Variant report

Variant	nsv1032732
Chromosome Location	chr5:58637179-58689010
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1046)
CpG islands
(count:122)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr5:58663693-58663944	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr5:58676057-58676572	GM12878	blood:	n/a	n/a
3	ATF2	chr5:58667411-58667779	GM12878	blood:	n/a	n/a
4	ATF2	chr5:58676085-58676588	GM12878	blood:	n/a	n/a
5	ATF2	chr5:58667352-58667796	GM12878	blood:	n/a	n/a
6	ATF3	chr5:58652777-58654067	A549	lung:	n/a	n/a
7	BATF	chr5:58667396-58667737	GM12878	blood:	n/a	chr5:58667586-58667597 chr5:58667587-58667597
8	BATF	chr5:58676204-58676489	GM12878	blood:	n/a	n/a
9	BATF	chr5:58676201-58676554	GM12878	blood:	n/a	n/a
10	BATF	chr5:58667359-58667749	GM12878	blood:	n/a	chr5:58667586-58667597 chr5:58667587-58667597
11	BCL11A	chr5:58676193-58676445	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:58676120-58676482	GM12878	blood:	n/a	chr5:58676143-58676152
13	BCL3	chr5:58652380-58654882	A549	lung:	n/a	chr5:58654065-58654072
14	BCL3	chr5:58657154-58657767	A549	lung:	n/a	n/a
15	BCL3	chr5:58676156-58676940	A549	lung:	n/a	n/a
16	BCL3	chr5:58655859-58656666	A549	lung:	n/a	n/a
17	BCL3	chr5:58653155-58654805	A549	lung:	n/a	chr5:58654065-58654072
18	BCLAF1	chr5:58676236-58676535	GM12878	blood:	n/a	n/a
19	BCLAF1	chr5:58676088-58676598	GM12878	blood:	n/a	chr5:58676143-58676152
20	BHLHE40	chr5:58676155-58676534	GM12878	blood:	n/a	n/a
21	BRCA1	chr5:58642865-58643197	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr5:58663710-58664021	HCT-116	colon:	n/a	n/a
23	CEBPB	chr5:58657316-58657613	MCF-7	breast:	n/a	n/a
24	CEBPB	chr5:58652711-58653861	A549	lung:	n/a	chr5:58653463-58653476
25	CEBPB	chr5:58676221-58676517	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:58655980-58656547	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
27	CEBPB	chr5:58655870-58656886	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
28	CEBPB	chr5:58653216-58653932	A549	lung:	n/a	chr5:58653463-58653476
29	CEBPB	chr5:58663663-58664162	A549	lung:	n/a	n/a
30	CEBPB	chr5:58642763-58643161	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:58658471-58658649	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:58648274-58648474	Hela-S3	cervix:	n/a	chr5:58648345-58648356
33	CEBPB	chr5:58648680-58648832	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:58658453-58658601	A549	lung:	n/a	n/a
35	CEBPB	chr5:58653597-58653845	MCF-7	breast:	n/a	n/a
36	CEBPB	chr5:58652378-58654781	A549	lung:	n/a	chr5:58654387-58654404 chr5:58653463-58653476
37	CEBPB	chr5:58659381-58659514	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:58648218-58648500	A549	lung:	n/a	chr5:58648345-58648356
39	CEBPB	chr5:58655968-58656493	A549	lung:	n/a	chr5:58656328-58656341 chr5:58656201-58656214
40	CEBPB	chr5:58654293-58654492	A549	lung:	n/a	chr5:58654387-58654404
41	CHD2	chr5:58676237-58676498	GM12878	blood:	n/a	n/a
42	CHD2	chr5:58652971-58652987	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr5:58663700-58663957	A549	lung:	n/a	n/a
44	CREB1	chr5:58676157-58676565	GM12878	blood:	n/a	n/a
45	CREB1	chr5:58653318-58653866	A549	lung:	n/a	n/a
46	CREB1	chr5:58676076-58676698	GM12878	blood:	n/a	n/a
47	CREB1	chr5:58667475-58667763	GM12878	blood:	n/a	n/a
48	CREB1	chr5:58654387-58654602	A549	lung:	n/a	n/a
49	CREB1	chr5:58667434-58667800	GM12878	blood:	n/a	n/a
