Variant report

Variant	nsv1034331
Chromosome Location	chr5:59678773-59773467
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:804)
CpG islands
(count:183)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:59742744-59743990	HepG2	liver:	n/a	chr5:59743535-59743551
2	ARID3A	chr5:59722961-59722993	K562	blood:	n/a	n/a
3	ARID3A	chr5:59759049-59759883	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:59769493-59769923	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:59712885-59714270	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	chr5:59699527-59699795	HepG2	liver:	n/a	n/a
13	BHLHE40	chr5:59742844-59743730	HepG2	liver:	n/a	n/a
14	BHLHE40	chr5:59758956-59759660	HepG2	liver:	n/a	n/a
15	BHLHE40	chr5:59699449-59699836	HepG2	liver:	n/a	n/a
16	BHLHE40	chr5:59743228-59743638	HepG2	liver:	n/a	n/a
17	BHLHE40	chr5:59743262-59743636	HepG2	liver:	n/a	n/a
18	BRCA1	chr5:59758918-59759295	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr5:59773450-59773510	GM12878	blood:	n/a	n/a
20	CCNT2	chr5:59747083-59747168	K562	blood:	n/a	n/a
21	CEBPB	chr5:59706378-59706655	HepG2	liver:	n/a	n/a
22	CEBPB	chr5:59699446-59699837	HepG2	liver:	n/a	chr5:59699638-59699649
23	CEBPB	chr5:59699385-59699839	HepG2	liver:	n/a	chr5:59699638-59699649
24	CEBPB	chr5:59700026-59700313	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:59759016-59759277	HepG2	liver:	n/a	chr5:59759173-59759184
26	CEBPB	chr5:59688801-59688993	A549	lung:	n/a	n/a
27	CEBPB	chr5:59699448-59699819	HepG2	liver:	n/a	chr5:59699638-59699649
28	CEBPB	chr5:59758972-59759399	MCF-7	breast:	n/a	chr5:59759173-59759184
29	CEBPB	chr5:59761806-59762009	A549	lung:	n/a	n/a
30	CEBPB	chr5:59759094-59759253	H1-hESC	embryonic stem cell:	n/a	chr5:59759173-59759184
31	CEBPB	chr5:59758954-59759375	A549	lung:	n/a	chr5:59759173-59759184
32	CEBPB	chr5:59680450-59680763	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:59758926-59759470	Hela-S3	cervix:	n/a	chr5:59759173-59759184
34	CEBPB	chr5:59738481-59738678	HepG2	liver:	n/a	chr5:59738605-59738616
35	CEBPB	chr5:59758780-59759728	A549	lung:	n/a	chr5:59759173-59759184 chr5:59758810-59758822 chr5:59758883-59758895
36	CEBPB	chr5:59699506-59699747	HepG2	liver:	n/a	chr5:59699638-59699649
37	CEBPB	chr5:59699965-59700344	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr5:59758957-59759712	HepG2	liver:	n/a	chr5:59759173-59759184
39	CEBPB	chr5:59758902-59759356	HepG2	liver:	n/a	chr5:59759173-59759184
40	CEBPB	chr5:59759013-59759326	MCF-7	breast:	n/a	chr5:59759173-59759184
41	CEBPB	chr5:59688730-59689045	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:59678604-59678926	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:59758997-59759365	IMR90	lung:	n/a	chr5:59759173-59759184
44	CEBPB	chr5:59680471-59680692	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr5:59699956-59700331	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr5:59699488-59699754	A549	lung:	n/a	chr5:59699638-59699649
47	CEBPB	chr5:59700052-59700274	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr5:59758865-59759496	A549	lung:	n/a	chr5:59759173-59759184 chr5:59758883-59758895
49	CEBPB	chr5:59758981-59759376	K562	blood:	n/a	chr5:59759173-59759184
50	CEBPB	chr5:59758995-59759301	K562	blood:	n/a	chr5:59759173-59759184

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59711350-59711400	HRE	kidney:	n/a
2	chr5:59711378-59711428	Jurkat	blood:	n/a
3	chr5:59711350-59711400	HRPEpiC	eye:	n/a
4	chr5:59727726-59727776	NB4	blood:	n/a
5	chr5:59727726-59727776	PFSK-1	brain:	n/a
6	chr5:59711378-59711428	MCF10A-Er-Src	breast:	n/a
7	chr5:59711350-59711400	HCM	heart:	n/a
8	chr5:59727726-59727776	NH-A	brain:	n/a
9	chr5:59711378-59711428	AG10803	skin:	n/a
10	chr5:59711378-59711428	HEEpiC	esophagus:	n/a
11	chr5:59711378-59711428	CMK	blood:	n/a
12	chr5:59727726-59727776	GM12878	blood:	n/a
13	chr5:59727726-59727776	AG04450	lung:	fetal
14	chr5:59727726-59727776	A549	lung:	n/a
15	chr5:59711378-59711428	NHBE	bronchial:	n/a
16	chr5:59711350-59711400	MCF-7	breast:	n/a
17	chr5:59711378-59711428	HRPEpiC	eye:	n/a
18	chr5:59727726-59727776	HEEpiC	esophagus:	n/a
19	chr5:59711350-59711400	HCPEpiC	choroid plexus:	n/a
20	chr5:59727726-59727776	HMEC	breast:	n/a
21	chr5:59711378-59711428	LNCaP	prostate:	n/a
22	chr5:59711378-59711428	T-47D	breast:	n/a
23	chr5:59711350-59711400	NHDF-neo	bronchial:	n/a
24	chr5:59711350-59711400	PFSK-1	brain:	n/a
25	chr5:59711350-59711400	HUVEC	blood vessel:	n/a
26	chr5:59727726-59727776	SK-N-SH_RA	brain:	n/a
27	chr5:59727726-59727776	HUVEC	blood vessel:	n/a
28	chr5:59711378-59711428	PANC-1	pancreas:	n/a
29	chr5:59727726-59727776	HRCEpiC	kidney:	n/a
30	chr5:59727726-59727776	HCT-116	colon:	n/a
31	chr5:59727726-59727776	ovcar-3	ovarian:	n/a
32	chr5:59727726-59727776	SKMC	muscle:	n/a
