Variant report

Variant	nsv6382
Chromosome Location	chr8:127845446-127890549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:367)
Chromatin interactive
region (count:28)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:127888902-127889101	K562	blood:	n/a	n/a
2	ARID3A	chr8:127888872-127889296	HepG2	liver:	n/a	n/a
3	ATF1	chr8:127868736-127868930	K562	blood:	n/a	n/a
4	ATF2	chr8:127888782-127889275	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr8:127874967-127875279	GM12878	blood:	n/a	n/a
6	ATF2	chr8:127888829-127889197	GM12878	blood:	n/a	n/a
7	ATF2	chr8:127874848-127875373	GM12878	blood:	n/a	n/a
8	ATF3	chr8:127888907-127889099	K562	blood:	n/a	n/a
9	BACH1	chr8:127860809-127860854	K562	blood:	n/a	n/a
10	BACH1	chr8:127865922-127865975	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr8:127874949-127875281	GM12878	blood:	n/a	n/a
12	BATF	chr8:127874875-127875324	GM12878	blood:	n/a	n/a
13	BATF	chr8:127883861-127884216	GM12878	blood:	n/a	n/a
14	BATF	chr8:127869508-127869773	GM12878	blood:	n/a	chr8:127869622-127869633 chr8:127869604-127869612
15	BATF	chr8:127869411-127869807	GM12878	blood:	n/a	chr8:127869622-127869633 chr8:127869604-127869612
16	BCL11A	chr8:127874989-127875200	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:127874946-127875320	GM12878	blood:	n/a	n/a
18	BCLAF1	chr8:127888896-127889223	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:127888907-127889156	K562	blood:	n/a	n/a
20	BHLHE40	chr8:127875020-127875324	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:127851280-127851404	GM12878	blood:	n/a	chr8:127851281-127851294 chr8:127851283-127851292 chr8:127851283-127851292
22	BHLHE40	chr8:127888839-127889164	GM12878	blood:	n/a	n/a
23	BRCA1	chr8:127888810-127889293	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:127868763-127868958	A549	lung:	n/a	n/a
25	CEBPB	chr8:127850790-127850808	K562	blood:	n/a	n/a
26	CEBPB	chr8:127855303-127855421	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:127869489-127869835	IMR90	lung:	n/a	n/a
28	CEBPB	chr8:127888959-127889134	K562	blood:	n/a	n/a
29	CEBPB	chr8:127846217-127846537	HepG2	liver:	n/a	n/a
30	CEBPB	chr8:127855716-127856069	HepG2	liver:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
31	CEBPB	chr8:127850197-127850202	A549	lung:	n/a	n/a
32	CEBPB	chr8:127855726-127856078	A549	lung:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
33	CEBPB	chr8:127874991-127875238	IMR90	lung:	n/a	n/a
34	CEBPB	chr8:127855734-127855989	Hela-S3	cervix:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
35	CEBPB	chr8:127845647-127846692	IMR90	lung:	n/a	n/a
36	CEBPB	chr8:127855291-127855387	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:127854860-127856058	IMR90	lung:	n/a	chr8:127855891-127855902 chr8:127855892-127855903 chr8:127855891-127855904
38	CEBPB	chr8:127870441-127870727	A549	lung:	n/a	chr8:127870614-127870625
39	CEBPB	chr8:127855243-127855498	A549	lung:	n/a	n/a
40	CHD1	chr8:127888703-127889347	IMR90	lung:	n/a	n/a
41	CHD2	chr8:127889022-127889027	K562	blood:	n/a	n/a
42	CHD2	chr8:127888983-127889305	HepG2	liver:	n/a	n/a
43	CHD2	chr8:127888877-127889222	Hela-S3	cervix:	n/a	n/a
44	CREB1	chr8:127888899-127889161	A549	lung:	n/a	n/a
45	CREB1	chr8:127860674-127861058	GM12878	blood:	n/a	n/a
46	CREB1	chr8:127860715-127861177	GM12878	blood:	n/a	n/a
47	CTCF	chr8:127881760-127881910	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr8:127881740-127881890	GM12875	blood:	n/a	n/a
49	CTCF	chr8:127881760-127881910	HCM	heart:	n/a	n/a
50	CTCF	chr8:127888851-127889151	GM19239	blood:	n/a	chr8:127888996-127889014 chr8:127888998-127889019

