Variant report

Variant	nsv1018431
Chromosome Location	chr5:59191099-59265363
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:62)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:59233475-59233811	GM12878	blood:	n/a	n/a
2	BATF	chr5:59233497-59233778	GM12878	blood:	n/a	n/a
3	BATF	chr5:59254698-59255037	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:59200990-59201371	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:59219392-59219534	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:59206397-59206520	Hela-S3	cervix:	n/a	chr5:59206458-59206469 chr5:59206458-59206467
7	CEBPB	chr5:59248870-59248976	A549	lung:	n/a	n/a
8	CHD2	chr5:59217858-59217860	GM12878	blood:	n/a	n/a
9	CHD2	chr5:59232866-59232942	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr5:59217708-59217917	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr5:59218334-59218341	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr5:59219400-59219550	AG04449	skin:	n/a	n/a
13	CTCF	chr5:59219460-59219610	HVMF	connective:	n/a	n/a
14	CTCF	chr5:59219500-59219650	MCF-7	breast:	n/a	n/a
15	CTCF	chr5:59219244-59219693	MCF-7	breast:	n/a	n/a
16	CTCF	chr5:59219406-59219571	LNCaP	prostate:	n/a	n/a
17	CTCF	chr5:59219438-59219533	Spleen_OC	spleen:	n/a	n/a
18	CTCF	chr5:59219540-59219690	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr5:59219400-59219550	AG09319	gingival:	n/a	n/a
20	CTCF	chr5:59219460-59219610	RPTEC	kidney:	n/a	n/a
21	CTCF	chr5:59219500-59219650	HFF-Myc	foreskin:	n/a	n/a
22	CTCF	chr5:59219433-59219536	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr5:59219299-59219691	IMR90	lung:	n/a	n/a
24	CTCF	chr5:59219400-59219550	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr5:59219400-59219550	AG09309	skin:	n/a	n/a
26	CTCF	chr5:59219380-59219530	HEK293	kidney:	n/a	n/a
27	CTCF	chr5:59219640-59219790	AG10803	skin:	n/a	n/a
28	CTCF	chr5:59219422-59219570	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr5:59219420-59219570	Caco-2	colon:	n/a	n/a
30	CTCF	chr5:59219520-59219670	NHLF	lung:	n/a	n/a
31	CTCF	chr5:59219180-59219330	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr5:59219374-59219622	Gliobla	brain:	n/a	n/a
33	CTCF	chr5:59207999-59208013	IMR90	lung:	n/a	n/a
34	CTCF	chr5:59219136-59219768	SK-N-SH	brain:	n/a	n/a
35	CTCF	chr5:59219460-59219610	HPF	lung:	n/a	n/a
36	CTCF	chr5:59219384-59219592	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr5:59219400-59219550	HPF	lung:	n/a	n/a
38	CTCF	chr5:59219400-59219550	Caco-2	colon:	n/a	n/a
39	CTCF	chr5:59219380-59219530	HUVEC	blood vessel:	n/a	n/a
40	CTCF	chr5:59219400-59219550	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr5:59219440-59219590	HMEC	breast:	n/a	n/a
42	CTCF	chr5:59219400-59219550	HCPEpiC	choroid plexus:	n/a	n/a
43	CTCF	chr5:59219277-59219670	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr5:59219380-59219530	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr5:59219440-59219590	AG09319	gingival:	n/a	n/a
46	CTCF	chr5:59219440-59219590	HVMF	connective:	n/a	n/a
47	CTCF	chr5:59219464-59219554	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr5:59219420-59219570	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr5:59219387-59219582	Fibrobl	skin:	n/a	n/a
50	CTCF	chr5:59219260-59219410	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59193490-59193540	SK-N-SH	brain:	n/a
2	chr5:59193490-59193540	SK-N-SH	brain:	n/a
3	chr5:59193490-59193540	Jurkat	blood:	n/a
4	chr5:59193490-59193540	HIPEpiC	eye:	n/a
5	chr5:59193490-59193540	SKMC	muscle:	n/a
6	chr5:59193490-59193540	NT2-D1	testis:	n/a
7	chr5:59193490-59193540	GM12878	blood:	n/a
8	chr5:59193490-59193540	SK-N-MC	brain:	n/a
9	chr5:59193490-59193540	HRCEpiC	kidney:	n/a
10	chr5:59193490-59193540	HCPEpiC	choroid plexus:	n/a
11	chr5:59193490-59193540	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:59193490-59193540	PFSK-1	brain:	n/a
13	chr5:59193490-59193540	NHDF-neo	bronchial:	n/a
14	chr5:59193490-59193540	ovcar-3	ovarian:	n/a
15	chr5:59193490-59193540	HepG2	liver:	n/a
16	chr5:59193490-59193540	H1-hESC	embryonic stem cell:	embryo
17	chr5:59193490-59193540	HEK293	kidney:	embryo
18	chr5:59193490-59193540	HCT-116	colon:	n/a
19	chr5:59193490-59193540	MCF-7	breast:	n/a
20	chr5:59193490-59193540	Caco-2	colon:	n/a
21	chr5:59193490-59193540	SAEC	small airway:	n/a
22	chr5:59193490-59193540	ECC-1	luminal epithelium:	n/a
23	chr5:59193490-59193540	LNCaP	prostate:	n/a
24	chr5:59193490-59193540	PrEC	prostate:	n/a
25	chr5:59193490-59193540	GM06990	blood:	n/a
26	chr5:59193490-59193540	AG09319	gingival:	n/a
27	chr5:59193490-59193540	Hepatocyte	liver:	n/a
28	chr5:59193490-59193540	HRE	kidney:	n/a
29	chr5:59193490-59193540	AG09309	skin:	n/a
30	chr5:59193490-59193540	MCF10A-Er-Src	breast:	n/a
31	chr5:59193490-59193540	HUVEC	blood vessel:	n/a
