Variant report

Variant	nsv1015490
Chromosome Location	chr8:124103255-124150990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:205)
CpG islands
(count:0)
Chromatin interactive
region (count:51)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:205 , 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	chr8:124118504-124118606	K562	blood:	n/a	n/a
2	ARID3A	chr8:124138713-124138945	K562	blood:	n/a	n/a
3	ARID3A	chr8:124115891-124116202	K562	blood:	n/a	n/a
4	ATF1	chr8:124138675-124138942	K562	blood:	n/a	n/a
5	ATF1	chr8:124125036-124125222	K562	blood:	n/a	n/a
6	ATF3	chr8:124115866-124116138	K562	blood:	n/a	n/a
7	BHLHE40	chr8:124116045-124116118	K562	blood:	n/a	n/a
8	BHLHE40	chr8:124118368-124118674	K562	blood:	n/a	n/a
9	CBX3	chr8:124115853-124116311	HCT-116	colon:	n/a	n/a
10	CCNT2	chr8:124115979-124116188	K562	blood:	n/a	n/a
11	CCNT2	chr8:124149754-124150113	K562	blood:	n/a	n/a
12	CEBPB	chr8:124142253-124142837	HCT-116	colon:	n/a	chr8:124142285-124142297
13	CEBPB	chr8:124146895-124147218	IMR90	lung:	n/a	n/a
14	CEBPB	chr8:124119212-124119235	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:124142398-124142714	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr8:124142461-124142661	K562	blood:	n/a	n/a
17	CEBPB	chr8:124142371-124142726	HCT-116	colon:	n/a	n/a
18	CEBPB	chr8:124146884-124147030	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:124146907-124147108	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr8:124118269-124118658	K562	blood:	n/a	n/a
21	CEBPB	chr8:124118373-124118640	K562	blood:	n/a	n/a
22	CEBPB	chr8:124146899-124147187	A549	lung:	n/a	n/a
23	CEBPB	chr8:124119140-124119203	A549	lung:	n/a	n/a
24	CEBPB	chr8:124118474-124118523	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:124146908-124147116	K562	blood:	n/a	n/a
26	CEBPB	chr8:124118423-124118661	A549	lung:	n/a	n/a
27	CEBPB	chr8:124142374-124142687	IMR90	lung:	n/a	n/a
28	CEBPB	chr8:124118395-124118625	K562	blood:	n/a	n/a
29	CEBPB	chr8:124146905-124147208	HepG2	liver:	n/a	n/a
30	CEBPB	chr8:124118437-124118645	HepG2	liver:	n/a	n/a
31	CEBPD	chr8:124149787-124150304	K562	blood:	n/a	n/a
32	CEBPD	chr8:124149827-124150242	K562	blood:	n/a	n/a
33	CHD2	chr8:124149799-124149965	K562	blood:	n/a	n/a
34	CTCF	chr8:124143485-124143506	GM10248	blood:	n/a	n/a
35	CTCF	chr8:124112400-124112550	GM12864	blood:	n/a	n/a
36	CTCF	chr8:124133242-124133246	GM20000	blood:	n/a	n/a
37	CTCF	chr8:124111220-124111370	GM12873	blood:	n/a	n/a
38	CTCF	chr8:124147240-124147339	GM20000	blood:	n/a	n/a
39	CTCF	chr8:124114460-124114610	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:124133247-124133320	GM20000	blood:	n/a	n/a
41	CUX1	chr8:124115998-124116329	K562	blood:	n/a	n/a
42	EBF1	chr8:124108200-124108747	GM12878	blood:	n/a	chr8:124108461-124108472
43	EBF1	chr8:124108235-124108684	GM12878	blood:	n/a	chr8:124108461-124108472
44	EBF1	chr8:124108253-124108646	GM12878	blood:	n/a	chr8:124108461-124108472
45	EP300	chr8:124138682-124138826	K562	blood:	n/a	n/a
46	EP300	chr8:124138659-124138977	K562	blood:	n/a	n/a
47	EP300	chr8:124142325-124142665	K562	blood:	n/a	n/a
48	EP300	chr8:124142396-124142755	Hela-S3	cervix:	n/a	chr8:124142720-124142734
49	EP300	chr8:124120105-124120264	K562	blood:	n/a	n/a
50	EP300	chr8:124149903-124150185	K562	blood:	n/a	n/a