33	chr5:59711350-59711400	HEK293	kidney:	embryo
34	chr5:59711350-59711400	Caco-2	colon:	n/a
35	chr5:59727726-59727776	HCF	heart:	n/a
36	chr5:59727726-59727776	NHBE	bronchial:	n/a
37	chr5:59711350-59711400	T-47D	breast:	n/a
38	chr5:59711350-59711400	NH-A	brain:	n/a
39	chr5:59711350-59711400	BJ	skin:	n/a
40	chr5:59711378-59711428	AoSMC	blood vessel:	n/a
41	chr5:59727726-59727776	MCF-7	breast:	n/a
42	chr5:59727726-59727776	U87	brain:	n/a
43	chr5:59711350-59711400	BE2_C	brain:	n/a
44	chr5:59727726-59727776	HL-60	blood:	n/a
45	chr5:59711378-59711428	AG04449	skin:	fetal
46	chr5:59711378-59711428	K562	blood:	n/a
47	chr5:59711378-59711428	AG09319	gingival:	n/a
48	chr5:59711378-59711428	IMR90	lung:	fetal
49	chr5:59727726-59727776	BJ	skin:	n/a
50	chr5:59727726-59727776	PrEC	prostate:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:59109590..59110214-chr5:59678255..59679111,2	MCF-7	breast:
2	chr5:59700212..59701783-chr5:59712786..59715237,2	K562	blood:
3	chr5:59105509..59106419-chr5:59678283..59679226,3	MCF-7	breast:
4	chr5:59689950..59691526-chr5:59697075..59698580,2	K562	blood:
5	chr5:59700212..59701783-chr5:59712786..59715237,2	K562	blood:
6	chr5:59590961..59591565-chr5:59678761..59679630,2	MCF-7	breast:
7	chr5:59678290..59679528-chr5:59881870..59883189,3	MCF-7	breast:
8	chr5:59689950..59691526-chr5:59697075..59698580,2	K562	blood:
9	chr5:59750546..59752966-chr5:59754525..59756849,2	K562	blood:
10	chr5:59590922..59592157-chr5:59678281..59679194,10	MCF-7	breast:

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: 3467 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3467 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568653971	chr5:59678836-59678837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558491893	chr5:59678851-59678852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75163750	chr5:59678853-59678854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185578618	chr5:59678859-59678860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs16877976	chr5:59678889-59678890	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs558650658	chr5:59678930-59678931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146052706	chr5:59678991-59678992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs372065998	chr5:59679059-59679060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541025036	chr5:59679082-59679083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114621314	chr5:59679100-59679101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529666928	chr5:59679177-59679178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543657061	chr5:59679205-59679206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs563460100	chr5:59679218-59679219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138717499	chr5:59679229-59679230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142729996	chr5:59679236-59679237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189893275	chr5:59679265-59679266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574573176	chr5:59679266-59679267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377538256	chr5:59679292-59679293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528608432	chr5:59679308-59679309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs548165807	chr5:59679322-59679323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568399941	chr5:59679343-59679344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373324949	chr5:59679387-59679388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376331020	chr5:59679414-59679415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79726374	chr5:59679417-59679418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557605040	chr5:59679457-59679458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182107973	chr5:59679464-59679465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186788978	chr5:59679465-59679466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs553650304	chr5:59679475-59679476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs77210116	chr5:59679478-59679479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527927648	chr5:59679480-59679481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371395830	chr5:59679569-59679570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370916769	chr5:59679574-59679575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117473377	chr5:59679594-59679595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574349678	chr5:59679596-59679597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs60962155	chr5:59679665-59679666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs563585842	chr5:59679671-59679672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs576757520	