Variant report

Variant	esv1819408
Chromosome Location	chr8:127835876-127898165
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1345)
CpG islands
(count:488)
Chromatin interactive
region (count:35)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:127836693-127836986	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:127888872-127889296	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:127888902-127889101	K562	blood:	n/a	n/a
4	ATF1	chr8:127840213-127840647	K562	blood:	n/a	n/a
5	ATF1	chr8:127868736-127868930	K562	blood:	n/a	n/a
6	ATF2	chr8:127874848-127875373	GM12878	blood:	n/a	n/a
7	ATF2	chr8:127888782-127889275	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr8:127888829-127889197	GM12878	blood:	n/a	n/a
9	ATF2	chr8:127874967-127875279	GM12878	blood:	n/a	n/a
10	ATF3	chr8:127888907-127889099	K562	blood:	n/a	n/a
11	BACH1	chr8:127836825-127836945	K562	blood:	n/a	n/a
12	BACH1	chr8:127841970-127841987	K562	blood:	n/a	n/a
13	BACH1	chr8:127865922-127865975	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:127860809-127860854	K562	blood:	n/a	n/a
15	BATF	chr8:127874949-127875281	GM12878	blood:	n/a	n/a
16	BATF	chr8:127874875-127875324	GM12878	blood:	n/a	n/a
17	BATF	chr8:127869411-127869807	GM12878	blood:	n/a	chr8:127869622-127869633 chr8:127869604-127869612
18	BATF	chr8:127869508-127869773	GM12878	blood:	n/a	chr8:127869622-127869633 chr8:127869604-127869612
19	BATF	chr8:127883861-127884216	GM12878	blood:	n/a	n/a
20	BCL11A	chr8:127874989-127875200	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:127874946-127875320	GM12878	blood:	n/a	n/a
22	BCLAF1	chr8:127888896-127889223	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:127888839-127889164	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:127875020-127875324	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:127888907-127889156	K562	blood:	n/a	n/a
26	BHLHE40	chr8:127851280-127851404	GM12878	blood:	n/a	chr8:127851281-127851294 chr8:127851283-127851292 chr8:127851283-127851292
27	BRCA1	chr8:127836660-127837161	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr8:127888810-127889293	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr8:127845197-127845222	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr8:127836609-127836949	K562	blood:	n/a	chr8:127836614-127836625
31	CCNT2	chr8:127840297-127840501	K562	blood:	n/a	n/a
32	CEBPB	chr8:127868763-127868958	A549	lung:	n/a	n/a
33	CEBPB	chr8:127854860-127856058	IMR90	lung:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
34	CEBPB	chr8:127855716-127856069	HepG2	liver:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
35	CEBPB	chr8:127850197-127850202	A549	lung:	n/a	n/a
36	CEBPB	chr8:127888959-127889134	K562	blood:	n/a	n/a
37	CEBPB	chr8:127855734-127855989	Hela-S3	cervix:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
38	CEBPB	chr8:127855726-127856078	A549	lung:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
39	CEBPB	chr8:127845647-127846692	IMR90	lung:	n/a	n/a
