Variant report

Variant	esv3385195
Chromosome Location	chr5:74810245-74843686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 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	ARID3A	chr5:74819121-74819443	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:74812604-74812638	K562	blood:	n/a	n/a
3	ARID3A	chr5:74814259-74814285	K562	blood:	n/a	n/a
4	ATF2	chr5:74819875-74820317	GM12878	blood:	n/a	n/a
5	ATF2	chr5:74819795-74820370	GM12878	blood:	n/a	n/a
6	BATF	chr5:74819890-74820272	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
7	BATF	chr5:74819848-74820276	GM12878	blood:	n/a	chr5:74820117-74820127 chr5:74820113-74820123
8	BATF	chr5:74822009-74822205	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:74819918-74820233	GM12878	blood:	n/a	n/a
10	BCLAF1	chr5:74819810-74820284	GM12878	blood:	n/a	n/a
11	BCLAF1	chr5:74819857-74820282	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:74809603-74810369	GM12878	blood:	n/a	n/a
13	BRCA1	chr5:74818279-74818351	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr5:74817009-74817397	HCT-116	colon:	n/a	n/a
15	CBX3	chr5:74817027-74817318	K562	blood:	n/a	n/a
16	CBX3	chr5:74816956-74817762	K562	blood:	n/a	n/a
17	CEBPB	chr5:74819823-74820008	K562	blood:	n/a	n/a
18	CEBPB	chr5:74819145-74819534	MCF-7	breast:	n/a	n/a
19	CEBPB	chr5:74818466-74818684	A549	lung:	n/a	chr5:74818555-74818566
20	CEBPB	chr5:74818438-74818707	H1-hESC	embryonic stem cell:	n/a	chr5:74818555-74818566
21	CEBPB	chr5:74818399-74818725	Hela-S3	cervix:	n/a	chr5:74818555-74818566
22	CEBPB	chr5:74834106-74834416	IMR90	lung:	n/a	chr5:74834262-74834275 chr5:74834262-74834273
23	CEBPB	chr5:74819136-74819467	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:74832035-74832295	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:74818420-74818788	A549	lung:	n/a	chr5:74818555-74818566
26	CEBPB	chr5:74818376-74818746	K562	blood:	n/a	chr5:74818555-74818566
27	CEBPB	chr5:74841366-74841566	K562	blood:	n/a	n/a
28	CEBPB	chr5:74818388-74818744	IMR90	lung:	n/a	chr5:74818555-74818566
29	CEBPB	chr5:74819947-74820171	GM12878	blood:	n/a	n/a
30	CEBPB	chr5:74834257-74834302	A549	lung:	n/a	chr5:74834262-74834275 chr5:74834262-74834273
31	CEBPB	chr5:74831987-74832299	K562	blood:	n/a	n/a
32	CEBPB	chr5:74818413-74818736	HepG2	liver:	n/a	chr5:74818555-74818566
33	CEBPB	chr5:74819770-74820410	GM12878	blood:	n/a	n/a
34	CREB1	chr5:74819891-74820498	GM12878	blood:	n/a	n/a
35	CTCF	chr5:74832935-74833014	A549	lung:	n/a	n/a
36	CTCF	chr5:74826660-74826749	Fibrobl	skin:	n/a	n/a
37	CTCF	chr5:74824900-74825050	GM12870	blood:	n/a	n/a
38	CTCF	chr5:74832939-74832983	NHEK	skin:	n/a	n/a
39	CTCF	chr5:74832982-74833014	GM12878	blood:	n/a	n/a
40	CTCF	chr5:74832916-74833027	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:74824480-74824630	GM12870	blood:	n/a	n/a
42	CTCF	chr5:74832910-74833001	MCF-7	breast:	n/a	n/a
43	CTCF	chr5:74832916-74833013	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:74832951-74832992	Fibrobl	skin:	n/a	n/a
45	CTCF	chr5:74832860-74833010	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr5:74832925-74833035	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:74832928-74833029	MCF-7	breast:	n/a	n/a
48	CUX1	chr5:74815813-74816013	GM12878	blood:	n/a	n/a
49	E2F4	chr5:74837273-74837576	MCF10A-Er-Src	breast:	n/a	chr5:74837523-74837532
50	EBF1	chr5:74812905-74812972	GM12878	blood:	n/a	chr5:74812923-74812934

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:74833385-74833435	ovcar-3	ovarian:	n/a
2	chr5:74833385-74833435	AG09319	gingival:	n/a
3	chr5:74833385-74833435	SK-N-SH	brain:	n/a
4	chr5:74811445-74811495	PFSK-1	brain:	n/a
5	chr5:74833385-74833435	AG09309	skin:	n/a
6	chr5:74833385-74833435	SK-N-MC	brain:	n/a
7	chr5:74811445-74811495	HMEC	breast:	n/a
8	chr5:74833385-74833435	GM12892	blood:	n/a
9	chr5:74833385-74833435	HMEC	breast:	n/a
10	chr5:74811445-74811495	GM12878	blood:	n/a
11	chr5:74811445-74811495	T-47D	breast:	n/a
12	chr5:74811445-74811495	HCM	heart:	n/a
