	Fetal Kidney	kidney
44	chr5:79952200-79954000	Weak transcription	Spleen	Spleen
45	chr5:79952200-79954800	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr5:79952200-79955800	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr5:79952200-79956400	Strong transcription	Fetal Muscle Leg	muscle
48	chr5:79952200-79956400	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr5:79952200-79964200	Weak transcription	Brain Angular Gyrus	brain
50	chr5:79952200-79964200	Strong transcription	Fetal Muscle Trunk	muscle

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