Variant report

Variant	esv15294
Chromosome Location	chr8:99017130-99025235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:138)
CpG islands
(count:122)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:138 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:99023326-99023735	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr8:99023245-99023773	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr8:99017769-99018265	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:99017909-99018344	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:99017904-99018110	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr8:99019713-99019830	K562	blood:	n/a	n/a
7	CEBPB	chr8:99023457-99024201	IMR90	lung:	n/a	n/a
8	CEBPB	chr8:99023423-99023760	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr8:99023586-99024104	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr8:99017849-99018338	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr8:99023084-99023794	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr8:99017502-99018449	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr8:99024680-99024830	BE2_C	brain:	n/a	n/a
14	CTCF	chr8:99024580-99024730	HCT-116	colon:	n/a	chr8:99024626-99024639
15	CTCF	chr8:99024680-99024830	HAc	cerebellar:	n/a	n/a
16	CTCF	chr8:99024600-99024750	HCPEpiC	choroid plexus:	n/a	chr8:99024626-99024639
17	CTCF	chr8:99024651-99024834	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr8:99024500-99024650	GM12871	blood:	n/a	chr8:99024626-99024639
19	CTCF	chr8:99024640-99024790	AG04450	lung:	n/a	n/a
20	CTCF	chr8:99024600-99024750	K562	blood:	n/a	chr8:99024626-99024639
21	CTCF	chr8:99024640-99024790	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr8:99024580-99024730	GM12865	blood:	n/a	chr8:99024626-99024639
23	CTCF	chr8:99024540-99024690	BE2_C	brain:	n/a	chr8:99024626-99024639
24	CTCF	chr8:99024660-99024810	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr8:99024620-99024770	HBMEC	blood vessel:	n/a	chr8:99024626-99024639
26	CTCF	chr8:99024580-99024730	NHDF-neo	bronchial:	n/a	chr8:99024626-99024639
27	CTCF	chr8:99024660-99024810	GM12864	blood:	n/a	n/a
28	CTCF	chr8:99024660-99024810	HepG2	liver:	n/a	n/a
29	CTCF	chr8:99024680-99024830	AG04449	skin:	n/a	n/a
30	CTCF	chr8:99017320-99017470	NHDF-neo	bronchial:	n/a	n/a
31	CTCF	chr8:99024471-99024891	H1-hESC	embryonic stem cell:	n/a	chr8:99024626-99024639
32	CTCF	chr8:99024640-99024790	GM12868	blood:	n/a	n/a
33	CTCF	chr8:99024680-99024830	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr8:99024600-99024750	SK-N-SH_RA	brain:	n/a	chr8:99024626-99024639
35	CTCF	chr8:99024640-99024790	HEK293	kidney:	n/a	n/a
36	CTCF	chr8:99024700-99024850	GM12871	blood:	n/a	n/a
37	CTCF	chr8:99022920-99023070	GM12866	blood:	n/a	n/a
38	CTCF	chr8:99017920-99018070	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr8:99024680-99024830	GM12872	blood:	n/a	n/a
40	CTCF	chr8:99024620-99024770	AG04449	skin:	n/a	chr8:99024626-99024639
41	CTCF	chr8:99024660-99024810	GM12873	blood:	n/a	n/a
42	EP300	chr8:99023247-99023766	H1-hESC	embryonic stem cell:	n/a	n/a
43	EP300	chr8:99023620-99024155	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr8:99021347-99021589	SK-N-SH_RA	brain:	n/a	n/a
45	EP300	chr8:99022726-99024445	SK-N-SH	brain:	n/a	chr8:99022797-99022811 chr8:99022795-99022804
46	EP300	chr8:99023640-99024271	SK-N-SH	brain:	n/a	n/a
47	EP300	chr8:99023621-99024205	SK-N-SH_RA	brain:	n/a	n/a
48	FOS	chr8:99021333-99021638	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr8:99021314-99021660	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr8:99023915-99024123	MCF10A-Er-Src	breast:	n/a	chr8:99024080-99024089

