Variant report

Variant	nsv6375
Chromosome Location	chr8:125056543-125087258
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:109)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:109 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:125083089-125083110	K562	blood:	n/a	n/a
2	BHLHE40	chr8:125083937-125084280	K562	blood:	n/a	n/a
3	CEBPB	chr8:125078226-125078448	IMR90	lung:	n/a	n/a
4	CEBPB	chr8:125073515-125073653	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:125060302-125060683	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr8:125060440-125060456	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:125073498-125073645	K562	blood:	n/a	n/a
8	CEBPB	chr8:125062053-125062472	ECC-1	luminal epithelium:	n/a	n/a
9	CHD2	chr8:125057469-125057522	GM12878	blood:	n/a	n/a
10	CTCF	chr8:125060600-125060750	AG04449	skin:	n/a	n/a
11	CTCF	chr8:125060540-125060690	HEK293	kidney:	n/a	n/a
12	CTCF	chr8:125060580-125060730	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr8:125060560-125060710	HMF	breast:	n/a	n/a
14	CTCF	chr8:125060560-125060710	GM12873	blood:	n/a	n/a
15	CTCF	chr8:125060320-125060470	RPTEC	kidney:	n/a	n/a
16	CTCF	chr8:125060660-125060810	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr8:125060600-125060750	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr8:125073580-125073730	HepG2	liver:	n/a	n/a
19	CTCF	chr8:125062740-125062890	HEK293	kidney:	n/a	chr8:125062778-125062791 chr8:125062789-125062798 chr8:125062785-125062798 chr8:125062780-125062790
20	CTCF	chr8:125060300-125060450	RPTEC	kidney:	n/a	n/a
21	CTCF	chr8:125073660-125073810	BE2_C	brain:	n/a	n/a
22	CTCF	chr8:125060660-125060810	HCFaa	heart:	n/a	n/a
23	CTCF	chr8:125060640-125060790	AG04450	lung:	n/a	n/a
24	CTCF	chr8:125083660-125083810	WI-38	lung:	n/a	n/a
25	CTCF	chr8:125060600-125060750	HPAF	blood vessel:	n/a	n/a
26	CTCF	chr8:125075084-125075190	K562	blood:	n/a	n/a
27	CTCF	chr8:125060620-125060770	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:125062660-125062810	GM12864	blood:	n/a	chr8:125062778-125062791 chr8:125062789-125062798 chr8:125062785-125062798 chr8:125062780-125062790
29	CTCF	chr8:125083155-125083180	GM20000	blood:	n/a	n/a
30	CTCF	chr8:125060600-125060750	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr8:125075020-125075170	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:125062680-125062830	GM12865	blood:	n/a	chr8:125062778-125062791 chr8:125062789-125062798 chr8:125062785-125062798 chr8:125062780-125062790
33	CTCF	chr8:125060620-125060770	GM12865	blood:	n/a	n/a
34	CTCF	chr8:125060600-125060750	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr8:125060620-125060770	AG04450	lung:	n/a	n/a
36	CTCF	chr8:125073940-125074090	SAEC	small airway:	n/a	n/a
