Variant report

Variant	nsv516190
Chromosome Location	chr8:125323011-125343441
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:59)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:59 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr8:125333164-125333217	A549	lung:	n/a	chr8:125333197-125333210 chr8:125333196-125333213
2	CEBPB	chr8:125332945-125333577	A549	lung:	n/a	chr8:125333197-125333210 chr8:125333196-125333213
3	CEBPB	chr8:125333049-125333366	K562	blood:	n/a	chr8:125333197-125333210 chr8:125333196-125333213
4	CTCF	chr8:125335132-125335182	MCF-7	breast:	n/a	n/a
5	CTCF	chr8:125340430-125340472	Kidney_OC	kidney:	n/a	n/a
6	CUX1	chr8:125337173-125337220	GM12878	blood:	n/a	n/a
7	E2F4	chr8:125341888-125342090	MCF10A-Er-Src	breast:	n/a	n/a
8	E2F4	chr8:125331165-125331447	MCF10A-Er-Src	breast:	n/a	n/a
9	EP300	chr8:125333515-125333884	SK-N-SH_RA	brain:	n/a	n/a
10	EP300	chr8:125333168-125333869	SK-N-SH	brain:	n/a	chr8:125333195-125333209
11	EP300	chr8:125329377-125329418	K562	blood:	n/a	n/a
12	EP300	chr8:125333450-125333773	SK-N-SH_RA	brain:	n/a	n/a
13	FOSL2	chr8:125333155-125333692	A549	lung:	n/a	n/a
14	FOSL2	chr8:125333090-125333633	SK-N-SH	brain:	n/a	n/a
15	FOXA1	chr8:125326435-125326560	T-47D	breast:	n/a	chr8:125326471-125326486
16	FOXA1	chr8:125326246-125326635	T-47D	breast:	n/a	chr8:125326471-125326486
17	GATA3	chr8:125333112-125333941	SK-N-SH	brain:	n/a	chr8:125333805-125333813 chr8:125333831-125333841
18	GATA3	chr8:125333028-125333980	SK-N-SH	brain:	n/a	chr8:125333805-125333813 chr8:125333831-125333841
19	GATA3	chr8:125326253-125326603	T-47D	breast:	n/a	chr8:125326340-125326356 chr8:125326337-125326354
20	GATA3	chr8:125322877-125323107	SH-SY5Y	brain:	n/a	chr8:125323038-125323051 chr8:125323044-125323065
21	GATA3	chr8:125332991-125333739	A549	lung:	n/a	n/a
22	JUN	chr8:125323334-125323441	K562	blood:	n/a	n/a
23	JUND	chr8:125333095-125333906	SK-N-SH	brain:	n/a	chr8:125333831-125333840
24	JUND	chr8:125333092-125333642	SK-N-SH	brain:	n/a	n/a
25	MAFF	chr8:125336418-125336668	HepG2	liver:	n/a	chr8:125336506-125336524
26	MAFK	chr8:125336358-125336669	HepG2	liver:	n/a	chr8:125336507-125336522
27	MAFK	chr8:125336349-125336652	HepG2	liver:	n/a	chr8:125336507-125336522
28	MAFK	chr8:125336366-125336679	IMR90	lung:	n/a	chr8:125336507-125336522
29	MAZ	chr8:125335894-125335957	HepG2	liver:	n/a	n/a
30	MEF2A	chr8:125323718-125324058	GM12878	blood:	n/a	n/a
31	NFIC	chr8:125333107-125333913	SK-N-SH	brain:	n/a	n/a
32	PBX3	chr8:125333397-125333865	SK-N-SH	brain:	n/a	n/a
33	PBX3	chr8:125333344-125333911	SK-N-SH	brain:	n/a	n/a
34	POLR2A	chr8:125335143-125335180	MCF-7	breast:	n/a	n/a
35	POLR2A	chr8:125328348-125328356	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr8:125335736-125335853	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr8:125340800-125340893	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr8:125338067-125338076	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr8:125337182-125337380	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr8:125342159-125342199	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr8:125331797-125331810	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr8:125323396-125323436	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr8:125329076-125329143	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr8:125328498-125328577	Hela-S3	cervix:	n/a	n/a
45	RCOR1	chr8:125339066-125339071	GM12878	blood:	n/a	n/a
46	RFX5	chr8:125335866-125335917	K562	blood:	n/a	n/a
47	RUNX3	chr8:125323602-125324063	GM12878	blood:	n/a	n/a
48	SP1	chr8:125333145-125333652	A549	lung:	n/a	n/a
49	STAT3	chr8:125335363-125335544	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr8:125336309-125336380	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:125331344-125331394	A549	lung:	n/a
2	chr8:125331344-125331394	MCF10A-Er-Src	breast:	n/a
3	chr8:125331344-125331394	SK-N-SH	brain:	n/a
4	chr8:125331344-125331394	Caco-2	colon:	n/a
5	chr8:125331344-125331394	NHDF-neo	bronchial:	n/a
6	chr8:125331344-125331394	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:125331344-125331394	LNCaP	prostate:	n/a
8	chr8:125331344-125331394	HepG2	liver:	n/a
9	chr8:125331344-125331394	GM06990	blood:	n/a
10	chr8:125331344-125331394	HIPEpiC	eye:	n/a
11	chr8:125331344-125331394	NH-A	brain:	n/a
