Variant report

Variant	esv3423266
Chromosome Location	chr8:69242023-69244571
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:165)
CpG islands
(count:918)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:165 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:69242862-69243752	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:69244369-69244445	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr8:69242704-69243064	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr8:69243419-69244042	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr8:69242636-69243750	H1-hESC	embryonic stem cell:	n/a	chr8:69243224-69243234 chr8:69243121-69243131
6	CREB1	chr8:69242735-69243268	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTBP2	chr8:69242647-69243935	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr8:69242842-69242995	MCF-7	breast:	n/a	n/a
9	CTCF	chr8:69243100-69243250	SAEC	small airway:	n/a	chr8:69243128-69243138
10	CTCF	chr8:69242820-69242970	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr8:69242836-69243288	ProgFib	skin:	n/a	chr8:69243128-69243138
12	CTCF	chr8:69243080-69243230	HCFaa	heart:	n/a	chr8:69243128-69243138
13	CTCF	chr8:69243051-69243217	MCF-7	breast:	n/a	chr8:69243128-69243138
14	CTCF	chr8:69242868-69243286	NHEK	skin:	n/a	chr8:69243128-69243138
15	CTCF	chr8:69242840-69242990	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr8:69243620-69243770	HMEC	breast:	n/a	n/a
17	CTCF	chr8:69242840-69242990	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr8:69243606-69243699	Medullo	brain:	n/a	n/a
19	CTCF	chr8:69243084-69243218	Medullo	brain:	n/a	chr8:69243128-69243138
20	CTCF	chr8:69243403-69243518	MCF-7	breast:	n/a	n/a
21	CTCF	chr8:69242866-69243346	MCF-7	breast:	n/a	chr8:69243128-69243138
22	CTCF	chr8:69242900-69243050	MCF-7	breast:	n/a	n/a
23	CTCF	chr8:69242740-69242890	HEK293	kidney:	n/a	n/a
24	CTCF	chr8:69243660-69243810	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr8:69243060-69243210	AG09319	gingival:	n/a	chr8:69243128-69243138
26	CTCF	chr8:69243584-69243871	MCF-7	breast:	n/a	n/a
27	CTCF	chr8:69243700-69243850	MCF-7	breast:	n/a	n/a
28	CTCF	chr8:69243060-69243210	RPTEC	kidney:	n/a	chr8:69243128-69243138
29	CTCF	chr8:69243080-69243230	HRE	kidney:	n/a	chr8:69243128-69243138
30	CTCF	chr8:69243040-69243190	HRE	kidney:	n/a	chr8:69243128-69243138
31	CTCF	chr8:69243107-69243173	LNCaP	prostate:	n/a	chr8:69243128-69243138
32	CTCF	chr8:69243100-69243250	BJ	skin:	n/a	chr8:69243128-69243138
33	CTCF	chr8:69242815-69243293	A549	lung:	n/a	chr8:69243128-69243138
34	CTCF	chr8:69243560-69243710	HEK293	kidney:	n/a	n/a
35	CTCF	chr8:69243879-69243881	A549	lung:	n/a	n/a
36	CTCF	chr8:69243040-69243190	NHDF-neo	bronchial:	n/a	chr8:69243128-69243138
37	CTCF	chr8:69242660-69242810	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr8:69243620-69243770	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr8:69243503-69243518	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:69243100-69243250	HRPEpiC	eye:	n/a	chr8:69243128-69243138
