Variant report

Variant	nsv549764
Chromosome Location	chr10:671495-704460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:203)
CpG islands
(count:3603)
Chromatin interactive
region (count:20)
LncRNA
region (count:9)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:203 , 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	chr10:695549-696087	HepG2	liver:	n/a	n/a
2	ATF1	chr10:691655-691733	K562	blood:	n/a	n/a
3	BACH1	chr10:699656-699670	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr10:673571-673899	K562	blood:	n/a	n/a
5	BHLHE40	chr10:695485-697003	HepG2	liver:	n/a	n/a
6	BHLHE40	chr10:695707-696007	HepG2	liver:	n/a	n/a
7	BHLHE40	chr10:679292-679487	HepG2	liver:	n/a	n/a
8	CEBPB	chr10:697228-697554	IMR90	lung:	n/a	n/a
9	CEBPB	chr10:695388-696030	A549	lung:	n/a	n/a
10	CEBPB	chr10:695464-696050	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:695684-696164	HepG2	liver:	n/a	n/a
12	CEBPB	chr10:695403-696085	HepG2	liver:	n/a	n/a
13	CEBPD	chr10:695811-696058	HepG2	liver:	n/a	n/a
14	CEBPD	chr10:695785-696331	HepG2	liver:	n/a	n/a
15	CHD2	chr10:688364-688501	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr10:695672-696183	HepG2	liver:	n/a	n/a
17	CREB1	chr10:695734-695984	A549	lung:	n/a	n/a
18	CREB1	chr10:695565-696794	HepG2	liver:	n/a	n/a
19	CREB1	chr10:695682-696078	A549	lung:	n/a	n/a
20	CTCF	chr10:704223-704291	GM10266	blood:	n/a	n/a
21	CTCF	chr10:700280-700430	GM12868	blood:	n/a	n/a
22	CTCF	chr10:671360-671510	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr10:700700-700850	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr10:679380-679530	RPTEC	kidney:	n/a	chr10:679446-679459
25	CTCF	chr10:700580-700730	HepG2	liver:	n/a	chr10:700699-700708
26	CTCF	chr10:693878-693957	GM13976	blood:	n/a	n/a
27	CTCF	chr10:700620-700770	BE2_C	brain:	n/a	chr10:700699-700708
28	CTCF	chr10:700380-700530	RPTEC	kidney:	n/a	n/a
29	CTCF	chr10:700640-700790	AG04450	lung:	n/a	chr10:700699-700708
30	CTCF	chr10:700660-700810	HRPEpiC	eye:	n/a	chr10:700699-700708
31	CTCF	chr10:698800-698950	MCF-7	breast:	n/a	n/a
32	CTCF	chr10:686801-686870	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr10:700620-700770	Caco-2	colon:	n/a	chr10:700699-700708
34	CTCF	chr10:700620-700770	MCF-7	breast:	n/a	chr10:700699-700708
35	CTCF	chr10:700620-700770	HBMEC	blood vessel:	n/a	chr10:700699-700708
36	CTCF	chr10:694301-694378	GM19239	blood:	n/a	n/a
37	CTCF	chr10:700600-700750	Caco-2	colon:	n/a	chr10:700699-700708
38	CTCF	chr10:683206-683264	Lung_OC	lung:	n/a	n/a
39	CTCF	chr10:704201-704255	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr10:700620-700770	HEK293	kidney:	n/a	chr10:700699-700708
41	ELF1	chr10:695680-696083	HepG2	liver:	n/a	n/a
42	ELF1	chr10:695777-696007	HepG2	liver:	n/a	n/a
43	EP300	chr10:695478-696062	HepG2	liver:	n/a	chr10:695903-695912 chr10:695896-695910 chr10:695984-696000 chr10:695902-695916
44	EP300	chr10:695726-696137	HepG2	liver:	n/a	chr10:695903-695912 chr10:695896-695910 chr10:695984-696000 chr10:695902-695916
45	ESR1	chr10:688220-688552	ECC-1	luminal epithelium:	n/a	n/a
46	ESR1	chr10:688108-688511	ECC-1	luminal epithelium:	n/a	n/a
47	FOSL2	chr10:695674-696085	HepG2	liver:	n/a	n/a
48	FOXA1	chr10:695712-696200	HepG2	liver:	n/a	n/a
49	FOXA1	chr10:695712-696170	HepG2	liver:	n/a	n/a
50	FOXA1	chr10:695677-696189	HepG2	liver:	n/a	n/a