12	chr8:125331344-125331394	BE2_C	brain:	n/a
13	chr8:125331344-125331394	H1-hESC	embryonic stem cell:	embryo
14	chr8:125331344-125331394	HCF	heart:	n/a
15	chr8:125331344-125331394	GM19239	blood:	n/a
16	chr8:125331344-125331394	HRE	kidney:	n/a
17	chr8:125331344-125331394	Hela-S3	cervix:	n/a
18	chr8:125331344-125331394	HNPCEpiC	eye:	n/a
19	chr8:125331344-125331394	HUVEC	blood vessel:	n/a
20	chr8:125331344-125331394	RPTEC	kidney:	n/a
21	chr8:125331344-125331394	GM12878	blood:	n/a
22	chr8:125331344-125331394	NHBE	bronchial:	n/a
23	chr8:125331344-125331394	HCT-116	colon:	n/a
24	chr8:125331344-125331394	MCF-7	breast:	n/a
25	chr8:125331344-125331394	SKMC	muscle:	n/a
26	chr8:125331344-125331394	SK-N-MC	brain:	n/a
27	chr8:125331344-125331394	Jurkat	blood:	n/a
28	chr8:125331344-125331394	U87	brain:	n/a
29	chr8:125331344-125331394	HAEpiC	amniotic membrane:	n/a
30	chr8:125331344-125331394	PFSK-1	brain:	n/a
31	chr8:125331344-125331394	HMEC	breast:	n/a
32	chr8:125331344-125331394	HEK293	kidney:	embryo
33	chr8:125331344-125331394	HCM	heart:	n/a
34	chr8:125331344-125331394	HL-60	blood:	n/a
35	chr8:125331344-125331394	Hepatocyte	liver:	n/a
36	chr8:125331344-125331394	NB4	blood:	n/a
37	chr8:125331344-125331394	HRPEpiC	eye:	n/a
38	chr8:125331344-125331394	K562	blood:	n/a
39	chr8:125331344-125331394	ProgFib	skin:	n/a
40	chr8:125331344-125331394	SK-N-SH_RA	brain:	n/a
41	chr8:125331344-125331394	GM12892	blood:	n/a
42	chr8:125331344-125331394	ECC-1	luminal epithelium:	n/a
43	chr8:125331344-125331394	PANC-1	pancreas:	n/a
44	chr8:125331344-125331394	SAEC	small airway:	n/a
45	chr8:125331344-125331394	ovcar-3	ovarian:	n/a
46	chr8:125331344-125331394	AG10803	skin:	n/a
47	chr8:125331344-125331394	T-47D	breast:	n/a
48	chr8:125331344-125331394	GM12891	blood:	n/a
49	chr8:125331344-125331394	IMR90	lung:	fetal
50	chr8:125331344-125331394	AG04450	lung:	fetal

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:125337424..125341244-chr8:125341867..125344494,3	K562	blood:
2	chr8:125324055..125327630-chr8:125328027..125332156,3	K562	blood:
3	chr8:125340865..125342625-chr8:125376929..125379138,2	MCF-7	breast:
4	chr8:125324055..125327630-chr8:125328027..125332156,3	K562	blood:
5	chr8:125323757..125325315-chr8:125327181..125329547,2	MCF-7	breast:
6	chr8:125325078..125328020-chr8:125382939..125385370,2	MCF-7	breast:
7	chr8:125326091..125328342-chr8:125340650..125343149,2	MCF-7	breast:
8	chr8:125338867..125341244-chr8:125341867..125344052,2	K562	blood:
9	chr8:125283005..125285047-chr8:125323215..125325556,2	MCF-7	breast:
10	chr8:125294360..125297357-chr8:125322539..125325121,3	MCF-7	breast:
11	chr8:125331715..125333377-chr8:125335165..125337220,2	K562	blood:
12	chr8:125334967..125336817-chr8:125345932..125347614,2	MCF-7	breast:
13	chr8:125337424..125341244-chr8:125341867..125344494,3	K562	blood:
14	chr8:125331184..125334552-chr8:125384168..125386612,3	MCF-7	breast:
15	chr8:125329487..125331943-chr8:125333452..125335110,2	K562	blood:
16	chr8:125323403..125327630-chr8:125328027..125332156,5	K562	blood:
17	chr8:125319313..125321023-chr8:125321990..125323812,2	MCF-7	breast:
18	chr8:125323403..125327630-chr8:125328027..125332156,5	K562	blood:
19	chr8:125338106..125341622-chr8:125346657..125350721,4	MCF-7	breast:
20	chr8:125338867..125341244-chr8:125341867..125344052,2	K562	blood:
21	chr8:125331715..125333377-chr8:125335165..125337220,2	K562	blood:
22	chr12:52595065..52596924-chr8:125324290..125327050,2	MCF-7	breast:
23	chr8:125322529..125324874-chr8:126203230..126205002,2	K562	blood:
24	chr8:125329487..125331943-chr8:125333452..125335110,2	K562	blood:
25	chr8:125342566..125344974-chr8:125348992..125350712,2	K562	blood:
26	chr8:125323757..125325315-chr8:125327181..125329547,2	MCF-7	breast:
27	chr8:125340663..125343070-chr8:125358970..125360934,2	K562	blood:
28	chr8:125312676..125315589-chr8:125327120..125329013,2	K562	blood:
29	chr8:125326091..125328342-chr8:125340650..125343149,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TMEM65	hsa-let-7b-5p	chr8:125326162-125326156
2	TMEM65	hsa-let-7b-5p	chr8:125326157-125326180

Variant related genes	Relation type
ENSG00000271975	TF binding region
ENSG00000271975	CpG island
ENSG00000237586	chromatin interactions
ENSG00000164983	chromatin interactions
ENSG00000271975	chromatin interactions
