Variant report

Variant	nsv1034355
Chromosome Location	chr8:39942179-39961432
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	chr8:39961368-39962195	HepG2	liver:	n/a	n/a
2	BCL3	chr8:39957043-39958074	A549	lung:	n/a	chr8:39957459-39957467
3	BCL3	chr8:39957020-39957794	A549	lung:	n/a	chr8:39957459-39957467
4	BRCA1	chr8:39957330-39958349	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr8:39961333-39962212	HepG2	liver:	n/a	chr8:39961965-39961976
6	CEBPB	chr8:39956448-39956786	A549	lung:	n/a	n/a
7	CEBPB	chr8:39957184-39958022	A549	lung:	n/a	chr8:39957324-39957332
8	CEBPB	chr8:39961324-39961763	A549	lung:	n/a	n/a
9	CEBPB	chr8:39957064-39958096	A549	lung:	n/a	chr8:39957324-39957332
10	CEBPB	chr8:39956411-39957859	IMR90	lung:	n/a	chr8:39957324-39957332
11	CEBPB	chr8:39957216-39958065	A549	lung:	n/a	chr8:39957324-39957332
12	CEBPB	chr8:39956378-39958069	Hela-S3	cervix:	n/a	chr8:39957324-39957332
13	CEBPB	chr8:39957555-39958015	MCF-7	breast:	n/a	n/a
14	CEBPB	chr8:39961335-39962165	IMR90	lung:	n/a	chr8:39961965-39961976
15	CEBPB	chr8:39956398-39956956	A549	lung:	n/a	n/a
16	CEBPB	chr8:39961335-39962187	HepG2	liver:	n/a	chr8:39961965-39961976
17	CEBPB	chr8:39961339-39962175	Hela-S3	cervix:	n/a	chr8:39961965-39961976
18	CEBPB	chr8:39961318-39962191	A549	lung:	n/a	chr8:39961965-39961976
19	CEBPB	chr8:39961420-39961660	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:39956452-39956873	A549	lung:	n/a	n/a
21	CEBPB	chr8:39961199-39962313	A549	lung:	n/a	chr8:39961965-39961976
22	CHD2	chr8:39956472-39956910	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr8:39957132-39957944	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr8:39948369-39948569	HepG2	liver:	n/a	n/a
25	E2F4	chr8:39957243-39957840	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr8:39954879-39955005	GM12878	blood:	n/a	chr8:39954961-39954972
27	EP300	chr8:39961418-39961792	HepG2	liver:	n/a	chr8:39961519-39961533
28	EP300	chr8:39961200-39962292	A549	lung:	n/a	chr8:39961519-39961533
29	EP300	chr8:39961382-39962122	Hela-S3	cervix:	n/a	chr8:39961519-39961533
30	EP300	chr8:39961298-39962225	HepG2	liver:	n/a	chr8:39961519-39961533
31	EP300	chr8:39956450-39958009	Hela-S3	cervix:	n/a	chr8:39957348-39957357
32	EP300	chr8:39957049-39958054	A549	lung:	n/a	chr8:39957348-39957357
33	EP300	chr8:39961374-39962265	HepG2	liver:	n/a	chr8:39961519-39961533
34	EP300	chr8:39961250-39961896	A549	lung:	n/a	chr8:39961519-39961533
35	EP300	chr8:39956332-39958124	A549	lung:	n/a	chr8:39957348-39957357
36	FOS	chr8:39955512-39955977	MCF10A-Er-Src	breast:	n/a	chr8:39955771-39955779
37	FOS	chr8:39955606-39955998	HUVEC	blood vessel:	n/a	chr8:39955771-39955779
38	FOS	chr8:39961340-39961634	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr8:39956583-39958053	MCF10A-Er-Src	breast:	n/a	chr8:39957313-39957324 chr8:39957814-39957824 chr8:39957316-39957326 chr8:39957811-39957822 chr8:39957316-39957326 chr8:39957316-39957326 chr8:39957814-39957824 chr8:39957815-39957823 chr8:39957316-39957326 chr8:39957315-39957326 chr8:39957814-39957824 chr8:39957315-39957327
40	FOS	chr8:39957190-39958005	MCF10A-Er-Src	breast:	n/a	chr8:39957313-39957324 chr8:39957814-39957824 chr8:39957316-39957326 chr8:39957811-39957822 chr8:39957316-39957326 chr8:39957316-39957326 chr8:39957814-39957824 chr8:39957815-39957823 chr8:39957316-39957326 chr8:39957315-39957326 chr8:39957814-39957824 chr8:39957315-39957327
41	FOS	chr8:39956559-39958091	MCF10A-Er-Src	breast:	n/a	chr8:39957313-39957324 chr8:39957814-39957824 chr8:39957316-39957326 chr8:39957811-39957822 chr8:39957316-39957326 chr8:39957316-39957326 chr8:39957814-39957824 chr8:39957815-39957823 chr8:39957316-39957326 chr8:39957315-39957326 chr8:39957814-39957824 chr8:39957315-39957327
42	FOS	chr8:39955508-39956000	MCF10A-Er-Src	breast:	n/a	chr8:39955771-39955779
43	FOS	chr8:39956456-39958092	MCF10A-Er-Src	breast:	n/a	chr8:39957313-39957324 chr8:39957814-39957824 chr8:39957316-39957326 chr8:39957811-39957822 chr8:39957316-39957326 chr8:39957316-39957326 chr8:39957814-39957824 chr8:39957815-39957823 chr8:39957316-39957326 chr8:39957315-39957326 chr8:39957814-39957824 chr8:39957315-39957327
44	FOS	chr8:39961367-39962106	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr8:39955567-39955964	MCF10A-Er-Src	breast:	n/a	chr8:39955771-39955779
46	FOS	chr8:39951663-39952070	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:39951699-39952069	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr8:39951682-39952049	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr8:39956423-39957505	HUVEC	blood vessel:	n/a	chr8:39957313-39957324 chr8:39957316-39957326 chr8:39957316-39957326 chr8:39957316-39957326 chr8:39957316-39957326 chr8:39957315-39957326 chr8:39957315-39957327
50	FOS	chr8:39961351-39961673	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39950015-39950065	HNPCEpiC	eye:	n/a
2	chr8:39950015-39950065	GM19239	blood:	n/a
3	chr8:39950015-39950065	PrEC	prostate:	n/a
4	chr8:39950015-39950065	PANC-1	pancreas:	n/a
5	chr8:39950015-39950065	Hela-S3	cervix:	n/a
6	chr8:39950015-39950065	GM12892	blood:	n/a
7	chr8:39950015-39950065	GM12891	blood:	n/a
8	chr8:39950015-39950065	SAEC	small airway:	n/a
9	chr8:39950015-39950065	Jurkat	blood:	n/a
10	chr8:39950015-39950065	T-47D	breast:	n/a
