Variant report

Variant	esv3350740
Chromosome Location	chr8:87080786-87083934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:30)
CpG islands
(count:610)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:30 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD1	chr8:87081828-87082117	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr8:87081436-87081897	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr8:87083800-87083842	LNCaP	prostate:	n/a	n/a
4	CTCF	chr8:87083346-87083409	LNCaP	prostate:	n/a	n/a
5	E2F6	chr8:87081288-87082136	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F6	chr8:87081467-87081963	H1-hESC	embryonic stem cell:	n/a	n/a
7	GTF2F1	chr8:87081614-87081623	H1-hESC	embryonic stem cell:	n/a	n/a
8	MAX	chr8:87081352-87081824	H1-hESC	embryonic stem cell:	n/a	chr8:87081650-87081659
9	MAX	chr8:87081326-87082025	H1-hESC	embryonic stem cell:	n/a	chr8:87081650-87081659
10	MAX	chr8:87081276-87081979	H1-hESC	embryonic stem cell:	n/a	chr8:87081650-87081659
11	MXI1	chr8:87081705-87081831	H1-hESC	embryonic stem cell:	n/a	n/a
12	MYC	chr8:87083494-87083585	GM12878	blood:	n/a	n/a
13	MYC	chr8:87081929-87082009	H1-hESC	embryonic stem cell:	n/a	n/a
14	POLR2A	chr8:87081455-87082095	H1-hESC	embryonic stem cell:	n/a	n/a
15	POLR2A	chr8:87081534-87082000	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr8:87083774-87083888	ProgFib	skin:	n/a	n/a
17	POLR2A	chr8:87081253-87081568	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr8:87081284-87081474	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr8:87083708-87083749	ProgFib	skin:	n/a	n/a
20	POLR2A	chr8:87081751-87081915	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr8:87081339-87081441	H1-hESC	embryonic stem cell:	n/a	n/a
22	TBP	chr8:87081415-87081971	H1-hESC	embryonic stem cell:	n/a	n/a
23	TCF12	chr8:87081214-87081622	H1-hESC	embryonic stem cell:	n/a	n/a
24	TCF12	chr8:87081377-87081638	H1-hESC	embryonic stem cell:	n/a	n/a
25	USF1	chr8:87081487-87081747	H1-hESC	embryonic stem cell:	n/a	n/a
26	USF1	chr8:87081408-87081771	H1-hESC	embryonic stem cell:	n/a	n/a
27	USF2	chr8:87081534-87081874	H1-hESC	embryonic stem cell:	n/a	n/a
28	YY1	chr8:87081072-87081495	H1-hESC	embryonic stem cell:	n/a	chr8:87081255-87081267
29	YY1	chr8:87080984-87081843	H1-hESC	embryonic stem cell:	n/a	chr8:87081255-87081267
30	ZNF143	chr8:87081296-87081748	H1-hESC	embryonic stem cell:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:87081553-87081603	AG09309	skin:	n/a
2	chr8:87082045-87082095	BJ	skin:	n/a
3	chr8:87082008-87082058	Hela-S3	cervix:	n/a
4	chr8:87081553-87081603	BE2_C	brain:	n/a
5	chr8:87081770-87081820	K562	blood:	n/a
6	chr8:87082065-87082115	GM12878	blood:	n/a
7	chr8:87081553-87081603	NB4	blood:	n/a
8	chr8:87082205-87082255	PFSK-1	brain:	n/a
9	chr8:87081978-87082028	MCF10A-Er-Src	breast:	n/a
10	chr8:87081978-87082028	SAEC	small airway:	n/a
11	chr8:87081553-87081603	SKMC	muscle:	n/a
12	chr8:87081978-87082028	ovcar-3	ovarian:	n/a
13	chr8:87082023-87082073	HRCEpiC	kidney:	n/a
14	chr8:87082045-87082095	GM12891	blood:	n/a
15	chr8:87082014-87082064	GM12878	blood:	n/a
16	chr8:87082008-87082058	LNCaP	prostate:	n/a
17	chr8:87081978-87082028	LNCaP	prostate:	n/a
18	chr8:87081978-87082028	HCPEpiC	choroid plexus:	n/a
19	chr8:87081770-87081820	NH-A	brain:	n/a
20	chr8:87082065-87082115	PFSK-1	brain:	n/a
21	chr8:87081978-87082028	GM12892	blood:	n/a
22	chr8:87081654-87081704	HAEpiC	amniotic membrane:	n/a
23	chr8:87082065-87082115	BE2_C	brain:	n/a
24	chr8:87081654-87081704	GM12891	blood:	n/a
25	chr8:87082045-87082095	Hepatocyte	liver:	n/a
26	chr8:87082023-87082073	AG04449	skin:	fetal
27	chr8:87081553-87081603	HRPEpiC	eye:	n/a
28	chr8:87082014-87082064	HUVEC	blood vessel:	n/a
29	chr8:87082023-87082073	BJ	skin:	n/a
30	chr8:87082014-87082064	HIPEpiC	eye:	n/a
31	chr8:87081978-87082028	GM12891	blood:	n/a
32	chr8:87082205-87082255	RPTEC	kidney:	n/a
33	chr8:87081654-87081704	SK-N-SH_RA	brain:	n/a
34	chr8:87082023-87082073	HPAEpiC	pulmonary alveolar:	n/a
35	chr8:87081978-87082028	HIPEpiC	eye:	n/a
36	chr8:87082014-87082064	AoSMC	blood vessel:	n/a
37	chr8:87081654-87081704	HMEC	breast:	n/a
38	chr8:87081654-87081704	AG09319	gingival:	n/a
39	chr8:87082023-87082073	HCT-116	colon:	n/a
40	chr8:87081770-87081820	HCPEpiC	choroid plexus:	n/a
41	chr8:87081654-87081704	HRCEpiC	kidney:	n/a
42	chr8:87082008-87082058	Hepatocyte	liver:	n/a
43	chr8:87082205-87082255	AG04449	skin:	fetal
44	chr8:87082008-87082058	AoSMC	blood vessel:	n/a
45	chr8:87082014-87082064	Hela-S3	cervix:	n/a
46	chr8:87082014-87082064	MCF-7	breast:	n/a
47	chr8:87081654-87081704	GM12892	blood:	n/a
48	chr8:87081553-87081603	ovcar-3	ovarian:	n/a
49	chr8:87082065-87082115	HRE	kidney:	n/a
50	chr8:87081654-87081704	HRPEpiC	eye:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:87079401..87081548-chr8:87093916..87096819,2	MCF-7	breast:
2	chr8:87076395..87078069-chr8:87079542..87081146,2	MCF-7	breast:
3	chr8:87078387..87081366-chr8:87083047..87085663,2	K562	blood:
4	chr8:87078387..87081366-chr8:87083047..87085663,2	K562	blood:

No data

Variant related genes	Relation type
PSKH2	TF binding region
ATP6V0D2	TF binding region
PSKH2	CpG island
ATP6V0D2	CpG island

Extended variants
information (count: 136 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:136 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183403339	chr8:87080801-87080802	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
2	rs573863635	chr8:87080820-87080821	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs79393815	chr8:87080864-87080865	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
4	rs549159208	chr8:87080973-87080974	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
5	rs528227785	chr8:87081004-87081005	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs13439162	chr8:87081010-87081011	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs13438947	chr8:87081027-87081028	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs530442691	chr8:87081065-87081066	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs375903860	chr8:87081069-87081070	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558833926	chr8:87081080-87081081	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs13439338	chr8:87081085-87081086	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs570043100	chr8:87081113-87081114	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187941977	chr8:87081117-87081118	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192803111	chr8:87081118-87081119	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs62509892	chr8:87081119-87081120	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs371270651	chr8:87081134-87081135	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569215751	chr8:87081153-87081154	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs375032069	chr8:87081156-87081157	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs565942817	chr8:87081176-87081177	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs535070233	chr8:87081187-87081188	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs141275352	chr8:87081195-87081196	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs146927882	chr8:87081220-87081221	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs183597573	chr8:87081232-87081233	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs557269646	chr8:87081237-87081238	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs113104542	chr8:87081266-87081267	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs574725495	chr8:87081272-87081273	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs542833360	chr8:87081284-87081285	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs553160986	chr8:87081300-87081301	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs189496586	chr8:87081332-87081333	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs192400064	chr8:87081335-87081336	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs10085963	chr8:87081336-87081337	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs530506480	chr8:87081339-87081340	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs543852384	chr8:87081341-87081342	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs150939580	chr8:87081395-87081396	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373140255	chr8:87081406-87081407	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs529505087	chr8:87081489-87081490	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs549269251	chr8:87081492-87081493	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs566237412	chr8:87081518-87081519	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs184834016	chr8:87081543-87081544	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs200126153	chr8:87081644-87081645	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs571676571	chr8:87081668-87081669	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs267602022	chr8:87081674-87081675	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs146243331	chr8:87081675-87081676	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
44	rs370321743	chr8:87081679-87081680	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs140592507	chr8:87081697-87081698	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs56204225	chr8:87081711-87081712	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs372808822	chr8:87081716-87081717	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs375810069	chr8:87081727-87081728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs567670091	chr8:87081748-87081749	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs370079446	chr8:87081758-87081759	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	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
Cancer	16751803	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
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:87076800-87087200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:87079600-87081000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:87080000-87081600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr8:87080200-87081000	Enhancers	Brain Germinal Matrix	brain
5	chr8:87080400-87081000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
6	chr8:87080400-87081000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:87080400-87081400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:87080400-87081400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:87080600-87080800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chr8:87080600-87081000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
11	chr8:87080800-87081000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
12	chr8:87080800-87081000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
13	chr8:87080800-87081000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
14	chr8:87080800-87081000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:87080800-87081200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
16	chr8:87080800-87081200	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
17	chr8:87080800-87081200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
18	chr8:87080800-87081400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
19	chr8:87081000-87081400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
20	chr8:87081000-87081400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
21	chr8:87081000-87081600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr8:87081000-87081600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
23	chr8:87081000-87081600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr8:87081000-87081600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
25	chr8:87081000-87081600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:87081000-87082000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
27	chr8:87081000-87082000	Bivalent Enhancer	Brain Germinal Matrix	brain
28	chr8:87081200-87081600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
29	chr8:87081200-87081600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr8:87081200-87081800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
31	chr8:87081200-87081800	Bivalent Enhancer	Fetal Heart	heart
32	chr8:87081200-87082200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
33	chr8:87081200-87082200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
34	chr8:87081400-87081600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
35	chr8:87081400-87081600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:87081400-87081600	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:87081400-87081800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr8:87081400-87081800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr8:87081400-87081800	Bivalent Enhancer	Left Ventricle	heart
40	chr8:87081400-87082000	Bivalent Enhancer	Fetal Brain Male	brain
41	chr8:87081400-87082000	Enhancers	Placenta Amnion	Placenta Amnion
42	chr8:87081400-87082200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
43	chr8:87081600-87081800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
44	chr8:87081600-87081800	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr8:87081600-87081800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr8:87081600-87081800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:87081600-87081800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:87081600-87081800	Bivalent Enhancer	Brain Hippocampus Middle	brain
49	chr8:87081600-87081800	Enhancers	Pancreas	Pancrea
50	chr8:87081600-87081800	Flanking Bivalent TSS/Enh	Right Ventricle	heart

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