Variant report

Variant	nsv831285
Chromosome Location	chr8:35485874-35648117
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	ATF1	chr8:35535442-35535506	K562	blood:	n/a	n/a
2	BACH1	chr8:35524193-35524227	K562	blood:	n/a	n/a
3	CCNT2	chr8:35527398-35527598	K562	blood:	n/a	n/a
4	CEBPB	chr8:35497562-35497821	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:35643318-35643686	HepG2	liver:	n/a	chr8:35643499-35643510
6	CEBPB	chr8:35587769-35588129	A549	lung:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
7	CEBPB	chr8:35490872-35490959	HepG2	liver:	n/a	chr8:35490916-35490929 chr8:35490917-35490928 chr8:35490916-35490927
8	CEBPB	chr8:35497542-35497841	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:35555536-35555860	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr8:35637840-35638217	H1-hESC	embryonic stem cell:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
11	CEBPB	chr8:35641050-35641476	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr8:35643317-35643677	Hela-S3	cervix:	n/a	chr8:35643499-35643510
13	CEBPB	chr8:35643317-35643693	IMR90	lung:	n/a	chr8:35643499-35643510
14	CEBPB	chr8:35497546-35497854	IMR90	lung:	n/a	n/a
15	CEBPB	chr8:35539752-35540073	HepG2	liver:	n/a	chr8:35539891-35539908 chr8:35539821-35539834
16	CEBPB	chr8:35637869-35638225	IMR90	lung:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
17	CEBPB	chr8:35643320-35643687	H1-hESC	embryonic stem cell:	n/a	chr8:35643499-35643510
18	CEBPB	chr8:35575000-35575611	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:35497599-35497849	A549	lung:	n/a	n/a
20	CEBPB	chr8:35643373-35643678	K562	blood:	n/a	chr8:35643499-35643510
21	CEBPB	chr8:35587803-35588127	H1-hESC	embryonic stem cell:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
22	CEBPB	chr8:35618307-35618518	A549	lung:	n/a	chr8:35618369-35618382
23	CEBPB	chr8:35637870-35638208	A549	lung:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
24	CEBPB	chr8:35637927-35638130	K562	blood:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
25	CEBPB	chr8:35643317-35643694	A549	lung:	n/a	chr8:35643499-35643510
26	CEBPB	chr8:35502473-35502530	A549	lung:	n/a	n/a
27	CEBPB	chr8:35555605-35555833	K562	blood:	n/a	n/a
28	CEBPB	chr8:35587790-35588138	IMR90	lung:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
29	CEBPB	chr8:35637878-35638216	HepG2	liver:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
30	CEBPB	chr8:35515200-35515231	HepG2	liver:	n/a	chr8:35515204-35515215
31	CEBPB	chr8:35643342-35643712	ECC-1	luminal epithelium:	n/a	chr8:35643499-35643510
32	CEBPB	chr8:35539839-35540086	A549	lung:	n/a	chr8:35539891-35539908
33	CEBPB	chr8:35555531-35555856	A549	lung:	n/a	n/a
34	CEBPB	chr8:35643368-35643653	ECC-1	luminal epithelium:	n/a	chr8:35643499-35643510
35	CEBPB	chr8:35587780-35588134	HepG2	liver:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
36	CEBPB	chr8:35602643-35602843	HepG2	liver:	n/a	chr8:35602724-35602735
37	CEBPB	chr8:35587784-35588055	K562	blood:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
38	CTBP2	chr8:35575428-35576630	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:35622640-35622790	GM12873	blood:	n/a	n/a
40	CTCF	chr8:35515240-35515247	GM13977	blood:	n/a	n/a
41	CTCF	chr8:35622640-35622790	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr8:35622699-35622822	Medullo	brain:	n/a	n/a
43	CTCF	chr8:35622760-35622910	HRE	kidney:	n/a	n/a
44	CTCF	chr8:35622580-35622730	GM12868	blood:	n/a	n/a
45	CTCF	chr8:35622620-35622770	RPTEC	kidney:	n/a	n/a
46	CTCF	chr8:35622546-35622840	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:35622700-35622850	SAEC	small airway:	n/a	n/a
48	CTCF	chr8:35622700-35622850	NB4	blood:	n/a	n/a
49	CTCF	chr8:35622526-35622930	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr8:35622760-35622910	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:35501934-35501984	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:35613299-35613349	AoSMC	blood vessel:	n/a
3	chr8:35580432-35580482	HEEpiC	esophagus:	n/a
4	chr8:35576222-35576272	HEEpiC	esophagus:	n/a
5	chr8:35598326-35598376	Hela-S3	cervix:	n/a
6	chr8:35598326-35598376	GM19239	blood:	n/a
7	chr8:35598326-35598376	ovcar-3	ovarian:	n/a
8	chr8:35540239-35540289	MCF10A-Er-Src	breast:	n/a
9	chr8:35580432-35580482	SK-N-SH	brain:	n/a
10	chr8:35598326-35598376	SK-N-MC	brain:	n/a
11	chr8:35580715-35580765	CMK	blood:	n/a
12	chr8:35581526-35581576	HCPEpiC	choroid plexus:	n/a
13	chr8:35613299-35613349	AG10803	skin:	n/a
14	chr8:35581526-35581576	Hela-S3	cervix:	n/a
15	chr8:35598326-35598376	A549	lung:	n/a
16	chr8:35580432-35580482	HEK293	kidney:	embryo
17	chr8:35580432-35580482	AG04450	lung:	fetal
18	chr8:35576222-35576272	Jurkat	blood:	n/a
19	chr8:35613299-35613349	SK-N-SH	brain:	n/a
20	chr8:35540239-35540289	HCPEpiC	choroid plexus:	n/a
21	chr8:35580432-35580482	CMK	blood:	n/a
22	chr8:35580432-35580482	HRCEpiC	kidney:	n/a
23	chr8:35613299-35613349	HCPEpiC	choroid plexus:	n/a
24	chr8:35580715-35580765	SK-N-SH	brain:	n/a
25	chr8:35581526-35581576	HAEpiC	amniotic membrane:	n/a
26	chr8:35540239-35540289	U87	brain:	n/a