11	chr8:39950015-39950065	MCF10A-Er-Src	breast:	n/a
12	chr8:39950015-39950065	SKMC	muscle:	n/a
13	chr8:39950015-39950065	NHBE	bronchial:	n/a
14	chr8:39950015-39950065	ovcar-3	ovarian:	n/a
15	chr8:39950015-39950065	NHDF-neo	bronchial:	n/a
16	chr8:39950015-39950065	HCF	heart:	n/a
17	chr8:39950015-39950065	AoSMC	blood vessel:	n/a
18	chr8:39950015-39950065	GM06990	blood:	n/a
19	chr8:39950015-39950065	HRE	kidney:	n/a
20	chr8:39950015-39950065	ECC-1	luminal epithelium:	n/a
21	chr8:39950015-39950065	A549	lung:	n/a
22	chr8:39950015-39950065	MCF-7	breast:	n/a
23	chr8:39950015-39950065	Caco-2	colon:	n/a
24	chr8:39950015-39950065	LNCaP	prostate:	n/a
25	chr8:39950015-39950065	HCPEpiC	choroid plexus:	n/a
26	chr8:39950015-39950065	CMK	blood:	n/a
27	chr8:39950015-39950065	AG09309	skin:	n/a
28	chr8:39950015-39950065	BJ	skin:	n/a
29	chr8:39950015-39950065	HCT-116	colon:	n/a
30	chr8:39950015-39950065	NB4	blood:	n/a
31	chr8:39950015-39950065	HAEpiC	amniotic membrane:	n/a
32	chr8:39950015-39950065	HUVEC	blood vessel:	n/a
33	chr8:39950015-39950065	AG09319	gingival:	n/a
34	chr8:39950015-39950065	HRCEpiC	kidney:	n/a
35	chr8:39950015-39950065	ProgFib	skin:	n/a
36	chr8:39950015-39950065	H1-hESC	embryonic stem cell:	embryo
37	chr8:39950015-39950065	RPTEC	kidney:	n/a
38	chr8:39950015-39950065	PFSK-1	brain:	n/a
39	chr8:39950015-39950065	HRPEpiC	eye:	n/a
40	chr8:39950015-39950065	Hepatocyte	liver:	n/a
41	chr8:39950015-39950065	HepG2	liver:	n/a
42	chr8:39950015-39950065	HL-60	blood:	n/a
43	chr8:39950015-39950065	AG10803	skin:	n/a
44	chr8:39950015-39950065	HEEpiC	esophagus:	n/a
45	chr8:39950015-39950065	HEK293	kidney:	embryo
46	chr8:39950015-39950065	SK-N-SH_RA	brain:	n/a
47	chr8:39950015-39950065	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:39950015-39950065	K562	blood:	n/a
49	chr8:39950015-39950065	U87	brain:	n/a
50	chr8:39950015-39950065	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:39956140..39958982-chr8:39975836..39978547,3	MCF-7	breast:
2	chr8:39957259..39959898-chr8:40032883..40035530,2	MCF-7	breast:
3	chr8:39958460..39961008-chr8:40021213..40023087,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM2-3	chr8:39949028-39949067	XLOC_007063

Variant related genes	Relation type
ENSG00000253381	TF binding region
ENSG00000253381	CpG island
STYX	miRNA target sites

Extended variants
information (count: 905 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:905 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546162824	chr8:39942191-39942192	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs187683300	chr8:39942218-39942219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560490160	chr8:39942299-39942300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191716629	chr8:39942303-39942304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141437153	chr8:39942304-39942305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548832331	chr8:39942313-39942314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184026980	chr8:39942317-39942318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529751190	chr8:39942321-39942322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs150824607	chr8:39942334-39942335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139641087	chr8:39942345-39942346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532163013	chr8:39942357-39942358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144278589	chr8:39942366-39942367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1904906	chr8:39942372-39942373	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs534925833	chr8:39942441-39942442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188757716	chr8:39942451-39942452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191964668	chr8:39942477-39942478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537139540	chr8:39942568-39942569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570950745	chr8:39942577-39942578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577145714	chr8:39942589-39942590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539789761	chr8:39942594-39942595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs552961938	chr8:39942596-39942597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573156178	chr8:39942614-39942615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185205072	chr8:39942635-39942636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1904907	chr8:39942659-39942660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs146082172	chr8:39942693-39942694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75507629	chr8:39942760-39942761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563369781	chr8:39942796-39942797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532123290	chr8:39942797-39942798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552162439	chr8:39942816-39942817	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs139919700	chr8:39942834-39942835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528392632	chr8:39942840-39942841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548542620	chr8:39942888-39942889	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149707951	