Variant report

Variant	esv3344377
Chromosome Location	chr8:125313371-125316194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:125313806-125313810	A549	lung:	n/a	n/a
2	E2F4	chr8:125315177-125315364	MCF10A-Er-Src	breast:	n/a	n/a
3	MYC	chr8:125313705-125313809	GM12878	blood:	n/a	n/a
4	MYC	chr8:125313813-125313835	GM12878	blood:	n/a	n/a
5	MYC	chr8:125313627-125314099	MCF-7	breast:	n/a	n/a
6	MYC	chr8:125313606-125314013	MCF-7	breast:	n/a	n/a
7	POLR2A	chr8:125313615-125313754	MCF-7	breast:	n/a	n/a
8	POLR2A	chr8:125313599-125314006	A549	lung:	n/a	n/a
9	POLR2A	chr8:125313672-125313810	K562	blood:	n/a	n/a
10	POLR2A	chr8:125313568-125313879	H1-hESC	embryonic stem cell:	n/a	n/a
11	POLR2A	chr8:125313607-125313613	MCF-7	breast:	n/a	n/a
12	POLR2A	chr8:125313578-125314075	MCF-7	breast:	n/a	n/a
13	POLR2A	chr8:125313420-125313726	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr8:125313594-125313710	ProgFib	skin:	n/a	n/a
15	POLR2A	chr8:125313889-125313940	ProgFib	skin:	n/a	n/a
16	POLR2A	chr8:125313539-125313918	A549	lung:	n/a	n/a
17	POLR2A	chr8:125313362-125314142	PFSK-1	brain:	n/a	n/a
18	POLR2A	chr8:125313798-125314064	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr8:125313589-125313741	A549	lung:	n/a	n/a
20	POLR2A	chr8:125313728-125313871	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr8:125313515-125314100	MCF-7	breast:	n/a	n/a
22	POLR2A	chr8:125313618-125313631	K562	blood:	n/a	n/a
23	POLR2A	chr8:125315960-125316590	A549	lung:	n/a	n/a
24	POLR2A	chr8:125315493-125315527	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr8:125316018-125316024	HepG2	liver:	n/a	n/a
26	POLR2A	chr8:125313764-125313787	MCF-7	breast:	n/a	n/a
27	RFX5	chr8:125316041-125316045	HepG2	liver:	n/a	n/a
28	SETDB1	chr8:125315896-125316170	U2OS	brain:	n/a	n/a
29	YY1	chr8:125315823-125316107	H1-hESC	embryonic stem cell:	n/a	chr8:125315978-125315990 chr8:125315959-125315971
30	YY1	chr8:125315824-125316135	K562	blood:	n/a	chr8:125315978-125315990 chr8:125315959-125315971
31	YY1	chr8:125315926-125316004	K562	blood:	n/a	chr8:125315978-125315990 chr8:125315959-125315971
32	YY1	chr8:125315817-125316187	K562	blood:	n/a	chr8:125315978-125315990 chr8:125315959-125315971

