Variant report

Variant	nsv1023842
Chromosome Location	chr5:104225365-104268400
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:128)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:128 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104255114-104255149	HepG2	liver:	n/a	n/a
2	BRCA1	chr5:104246667-104246983	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr5:104246629-104247018	Hela-S3	cervix:	n/a	n/a
4	CHD2	chr5:104246611-104246974	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr5:104230760-104230910	Caco-2	colon:	n/a	n/a
6	CTCF	chr5:104268258-104268288	MCF-7	breast:	n/a	n/a
7	CTCF	chr5:104268246-104268249	MCF-7	breast:	n/a	n/a
8	CTCF	chr5:104268295-104268333	MCF-7	breast:	n/a	n/a
9	CTCF	chr5:104268319-104268324	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr5:104268240-104268390	Caco-2	colon:	n/a	n/a
11	CTCF	chr5:104268240-104268390	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:104268274-104268340	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:104234611-104234636	Lung_OC	lung:	n/a	n/a
14	CTCF	chr5:104249600-104249750	BE2_C	brain:	n/a	n/a
15	CTCF	chr5:104249560-104249710	BE2_C	brain:	n/a	n/a
16	CTCF	chr5:104268257-104268260	Gliobla	brain:	n/a	n/a
17	CTCF	chr5:104268250-104268254	MCF-7	breast:	n/a	n/a
18	CTCF	chr5:104268210-104268328	LNCaP	prostate:	n/a	n/a
19	CTCF	chr5:104268261-104268324	Gliobla	brain:	n/a	n/a
20	CTCF	chr5:104268256-104268367	MCF-7	breast:	n/a	n/a
21	E2F4	chr5:104253014-104253201	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr5:104246543-104247084	MCF-7	breast:	n/a	n/a
23	EP300	chr5:104226355-104226980	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr5:104245533-104245803	SK-N-SH_RA	brain:	n/a	chr5:104245546-104245555
25	EP300	chr5:104249508-104249809	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr5:104226436-104226922	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr5:104249508-104249993	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr5:104249074-104250805	SK-N-SH	brain:	n/a	chr5:104250292-104250306 chr5:104250761-104250769 chr5:104249376-104249390 chr5:104250723-104250731
29	EP300	chr5:104246519-104247127	MCF-7	breast:	n/a	n/a
30	EP300	chr5:104242180-104242326	K562	blood:	n/a	n/a
31	EP300	chr5:104226150-104227492	SK-N-SH	brain:	n/a	n/a
32	EP300	chr5:104245506-104245885	SK-N-SH_RA	brain:	n/a	chr5:104245546-104245555
33	FOS	chr5:104246554-104246964	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr5:104246550-104246973	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr5:104246641-104246949	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr5:104246661-104246934	MCF10A-Er-Src	breast:	n/a	n/a
37	FOSL2	chr5:104246547-104246999	MCF-7	breast:	n/a	n/a
38	FOXA1	chr5:104246614-104246888	T-47D	breast:	n/a	n/a
39	FOXA2	chr5:104246524-104247092	A549	lung:	n/a	n/a
40	FOXA2	chr5:104240164-104240520	A549	lung:	n/a	n/a
41	FOXA2	chr5:104246546-104246969	A549	lung:	n/a	n/a
42	FOXP2	chr5:104246693-104246885	PFSK-1	brain:	n/a	n/a
43	FOXP2	chr5:104246597-104247029	SK-N-MC	brain:	n/a	n/a
44	GATA2	chr5:104249430-104250872	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr5:104249372-104250066	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr5:104240355-104240546	MCF-7	breast:	n/a	n/a
47	GATA3	chr5:104246471-104247244	MCF-7	breast:	n/a	n/a
48	GATA3	chr5:104240225-104240611	MCF-7	breast:	n/a	n/a
49	GATA3	chr5:104248237-104248859	SH-SY5Y	brain:	n/a	n/a
50	GATA3	chr5:104250257-104250677	SH-SY5Y	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104265747-104265797	HPAEpiC	pulmonary alveolar:	n/a
2	chr5:104265747-104265797	SK-N-SH_RA	brain:	n/a
3	chr5:104265747-104265797	BE2_C	brain:	n/a
4	chr5:104265747-104265797	ECC-1	luminal epithelium:	n/a
5	chr5:104265747-104265797	SAEC	small airway:	n/a
6	chr5:104265747-104265797	Hepatocyte	liver:	n/a
7	chr5:104265747-104265797	H1-hESC	embryonic stem cell:	embryo
8	chr5:104265747-104265797	Caco-2	colon:	n/a
9	chr5:104265747-104265797	HRE	kidney:	n/a
10	chr5:104265747-104265797	MCF-7	breast:	n/a
11	chr5:104265747-104265797	BJ	skin:	n/a
12	chr5:104265747-104265797	RPTEC	kidney:	n/a
13	chr5:104265747-104265797	Jurkat	blood:	n/a
14	chr5:104265747-104265797	AoSMC	blood vessel:	n/a
15	chr5:104265747-104265797	HL-60	blood:	n/a
16	chr5:104265747-104265797	GM12892	blood:	n/a
17	chr5:104265747-104265797	AG09309	skin:	n/a
18	chr5:104265747-104265797	NB4	blood:	n/a
19	chr5:104265747-104265797	PFSK-1	brain:	n/a
20	chr5:104265747-104265797	HCM	heart:	n/a
21	chr5:104265747-104265797	HUVEC	blood vessel:	n/a
22	chr5:104265747-104265797	Hela-S3	cervix:	n/a
23	chr5:104265747-104265797	AG04450	lung:	fetal
24	chr5:104265747-104265797	HEEpiC	esophagus:	n/a
25	chr5:104265747-104265797	MCF10A-Er-Src	breast:	n/a
26	chr5:104265747-104265797	GM19239	blood:	n/a
27	chr5:104265747-104265797	SK-N-SH	brain:	n/a
28	chr5:104265747-104265797	ovcar-3	ovarian:	n/a
29	chr5:104265747-104265797	HEK293	kidney:	embryo
30	chr5:104265747-104265797	SKMC	muscle:	n/a
31	chr5:104265747-104265797	HCF	heart:	n/a
32	chr5:104265747-104265797	AG10803	skin:	n/a
33	chr5:104265747-104265797	A549	lung:	n/a
34	chr5:104265747-104265797	IMR90	lung:	fetal
