Variant report

Variant	nsv882209
Chromosome Location	chr5:76004933-76034355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1043)
CpG islands
(count:1528)
Chromatin interactive
region (count:31)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1043 , 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	ARID3A	chr5:76032333-76032391	K562	blood:	n/a	n/a
2	ARID3A	chr5:76012650-76012879	K562	blood:	n/a	n/a
3	ARID3A	chr5:76028995-76029090	HepG2	liver:	n/a	n/a
4	ATF1	chr5:76006712-76006792	K562	blood:	n/a	n/a
5	ATF2	chr5:76006685-76007268	GM12878	blood:	n/a	n/a
6	ATF2	chr5:76032833-76033458	GM12878	blood:	n/a	n/a
7	ATF2	chr5:76016921-76017407	GM12878	blood:	n/a	n/a
8	ATF2	chr5:76028650-76029329	GM12878	blood:	n/a	n/a
9	ATF2	chr5:76028730-76029343	GM12878	blood:	n/a	n/a
10	ATF2	chr5:76016930-76017421	GM12878	blood:	n/a	n/a
11	ATF2	chr5:76032784-76033389	GM12878	blood:	n/a	n/a
12	BACH1	chr5:76011198-76012110	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:76012439-76012495	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:76012806-76012850	K562	blood:	n/a	n/a
15	BATF	chr5:76006786-76007128	GM12878	blood:	n/a	n/a
16	BATF	chr5:76028784-76029299	GM12878	blood:	n/a	n/a
17	BATF	chr5:76032874-76033224	GM12878	blood:	n/a	n/a
18	BATF	chr5:76006839-76007140	GM12878	blood:	n/a	n/a
19	BATF	chr5:76032943-76033304	GM12878	blood:	n/a	n/a
20	BATF	chr5:76007285-76007597	GM12878	blood:	n/a	n/a
21	BATF	chr5:76028286-76029317	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:76028740-76029285	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:76017111-76017347	GM12878	blood:	n/a	chr5:76017208-76017217
24	BCL11A	chr5:76016959-76017354	GM12878	blood:	n/a	chr5:76017208-76017217
25	BCL11A	chr5:76032791-76033363	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:76007318-76007526	GM12878	blood:	n/a	n/a
27	BCL11A	chr5:76032814-76033372	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:76028798-76029240	GM12878	blood:	n/a	n/a
29	BCL3	chr5:76017038-76017363	GM12878	blood:	n/a	chr5:76017208-76017217
30	BCL3	chr5:76032889-76033230	GM12878	blood:	n/a	n/a
31	BCLAF1	chr5:76028811-76029276	GM12878	blood:	n/a	n/a
32	BCLAF1	chr5:76028701-76029388	GM12878	blood:	n/a	n/a
33	BCLAF1	chr5:76016982-76017402	GM12878	blood:	n/a	chr5:76017208-76017217
34	BCLAF1	chr5:76016997-76017352	GM12878	blood:	n/a	chr5:76017208-76017217
35	BCLAF1	chr5:76032829-76033381	GM12878	blood:	n/a	n/a
36	BCLAF1	chr5:76032790-76033225	GM12878	blood:	n/a	n/a
37	BHLHE40	chr5:76016850-76017430	GM12878	blood:	n/a	n/a
38	BHLHE40	chr5:76011162-76011402	GM12878	blood:	n/a	chr5:76011187-76011203
39	BHLHE40	chr5:76011814-76012537	K562	blood:	n/a	n/a
40	BHLHE40	chr5:76028739-76029497	GM12878	blood:	n/a	n/a
41	BHLHE40	chr5:76011840-76012523	HepG2	liver:	n/a	n/a
42	BHLHE40	chr5:76011789-76012488	GM12878	blood:	n/a	n/a
43	BHLHE40	chr5:76032774-76033431	GM12878	blood:	n/a	n/a
44	CBX3	chr5:76025553-76025995	K562	blood:	n/a	n/a
45	CBX3	chr5:76011474-76011745	K562	blood:	n/a	n/a
46	CBX3	chr5:76011795-76012198	K562	blood:	n/a	n/a
47	CCNT2	chr5:76012665-76012819	K562	blood:	n/a	n/a
48	CCNT2	chr5:76011492-76012388	K562	blood:	n/a	n/a
49	CCNT2	chr5:76011117-76011292	K562	blood:	n/a	n/a
50	CEBPB	chr5:76020821-76021204	IMR90	lung:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76011836-76011886	HCF	heart:	n/a
2	chr5:76008361-76008411	HRE	kidney:	n/a
3	chr5:76029522-76029572	HCF	heart:	n/a
4	chr5:76011836-76011886	HCF	heart:	n/a
5	chr5:76008361-76008411	HRE	kidney:	n/a
6	chr5:76029522-76029572	HCF	heart:	n/a
7	chr5:76012827-76012877	HEEpiC	esophagus:	n/a
8	chr5:76011849-76011899	HRE	kidney:	n/a
9	chr5:76010444-76010494	HNPCEpiC	eye:	n/a
10	chr5:76012757-76012807	HCPEpiC	choroid plexus:	n/a
11	chr5:76012246-76012296	HMEC	breast:	n/a
12	chr5:76012757-76012807	HCF	heart:	n/a
13	chr5:76011643-76011693	GM12892	blood:	n/a
14	chr5:76011698-76011748	HCF	heart:	n/a
15	chr5:76011304-76011354	ECC-1	luminal epithelium:	n/a
16	chr5:76012591-76012641	ovcar-3	ovarian:	n/a
17	chr5:76011304-76011354	CMK	blood:	n/a
18	chr5:76028950-76029000	HCPEpiC	choroid plexus:	n/a
