Variant report

Variant	nsv882559
Chromosome Location	chr5:104242877-104390848
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:123)
Chromatin interactive
region (count:29)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:370 , 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	chr5:104255114-104255149	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:104369169-104369636	K562	blood:	n/a	n/a
3	ATF1	chr5:104373680-104373755	K562	blood:	n/a	n/a
4	ATF1	chr5:104370024-104370214	K562	blood:	n/a	n/a
5	BHLHE40	chr5:104369418-104369675	K562	blood:	n/a	n/a
6	BRCA1	chr5:104325896-104325918	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr5:104246667-104246983	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr5:104317800-104317805	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
10	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
11	CCNT2	chr5:104306891-104307038	K562	blood:	n/a	n/a
12	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
13	CEBPB	chr5:104370063-104370467	A549	lung:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
14	CEBPB	chr5:104278321-104278989	MCF-7	breast:	n/a	n/a
15	CEBPB	chr5:104297579-104297662	HepG2	liver:	n/a	chr5:104297618-104297629 chr5:104297617-104297630
16	CEBPB	chr5:104321962-104322422	MCF-7	breast:	n/a	n/a
17	CEBPB	chr5:104334377-104334640	K562	blood:	n/a	chr5:104334524-104334537
18	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a
19	CEBPB	chr5:104246629-104247018	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:104369982-104370331	K562	blood:	n/a	n/a
21	CEBPB	chr5:104288117-104288374	HepG2	liver:	n/a	chr5:104288258-104288271 chr5:104288258-104288269
22	CEBPB	chr5:104369987-104370554	Hela-S3	cervix:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
23	CEBPB	chr5:104278464-104278803	MCF-7	breast:	n/a	n/a
24	CEBPB	chr5:104370108-104370517	ECC-1	luminal epithelium:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
25	CEBPB	chr5:104278381-104278967	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:104273290-104273692	Hela-S3	cervix:	n/a	chr5:104273426-104273439 chr5:104273423-104273440
27	CEBPB	chr5:104369173-104369683	K562	blood:	n/a	chr5:104369288-104369301
28	CEBPB	chr5:104369993-104370525	K562	blood:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
29	CEBPB	chr5:104370011-104370528	HepG2	liver:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
30	CEBPB	chr5:104370069-104370367	H1-hESC	embryonic stem cell:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
31	CEBPD	chr5:104369352-104369808	K562	blood:	n/a	n/a
32	CEBPD	chr5:104322765-104323144	K562	blood:	n/a	n/a
33	CHD2	chr5:104323100-104323131	K562	blood:	n/a	n/a
34	CHD2	chr5:104246611-104246974	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr5:104278471-104278830	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr5:104322260-104322410	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:104268319-104268324	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr5:104300088-104300155	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:104311457-104311553	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:104268274-104268340	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:104268261-104268324	Gliobla	brain:	n/a	n/a
42	CTCF	chr5:104268240-104268390	Caco-2	colon:	n/a	n/a
43	CTCF	chr5:104311439-104311504	GM12892	blood:	n/a	n/a
44	CTCF	chr5:104300157-104300162	LNCaP	prostate:	n/a	n/a
45	CTCF	chr5:104281767-104281872	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr5:104288608-104288628	Medullo	brain:	n/a	n/a
47	CTCF	chr5:104386370-104386472	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr5:104386380-104386454	GM10248	blood:	n/a	n/a
49	CTCF	chr5:104322470-104322512	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr5:104268256-104268367	MCF-7	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104265747-104265797	NHBE	bronchial:	n/a
2	chr5:104265747-104265797	NHBE	bronchial:	n/a
3	chr5:104265747-104265797	HL-60	blood:	n/a
4	chr5:104345171-104345221	H1-hESC	embryonic stem cell:	embryo
5	chr5:104265747-104265797	HIPEpiC	eye:	n/a
