Variant report

Variant	nsv1033344
Chromosome Location	chr5:59710033-59773467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:390)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:390 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59712885-59714270	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:59759049-59759883	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:59722961-59722993	K562	blood:	n/a	n/a
4	ARID3A	chr5:59742744-59743990	HepG2	liver:	n/a	chr5:59743535-59743551
5	ARID3A	chr5:59769493-59769923	HepG2	liver:	n/a	n/a
6	ATF3	chr5:59758895-59759556	A549	lung:	n/a	n/a
7	BATF	chr5:59712137-59712393	GM12878	blood:	n/a	n/a
8	BCL11A	chr5:59712066-59712395	GM12878	blood:	n/a	n/a
9	BCL3	chr5:59758809-59759695	A549	lung:	n/a	chr5:59759578-59759587
10	BCL3	chr5:59758832-59759533	A549	lung:	n/a	n/a
11	BHLHE40	chr5:59758972-59759353	A549	lung:	n/a	n/a
12	BHLHE40	chr5:59742844-59743730	HepG2	liver:	n/a	n/a
13	BHLHE40	chr5:59743262-59743636	HepG2	liver:	n/a	n/a
14	BHLHE40	chr5:59743228-59743638	HepG2	liver:	n/a	n/a
15	BHLHE40	chr5:59758956-59759660	HepG2	liver:	n/a	n/a
16	BRCA1	chr5:59773450-59773510	GM12878	blood:	n/a	n/a
17	BRCA1	chr5:59758918-59759295	Hela-S3	cervix:	n/a	n/a
18	CCNT2	chr5:59747083-59747168	K562	blood:	n/a	n/a
19	CEBPB	chr5:59761806-59762009	A549	lung:	n/a	n/a
20	CEBPB	chr5:59758957-59759712	HepG2	liver:	n/a	chr5:59759173-59759184
21	CEBPB	chr5:59758902-59759356	HepG2	liver:	n/a	chr5:59759173-59759184
22	CEBPB	chr5:59759094-59759253	H1-hESC	embryonic stem cell:	n/a	chr5:59759173-59759184
23	CEBPB	chr5:59744444-59744829	Hela-S3	cervix:	n/a	chr5:59744753-59744765
24	CEBPB	chr5:59758981-59759376	K562	blood:	n/a	chr5:59759173-59759184
25	CEBPB	chr5:59758780-59759728	A549	lung:	n/a	chr5:59759173-59759184 chr5:59758810-59758822 chr5:59758883-59758895
26	CEBPB	chr5:59758952-59759391	HepG2	liver:	n/a	chr5:59759173-59759184
27	CEBPB	chr5:59744195-59744769	A549	lung:	n/a	chr5:59744753-59744765
28	CEBPB	chr5:59758997-59759365	IMR90	lung:	n/a	chr5:59759173-59759184
29	CEBPB	chr5:59759013-59759326	MCF-7	breast:	n/a	chr5:59759173-59759184
30	CEBPB	chr5:59738481-59738678	HepG2	liver:	n/a	chr5:59738605-59738616
31	CEBPB	chr5:59758972-59759399	MCF-7	breast:	n/a	chr5:59759173-59759184
32	CEBPB	chr5:59759016-59759277	HepG2	liver:	n/a	chr5:59759173-59759184
33	CEBPB	chr5:59758954-59759375	A549	lung:	n/a	chr5:59759173-59759184
34	CEBPB	chr5:59713572-59713952	HepG2	liver:	n/a	chr5:59713769-59713780
35	CEBPB	chr5:59740891-59741112	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr5:59758865-59759496	A549	lung:	n/a	chr5:59759173-59759184 chr5:59758883-59758895
37	CEBPB	chr5:59758995-59759301	K562	blood:	n/a	chr5:59759173-59759184
38	CEBPB	chr5:59758926-59759470	Hela-S3	cervix:	n/a	chr5:59759173-59759184
39	CHD2	chr5:59759045-59759296	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr5:59754497-59754924	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:59712430-59712460	GM10248	blood:	n/a	n/a
42	CTCF	chr5:59754580-59754730	HepG2	liver:	n/a	n/a
43	CTCF	chr5:59754610-59754792	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:59754590-59754775	HepG2	liver:	n/a	n/a
45	CTCF	chr5:59754560-59754710	BE2_C	brain:	n/a	n/a
46	CTCF	chr5:59754660-59754810	BE2_C	brain:	n/a	n/a
47	CTCF	chr5:59754640-59754790	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr5:59718802-59718835	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr5:59754620-59754770	Caco-2	colon:	n/a	n/a
50	CTCF	chr5:59754111-59754159	Fibrobl	skin:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59727726-59727776	HIPEpiC	eye:	n/a
2	chr5:59711378-59711428	Caco-2	colon:	n/a
3	chr5:59727726-59727776	HRPEpiC	eye:	n/a
4	chr5:59711378-59711428	RPTEC	kidney:	n/a
5	chr5:59727726-59727776	SK-N-SH	brain:	n/a
6	chr5:59711350-59711400	HRE	kidney:	n/a
7	chr5:59711378-59711428	NHDF-neo	bronchial:	n/a
8	chr5:59711350-59711400	HepG2	liver:	n/a
9	chr5:59727726-59727776	ovcar-3	ovarian:	n/a
10	chr5:59727726-59727776	IMR90	lung:	fetal
11	chr5:59711350-59711400	NHDF-neo	bronchial:	n/a
12	chr5:59727726-59727776	Hepatocyte	liver:	n/a
13	chr5:59711350-59711400	Caco-2	colon:	n/a
14	chr5:59711350-59711400	GM06990	blood:	n/a
15	chr5:59711350-59711400	Hepatocyte	liver:	n/a
16	chr5:59727726-59727776	U87	brain:	n/a
17	chr5:59727726-59727776	LNCaP	prostate:	n/a
18	chr5:59727726-59727776	Hela-S3	cervix:	n/a
19	chr5:59711378-59711428	AG09319	gingival:	n/a
20	chr5:59727726-59727776	HCT-116	colon:	n/a
21	chr5:59711378-59711428	A549	lung:	n/a
22	chr5:59727726-59727776	MCF10A-Er-Src	breast:	n/a
23	chr5:59727726-59727776	HUVEC	blood vessel:	n/a
24	chr5:59711378-59711428	Hela-S3	cervix:	n/a
25	chr5:59727726-59727776	T-47D	breast:	n/a
26	chr5:59711378-59711428	H1-hESC	embryonic stem cell:	embryo