27	chr8:35598326-35598376	HNPCEpiC	eye:	n/a
28	chr8:35580715-35580765	MCF10A-Er-Src	breast:	n/a
29	chr8:35540239-35540289	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:35581526-35581576	GM12878	blood:	n/a
31	chr8:35580432-35580482	HNPCEpiC	eye:	n/a
32	chr8:35580715-35580765	AoSMC	blood vessel:	n/a
33	chr8:35580715-35580765	HMEC	breast:	n/a
34	chr8:35581526-35581576	ProgFib	skin:	n/a
35	chr8:35540239-35540289	Jurkat	blood:	n/a
36	chr8:35501934-35501984	ProgFib	skin:	n/a
37	chr8:35598326-35598376	NB4	blood:	n/a
38	chr8:35613299-35613349	BJ	skin:	n/a
39	chr8:35501934-35501984	Jurkat	blood:	n/a
40	chr8:35501934-35501984	HAEpiC	amniotic membrane:	n/a
41	chr8:35581526-35581576	BJ	skin:	n/a
42	chr8:35576222-35576272	SK-N-SH	brain:	n/a
43	chr8:35576222-35576272	GM12878	blood:	n/a
44	chr8:35501934-35501984	SAEC	small airway:	n/a
45	chr8:35598326-35598376	SAEC	small airway:	n/a
46	chr8:35598326-35598376	CMK	blood:	n/a
47	chr8:35576222-35576272	NB4	blood:	n/a
48	chr8:35581526-35581576	GM12891	blood:	n/a
49	chr8:35576222-35576272	Hela-S3	cervix:	n/a
50	chr8:35581526-35581576	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:35497530..35499054-chr8:35564853..35566842,2	K562	blood:
2	chr8:35497530..35499054-chr8:35564853..35566842,2	K562	blood:
3	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
4	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:
5	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:
6	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:
7	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
8	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:

Variant related genes	Relation type
UNC5D	TF binding region
ENSG00000233863	TF binding region
UNC5D	CpG island
ENSG00000233863	CpG island

Extended variants
information (count: 5325 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:5325 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557207434	chr8:35485877-35485878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575548057	chr8:35485909-35485910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs59214815	chr8:35485937-35485938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563473982	chr8:35485978-35485979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545353479	chr8:35485985-35485986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564113634	chr8:35486021-35486022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530744697	chr8:35486029-35486030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548829311	chr8:35486129-35486130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374194882	chr8:35486167-35486168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559910305	chr8:35486186-35486187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2978585	chr8:35486208-35486209	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs191329821	chr8:35486266-35486267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs180851430	chr8:35486272-35486273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550809618	chr8:35486284-35486285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148479606	chr8:35486290-35486291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185506945	chr8:35486332-35486333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551745078	chr8:35486405-35486406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs189868893	chr8:35486427-35486428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561052873	chr8:35486453-35486454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570818016	chr8:35486458-35486459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117822517	chr8:35486477-35486478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377161682	chr8:35486503-35486504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs546298104	chr8:35486531-35486532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568486048	chr8:35486546-35486547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs183249721	chr8:35486570-35486571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs142729547	chr8:35486640-35486641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188838240	chr8:35486649-35486650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546315893	chr8:35486679-35486680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs191726060	chr8:35486715-35486716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs558200048	chr8:35486744-35486745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs572774421	chr8:35486770-35486771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10283043	chr8:35486779-35486780	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs555405966	chr8:35486782-35486783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538722890	chr8:35486824-35486825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183558595	chr8:35486862-35486863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs139470850	chr8:35486880-35486881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370350947	chr8:35486881-35486882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562667217	