35	chr5:104265747-104265797	CMK	blood:	n/a
36	chr5:104265747-104265797	HCPEpiC	choroid plexus:	n/a
37	chr5:104265747-104265797	NHBE	bronchial:	n/a
38	chr5:104265747-104265797	GM06990	blood:	n/a
39	chr5:104265747-104265797	GM12891	blood:	n/a
40	chr5:104265747-104265797	PrEC	prostate:	n/a
41	chr5:104265747-104265797	T-47D	breast:	n/a
42	chr5:104265747-104265797	HepG2	liver:	n/a
43	chr5:104265747-104265797	LNCaP	prostate:	n/a
44	chr5:104265747-104265797	ProgFib	skin:	n/a
45	chr5:104265747-104265797	U87	brain:	n/a
46	chr5:104265747-104265797	GM12878	blood:	n/a
47	chr5:104265747-104265797	AG04449	skin:	fetal
48	chr5:104265747-104265797	HIPEpiC	eye:	n/a
49	chr5:104265747-104265797	NHDF-neo	bronchial:	n/a
50	chr5:104265747-104265797	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
2	chr5:104227529..104229773-chr5:104240979..104242491,2	MCF-7	breast:
3	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
4	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
5	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:
6	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
7	chr5:104223049..104225474-chr5:104235768..104238593,2	MCF-7	breast:
8	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
9	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
10	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
11	chr17:57939158..57941470-chr5:104246724..104248724,2	MCF-7	breast:
12	chr5:104226367..104227906-chr5:104228376..104230821,2	MCF-7	breast:
13	chr5:104256936..104259316-chr5:104275958..104278631,2	K562	blood:
14	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
15	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
16	chr5:104234931..104236476-chr5:104238248..104241105,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104253193-104253599	ENSG00000253584
2	lnc-NUDT12-6	chr5:104246363-104246434	ENSG00000251574

No data

Variant related genes	Relation type
ENSG00000251574	TF binding region
ENSG00000251574	CpG island

Extended variants
information (count: 905 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:905 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56185843	chr5:104234409-104234410	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs527875922	chr5:104234441-104234442	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548140855	chr5:104234446-104234447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs367935872	chr5:104234485-104234486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187199898	chr5:104234499-104234500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539839339	chr5:104234542-104234543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542047428	chr5:104234550-104234551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs193017263	chr5:104234559-104234560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79466400	chr5:104234595-104234596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370556292	chr5:104234611-104234612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570139926	chr5:104234630-104234631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs319906	chr5:104234635-104234636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs555433743	chr5:104234648-104234649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566827730	chr5:104234649-104234650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574327942	chr5:104234665-104234666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531345507	chr5:104234668-104234669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549856700	chr5:104234727-104234728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115540395	chr5:104234759-104234760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535793150	chr5:104234783-104234784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577029595	chr5:104234785-104234786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371815587	chr5:104234839-104234840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564780787	chr5:104234872-104234873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs562296835	chr5:104234886-104234887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575985314	chr5:104234891-104234892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10063729	chr5:104234912-104234913	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs185153478	chr5:104234928-104234929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527912729	chr5:104234984-104234985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs190389770	chr5:104234991-104234992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569871845	chr5:104235001-104235002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs319907	chr5:104235042-104235043	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs533414183	chr5:104235045-104235046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550447808	chr5:104235057-104235058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs115645753	chr5:104235071-104235072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535443421	chr5:104235117-104235118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566010348	