Variant report

Variant	nsv882208
Chromosome Location	chr5:75997213-76034355
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1184)
CpG islands
(count:1587)
Chromatin interactive
region (count:37)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1184 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:76012650-76012879	K562	blood:	n/a	n/a
2	ARID3A	chr5:76028995-76029090	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:76032333-76032391	K562	blood:	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	chr5:76016930-76017421	GM12878	blood:	n/a	n/a
7	ATF2	chr5:76028650-76029329	GM12878	blood:	n/a	n/a
8	ATF2	chr5:76016921-76017407	GM12878	blood:	n/a	n/a
9	ATF2	chr5:76032784-76033389	GM12878	blood:	n/a	n/a
10	ATF2	chr5:76028730-76029343	GM12878	blood:	n/a	n/a
11	ATF2	chr5:76032833-76033458	GM12878	blood:	n/a	n/a
12	BACH1	chr5:76012439-76012495	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:76011198-76012110	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr5:76012806-76012850	K562	blood:	n/a	n/a
15	BATF	chr5:76032943-76033304	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	chr5:76028286-76029317	GM12878	blood:	n/a	n/a
19	BATF	chr5:76006839-76007140	GM12878	blood:	n/a	n/a
20	BATF	chr5:76006786-76007128	GM12878	blood:	n/a	n/a
21	BATF	chr5:76007285-76007597	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:76028798-76029240	GM12878	blood:	n/a	n/a
23	BCL11A	chr5:76028740-76029285	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:76032791-76033363	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:76016959-76017354	GM12878	blood:	n/a	chr5:76017208-76017217
26	BCL11A	chr5:76032814-76033372	GM12878	blood:	n/a	n/a
27	BCL11A	chr5:76007318-76007526	GM12878	blood:	n/a	n/a
28	BCL11A	chr5:76017111-76017347	GM12878	blood:	n/a	chr5:76017208-76017217
29	BCL3	chr5:76032889-76033230	GM12878	blood:	n/a	n/a
30	BCL3	chr5:76017038-76017363	GM12878	blood:	n/a	chr5:76017208-76017217
31	BCLAF1	chr5:76028701-76029388	GM12878	blood:	n/a	n/a
32	BCLAF1	chr5:76028811-76029276	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	chr5:76011840-76012523	HepG2	liver:	n/a	n/a
38	BHLHE40	chr5:76011162-76011402	GM12878	blood:	n/a	chr5:76011187-76011203
39	BHLHE40	chr5:76032774-76033431	GM12878	blood:	n/a	n/a
40	BHLHE40	chr5:76011814-76012537	K562	blood:	n/a	n/a
41	BHLHE40	chr5:76011789-76012488	GM12878	blood:	n/a	n/a
42	BHLHE40	chr5:76028739-76029497	GM12878	blood:	n/a	n/a
43	BHLHE40	chr5:76016850-76017430	GM12878	blood:	n/a	n/a
44	CBX3	chr5:76011795-76012198	K562	blood:	n/a	n/a
45	CBX3	chr5:76025553-76025995	K562	blood:	n/a	n/a
46	CBX3	chr5:76011474-76011745	K562	blood:	n/a	n/a
47	CCNT2	chr5:76012665-76012819	K562	blood:	n/a	n/a
48	CCNT2	chr5:76011117-76011292	K562	blood:	n/a	n/a
49	CCNT2	chr5:76011492-76012388	K562	blood:	n/a	n/a
50	CEBPB	chr5:75997087-75997453	HepG2	liver:	n/a	chr5:75997251-75997264 chr5:75997252-75997263 chr5:75997251-75997264 chr5:75997251-75997262

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76028910-76028960	GM19239	blood:	n/a
2	chr5:76028910-76028960	GM19239	blood:	n/a
3	chr5:76012757-76012807	HNPCEpiC	eye:	n/a
4	chr5:76003762-76003812	HL-60	blood:	n/a
5	chr5:76011643-76011693	SK-N-MC	brain:	n/a
6	chr5:76010658-76010708	NHBE	bronchial:	n/a
7	chr5:76010472-76010522	SKMC	muscle:	n/a
8	chr5:76012757-76012807	AG04450	lung:	fetal
9	chr5:76010598-76010648	HL-60	blood:	n/a
10	chr5:76010444-76010494	LNCaP	prostate:	n/a
11	chr5:76005699-76005749	NB4	blood:	n/a
12	chr5:76003762-76003812	AoSMC	blood vessel:	n/a
13	chr5:76008361-76008411	BE2_C	brain:	n/a
14	chr5:76011698-76011748	SK-N-SH	brain:	n/a
15	chr5:76010444-76010494	ECC-1	luminal epithelium:	n/a
16	chr5:76011127-76011177	AG04450	lung:	fetal
17	chr5:76011922-76011972	PANC-1	pancreas:	n/a
18	chr5:76011698-76011748	HAEpiC	amniotic membrane:	n/a
19	chr5:76010472-76010522	HRCEpiC	kidney:	n/a
20	chr5:76011922-76011972	GM12891	blood:	n/a
21	chr5:76012246-76012296	HRPEpiC	eye:	n/a
22	chr5:76012591-76012641	HPAEpiC	pulmonary alveolar:	n/a
23	chr5:76005699-76005749	Jurkat	blood:	n/a
24	chr5:76010472-76010522	PrEC	prostate:	n/a
25	chr5:76011922-76011972	GM12878	blood:	n/a