27	chr5:59711350-59711400	BJ	skin:	n/a
28	chr5:59727726-59727776	HAEpiC	amniotic membrane:	n/a
29	chr5:59711350-59711400	HAEpiC	amniotic membrane:	n/a
30	chr5:59711378-59711428	SAEC	small airway:	n/a
31	chr5:59727726-59727776	SKMC	muscle:	n/a
32	chr5:59711378-59711428	SK-N-SH_RA	brain:	n/a
33	chr5:59727726-59727776	MCF-7	breast:	n/a
34	chr5:59711350-59711400	HEEpiC	esophagus:	n/a
35	chr5:59727726-59727776	HCPEpiC	choroid plexus:	n/a
36	chr5:59711350-59711400	SKMC	muscle:	n/a
37	chr5:59727726-59727776	AG09309	skin:	n/a
38	chr5:59727726-59727776	AG09319	gingival:	n/a
39	chr5:59727726-59727776	BJ	skin:	n/a
40	chr5:59711350-59711400	ovcar-3	ovarian:	n/a
41	chr5:59727726-59727776	HPAEpiC	pulmonary alveolar:	n/a
42	chr5:59711350-59711400	AG04450	lung:	fetal
43	chr5:59727726-59727776	PANC-1	pancreas:	n/a
44	chr5:59711378-59711428	SK-N-MC	brain:	n/a
45	chr5:59727726-59727776	K562	blood:	n/a
46	chr5:59711378-59711428	HNPCEpiC	eye:	n/a
47	chr5:59727726-59727776	HCF	heart:	n/a
48	chr5:59727726-59727776	NT2-D1	testis:	n/a
49	chr5:59727726-59727776	HEEpiC	esophagus:	n/a
50	chr5:59727726-59727776	HEK293	kidney:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:59700212..59701783-chr5:59712786..59715237,2	K562	blood:
2	chr5:59750546..59752966-chr5:59754525..59756849,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000213896	TF binding region
ENSG00000224838	TF binding region
SETP21	TF binding region
PDE4D	TF binding region
ENSG00000213896	CpG island
ENSG00000224838	CpG island
SETP21	CpG island
PDE4D	CpG island
ENSG00000214244	chromatin interactions

Extended variants
information (count: 2409 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2409 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6864442	chr5:59710033-59710034	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs546267955	chr5:59710070-59710071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553693221	chr5:59710072-59710073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140477620	chr5:59710102-59710103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369942676	chr5:59710139-59710140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377157074	chr5:59710158-59710159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554976107	chr5:59710160-59710161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560759054	chr5:59710275-59710276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150430178	chr5:59710356-59710357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527865037	chr5:59710367-59710368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531028823	chr5:59710404-59710405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs190796897	chr5:59710419-59710420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537266494	chr5:59710506-59710507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138128969	chr5:59710509-59710510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531969351	chr5:59710523-59710524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551712676	chr5:59710601-59710602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183029230	chr5:59710655-59710656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528357601	chr5:59710664-59710665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548201920	chr5:59710693-59710694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568228119	chr5:59710720-59710721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187561846	chr5:59710768-59710769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536877348	chr5:59710835-59710836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs557487500	chr5:59710987-59710988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193287083	chr5:59711034-59711035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570998184	chr5:59711046-59711047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs539949124	chr5:59711091-59711092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs553358540	chr5:59711105-59711106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573297810	chr5:59711152-59711153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373862431	chr5:59711154-59711155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564758906	chr5:59711224-59711225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113048083	chr5:59711244-59711245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199970694	chr5:59711246-59711247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573376906	chr5:59711252-59711253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575775289	chr5:59711269-59711270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs544529038	chr5:59711297-59711298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28460011	