13	chr5:74833385-74833435	HCM	heart:	n/a
14	chr5:74811445-74811495	K562	blood:	n/a
15	chr5:74811445-74811495	SKMC	muscle:	n/a
16	chr5:74811445-74811495	SK-N-MC	brain:	n/a
17	chr5:74833385-74833435	CMK	blood:	n/a
18	chr5:74833385-74833435	Caco-2	colon:	n/a
19	chr5:74833385-74833435	PANC-1	pancreas:	n/a
20	chr5:74811445-74811495	HCT-116	colon:	n/a
21	chr5:74811445-74811495	HIPEpiC	eye:	n/a
22	chr5:74811445-74811495	PrEC	prostate:	n/a
23	chr5:74811445-74811495	ovcar-3	ovarian:	n/a
24	chr5:74833385-74833435	HCT-116	colon:	n/a
25	chr5:74833385-74833435	GM12878	blood:	n/a
26	chr5:74811445-74811495	LNCaP	prostate:	n/a
27	chr5:74811445-74811495	HRCEpiC	kidney:	n/a
28	chr5:74811445-74811495	GM12892	blood:	n/a
29	chr5:74811445-74811495	MCF-7	breast:	n/a
30	chr5:74833385-74833435	Hela-S3	cervix:	n/a
31	chr5:74811445-74811495	SK-N-SH	brain:	n/a
32	chr5:74833385-74833435	Hepatocyte	liver:	n/a
33	chr5:74811445-74811495	AG09319	gingival:	n/a
34	chr5:74833385-74833435	HepG2	liver:	n/a
35	chr5:74833385-74833435	HRPEpiC	eye:	n/a
36	chr5:74833385-74833435	RPTEC	kidney:	n/a
37	chr5:74811445-74811495	AG09309	skin:	n/a
38	chr5:74833385-74833435	NHDF-neo	bronchial:	n/a
39	chr5:74833385-74833435	HIPEpiC	eye:	n/a
40	chr5:74811445-74811495	HCPEpiC	choroid plexus:	n/a
41	chr5:74811445-74811495	RPTEC	kidney:	n/a
42	chr5:74833385-74833435	GM12891	blood:	n/a
43	chr5:74811445-74811495	NHBE	bronchial:	n/a
44	chr5:74833385-74833435	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:74811445-74811495	MCF10A-Er-Src	breast:	n/a
46	chr5:74833385-74833435	MCF-7	breast:	n/a
47	chr5:74833385-74833435	HEEpiC	esophagus:	n/a
48	chr5:74833385-74833435	SKMC	muscle:	n/a
49	chr5:74811445-74811495	NHDF-neo	bronchial:	n/a
50	chr5:74811445-74811495	HUVEC	blood vessel:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:74815294..74818982-chr5:74820247..74823584,4	K562	blood:
2	chr5:74808217..74810593-chr5:74816041..74817596,2	K562	blood:
3	chr5:74839175..74841677-chr5:74843205..74845206,2	K562	blood:
4	chr5:74808217..74810593-chr5:74816041..74817596,2	K562	blood:
5	chr5:74805731..74808646-chr5:74817149..74819644,4	MCF-7	breast:
6	chr5:74839175..74841677-chr5:74843205..74845206,2	K562	blood:
7	chr5:74805305..74807843-chr5:74822655..74824255,2	MCF-7	breast:
8	chr5:74835008..74837584-chr5:74853567..74856265,2	K562	blood:
9	chr5:74828971..74830534-chr5:74850595..74852572,2	K562	blood:
10	chr5:74818089..74820423-chr5:74844136..74846157,2	MCF-7	breast:
11	chr5:74806414..74809041-chr5:74824381..74827349,2	K562	blood:
12	chr5:74811101..74813110-chr5:74815287..74817345,2	K562	blood:
13	chr5:74840733..74842326-chr5:74845611..74848333,2	K562	blood:
14	chr5:74815294..74818982-chr5:74820247..74823584,4	K562	blood:
15	chr5:74820287..74822535-chr5:74827846..74830107,2	K562	blood:
16	chr5:74819271..74821743-chr5:74831867..74834038,2	MCF-7	breast:
17	chr5:74808667..74810597-chr5:74818060..74820048,3	K562	blood:
18	chr5:74811981..74814673-chr5:74874113..74876597,2	K562	blood:
19	chr5:74808667..74810597-chr5:74818060..74820048,3	K562	blood:
20	chr5:74811101..74813110-chr5:74815287..74817345,2	K562	blood:
21	chr5:74820287..74822535-chr5:74827846..74830107,2	K562	blood:
22	chr5:74819271..74821743-chr5:74831867..74834038,2	MCF-7	breast:
23	chr5:74793165..74795664-chr5:74814824..74817209,2	K562	blood:

No data

Variant related genes	Relation type
POLK	TF binding region
COL4A3BP	TF binding region
RNU7-175P	TF binding region
POLK	CpG island
COL4A3BP	CpG island
RNU7-175P	CpG island
ENSG00000113163	chromatin interactions
ENSG00000122008	chromatin interactions

Extended variants
