Variant report

Variant	nsv465271
Chromosome Location	chr8:1037264-1082750
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	BACH1	chr8:1067672-1067993	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr8:1060374-1060612	HepG2	liver:	n/a	n/a
3	BHLHE40	chr8:1058414-1058822	K562	blood:	n/a	n/a
4	BHLHE40	chr8:1060509-1060574	K562	blood:	n/a	n/a
5	BHLHE40	chr8:1058357-1058815	HepG2	liver:	n/a	n/a
6	BHLHE40	chr8:1081205-1081343	K562	blood:	n/a	chr8:1081230-1081239 chr8:1081229-1081238 chr8:1081224-1081245 chr8:1081230-1081239 chr8:1081231-1081240
7	CEBPB	chr8:1079259-1079453	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr8:1067504-1067974	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr8:1060008-1060039	Spleen_OC	spleen:	n/a	n/a
10	CTCF	chr8:1039115-1039202	GM13976	blood:	n/a	n/a
11	CTCF	chr8:1057833-1057976	LNCaP	prostate:	n/a	n/a
12	CTCF	chr8:1058932-1059061	LNCaP	prostate:	n/a	n/a
13	CTCF	chr8:1057832-1057905	LNCaP	prostate:	n/a	n/a
14	CTCF	chr8:1076460-1076610	WERI-Rb-1	eye:	n/a	n/a
15	CTCF	chr8:1055977-1056033	GM10248	blood:	n/a	n/a
16	CTCF	chr8:1076284-1076397	Lung_OC	lung:	n/a	n/a
17	CTCF	chr8:1059618-1059698	Lung_OC	lung:	n/a	n/a
18	CTCF	chr8:1067705-1067709	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr8:1059578-1059721	LNCaP	prostate:	n/a	n/a
20	E2F4	chr8:1073353-1073841	MCF10A-Er-Src	breast:	n/a	n/a
21	EGR1	chr8:1048458-1048712	K562	blood:	n/a	n/a
22	EGR1	chr8:1048717-1048925	K562	blood:	n/a	n/a
23	FOSL1	chr8:1080408-1080586	K562	blood:	n/a	chr8:1080522-1080529 chr8:1080517-1080528 chr8:1080518-1080527 chr8:1080517-1080529 chr8:1080518-1080528
24	GABPA	chr8:1059101-1059478	GM12878	blood:	n/a	n/a
25	GATA2	chr8:1074569-1074858	SH-SY5Y	brain:	n/a	n/a
26	GATA2	chr8:1080135-1080989	SH-SY5Y	brain:	n/a	chr8:1080520-1080529 chr8:1080461-1080478
27	GATA3	chr8:1080182-1080864	SH-SY5Y	brain:	n/a	chr8:1080520-1080529 chr8:1080461-1080478
28	GATA3	chr8:1074522-1074772	SH-SY5Y	brain:	n/a	n/a
29	GATA3	chr8:1081606-1082057	SH-SY5Y	brain:	n/a	chr8:1081870-1081879
30	HDAC2	chr8:1067620-1067928	H1-hESC	embryonic stem cell:	n/a	chr8:1067869-1067883 chr8:1067872-1067886 chr8:1067871-1067885
31	HEY1	chr8:1059048-1059466	K562	blood:	n/a	n/a
32	JUND	chr8:1059067-1059401	HepG2	liver:	n/a	n/a
33	JUND	chr8:1081130-1081281	H1-hESC	embryonic stem cell:	n/a	chr8:1081211-1081222
34	JUND	chr8:1080368-1080687	K562	blood:	n/a	chr8:1080522-1080529 chr8:1080518-1080527 chr8:1080517-1080528 chr8:1080517-1080529 chr8:1080518-1080528
35	JUND	chr8:1080369-1080629	HepG2	liver:	n/a	chr8:1080522-1080529 chr8:1080518-1080527 chr8:1080517-1080528 chr8:1080517-1080529 chr8:1080518-1080528
36	MAFF	chr8:1081760-1081953	K562	blood:	n/a	n/a
37	MAFF	chr8:1069881-1070035	K562	blood:	n/a	chr8:1069976-1069994
38	MAFF	chr8:1069854-1070071	HepG2	liver:	n/a	chr8:1069976-1069994
39	MAFK	chr8:1069862-1070120	IMR90	lung:	n/a	chr8:1069977-1069992 chr8:1069981-1069992 chr8:1069982-1069993 chr8:1069981-1069992 chr8:1069982-1069993 chr8:1069980-1069994
40	MAFK	chr8:1069822-1070139	HepG2	liver:	n/a	chr8:1069977-1069992 chr8:1069981-1069992 chr8:1069982-1069993 chr8:1069981-1069992 chr8:1069982-1069993 chr8:1069980-1069994
41	MAFK	chr8:1081749-1082062	H1-hESC	embryonic stem cell:	n/a	chr8:1081867-1081877 chr8:1081867-1081876
42	MAFK	chr8:1069875-1069990	K562	blood:	n/a	n/a
43	MAFK	chr8:1069814-1070147	HepG2	liver:	n/a	chr8:1069977-1069992 chr8:1069981-1069992 chr8:1069982-1069993 chr8:1069981-1069992 chr8:1069982-1069993 chr8:1069980-1069994
44	MAX	chr8:1060342-1060582	K562	blood:	n/a	chr8:1060475-1060485
45	MAX	chr8:1060167-1060648	HUVEC	blood vessel:	n/a	chr8:1060475-1060485
46	MAX	chr8:1060317-1060670	NB4	blood:	n/a	chr8:1060475-1060485
47	MYC	chr8:1042358-1042396	H1-hESC	embryonic stem cell:	n/a	n/a
48	MYC	chr8:1078086-1078140	MCF-7	breast:	n/a	n/a
49	MYC	chr8:1051760-1051807	MCF-7	breast:	n/a	n/a
50	MYC	chr8:1078150-1078155	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:1054065-1054115	BJ	skin:	n/a
2	chr8:1049901-1049951	SKMC	muscle:	n/a
3	chr8:1080669-1080719	Hela-S3	cervix:	n/a
4	chr8:1054065-1054115	BJ	skin:	n/a
5	chr8:1049901-1049951	SKMC	muscle:	n/a
6	chr8:1080669-1080719	Hela-S3	cervix:	n/a
7	chr8:1082686-1082736	NHBE	bronchial:	n/a
8	chr8:1049394-1049444	AG04449	skin:	fetal
9	chr8:1046358-1046408	HEEpiC	esophagus:	n/a
10	chr8:1054065-1054115	HCPEpiC	choroid plexus:	n/a
11	chr8:1049477-1049527	U87	brain:	n/a
12	chr8:1051585-1051635	T-47D	breast:	n/a
13	chr8:1048135-1048185	AG09319	gingival:	n/a
14	chr8:1051585-1051635	HCT-116	colon:	n/a
15	chr8:1048135-1048185	NHBE	bronchial:	n/a
16	chr8:1053439-1053489	Caco-2	colon:	n/a
17	chr8:1051728-1051778	HAEpiC	amniotic membrane:	n/a
18	chr8:1046358-1046408	PrEC	prostate:	n/a
19	chr8:1041336-1041386	ECC-1	luminal epithelium:	n/a
20	chr8:1045563-1045613	GM12878	blood:	n/a
21	chr8:1051510-1051560	HEK293	kidney:	embryo
