Variant report

Variant	nsv831443
Chromosome Location	chr8:119390590-119590662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2222)
CpG islands
(count:977)
Chromatin interactive
region (count:27)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2222 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:119517559-119518077	GM12878	blood:	n/a	n/a
2	ATF2	chr8:119519482-119520197	GM12878	blood:	n/a	n/a
3	ATF2	chr8:119521329-119521939	GM12878	blood:	n/a	n/a
4	ATF2	chr8:119517591-119518023	GM12878	blood:	n/a	n/a
5	ATF2	chr8:119511318-119511888	GM12878	blood:	n/a	n/a
6	ATF2	chr8:119520504-119521077	GM12878	blood:	n/a	n/a
7	ATF2	chr8:119535305-119535725	GM12878	blood:	n/a	n/a
8	ATF2	chr8:119511264-119511958	GM12878	blood:	n/a	n/a
9	ATF2	chr8:119519544-119520274	GM12878	blood:	n/a	n/a
10	ATF2	chr8:119520457-119520968	GM12878	blood:	n/a	n/a
11	ATF2	chr8:119575980-119576542	GM12878	blood:	n/a	n/a
12	ATF2	chr8:119535259-119535767	GM12878	blood:	n/a	n/a
13	ATF3	chr8:119451865-119452446	HCT-116	colon:	n/a	n/a
14	BACH1	chr8:119431288-119431480	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr8:119537021-119537398	GM12878	blood:	n/a	n/a
16	BATF	chr8:119519809-119520158	GM12878	blood:	n/a	chr8:119519929-119519940
17	BATF	chr8:119576054-119576428	GM12878	blood:	n/a	n/a
18	BATF	chr8:119520465-119520851	GM12878	blood:	n/a	chr8:119520640-119520650
19	BATF	chr8:119520452-119521181	GM12878	blood:	n/a	chr8:119520640-119520650
20	BATF	chr8:119589703-119590043	GM12878	blood:	n/a	n/a
21	BATF	chr8:119517565-119518009	GM12878	blood:	n/a	n/a
22	BATF	chr8:119519237-119519552	GM12878	blood:	n/a	n/a
23	BATF	chr8:119519765-119520177	GM12878	blood:	n/a	chr8:119519929-119519940
24	BATF	chr8:119517547-119518039	GM12878	blood:	n/a	n/a
25	BATF	chr8:119450837-119451208	GM12878	blood:	n/a	n/a
26	BATF	chr8:119450865-119451222	GM12878	blood:	n/a	n/a
27	BATF	chr8:119589681-119589990	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:119576030-119576753	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:119519865-119520147	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:119567570-119567812	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr8:119566177-119566360	GM12878	blood:	n/a	n/a
32	BCL11A	chr8:119511374-119511931	GM12878	blood:	n/a	chr8:119511634-119511643
33	BCL11A	chr8:119535317-119535666	GM12878	blood:	n/a	chr8:119535494-119535503
34	BCL11A	chr8:119576068-119576701	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:119519836-119520246	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:119511379-119511825	GM12878	blood:	n/a	chr8:119511634-119511643
37	BCL3	chr8:119519902-119520189	GM12878	blood:	n/a	n/a
38	BCL3	chr8:119427636-119428450	A549	lung:	n/a	chr8:119428152-119428161 chr8:119428153-119428162
39	BCL3	chr8:119520522-119520919	GM12878	blood:	n/a	n/a
40	BCL3	chr8:119519844-119520253	GM12878	blood:	n/a	n/a
41	BCL3	chr8:119427814-119428398	A549	lung:	n/a	chr8:119428152-119428161 chr8:119428153-119428162
42	BCLAF1	chr8:119511241-119511922	GM12878	blood:	n/a	chr8:119511634-119511643
43	BCLAF1	chr8:119576016-119576692	GM12878	blood:	n/a	n/a
44	BCLAF1	chr8:119521457-119521955	GM12878	blood:	n/a	n/a
45	BCLAF1	chr8:119511312-119511859	GM12878	blood:	n/a	chr8:119511634-119511643
46	BCLAF1	chr8:119519717-119520259	GM12878	blood:	n/a	n/a
47	BCLAF1	chr8:119517431-119518061	GM12878	blood:	n/a	n/a
48	BCLAF1	chr8:119576030-119576911	GM12878	blood:	n/a	n/a
49	BHLHE40	chr8:119516979-119518013	GM12878	blood:	n/a	n/a
50	BHLHE40	chr8:119589915-119590053	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:119567541-119567591	Hepatocyte	liver:	n/a
2	chr8:119567541-119567591	Hepatocyte	liver:	n/a
3	chr8:119531106-119531156	HNPCEpiC	eye:	n/a
4	chr8:119560948-119560998	ECC-1	luminal epithelium:	n/a
5	chr8:119517944-119517994	BE2_C	brain:	n/a
6	chr8:119561032-119561082	LNCaP	prostate:	n/a
7	chr8:119500053-119500103	GM19239	blood:	n/a
8	chr8:119392871-119392921	SKMC	muscle:	n/a
9	chr8:119392871-119392921	GM06990	blood:	n/a
10	chr8:119456570-119456620	AG09319	gingival:	n/a
11	chr8:119567541-119567591	HCT-116	colon:	n/a
12	chr8:119504312-119504362	IMR90	lung:	fetal
13	chr8:119392871-119392921	ProgFib	skin:	n/a
14	chr8:119561032-119561082	CMK	blood:	n/a
15	chr8:119476471-119476521	A549	lung:	n/a
16	chr8:119392871-119392921	H1-hESC	embryonic stem cell:	embryo
17	chr8:119500053-119500103	HL-60	blood:	n/a