40	CEBPB	chr8:127855291-127855387	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:127839991-127840503	IMR90	lung:	n/a	n/a
42	CEBPB	chr8:127874991-127875238	IMR90	lung:	n/a	n/a
43	CEBPB	chr8:127846217-127846537	HepG2	liver:	n/a	n/a
44	CEBPB	chr8:127855303-127855421	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:127855243-127855498	A549	lung:	n/a	n/a
46	CEBPB	chr8:127850790-127850808	K562	blood:	n/a	n/a
47	CEBPB	chr8:127869489-127869835	IMR90	lung:	n/a	n/a
48	CEBPB	chr8:127870441-127870727	A549	lung:	n/a	chr8:127870614-127870625
49	CHD1	chr8:127888703-127889347	IMR90	lung:	n/a	n/a
50	CHD2	chr8:127888877-127889222	Hela-S3	cervix:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:127839581-127839631	GM19239	blood:	n/a
2	chr8:127889050-127889100	GM06990	blood:	n/a
3	chr8:127889295-127889345	ECC-1	luminal epithelium:	n/a
4	chr8:127846077-127846127	SK-N-SH	brain:	n/a
5	chr8:127866047-127866097	GM12878	blood:	n/a
6	chr8:127889295-127889345	A549	lung:	n/a
7	chr8:127846077-127846127	AG10803	skin:	n/a
8	chr8:127839581-127839631	HCT-116	colon:	n/a
9	chr8:127889050-127889100	T-47D	breast:	n/a
10	chr8:127889025-127889075	GM12892	blood:	n/a
11	chr8:127889050-127889100	AG09319	gingival:	n/a
12	chr8:127846077-127846127	GM06990	blood:	n/a
13	chr8:127846077-127846127	NH-A	brain:	n/a
14	chr8:127889025-127889075	BJ	skin:	n/a
15	chr8:127889050-127889100	LNCaP	prostate:	n/a
16	chr8:127889025-127889075	HRCEpiC	kidney:	n/a
17	chr8:127889050-127889100	CMK	blood:	n/a
18	chr8:127866047-127866097	A549	lung:	n/a
19	chr8:127889025-127889075	HepG2	liver:	n/a
20	chr8:127846077-127846127	HRCEpiC	kidney:	n/a
21	chr8:127839581-127839631	PrEC	prostate:	n/a
22	chr8:127889295-127889345	ProgFib	skin:	n/a
23	chr8:127889050-127889100	HRE	kidney:	n/a
24	chr8:127846077-127846127	IMR90	lung:	fetal
25	chr8:127839581-127839631	MCF-7	breast:	n/a
26	chr8:127889025-127889075	SK-N-MC	brain:	n/a
27	chr8:127889295-127889345	NHDF-neo	bronchial:	n/a
28	chr8:127846077-127846127	NB4	blood:	n/a
29	chr8:127837199-127837249	Jurkat	blood:	n/a
30	chr8:127889010-127889060	GM12878	blood:	n/a
31	chr8:127889010-127889060	HL-60	blood:	n/a
32	chr8:127889295-127889345	SAEC	small airway:	n/a
33	chr8:127889025-127889075	GM19239	blood:	n/a
34	chr8:127837199-127837249	ovcar-3	ovarian:	n/a
35	chr8:127866047-127866097	HRPEpiC	eye:	n/a
36	chr8:127846077-127846127	PANC-1	pancreas:	n/a
37	chr8:127839581-127839631	U87	brain:	n/a
38	chr8:127846077-127846127	SAEC	small airway:	n/a
39	chr8:127839581-127839631	HEK293	kidney:	embryo
40	chr8:127866047-127866097	ECC-1	luminal epithelium:	n/a
41	chr8:127846077-127846127	HEK293	kidney:	embryo
42	chr8:127837199-127837249	IMR90	lung:	fetal
43	chr8:127837199-127837249	SK-N-SH_RA	brain:	n/a
44	chr8:127889010-127889060	AG04450	lung:	fetal
45	chr8:127889025-127889075	MCF10A-Er-Src	breast:	n/a
46	chr8:127839581-127839631	HUVEC	blood vessel:	n/a
47	chr8:127846077-127846127	HRE	kidney:	n/a
48	chr8:127839581-127839631	AG10803	skin:	n/a
49	chr8:127837199-127837249	BE2_C	brain:	n/a
50	chr8:127889295-127889345	AG04450	lung:	fetal