6	chr5:104265747-104265797	SK-N-SH_RA	brain:	n/a
7	chr5:104265747-104265797	AoSMC	blood vessel:	n/a
8	chr5:104345171-104345221	HEK293	kidney:	embryo
9	chr5:104265747-104265797	A549	lung:	n/a
10	chr5:104345171-104345221	HEEpiC	esophagus:	n/a
11	chr5:104265747-104265797	AG04449	skin:	fetal
12	chr5:104265747-104265797	SK-N-SH	brain:	n/a
13	chr5:104345171-104345221	IMR90	lung:	fetal
14	chr5:104345171-104345221	NB4	blood:	n/a
15	chr5:104345171-104345221	GM19239	blood:	n/a
16	chr5:104265747-104265797	Hepatocyte	liver:	n/a
17	chr5:104345171-104345221	ECC-1	luminal epithelium:	n/a
18	chr5:104265747-104265797	AG09309	skin:	n/a
19	chr5:104345171-104345221	CMK	blood:	n/a
20	chr5:104345171-104345221	U87	brain:	n/a
21	chr5:104345171-104345221	NH-A	brain:	n/a
22	chr5:104265747-104265797	HRE	kidney:	n/a
23	chr5:104265747-104265797	HNPCEpiC	eye:	n/a
24	chr5:104345171-104345221	HUVEC	blood vessel:	n/a
25	chr5:104265747-104265797	LNCaP	prostate:	n/a
26	chr5:104345171-104345221	AG09319	gingival:	n/a
27	chr5:104345171-104345221	AG10803	skin:	n/a
28	chr5:104265747-104265797	SAEC	small airway:	n/a
29	chr5:104265747-104265797	HUVEC	blood vessel:	n/a
30	chr5:104265747-104265797	GM12891	blood:	n/a
31	chr5:104345171-104345221	HMEC	breast:	n/a
32	chr5:104345171-104345221	HCT-116	colon:	n/a
33	chr5:104265747-104265797	HRCEpiC	kidney:	n/a
34	chr5:104265747-104265797	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:104345171-104345221	AG09309	skin:	n/a
36	chr5:104265747-104265797	AG10803	skin:	n/a
37	chr5:104265747-104265797	SK-N-MC	brain:	n/a
38	chr5:104265747-104265797	ProgFib	skin:	n/a
39	chr5:104265747-104265797	Hela-S3	cervix:	n/a
40	chr5:104345171-104345221	NT2-D1	testis:	n/a
41	chr5:104265747-104265797	PrEC	prostate:	n/a
42	chr5:104345171-104345221	HRPEpiC	eye:	n/a
43	chr5:104345171-104345221	GM12892	blood:	n/a
44	chr5:104345171-104345221	Hepatocyte	liver:	n/a
45	chr5:104345171-104345221	K562	blood:	n/a
46	chr5:104265747-104265797	IMR90	lung:	fetal
47	chr5:104345171-104345221	SK-N-SH_RA	brain:	n/a
48	chr5:104345171-104345221	HAEpiC	amniotic membrane:	n/a
49	chr5:104265747-104265797	AG09319	gingival:	n/a
50	chr5:104265747-104265797	HRPEpiC	eye:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
2	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
3	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
4	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
5	chr5:104271936..104274851-chr5:104276428..104278480,3	MCF-7	breast:
6	chr5:104308244..104309781-chr5:104310392..104313289,2	K562	blood:
7	chr5:104256936..104259316-chr5:104275958..104278631,2	K562	blood:
8	chr17:57921408..57924296-chr5:104291652..104294224,2	MCF-7	breast:
9	chr5:104270441..104272983-chr5:104273696..104275223,2	K562	blood:
10	chr5:104296966..104298915-chr5:104301513..104303519,2	K562	blood:
11	chr5:104248370..104250240-chr5:104261197..104262793,2	MCF-7	breast:
12	chr5:104302225..104304920-chr5:104306783..104309637,2	MCF-7	breast:
13	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:
14	chr5:104271936..104274851-chr5:104276428..104278480,3	MCF-7	breast:
15	chr5:104256936..104259316-chr5:104275958..104278631,2	K562	blood:
16	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
17	chr5:104270441..104272983-chr5:104273696..104275223,2	K562	blood:
18	chr5:104277822..104279427-chr5:104300449..104302157,2	MCF-7	breast:
19	chr5:104277822..104279427-chr5:104300449..104302157,2	MCF-7	breast:
20	chr5:104369671..104371200-chr5:104727235..104729208,2	K562	blood:
21	chr5:104294786..104295742-chr9:99125283..99126098,2	MCF-7	breast:
22	chr5:104239889..104241844-chr5:104241951..104244541,2	MCF-7	breast:
23	chr5:104296966..104298915-chr5:104301513..104303519,2	K562	blood:
24	chr17:57939158..57941470-chr5:104246724..104248724,2	MCF-7	breast:
25	chr5:104302225..104304920-chr5:104306783..104309637,2	MCF-7	breast:
26	chr5:104245189..104247786-chr5:104277262..104279951,2	MCF-7	breast:
27	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
28	chr5:104308244..104309781-chr5:104310392..104313289,2	K562	blood:
29	chr5:104246978..104249905-chr5:104251799..104254646,2	MCF-7	breast:

(count:7 , 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
3	lnc-NUDT12-7	chr5:104308988-104309359	ENSG00000253584
4	lnc-NUDT12-7	chr5:104315392-104315477	ENSG00000253584
5	lnc-NUDT12-7	chr5:104311375-104311586	ENSG00000253584
6	lnc-NUDT12-7	chr5:104344562-104344612	ENSG00000253584
7	lnc-NUDT12-7	chr5:104344562-104344618	ENSG00000253584

No data

Variant related genes	Relation type
ENSG00000253584	TF binding region
ENSG00000251574	TF binding region
ENSG00000253584	CpG island
ENSG00000251574	CpG island
ENSG00000251574	chromatin interactions

Extended variants
information (count: 1736 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1736 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs410181	chr5:104242877-104242878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs529346079	chr5:104242919-104242920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs371352348	chr5:104242928-104242929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565354901	chr5:104242930-104242931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533181588	chr5:104242995-104242996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs549963729	chr5:104243006-104243007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs189851761	chr5:104243023-104243024	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529237174	chr5:104243034-104243035	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1152318	chr5:104243053-104243054	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs577945964	chr5:104243062-104243063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528055360	chr5:104243216-104243217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551476916	chr5:104243217-104243218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs570974126	chr5:104243231-104243232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537255389	chr5:104243254-104243255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs562946487	chr5:104243255-104243256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557085156	chr5:104243306-104243307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567516721	chr5:104243355-104243356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555977778	chr5:104243357-104243358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs536990862	chr5:104243381-104243382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553373405	chr5:104243383-104243384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181424083	chr5:104243401-104243402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs574632242	chr5:104243414-104243415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs573215696	chr5:104243444-104243445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116485174	chr5:104243461-104243462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs1152319	chr5:104243462-104243463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs575764378	chr5:104243495-104243496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556977850	chr5:104243619-104243620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544718049	chr5:104243629-104243630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575136047	chr5:104243679-104243680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529063153	chr5:104243706-104243707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542936474	chr5:104243727-104243728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563238980	chr5:104243739-104243740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545754930	chr5:104243744-104243745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548725972	chr5:104243766-104243767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528355028	chr5:104243767-104243768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559358587	chr5:104243769-104243770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528106966	chr5:104243771-104243772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550920636	chr5:104243772-104243773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571012586	chr5:104243791-104243792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35058344	chr5:104243815-104243816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530565975	chr5:104243838-104243839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550251916	chr5:104243856-104243857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141019952	chr5:104243988-104243989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs6882561	chr5:104243992-104243993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567879544	chr5:104244022-104244023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs151013988	chr5:104244057-104244058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140814449	chr5:104244111-104244112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572785351	chr5:104244181-104244182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377730177	chr5:104244210-104244211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs567016909	chr5:104244278-104244279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104237800-104245400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:104243000-104243200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr5:104243200-104245400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr5:104245400-104246800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:104245400-104247200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:104245600-104246400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:104245600-104246600	Enhancers	Hela-S3	cervix
8	chr5:104245600-104247800	Active TSS	A549	lung
9	chr5:104245800-104246200	Enhancers	NHEK	skin
10	chr5:104245800-104247600	Enhancers	HMEC	breast
11	chr5:104246000-104246600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:104246000-104247000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr5:104246200-104246600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr5:104246200-104247000	Flanking Active TSS	NHEK	skin
15	chr5:104246400-104246600	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr5:104246400-104246600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:104246400-104247600	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr5:104246600-104246800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr5:104246600-104246800	Flanking Active TSS	Hela-S3	cervix
20	chr5:104246600-104247000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr5:104246600-104247000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr5:104246800-104247000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr5:104246800-104247000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr5:104246800-104247200	Active TSS	Hela-S3	cervix
25	chr5:104247000-104247200	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr5:104247000-104247200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr5:104247000-104247200	Enhancers	NHEK	skin
28	chr5:104247000-104247400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr5:104247200-104247800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:104247400-104247600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:104247800-104250400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr5:104249400-104251600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr5:104249600-104250000	Enhancers	Fetal Brain Male	brain
34	chr5:104249600-104251000	Enhancers	Brain Germinal Matrix	brain
35	chr5:104250400-104251000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr5:104250800-104251400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:104255800-104256200	Enhancers	Breast Myoepithelial Primary Cells	Breast
38	chr5:104260000-104260800	Enhancers	Fetal Intestine Large	intestine
39	chr5:104264600-104265200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:104265200-104268200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:104268200-104268400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr5:104268200-104268400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:104268400-104268600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr5:104277200-104277400	Enhancers	Fetal Intestine Large	intestine
45	chr5:104277200-104277400	Enhancers	Fetal Intestine Small	intestine
46	chr5:104277400-104278400	Weak transcription	Fetal Intestine Large	intestine
47	chr5:104277600-104283000	Weak transcription	Fetal Intestine Small	intestine
48	chr5:104277800-104278600	Enhancers	Hela-S3	cervix
49	chr5:104278200-104278800	Enhancers	Colon Smooth Muscle	Colon
50	chr5:104278400-104279200	Enhancers	Fetal Intestine Large	intestine

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