Variant report

Variant	nsv889702
Chromosome Location	chr8:1457884-1507521
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:238)
CpG islands
(count:3545)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:238 , 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	ATF1	chr8:1506879-1507048	K562	blood:	n/a	n/a
2	BCL3	chr8:1463690-1465073	GM12878	blood:	n/a	n/a
3	BCL3	chr8:1464008-1465001	GM12878	blood:	n/a	n/a
4	BCL3	chr8:1506504-1507147	GM12878	blood:	n/a	n/a
5	BCL3	chr8:1506622-1507133	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:1462786-1462853	K562	blood:	n/a	n/a
7	CTCF	chr8:1484980-1485130	Hela-S3	cervix:	n/a	chr8:1485008-1485021 chr8:1485005-1485023
8	CTCF	chr8:1476280-1476430	HepG2	liver:	n/a	n/a
9	CTCF	chr8:1476250-1476411	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr8:1476154-1476503	K562	blood:	n/a	n/a
11	CTCF	chr8:1464737-1464823	LNCaP	prostate:	n/a	n/a
12	CTCF	chr8:1476280-1476430	A549	lung:	n/a	n/a
13	CTCF	chr8:1500520-1500670	SK-N-SH_RA	brain:	n/a	chr8:1500560-1500578
14	CTCF	chr8:1476240-1476390	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr8:1462635-1462855	HepG2	liver:	n/a	chr8:1462756-1462769
16	CTCF	chr8:1459401-1459433	Pancreas_OC	pancreas:	n/a	n/a
17	CTCF	chr8:1476283-1476372	MCF-7	breast:	n/a	n/a
18	CTCF	chr8:1462740-1462890	HCT-116	colon:	n/a	chr8:1462756-1462769
19	CTCF	chr8:1496744-1497092	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr8:1462720-1462870	MCF-7	breast:	n/a	chr8:1462756-1462769
21	CTCF	chr8:1459400-1459549	GM10248	blood:	n/a	n/a
22	CTCF	chr8:1462670-1462838	K562	blood:	n/a	chr8:1462756-1462769
23	CTCF	chr8:1500560-1500710	SK-N-SH_RA	brain:	n/a	chr8:1500560-1500578
24	CTCF	chr8:1476271-1476386	HepG2	liver:	n/a	n/a
25	CTCF	chr8:1459314-1459379	GM13976	blood:	n/a	n/a
26	CTCF	chr8:1496751-1497094	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr8:1476253-1476405	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:1462974-1463010	LNCaP	prostate:	n/a	chr8:1462985-1462998
29	CTCF	chr8:1462762-1462768	MCF-7	breast:	n/a	n/a
30	CTCF	chr8:1496833-1497035	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr8:1476300-1476356	Gliobla	brain:	n/a	n/a
32	CTCF	chr8:1459529-1459564	GM13976	blood:	n/a	n/a
33	CTCF	chr8:1485438-1485455	GM10248	blood:	n/a	n/a
34	CTCF	chr8:1484980-1485130	K562	blood:	n/a	chr8:1485008-1485021 chr8:1485005-1485023
35	CTCF	chr8:1476289-1476381	LNCaP	prostate:	n/a	n/a
36	CTCF	chr8:1462660-1462810	WERI-Rb-1	eye:	n/a	chr8:1462756-1462769
37	CTCF	chr8:1476280-1476430	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr8:1459747-1459751	LNCaP	prostate:	n/a	n/a
39	CTCF	chr8:1484845-1485086	H1-hESC	embryonic stem cell:	n/a	chr8:1485008-1485021 chr8:1485005-1485023
40	CTCF	chr8:1484053-1484067	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr8:1485240-1485390	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr8:1476226-1476431	K562	blood:	n/a	n/a
43	CTCF	chr8:1462716-1462833	MCF-7	breast:	n/a	chr8:1462756-1462769
44	CTCF	chr8:1483040-1483190	GM12875	blood:	n/a	n/a
45	CTCF	chr8:1484933-1485068	K562	blood:	n/a	chr8:1485008-1485021 chr8:1485005-1485023
46	CTCF	chr8:1462660-1462810	Caco-2	colon:	n/a	chr8:1462756-1462769
47	CTCF	chr8:1462668-1462841	HepG2	liver:	n/a	chr8:1462756-1462769
48	CTCF	chr8:1462740-1462890	MCF-7	breast:	n/a	chr8:1462756-1462769
49	CTCF	chr8:1476280-1476430	K562	blood:	n/a	n/a
50	CTCF	chr8:1484940-1485090	HCT-116	colon:	n/a	chr8:1485008-1485021 chr8:1485005-1485023