18	chr8:119560948-119560998	HRE	kidney:	n/a
19	chr8:119517944-119517994	HCF	heart:	n/a
20	chr8:119558921-119558971	ovcar-3	ovarian:	n/a
21	chr8:119500053-119500103	MCF10A-Er-Src	breast:	n/a
22	chr8:119428220-119428270	H1-hESC	embryonic stem cell:	embryo
23	chr8:119517944-119517994	PFSK-1	brain:	n/a
24	chr8:119456570-119456620	SKMC	muscle:	n/a
25	chr8:119576599-119576649	AoSMC	blood vessel:	n/a
26	chr8:119586905-119586955	GM19239	blood:	n/a
27	chr8:119531106-119531156	PANC-1	pancreas:	n/a
28	chr8:119531106-119531156	GM12892	blood:	n/a
29	chr8:119500053-119500103	NHDF-neo	bronchial:	n/a
30	chr8:119504312-119504362	SK-N-SH	brain:	n/a
31	chr8:119531106-119531156	BE2_C	brain:	n/a
32	chr8:119567541-119567591	AG09319	gingival:	n/a
33	chr8:119476471-119476521	HUVEC	blood vessel:	n/a
34	chr8:119504312-119504362	NT2-D1	testis:	n/a
35	chr8:119558921-119558971	RPTEC	kidney:	n/a
36	chr8:119504312-119504362	CMK	blood:	n/a
37	chr8:119456570-119456620	SK-N-SH	brain:	n/a
38	chr8:119450829-119450879	Jurkat	blood:	n/a
39	chr8:119537610-119537660	HCF	heart:	n/a
40	chr8:119531106-119531156	HIPEpiC	eye:	n/a
41	chr8:119561032-119561082	SAEC	small airway:	n/a
42	chr8:119517944-119517994	A549	lung:	n/a
43	chr8:119500053-119500103	AG04450	lung:	fetal
44	chr8:119558921-119558971	NB4	blood:	n/a
45	chr8:119537610-119537660	H1-hESC	embryonic stem cell:	embryo
46	chr8:119567541-119567591	HIPEpiC	eye:	n/a
47	chr8:119504312-119504362	AG10803	skin:	n/a
48	chr8:119576599-119576649	HNPCEpiC	eye:	n/a
49	chr8:119586905-119586955	Caco-2	colon:	n/a
50	chr8:119560948-119560998	HEEpiC	esophagus:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:118486317..118487175-chr8:119426958..119427783,2	MCF-7	breast:
2	chr8:118627506..118628166-chr8:119431178..119431899,3	MCF-7	breast:
3	chr8:119568051..119569877-chr8:119570145..119573095,2	MCF-7	breast:
4	chr8:119506168..119508828-chr8:119515870..119518341,2	MCF-7	breast:
5	chr8:118342111..118342745-chr8:119522687..119523228,2	MCF-7	breast:
6	chr8:119453959..119456833-chr8:119457362..119459167,2	MCF-7	breast:
7	chr8:119506168..119508828-chr8:119515870..119518341,2	MCF-7	breast:
8	chr17:41380614..41382191-chr8:119586621..119588121,2	K562	blood:
9	chr8:119568051..119569877-chr8:119570145..119573095,2	MCF-7	breast:
10	chr8:119122872..119125708-chr8:119413009..119415201,2	MCF-7	breast:
11	chr8:119122848..119125594-chr8:119426689..119430299,4	MCF-7	breast:
12	chr8:119453959..119456833-chr8:119457362..119459167,2	MCF-7	breast:
13	chr8:119572899..119575048-chr8:119586649..119588943,2	MCF-7	breast:
14	chr8:119390887..119392746-chr8:119398566..119401528,2	MCF-7	breast:
15	chr8:119424882..119426911-chr8:119926050..119928623,2	MCF-7	breast:
16	chr2:48510170..48510784-chr8:119556555..119557269,2	MCF-7	breast:
17	chr8:118875517..118876420-chr8:119426479..119427389,2	MCF-7	breast:
18	chr8:119428165..119429775-chr8:119429959..119432245,2	K562	blood:
19	chr8:119428165..119429775-chr8:119429959..119432245,2	K562	blood:
20	chr8:119572899..119575048-chr8:119586649..119588943,2	MCF-7	breast:
21	chr8:119122724..119126766-chr8:119426367..119429330,6	MCF-7	breast:
22	chr8:119132642..119133483-chr8:119426942..119427821,2	MCF-7	breast:
23	chr8:119122868..119126675-chr8:119423984..119426561,3	MCF-7	breast:
24	chr17:41399379..41402179-chr8:119586621..119589601,3	K562	blood:
25	chr17:41465859..41468087-chr8:119586601..119588121,2	MCF-7	breast:
26	chr17:41398945..41402179-chr8:119586621..119589621,3	K562	blood:
27	chr19:47291444..47292264-chr8:119550884..119551384,2	NB4	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TNFRSF11B-4	chr8:119573406-119576339	NONHSAT128411
2	lnc-AC023590.1.1-1	chr8:119412516-119412844	NONHSAT128409
3	lnc-EXT1-7	chr8:119391799-119391844	NONHSAT128410
4	lnc-AC023590.1.1-1	chr8:119407024-119407231	NONHSAT128409

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SAMD12	hsa-miR-340-5p	chr8:119391192-119391214

Variant related genes	Relation type
SAMD12	TF binding region
SAMD12	CpG island
ENSG00000177570	chromatin interactions
