Variant report

Variant	nsv890933
Chromosome Location	chr8:58005923-58084006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58026284-58026534	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58033807-58033945	K562	blood:	n/a	n/a
3	BACH1	chr8:58049285-58049314	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr8:58026404-58026491	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:58061093-58061371	HepG2	liver:	n/a	chr8:58061133-58061146
6	CEBPB	chr8:58021346-58021751	HepG2	liver:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
7	CEBPB	chr8:58021305-58021663	HepG2	liver:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
8	CEBPB	chr8:58053930-58054161	K562	blood:	n/a	n/a
9	CEBPB	chr8:58021203-58021733	MCF-7	breast:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
10	CEBPB	chr8:58061084-58061385	IMR90	lung:	n/a	chr8:58061133-58061146
11	CEBPB	chr8:58027864-58027874	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:58016896-58017245	HepG2	liver:	n/a	chr8:58017060-58017071
13	CEBPB	chr8:58061157-58061275	K562	blood:	n/a	n/a
14	CEBPB	chr8:58021373-58021734	HepG2	liver:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
15	CEBPB	chr8:58053850-58054200	A549	lung:	n/a	n/a
16	CEBPB	chr8:58021361-58021734	A549	lung:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
17	CEBPB	chr8:58021311-58021749	A549	lung:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
18	CEBPB	chr8:58021351-58021744	IMR90	lung:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
19	CEBPB	chr8:58021345-58021739	K562	blood:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
20	CEBPB	chr8:58021280-58021759	Hela-S3	cervix:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
21	CEBPB	chr8:58053880-58054182	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr8:58021314-58021703	ECC-1	luminal epithelium:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
23	CEBPB	chr8:58021347-58021716	ECC-1	luminal epithelium:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
24	CEBPB	chr8:58021368-58021650	K562	blood:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
25	CEBPB	chr8:58021285-58021779	MCF-7	breast:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
26	CEBPB	chr8:58021423-58021631	K562	blood:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
27	CEBPB	chr8:58021365-58021694	H1-hESC	embryonic stem cell:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
28	CEBPB	chr8:58059648-58059906	MCF-7	breast:	n/a	chr8:58059752-58059765 chr8:58059752-58059763
29	CEBPB	chr8:58016949-58017131	HepG2	liver:	n/a	chr8:58017060-58017071
30	CEBPB	chr8:58021417-58021636	HepG2	liver:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
31	CEBPB	chr8:58021292-58021801	A549	lung:	n/a	chr8:58021533-58021544 chr8:58021548-58021559
32	CEBPB	chr8:58053895-58054196	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:58053845-58054196	HepG2	liver:	n/a	n/a
34	CEBPD	chr8:58021363-58021605	HepG2	liver:	n/a	n/a
35	CEBPD	chr8:58016947-58017178	HepG2	liver:	n/a	n/a
36	CTCF	chr8:58033840-58034070	HMEC	breast:	n/a	chr8:58033873-58033882
37	CTCF	chr8:58026360-58026510	HFF-Myc	foreskin:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
38	CTCF	chr8:58026380-58026530	GM12869	blood:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
39	CTCF	chr8:58020200-58020350	HCT-116	colon:	n/a	n/a
40	CTCF	chr8:58026360-58026510	GM12872	blood:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
41	CTCF	chr8:58026380-58026530	HMF	breast:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
42	CTCF	chr8:58026360-58026510	HBMEC	blood vessel:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
43	CTCF	chr8:58026400-58026550	GM12867	blood:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
44	CTCF	chr8:58026360-58026510	GM12864	blood:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
45	CTCF	chr8:58033806-58033916	GM12878	blood:	n/a	chr8:58033873-58033882
46	CTCF	chr8:58033800-58033950	HRE	kidney:	n/a	chr8:58033873-58033882
47	CTCF	chr8:58026360-58026510	HPAF	blood vessel:	n/a	chr8:58026431-58026452 chr8:58026436-58026454
48	CTCF	chr8:58033850-58033903	HepG2	liver:	n/a	chr8:58033873-58033882
49	CTCF	chr8:58077023-58077061	GM10248	blood:	n/a	n/a
50	CTCF	chr8:58058026-58058106	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58055876-58055926	AG04450	lung:	fetal
2	chr8:58055876-58055926	AG04450	lung:	fetal
3	chr8:58055168-58055218	PrEC	prostate:	n/a
4	chr8:58055024-58055074	BE2_C	brain:	n/a
5	chr8:58056113-58056163	HNPCEpiC	eye:	n/a
6	chr8:58056026-58056076	HCF	heart:	n/a
7	chr8:58055876-58055926	SK-N-MC	brain:	n/a
8	chr8:58053663-58053713	BE2_C	brain:	n/a
9	chr8:58055168-58055218	LNCaP	prostate:	n/a
10	chr8:58056026-58056076	SK-N-SH	brain:	n/a
11	chr8:58057665-58057715	NB4	blood:	n/a
12	chr8:58057665-58057715	HAEpiC	amniotic membrane:	n/a
13	chr8:58056175-58056225	H1-hESC	embryonic stem cell:	embryo
14	chr8:58056751-58056801	MCF-7	breast:	n/a
15	chr8:58054756-58054806	HRE	kidney:	n/a
16	chr8:58056113-58056163	ovcar-3	ovarian:	n/a
17	chr8:58055024-58055074	NT2-D1	testis:	n/a
18	chr8:58056026-58056076	HCT-116	colon:	n/a
19	chr8:58057665-58057715	IMR90	lung:	fetal
20	chr8:58057665-58057715	HCPEpiC	choroid plexus:	n/a
21	chr8:58055591-58055641	HRCEpiC	kidney:	n/a
22	chr8:58056113-58056163	HCM	heart:	n/a