chr8:39942926-39942927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537276714	chr8:39942929-39942930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145664299	chr8:39942937-39942938	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570887161	chr8:39942942-39942943	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574741118	chr8:39942943-39942944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552949449	chr8:39942985-39942986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190601478	chr8:39942991-39942992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535733504	chr8:39943131-39943132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs80062688	chr8:39943136-39943137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575871480	chr8:39943184-39943185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs61048623	chr8:39943215-39943216	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539862750	chr8:39943227-39943228	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113748764	chr8:39943254-39943255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564534532	chr8:39943314-39943315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141913882	chr8:39943344-39943345	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576825709	chr8:39943415-39943416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116681778	chr8:39943512-39943513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56347116	chr8:39943527-39943528	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Melanoma	18172304	CNVD
Medulloblastoma	21979893	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Medulloblastoma	19270706	CNVD
Cancer	20164919	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21045282	CNVD
Lung cancer	17925434	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39939400-39943600	Weak transcription	Fetal Stomach	stomach
2	chr8:39939600-39943400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr8:39939600-39943600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr8:39939800-39942200	Weak transcription	Fetal Brain Male	brain
5	chr8:39940000-39942800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:39940000-39950000	Weak transcription	A549	lung
7	chr8:39940200-39943200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:39940600-39945000	Weak transcription	Ovary	ovary
9	chr8:39941000-39945000	Enhancers	Fetal Lung	lung
10	chr8:39941800-39944000	Weak transcription	HepG2	liver
11	chr8:39942000-39943400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr8:39942000-39943600	Weak transcription	Colon Smooth Muscle	Colon
13	chr8:39942200-39942400	Enhancers	Fetal Brain Male	brain
14	chr8:39942800-39944600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:39943200-39944600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr8:39943400-39944000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:39943400-39944400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:39943400-39944600	Enhancers	Rectal Smooth Muscle	rectum
19	chr8:39943600-39944000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr8:39943600-39944200	Enhancers	Colon Smooth Muscle	Colon
21	chr8:39943600-39944600	Enhancers	Fetal Stomach	stomach
22	chr8:39943800-39944000	Enhancers	Stomach Smooth Muscle	stomach
23	chr8:39944000-39945200	Enhancers	HepG2	liver
24	chr8:39944000-39950800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr8:39944200-39949800	Weak transcription	Colon Smooth Muscle	Colon
26	chr8:39944600-39948200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr8:39944600-39948200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr8:39944600-39950200	Weak transcription	Rectal Smooth Muscle	rectum
29	chr8:39945000-39945200	Enhancers	Ovary	ovary
30	chr8:39945200-39948200	Weak transcription	HepG2	liver
31	chr8:39946200-39946400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr8:39946400-39946600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr8:39946600-39948200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr8:39948200-39948400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr8:39948200-39948400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr8:39948200-39948400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:39948200-39948600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr8:39948200-39948600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr8:39948200-39948600	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr8:39948200-39948600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr8:39948200-39948600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:39948200-39948600	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr8:39948200-39948800	Enhancers	HepG2	liver
44	chr8:39948200-39949000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr8:39948200-39949200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:39948200-39949200	Enhancers	Stomach Mucosa	stomach
47	chr8:39948200-39950800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr8:39948200-39951000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr8:39948400-39948600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr8:39948400-39948600	Enhancers	iPS-15b Cell Line	embryonic stem cell

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