chr5:104235144-104235145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565807506	chr5:104235176-104235177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs200991068	chr5:104235800-104235801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188033383	chr5:104235807-104235808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs180912435	chr5:104235815-104235816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565846906	chr5:104235818-104235819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564139866	chr5:104235845-104235846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569622875	chr5:104235846-104235847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528518016	chr5:104235847-104235848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs62369094	chr5:104235857-104235858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs551848204	chr5:104235941-104235942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185315033	chr5:104236011-104236012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539602545	chr5:104236033-104236034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs1230734	chr5:104236045-104236046	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs79801231	chr5:104236077-104236078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535454569	chr5:104236079-104236080	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
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	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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	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
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104234400-104235200	Enhancers	Placenta Amnion	Placenta Amnion
2	chr5:104235800-104236400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:104235800-104236600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr5:104236000-104236400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr5:104236000-104236600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr5:104236000-104237800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:104236200-104236800	Enhancers	Brain Anterior Caudate	brain
8	chr5:104236200-104237000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:104237800-104245400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:104239600-104240600	Enhancers	A549	lung
11	chr5:104240200-104240800	Enhancers	HepG2	liver
12	chr5:104243000-104243200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr5:104243200-104245400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr5:104245400-104246800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:104245400-104247200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr5:104245600-104246400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:104245600-104246600	Enhancers	Hela-S3	cervix
18	chr5:104245600-104247800	Active TSS	A549	lung
19	chr5:104245800-104246200	Enhancers	NHEK	skin
20	chr5:104245800-104247600	Enhancers	HMEC	breast
21	chr5:104246000-104246600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr5:104246000-104247000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:104246200-104246600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr5:104246200-104247000	Flanking Active TSS	NHEK	skin
25	chr5:104246400-104246600	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr5:104246400-104246600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:104246400-104247600	Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr5:104246600-104246800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr5:104246600-104246800	Flanking Active TSS	Hela-S3	cervix
30	chr5:104246600-104247000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:104246600-104247000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:104246800-104247000	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr5:104246800-104247000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:104246800-104247200	Active TSS	Hela-S3	cervix
35	chr5:104247000-104247200	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr5:104247000-104247200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr5:104247000-104247200	Enhancers	NHEK	skin
38	chr5:104247000-104247400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr5:104247200-104247800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr5:104247400-104247600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:104247800-104250400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr5:104249400-104251600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr5:104249600-104250000	Enhancers	Fetal Brain Male	brain
44	chr5:104249600-104251000	Enhancers	Brain Germinal Matrix	brain
45	chr5:104250400-104251000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr5:104250800-104251400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:104255800-104256200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr5:104260000-104260800	Enhancers	Fetal Intestine Large	intestine
49	chr5:104264600-104265200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:104265200-104268200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links