(count:3545 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1460268-1460318	AG09319	gingival:	n/a
2	chr8:1495289-1495339	PrEC	prostate:	n/a
3	chr8:1494546-1494596	HepG2	liver:	n/a
4	chr8:1462903-1462953	HL-60	blood:	n/a
5	chr8:1500789-1500839	ECC-1	luminal epithelium:	n/a
6	chr8:1497078-1497128	NT2-D1	testis:	n/a
7	chr8:1498266-1498316	Hela-S3	cervix:	n/a
8	chr8:1460268-1460318	AG09319	gingival:	n/a
9	chr8:1495289-1495339	PrEC	prostate:	n/a
10	chr8:1494546-1494596	HepG2	liver:	n/a
11	chr8:1462903-1462953	HL-60	blood:	n/a
12	chr8:1500789-1500839	ECC-1	luminal epithelium:	n/a
13	chr8:1497078-1497128	NT2-D1	testis:	n/a
14	chr8:1498266-1498316	Hela-S3	cervix:	n/a
15	chr8:1468625-1468675	HMEC	breast:	n/a
16	chr8:1501640-1501690	Hela-S3	cervix:	n/a
17	chr8:1496751-1496801	AG09309	skin:	n/a
18	chr8:1497307-1497357	HNPCEpiC	eye:	n/a
19	chr8:1495185-1495235	AG09319	gingival:	n/a
20	chr8:1494546-1494596	HRE	kidney:	n/a
21	chr8:1495025-1495075	HNPCEpiC	eye:	n/a
22	chr8:1497078-1497128	NB4	blood:	n/a
23	chr8:1496052-1496102	K562	blood:	n/a
24	chr8:1472161-1472211	HL-60	blood:	n/a
25	chr8:1495289-1495339	HEEpiC	esophagus:	n/a
26	chr8:1501226-1501276	HRCEpiC	kidney:	n/a
27	chr8:1496052-1496102	GM12891	blood:	n/a
28	chr8:1501898-1501948	AG04450	lung:	fetal
29	chr8:1468625-1468675	NB4	blood:	n/a
30	chr8:1501898-1501948	HAEpiC	amniotic membrane:	n/a
31	chr8:1458119-1458169	ProgFib	skin:	n/a
32	chr8:1502766-1502816	AG09319	gingival:	n/a
33	chr8:1495289-1495339	SK-N-SH	brain:	n/a
34	chr8:1501640-1501690	SK-N-SH	brain:	n/a
35	chr8:1458508-1458558	HCF	heart:	n/a
36	chr8:1463125-1463175	HNPCEpiC	eye:	n/a
37	chr8:1497608-1497658	RPTEC	kidney:	n/a
38	chr8:1500789-1500839	IMR90	lung:	fetal
39	chr8:1498266-1498316	HRCEpiC	kidney:	n/a
40	chr8:1497878-1497928	NHDF-neo	bronchial:	n/a
41	chr8:1462903-1462953	AG04449	skin:	fetal
42	chr8:1472161-1472211	HCT-116	colon:	n/a
43	chr8:1495169-1495219	IMR90	lung:	fetal
44	chr8:1497307-1497357	HRCEpiC	kidney:	n/a
45	chr8:1505031-1505081	MCF10A-Er-Src	breast:	n/a
46	chr8:1496052-1496102	AG04449	skin:	fetal
47	chr8:1470122-1470172	GM06990	blood:	n/a
48	chr8:1496711-1496761	SK-N-SH_RA	brain:	n/a
49	chr8:1494546-1494596	HEK293	kidney:	embryo
50	chr8:1501670-1501720	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:1483969..1486472-chr8:1489683..1491378,2	K562	blood:
2	chr8:1483969..1486472-chr8:1489683..1491378,2	K562	blood:

No data

Variant related genes	Relation type
DLGAP2	TF binding region
DLGAP2	CpG island

Extended variants
information (count: 2829 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:2829 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4875868	chr8:1457884-1457885	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs191273669	chr8:1457889-1457890	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs143985129	chr8:1457900-1457901	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs372948117	chr8:1457926-1457927	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs147302143	chr8:1457932-1457933	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs182901999	chr8:1457941-1457942	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs140349011	chr8:1457974-1457975	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs187535338	chr8:1458008-1458009	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs560956102	chr8:1458020-1458021	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs529988693	chr8:1458034-1458035	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs75015721	chr8:1458038-1458039	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs4875869	chr8:1458045-1458046	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs531555753	chr8:1458061-1458062	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs551375133	chr8:1458085-1458086	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs4876077	chr8:1458101-1458102	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs527810190	chr8:1458107-1458108	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs113466740	chr8:1458109-1458110	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs190428439	chr8:1458129-1458130	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs536948172	chr8:1458162-1458163	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs556849132	chr8:1458164-1458165	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs144327768	chr8:1458171-1458172	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs144422896	chr8:1458180-1458181	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs148398001	chr8:1458206-1458207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572087515	chr8:1458225-1458226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534456748	chr8:1458227-1458228	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183379981	chr8:1458234-1458235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577652560	chr8:1458237-1458238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs59220237	chr8:1458261-1458262	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs563204816	chr8:1458290-1458291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576747376	chr8:1458297-1458298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188932955	chr8:1458298-1458299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs192375123	chr8:1458314-1458315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184282405	chr8:1458330-1458331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547620932	chr8:1458331-1458332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34546033	chr8:1458343-1458344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568594197	chr8:1458348-1458349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs61678583	chr8:1458351-1458352	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs530276622	chr8:1458392-1458393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538667705	chr8:1458395-1458396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552731030	chr8:1458482-1458483	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142524874	chr8:1458485-1458486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570338066	chr8:1458496-1458497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550765163	chr8:1458516-1458517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539371169	chr8:1458555-1458556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187992078	chr8:1458589-1458590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75670453	chr8:1458591-1458592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151009235	chr8:1458594-1458595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554324659	chr8:1458596-1458597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112340890	chr8:1458620-1458621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141155134	chr8:1458647-1458648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Cancer	18840272	CNVD
Pilocytic astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Breast cancer	20932292	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1449200-1465200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:1455800-1458200	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:1456200-1458400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
4	chr8:1456200-1471400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:1457200-1458200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr8:1457200-1458200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
7	chr8:1457400-1458200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr8:1457400-1458200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr8:1457400-1458200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr8:1457600-1458000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr8:1457600-1458800	Enhancers	Fetal Brain Male	brain
12	chr8:1457600-1458800	Enhancers	Pancreas	Pancrea
13	chr8:1458800-1462600	Weak transcription	Brain Angular Gyrus	brain
14	chr8:1460000-1460400	Enhancers	Colon Smooth Muscle	Colon
15	chr8:1460200-1461000	Enhancers	Rectal Smooth Muscle	rectum
16	chr8:1460400-1460800	Active TSS	Colon Smooth Muscle	Colon
17	chr8:1460800-1461000	Flanking Active TSS	Colon Smooth Muscle	Colon
18	chr8:1461000-1461200	Enhancers	Colon Smooth Muscle	Colon
19	chr8:1465200-1465400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:1465400-1465800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr8:1465800-1466000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr8:1466000-1470400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:1467200-1467400	Bivalent Enhancer	Fetal Stomach	stomach
24	chr8:1471400-1471600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:1471600-1472400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr8:1472200-1473000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr8:1472400-1472800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr8:1472800-1475000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr8:1475000-1475400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:1482400-1483000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:1485000-1485200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
32	chr8:1485000-1485400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr8:1485000-1485800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
34	chr8:1485200-1486200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr8:1486400-1487000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:1486600-1486800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr8:1486600-1487000	Enhancers	Fetal Brain Female	brain
38	chr8:1486800-1488800	Enhancers	Fetal Brain Male	brain
39	chr8:1487000-1505200	Weak transcription	Fetal Brain Female	brain
40	chr8:1487800-1488200	Enhancers	Spleen	Spleen
41	chr8:1488000-1488400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:1489800-1490200	Bivalent Enhancer	HepG2	liver
43	chr8:1494400-1494600	Enhancers	Brain Germinal Matrix	brain
44	chr8:1494400-1494800	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:1494400-1495000	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr8:1494600-1495000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr8:1494600-1497200	Weak transcription	Brain Germinal Matrix	brain
48	chr8:1494800-1495200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr8:1494800-1495200	ZNF genes & repeats	Right Atrium	heart
50	chr8:1495000-1495600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links