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125313573-125313623	HAEpiC	amniotic membrane:	n/a
2	chr8:125313940-125313990	SK-N-MC	brain:	n/a
3	chr8:125313940-125313990	NHDF-neo	bronchial:	n/a
4	chr8:125315065-125315115	AG04450	lung:	fetal
5	chr8:125313885-125313935	A549	lung:	n/a
6	chr8:125313940-125313990	U87	brain:	n/a
7	chr8:125313573-125313623	ProgFib	skin:	n/a
8	chr8:125313573-125313623	SKMC	muscle:	n/a
9	chr8:125313573-125313623	MCF-7	breast:	n/a
10	chr8:125313573-125313623	ovcar-3	ovarian:	n/a
11	chr8:125313573-125313623	LNCaP	prostate:	n/a
12	chr8:125313940-125313990	SK-N-SH	brain:	n/a
13	chr8:125315065-125315115	NB4	blood:	n/a
14	chr8:125315065-125315115	CMK	blood:	n/a
15	chr8:125313573-125313623	Hepatocyte	liver:	n/a
16	chr8:125313940-125313990	PFSK-1	brain:	n/a
17	chr8:125313573-125313623	HepG2	liver:	n/a
18	chr8:125313940-125313990	HUVEC	blood vessel:	n/a
19	chr8:125313885-125313935	NHBE	bronchial:	n/a
20	chr8:125313940-125313990	HCT-116	colon:	n/a
21	chr8:125313940-125313990	HPAEpiC	pulmonary alveolar:	n/a
22	chr8:125315065-125315115	SK-N-SH_RA	brain:	n/a
23	chr8:125315065-125315115	ovcar-3	ovarian:	n/a
24	chr8:125315065-125315115	HCF	heart:	n/a
25	chr8:125313885-125313935	SK-N-SH	brain:	n/a
26	chr8:125313885-125313935	MCF10A-Er-Src	breast:	n/a
27	chr8:125313885-125313935	GM12891	blood:	n/a
28	chr8:125313940-125313990	MCF-7	breast:	n/a
29	chr8:125313573-125313623	T-47D	breast:	n/a
30	chr8:125315065-125315115	GM12878	blood:	n/a
31	chr8:125313573-125313623	NHDF-neo	bronchial:	n/a
32	chr8:125313940-125313990	HEK293	kidney:	embryo
33	chr8:125313573-125313623	AG04449	skin:	fetal
34	chr8:125313940-125313990	ovcar-3	ovarian:	n/a
35	chr8:125313573-125313623	NHBE	bronchial:	n/a
36	chr8:125313885-125313935	AG10803	skin:	n/a
37	chr8:125313573-125313623	NH-A	brain:	n/a
38	chr8:125313573-125313623	Hela-S3	cervix:	n/a
39	chr8:125315065-125315115	GM19239	blood:	n/a
40	chr8:125315065-125315115	NHBE	bronchial:	n/a
41	chr8:125313885-125313935	ECC-1	luminal epithelium:	n/a
42	chr8:125313573-125313623	AG10803	skin:	n/a
43	chr8:125313885-125313935	IMR90	lung:	fetal
44	chr8:125315065-125315115	HEEpiC	esophagus:	n/a
45	chr8:125313573-125313623	IMR90	lung:	fetal
46	chr8:125315065-125315115	Caco-2	colon:	n/a
47	chr8:125313573-125313623	HCF	heart:	n/a
48	chr8:125313885-125313935	HEEpiC	esophagus:	n/a
49	chr8:125313573-125313623	CMK	blood:	n/a
50	chr8:125313940-125313990	Jurkat	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:125307762..125311080-chr8:125313612..125318794,4	K562	blood:
2	chr8:125292376..125294565-chr8:125310968..125313467,2	MCF-7	breast:
3	chr8:125309455..125311025-chr8:125315072..125317526,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000237586	TF binding region
ENSG00000237586	CpG island