26	chr5:76005699-76005749	AG04449	skin:	fetal
27	chr5:76011698-76011748	U87	brain:	n/a
28	chr5:76011138-76011188	HPAEpiC	pulmonary alveolar:	n/a
29	chr5:76012246-76012296	SAEC	small airway:	n/a
30	chr5:76011304-76011354	GM12878	blood:	n/a
31	chr5:76015832-76015882	U87	brain:	n/a
32	chr5:76011304-76011354	NB4	blood:	n/a
33	chr5:76010472-76010522	HCT-116	colon:	n/a
34	chr5:76008361-76008411	HRCEpiC	kidney:	n/a
35	chr5:76011428-76011478	HEK293	kidney:	embryo
36	chr5:76010444-76010494	AG04450	lung:	fetal
37	chr5:76012827-76012877	SK-N-SH_RA	brain:	n/a
38	chr5:76012827-76012877	NT2-D1	testis:	n/a
39	chr5:76011304-76011354	PFSK-1	brain:	n/a
40	chr5:76011323-76011373	Jurkat	blood:	n/a
41	chr5:76011304-76011354	PANC-1	pancreas:	n/a
42	chr5:76007292-76007342	HL-60	blood:	n/a
43	chr5:76012246-76012296	NHDF-neo	bronchial:	n/a
44	chr5:76029522-76029572	GM06990	blood:	n/a
45	chr5:76011849-76011899	HCT-116	colon:	n/a
46	chr5:76011304-76011354	HNPCEpiC	eye:	n/a
47	chr5:76011698-76011748	A549	lung:	n/a
48	chr5:76011698-76011748	AoSMC	blood vessel:	n/a
49	chr5:76011643-76011693	HRCEpiC	kidney:	n/a
50	chr5:76015832-76015882	SK-N-SH	brain:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75997956..76000044-chr5:76012205..76013755,2	K562	blood:
2	chr5:75937138..75939935-chr5:76031767..76034422,2	K562	blood:
3	chr5:76017345..76018968-chr5:76030272..76032343,2	K562	blood:
4	chr5:76032426..76034462-chr5:76050771..76053290,2	K562	blood:
5	chr5:76023117..76024949-chr5:76027820..76030063,2	K562	blood:
6	chr5:76015537..76017446-chr5:76018404..76021830,3	K562	blood:
7	chr5:75997963..75999602-chr5:76001084..76003295,2	K562	blood:
8	chr5:75994843..75996595-chr5:75999290..76000905,2	K562	blood:
9	chr5:76015537..76017446-chr5:76018404..76021830,3	K562	blood:
10	chr5:76023117..76024949-chr5:76027820..76030063,2	K562	blood:
11	chr5:76009018..76015131-chr5:76017344..76021190,10	K562	blood:
12	chr5:75997963..75999602-chr5:76001084..76003295,2	K562	blood:
13	chr5:75994284..75996873-chr5:76003044..76005925,2	K562	blood:
14	chr5:76023449..76027739-chr5:76027820..76030075,3	K562	blood:
15	chr5:76023449..76027739-chr5:76027820..76030075,3	K562	blood:
16	chr5:76003087..76005831-chr5:76008202..76010428,3	K562	blood:
17	chr5:76003087..76005831-chr5:76008202..76010428,3	K562	blood:
18	chr5:76025270..76027765-chr5:76030412..76033336,2	K562	blood:
19	chr5:76015744..76018157-chr5:76033229..76035001,2	K562	blood:
20	chr5:76010538..76012430-chr5:76033988..76036360,2	K562	blood:
21	chr5:76008537..76011393-chr5:76015076..76017245,2	K562	blood:
22	chr5:75999626..76001193-chr5:76002923..76004547,2	K562	blood:
23	chr5:76021774..76024376-chr5:76030614..76032176,2	K562	blood:
24	chr5:75999626..76001193-chr5:76002923..76004547,2	K562	blood:
25	chr5:76015491..76019327-chr5:76037164..76040900,3	K562	blood:
26	chr5:76008537..76011393-chr5:76015076..76017245,2	K562	blood:
27	chr5:76025270..76027765-chr5:76030412..76033336,2	K562	blood:
28	chr5:76021774..76024376-chr5:76030614..76032176,2	K562	blood:
29	chr5:76019532..76021733-chr5:76028622..76031324,3	K562	blood:
30	chr5:76011354..76013576-chr5:76033498..76036303,3	K562	blood:
31	chr5:75964145..75966782-chr5:76017309..76019547,2	K562	blood:
32	chr5:76017345..76018968-chr5:76030272..76032343,2	K562	blood:
33	chr5:76028712..76031262-chr5:76040651..76044472,3	K562	blood:
34	chr5:76019532..76021733-chr5:76028622..76031324,3	K562	blood:
35	chr5:76011844..76018485-chr5:76019035..76024574,8	K562	blood:
36	chr5:75997956..76000044-chr5:76012205..76013755,2	K562	blood:
37	chr5:76015744..76018157-chr5:76033229..76035001,2	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	chr5:76008228-76008713	NONHSAT102247
4	lnc-F2R-1	chr5:76007763-76008686	NONHSAT102246

No data

Variant related genes	Relation type
F2R	TF binding region
IQGAP2	TF binding region
ENSG00000225407	TF binding region
F2R	CpG island
IQGAP2	CpG island
ENSG00000225407	CpG island
ENSG00000181104	chromatin interactions
ENSG00000225407	chromatin interactions
ENSG00000145703	chromatin interactions
MCM5	miRNA target sites

Extended variants