(count:3603 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:695859-695909	U87	brain:	n/a
2	chr10:679221-679271	Jurkat	blood:	n/a
3	chr10:671497-671547	HepG2	liver:	n/a
4	chr10:693439-693489	GM12878	blood:	n/a
5	chr10:695859-695909	U87	brain:	n/a
6	chr10:679221-679271	Jurkat	blood:	n/a
7	chr10:671497-671547	HepG2	liver:	n/a
8	chr10:693439-693489	GM12878	blood:	n/a
9	chr10:695403-695453	CMK	blood:	n/a
10	chr10:686762-686812	SKMC	muscle:	n/a
11	chr10:676740-676790	ovcar-3	ovarian:	n/a
12	chr10:678920-678970	AG04449	skin:	fetal
13	chr10:685091-685141	AG09309	skin:	n/a
14	chr10:677269-677319	HUVEC	blood vessel:	n/a
15	chr10:697901-697951	Hepatocyte	liver:	n/a
16	chr10:677369-677419	AG10803	skin:	n/a
17	chr10:682125-682175	HCT-116	colon:	n/a
18	chr10:673730-673780	GM06990	blood:	n/a
19	chr10:682486-682536	ECC-1	luminal epithelium:	n/a
20	chr10:695853-695903	CMK	blood:	n/a
21	chr10:685357-685407	NT2-D1	testis:	n/a
22	chr10:678920-678970	AoSMC	blood vessel:	n/a
23	chr10:686201-686251	GM12878	blood:	n/a
24	chr10:682841-682891	SK-N-SH_RA	brain:	n/a
25	chr10:693439-693489	NB4	blood:	n/a
26	chr10:694898-694948	SKMC	muscle:	n/a
27	chr10:675907-675957	SAEC	small airway:	n/a
28	chr10:678920-678970	BJ	skin:	n/a
29	chr10:695844-695894	MCF10A-Er-Src	breast:	n/a
30	chr10:673310-673360	LNCaP	prostate:	n/a
31	chr10:698258-698308	NH-A	brain:	n/a
32	chr10:676740-676790	NH-A	brain:	n/a
33	chr10:682147-682197	HCT-116	colon:	n/a
34	chr10:696332-696382	MCF10A-Er-Src	breast:	n/a
35	chr10:675907-675957	GM19239	blood:	n/a
36	chr10:693439-693489	GM06990	blood:	n/a
37	chr10:677269-677319	NB4	blood:	n/a
38	chr10:679221-679271	HCPEpiC	choroid plexus:	n/a
39	chr10:680352-680402	HIPEpiC	eye:	n/a
40	chr10:682125-682175	HCM	heart:	n/a
41	chr10:679322-679372	U87	brain:	n/a
42	chr10:695844-695894	SK-N-MC	brain:	n/a
43	chr10:682147-682197	GM12891	blood:	n/a
44	chr10:682449-682499	T-47D	breast:	n/a
45	chr10:698258-698308	GM06990	blood:	n/a
46	chr10:682486-682536	PrEC	prostate:	n/a
47	chr10:675888-675938	NHDF-neo	bronchial:	n/a
48	chr10:673730-673780	SK-N-SH_RA	brain:	n/a
49	chr10:678920-678970	HCT-116	colon:	n/a
50	chr10:676761-676811	AG09309	skin:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:667961..671852-chr10:732081..736425,5	MCF-7	breast:
2	chr10:698785..701781-chr10:833421..835495,2	MCF-7	breast:
3	chr10:692996..695820-chr10:700101..701896,2	MCF-7	breast:
4	chr10:687008..688714-chr10:699568..702258,2	MCF-7	breast:
5	chr10:668740..670601-chr10:679784..682752,2	K562	blood:
6	chr10:678262..679765-chr10:686218..688304,2	MCF-7	breast:
7	chr10:676250..679405-chr10:680596..683070,3	MCF-7	breast:
8	chr10:701409..702201-chr19:4341065..4341565,2	MCF-7	breast:
9	chr10:670049..672648-chr10:675180..678695,4	MCF-7	breast:
10	chr10:684852..686965-chr10:1094186..1096344,2	MCF-7	breast:
11	chr10:663652..666584-chr10:669645..672597,2	MCF-7	breast:
12	chr10:591027..592678-chr10:670118..672515,2	MCF-7	breast:
13	chr10:660244..661956-chr10:668793..671774,2	MCF-7	breast:
14	chr10:678817..681667-chr10:734486..736272,2	MCF-7	breast:
15	chr10:692009..694331-chr10:706518..708449,2	MCF-7	breast:
16	chr10:670049..672648-chr10:675180..678695,4	MCF-7	breast:
17	chr10:692996..695820-chr10:700101..701896,2	MCF-7	breast:
18	chr10:691751..694285-chr10:694356..695999,2	K562	blood:
19	chr10:676250..679405-chr10:680596..683070,3	MCF-7	breast:
20	chr10:674481..678808-chr10:734028..737251,4	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf108-2	chr10:674578-674837	ENSG00000225140.1
2	lnc-C10orf108-1	chr10:696017-696382	NR_027152
3	lnc-C10orf108-1	chr10:695888-696118	NONHSAT010867
4	lnc-C10orf108-2	chr10:675799-677195	ENSG00000225140.1
5	lnc-C10orf108-1	chr10:697051-698595	NONHSAT010867
6	lnc-C10orf108-2	chr10:674578-674837	NONHSAT010863
7	lnc-C10orf108-2	chr10:675799-676319	NONHSAT010863
8	lnc-C10orf108-2	chr10:676345-677195	NONHSAT010863
9	lnc-C10orf108-1	chr10:696231-696382	NONHSAT010867

