Variant report

Variant	nsv611672
Chromosome Location	chr8:86846445-86886950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:577)
CpG islands
(count:0)
Chromatin interactive
region (count:59)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:577 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86860057-86860260	K562	blood:	n/a	n/a
2	ARID3A	chr8:86878872-86879538	K562	blood:	n/a	n/a
3	ARID3A	chr8:86877891-86877975	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:86860947-86861211	K562	blood:	n/a	n/a
5	ARID3A	chr8:86860674-86860711	K562	blood:	n/a	n/a
6	ARID3A	chr8:86868281-86868466	K562	blood:	n/a	n/a
7	ARID3A	chr8:86855400-86856788	K562	blood:	n/a	chr8:86856408-86856424
8	ARID3A	chr8:86873919-86874476	K562	blood:	n/a	n/a
9	ARID3A	chr8:86854067-86854193	K562	blood:	n/a	n/a
10	ARID3A	chr8:86848202-86848466	K562	blood:	n/a	n/a
11	ARID3A	chr8:86851632-86852291	K562	blood:	n/a	n/a
12	ATF1	chr8:86851680-86851940	K562	blood:	n/a	n/a
13	ATF1	chr8:86858572-86858850	K562	blood:	n/a	n/a
14	ATF3	chr8:86853960-86854338	K562	blood:	n/a	n/a
15	ATF3	chr8:86848176-86848532	K562	blood:	n/a	n/a
16	BACH1	chr8:86878970-86879079	K562	blood:	n/a	n/a
17	BACH1	chr8:86873787-86874392	K562	blood:	n/a	n/a
18	BACH1	chr8:86873756-86874253	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:86854704-86854857	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr8:86848360-86848557	K562	blood:	n/a	n/a
21	BACH1	chr8:86855556-86855909	K562	blood:	n/a	n/a
22	BHLHE40	chr8:86860851-86861210	K562	blood:	n/a	n/a
23	BHLHE40	chr8:86848213-86848489	K562	blood:	n/a	n/a
24	BHLHE40	chr8:86851452-86852081	K562	blood:	n/a	n/a
25	BHLHE40	chr8:86878900-86879572	K562	blood:	n/a	n/a
26	BHLHE40	chr8:86864850-86864971	K562	blood:	n/a	n/a
27	CBX3	chr8:86882637-86883016	K562	blood:	n/a	n/a
28	CBX3	chr8:86878808-86879237	K562	blood:	n/a	n/a
29	CBX3	chr8:86855246-86855994	K562	blood:	n/a	n/a
30	CBX3	chr8:86848116-86848555	K562	blood:	n/a	n/a
31	CCNT2	chr8:86851412-86851908	K562	blood:	n/a	n/a
32	CCNT2	chr8:86855767-86856007	K562	blood:	n/a	n/a
33	CCNT2	chr8:86878585-86879466	K562	blood:	n/a	chr8:86879008-86879028
34	CEBPB	chr8:86855387-86855903	K562	blood:	n/a	n/a
35	CEBPB	chr8:86855406-86856007	MCF-7	breast:	n/a	n/a
36	CEBPB	chr8:86874027-86874656	Hela-S3	cervix:	n/a	chr8:86874482-86874493
37	CEBPB	chr8:86874245-86874687	MCF-7	breast:	n/a	chr8:86874482-86874493
38	CEBPB	chr8:86847793-86848810	A549	lung:	n/a	chr8:86848372-86848383
39	CEBPB	chr8:86847697-86849448	Hela-S3	cervix:	n/a	chr8:86848372-86848383
40	CEBPB	chr8:86847845-86848785	K562	blood:	n/a	chr8:86848372-86848383
41	CEBPB	chr8:86874396-86874633	K562	blood:	n/a	chr8:86874482-86874493
42	CEBPB	chr8:86848109-86848565	ECC-1	luminal epithelium:	n/a	chr8:86848372-86848383
43	CEBPB	chr8:86858898-86859037	HepG2	liver:	n/a	chr8:86858989-86859000
44	CEBPB	chr8:86874267-86874692	ECC-1	luminal epithelium:	n/a	chr8:86874482-86874493
45	CEBPB	chr8:86854020-86854265	K562	blood:	n/a	n/a
46	CEBPB	chr8:86848192-86848660	H1-hESC	embryonic stem cell:	n/a	chr8:86848372-86848383
47	CEBPB	chr8:86874268-86874695	ECC-1	luminal epithelium:	n/a	chr8:86874482-86874493
48	CEBPB	chr8:86877329-86877486	K562	blood:	n/a	n/a
49	CEBPB	chr8:86848166-86848569	HepG2	liver:	n/a	chr8:86848372-86848383
50	CEBPB	chr8:86852955-86853850	MCF-7	breast:	n/a	chr8:86853134-86853151

