Variant report

Variant	esv3321933
Chromosome Location	chr8:131438670-131443068
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:131438707-131439423	HepG2	liver:	n/a	n/a
2	BRCA1	chr8:131438888-131439094	HepG2	liver:	n/a	n/a
3	CEBPB	chr8:131439062-131439214	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:131438949-131439386	HepG2	liver:	n/a	n/a
5	CHD2	chr8:131439005-131439165	HepG2	liver:	n/a	n/a
6	CTCF	chr8:131440902-131440981	NHEK	skin:	n/a	n/a
7	CTCF	chr8:131442120-131442270	AG09319	gingival:	n/a	n/a
8	CTCF	chr8:131440834-131440943	GM19239	blood:	n/a	n/a
9	E2F4	chr8:131442020-131442278	MCF10A-Er-Src	breast:	n/a	n/a
10	EP300	chr8:131438990-131439383	HepG2	liver:	n/a	n/a
11	EP300	chr8:131438839-131439366	HepG2	liver:	n/a	n/a
12	EP300	chr8:131438934-131439357	HepG2	liver:	n/a	n/a
13	ESR1	chr8:131441992-131442406	T-47D	breast:	n/a	chr8:131442197-131442214
14	ESR1	chr8:131441996-131442321	T-47D	breast:	n/a	chr8:131442197-131442214
15	ESR1	chr8:131442022-131442421	T-47D	breast:	n/a	chr8:131442197-131442214
16	FOS	chr8:131441935-131442345	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
17	FOS	chr8:131440236-131440466	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
18	FOS	chr8:131440193-131440467	HUVEC	blood vessel:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
19	FOS	chr8:131440195-131440466	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
20	FOS	chr8:131441939-131442342	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
21	FOS	chr8:131440174-131440520	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
22	FOS	chr8:131440216-131440464	MCF10A-Er-Src	breast:	n/a	chr8:131440324-131440335 chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
23	FOS	chr8:131441941-131442313	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
24	FOS	chr8:131441926-131442345	MCF10A-Er-Src	breast:	n/a	chr8:131442086-131442098
25	FOSL2	chr8:131440106-131440559	A549	lung:	n/a	chr8:131440327-131440338 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
26	FOXA1	chr8:131438861-131439343	HepG2	liver:	n/a	n/a
27	FOXA1	chr8:131438800-131439411	HepG2	liver:	n/a	n/a
28	FOXA1	chr8:131438853-131439472	HepG2	liver:	n/a	n/a
29	FOXA1	chr8:131438864-131439711	HepG2	liver:	n/a	n/a
30	FOXA2	chr8:131438892-131439397	HepG2	liver:	n/a	n/a
31	FOXA2	chr8:131439462-131439736	HepG2	liver:	n/a	n/a
32	FOXA2	chr8:131438788-131439711	HepG2	liver:	n/a	n/a
33	GABPA	chr8:131443021-131443458	A549	lung:	n/a	n/a
34	GATA3	chr8:131441711-131442411	T-47D	breast:	n/a	n/a
35	GATA3	chr8:131441658-131442319	T-47D	breast:	n/a	n/a
36	HDAC2	chr8:131438850-131439436	HepG2	liver:	n/a	n/a
37	HDAC2	chr8:131438927-131439369	HepG2	liver:	n/a	n/a
38	HNF4A	chr8:131439054-131439267	HepG2	liver:	n/a	chr8:131439146-131439161
39	HNF4A	chr8:131438972-131439268	HepG2	liver:	n/a	chr8:131439146-131439161
40	HNF4G	chr8:131438991-131439341	HepG2	liver:	n/a	chr8:131439145-131439160
41	JUND	chr8:131440176-131440512	HepG2	liver:	n/a	chr8:131440327-131440338 chr8:131440324-131440335 chr8:131440324-131440336 chr8:131440325-131440334 chr8:131440325-131440335
42	JUND	chr8:131439004-131439387	HepG2	liver:	n/a	n/a
43	MAFF	chr8:131438793-131439308	HepG2	liver:	n/a	n/a
44	MAFK	chr8:131438834-131439282	HepG2	liver:	n/a	n/a
45	MAFK	chr8:131438847-131439282	HepG2	liver:	n/a	n/a
46	MAX	chr8:131438606-131439445	HepG2	liver:	n/a	n/a
47	MAX	chr8:131439091-131439291	HepG2	liver:	n/a	n/a
48	MAZ	chr8:131438964-131439253	HepG2	liver:	n/a	n/a
49	MBD4	chr8:131438912-131439358	HepG2	liver:	n/a	n/a
50	MXI1	chr8:131438721-131439436	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:131439096-131439146	RPTEC	kidney:	n/a
2	chr8:131439096-131439146	RPTEC	kidney:	n/a
3	chr8:131441413-131441463	T-47D	breast:	n/a
4	chr8:131439096-131439146	ovcar-3	ovarian:	n/a
5	chr8:131439812-131439862	CMK	blood:	n/a
6	chr8:131440305-131440355	SK-N-SH_RA	brain:	n/a
7	chr8:131440305-131440355	GM12891	blood:	n/a
8	chr8:131441413-131441463	Caco-2	colon:	n/a
9	chr8:131441413-131441463	HMEC	breast:	n/a
10	chr8:131441413-131441463	GM06990	blood:	n/a
11	chr8:131441413-131441463	ovcar-3	ovarian:	n/a
12	chr8:131439812-131439862	GM12892	blood:	n/a
13	chr8:131439096-131439146	AoSMC	blood vessel:	n/a
14	chr8:131439096-131439146	ProgFib	skin:	n/a
15	chr8:131440305-131440355	HNPCEpiC	eye:	n/a
16	chr8:131441413-131441463	NHBE	bronchial:	n/a
17	chr8:131441413-131441463	HUVEC	blood vessel:	n/a
18	chr8:131439812-131439862	HepG2	liver:	n/a
19	chr8:131439096-131439146	NH-A	brain:	n/a
20	chr8:131440305-131440355	T-47D	breast:	n/a
21	chr8:131440305-131440355	LNCaP	prostate:	n/a
22	chr8:131439812-131439862	HCT-116	colon:	n/a
23	chr8:131440305-131440355	HAEpiC	amniotic membrane:	n/a
24	chr8:131439812-131439862	PrEC	prostate:	n/a
25	chr8:131441413-131441463	PFSK-1	brain:	n/a
26	chr8:131441413-131441463	PrEC	prostate:	n/a
27	chr8:131440305-131440355	Hela-S3	cervix:	n/a
28	chr8:131440305-131440355	AG04449	skin:	fetal
29	chr8:131441413-131441463	HEEpiC	esophagus:	n/a
30	chr8:131440305-131440355	NHBE	bronchial:	n/a