chr5:59711334-59711335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs142781521	chr5:59711344-59711345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549750849	chr5:59711357-59711358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs28635931	chr5:59711361-59711362	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs528106848	chr5:59711397-59711398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548442953	chr5:59711400-59711401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535549519	chr5:59711401-59711402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187583950	chr5:59711418-59711419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376485871	chr5:59711432-59711433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112780521	chr5:59711440-59711441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs369343684	chr5:59711455-59711456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192012346	chr5:59711460-59711461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373153551	chr5:59711476-59711477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115760413	chr5:59711503-59711504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376951451	chr5:59711508-59711509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	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
Hepatocellular carcinoma	16750200	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
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59695000-59712600	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59696000-59713200	Weak transcription	Aorta	Aorta
3	chr5:59707200-59712400	Weak transcription	HepG2	liver
4	chr5:59712200-59713000	Enhancers	Primary B cells from peripheral blood	blood
5	chr5:59712400-59713000	Enhancers	GM12878-XiMat	blood
6	chr5:59712400-59716800	Enhancers	HepG2	liver
7	chr5:59712600-59713200	Enhancers	Primary B cells from cord blood	blood
8	chr5:59712600-59713200	Enhancers	Primary hematopoietic stem cells	blood
9	chr5:59712800-59713400	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr5:59713000-59713200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
11	chr5:59713200-59713600	Enhancers	Aorta	Aorta
12	chr5:59713200-59716000	Weak transcription	Primary B cells from cord blood	blood
13	chr5:59716000-59716600	ZNF genes & repeats	Primary B cells from cord blood	blood
14	chr5:59716400-59716800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr5:59716400-59716800	ZNF genes & repeats	Pancreas	Pancrea
16	chr5:59716800-59717000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:59717000-59730000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr5:59727200-59766600	Weak transcription	Primary B cells from cord blood	blood
19	chr5:59730000-59730400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:59730400-59731000	Enhancers	Colon Smooth Muscle	Colon
21	chr5:59730400-59731800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:59730400-59733200	Enhancers	HepG2	liver
23	chr5:59731800-59732000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:59732000-59732400	Enhancers	GM12878-XiMat	blood
25	chr5:59732400-59733000	Enhancers	Primary B cells from peripheral blood	blood
26	chr5:59732400-59733400	Flanking Active TSS	GM12878-XiMat	blood
27	chr5:59732800-59733000	Enhancers	Aorta	Aorta
28	chr5:59733000-59742600	Weak transcription	Aorta	Aorta
29	chr5:59733200-59738800	Weak transcription	HepG2	liver
30	chr5:59733400-59733800	Enhancers	GM12878-XiMat	blood
31	chr5:59734000-59734400	Enhancers	Fetal Kidney	kidney
32	chr5:59738800-59742800	Enhancers	HepG2	liver
33	chr5:59740000-59741200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:59740000-59741600	Enhancers	Fetal Brain Male	brain
35	chr5:59740200-59740600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr5:59740400-59741000	Enhancers	Fetal Brain Female	brain
37	chr5:59740400-59741000	Enhancers	Hela-S3	cervix
38	chr5:59740600-59740800	Enhancers	Gastric	stomach
39	chr5:59741000-59744200	Weak transcription	Hela-S3	cervix
40	chr5:59741200-59741600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:59741600-59741800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr5:59741600-59743200	Enhancers	Stomach Mucosa	stomach
43	chr5:59741600-59744800	Weak transcription	Fetal Brain Male	brain
44	chr5:59741800-59783200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:59742600-59743000	Enhancers	Aorta	Aorta
46	chr5:59742600-59743000	Enhancers	A549	lung
47	chr5:59742600-59744400	Enhancers	Gastric	stomach
48	chr5:59742800-59743200	Flanking Active TSS	HepG2	liver
49	chr5:59743000-59743600	Flanking Active TSS	A549	lung
50	chr5:59743000-59743800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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