32	chr5:59193490-59193540	HNPCEpiC	eye:	n/a
33	chr5:59193490-59193540	PANC-1	pancreas:	n/a
34	chr5:59193490-59193540	AG04450	lung:	fetal
35	chr5:59193490-59193540	GM12892	blood:	n/a
36	chr5:59193490-59193540	BJ	skin:	n/a
37	chr5:59193490-59193540	NB4	blood:	n/a
38	chr5:59193490-59193540	HCF	heart:	n/a
39	chr5:59193490-59193540	HMEC	breast:	n/a
40	chr5:59193490-59193540	SK-N-SH_RA	brain:	n/a
41	chr5:59193490-59193540	HEEpiC	esophagus:	n/a
42	chr5:59193490-59193540	AG10803	skin:	n/a
43	chr5:59193490-59193540	HL-60	blood:	n/a
44	chr5:59193490-59193540	IMR90	lung:	fetal
45	chr5:59193490-59193540	A549	lung:	n/a
46	chr5:59193490-59193540	HAEpiC	amniotic membrane:	n/a
47	chr5:59193490-59193540	HCM	heart:	n/a
48	chr5:59193490-59193540	RPTEC	kidney:	n/a
49	chr5:59193490-59193540	NHBE	bronchial:	n/a
50	chr5:59193490-59193540	BE2_C	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:59200694..59202492-chr5:59202727..59205702,2	K562	blood:
2	chr5:59235055..59237552-chr5:59238015..59240745,2	MCF-7	breast:
3	chr5:59196889..59199265-chr5:59202553..59204106,2	K562	blood:
4	chr5:59235055..59237552-chr5:59238015..59240745,2	MCF-7	breast:
5	chr5:59204919..59207898-chr5:59228269..59230906,2	K562	blood:
6	chr5:59204919..59207898-chr5:59228269..59230906,2	K562	blood:
7	chr5:59200694..59202492-chr5:59202727..59205702,2	K562	blood:
8	chr5:59109451..59110017-chr5:59219079..59219734,2	MCF-7	breast:
9	chr5:59196889..59199265-chr5:59202553..59204106,2	K562	blood:

No data

Variant related genes	Relation type
PDE4D	TF binding region
PDE4D	CpG island

Extended variants
information (count: 2450 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2450 , 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	rs16890345	chr5:59191099-59191100	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537287941	chr5:59191100-59191101	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs557528243	chr5:59191101-59191102	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs574762206	chr5:59191129-59191130	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs182461270	chr5:59191191-59191192	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs187188875	chr5:59191199-59191200	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs114712430	chr5:59191201-59191202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572094716	chr5:59191245-59191246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142980284	chr5:59191275-59191276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374766574	chr5:59191409-59191410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35593116	chr5:59191433-59191434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370219076	chr5:59191454-59191455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529790672	chr5:59191498-59191499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543278285	chr5:59191517-59191518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76500476	chr5:59191522-59191523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532174121	chr5:59191540-59191541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552466938	chr5:59191553-59191554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192697078	chr5:59191561-59191562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs565590665	chr5:59191572-59191573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs159616	chr5:59191612-59191613	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs548170017	chr5:59191650-59191651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs13175909	chr5:59191751-59191752	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs557187375	chr5:59191803-59191804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557307165	chr5:59191867-59191868	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs73761038	chr5:59191947-59191948	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs184144166	chr5:59191949-59191950	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs539620083	chr5:59192005-59192006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs147450519	chr5:59192010-59192011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs573538397	chr5:59192107-59192108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187881518	chr5:59192110-59192111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7700565	chr5:59192127-59192128	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs554581386	chr5:59192132-59192133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139262686	chr5:59192148-59192149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545035431	chr5:59192152-59192153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs149732635	chr5:59192289-59192290	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs563208011	chr5:59192325-59192326	