information (count: 1160 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188763467	chr5:74810247-74810248	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs140150648	chr5:74810273-74810274	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs181610268	chr5:74810345-74810346	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs550908362	chr5:74810355-74810356	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs567596713	chr5:74810383-74810384	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs10059022	chr5:74810384-74810385	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs371796928	chr5:74810404-74810405	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs556416782	chr5:74810447-74810448	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs79996311	chr5:74810448-74810449	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs565624767	chr5:74810485-74810486	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs187247453	chr5:74810505-74810506	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs111998238	chr5:74810558-74810559	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs571516709	chr5:74810560-74810561	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537222168	chr5:74810591-74810592	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs151176935	chr5:74810618-74810619	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs532797657	chr5:74810742-74810743	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs140219440	chr5:74810750-74810751	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs374300815	chr5:74810774-74810775	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs191914341	chr5:74810809-74810810	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs112269749	chr5:74810824-74810825	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182501369	chr5:74810837-74810838	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs185914382	chr5:74810910-74810911	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs189883153	chr5:74810924-74810925	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs545212736	chr5:74810925-74810926	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs565034468	chr5:74810955-74810956	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs531037169	chr5:74811069-74811070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577905120	chr5:74811085-74811086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561118997	chr5:74811121-74811122	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530330642	chr5:74811181-74811182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34132581	chr5:74811195-74811196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547231598	chr5:74811220-74811221	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs112096843	chr5:74811258-74811259	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs560011221	chr5:74811278-74811279	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs368372658	chr5:74811284-74811285	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs528088532	chr5:74811307-74811308	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs182500082	chr5:74811320-74811321	Weak transcription Enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574423855	chr5:74811445-74811446	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs568396009	chr5:74811446-74811447	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs535504156	chr5:74811448-74811449	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs9293653	chr5:74811497-74811498	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs377145881	chr5:74811501-74811502	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs549633383	chr5:74811506-74811507	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs537106123	chr5:74811631-74811632	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs187248500	chr5:74811688-74811689	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs75376232	chr5:74811689-74811690	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs80180254	chr5:74811697-74811698	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs553222807	chr5:74811699-74811700	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs573203042	chr5:74811708-74811709	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs560232704	chr5:74811711-74811712	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs544978114	chr5:74811719-74811720	Weak transcription Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	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