information (count: 1399 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1399 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10063791	chr5:75997213-75997214	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553284045	chr5:75997219-75997220	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs562095035	chr5:75997263-75997264	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs145487036	chr5:75997350-75997351	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs545091517	chr5:75997385-75997386	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs148990343	chr5:75997388-75997389	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs565073662	chr5:75997430-75997431	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs532943110	chr5:75997440-75997441	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs113695873	chr5:75997441-75997442	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs2435055	chr5:75997443-75997444	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs563353174	chr5:75997489-75997490	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs182968487	chr5:75997502-75997503	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142585549	chr5:75997507-75997508	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs188628770	chr5:75997546-75997547	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs537907358	chr5:75997639-75997640	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs28609562	chr5:75997678-75997679	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs13168057	chr5:75997698-75997699	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs536762390	chr5:75997720-75997721	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs551110085	chr5:75997815-75997816	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs11956898	chr5:75997831-75997832	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs377654468	chr5:75997832-75997833	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs372430084	chr5:75997853-75997854	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs147926084	chr5:75997877-75997878	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs13181615	chr5:75997880-75997881	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs11950408	chr5:75997898-75997899	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs546015610	chr5:75997912-75997913	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs193284546	chr5:75997914-75997915	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs576165271	chr5:75997917-75997918	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs542261303	chr5:75997920-75997921	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs558552708	chr5:75997925-75997926	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs575660686	chr5:75997926-75997927	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs544389627	chr5:75997931-75997932	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs562062301	chr5:75997966-75997967	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs573801440	chr5:75997977-75997978	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs184220627	chr5:75998023-75998024	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs373761527	chr5:75998049-75998050	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs138560214	chr5:75998053-75998054	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs2307122	chr5:75998096-75998097	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs528417782	chr5:75998117-75998118	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs114417222	chr5:75998143-75998144	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs564881218	chr5:75998177-75998178	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs530577495	chr5:75998180-75998181	Weak transcription Strong transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs34954	chr5:75998201-75998202	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs368611155	chr5:75998258-75998259	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs371698173	chr5:75998265-75998266	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs115903872	chr5:75998280-75998281	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs376268244	chr5:75998281-75998282	