31	chr8:131439812-131439862	AG04450	lung:	fetal
32	chr8:131441413-131441463	AoSMC	blood vessel:	n/a
33	chr8:131439812-131439862	SK-N-SH_RA	brain:	n/a
34	chr8:131440305-131440355	CMK	blood:	n/a
35	chr8:131439812-131439862	AG09309	skin:	n/a
36	chr8:131440305-131440355	MCF-7	breast:	n/a
37	chr8:131439812-131439862	HCPEpiC	choroid plexus:	n/a
38	chr8:131440305-131440355	ECC-1	luminal epithelium:	n/a
39	chr8:131440305-131440355	HCF	heart:	n/a
40	chr8:131439096-131439146	BE2_C	brain:	n/a
41	chr8:131439812-131439862	AG04449	skin:	fetal
42	chr8:131441413-131441463	K562	blood:	n/a
43	chr8:131439812-131439862	HNPCEpiC	eye:	n/a
44	chr8:131439812-131439862	Hela-S3	cervix:	n/a
45	chr8:131439812-131439862	HMEC	breast:	n/a
46	chr8:131440305-131440355	HRCEpiC	kidney:	n/a
47	chr8:131439096-131439146	SK-N-MC	brain:	n/a
48	chr8:131439812-131439862	H1-hESC	embryonic stem cell:	embryo
49	chr8:131441413-131441463	NB4	blood:	n/a
50	chr8:131440305-131440355	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:131442195..131445335-chr8:131452635..131456457,4	MCF-7	breast:
2	chr8:131436507..131441847-chr8:131454010..131456873,7	MCF-7	breast:
3	chr8:131442808..131445703-chr8:131454691..131456819,2	MCF-7	breast:
4	chr8:131441459..131443636-chr8:131445223..131447112,2	K562	blood:
5	chr8:131442973..131445344-chr8:131451202..131452908,2	MCF-7	breast:

Variant related genes	Relation type
ASAP1	TF binding region
ASAP1	CpG island
ENSG00000153317	chromatin interactions

Extended variants
information (count: 181 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:181 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56287696	chr8:131438671-131438672	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs78676282	chr8:131438679-131438680	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535403621	chr8:131438743-131438744	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs146715835	chr8:131438788-131438789	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139328126	chr8:131438814-131438815	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs572809561	chr8:131438835-131438836	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540115972	chr8:131438849-131438850	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558436911	chr8:131438884-131438885	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576700758	chr8:131438891-131438892	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556459969	chr8:131438899-131438900	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs575678099	chr8:131439011-131439012	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562163623	chr8:131439029-131439030	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs144018166	chr8:131439095-131439096	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs77582488	chr8:131439113-131439114	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs568258929	chr8:131439144-131439145	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs77354712	chr8:131439198-131439199	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187766650	chr8:131439204-131439205	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563951051	chr8:131439220-131439221	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531487419	chr8:131439322-131439323	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs549633118	chr8:131439333-131439334	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568114917	chr8:131439366-131439367	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535184358	chr8:131439394-131439395	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547443406	chr8:131439395-131439396	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565675533	chr8:131439469-131439470	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs191208865	chr8:131439496-131439497	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs540176411	chr8:131439524-131439525	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs183420418	chr8:131439528-131439529	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs187958635	chr8:131439582-131439583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs193180599	chr8:131439586-131439587	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs555593106	chr8:131439607-131439608	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557863226	chr8:131439626-131439627	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146457316	chr8:131439674-131439675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs541165037	chr8:131439676-131439677	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs559364127	chr8:131439677-131439678	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577577348	chr8:131439691-131439692	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545694991	chr8:131439694-131439695	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs11775398	chr8:131439767-131439768	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs74724856	chr8:131439805-131439806	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs73711702	