23	chr8:58055024-58055074	HL-60	blood:	n/a
24	chr8:58055876-58055926	BJ	skin:	n/a
25	chr8:58059068-58059118	HEK293	kidney:	embryo
26	chr8:58057665-58057715	SKMC	muscle:	n/a
27	chr8:58055591-58055641	HCPEpiC	choroid plexus:	n/a
28	chr8:58053663-58053713	HRPEpiC	eye:	n/a
29	chr8:58055024-58055074	MCF-7	breast:	n/a
30	chr8:58054756-58054806	IMR90	lung:	fetal
31	chr8:58056751-58056801	HCT-116	colon:	n/a
32	chr8:58056751-58056801	Hela-S3	cervix:	n/a
33	chr8:58056175-58056225	NHBE	bronchial:	n/a
34	chr8:58055591-58055641	HL-60	blood:	n/a
35	chr8:58055876-58055926	HUVEC	blood vessel:	n/a
36	chr8:58056751-58056801	SAEC	small airway:	n/a
37	chr8:58056113-58056163	LNCaP	prostate:	n/a
38	chr8:58055024-58055074	IMR90	lung:	fetal
39	chr8:58056026-58056076	PrEC	prostate:	n/a
40	chr8:58056175-58056225	SK-N-SH_RA	brain:	n/a
41	chr8:58056751-58056801	HL-60	blood:	n/a
42	chr8:58056501-58056551	HPAEpiC	pulmonary alveolar:	n/a
43	chr8:58053663-58053713	PANC-1	pancreas:	n/a
44	chr8:58057665-58057715	HepG2	liver:	n/a
45	chr8:58053663-58053713	IMR90	lung:	fetal
46	chr8:58056751-58056801	NHDF-neo	bronchial:	n/a
47	chr8:58055168-58055218	ovcar-3	ovarian:	n/a
48	chr8:58056026-58056076	NT2-D1	testis:	n/a
49	chr8:58056113-58056163	AG09309	skin:	n/a
50	chr8:58054756-58054806	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:58048196..58050433-chr8:58051015..58053775,2	K562	blood:
2	chr8:57905221..57907345-chr8:58041168..58043040,2	MCF-7	breast:
3	chr8:58027851..58030791-chr8:58031054..58032684,2	K562	blood:
4	chr8:58027851..58030791-chr8:58031054..58032684,2	K562	blood:
5	chr8:57883085..57884006-chr8:58025963..58027168,5	K562	blood:
6	chr8:57902387..57904313-chr8:58024035..58025722,2	K562	blood:
7	chr8:57905281..57908355-chr8:58026023..58027939,4	MCF-7	breast:
8	chr8:58048196..58050433-chr8:58051015..58053775,2	K562	blood:
9	chr8:57904454..57906209-chr8:58005656..58007694,2	MCF-7	breast:
10	chr8:57360390..57360959-chr8:58025976..58026484,2	K562	blood:
11	chr8:57904494..57906822-chr8:58031187..58033221,2	MCF-7	breast:
12	chr8:57883252..57884200-chr8:58025868..58026858,2	MCF-7	breast:
13	chr8:58076519..58079288-chr8:58083789..58085655,2	K562	blood:
14	chr8:58076519..58079288-chr8:58083789..58085655,2	K562	blood:
15	chr8:58057960..58058531-chr8:58255912..58256499,2	MCF-7	breast:
16	chr8:58083900..58086328-chr8:58091891..58093782,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58055271-58055444	NONHSAT126727
2	lnc-FAM110B-8	chr8:58063159-58063293	NONHSAT126727

Variant related genes	Relation type
ENSG00000253301	TF binding region
RNA5SP266	TF binding region
ENSG00000253301	CpG island
RNA5SP266	CpG island
ENSG00000104331	chromatin interactions
ENSG00000253871	chromatin interactions

Extended variants
information (count: 1240 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1240 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7835839	chr8:58005923-58005924	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192480773	chr8:58005925-58005926	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201621590	chr8:58005983-58005984	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369189688	chr8:58005984-58005985	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs10525817	chr8:58006009-58006010	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs374097526	chr8:58006010-58006011	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs377167516	chr8:58006011-58006012	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs117261786	chr8:58006013-58006014	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557207238	chr8:58006016-58006017	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183680165	chr8:58006124-58006125	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs35194521	chr8:58006154-58006155	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs187534386	chr8:58006165-58006166	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs141059111	chr8:58006214-58006215	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572532922	chr8:58006242-58006243	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs541559308	chr8:58006260-58006261	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374208949	chr8:58006278-58006279	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574854323	chr8:58006305-58006306	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144870572	chr8:58006326-58006327	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs578058309	chr8:58006361-58006362	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs543479945	chr8:58006448-58006449	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534171857	chr8:58006513-58006514	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs76906836	chr8:58006523-58006524	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190534900	chr8:58006536-58006537	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs10093153	chr8:58006613-58006614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs182970031	chr8:58006653-58006654	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559521120	chr8:58006666-58006667	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs116225204	chr8:58006712-58006713	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs551080238	chr8:58006717-58006718	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs201524884	