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:127834592..127842945-chr8:128745185..128752445,14	MCF-7	breast:
2	chr8:127863317..127865201-chr8:127865656..127867797,3	K562	blood:
3	chr8:127897687..127899780-chr8:128012321..128014197,2	MCF-7	breast:
4	chr8:127858088..127860526-chr8:127861432..127863548,2	MCF-7	breast:
5	chr8:127889004..127891889-chr8:127895574..127897530,2	K562	blood:
6	chr8:127840741..127842385-chr8:128747394..128749992,2	MCF-7	breast:
7	chr8:127836631..127837289-chr8:127881392..127882026,2	MCF-7	breast:
8	chr8:127888513..127889240-chr8:128174738..128175621,2	MCF-7	breast:
9	chr8:127889004..127891889-chr8:127895574..127897530,2	K562	blood:
10	chr8:127850550..127853245-chr8:127857411..127860204,2	K562	blood:
11	chr8:127888435..127891716-chr8:128747434..128751329,3	MCF-7	breast:
12	chr8:127890394..127893328-chr8:128049298..128051966,2	MCF-7	breast:
13	chr8:127888506..127889510-chr8:128190851..128191526,3	K562	blood:
14	chr8:127888555..127889369-chr8:128050671..128051188,2	MCF-7	breast:
15	chr8:127888650..127889474-chr8:128219262..128219815,3	MCF-7	breast:
16	chr8:127888573..127889987-chr8:128190304..128191389,7	MCF-7	breast:
17	chr8:127887780..127894023-chr8:128746795..128750796,8	MCF-7	breast:
18	chr8:127863317..127865201-chr8:127865656..127867797,3	K562	blood:
19	chr8:127872138..127873999-chr8:127878961..127881315,2	K562	blood:
20	chr8:127844604..127847451-chr8:127850237..127852011,2	MCF-7	breast:
21	chr8:127888611..127889740-chr8:128174743..128176385,8	MCF-7	breast:
22	chr8:127836927..127839136-chr8:127848377..127851052,2	K562	blood:
23	chr8:127872138..127873999-chr8:127878961..127881315,2	K562	blood:
24	chr8:127881390..127882102-chr8:130693928..130694709,3	K562	blood:
25	chr8:127844604..127847451-chr8:127850237..127852011,2	MCF-7	breast:
26	chr8:127887627..127889305-chr8:128171709..128173869,2	MCF-7	breast:
27	chr8:127888486..127889437-chr8:128046877..128047818,8	MCF-7	breast:
28	chr8:127888783..127889396-chr8:128190557..128191077,3	MCF-7	breast:
29	chr8:127836311..127837281-chr8:127888680..127889401,2	MCF-7	breast:
30	chr8:127836311..127837281-chr8:127888680..127889401,2	MCF-7	breast:
31	chr8:127888564..127889446-chr8:130699431..130700261,2	K562	blood:
32	chr8:127836927..127839136-chr8:127848377..127851052,2	K562	blood:
33	chr8:127836631..127837289-chr8:127881392..127882026,2	MCF-7	breast:
34	chr8:127849961..127854048-chr8:127854713..127860204,4	K562	blood:
35	chr8:127888960..127889471-chr8:128508382..128509088,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM84B-3	chr8:127857516-127857628	XLOC_007212
2	lnc-POU5F1B-2	chr8:127889917-127890077	NONHSAT129013
3	lnc-POU5F1B-2	chr8:127859300-127859333	ENSG00000253438
4	lnc-POU5F1B-2	chr8:127889400-127889489	NONHSAT129013
5	lnc-FAM84B-3	chr8:127859120-127859220	XLOC_007212
6	lnc-POU5F1B-2	chr8:127890620-127890725	ENSG00000253438
7	lnc-POU5F1B-2	chr8:127889917-127890035	ENSG00000253438