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs532337296	chr5:59192336-59192337	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs144648845	chr5:59192417-59192418	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs559265195	chr5:59192482-59192483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs368735407	chr5:59192514-59192515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193046668	chr5:59192540-59192541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs528367426	chr5:59192541-59192542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548206718	chr5:59192547-59192548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543187064	chr5:59192629-59192630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568427127	chr5:59192657-59192658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17313920	chr5:59192661-59192662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs13177266	chr5:59192701-59192702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557523052	chr5:59192712-59192713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561122706	chr5:59192778-59192779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185048442	chr5:59192825-59192826	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59190600-59191200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr5:59191200-59193000	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr5:59191400-59191600	Enhancers	Fetal Brain Male	brain
4	chr5:59193000-59193200	Enhancers	Brain Germinal Matrix	brain
5	chr5:59193000-59200800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:59194200-59194400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:59197000-59197200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:59200800-59201200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr5:59201200-59202000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:59201200-59202200	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr5:59202200-59202400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr5:59206400-59278800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr5:59209000-59210600	Weak transcription	Aorta	Aorta
14	chr5:59210600-59210800	Enhancers	Aorta	Aorta
15	chr5:59215000-59215600	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr5:59215000-59215600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr5:59215000-59215800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr5:59215200-59215600	Enhancers	Primary hematopoietic stem cells	blood
19	chr5:59215600-59218200	Weak transcription	Primary hematopoietic stem cells	blood
20	chr5:59216400-59216800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:59216800-59217200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr5:59217000-59218600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr5:59217200-59218600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr5:59217400-59218200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr5:59217400-59218800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:59217400-59218800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr5:59217600-59218200	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr5:59217600-59218600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr5:59217800-59218400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr5:59217800-59218400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:59217800-59218400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:59217800-59218600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr5:59217800-59218600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr5:59217800-59219000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:59218000-59218400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr5:59218200-59218600	Enhancers	Primary hematopoietic stem cells	blood
37	chr5:59218200-59218600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:59218200-59218800	Enhancers	Adipose Nuclei	Adipose
39	chr5:59218400-59219200	Enhancers	Hela-S3	cervix
40	chr5:59218600-59219400	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr5:59219400-59221000	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr5:59223200-59223800	Enhancers	Fetal Brain Male	brain
43	chr5:59223200-59224000	Enhancers	Brain Germinal Matrix	brain
44	chr5:59223600-59224000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr5:59232200-59232800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr5:59232600-59232800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr5:59232600-59233400	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:59237600-59238800	Enhancers	Adipose Nuclei	Adipose
49	chr5:59238400-59242800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr5:59238800-59239600	Weak transcription	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links