No data

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:86866655..86868927-chr8:86870590..86874049,3	K562	blood:
2	chr8:86373353..86377706-chr8:86848632..86856784,15	MCF-7	breast:
3	chr8:86877063..86879169-chr8:86913425..86915050,2	K562	blood:
4	chr8:86852733..86854770-chr8:86972857..86974930,2	K562	blood:
5	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
6	chr16:75285561..75287264-chr8:86851129..86852972,2	MCF-7	breast:
7	chr8:86864135..86865739-chr8:86867994..86869726,2	K562	blood:
8	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
9	chr8:86850726..86853148-chr8:86853230..86857704,4	K562	blood:
10	chr8:86464673..86465447-chr8:86852772..86853973,3	MCF-7	breast:
11	chr8:86854974..86856986-chr8:86861959..86864314,2	MCF-7	breast:
12	chr8:86852831..86853539-chr8:86919503..86920015,2	MCF-7	breast:
13	chr8:86852235..86854715-chr8:86982807..86985769,2	MCF-7	breast:
14	chr8:86849418..86851109-chr8:86874092..86876828,2	MCF-7	breast:
15	chr8:86852107..86854370-chr8:86972859..86974722,2	MCF-7	breast:
16	chr8:86863160..86866224-chr8:86868226..86872946,5	K562	blood:
17	chr8:86855854..86858675-chr8:86858692..86862985,4	K562	blood:
18	chr8:86853239..86855144-chr8:86935082..86937255,2	MCF-7	breast:
19	chr8:86865438..86867152-chr8:86874296..86876870,2	MCF-7	breast:
20	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:
21	chr8:86876992..86879169-chr8:86912945..86915050,2	K562	blood:
22	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
23	chr8:86852831..86853452-chr8:86919492..86920015,2	MCF-7	breast:
24	chr8:86866655..86868927-chr8:86870590..86874049,3	K562	blood:
25	chr8:86848347..86850172-chr8:86983643..86985301,2	MCF-7	breast:
26	chr8:86842328..86846143-chr8:86846375..86849662,4	K562	blood:
27	chr8:86854583..86856864-chr8:86887493..86890271,2	MCF-7	breast:
28	chr8:86375109..86376361-chr8:86852746..86853757,4	MCF-7	breast:
29	chr8:86849418..86851109-chr8:86874092..86876828,2	MCF-7	breast:
30	chr8:86866810..86870482-chr8:86870568..86874255,4	K562	blood:
31	chr8:86864135..86865739-chr8:86867994..86869726,2	K562	blood:
32	chr8:86853239..86855562-chr8:86941096..86942635,2	MCF-7	breast:
33	chr8:86855854..86858107-chr8:86860014..86862808,3	K562	blood:
34	chr8:86843222..86846042-chr8:86847745..86849520,2	K562	blood:
35	chr8:86863160..86866224-chr8:86868226..86872946,5	K562	blood:
36	chr8:86853468..86855962-chr8:86866121..86867816,2	MCF-7	breast:
37	chr8:86849344..86852342-chr8:86863151..86865379,2	K562	blood:
38	chr8:86847849..86857260-chr8:86866079..86880479,25	MCF-7	breast:
39	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:
40	chr8:86853963..86856746-chr8:86949985..86952408,2	K562	blood:
41	chr8:86867877..86870175-chr8:86957602..86960658,3	K562	blood:
42	chr8:86854256..86855844-chr8:86962935..86965322,2	K562	blood:
43	chr8:86853963..86856698-chr8:86950908..86953530,2	K562	blood:
44	chr8:86849039..86851736-chr8:87015052..87016845,2	MCF-7	breast:
45	chr3:61613244..61613971-chr8:86852933..86853873,2	MCF-7	breast:
46	chr8:86873909..86875817-chr8:86877327..86879783,3	K562	blood:
47	chr8:86868209..86870416-chr8:86917445..86919044,2	K562	blood:
48	chr8:86852142..86856180-chr8:86917083..86921619,8	MCF-7	breast:
49	chr8:86864951..86867156-chr8:86950288..86952196,2	K562	blood:
50	chr8:86855992..86858469-chr8:86859660..86861283,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-REXO1L2P-2	chr8:86866739-86866829	XLOC_007141
2	lnc-REXO1L2P-2	chr8:86864119-86865001	XLOC_007141
3	lnc-ATP6V0D2-2	chr8:86851934-86852014	NONHSAT127540
4	lnc-ATP6V0D2-2	chr8:86851934-86852014	ENSG00000253154