No data

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:124053046..124055270-chr8:124104055..124106373,2	MCF-7	breast:
2	chr8:124096600..124098106-chr8:124124370..124126385,2	MCF-7	breast:
3	chr8:124101865..124103695-chr8:124134066..124136996,2	K562	blood:
4	chr8:124098071..124099602-chr8:124102319..124104778,2	MCF-7	breast:
5	chr8:124113489..124116469-chr8:124118656..124121514,2	K562	blood:
6	chr8:124136116..124138803-chr8:124140599..124142133,2	K562	blood:
7	chr8:124102688..124105336-chr8:124111816..124114420,2	K562	blood:
8	chr8:124103620..124105576-chr8:124111193..124113451,2	MCF-7	breast:
9	chr8:124133634..124135408-chr8:124138761..124140483,2	K562	blood:
10	chr8:124127687..124130372-chr8:124131606..124133579,2	MCF-7	breast:
11	chr8:124131670..124133659-chr8:124135083..124137190,3	MCF-7	breast:
12	chr8:124113205..124115254-chr8:124116735..124119002,2	K562	blood:
13	chr8:124131028..124133597-chr8:124144935..124147901,2	K562	blood:
14	chr8:124143178..124145136-chr8:124155401..124158331,2	MCF-7	breast:
15	chr8:124127687..124130372-chr8:124131606..124133579,2	MCF-7	breast:
16	chr8:124136612..124138190-chr8:124144199..124146397,2	K562	blood:
17	chr8:124150012..124152618-chr8:124154439..124156417,2	K562	blood:
18	chr8:124136116..124138803-chr8:124140599..124142133,2	K562	blood:
19	chr8:124148204..124150384-chr8:124166803..124168730,2	K562	blood:
20	chr8:124094220..124096986-chr8:124125949..124128306,2	K562	blood:
21	chr8:124050657..124053142-chr8:124135832..124138315,2	MCF-7	breast:
22	chr8:124101511..124104352-chr8:124116261..124118453,2	MCF-7	breast:
23	chr8:124113359..124117721-chr8:124119367..124124584,5	K562	blood:
24	chr8:124107106..124109057-chr8:124110948..124112653,2	K562	blood:
25	chr8:124119976..124122130-chr8:124122257..124124214,3	K562	blood:
26	chr8:124089689..124091301-chr8:124118669..124120811,2	K562	blood:
27	chr8:124099494..124101428-chr8:124118958..124120989,2	MCF-7	breast:
28	chr8:124131028..124133597-chr8:124144935..124147901,2	K562	blood:
29	chr8:124146952..124149281-chr8:124151497..124153020,2	MCF-7	breast:
30	chr8:124140421..124142516-chr8:124160031..124161914,2	MCF-7	breast:
31	chr8:124085491..124088248-chr8:124107597..124109815,2	K562	blood:
32	chr8:124136088..124138990-chr8:124140996..124143260,2	MCF-7	breast:
33	chr8:124107106..124109057-chr8:124110948..124112653,2	K562	blood:
34	chr8:124136088..124138990-chr8:124140996..124143260,2	MCF-7	breast:
35	chr8:124138462..124140007-chr8:124160075..124163019,2	K562	blood:
36	chr8:124132830..124135364-chr8:124139442..124142284,2	K562	blood:
37	chr8:124115548..124117952-chr8:124139707..124141973,2	K562	blood:
38	chr8:124132830..124135364-chr8:124139442..124142284,2	K562	blood:
39	chr8:124144944..124147685-chr8:124154381..124156517,2	K562	blood:
40	chr8:124113205..124115254-chr8:124116735..124119002,2	K562	blood:
41	chr8:124092114..124093955-chr8:124121687..124124209,2	K562	blood:
42	chr8:124113489..124116469-chr8:124118656..124121514,2	K562	blood:
43	chr8:124134100..124136026-chr8:124142874..124145469,2	MCF-7	breast:
44	chr8:124101511..124104352-chr8:124116261..124118453,2	MCF-7	breast:
45	chr8:124118101..124120061-chr8:124161025..124163344,2	MCF-7	breast:
46	chr8:124120136..124121650-chr8:124122714..124125221,2	K562	blood:
47	chr8:124086536..124087317-chr8:124124621..124125454,2	MCF-7	breast:
48	chr8:124098570..124100865-chr8:124113494..124116382,2	MCF-7	breast:
49	chr8:124136612..124138190-chr8:124144199..124146397,2	K562	blood:
50	chr8:124133634..124135408-chr8:124138761..124140483,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM83A-5	chr8:124135346-124135922	NONHSAT128512

No data

Variant related genes	Relation type
HMGB1P19	TF binding region
TBC1D31	TF binding region
ENSG00000253463	chromatin interactions
ENSG00000136986	chromatin interactions
ENSG00000156787	chromatin interactions