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:127889050-127889100	GM06990	blood:	n/a
2	chr8:127889050-127889100	GM06990	blood:	n/a
3	chr8:127889010-127889060	MCF10A-Er-Src	breast:	n/a
4	chr8:127866047-127866097	HCF	heart:	n/a
5	chr8:127889295-127889345	SK-N-SH_RA	brain:	n/a
6	chr8:127889295-127889345	HCF	heart:	n/a
7	chr8:127889050-127889100	ProgFib	skin:	n/a
8	chr8:127889050-127889100	PFSK-1	brain:	n/a
9	chr8:127866047-127866097	HEEpiC	esophagus:	n/a
10	chr8:127889025-127889075	AoSMC	blood vessel:	n/a
11	chr8:127889295-127889345	NH-A	brain:	n/a
12	chr8:127846077-127846127	AG09309	skin:	n/a
13	chr8:127866047-127866097	HRPEpiC	eye:	n/a
14	chr8:127889295-127889345	HepG2	liver:	n/a
15	chr8:127866047-127866097	AG10803	skin:	n/a
16	chr8:127889295-127889345	Caco-2	colon:	n/a
17	chr8:127889025-127889075	HRCEpiC	kidney:	n/a
18	chr8:127889295-127889345	BE2_C	brain:	n/a
19	chr8:127889050-127889100	PrEC	prostate:	n/a
20	chr8:127889295-127889345	GM12891	blood:	n/a
21	chr8:127889010-127889060	AG04450	lung:	fetal
22	chr8:127889295-127889345	NT2-D1	testis:	n/a
23	chr8:127889010-127889060	PANC-1	pancreas:	n/a
24	chr8:127889025-127889075	HNPCEpiC	eye:	n/a
25	chr8:127889025-127889075	NHBE	bronchial:	n/a
26	chr8:127889050-127889100	HIPEpiC	eye:	n/a
27	chr8:127889050-127889100	Jurkat	blood:	n/a
28	chr8:127889050-127889100	T-47D	breast:	n/a
29	chr8:127889025-127889075	PFSK-1	brain:	n/a
30	chr8:127889050-127889100	AG10803	skin:	n/a
31	chr8:127889010-127889060	GM12892	blood:	n/a
32	chr8:127889025-127889075	HUVEC	blood vessel:	n/a
33	chr8:127889025-127889075	GM12891	blood:	n/a
34	chr8:127889010-127889060	SK-N-SH_RA	brain:	n/a
35	chr8:127889010-127889060	RPTEC	kidney:	n/a
36	chr8:127889010-127889060	H1-hESC	embryonic stem cell:	embryo
37	chr8:127889025-127889075	Jurkat	blood:	n/a
38	chr8:127889025-127889075	SKMC	muscle:	n/a
39	chr8:127889050-127889100	GM19239	blood:	n/a
40	chr8:127866047-127866097	BJ	skin:	n/a
41	chr8:127889050-127889100	HEK293	kidney:	embryo
42	chr8:127866047-127866097	HepG2	liver:	n/a
43	chr8:127866047-127866097	Jurkat	blood:	n/a
44	chr8:127889025-127889075	HL-60	blood:	n/a
45	chr8:127889025-127889075	PrEC	prostate:	n/a
46	chr8:127889050-127889100	CMK	blood:	n/a
47	chr8:127866047-127866097	AG04449	skin:	fetal
48	chr8:127889050-127889100	HAEpiC	amniotic membrane:	n/a
49	chr8:127846077-127846127	GM06990	blood:	n/a
50	chr8:127889010-127889060	HL-60	blood:	n/a