No data

Variant related genes	Relation type
ENSG00000253154	TF binding region
ENSG00000050820	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000253154	chromatin interactions
ENSG00000104267	chromatin interactions

Extended variants
information (count: 1439 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1439 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2980372	chr8:86846445-86846446	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs545926177	chr8:86846556-86846557	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549240684	chr8:86846566-86846567	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs192039414	chr8:86846572-86846573	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs115887813	chr8:86846597-86846598	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs4378008	chr8:86846628-86846629	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs571837491	chr8:86846672-86846673	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs4563937	chr8:86846748-86846749	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs372070565	chr8:86846771-86846772	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs184229172	chr8:86846838-86846839	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs567635299	chr8:86846850-86846851	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs79640873	chr8:86846862-86846863	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs10097187	chr8:86846863-86846864	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573165010	chr8:86846872-86846873	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188808236	chr8:86846939-86846940	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs11783525	chr8:86846945-86846946	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs62511141	chr8:86846953-86846954	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs575848970	chr8:86846968-86846969	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs376773783	chr8:86846971-86846972	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543939303	chr8:86846980-86846981	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs546447003	chr8:86846984-86846985	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560673451	chr8:86847012-86847013	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369638660	chr8:86847047-86847048	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs73267429	chr8:86847087-86847088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs559758791	chr8:86847088-86847089	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs528735877	chr8:86847089-86847090	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs564538343	chr8:86847095-86847096	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs74749629	chr8:86847128-86847129	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs55994428	chr8:86847151-86847152	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550750612	chr8:86847244-86847245	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs567769655	chr8:86847245-86847246	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs74547821	chr8:86847330-86847331	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs547012274	chr8:86847346-86847347	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs147080186	chr8:86847391-86847392	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs555907003	chr8:86847399-86847400	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs538542465	chr8:86847447-86847448	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs558830019	chr8:86847504-86847505	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs568930740	chr8:86847514-86847515	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs538050859	chr8:86847530-86847531	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs375493690	chr8:86847567-86847568	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs73688535	chr8:86847606-86847607	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs574187389	chr8:86847613-86847614	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs151093564	chr8:86847622-86847623	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs374932026	chr8:86847628-86847629	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs140967265	chr8:86847698-86847699	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs576785154	chr8:86847705-86847706	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs546766597	chr8:86847724-86847725	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs545346348	chr8:86847742-86847743	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs565575592	chr8:86847749-86847750	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs530971818	chr8:86847771-86847772	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD

Chromatin state (count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86843000-86846800	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr8:86843000-86847200	Weak transcription	Brain Hippocampus Middle	brain
3	chr8:86843000-86848600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr8:86843000-86848800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr8:86843200-86848400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr8:86843400-86847000	Weak transcription	NHEK	skin
7	chr8:86843600-86846800	Weak transcription	HMEC	breast
8	chr8:86843600-86847000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:86843600-86847600	Weak transcription	Brain Anterior Caudate	brain
10	chr8:86843600-86847800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:86843600-86849000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:86843800-86846800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:86843800-86846800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:86843800-86846800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr8:86843800-86847000	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr8:86844000-86847800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr8:86844200-86846800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr8:86844200-86849200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr8:86844600-86849000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:86845000-86848800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:86845200-86848000	Weak transcription	Brain Substantia Nigra	brain
22	chr8:86845800-86846600	Weak transcription	Primary monocytes fromperipheralblood	blood
23	chr8:86845800-86848400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr8:86845800-86848600	Enhancers	Fetal Lung	lung
25	chr8:86845800-86849000	Weak transcription	HSMM	muscle
26	chr8:86845800-86849400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:86846000-86847000	Weak transcription	Placenta	Placenta
28	chr8:86846000-86847800	Weak transcription	K562	blood
29	chr8:86846200-86847000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:86846200-86847800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr8:86846200-86848000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr8:86846200-86848600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr8:86846200-86848600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr8:86846200-86848600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:86846400-86846800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr8:86846400-86848000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr8:86846600-86847600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:86846600-86849400	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr8:86846800-86847400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr8:86846800-86847800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:86846800-86847800	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr8:86846800-86848000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr8:86846800-86848000	Enhancers	HMEC	breast
44	chr8:86846800-86848400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:86846800-86850400	Enhancers	Placenta Amnion	Placenta Amnion
46	chr8:86846800-86851600	Enhancers	Cortex derived primary cultured neurospheres	brain
47	chr8:86847000-86847200	Enhancers	Placenta	Placenta
48	chr8:86847000-86848200	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr8:86847000-86848400	Enhancers	NHDF-Ad	bronchial
50	chr8:86847000-86848800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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