chr8:35486900-35486901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188222739	chr8:35486987-35486988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149681870	chr8:35486997-35486998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146696162	chr8:35487023-35487024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570197389	chr8:35487054-35487055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58748125	chr8:35487063-35487064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs140312188	chr8:35487075-35487076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556051093	chr8:35487104-35487105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568175398	chr8:35487136-35487137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375238599	chr8:35487152-35487153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569930345	chr8:35487166-35487167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550710155	chr8:35487169-35487170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574095469	chr8:35487186-35487187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	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
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
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
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	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
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21785460	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35483400-35489400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr8:35483600-35489600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr8:35483600-35493800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr8:35484200-35489400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr8:35484200-35489600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:35484200-35490000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:35484600-35489000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:35484800-35486000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr8:35484800-35488000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr8:35485000-35486000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr8:35485800-35486400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr8:35486000-35486200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr8:35486000-35486600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:35486200-35486600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr8:35486400-35489000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr8:35486600-35486800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr8:35486600-35494000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:35486800-35494200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr8:35487800-35489000	Enhancers	Adipose Nuclei	Adipose
20	chr8:35488000-35488400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr8:35488400-35489600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:35489000-35490000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr8:35489000-35490400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr8:35489000-35490800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:35489000-35491200	Weak transcription	Adipose Nuclei	Adipose
26	chr8:35489400-35489600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr8:35489400-35490000	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr8:35489400-35490400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:35489400-35490600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:35489600-35490000	Enhancers	H9 Cell Line	embryonic stem cell
31	chr8:35489600-35490200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr8:35489600-35490200	Enhancers	H1 Cell Line	embryonic stem cell
33	chr8:35489600-35490400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr8:35489600-35494200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr8:35490000-35490400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr8:35490000-35490600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:35490000-35493800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr8:35490000-35494000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr8:35490000-35494400	Enhancers	Fetal Heart	heart
40	chr8:35490200-35491800	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr8:35490200-35493800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr8:35490400-35491400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr8:35490400-35493800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr8:35490400-35493800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:35490600-35490800	Enhancers	Colon Smooth Muscle	Colon
46	chr8:35490600-35494400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:35490800-35492800	Weak transcription	Colon Smooth Muscle	Colon
48	chr8:35491200-35491600	Enhancers	Adipose Nuclei	Adipose
49	chr8:35491200-35492200	Enhancers	Fetal Lung	lung
50	chr8:35491400-35492000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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