22	chr8:1049335-1049385	HPAEpiC	pulmonary alveolar:	n/a
23	chr8:1080916-1080966	NT2-D1	testis:	n/a
24	chr8:1049215-1049265	RPTEC	kidney:	n/a
25	chr8:1041611-1041661	NB4	blood:	n/a
26	chr8:1057632-1057682	GM06990	blood:	n/a
27	chr8:1053508-1053558	HRE	kidney:	n/a
28	chr8:1050972-1051022	GM12878	blood:	n/a
29	chr8:1049167-1049217	HCT-116	colon:	n/a
30	chr8:1054786-1054836	CMK	blood:	n/a
31	chr8:1068250-1068300	SK-N-SH_RA	brain:	n/a
32	chr8:1049477-1049527	NHDF-neo	bronchial:	n/a
33	chr8:1049901-1049951	AoSMC	blood vessel:	n/a
34	chr8:1050972-1051022	HRCEpiC	kidney:	n/a
35	chr8:1051814-1051864	SK-N-SH	brain:	n/a
36	chr8:1048765-1048815	HEEpiC	esophagus:	n/a
37	chr8:1046622-1046672	SKMC	muscle:	n/a
38	chr8:1048765-1048815	NH-A	brain:	n/a
39	chr8:1053508-1053558	AG04450	lung:	fetal
40	chr8:1054048-1054098	GM12878	blood:	n/a
41	chr8:1054065-1054115	SK-N-MC	brain:	n/a
42	chr8:1053508-1053558	HRPEpiC	eye:	n/a
43	chr8:1068250-1068300	HCPEpiC	choroid plexus:	n/a
44	chr8:1053508-1053558	Hepatocyte	liver:	n/a
45	chr8:1048135-1048185	LNCaP	prostate:	n/a
46	chr8:1054048-1054098	HUVEC	blood vessel:	n/a
47	chr8:1049335-1049385	HRE	kidney:	n/a
48	chr8:1048844-1048894	RPTEC	kidney:	n/a
49	chr8:1054786-1054836	MCF-7	breast:	n/a
50	chr8:1046622-1046672	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr8:1012791..1015412-chr8:1066556..1068717,2	K562	blood:
2	chr8:1055778..1058022-chr8:1059688..1062614,2	K562	blood:
3	chr8:1055778..1058022-chr8:1059688..1062614,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO25-5	chr8:1054883-1055066	ENSG00000237647.4
2	lnc-FBXO25-5	chr8:1054882-1055066	ENSG00000254269

Variant related genes	Relation type
ENSG00000254269	TF binding region
ENSG00000254269	CpG island

Extended variants
information (count: 2768 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:2768 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4735837	chr8:1037264-1037265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs74557192	chr8:1037274-1037275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188240117	chr8:1037288-1037289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549118178	chr8:1037308-1037309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569106070	chr8:1037319-1037320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs144553403	chr8:1037330-1037331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557812917	chr8:1037333-1037334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532598411	chr8:1037335-1037336	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373235623	chr8:1037336-1037337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs577977697	chr8:1037337-1037338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs377330918	chr8:1037344-1037345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs534162165	chr8:1037362-1037363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs553003111	chr8:1037391-1037392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs180699536	chr8:1037410-1037411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573046714	chr8:1037423-1037424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs533636627	chr8:1037447-1037448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541756741	chr8:1037454-1037455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545276250	chr8:1037492-1037493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184480582	chr8:1037524-1037525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535340470	chr8:1037542-1037543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575060799	chr8:1037554-1037555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113387843	chr8:1037555-1037556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59208645	chr8:1037560-1037561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397797168	chr8:1037566-1037567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575498245	chr8:1037582-1037583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530578189	chr8:1037584-1037585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189452890	chr8:1037594-1037595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532801908	chr8:1037597-1037598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114946051	chr8:1037602-1037603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181446383	chr8:1037610-1037611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs543513108	chr8:1037700-1037701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529637355	chr8:1037705-1037706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565005973	chr8:1037724-1037725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549256859	chr8:1037739-1037740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75183721	chr8:1037741-1037742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185803871	