chr8:58006764-58006765	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs75173158	chr8:58006765-58006766	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs564394803	chr8:58006776-58006777	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571046081	chr8:58006778-58006779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs537031140	chr8:58006785-58006786	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs550353059	chr8:58006788-58006789	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567544444	chr8:58006844-58006845	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575948290	chr8:58006890-58006891	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs553086046	chr8:58006899-58006900	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs567855157	chr8:58006920-58006921	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs543871559	chr8:58006921-58006922	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573090346	chr8:58006962-58006963	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs538870096	chr8:58006989-58006990	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs77676700	chr8:58006996-58006997	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541833593	chr8:58006997-58006998	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs192693000	chr8:58007075-58007076	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs370284199	chr8:58007152-58007153	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs398067849	chr8:58007167-58007168	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs397945163	chr8:58007168-58007169	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs578177697	chr8:58007183-58007184	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs377403570	chr8:58007193-58007194	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs371049867	chr8:58007230-58007231	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:130 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58005800-58006200	Enhancers	Rectal Mucosa Donor 31	rectum
2	chr8:58007000-58007600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr8:58012000-58012800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:58012000-58012800	Enhancers	Lung	lung
5	chr8:58012000-58012800	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr8:58012200-58012600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr8:58015800-58017800	Enhancers	Liver	Liver
8	chr8:58016000-58017400	Enhancers	HepG2	liver
9	chr8:58016800-58017200	Active TSS	Psoas Muscle	Psoas
10	chr8:58017400-58021000	Weak transcription	HepG2	liver
11	chr8:58017800-58020800	Weak transcription	Liver	Liver
12	chr8:58018800-58020000	Enhancers	Fetal Kidney	kidney
13	chr8:58019200-58020400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr8:58019200-58020400	Enhancers	Fetal Lung	lung
15	chr8:58020200-58020800	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr8:58020400-58020800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr8:58020400-58021000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr8:58020400-58021200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr8:58020400-58024200	Weak transcription	Fetal Lung	lung
20	chr8:58020600-58022000	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr8:58020800-58021200	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr8:58020800-58022000	Enhancers	Liver	Liver
23	chr8:58020800-58025800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:58021000-58021400	Enhancers	HepG2	liver
25	chr8:58021000-58021800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:58021200-58021800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:58021200-58021800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
28	chr8:58021800-58022400	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr8:58021800-58026000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:58022000-58026000	Weak transcription	Liver	Liver
31	chr8:58024200-58024600	Enhancers	Fetal Lung	lung
32	chr8:58024400-58024800	Enhancers	Fetal Brain Male	brain
33	chr8:58025800-58026200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr8:58026000-58026400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr8:58026000-58026400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr8:58026000-58026600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:58026000-58028200	Enhancers	Liver	Liver
38	chr8:58027200-58028200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr8:58028600-58029800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:58035400-58035600	Enhancers	Psoas Muscle	Psoas
41	chr8:58035600-58036600	Weak transcription	Psoas Muscle	Psoas
42	chr8:58036600-58037200	Enhancers	Fetal Muscle Leg	muscle
43	chr8:58036600-58037200	Enhancers	Skeletal Muscle Male	skeletal muscle
44	chr8:58036600-58037400	Enhancers	Psoas Muscle	Psoas
45	chr8:58036600-58037800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr8:58038200-58038400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:58043200-58043800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr8:58043200-58043800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:58047000-58047600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr8:58054600-58055000	Bivalent Enhancer	Fetal Muscle Leg	muscle

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