chr8:131439852-131439853	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs561709607	chr8:131439856-131439857	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529030124	chr8:131440032-131440033	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs547506129	chr8:131440074-131440075	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs75191282	chr8:131440087-131440088	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs184276371	chr8:131440109-131440110	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs552121846	chr8:131440224-131440225	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs545700889	chr8:131440265-131440266	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs140698505	chr8:131440306-131440307	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537327237	chr8:131440315-131440316	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs555974812	chr8:131440336-131440337	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs187812735	chr8:131440347-131440348	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:156)

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
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
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	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
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Gastrointestinal stromal cancer	20818650	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131417000-131440600	Weak transcription	Fetal Kidney	kidney
2	chr8:131429000-131446800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:131429000-131454800	Weak transcription	Aorta	Aorta
4	chr8:131429200-131444800	Weak transcription	HSMMtube	muscle
5	chr8:131429400-131440200	Weak transcription	Pancreas	Pancrea
6	chr8:131429400-131442600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr8:131429400-131447200	Weak transcription	Gastric	stomach
8	chr8:131429400-131449400	Weak transcription	Brain Hippocampus Middle	brain
9	chr8:131429600-131453800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr8:131431600-131442600	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr8:131432000-131438800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr8:131432000-131445000	Weak transcription	Psoas Muscle	Psoas
13	chr8:131432200-131439800	Weak transcription	NHDF-Ad	bronchial
14	chr8:131432200-131449400	Weak transcription	Ovary	ovary
15	chr8:131432400-131441600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr8:131432400-131441600	Weak transcription	Osteobl	bone
17	chr8:131432400-131442000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr8:131433800-131440800	Weak transcription	Right Ventricle	heart
19	chr8:131434000-131443000	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr8:131434200-131443000	Weak transcription	Brain Substantia Nigra	brain
21	chr8:131434600-131441600	Weak transcription	Hela-S3	cervix
22	chr8:131434600-131447000	Weak transcription	HSMM	muscle
23	chr8:131434600-131447200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:131434800-131438800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr8:131434800-131442000	Weak transcription	Fetal Stomach	stomach
26	chr8:131434800-131442200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:131434800-131453000	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr8:131435000-131441400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr8:131435000-131446600	Weak transcription	NH-A	brain
30	chr8:131435200-131440800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:131435200-131441400	Weak transcription	Fetal Muscle Leg	muscle
32	chr8:131435200-131442000	Weak transcription	HUVEC	blood vessel
33	chr8:131435200-131442200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:131435200-131442200	Weak transcription	Left Ventricle	heart
35	chr8:131435200-131443400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:131435600-131439000	Weak transcription	NHLF	lung
37	chr8:131435800-131439800	Weak transcription	HMEC	breast
38	chr8:131435800-131441000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:131435800-131441600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr8:131435800-131443200	Weak transcription	Stomach Smooth Muscle	stomach
41	chr8:131436400-131439200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr8:131436800-131438800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr8:131436800-131438800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr8:131437000-131438800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr8:131437000-131439200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr8:131437000-131440000	Weak transcription	Lung	lung
47	chr8:131437000-131440600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr8:131437000-131441200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr8:131437000-131442600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:131437000-131449800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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