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs141420081	chr5:75998324-75998325	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs368828240	chr5:75998335-75998336	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs547415830	chr5:75998348-75998349	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	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:1577 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75945200-76001000	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr5:75946400-76001000	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr5:75948000-76004600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr5:75950800-75999400	Weak transcription	Ovary	ovary
5	chr5:75951800-76001400	Weak transcription	Rectal Smooth Muscle	rectum
6	chr5:75969800-75999600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr5:75975600-75999600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:75977600-76003400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr5:75978400-76001600	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr5:75978400-76004400	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr5:75978600-76003400	Strong transcription	Primary T helper cells PMA-I stimulated	--
12	chr5:75980600-76002600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr5:75980800-76000200	Strong transcription	Primary hematopoietic stem cells	blood
14	chr5:75981200-76001600	Weak transcription	Primary B cells from peripheral blood	blood
15	chr5:75985800-76004400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr5:75986600-76000000	Strong transcription	Primary B cells from cord blood	blood
17	chr5:75987600-76001200	Weak transcription	Small Intestine	intestine
18	chr5:75987800-76001400	Weak transcription	Fetal Lung	lung
19	chr5:75988000-75999200	Weak transcription	Stomach Mucosa	stomach
20	chr5:75988200-75999400	Strong transcription	Placenta	Placenta
21	chr5:75988200-75999600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:75988400-75998600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
23	chr5:75988400-76004600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
24	chr5:75988600-76001800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr5:75988600-76007800	Weak transcription	Fetal Intestine Large	intestine
26	chr5:75988800-75999000	Weak transcription	Fetal Kidney	kidney
27	chr5:75988800-76006600	Weak transcription	Fetal Muscle Trunk	muscle
28	chr5:75988800-76011000	Weak transcription	Lung	lung
29	chr5:75989000-75997800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr5:75989200-76000000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr5:75989600-76010400	Weak transcription	Fetal Intestine Small	intestine
32	chr5:75990600-75999600	Weak transcription	Adipose Nuclei	Adipose
33	chr5:75990800-75999600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr5:75991000-76000800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr5:75991400-76010600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr5:75991600-76005800	Weak transcription	Fetal Muscle Leg	muscle
37	chr5:75992800-76000400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:75993000-75999600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr5:75993000-76000200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr5:75993000-76000400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:75993200-75998400	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr5:75993200-76000400	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr5:75993400-75997600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
44	chr5:75993400-76001400	Strong transcription	Primary T cells from cord blood	blood
45	chr5:75993800-76001600	Weak transcription	K562	blood
46	chr5:75993800-76004200	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr5:75994200-76006400	Weak transcription	GM12878-XiMat	blood
48	chr5:75994400-75998800	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr5:75994400-75999800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr5:75995800-76004000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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