No data

Variant related genes	Relation type
PCAT1	TF binding region
PCAT1	CpG island
ENSG00000136997	chromatin interactions
ENSG00000249375	chromatin interactions
ENSG00000253438	chromatin interactions
ADCY6	miRNA target sites

Extended variants
information (count: 2498 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:2498 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559478177	chr8:127835900-127835901	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs6983290	chr8:127835936-127835937	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7003659	chr8:127835986-127835987	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs6983330	chr8:127836007-127836008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs6983599	chr8:127836035-127836036	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs555639699	chr8:127836039-127836040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs568187810	chr8:127836050-127836051	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs539680498	chr8:127836064-127836065	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs559128528	chr8:127836103-127836104	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186422836	chr8:127836105-127836106	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs112132806	chr8:127836117-127836118	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs144044556	chr8:127836122-127836123	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs7003931	chr8:127836137-127836138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555632559	chr8:127836154-127836155	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs189848859	chr8:127836155-127836156	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs7003948	chr8:127836164-127836165	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs6983660	chr8:127836207-127836208	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs148654166	chr8:127836271-127836272	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144402036	chr8:127836272-127836273	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs6984346	chr8:127836337-127836338	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs6984351	chr8:127836348-127836349	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs147442853	chr8:127836432-127836433	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs72722260	chr8:127836496-127836497	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs139742177	chr8:127836521-127836522	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs10216757	chr8:127836529-127836530	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs550806069	chr8:127836552-127836553	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs570779404	chr8:127836594-127836595	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs35115206	chr8:127836597-127836598	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs145061126	chr8:127836698-127836699	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs547059289	chr8:127836751-127836752	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs10216375	chr8:127836765-127836766	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535773737	chr8:127836801-127836802	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs116929665	chr8:127836841-127836842	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs368238263	chr8:127836852-127836853	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs373075394	chr8:127836854-127836855	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556959246	chr8:127836859-127836860	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs376384752	chr8:127836865-127836866	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs568970838	chr8:127836870-127836871	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs537904968	chr8:127836871-127836872	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557569841	chr8:127836914-127836915	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs201916899	chr8:127836925-127836926	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs57588856	chr8:127836926-127836927	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs398096133	chr8:127836928-127836929	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs150921660	chr8:127836946-127836947	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs77287339	chr8:127836969-127836970	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140788028	chr8:127836981-127836982	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs149680320	chr8:127837010-127837011	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs542133310	chr8:127837026-127837027	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144742529	chr8:127837032-127837033	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs16901727	chr8:127837072-127837073	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:157)

Disease	PMID	Source
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
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	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
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Gastric cancer	21635755	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD

Chromatin state (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:127827000-127837200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:127832000-127836600	Enhancers	Osteobl	bone
3	chr8:127832600-127836600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:127832600-127836600	Weak transcription	Fetal Lung	lung
5	chr8:127833000-127836200	Weak transcription	NHDF-Ad	bronchial
6	chr8:127833200-127837000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr8:127833400-127836400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr8:127833400-127836400	Weak transcription	Fetal Muscle Leg	muscle
9	chr8:127833600-127836200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:127833600-127836400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr8:127833600-127836800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr8:127833600-127839800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr8:127833800-127836600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr8:127833800-127837000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr8:127833800-127837000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:127834000-127836800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr8:127834200-127836400	Weak transcription	Fetal Heart	heart
18	chr8:127834200-127836800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:127834400-127836200	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr8:127834400-127836400	Weak transcription	NH-A	brain
21	chr8:127834400-127836400	Weak transcription	NHEK	skin
22	chr8:127835800-127836400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr8:127836200-127836400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr8:127836200-127836400	Enhancers	NHDF-Ad	bronchial
25	chr8:127836200-127836800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr8:127836400-127836600	Enhancers	A549	lung
27	chr8:127836400-127836600	Enhancers	Hela-S3	cervix
28	chr8:127836400-127836800	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr8:127836400-127836800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:127836400-127836800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr8:127836400-127836800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:127836400-127836800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:127836400-127836800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr8:127836400-127836800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr8:127836400-127836800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:127836400-127836800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr8:127836400-127836800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr8:127836400-127836800	Enhancers	Fetal Muscle Leg	muscle
39	chr8:127836400-127836800	Enhancers	HSMMtube	muscle
40	chr8:127836400-127836800	Enhancers	HUVEC	blood vessel
41	chr8:127836400-127836800	Enhancers	NH-A	brain
42	chr8:127836400-127836800	Flanking Active TSS	NHDF-Ad	bronchial
43	chr8:127836400-127836800	Enhancers	NHEK	skin
44	chr8:127836400-127837000	Enhancers	Fetal Heart	heart
45	chr8:127836400-127837000	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr8:127836400-127837000	Active TSS	K562	blood
47	chr8:127836400-127837000	Enhancers	NHLF	lung
48	chr8:127836600-127836800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr8:127836600-127836800	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr8:127836600-127836800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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