ENSG00000253227	chromatin interactions

Extended variants
information (count: 654 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:654 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12707907	chr8:125323011-125323012	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs566467505	chr8:125323022-125323023	Weak transcription Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs528855869	chr8:125323143-125323144	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs182779292	chr8:125323149-125323150	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146994842	chr8:125323260-125323261	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs80186682	chr8:125323295-125323296	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs138086296	chr8:125323322-125323323	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs571688642	chr8:125323377-125323378	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs534306369	chr8:125323388-125323389	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553928503	chr8:125323391-125323392	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs573998977	chr8:125323405-125323406	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187494009	chr8:125323442-125323443	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs555728520	chr8:125323453-125323454	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575610212	chr8:125323488-125323489	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs191122443	chr8:125323497-125323498	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs564282670	chr8:125323498-125323499	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs202058825	chr8:125323500-125323501	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs183653347	chr8:125323507-125323508	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs540346047	chr8:125323534-125323535	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs149544104	chr8:125323578-125323579	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs79362569	chr8:125323637-125323638	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs187796264	chr8:125323675-125323676	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs76875381	chr8:125323711-125323712	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs76653209	chr8:125323715-125323716	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs34051865	chr8:125323752-125323753	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543612687	chr8:125323755-125323756	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs569256186	chr8:125323797-125323798	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs73332134	chr8:125323850-125323851	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551614908	chr8:125323948-125323949	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs571811673	chr8:125323982-125323983	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs534102886	chr8:125324009-125324010	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs554254153	chr8:125324013-125324014	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs567634259	chr8:125324045-125324046	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs143018563	chr8:125324046-125324047	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556589996	chr8:125324048-125324049	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs148198613	chr8:125324205-125324206	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544522034	chr8:125324325-125324326	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs200762629	chr8:125324366-125324367	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370445885	chr8:125324371-125324372	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377179427	chr8:125324372-125324373	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs72721440	chr8:125324373-125324374	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs373651119	chr8:125324426-125324427	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs141190259	chr8:125324452-125324453	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs117221313	chr8:125324468-125324469	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573650682	chr8:125324470-125324471	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs200230809	chr8:125324489-125324490	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369894660	chr8:125324496-125324497	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559769404	chr8:125324516-125324517	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs66480306	chr8:125324529-125324530	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs374281482	chr8:125324546-125324547	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:142)