(count:28 , 50 per page) page: 1

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

(count:6 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1828 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:1828 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569608278	chr8:127845461-127845462	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs538424113	chr8:127845492-127845493	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs367823481	chr8:127845568-127845569	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs200681917	chr8:127845580-127845581	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs61676572	chr8:127845581-127845582	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs73705595	chr8:127845620-127845621	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184336522	chr8:127845660-127845661	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs35507366	chr8:127845675-127845676	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs986046	chr8:127845702-127845703	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs563694922	chr8:127845760-127845761	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs141792208	chr8:127845787-127845788	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs565825714	chr8:127845848-127845849	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs188771800	chr8:127845861-127845862	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs542703901	chr8:127845878-127845879	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs79866348	chr8:127845906-127845907	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs79418862	chr8:127845907-127845908	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs75263754	chr8:127845910-127845911	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs562793365	chr8:127845974-127845975	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs527517183	chr8:127846002-127846003	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531527006	chr8:127846012-127846013	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs544775161	chr8:127846033-127846034	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs564753535	chr8:127846059-127846060	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs369168267	chr8:127846065-127846066	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs150599218	chr8:127846078-127846079	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs547469253	chr8:127846089-127846090	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs71578557	chr8:127846109-127846110	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs142859749	chr8:127846110-127846111	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs570429419	chr8:127846113-127846114	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs151072172	chr8:127846118-127846119	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs35053742	chr8:127846120-127846121	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs537710249	chr8:127846130-127846131	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs116015390	chr8:127846138-127846139	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs77677907	chr8:127846157-127846158	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs181320698	chr8:127846176-127846177	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs185467420	chr8:127846229-127846230	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs16901753	chr8:127846275-127846276	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs558351813	chr8:127846306-127846307	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs16901755	chr8:127846315-127846316	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs139619659	chr8:127846334-127846335	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553946323	chr8:127846336-127846337	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs116127313	chr8:127846340-127846341	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574092590	chr8:127846423-127846424	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10090865	chr8:127846474-127846475	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs189294406	chr8:127846497-127846498	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149254279	chr8:127846522-127846523	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146172684	chr8:127846539-127846540	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567307234	chr8:127846550-127846551	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139225006	chr8:127846627-127846628	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs536563170	chr8:127846658-127846659	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs80215429	chr8:127846687-127846688	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	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:583 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:127837800-127845600	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr8:127837800-127845800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr8:127837800-127845800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr8:127840400-127845800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:127840600-127845800	Weak transcription	Fetal Kidney	kidney
6	chr8:127840800-127845600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:127840800-127845600	Weak transcription	Left Ventricle	heart
8	chr8:127840800-127845800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr8:127840800-127845800	Enhancers	Muscle Satellite Cultured Cells	--
10	chr8:127840800-127845800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr8:127840800-127845800	Enhancers	HSMM	muscle
12	chr8:127841000-127845600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:127841000-127845600	Weak transcription	Fetal Thymus	thymus
14	chr8:127841000-127845800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr8:127841000-127845800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:127842400-127847000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr8:127843800-127845800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:127844000-127845600	Weak transcription	HMEC	breast
19	chr8:127844000-127845800	Weak transcription	NHEK	skin
20	chr8:127844200-127845600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:127844400-127847800	Enhancers	Fetal Muscle Leg	muscle
22	chr8:127844400-127848000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:127844600-127845600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr8:127844600-127845800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:127844800-127847200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr8:127845000-127845600	Enhancers	NH-A	brain
27	chr8:127845000-127845600	Enhancers	NHDF-Ad	bronchial
28	chr8:127845000-127845800	Enhancers	HUVEC	blood vessel
29	chr8:127845000-127845800	Enhancers	NHLF	lung
30	chr8:127845000-127846000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr8:127845000-127846200	Enhancers	Spleen	Spleen
32	chr8:127845000-127846600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:127845000-127846800	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr8:127845000-127846800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:127845000-127846800	Enhancers	Psoas Muscle	Psoas
36	chr8:127845000-127847000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:127845000-127847200	Enhancers	Fetal Muscle Trunk	muscle
38	chr8:127845200-127845600	Flanking Active TSS	HSMMtube	muscle
39	chr8:127845200-127846800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr8:127845200-127846800	Enhancers	Fetal Heart	heart
41	chr8:127845400-127845600	Enhancers	Osteobl	bone
42	chr8:127845400-127845800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr8:127845400-127845800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
44	chr8:127845400-127846000	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr8:127845400-127846600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr8:127845400-127846600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr8:127845400-127846800	Enhancers	Colon Smooth Muscle	Colon
48	chr8:127845400-127846800	Enhancers	Fetal Lung	lung
49	chr8:127845400-127846800	Enhancers	Fetal Stomach	stomach
50	chr8:127845400-127847000	Enhancers	Placenta	Placenta

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