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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	22355333	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:893 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74808000-74814600	Weak transcription	Gastric	stomach
2	chr5:74808200-74814600	Weak transcription	Left Ventricle	heart
3	chr5:74808200-74814600	Weak transcription	Pancreas	Pancrea
4	chr5:74808200-74814800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:74808200-74817600	Weak transcription	Esophagus	oesophagus
6	chr5:74808400-74812000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr5:74808400-74812000	Enhancers	Primary B cells from cord blood	blood
8	chr5:74808400-74812400	Enhancers	Primary B cells from peripheral blood	blood
9	chr5:74808600-74810400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr5:74808600-74814600	Weak transcription	Right Ventricle	heart
11	chr5:74808600-74817600	Weak transcription	Thymus	Thymus
12	chr5:74808600-74819000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr5:74808800-74810600	Enhancers	Duodenum Mucosa	Duodenum
14	chr5:74808800-74814400	Weak transcription	Fetal Muscle Trunk	muscle
15	chr5:74808800-74814600	Weak transcription	Lung	lung
16	chr5:74808800-74816200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr5:74808800-74816200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr5:74808800-74817600	Weak transcription	Aorta	Aorta
19	chr5:74808800-74817600	Weak transcription	Fetal Thymus	thymus
20	chr5:74808800-74817800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr5:74808800-74849600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr5:74809000-74810400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:74809000-74810400	Enhancers	Hela-S3	cervix
24	chr5:74809000-74810400	Enhancers	HepG2	liver
25	chr5:74809000-74811600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr5:74809000-74812000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:74809000-74813000	Weak transcription	Fetal Brain Male	brain
28	chr5:74809000-74815600	Weak transcription	Fetal Intestine Large	intestine
29	chr5:74809000-74816200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr5:74809000-74816200	Weak transcription	Small Intestine	intestine
31	chr5:74809000-74819600	Weak transcription	Placenta	Placenta
32	chr5:74809000-74820000	Weak transcription	Colonic Mucosa	Colon
33	chr5:74809400-74814600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr5:74809400-74814600	Weak transcription	Fetal Intestine Small	intestine
35	chr5:74809400-74814600	Weak transcription	Right Atrium	heart
36	chr5:74809400-74814800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr5:74809400-74815200	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr5:74809400-74815800	Weak transcription	Primary T cells from cord blood	blood
39	chr5:74809400-74816200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr5:74809400-74816200	Weak transcription	Ovary	ovary
41	chr5:74809400-74816400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr5:74809400-74816400	Weak transcription	Osteobl	bone
43	chr5:74809400-74817600	Weak transcription	HSMM	muscle
44	chr5:74809400-74817800	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr5:74809400-74830600	Weak transcription	Fetal Kidney	kidney
46	chr5:74809600-74811400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr5:74809600-74812000	Weak transcription	Primary hematopoietic stem cells	blood
48	chr5:74809600-74814800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr5:74809600-74814800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr5:74809600-74816200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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