37	CTCF	chr8:125073600-125073750	HAc	cerebellar:	n/a	n/a
38	CTCF	chr8:125060600-125060750	HCM	heart:	n/a	n/a
39	E2F4	chr8:125058814-125058836	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F6	chr8:125065827-125066182	H1-hESC	embryonic stem cell:	n/a	n/a
41	EP300	chr8:125061830-125062640	ECC-1	luminal epithelium:	n/a	chr8:125061831-125061845
42	EP300	chr8:125061902-125062582	ECC-1	luminal epithelium:	n/a	n/a
43	EP300	chr8:125056656-125057168	SK-N-SH_RA	brain:	n/a	chr8:125056856-125056872
44	EP300	chr8:125056655-125057203	SK-N-SH_RA	brain:	n/a	chr8:125056856-125056872
45	EP300	chr8:125056618-125057371	ECC-1	luminal epithelium:	n/a	chr8:125056856-125056872
46	ESR1	chr8:125056690-125057160	ECC-1	luminal epithelium:	n/a	n/a
47	ESR1	chr8:125061992-125062444	ECC-1	luminal epithelium:	n/a	n/a
48	ESR1	chr8:125056619-125057258	ECC-1	luminal epithelium:	n/a	n/a
49	ESR1	chr8:125061960-125062376	ECC-1	luminal epithelium:	n/a	n/a
50	ESR1	chr8:125061991-125062541	ECC-1	luminal epithelium:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr8:125066429..125069307-chr8:125073491..125075703,2	K562	blood:
2	chr8:125056975..125059050-chr8:125064590..125067107,2	MCF-7	breast:
3	chr8:125066429..125069307-chr8:125073491..125075703,2	K562	blood:
4	chr8:125052912..125056665-chr8:125383684..125385533,3	MCF-7	breast:
5	chr8:125078998..125082255-chr8:125082852..125085569,3	MCF-7	breast:
6	chr8:125067696..125069219-chr8:125081957..125084007,2	MCF-7	breast:
7	chr8:125079170..125082101-chr8:125082699..125084464,2	K562	blood:
8	chr8:125056975..125059050-chr8:125064590..125067107,2	MCF-7	breast:
9	chr8:125055470..125057405-chr8:125059184..125061018,2	K562	blood:
10	chr8:125066380..125069161-chr8:125069847..125072884,3	MCF-7	breast:
11	chr8:125055470..125057405-chr8:125059184..125061018,2	K562	blood:
12	chr8:125073277..125075066-chr8:125078530..125080434,2	K562	blood:
13	chr8:125079170..125082101-chr8:125082699..125084464,2	K562	blood:
14	chr8:125067696..125069219-chr8:125081957..125084007,2	MCF-7	breast:
15	chr8:125080809..125082492-chr8:125157999..125159766,2	MCF-7	breast:
16	chr8:125078998..125082255-chr8:125082852..125085569,3	MCF-7	breast:
17	chr8:125048985..125052591-chr8:125053625..125056640,3	MCF-7	breast:
18	chr8:125073277..125075066-chr8:125078530..125080434,2	K562	blood:
19	chr8:125053217..125056265-chr8:125057070..125060007,3	MCF-7	breast:
20	chr8:125066380..125069161-chr8:125069847..125072884,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM65-2	chr8:125058852-125059017	NONHSAT128575
2	lnc-TMEM65-5	chr8:125085611-125085653	ucscGeneNc_uc003yqx_1
3	lnc-TMEM65-5	chr8:125065559-125067194	ucscGeneNc_uc003yqx_1
4	lnc-TMEM65-2	chr8:125059798-125060310	NONHSAT128575