Extended variants
information (count: 1640 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:1640 , 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	rs138517508	chr8:124103268-124103269	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs559528207	chr8:124103305-124103306	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs540316197	chr8:124103316-124103317	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs528203846	chr8:124103318-124103319	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs542361799	chr8:124103333-124103334	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs1878776	chr8:124103395-124103396	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs188716776	chr8:124103409-124103410	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs144018662	chr8:124103445-124103446	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531200269	chr8:124103449-124103450	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs34076598	chr8:124103451-124103452	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs191560349	chr8:124103629-124103630	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570492553	chr8:124103727-124103728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs533201261	chr8:124103765-124103766	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs546680455	chr8:124103766-124103767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147287436	chr8:124103804-124103805	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535559366	chr8:124103842-124103843	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182541461	chr8:124103926-124103927	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs148641226	chr8:124103973-124103974	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs141199212	chr8:124103998-124103999	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557019095	chr8:124104036-124104037	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs75649096	chr8:124104045-124104046	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs62521770	chr8:124104070-124104071	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs28654188	chr8:124104084-124104085	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs373686234	chr8:124104098-124104099	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531462846	chr8:124104112-124104113	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs576269308	chr8:124104198-124104199	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541574968	chr8:124104270-124104271	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs544849705	chr8:124104283-124104284	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs150731148	chr8:124104315-124104316	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs531041035	chr8:124104316-124104317	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs191247404	chr8:124104352-124104353	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs564481384	chr8:124104380-124104381	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs368338997	chr8:124104400-124104401	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533457484	chr8:124104410-124104411	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs546545682	chr8:124104415-124104416	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs371880006	chr8:124104436-124104437	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs564727744	chr8:124104443-124104444	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs529356133	chr8:124104460-124104461	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs113045111	chr8:124104586-124104587	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs549236819	chr8:124104624-124104625	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568240345	chr8:124104639-124104640	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs139014939	chr8:124104648-124104649	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547845846	chr8:124104657-124104658	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs115036262	chr8:124104704-124104705	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539766071	chr8:124104772-124104773	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561982315	chr8:124104786-124104787	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs529052056	chr8:124104814-124104815	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs115995294	chr8:124104832-124104833	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572909565	chr8:124104834-124104835	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535513632	chr8:124104913-124104914	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:144)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:993 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124085800-124118800	Weak transcription	Small Intestine	intestine
2	chr8:124086000-124108600	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr8:124086000-124109600	Weak transcription	HMEC	breast
4	chr8:124086000-124111200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr8:124086000-124112400	Weak transcription	NH-A	brain
6	chr8:124086000-124113400	Weak transcription	Brain Angular Gyrus	brain
7	chr8:124086000-124115600	Weak transcription	Right Ventricle	heart
8	chr8:124086000-124115800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:124086000-124116200	Weak transcription	Brain Substantia Nigra	brain
10	chr8:124086000-124116600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr8:124086000-124117200	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr8:124086000-124117200	Weak transcription	HSMMtube	muscle
13	chr8:124086000-124146400	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr8:124086000-124154600	Weak transcription	Aorta	Aorta
15	chr8:124086000-124158400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:124086000-124168800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr8:124086000-124169000	Weak transcription	Colon Smooth Muscle	Colon
18	chr8:124086200-124115800	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr8:124086200-124122000	Weak transcription	Spleen	Spleen
20	chr8:124086200-124142200	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr8:124086200-124146400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr8:124086200-124168800	Weak transcription	Esophagus	oesophagus
23	chr8:124086400-124112000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr8:124086600-124145200	Weak transcription	Fetal Brain Male	brain
25	chr8:124086600-124168800	Weak transcription	Lung	lung
26	chr8:124086800-124114000	Weak transcription	Psoas Muscle	Psoas
27	chr8:124087000-124110200	Weak transcription	Brain Germinal Matrix	brain
28	chr8:124087200-124112400	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr8:124087200-124143800	Weak transcription	Fetal Kidney	kidney
30	chr8:124088600-124115800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:124089400-124116400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:124094200-124111200	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr8:124095200-124107400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr8:124095600-124111600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr8:124095600-124118000	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr8:124095800-124142800	Weak transcription	Fetal Intestine Small	intestine
37	chr8:124096200-124112800	Weak transcription	HSMM	muscle
38	chr8:124096200-124168800	Weak transcription	Liver	Liver
39	chr8:124096400-124118000	Weak transcription	Brain Anterior Caudate	brain
40	chr8:124096600-124108400	Weak transcription	HepG2	liver
41	chr8:124096600-124110000	Weak transcription	Duodenum Mucosa	Duodenum
42	chr8:124096600-124111600	Weak transcription	Fetal Brain Female	brain
43	chr8:124096600-124114000	Weak transcription	Fetal Lung	lung
44	chr8:124096600-124115800	Weak transcription	NHLF	lung
45	chr8:124096800-124110000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr8:124096800-124111000	Weak transcription	Fetal Intestine Large	intestine
47	chr8:124096800-124113200	Weak transcription	Adipose Nuclei	Adipose
48	chr8:124096800-124113400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr8:124097000-124108400	Weak transcription	NHEK	skin
50	chr8:124097000-124109400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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