19	chr5:76012246-76012296	RPTEC	kidney:	n/a
20	chr5:76012827-76012877	HL-60	blood:	n/a
21	chr5:76010472-76010522	GM12878	blood:	n/a
22	chr5:76012591-76012641	BE2_C	brain:	n/a
23	chr5:76012827-76012877	Jurkat	blood:	n/a
24	chr5:76011836-76011886	SK-N-SH_RA	brain:	n/a
25	chr5:76010658-76010708	HCF	heart:	n/a
26	chr5:76011304-76011354	HCM	heart:	n/a
27	chr5:76007292-76007342	HCM	heart:	n/a
28	chr5:76028950-76029000	MCF10A-Er-Src	breast:	n/a
29	chr5:76011127-76011177	Jurkat	blood:	n/a
30	chr5:76011304-76011354	HIPEpiC	eye:	n/a
31	chr5:76011138-76011188	AoSMC	blood vessel:	n/a
32	chr5:76011849-76011899	Jurkat	blood:	n/a
33	chr5:76028950-76029000	Hela-S3	cervix:	n/a
34	chr5:76028910-76028960	AG04450	lung:	fetal
35	chr5:76012591-76012641	NT2-D1	testis:	n/a
36	chr5:76011922-76011972	GM12878	blood:	n/a
37	chr5:76028950-76029000	Caco-2	colon:	n/a
38	chr5:76010472-76010522	HUVEC	blood vessel:	n/a
39	chr5:76008361-76008411	PrEC	prostate:	n/a
40	chr5:76010598-76010648	AoSMC	blood vessel:	n/a
41	chr5:76011836-76011886	CMK	blood:	n/a
42	chr5:76012246-76012296	ovcar-3	ovarian:	n/a
43	chr5:76012827-76012877	LNCaP	prostate:	n/a
44	chr5:76011304-76011354	MCF-7	breast:	n/a
45	chr5:76012827-76012877	NHBE	bronchial:	n/a
46	chr5:76005699-76005749	MCF-7	breast:	n/a
47	chr5:76011698-76011748	HCM	heart:	n/a
48	chr5:76011323-76011373	HRCEpiC	kidney:	n/a
49	chr5:76011127-76011177	K562	blood:	n/a
50	chr5:76011836-76011886	HAEpiC	amniotic membrane:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:76011354..76013576-chr5:76033498..76036303,3	K562	blood:
2	chr5:76019532..76021733-chr5:76028622..76031324,3	K562	blood:
3	chr5:76028712..76031262-chr5:76040651..76044472,3	K562	blood:
4	chr5:76015537..76017446-chr5:76018404..76021830,3	K562	blood:
5	chr5:76015537..76017446-chr5:76018404..76021830,3	K562	blood:
6	chr5:75964145..75966782-chr5:76017309..76019547,2	K562	blood:
7	chr5:75997956..76000044-chr5:76012205..76013755,2	K562	blood:
8	chr5:76015744..76018157-chr5:76033229..76035001,2	K562	blood:
9	chr5:76025270..76027765-chr5:76030412..76033336,2	K562	blood:
10	chr5:76021774..76024376-chr5:76030614..76032176,2	K562	blood:
11	chr5:76010538..76012430-chr5:76033988..76036360,2	K562	blood:
12	chr5:75937138..75939935-chr5:76031767..76034422,2	K562	blood:
13	chr5:76008537..76011393-chr5:76015076..76017245,2	K562	blood:
14	chr5:75994284..75996873-chr5:76003044..76005925,2	K562	blood:
15	chr5:76003087..76005831-chr5:76008202..76010428,3	K562	blood:
16	chr5:76017345..76018968-chr5:76030272..76032343,2	K562	blood:
17	chr5:76023449..76027739-chr5:76027820..76030075,3	K562	blood:
18	chr5:76021774..76024376-chr5:76030614..76032176,2	K562	blood:
19	chr5:76025270..76027765-chr5:76030412..76033336,2	K562	blood:
20	chr5:76023117..76024949-chr5:76027820..76030063,2	K562	blood:
21	chr5:76009018..76015131-chr5:76017344..76021190,10	K562	blood:
22	chr5:76011844..76018485-chr5:76019035..76024574,8	K562	blood:
23	chr5:76015491..76019327-chr5:76037164..76040900,3	K562	blood:
24	chr5:76003087..76005831-chr5:76008202..76010428,3	K562	blood:
25	chr5:76008537..76011393-chr5:76015076..76017245,2	K562	blood:
26	chr5:76032426..76034462-chr5:76050771..76053290,2	K562	blood:
27	chr5:76017345..76018968-chr5:76030272..76032343,2	K562	blood:
28	chr5:76019532..76021733-chr5:76028622..76031324,3	K562	blood:
29	chr5:76015744..76018157-chr5:76033229..76035001,2	K562	blood:
30	chr5:76023449..76027739-chr5:76027820..76030075,3	K562	blood:
31	chr5:76023117..76024949-chr5:76027820..76030063,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F2R-1	chr5:76007762-76008686	ncR-uPAR
2	lnc-F2RL2-2	chr5:76012002-76012040	ENSG00000225407
3	lnc-F2R-1	chr5:76007763-76008686	NONHSAT102246
4	lnc-F2R-1	chr5:76008228-76008713	NONHSAT102247

No data

Variant related genes	Relation type
F2R	TF binding region
ENSG00000225407	TF binding region
F2R	CpG island
ENSG00000225407	CpG island
ENSG00000181104	chromatin interactions
ENSG00000145703	chromatin interactions
ENSG00000225407	chromatin interactions
MCM5	miRNA target sites

Extended variants