Extended variants
information (count: 156 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:156 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374792504	chr8:125313392-125313393	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs565604721	chr8:125313393-125313394	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542058810	chr8:125313397-125313398	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs78364264	chr8:125313398-125313399	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs554445122	chr8:125313415-125313416	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs149896986	chr8:125313466-125313467	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs536736531	chr8:125313490-125313491	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs556975556	chr8:125313503-125313504	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs576907844	chr8:125313510-125313511	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs545785161	chr8:125313528-125313529	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549718279	chr8:125313532-125313533	ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs573558540	chr8:125313558-125313559	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs143958075	chr8:125313593-125313594	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs79897377	chr8:125313634-125313635	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562134809	chr8:125313656-125313657	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs529207572	chr8:125313661-125313662	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531094911	chr8:125313677-125313678	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191800089	chr8:125313695-125313696	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372082355	chr8:125313747-125313748	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533171544	chr8:125313748-125313749	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113553967	chr8:125313773-125313774	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6991465	chr8:125313780-125313781	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs528370976	chr8:125313817-125313818	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548404204	chr8:125313853-125313854	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs557244863	chr8:125313909-125313910	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs367594612	chr8:125313922-125313923	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537201229	chr8:125313924-125313925	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556798449	chr8:125313938-125313939	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115222318	chr8:125313940-125313941	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs55962822	chr8:125313943-125313944	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539471169	chr8:125313948-125313949	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553003625	chr8:125313956-125313957	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573621631	chr8:125313977-125313978	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs61733521	chr8:125314015-125314016	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs74890352	chr8:125314055-125314056	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs368511004	chr8:125314111-125314112	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs575772136	chr8:125314131-125314132	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs142922914	chr8:125314158-125314159	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs564274847	chr8:125314174-125314175	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs533230853	chr8:125314187-125314188	ZNF genes & repeats Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs372124688	chr8:125314230-125314231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377542038	chr8:125314237-125314238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13268480	chr8:125314259-125314260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs370787513	chr8:125314260-125314261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13270868	chr8:125314261-125314262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs13270881	chr8:125314268-125314269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375828869	chr8:125314269-125314270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13268492	chr8:125314270-125314271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543673452	chr8:125314287-125314288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561545407	chr8:125314301-125314302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

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
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125301400-125329800	Weak transcription	HSMMtube	muscle
2	chr8:125304400-125313600	Weak transcription	Left Ventricle	heart
3	chr8:125304600-125317800	Weak transcription	Fetal Heart	heart
4	chr8:125306200-125328000	Weak transcription	A549	lung
5	chr8:125309400-125331000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr8:125311200-125333600	Weak transcription	Right Ventricle	heart
7	chr8:125312000-125320200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr8:125312000-125323800	Weak transcription	Aorta	Aorta
9	chr8:125312000-125330800	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr8:125312400-125313600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr8:125312400-125319400	Weak transcription	Primary T cells from cord blood	blood
12	chr8:125312400-125331000	Weak transcription	Duodenum Mucosa	Duodenum
13	chr8:125312600-125326000	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr8:125312600-125328000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr8:125312600-125329800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr8:125312600-125329800	Weak transcription	Thymus	Thymus
17	chr8:125312600-125330000	Weak transcription	Fetal Stomach	stomach
18	chr8:125312600-125333000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr8:125312600-125346000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr8:125312800-125313400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:125312800-125316400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:125312800-125319200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:125312800-125323600	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr8:125312800-125329800	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr8:125312800-125329800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr8:125312800-125331600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr8:125312800-125337800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr8:125313000-125313400	Active TSS	Placenta	Placenta
29	chr8:125313400-125313600	Flanking Active TSS	Placenta	Placenta
30	chr8:125313400-125314200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr8:125313400-125314200	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr8:125313400-125314200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr8:125313400-125329800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr8:125313600-125314000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:125313600-125314000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:125313600-125314000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
37	chr8:125313600-125314000	Flanking Bivalent TSS/Enh	Placenta	Placenta
38	chr8:125313600-125314000	Genic enhancers	Left Ventricle	heart
39	chr8:125313600-125314200	ZNF genes & repeats	Fetal Intestine Small	intestine
40	chr8:125314000-125314200	Flanking Active TSS	Placenta	Placenta
41	chr8:125314000-125320200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr8:125314000-125326200	Weak transcription	Colon Smooth Muscle	Colon
43	chr8:125314000-125330000	Weak transcription	Left Ventricle	heart
44	chr8:125314200-125316400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr8:125314200-125330000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr8:125314200-125332000	Weak transcription	Fetal Intestine Small	intestine
47	chr8:125314200-125340200	Weak transcription	Placenta	Placenta
48	chr8:125315800-125333000	Weak transcription	NH-A	brain

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