41	CTCF	chr8:69242960-69243110	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr8:69243140-69243290	AG10803	skin:	n/a	n/a
43	CTCF	chr8:69243100-69243250	HFF	foreskin:	n/a	chr8:69243128-69243138
44	CTCF	chr8:69243117-69243205	Pancreas_OC	pancreas:	n/a	chr8:69243128-69243138
45	CTCF	chr8:69242863-69243298	Fibrobl	skin:	n/a	chr8:69243128-69243138
46	CTCF	chr8:69243080-69243230	GM12874	blood:	n/a	chr8:69243128-69243138
47	CTCF	chr8:69243100-69243250	GM12866	blood:	n/a	chr8:69243128-69243138
48	CTCF	chr8:69243060-69243210	HEK293	kidney:	n/a	chr8:69243128-69243138
49	CTCF	chr8:69243020-69243170	HMEC	breast:	n/a	chr8:69243128-69243138
50	CTCF	chr8:69243566-69243899	NHEK	skin:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:69242921-69242971	MCF10A-Er-Src	breast:	n/a
2	chr8:69244553-69244603	HRE	kidney:	n/a
3	chr8:69244152-69244202	U87	brain:	n/a
4	chr8:69242921-69242971	MCF10A-Er-Src	breast:	n/a
5	chr8:69244553-69244603	HRE	kidney:	n/a
6	chr8:69244152-69244202	U87	brain:	n/a
7	chr8:69243398-69243448	HCM	heart:	n/a
8	chr8:69243752-69243802	GM19239	blood:	n/a
9	chr8:69244205-69244255	T-47D	breast:	n/a
10	chr8:69242921-69242971	ovcar-3	ovarian:	n/a
11	chr8:69243752-69243802	MCF-7	breast:	n/a
12	chr8:69243904-69243954	H1-hESC	embryonic stem cell:	embryo
13	chr8:69244205-69244255	BJ	skin:	n/a
14	chr8:69242974-69243024	HPAEpiC	pulmonary alveolar:	n/a
15	chr8:69244152-69244202	SAEC	small airway:	n/a
16	chr8:69242974-69243024	A549	lung:	n/a
17	chr8:69244343-69244393	Jurkat	blood:	n/a
18	chr8:69243602-69243652	HCPEpiC	choroid plexus:	n/a
19	chr8:69243398-69243448	HIPEpiC	eye:	n/a
20	chr8:69243602-69243652	ECC-1	luminal epithelium:	n/a
21	chr8:69243602-69243652	K562	blood:	n/a
22	chr8:69242974-69243024	BJ	skin:	n/a
23	chr8:69244205-69244255	AoSMC	blood vessel:	n/a
24	chr8:69243398-69243448	GM12892	blood:	n/a
25	chr8:69243510-69243560	HCM	heart:	n/a
26	chr8:69243602-69243652	AG09319	gingival:	n/a
27	chr8:69243602-69243652	HRPEpiC	eye:	n/a
28	chr8:69243285-69243335	PFSK-1	brain:	n/a
29	chr8:69243752-69243802	AG04450	lung:	fetal
30	chr8:69242974-69243024	HUVEC	blood vessel:	n/a
31	chr8:69242974-69243024	AG10803	skin:	n/a
32	chr8:69243752-69243802	PrEC	prostate:	n/a
33	chr8:69244510-69244560	HRCEpiC	kidney:	n/a
34	chr8:69243486-69243536	HCPEpiC	choroid plexus:	n/a
35	chr8:69244553-69244603	Hepatocyte	liver:	n/a
36	chr8:69243752-69243802	LNCaP	prostate:	n/a
37	chr8:69244553-69244603	K562	blood:	n/a
38	chr8:69244343-69244393	NH-A	brain:	n/a
39	chr8:69243285-69243335	HEEpiC	esophagus:	n/a
40	chr8:69242509-69242559	AG04449	skin:	fetal
41	chr8:69244510-69244560	AG04449	skin:	fetal
42	chr8:69243510-69243560	SKMC	muscle:	n/a
43	chr8:69244553-69244603	ProgFib	skin:	n/a
44	chr8:69243398-69243448	NHBE	bronchial:	n/a
45	chr8:69244205-69244255	AG09319	gingival:	n/a
46	chr8:69244152-69244202	H1-hESC	embryonic stem cell:	embryo
47	chr8:69243285-69243335	LNCaP	prostate:	n/a
48	chr8:69243398-69243448	AG04450	lung:	fetal
49	chr8:69243602-69243652	AG04450	lung:	fetal
50	chr8:69244343-69244393	HCF	heart:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-664D7.4.1-4	chr8:69243542-69243726	NR_038877