chr8:1037765-1037766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146635115	chr8:1037786-1037787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141379940	chr8:1037796-1037797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs144609949	chr8:1037797-1037798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142085434	chr8:1037814-1037815	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs554188433	chr8:1037844-1037845	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs373589577	chr8:1037863-1037864	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs138362708	chr8:1037884-1037885	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs535785901	chr8:1037901-1037902	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs76120699	chr8:1037916-1037917	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs575530323	chr8:1037928-1037929	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs73180697	chr8:1037929-1037930	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs79709816	chr8:1037939-1037940	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs577618831	chr8:1037947-1037948	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs148857789	chr8:1037966-1037967	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Schizophrenia	23813976	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Autism	20531469	CNVD
Breast cancer	20932292	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:1022400-1039200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr8:1030600-1040000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:1034800-1037800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr8:1036800-1040000	Enhancers	Fetal Lung	lung
5	chr8:1037600-1040200	Enhancers	Fetal Brain Male	brain
6	chr8:1037800-1038000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr8:1037800-1038000	Enhancers	Duodenum Mucosa	Duodenum
8	chr8:1037800-1038000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
9	chr8:1037800-1038000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
10	chr8:1038000-1038200	Enhancers	Fetal Brain Female	brain
11	chr8:1038000-1038200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
12	chr8:1038000-1039200	Weak transcription	Duodenum Mucosa	Duodenum
13	chr8:1038000-1039400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr8:1038200-1039800	Enhancers	Fetal Muscle Leg	muscle
15	chr8:1038200-1043000	Weak transcription	Fetal Brain Female	brain
16	chr8:1038600-1038800	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr8:1038800-1039200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
18	chr8:1038800-1039400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr8:1038800-1039600	Enhancers	Spleen	Spleen
20	chr8:1039000-1039200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr8:1039000-1039200	Active TSS	Adipose Nuclei	Adipose
22	chr8:1039000-1039400	Active TSS	Colon Smooth Muscle	Colon
23	chr8:1039000-1039400	Active TSS	Rectal Mucosa Donor 29	rectum
24	chr8:1039000-1039400	Active TSS	Rectal Smooth Muscle	rectum
25	chr8:1039000-1039600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:1039000-1039600	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr8:1039000-1039600	Bivalent/Poised TSS	Hela-S3	cervix
28	chr8:1039000-1042200	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr8:1039200-1039400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:1039200-1039400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr8:1039200-1039400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
32	chr8:1039200-1039400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
33	chr8:1039200-1039600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:1039200-1039600	Flanking Active TSS	Adipose Nuclei	Adipose
35	chr8:1039200-1039600	Active TSS	Colonic Mucosa	Colon
36	chr8:1039200-1039600	Flanking Active TSS	Duodenum Mucosa	Duodenum
37	chr8:1039200-1039600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr8:1039200-1039600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
39	chr8:1039200-1040600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr8:1039400-1039600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr8:1039400-1039600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr8:1039400-1039600	Bivalent Enhancer	Brain Anterior Caudate	brain
43	chr8:1039400-1039600	Flanking Active TSS	Colon Smooth Muscle	Colon
44	chr8:1039400-1039600	Flanking Active TSS	Rectal Smooth Muscle	rectum
45	chr8:1039400-1039600	Bivalent Enhancer	Right Ventricle	heart
46	chr8:1039400-1039600	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
47	chr8:1039400-1039600	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
48	chr8:1039400-1039800	Bivalent Enhancer	Fetal Stomach	stomach
49	chr8:1039400-1040000	Enhancers	Lung	lung
50	chr8:1039400-1043600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

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