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99023869-99023919	H1-hESC	embryonic stem cell:	embryo
2	chr8:99017690-99017740	HepG2	liver:	n/a
3	chr8:99017690-99017740	GM12891	blood:	n/a
4	chr8:99023869-99023919	SK-N-SH_RA	brain:	n/a
5	chr8:99023869-99023919	RPTEC	kidney:	n/a
6	chr8:99023869-99023919	MCF10A-Er-Src	breast:	n/a
7	chr8:99017690-99017740	H1-hESC	embryonic stem cell:	embryo
8	chr8:99017690-99017740	HNPCEpiC	eye:	n/a
9	chr8:99017690-99017740	HRPEpiC	eye:	n/a
10	chr8:99023869-99023919	GM12878	blood:	n/a
11	chr8:99023869-99023919	ovcar-3	ovarian:	n/a
12	chr8:99023869-99023919	T-47D	breast:	n/a
13	chr8:99017690-99017740	AG04450	lung:	fetal
14	chr8:99017690-99017740	SK-N-MC	brain:	n/a
15	chr8:99023869-99023919	PANC-1	pancreas:	n/a
16	chr8:99017690-99017740	GM12892	blood:	n/a
17	chr8:99017690-99017740	AG09309	skin:	n/a
18	chr8:99023869-99023919	A549	lung:	n/a
19	chr8:99023869-99023919	CMK	blood:	n/a
20	chr8:99017690-99017740	NH-A	brain:	n/a
21	chr8:99017690-99017740	Hepatocyte	liver:	n/a
22	chr8:99017690-99017740	K562	blood:	n/a
23	chr8:99017690-99017740	IMR90	lung:	fetal
24	chr8:99023869-99023919	Caco-2	colon:	n/a
25	chr8:99023869-99023919	AG09319	gingival:	n/a
26	chr8:99017690-99017740	NHBE	bronchial:	n/a
27	chr8:99017690-99017740	U87	brain:	n/a
28	chr8:99023869-99023919	LNCaP	prostate:	n/a
29	chr8:99017690-99017740	HAEpiC	amniotic membrane:	n/a
30	chr8:99023869-99023919	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:99017690-99017740	ovcar-3	ovarian:	n/a
32	chr8:99023869-99023919	GM19239	blood:	n/a
33	chr8:99017690-99017740	PFSK-1	brain:	n/a
34	chr8:99023869-99023919	HepG2	liver:	n/a
35	chr8:99023869-99023919	MCF-7	breast:	n/a
36	chr8:99023869-99023919	U87	brain:	n/a
37	chr8:99023869-99023919	NT2-D1	testis:	n/a
38	chr8:99017690-99017740	NT2-D1	testis:	n/a
39	chr8:99017690-99017740	NB4	blood:	n/a
40	chr8:99017690-99017740	AG04449	skin:	fetal
41	chr8:99023869-99023919	Hepatocyte	liver:	n/a
42	chr8:99017690-99017740	BE2_C	brain:	n/a
43	chr8:99017690-99017740	HMEC	breast:	n/a
44	chr8:99023869-99023919	HRE	kidney:	n/a
45	chr8:99023869-99023919	GM06990	blood:	n/a
46	chr8:99023869-99023919	HAEpiC	amniotic membrane:	n/a
47	chr8:99017690-99017740	SK-N-SH	brain:	n/a
48	chr8:99023869-99023919	BJ	skin:	n/a
49	chr8:99023869-99023919	HCM	heart:	n/a
50	chr8:99023869-99023919	HMEC	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:99024327..99027909-chr8:99029199..99033016,4	MCF-7	breast:
2	chr8:98917300..98918803-chr8:99024235..99026797,2	MCF-7	breast:
3	chr8:99020262..99022328-chr8:99024233..99025913,2	K562	blood:
4	chr8:98881503..98883125-chr8:99023785..99026314,2	MCF-7	breast:
5	chr8:99014119..99017352-chr8:99021059..99024142,3	MCF-7	breast:
6	chr8:99015593..99019656-chr8:99049212..99053715,4	MCF-7	breast:
7	chr8:99014119..99017352-chr8:99021059..99024142,3	MCF-7	breast:
8	chr8:99020262..99022328-chr8:99024233..99025913,2	K562	blood:
9	chr8:98880171..98881728-chr8:99021126..99023057,2	MCF-7	breast:

No data

Variant related genes	Relation type
MATN2	TF binding region
MATN2	CpG island
ENSG00000132561	chromatin interactions