information (count: 1106 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1106 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7728560	chr5:76004933-76004934	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552900597	chr5:76004948-76004949	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572949223	chr5:76004980-76004981	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147733612	chr5:76005046-76005047	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs558819192	chr5:76005073-76005074	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs77937167	chr5:76005074-76005075	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs149218123	chr5:76005088-76005089	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs73127587	chr5:76005113-76005114	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs532053801	chr5:76005114-76005115	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs573943028	chr5:76005164-76005165	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs114307326	chr5:76005166-76005167	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs35265530	chr5:76005194-76005195	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs560111830	chr5:76005202-76005203	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559379059	chr5:76005248-76005249	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143410236	chr5:76005259-76005260	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187108359	chr5:76005309-76005310	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs27951	chr5:76005321-76005322	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs564800958	chr5:76005370-76005371	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530644909	chr5:76005447-76005448	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs191873379	chr5:76005471-76005472	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs75100871	chr5:76005512-76005513	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs564148209	chr5:76005537-76005538	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs185164862	chr5:76005594-76005595	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs546931256	chr5:76005646-76005647	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs190405152	chr5:76005656-76005657	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs538685105	chr5:76005660-76005661	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs558935317	chr5:76005682-76005683	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs376958012	chr5:76005709-76005710	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs554139351	chr5:76005725-76005726	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs371214792	chr5:76005736-76005737	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs192925687	chr5:76005808-76005809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185508997	chr5:76005891-76005892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573921686	chr5:76005940-76005941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559530817	chr5:76005975-76005976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs542925379	chr5:76005984-76005985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs573049261	chr5:76006072-76006073	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs377580875	chr5:76006074-76006075	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs189421923	chr5:76006086-76006087	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs573111356	chr5:76006161-76006162	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs27903	chr5:76006172-76006173	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs549856895	chr5:76006213-76006214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564905409	chr5:76006225-76006226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569503194	chr5:76006269-76006270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs530475413	chr5:76006299-76006300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs544340417	chr5:76006315-76006316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140455752	chr5:76006333-76006334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180729057	chr5:76006354-76006355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546868186	chr5:76006398-76006399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs145672977	chr5:76006410-76006411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61370375	chr5:76006411-76006412	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