No data

Variant related genes	Relation type
ENSG00000254249	TF binding region
FER1L6-AS1	TF binding region
FER1L6-AS2	TF binding region
ENSG00000164983	chromatin interactions

Extended variants
information (count: 1175 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144588562	chr8:125056547-125056548	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs73328348	chr8:125056566-125056567	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs139432382	chr8:125056581-125056582	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs200242174	chr8:125056604-125056605	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs536890544	chr8:125056610-125056611	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs143967838	chr8:125056616-125056617	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs569842018	chr8:125056649-125056650	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs117954004	chr8:125056660-125056661	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs558544266	chr8:125056666-125056667	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs572365750	chr8:125056679-125056680	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs139840845	chr8:125056719-125056720	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs554082618	chr8:125056751-125056752	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs573845664	chr8:125056894-125056895	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs373577685	chr8:125056912-125056913	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs563234876	chr8:125056938-125056939	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs72714691	chr8:125056958-125056959	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs7003992	chr8:125056969-125056970	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs576229117	chr8:125056973-125056974	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs6984093	chr8:125056977-125056978	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs564726568	chr8:125057002-125057003	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs528342963	chr8:125057109-125057110	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs527326012	chr8:125057163-125057164	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs34517865	chr8:125057181-125057182	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs376615643	chr8:125057238-125057239	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs142109360	chr8:125057327-125057328	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs529209905	chr8:125057359-125057360	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs188906223	chr8:125057412-125057413	Bivalent Enhancer Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs193105690	chr8:125057483-125057484	Bivalent Enhancer Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs117633508	chr8:125057646-125057647	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185087581	chr8:125057673-125057674	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs151178562	chr8:125057700-125057701	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4871455	chr8:125057728-125057729	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs113399895	chr8:125057771-125057772	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs141032918	chr8:125057807-125057808	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs370377100	chr8:125057808-125057809	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545240128	chr8:125057834-125057835	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs149831272	chr8:125057847-125057848	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs145849116	chr8:125057881-125057882	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs189266336	chr8:125057884-125057885	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141869762	chr8:125057931-125057932	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs376667664	chr8:125057957-125057958	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs369117933	chr8:125057965-125057966	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373865928	chr8:125057977-125057978	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377618004	chr8:125057990-125057991	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs147024606	chr8:125058000-125058001	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs576255432	chr8:125058008-125058009	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs369635878	chr8:125058025-125058026	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373287444	chr8:125058037-125058038	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545218503	chr8:125058086-125058087	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs377489908	chr8:125058091-125058092	Weak transcription Strong transcription Enhancers	n/a	n/a	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
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
Schizophrenia	23813976	CNVD
Gastric cancer	18160780	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125052600-125083600	Weak transcription	Gastric	stomach
2	chr8:125053000-125060400	Weak transcription	Left Ventricle	heart
3	chr8:125053600-125058600	Enhancers	Fetal Heart	heart
4	chr8:125053800-125059800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:125053800-125062400	Weak transcription	Stomach Mucosa	stomach
6	chr8:125054200-125061000	Weak transcription	Fetal Stomach	stomach
7	chr8:125054400-125056600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:125054400-125056800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:125054600-125066800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr8:125055200-125057800	Enhancers	Fetal Intestine Small	intestine
11	chr8:125055400-125059400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:125056000-125057600	Enhancers	Fetal Intestine Large	intestine
13	chr8:125056200-125057200	Enhancers	Duodenum Mucosa	Duodenum
14	chr8:125056400-125056800	Enhancers	A549	lung
15	chr8:125056400-125057400	Enhancers	HepG2	liver
16	chr8:125056400-125060200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr8:125056600-125057200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:125056800-125057200	Enhancers	Pancreas	Pancrea
19	chr8:125056800-125057200	Enhancers	Sigmoid Colon	Sigmoid Colon
20	chr8:125056800-125057200	Flanking Active TSS	A549	lung
21	chr8:125056800-125057800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:125057000-125057200	Enhancers	Brain Germinal Matrix	brain
23	chr8:125057200-125057800	Enhancers	A549	lung
24	chr8:125057400-125057600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:125057800-125059400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:125057800-125062600	Weak transcription	Fetal Intestine Small	intestine
27	chr8:125058600-125059400	Weak transcription	Fetal Heart	heart
28	chr8:125059000-125065600	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr8:125059400-125060200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr8:125059400-125060200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr8:125059400-125060600	Enhancers	Fetal Heart	heart
32	chr8:125059800-125060400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:125059800-125060600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:125060200-125060600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:125060200-125060600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:125060200-125061200	Enhancers	Fetal Muscle Leg	muscle
37	chr8:125060400-125060800	Enhancers	Left Ventricle	heart
38	chr8:125060400-125061800	Bivalent Enhancer	HSMMtube	muscle
39	chr8:125060600-125061200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:125060600-125061800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:125061000-125062400	Strong transcription	Fetal Stomach	stomach
42	chr8:125061200-125064800	Weak transcription	Fetal Muscle Leg	muscle
43	chr8:125061800-125065400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr8:125062000-125062400	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr8:125062400-125064400	Strong transcription	Stomach Mucosa	stomach
46	chr8:125062400-125065400	Weak transcription	Fetal Stomach	stomach
47	chr8:125064400-125078600	Weak transcription	Stomach Mucosa	stomach
48	chr8:125064800-125067000	Enhancers	Fetal Muscle Leg	muscle
49	chr8:125065200-125065600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr8:125065200-125067200	Enhancers	Cortex derived primary cultured neurospheres	brain

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