ENSG00000105281	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000182197	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 7862 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:7862 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370742939	chr8:119390592-119390593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373768405	chr8:119390612-119390613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190026167	chr8:119390643-119390644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182705208	chr8:119390687-119390688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs16890917	chr8:119390715-119390716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs145314681	chr8:119390716-119390717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138053744	chr8:119390731-119390732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142540257	chr8:119390771-119390772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529313923	chr8:119390783-119390784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577272691	chr8:119390784-119390785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs12541679	chr8:119390889-119390890	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374501862	chr8:119390943-119390944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150599149	chr8:119390957-119390958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550168364	chr8:119390958-119390959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs202050040	chr8:119390971-119390972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543734480	chr8:119390975-119390976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138641259	chr8:119390990-119390991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188348523	chr8:119391036-119391037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564020363	chr8:119391051-119391052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs193166161	chr8:119391059-119391060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528089240	chr8:119391060-119391061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552198735	chr8:119391071-119391072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185388824	chr8:119391077-119391078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149311468	chr8:119391220-119391221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562027980	chr8:119391246-119391247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548976846	chr8:119391263-119391264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189154911	chr8:119391269-119391270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11992702	chr8:119391277-119391278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs74961998	chr8:119391305-119391306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575496723	chr8:119391311-119391312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539347661	chr8:119391362-119391363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558947799	chr8:119391365-119391366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs577150107	chr8:119391394-119391395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568068793	chr8:119391395-119391396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541152879	chr8:119391405-119391406	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs17749211	chr8:119391409-119391410	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
37	rs191277224	chr8:119391410-119391411	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs542024600	chr8:119391413-119391414	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs563729043	chr8:119391439-119391440	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs531277684	chr8:119391465-119391466	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs111562087	chr8:119391470-119391471	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs183717283	chr8:119391483-119391484	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs528837682	chr8:119391489-119391490	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs144238167	chr8:119391523-119391524	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs148708189	chr8:119391530-119391531	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs546584960	chr8:119391533-119391534	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs371982803	chr8:119391547-119391548	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs574452293	chr8:119391564-119391565	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs201880599	chr8:119391606-119391607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs371498471	chr8:119391613-119391614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:146)

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
