Variant report

Variant	nsv971700
Chromosome Location	chr8:125575569-125576444
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:48)
CpG islands
(count:62)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:48 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:125575830-125576206	HepG2	liver:	n/a	chr8:125575860-125575876
2	BCL3	chr8:125575859-125576156	GM12878	blood:	n/a	n/a
3	BCL3	chr8:125575852-125576113	GM12878	blood:	n/a	n/a
4	BHLHE40	chr8:125575860-125576236	HepG2	liver:	n/a	n/a
5	CBX3	chr8:125576389-125577323	K562	blood:	n/a	n/a
6	CEBPB	chr8:125575909-125576108	HepG2	liver:	n/a	n/a
7	EP300	chr8:125575698-125576276	T-47D	breast:	n/a	chr8:125576028-125576035 chr8:125575987-125575997 chr8:125576005-125576015
8	EP300	chr8:125575429-125576314	T-47D	breast:	n/a	chr8:125576028-125576035 chr8:125575987-125575997 chr8:125576005-125576015
9	ESR1	chr8:125575742-125576153	T-47D	breast:	n/a	n/a
10	ESR1	chr8:125575515-125576233	T-47D	breast:	n/a	n/a
11	ESR1	chr8:125575518-125576196	T-47D	breast:	n/a	n/a
12	ESR1	chr8:125575496-125576161	T-47D	breast:	n/a	n/a
13	ESR1	chr8:125575526-125576177	T-47D	breast:	n/a	n/a
14	FOSL2	chr8:125575774-125576184	HepG2	liver:	n/a	n/a
15	FOSL2	chr8:125575745-125576349	MCF-7	breast:	n/a	n/a
16	FOSL2	chr8:125575857-125576239	HepG2	liver:	n/a	n/a
17	FOXA1	chr8:125575668-125576282	HepG2	liver:	n/a	chr8:125576004-125576019 chr8:125575982-125575997
18	FOXA1	chr8:125575693-125576283	HepG2	liver:	n/a	chr8:125576004-125576019 chr8:125575982-125575997
19	FOXA1	chr8:125575692-125576167	HepG2	liver:	n/a	chr8:125576004-125576019 chr8:125575982-125575997
20	FOXA1	chr8:125575845-125576185	HepG2	liver:	n/a	chr8:125576004-125576019 chr8:125575982-125575997
21	FOXA1	chr8:125575576-125576185	T-47D	breast:	n/a	chr8:125576004-125576019 chr8:125575982-125575997
22	FOXA1	chr8:125575760-125576232	T-47D	breast:	n/a	chr8:125576004-125576019 chr8:125575982-125575997
23	FOXA2	chr8:125575844-125576193	A549	lung:	n/a	n/a
24	FOXA2	chr8:125575872-125576127	HepG2	liver:	n/a	n/a
25	FOXA2	chr8:125575852-125576179	A549	lung:	n/a	n/a
26	FOXA2	chr8:125575470-125576393	HepG2	liver:	n/a	n/a
27	GATA3	chr8:125575521-125576275	T-47D	breast:	n/a	n/a
28	GATA3	chr8:125575552-125576244	T-47D	breast:	n/a	n/a
29	HNF4A	chr8:125575888-125576182	HepG2	liver:	n/a	chr8:125575986-125575994
30	JUND	chr8:125575949-125576025	HepG2	liver:	n/a	n/a
31	JUND	chr8:125575909-125576130	HepG2	liver:	n/a	n/a
32	MAFF	chr8:125575754-125575950	HepG2	liver:	n/a	n/a
33	MAFK	chr8:125575692-125576083	HepG2	liver:	n/a	n/a
34	MAFK	chr8:125575876-125576076	HepG2	liver:	n/a	n/a
35	MAX	chr8:125575095-125576266	MCF-7	breast:	n/a	n/a
36	MAX	chr8:125575417-125576297	HepG2	liver:	n/a	n/a
37	MAX	chr8:125575886-125576045	HepG2	liver:	n/a	n/a
38	MBD4	chr8:125575748-125576165	HepG2	liver:	n/a	n/a
39	MXI1	chr8:125575625-125576185	HepG2	liver:	n/a	chr8:125575708-125575717
40	MYBL2	chr8:125575543-125576229	HepG2	liver:	n/a	n/a
41	NFIC	chr8:125575578-125576188	HepG2	liver:	n/a	n/a
42	PBX3	chr8:125575827-125576033	GM12878	blood:	n/a	n/a
43	POLR2A	chr8:125576076-125576346	HepG2	liver:	n/a	n/a
44	POLR2A	chr8:125575632-125575898	HepG2	liver:	n/a	n/a
45	POLR2A	chr8:125575278-125575831	HepG2	liver:	n/a	n/a
46	RCOR1	chr8:125576014-125576149	HepG2	liver:	n/a	n/a
47	RXRA	chr8:125575822-125576137	HepG2	liver:	n/a	n/a