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
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
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	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
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125301400-125329800	Weak transcription	HSMMtube	muscle
2	chr8:125306200-125328000	Weak transcription	A549	lung
3	chr8:125309400-125331000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr8:125311200-125333600	Weak transcription	Right Ventricle	heart
5	chr8:125312000-125323800	Weak transcription	Aorta	Aorta
6	chr8:125312000-125330800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr8:125312400-125331000	Weak transcription	Duodenum Mucosa	Duodenum
8	chr8:125312600-125326000	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr8:125312600-125328000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr8:125312600-125329800	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr8:125312600-125329800	Weak transcription	Thymus	Thymus
12	chr8:125312600-125330000	Weak transcription	Fetal Stomach	stomach
13	chr8:125312600-125333000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr8:125312600-125346000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr8:125312800-125323600	Weak transcription	Primary T helper cells PMA-I stimulated	--
16	chr8:125312800-125329800	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr8:125312800-125329800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr8:125312800-125331600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr8:125312800-125337800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr8:125313400-125329800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
21	chr8:125314000-125326200	Weak transcription	Colon Smooth Muscle	Colon
22	chr8:125314000-125330000	Weak transcription	Left Ventricle	heart
23	chr8:125314200-125330000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:125314200-125332000	Weak transcription	Fetal Intestine Small	intestine
25	chr8:125314200-125340200	Weak transcription	Placenta	Placenta
26	chr8:125315800-125333000	Weak transcription	NH-A	brain
27	chr8:125316400-125333800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr8:125316600-125323600	Weak transcription	HSMM	muscle
29	chr8:125316600-125329800	Weak transcription	Ovary	ovary
30	chr8:125316600-125333600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:125317000-125333000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:125317400-125335000	Weak transcription	Fetal Thymus	thymus
33	chr8:125317600-125330400	Weak transcription	Lung	lung
34	chr8:125317800-125328400	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr8:125318000-125331000	Weak transcription	Fetal Lung	lung
36	chr8:125318200-125331800	Weak transcription	Primary B cells from cord blood	blood
37	chr8:125318200-125333400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr8:125318200-125333400	Weak transcription	HMEC	breast
39	chr8:125318400-125332800	Weak transcription	Liver	Liver
40	chr8:125318400-125336600	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr8:125318600-125328400	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr8:125318600-125329800	Weak transcription	Fetal Muscle Leg	muscle
43	chr8:125319200-125329200	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr8:125319800-125328600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:125320000-125338200	Weak transcription	Fetal Muscle Trunk	muscle
46	chr8:125320400-125323600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr8:125320400-125323800	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr8:125320400-125329800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
49	chr8:125320400-125333400	Weak transcription	Brain Hippocampus Middle	brain
50	chr8:125320600-125323200	Weak transcription	Rectal Mucosa Donor 31	rectum

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