Acute myeloid leukemia	20729466	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
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
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
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
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	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
Chronic myeloid leukemia	21384125	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	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
Oral squamous cell carcinoma	21853135	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Breast cancer	18698023	CNVD
Multiple myeloma	16461302	CNVD
Uveal melanoma	20484589	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Breast cancer	19181860	CNVD
Endometrial cancer	23636398	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:1462 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:119323000-119394000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr8:119359600-119398600	Weak transcription	Lung	lung
3	chr8:119362600-119395400	Weak transcription	Pancreas	Pancrea
4	chr8:119362800-119398200	Weak transcription	GM12878-XiMat	blood
5	chr8:119366200-119394000	Weak transcription	Gastric	stomach
6	chr8:119381200-119393600	Weak transcription	Fetal Intestine Small	intestine
7	chr8:119382800-119395200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:119383000-119399400	Weak transcription	Brain Cingulate Gyrus	brain
9	chr8:119384200-119392600	Weak transcription	Esophagus	oesophagus
10	chr8:119385200-119399000	Weak transcription	Brain Angular Gyrus	brain
11	chr8:119385800-119391400	Weak transcription	Aorta	Aorta
12	chr8:119386200-119395200	Weak transcription	Fetal Intestine Large	intestine
13	chr8:119386600-119393600	Weak transcription	Liver	Liver
14	chr8:119387200-119399800	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr8:119387400-119391400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr8:119388000-119394000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr8:119389000-119391600	Weak transcription	A549	lung
18	chr8:119389000-119391800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr8:119389400-119392800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr8:119389600-119391800	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:119389600-119394400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr8:119390000-119393800	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr8:119390400-119404000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr8:119391400-119391600	ZNF genes & repeats	Aorta	Aorta
25	chr8:119391400-119391600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr8:119391400-119392800	Enhancers	NHEK	skin
27	chr8:119391400-119393000	Enhancers	Hela-S3	cervix
28	chr8:119391400-119394400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr8:119391600-119392400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr8:119391600-119392600	Enhancers	A549	lung
31	chr8:119391600-119392800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:119391600-119399000	Weak transcription	Aorta	Aorta
33	chr8:119391800-119392600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr8:119391800-119392600	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr8:119391800-119392600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr8:119391800-119392600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr8:119391800-119392600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr8:119391800-119392600	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr8:119391800-119392800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:119391800-119392800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr8:119391800-119392800	Enhancers	HMEC	breast
42	chr8:119391800-119392800	Enhancers	NHDF-Ad	bronchial
43	chr8:119391800-119392800	Enhancers	NHLF	lung
44	chr8:119391800-119393000	Enhancers	Osteobl	bone
45	chr8:119391800-119397000	Enhancers	HUVEC	blood vessel
46	chr8:119392000-119392600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr8:119392000-119392600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:119392000-119392800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr8:119392000-119392800	Enhancers	NH-A	brain
50	chr8:119392200-119392600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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