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	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1386 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75988600-76007800	Weak transcription	Fetal Intestine Large	intestine
2	chr5:75988800-76006600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr5:75988800-76011000	Weak transcription	Lung	lung
4	chr5:75989600-76010400	Weak transcription	Fetal Intestine Small	intestine
5	chr5:75991400-76010600	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr5:75991600-76005800	Weak transcription	Fetal Muscle Leg	muscle
7	chr5:75994200-76006400	Weak transcription	GM12878-XiMat	blood
8	chr5:75997200-76010400	Weak transcription	HepG2	liver
9	chr5:75997800-76010000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr5:75997800-76010800	Weak transcription	Gastric	stomach
11	chr5:75997800-76010800	Weak transcription	Pancreas	Pancrea
12	chr5:75998000-76007400	Weak transcription	Fetal Stomach	stomach
13	chr5:75998200-76010000	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr5:75998400-76010800	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr5:75998600-76009200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr5:75998600-76010000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr5:75998600-76010600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr5:75999600-76010400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr5:75999800-76007200	Weak transcription	Stomach Mucosa	stomach
20	chr5:76000400-76007200	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr5:76001600-76007200	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr5:76001800-76005000	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr5:76001800-76005800	Strong transcription	Primary hematopoietic stem cells	blood
24	chr5:76001800-76010200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr5:76002000-76005600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr5:76002000-76005600	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr5:76002600-76005200	Strong transcription	Liver	Liver
28	chr5:76002800-76005400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr5:76003000-76010400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr5:76003400-76008600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr5:76003400-76008800	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr5:76004000-76005000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr5:76004000-76005000	Strong transcription	Placenta	Placenta
34	chr5:76004000-76005200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr5:76004000-76005200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr5:76004000-76005800	Bivalent Enhancer	NHDF-Ad	bronchial
37	chr5:76004200-76005000	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr5:76004200-76005400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr5:76004200-76005600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr5:76004200-76006600	Enhancers	NHEK	skin
41	chr5:76004200-76006800	Enhancers	HMEC	breast
42	chr5:76004200-76007000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr5:76004200-76007600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr5:76004200-76007600	Enhancers	NHLF	lung
45	chr5:76004400-76006800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr5:76004400-76007600	Weak transcription	Primary B cells from cord blood	blood
47	chr5:76004400-76010000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr5:76004600-76005000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr5:76004600-76006400	Weak transcription	Duodenum Mucosa	Duodenum
50	chr5:76004600-76007400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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