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5699-5p	chr10:687688-687709	MIMAT0027103
hsa-miR-5699-3p	chr10:687639-687660	MIMAT0022492

No data

Variant related genes	Relation type
MIR5699	TF binding region
PRR26	TF binding region
ENSG00000225140	TF binding region
MIR5699	CpG island
PRR26	CpG island
ENSG00000225140	CpG island
ENSG00000067064	chromatin interactions
ENSG00000263511	chromatin interactions
ENSG00000180525	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000151240	chromatin interactions

Extended variants
information (count: 1620 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1620 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12248693	chr10:671495-671496	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs555686123	chr10:671498-671499	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs73588195	chr10:671537-671538	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs142703871	chr10:671572-671573	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs78358730	chr10:671584-671585	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs576604664	chr10:671593-671594	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs73588197	chr10:671601-671602	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs562355575	chr10:671629-671630	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531280612	chr10:671634-671635	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs115962906	chr10:671645-671646	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs74115083	chr10:671650-671651	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs527339557	chr10:671662-671663	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs549620417	chr10:671681-671682	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs186646219	chr10:671688-671689	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs571191646	chr10:671689-671690	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs576863519	chr10:671755-671756	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539464894	chr10:671758-671759	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs371541767	chr10:671766-671767	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs569900535	chr10:671892-671893	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs533550078	chr10:671914-671915	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs550364611	chr10:671960-671961	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs570266144	chr10:671965-671966	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs535902558	chr10:671977-671978	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs555619500	chr10:671995-671996	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs566060436	chr10:672042-672043	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs529066063	chr10:672043-672044	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs59939816	chr10:672047-672048	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs114188134	chr10:672048-672049	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs576689627	chr10:672049-672050	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs534669364	chr10:672052-672053	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs118161052	chr10:672056-672057	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs372615045	chr10:672067-672068	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs550863510	chr10:672074-672075	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs202054307	chr10:672090-672091	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs189964159	chr10:672123-672124	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561680317	chr10:672129-672130	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs571986819	chr10:672158-672159	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs540704112	chr10:672206-672207	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs564086807	chr10:672238-672239	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs375900898	chr10:672256-672257	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs533618567	chr10:672312-672313	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs550504781	chr10:672321-672322	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs200313019	chr10:672323-672324	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs563861811	chr10:672335-672336	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs557894049	chr10:672369-672370	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs113435321	chr10:672382-672383	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs148421712	chr10:672384-672385	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs369658675	chr10:672397-672398	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs2794955	chr10:672398-672399	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs114008859	chr10:672409-672410	Enhancers Weak transcription Flanking Active TSS Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1225 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:657200-673000	Enhancers	Fetal Muscle Leg	muscle
2	chr10:658400-672800	Enhancers	Left Ventricle	heart
3	chr10:660200-673000	Enhancers	Fetal Heart	heart
4	chr10:660800-673200	Enhancers	Brain Germinal Matrix	brain
5	chr10:666400-672600	Enhancers	Fetal Brain Male	brain
6	chr10:667400-672800	Enhancers	Fetal Brain Female	brain
7	chr10:667400-673200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr10:667600-672600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:667600-679200	Weak transcription	Gastric	stomach
10	chr10:667800-671800	Enhancers	Fetal Stomach	stomach
11	chr10:667800-672200	Enhancers	Ovary	ovary
12	chr10:668400-672200	Enhancers	Pancreas	Pancrea
13	chr10:668800-672800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr10:669000-672800	Enhancers	NHDF-Ad	bronchial
15	chr10:669000-673200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:669200-672600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr10:669200-680000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr10:669400-674000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr10:669800-672200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr10:669800-672600	Enhancers	Esophagus	oesophagus
21	chr10:669800-672600	Enhancers	NHLF	lung
22	chr10:670000-671600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr10:670000-671600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr10:670000-672200	Enhancers	Stomach Mucosa	stomach
25	chr10:670000-672200	Flanking Active TSS	Stomach Smooth Muscle	stomach
26	chr10:670000-672600	Enhancers	Placenta	Placenta
27	chr10:670000-672800	Enhancers	Colonic Mucosa	Colon
28	chr10:670000-673000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr10:670000-673800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr10:670200-671600	Flanking Active TSS	Rectal Smooth Muscle	rectum
31	chr10:670200-671800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
32	chr10:670200-672200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr10:670200-672200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr10:670200-672200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr10:670200-672800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr10:670200-672800	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr10:670200-673000	Flanking Active TSS	Brain Anterior Caudate	brain
38	chr10:670400-671600	Flanking Active TSS	NH-A	brain
39	chr10:670400-671800	Flanking Active TSS	HSMMtube	muscle
40	chr10:670400-672600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
41	chr10:670600-672000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr10:670600-672000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
43	chr10:670600-672400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr10:670600-679400	Weak transcription	Aorta	Aorta
45	chr10:670800-671600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr10:670800-671600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
47	chr10:670800-671600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr10:670800-671800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr10:670800-671800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr10:670800-671800	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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