Extended variants
information (count: 330 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190389774	chr8:99017177-99017178	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs182079672	chr8:99017178-99017179	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546662467	chr8:99017284-99017285	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs544512623	chr8:99017290-99017291	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187579149	chr8:99017326-99017327	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs35316041	chr8:99017335-99017336	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149547143	chr8:99017349-99017350	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2444892	chr8:99017396-99017397	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs569000966	chr8:99017421-99017422	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs146033560	chr8:99017422-99017423	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs557013273	chr8:99017460-99017461	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs570657770	chr8:99017505-99017506	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs577961999	chr8:99017510-99017511	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs370913174	chr8:99017542-99017543	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs539438204	chr8:99017545-99017546	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs10955146	chr8:99017548-99017549	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs16896537	chr8:99017559-99017560	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370198118	chr8:99017588-99017589	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs11987110	chr8:99017609-99017610	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs555799012	chr8:99017637-99017638	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs12550104	chr8:99017665-99017666	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs139894422	chr8:99017674-99017675	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188083528	chr8:99017685-99017686	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs143401530	chr8:99017702-99017703	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs560884671	chr8:99017703-99017704	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs540336108	chr8:99017730-99017731	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs111596668	chr8:99017815-99017816	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs74570477	chr8:99017843-99017844	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs549245824	chr8:99017844-99017845	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs529047850	chr8:99017887-99017888	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs549758167	chr8:99017929-99017930	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs562666614	chr8:99017930-99017931	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs531397896	chr8:99017995-99017996	Weak transcription Enhancers Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs549153993	chr8:99018036-99018037	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs180893819	chr8:99018150-99018151	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs571118957	chr8:99018205-99018206	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs549090802	chr8:99018347-99018348	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs185349298	chr8:99018369-99018370	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs546800117	chr8:99018373-99018374	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs6651180	chr8:99018395-99018396	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs535510314	chr8:99018397-99018398	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs371447633	chr8:99018411-99018412	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs556023613	chr8:99018435-99018436	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs576048315	chr8:99018460-99018461	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74615699	chr8:99018471-99018472	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375060395	chr8:99018479-99018480	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190115883	chr8:99018486-99018487	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113162454	chr8:99018487-99018488	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs7831921	chr8:99018488-99018489	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs540291438	chr8:99018540-99018541	Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
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
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	22341455	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD

Chromatin state (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:98992600-99019400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:99008400-99045000	Weak transcription	Colonic Mucosa	Colon
3	chr8:99009000-99030000	Weak transcription	Pancreas	Pancrea
4	chr8:99009000-99030200	Weak transcription	Esophagus	oesophagus
5	chr8:99009600-99022600	Weak transcription	Rectal Smooth Muscle	rectum
6	chr8:99012000-99017200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:99012000-99028800	Weak transcription	Aorta	Aorta
8	chr8:99012000-99032000	Weak transcription	Gastric	stomach
9	chr8:99012400-99028800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr8:99013800-99018600	Weak transcription	Fetal Intestine Small	intestine
11	chr8:99014000-99022400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr8:99014200-99025400	Genic enhancers	Fetal Muscle Leg	muscle
13	chr8:99014200-99029600	Weak transcription	Fetal Intestine Large	intestine
14	chr8:99014400-99018000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr8:99014600-99017200	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr8:99014600-99019600	Weak transcription	Liver	Liver
17	chr8:99014600-99019800	Weak transcription	Fetal Lung	lung
18	chr8:99014600-99020000	Weak transcription	HSMM	muscle
19	chr8:99014600-99021200	Enhancers	Brain Cingulate Gyrus	brain
20	chr8:99014600-99021400	Enhancers	Brain Hippocampus Middle	brain
21	chr8:99014800-99017400	Weak transcription	Ovary	ovary
22	chr8:99014800-99018000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:99014800-99018000	Weak transcription	Adipose Nuclei	Adipose
24	chr8:99014800-99018200	Weak transcription	NH-A	brain
25	chr8:99014800-99022600	Strong transcription	Placenta Amnion	Placenta Amnion
26	chr8:99014800-99023000	Weak transcription	Colon Smooth Muscle	Colon
27	chr8:99015000-99017200	Weak transcription	NHLF	lung
28	chr8:99015000-99017800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr8:99015000-99018200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr8:99015000-99019800	Weak transcription	NHDF-Ad	bronchial
31	chr8:99015000-99020000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:99015000-99034400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr8:99015200-99022000	Weak transcription	Stomach Smooth Muscle	stomach
34	chr8:99015200-99023600	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr8:99015400-99018800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr8:99015400-99021200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr8:99015800-99023800	Weak transcription	Spleen	Spleen
38	chr8:99016000-99017400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr8:99016400-99017800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:99016400-99021400	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr8:99016400-99021400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
42	chr8:99016600-99018800	Genic enhancers	Fetal Stomach	stomach
43	chr8:99016600-99019800	Enhancers	Brain Substantia Nigra	brain
44	chr8:99016600-99020600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr8:99016600-99021400	Enhancers	Brain Angular Gyrus	brain
46	chr8:99016600-99021400	Enhancers	Brain Anterior Caudate	brain
47	chr8:99016800-99017800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr8:99016800-99017800	Enhancers	Placenta	Placenta
49	chr8:99016800-99018000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr8:99016800-99018400	Enhancers	HUES64 Cell Line	embryonic stem cell

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