50	CREB1	chr5:58653258-58653846	A549	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:58653624-58653674	Hepatocyte	liver:	n/a
2	chr5:58653624-58653674	HRE	kidney:	n/a
3	chr5:58652808-58652858	ECC-1	luminal epithelium:	n/a
4	chr5:58652808-58652858	AoSMC	blood vessel:	n/a
5	chr5:58652808-58652858	HCT-116	colon:	n/a
6	chr5:58653624-58653674	MCF-7	breast:	n/a
7	chr5:58653624-58653674	HCPEpiC	choroid plexus:	n/a
8	chr5:58652808-58652858	CMK	blood:	n/a
9	chr5:58653624-58653674	GM19239	blood:	n/a
10	chr5:58653624-58653674	RPTEC	kidney:	n/a
11	chr5:58652808-58652858	HepG2	liver:	n/a
12	chr5:58652808-58652858	LNCaP	prostate:	n/a
13	chr5:58653624-58653674	GM06990	blood:	n/a
14	chr5:58652808-58652858	NB4	blood:	n/a
15	chr5:58653624-58653674	GM12891	blood:	n/a
16	chr5:58653624-58653674	Hela-S3	cervix:	n/a
17	chr5:58653624-58653674	K562	blood:	n/a
18	chr5:58653624-58653674	HAEpiC	amniotic membrane:	n/a
19	chr5:58653624-58653674	HUVEC	blood vessel:	n/a
20	chr5:58652808-58652858	IMR90	lung:	fetal
21	chr5:58652808-58652858	MCF-7	breast:	n/a
22	chr5:58653624-58653674	HCT-116	colon:	n/a
23	chr5:58653624-58653674	U87	brain:	n/a
24	chr5:58653624-58653674	A549	lung:	n/a
25	chr5:58653624-58653674	HEK293	kidney:	embryo
26	chr5:58653624-58653674	HMEC	breast:	n/a
27	chr5:58652808-58652858	NH-A	brain:	n/a
28	chr5:58652808-58652858	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:58653624-58653674	ProgFib	skin:	n/a
30	chr5:58652808-58652858	K562	blood:	n/a
31	chr5:58653624-58653674	SAEC	small airway:	n/a
32	chr5:58652808-58652858	AG10803	skin:	n/a
33	chr5:58652808-58652858	AG04450	lung:	fetal
34	chr5:58652808-58652858	PFSK-1	brain:	n/a
35	chr5:58653624-58653674	H1-hESC	embryonic stem cell:	embryo
36	chr5:58653624-58653674	NH-A	brain:	n/a
37	chr5:58652808-58652858	SK-N-SH	brain:	n/a
38	chr5:58652808-58652858	GM12878	blood:	n/a
39	chr5:58652808-58652858	ProgFib	skin:	n/a
40	chr5:58653624-58653674	HEEpiC	esophagus:	n/a
41	chr5:58652808-58652858	GM06990	blood:	n/a
42	chr5:58652808-58652858	HCM	heart:	n/a
43	chr5:58652808-58652858	HNPCEpiC	eye:	n/a
44	chr5:58653624-58653674	SKMC	muscle:	n/a
45	chr5:58652808-58652858	T-47D	breast:	n/a
46	chr5:58653624-58653674	PrEC	prostate:	n/a
47	chr5:58653624-58653674	HIPEpiC	eye:	n/a
48	chr5:58653624-58653674	NHDF-neo	bronchial:	n/a
49	chr5:58653624-58653674	AoSMC	blood vessel:	n/a
50	chr5:58652808-58652858	AG09309	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:58645161..58647091-chr5:58651070..58653977,2	K562	blood:
2	chr5:58685998..58686505-chr5:58956311..58957192,2	MCF-7	breast:
3	chr3:39446942..39449413-chr5:58640294..58641815,3	K562	blood:
4	chr5:58517841..58518362-chr5:58663716..58664223,2	MCF-7	breast:
5	chr5:58484203..58484779-chr5:58676055..58676926,3	MCF-7	breast:
6	chr5:58483931..58484785-chr5:58663381..58664456,4	MCF-7	breast:
7	chr5:58657123..58657869-chr5:58676349..58676935,2	MCF-7	breast:
8	chr5:58657123..58657869-chr5:58676349..58676935,2	MCF-7	breast:
9	chr5:58514307..58514912-chr5:58675986..58677121,4	MCF-7	breast:
10	chr3:39447705..39449413-chr5:58640294..58641815,2	K562	blood:
11	chr5:58513952..58514913-chr5:58663432..58664673,5	MCF-7	breast:
12	chr5:58631024..58631593-chr5:58663326..58663872,2	MCF-7	breast:
13	chr5:58685562..58686590-chr5:58792342..58793267,6	MCF-7	breast:
14	chr5:58484022..58484971-chr5:58675909..58676491,2	MCF-7	breast:
15	chr5:58623297..58625750-chr5:58642406..58644812,2	MCF-7	breast:
16	chr5:58651518..58653116-chr5:58654954..58657664,2	K562	blood:

No data

Variant related genes	Relation type
PDE4D	TF binding region
PDE4D	CpG island
ENSG00000168028	chromatin interactions
ENSG00000113448	chromatin interactions

Extended variants
information (count: 1857 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568220215	chr5:58637183-58637184	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138257768	chr5:58637251-58637252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs537393494	chr5:58637262-58637263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373677713	chr5:58637455-58637456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540139254	chr5:58637467-58637468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184942170	chr5:58637497-58637498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559746251	chr5:58637503-58637504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113295547	chr5:58637513-58637514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577347583	chr5:58637518-58637519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73092947	chr5:58637523-58637524	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs553164839	chr5:58637533-58637534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34715930	chr5:58637552-58637553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372633971	chr5:58637597-58637598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542018046	chr5:58637617-58637618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562309680	chr5:58637646-58637647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533356665	chr5:58637649-58637650	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544543147	chr5:58637654-58637655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115972369	chr5:58637664-58637665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs563725570	chr5:58637699-58637700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138870558	chr5:58637701-58637702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551776021	chr5:58637719-58637720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565601383	chr5:58637749-58637750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528196663	chr5:58637776-58637777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188190580	chr5:58637790-58637791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373240379	chr5:58637814-58637815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs244574	chr5:58637853-58637854	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs140473242	chr5:58637933-58637934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145627619	chr5:58637946-58637947	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570783749	chr5:58638019-58638020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76248500	chr5:58638024-58638025	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371036986	chr5:58638081-58638082	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs553341609	chr5:58638097-58638098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375574885	chr5:58638139-58638140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs141842048	chr5:58638141-58638142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542355579	chr5:58638168-58638169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555670746	chr5:58638188-58638189	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575466292	chr5:58638189-58638190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544479642	chr5:58638200-58638201	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7736808	chr5:58638212-58638213	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs577930484	chr5:58638243-58638244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376914140	chr5:58638246-58638247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559349783	chr5:58638260-58638261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs144650131	chr5:58638273-58638274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs548302399	chr5:58638335-58638336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181730811	chr5:58638359-58638360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs244575	chr5:58638410-58638411	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs10471469	chr5:58638411-58638412	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs115639274	chr5:58638442-58638443	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539748307	chr5:58638539-58638540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546673522	chr5:58638551-58638552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	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
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	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
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	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
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:58625000-58644600	Weak transcription	Left Ventricle	heart
2	chr5:58627400-58641600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr5:58634400-58647800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:58635200-58640200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr5:58635200-58652600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr5:58635600-58637400	Weak transcription	Fetal Brain Male	brain
7	chr5:58636000-58637400	Weak transcription	Fetal Heart	heart
8	chr5:58636800-58637200	Enhancers	Psoas Muscle	Psoas
9	chr5:58636800-58637200	Strong transcription	A549	lung
10	chr5:58637200-58638600	Weak transcription	A549	lung
11	chr5:58637200-58646000	Weak transcription	Psoas Muscle	Psoas
12	chr5:58637400-58638400	Enhancers	Fetal Heart	heart
13	chr5:58637400-58639200	Enhancers	Fetal Brain Male	brain
14	chr5:58637600-58638600	Enhancers	Primary T cells from cord blood	blood
15	chr5:58637600-58638600	Enhancers	Fetal Thymus	thymus
16	chr5:58638200-58638600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr5:58638400-58640400	Weak transcription	Fetal Heart	heart
18	chr5:58638600-58639000	Enhancers	A549	lung
19	chr5:58639000-58639200	Flanking Active TSS	A549	lung
20	chr5:58639200-58639800	Genic enhancers	A549	lung
21	chr5:58639200-58640200	Weak transcription	Fetal Brain Male	brain
22	chr5:58639800-58640800	Enhancers	A549	lung
23	chr5:58640000-58640200	Enhancers	Right Ventricle	heart
24	chr5:58640000-58641800	Enhancers	Fetal Brain Female	brain
25	chr5:58640200-58640400	Enhancers	Fetal Brain Male	brain
26	chr5:58640200-58640600	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr5:58640200-58646000	Weak transcription	Right Ventricle	heart
28	chr5:58640400-58640800	Weak transcription	Fetal Brain Male	brain
29	chr5:58640400-58642800	Enhancers	Fetal Heart	heart
30	chr5:58640600-58641600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr5:58640800-58641000	Enhancers	Fetal Brain Male	brain
32	chr5:58640800-58641200	Weak transcription	A549	lung
33	chr5:58641000-58642200	Weak transcription	Fetal Brain Male	brain
34	chr5:58641200-58648000	Enhancers	A549	lung
35	chr5:58641400-58642200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr5:58641400-58642600	Enhancers	Brain Cingulate Gyrus	brain
37	chr5:58641400-58642800	Enhancers	Hela-S3	cervix
38	chr5:58641400-58643200	Enhancers	Colon Smooth Muscle	Colon
39	chr5:58641600-58641800	Enhancers	Brain Angular Gyrus	brain
40	chr5:58641600-58642000	Enhancers	Brain Substantia Nigra	brain
41	chr5:58641600-58643200	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr5:58641600-58643800	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr5:58641800-58642200	Weak transcription	Brain Angular Gyrus	brain
44	chr5:58641800-58643200	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr5:58641800-58646600	Weak transcription	Fetal Brain Female	brain
46	chr5:58642000-58642200	Weak transcription	Brain Substantia Nigra	brain
47	chr5:58642200-58642400	Active TSS	Brain Hippocampus Middle	brain
48	chr5:58642200-58642600	Active TSS	Brain Angular Gyrus	brain
49	chr5:58642200-58642600	Enhancers	Fetal Brain Male	brain
50	chr5:58642200-58643200	Enhancers	Brain Substantia Nigra	brain

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