chr5:59679820-59679821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147379262	chr5:59679872-59679873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192473929	chr5:59679916-59679917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528277562	chr5:59679954-59679955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577006090	chr5:59680021-59680022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548615414	chr5:59680181-59680182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562062158	chr5:59680211-59680212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs532048505	chr5:59680249-59680250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs530899967	chr5:59680251-59680252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114306352	chr5:59680337-59680338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550732337	chr5:59680343-59680344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571158188	chr5:59680384-59680385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139005531	chr5:59680412-59680413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183808008	chr5:59680444-59680445	Weak transcription Enhancers	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:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59647200-59694200	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59662600-59680200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr5:59675800-59680200	Weak transcription	Aorta	Aorta
4	chr5:59678400-59678800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr5:59678400-59678800	Enhancers	GM12878-XiMat	blood
6	chr5:59678400-59679000	Enhancers	Colon Smooth Muscle	Colon
7	chr5:59678600-59678800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:59678600-59678800	Enhancers	Small Intestine	intestine
9	chr5:59678600-59679400	Enhancers	Rectal Smooth Muscle	rectum
10	chr5:59679000-59680800	Weak transcription	Colon Smooth Muscle	Colon
11	chr5:59679400-59680200	Weak transcription	Rectal Smooth Muscle	rectum
12	chr5:59680200-59680400	Enhancers	Rectal Smooth Muscle	rectum
13	chr5:59680200-59680800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr5:59680200-59682600	Enhancers	Aorta	Aorta
15	chr5:59680200-59683800	Enhancers	Stomach Smooth Muscle	stomach
16	chr5:59680400-59680600	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr5:59680400-59680800	Weak transcription	Rectal Smooth Muscle	rectum
18	chr5:59680600-59681200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr5:59680600-59681600	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr5:59680800-59681000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr5:59680800-59681000	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:59680800-59683800	Enhancers	Rectal Smooth Muscle	rectum
23	chr5:59680800-59684200	Enhancers	Colon Smooth Muscle	Colon
24	chr5:59681000-59681200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr5:59681000-59683000	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:59681200-59681400	Enhancers	Fetal Stomach	stomach
27	chr5:59681200-59681400	Enhancers	A549	lung
28	chr5:59681200-59682200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:59681200-59683200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr5:59681200-59683600	Enhancers	Fetal Brain Male	brain
31	chr5:59681400-59681800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:59681400-59681800	Enhancers	Adipose Nuclei	Adipose
33	chr5:59681400-59682400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr5:59681400-59682400	Weak transcription	Fetal Stomach	stomach
35	chr5:59681400-59682600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr5:59681400-59682800	Weak transcription	A549	lung
37	chr5:59681400-59683000	Enhancers	Fetal Brain Female	brain
38	chr5:59681600-59683000	Enhancers	Brain Germinal Matrix	brain
39	chr5:59681600-59683400	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr5:59682200-59682400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:59682200-59682600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr5:59682200-59682600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr5:59682200-59682600	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr5:59682200-59683000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr5:59682200-59683200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr5:59682400-59682800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr5:59682400-59682800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr5:59682400-59682800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr5:59682400-59684000	Enhancers	Fetal Stomach	stomach
50	chr5:59682600-59683000	Enhancers	iPS-15b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links