No data

Variant related genes	Relation type
C8orf34	TF binding region
ENSG00000248801	TF binding region
C8orf34	CpG island
ENSG00000248801	CpG island

Extended variants
information (count: 114 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:114 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552207476	chr8:69242023-69242024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs137883534	chr8:69242030-69242031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370096850	chr8:69242122-69242123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551730644	chr8:69242126-69242127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534591603	chr8:69242148-69242149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371581401	chr8:69242165-69242166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs705992	chr8:69242226-69242227	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs527298258	chr8:69242242-69242243	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs193177868	chr8:69242304-69242305	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs567358630	chr8:69242339-69242340	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs141361872	chr8:69242351-69242352	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs113848195	chr8:69242389-69242390	Bivalent/Poised TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs185417837	chr8:69242407-69242408	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs77323698	chr8:69242430-69242431	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs28589928	chr8:69242432-69242433	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs150259417	chr8:69242460-69242461	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs868546	chr8:69242537-69242538	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs138950723	chr8:69242539-69242540	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs149442563	chr8:69242578-69242579	Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs574883068	chr8:69242638-69242639	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs543983488	chr8:69242654-69242655	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs563752263	chr8:69242687-69242688	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs375145268	chr8:69242705-69242706	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs557337355	chr8:69242727-69242728	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs545191867	chr8:69242761-69242762	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs190669270	chr8:69242763-69242764	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs527546784	chr8:69242779-69242780	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs547379577	chr8:69242782-69242783	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs560763460	chr8:69242789-69242790	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs368232723	chr8:69242799-69242800	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs180682881	chr8:69242958-69242959	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs10090284	chr8:69242960-69242961	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs113110777	chr8:69242961-69242962	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs73683492	chr8:69242966-69242967	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs116317841	chr8:69242974-69242975	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs1971527	chr8:69242983-69242984	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs73254829	chr8:69243014-69243015	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs149389557	chr8:69243017-69243018	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs564652660	chr8:69243021-69243022	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs186967489	chr8:69243029-69243030	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs370913539	chr8:69243030-69243031	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs201838391	chr8:69243040-69243041	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs555244228	chr8:69243043-69243044	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs568392624	chr8:69243059-69243060	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs537429299	chr8:69243062-69243063	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs375050527	chr8:69243063-69243064	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs557508106	chr8:69243119-69243120	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs76049615	chr8:69243170-69243171	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs1971404	chr8:69243173-69243174	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs117404630	chr8:69243175-69243176	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
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
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
Cancer	16751803	CNVD
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	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
Colorectal cancer	16272173	CNVD
Melanoma	22183965	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Colorectal cancer	21645411	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69240400-69242400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr8:69240800-69242400	Weak transcription	Aorta	Aorta
3	chr8:69242200-69242400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:69242200-69243000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
5	chr8:69242200-69246200	Active TSS	Brain Anterior Caudate	brain
6	chr8:69242200-69246200	Active TSS	Fetal Brain Female	brain
7	chr8:69242400-69242600	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
8	chr8:69242400-69242600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:69242400-69242600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr8:69242400-69242600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:69242400-69242600	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
12	chr8:69242400-69242600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
13	chr8:69242400-69242600	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
14	chr8:69242400-69242600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
15	chr8:69242400-69242600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr8:69242400-69242600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr8:69242400-69242600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:69242400-69242600	Enhancers	Adipose Nuclei	Adipose
19	chr8:69242400-69242600	Enhancers	Aorta	Aorta
20	chr8:69242400-69242600	Bivalent Enhancer	Fetal Kidney	kidney
21	chr8:69242400-69242600	Bivalent Enhancer	Fetal Lung	lung
22	chr8:69242400-69242600	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr8:69242400-69242800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr8:69242400-69242800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr8:69242400-69242800	Active TSS	Brain Cingulate Gyrus	brain
26	chr8:69242400-69243000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr8:69242400-69243400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr8:69242400-69243400	Active TSS	Brain Inferior Temporal Lobe	brain
29	chr8:69242400-69243400	Active TSS	Brain Substantia Nigra	brain
30	chr8:69242400-69243400	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
31	chr8:69242400-69244200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:69242400-69244200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr8:69242400-69244800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr8:69242400-69244800	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:69242400-69244800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
36	chr8:69242400-69245000	Active TSS	H9 Cell Line	embryonic stem cell
37	chr8:69242400-69245000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
38	chr8:69242400-69245000	Active TSS	Brain Angular Gyrus	brain
39	chr8:69242400-69245200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:69242400-69245200	Active TSS	Brain Hippocampus Middle	brain
41	chr8:69242600-69242800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr8:69242600-69242800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:69242600-69242800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
44	chr8:69242600-69242800	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
45	chr8:69242600-69242800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
46	chr8:69242600-69242800	Enhancers	Fetal Brain Male	brain
47	chr8:69242600-69242800	Flanking Active TSS	Placenta Amnion	Placenta Amnion
48	chr8:69242600-69242800	Active TSS	Right Atrium	heart
49	chr8:69242600-69242800	Flanking Bivalent TSS/Enh	Right Ventricle	heart
50	chr8:69242600-69242800	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle

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