48	SP1	chr8:125575739-125576130	HepG2	liver:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125576109-125576159	H1-hESC	embryonic stem cell:	embryo
2	chr8:125576109-125576159	H1-hESC	embryonic stem cell:	embryo
3	chr8:125576109-125576159	AG09309	skin:	n/a
4	chr8:125576109-125576159	NB4	blood:	n/a
5	chr8:125576109-125576159	T-47D	breast:	n/a
6	chr8:125576109-125576159	HAEpiC	amniotic membrane:	n/a
7	chr8:125576109-125576159	GM12891	blood:	n/a
8	chr8:125576109-125576159	GM12892	blood:	n/a
9	chr8:125576109-125576159	HCPEpiC	choroid plexus:	n/a
10	chr8:125576109-125576159	MCF-7	breast:	n/a
11	chr8:125576109-125576159	HL-60	blood:	n/a
12	chr8:125576109-125576159	HRCEpiC	kidney:	n/a
13	chr8:125576109-125576159	BJ	skin:	n/a
14	chr8:125576109-125576159	HNPCEpiC	eye:	n/a
15	chr8:125576109-125576159	BE2_C	brain:	n/a
16	chr8:125576109-125576159	AG04450	lung:	fetal
17	chr8:125576109-125576159	HIPEpiC	eye:	n/a
18	chr8:125576109-125576159	NHDF-neo	bronchial:	n/a
19	chr8:125576109-125576159	PrEC	prostate:	n/a
20	chr8:125576109-125576159	U87	brain:	n/a
21	chr8:125576109-125576159	NHBE	bronchial:	n/a
22	chr8:125576109-125576159	MCF10A-Er-Src	breast:	n/a
23	chr8:125576109-125576159	HepG2	liver:	n/a
24	chr8:125576109-125576159	ProgFib	skin:	n/a
25	chr8:125576109-125576159	HEK293	kidney:	embryo
26	chr8:125576109-125576159	HCT-116	colon:	n/a
27	chr8:125576109-125576159	NT2-D1	testis:	n/a
28	chr8:125576109-125576159	AG04449	skin:	fetal
29	chr8:125576109-125576159	Hela-S3	cervix:	n/a
30	chr8:125576109-125576159	K562	blood:	n/a
31	chr8:125576109-125576159	PANC-1	pancreas:	n/a
32	chr8:125576109-125576159	CMK	blood:	n/a
33	chr8:125576109-125576159	HEEpiC	esophagus:	n/a
34	chr8:125576109-125576159	Caco-2	colon:	n/a
35	chr8:125576109-125576159	SAEC	small airway:	n/a
36	chr8:125576109-125576159	IMR90	lung:	fetal
37	chr8:125576109-125576159	LNCaP	prostate:	n/a
38	chr8:125576109-125576159	HCF	heart:	n/a
39	chr8:125576109-125576159	SK-N-MC	brain:	n/a
40	chr8:125576109-125576159	GM19239	blood:	n/a
41	chr8:125576109-125576159	HCM	heart:	n/a
42	chr8:125576109-125576159	ovcar-3	ovarian:	n/a
43	chr8:125576109-125576159	HMEC	breast:	n/a
44	chr8:125576109-125576159	ECC-1	luminal epithelium:	n/a
45	chr8:125576109-125576159	AG10803	skin:	n/a
46	chr8:125576109-125576159	A549	lung:	n/a
47	chr8:125576109-125576159	GM12878	blood:	n/a
48	chr8:125576109-125576159	HRE	kidney:	n/a
49	chr8:125576109-125576159	SKMC	muscle:	n/a
50	chr8:125576109-125576159	SK-N-SH	brain:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:125549460..125555106-chr8:125573452..125578755,9	MCF-7	breast:
2	chr8:125574370..125578079-chr8:125630160..125632086,3	MCF-7	breast:
3	chr8:125572972..125577628-chr8:125578200..125582090,6	MCF-7	breast:
4	chr8:125486165..125488789-chr8:125574025..125577553,3	MCF-7	breast:
5	chr8:125560928..125566588-chr8:125566852..125577107,17	MCF-7	breast:
6	chr8:125575430..125576994-chr8:125827635..125829466,2	K562	blood:
7	chr8:125576007..125577952-chr8:125590257..125591907,2	MCF-7	breast:
8	chr8:125573757..125577202-chr8:125578987..125583404,3	MCF-7	breast:
9	chr8:125572673..125575871-chr8:125577015..125582400,6	K562	blood:
10	chr8:125567601..125570100-chr8:125573465..125576752,3	MCF-7	breast:
11	chr8:125548205..125551096-chr8:125575812..125578141,2	MCF-7	breast:
12	chr8:125569223..125571926-chr8:125574045..125576529,2	K562	blood:

No data

Variant related genes	Relation type
MTSS1	TF binding region
MTSS1	CpG island
ENSG00000147687	chromatin interactions
ENSG00000147684	chromatin interactions
ENSG00000170873	chromatin interactions
ENSG00000255491	chromatin interactions
ENSG00000170881	chromatin interactions
ENSG00000245149	chromatin interactions
ENSG00000272486	chromatin interactions

Extended variants
information (count: 36 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:36 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139091013	chr8:125575585-125575586	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs10110655	chr8:125575619-125575620	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561002071	chr8:125575648-125575649	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs16899704	chr8:125575651-125575652	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs569461160	chr8:125575660-125575661	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs188250434	chr8:125575664-125575665	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs144010996	chr8:125575696-125575697	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs373091206	chr8:125575703-125575704	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs578261595	chr8:125575742-125575743	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs72714721	chr8:125575777-125575778	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs180713115	chr8:125575791-125575792	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs11783209	chr8:125575803-125575804	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs539361735	chr8:125575825-125575826	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs558865650	chr8:125575947-125575948	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs184359696	chr8:125575962-125575963	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs146441602	chr8:125575978-125575979	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs190517527	chr8:125576004-125576005	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs182263652	chr8:125576017-125576018	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs10099056	chr8:125576082-125576083	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs10099060	chr8:125576094-125576095	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185786340	chr8:125576126-125576127	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs528943809	chr8:125576142-125576143	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs546185593	chr8:125576143-125576144	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs370837581	chr8:125576144-125576145	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs559264526	chr8:125576149-125576150	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs550904363	chr8:125576184-125576185	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs373162010	chr8:125576185-125576186	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs529795036	chr8:125576189-125576190	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs373504576	chr8:125576214-125576215	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs139867272	chr8:125576228-125576229	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs376033190	chr8:125576287-125576288	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs142908389	chr8:125576347-125576348	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs190688261	chr8:125576358-125576359	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs550319451	chr8:125576365-125576366	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs574540011	chr8:125576371-125576372	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs57897740	chr8:125576392-125576393	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:146)

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
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
Acute myeloid leukemia	20729466	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
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21240255	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125553800-125581200	Strong transcription	Fetal Brain Female	brain
2	chr8:125554200-125576200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr8:125554400-125576200	Strong transcription	Fetal Intestine Large	intestine
4	chr8:125554600-125575800	Strong transcription	Stomach Smooth Muscle	stomach
5	chr8:125556800-125576800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:125558000-125575600	Weak transcription	Stomach Mucosa	stomach
7	chr8:125561400-125575600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:125563600-125575600	Strong transcription	Fetal Stomach	stomach
9	chr8:125564000-125575600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:125564400-125576800	Strong transcription	Fetal Intestine Small	intestine
11	chr8:125566000-125576400	Weak transcription	GM12878-XiMat	blood
12	chr8:125566000-125602400	Weak transcription	Aorta	Aorta
13	chr8:125566200-125575800	Weak transcription	NHDF-Ad	bronchial
14	chr8:125566200-125590400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:125566400-125575800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr8:125566400-125575800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr8:125566400-125577600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:125566400-125577800	Weak transcription	Small Intestine	intestine
19	chr8:125566400-125600600	Weak transcription	NHEK	skin
20	chr8:125566600-125576400	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr8:125566600-125577200	Weak transcription	Osteobl	bone
22	chr8:125566800-125581400	Weak transcription	HSMM	muscle
23	chr8:125567000-125590200	Weak transcription	Fetal Brain Male	brain
24	chr8:125567200-125576200	Weak transcription	Fetal Heart	heart
25	chr8:125568200-125575600	Weak transcription	Duodenum Mucosa	Duodenum
26	chr8:125568200-125577000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr8:125568400-125575800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr8:125568600-125576400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:125568800-125575600	Weak transcription	Ovary	ovary
30	chr8:125568800-125576400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr8:125570000-125584800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:125570800-125575600	Strong transcription	Brain Inferior Temporal Lobe	brain
33	chr8:125570800-125605000	Weak transcription	Colon Smooth Muscle	Colon
34	chr8:125571400-125575600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr8:125571800-125581200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:125572000-125577000	Weak transcription	NHLF	lung
37	chr8:125572400-125575800	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr8:125572400-125575800	Weak transcription	Brain Substantia Nigra	brain
39	chr8:125572400-125576400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr8:125573400-125575800	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr8:125573800-125575600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr8:125573800-125575800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:125574000-125575600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr8:125574000-125575600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
45	chr8:125574000-125575600	Strong transcription	Brain Anterior Caudate	brain
46	chr8:125574200-125575600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr8:125574200-125575600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr8:125574200-125575600	Genic enhancers	Fetal Kidney	kidney
49	chr8:125574200-125576000	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr8:125574200-125576000	Weak transcription	Colonic Mucosa	Colon

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