Variant report

Variant	nsv1024251
Chromosome Location	chr8:92118995-92186057
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:92119585-92120834	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:92130895-92131095	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:92121937-92122001	HepG2	liver:	n/a	n/a
4	ATF1	chr8:92126805-92126814	K562	blood:	n/a	n/a
5	ATF2	chr8:92157649-92158115	GM12878	blood:	n/a	n/a
6	BACH1	chr8:92130210-92130270	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr8:92120097-92120425	HepG2	liver:	n/a	n/a
8	BHLHE40	chr8:92119659-92120741	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:92148653-92148976	IMR90	lung:	n/a	chr8:92148804-92148815
10	CEBPB	chr8:92119569-92119750	HepG2	liver:	n/a	n/a
11	CEBPB	chr8:92152343-92152575	HepG2	liver:	n/a	chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152447-92152458 chr8:92152445-92152456 chr8:92152447-92152458
12	CEBPB	chr8:92120574-92120772	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:92148672-92148965	HepG2	liver:	n/a	chr8:92148804-92148815
14	CEBPB	chr8:92120050-92120860	HepG2	liver:	n/a	chr8:92120199-92120211
15	CEBPB	chr8:92164320-92164536	A549	lung:	n/a	n/a
16	CEBPB	chr8:92148613-92148967	MCF-7	breast:	n/a	chr8:92148804-92148815
17	CEBPB	chr8:92130918-92131377	IMR90	lung:	n/a	n/a
18	CEBPB	chr8:92148557-92148979	MCF-7	breast:	n/a	chr8:92148804-92148815
19	CEBPB	chr8:92123908-92124201	HepG2	liver:	n/a	n/a
20	CEBPB	chr8:92148641-92148988	K562	blood:	n/a	chr8:92148804-92148815
21	CEBPB	chr8:92152325-92152560	IMR90	lung:	n/a	chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152445-92152458 chr8:92152447-92152456 chr8:92152447-92152456 chr8:92152447-92152458 chr8:92152445-92152456 chr8:92152447-92152458
22	CHD2	chr8:92179540-92179627	K562	blood:	n/a	n/a
23	CHD2	chr8:92124549-92124557	HepG2	liver:	n/a	n/a
24	CHD2	chr8:92120111-92120465	HepG2	liver:	n/a	n/a
25	CREB1	chr8:92157732-92158202	GM12878	blood:	n/a	n/a
26	CTCF	chr8:92120460-92120610	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr8:92120400-92120550	BE2_C	brain:	n/a	n/a
28	CTCF	chr8:92129920-92130070	AG09309	skin:	n/a	n/a
29	CTCF	chr8:92120500-92120650	HepG2	liver:	n/a	n/a
30	CTCF	chr8:92129900-92130050	AG10803	skin:	n/a	n/a
31	CTCF	chr8:92120477-92120670	MCF-7	breast:	n/a	n/a
32	CTCF	chr8:92120480-92120630	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr8:92120564-92120587	GM12878	blood:	n/a	n/a
34	CTCF	chr8:92120480-92120630	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:92120435-92120667	GM12878	blood:	n/a	n/a
36	CTCF	chr8:92120520-92120670	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:92120385-92120778	K562	blood:	n/a	n/a
38	CTCF	chr8:92120500-92120650	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr8:92120420-92120570	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr8:92120440-92120590	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr8:92120440-92120590	Caco-2	colon:	n/a	n/a
42	CTCF	chr8:92120530-92120626	LNCaP	prostate:	n/a	n/a
43	CTCF	chr8:92129900-92130050	AG04449	skin:	n/a	n/a
44	CTCF	chr8:92120517-92120624	HepG2	liver:	n/a	n/a
45	CTCF	chr8:92120460-92120610	BE2_C	brain:	n/a	n/a
46	CTCF	chr8:92129980-92130130	AG04449	skin:	n/a	n/a
47	CTCF	chr8:92142688-92142737	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr8:92120461-92120857	MCF-7	breast:	n/a	n/a
49	CTCF	chr8:92120500-92120650	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr8:92120600-92120750	RPTEC	kidney:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:92177481-92177531	SKMC	muscle:	n/a
2	chr8:92129661-92129711	NB4	blood:	n/a
3	chr8:92177481-92177531	HCM	heart:	n/a
4	chr8:92130025-92130075	HEEpiC	esophagus:	n/a
5	chr8:92130454-92130504	HRE	kidney:	n/a
6	chr8:92130454-92130504	GM19239	blood:	n/a
7	chr8:92177481-92177531	GM06990	blood:	n/a
8	chr8:92129661-92129711	IMR90	lung:	fetal
9	chr8:92129661-92129711	AoSMC	blood vessel:	n/a
10	chr8:92177481-92177531	GM12892	blood:	n/a
11	chr8:92130025-92130075	PANC-1	pancreas:	n/a
12	chr8:92130025-92130075	SK-N-SH	brain:	n/a
13	chr8:92130454-92130504	PANC-1	pancreas:	n/a
14	chr8:92130025-92130075	HL-60	blood:	n/a
15	chr8:92177481-92177531	H1-hESC	embryonic stem cell:	embryo
16	chr8:92130454-92130504	ProgFib	skin:	n/a
17	chr8:92177481-92177531	HPAEpiC	pulmonary alveolar:	n/a
18	chr8:92129661-92129711	ovcar-3	ovarian:	n/a
19	chr8:92130454-92130504	HEEpiC	esophagus:	n/a
20	chr8:92130454-92130504	Hela-S3	cervix:	n/a
21	chr8:92130025-92130075	MCF10A-Er-Src	breast:	n/a
22	chr8:92177481-92177531	MCF10A-Er-Src	breast:	n/a
23	chr8:92129661-92129711	U87	brain:	n/a
24	chr8:92130454-92130504	BJ	skin:	n/a
25	chr8:92129661-92129711	HEK293	kidney:	embryo
26	chr8:92130454-92130504	AG04449	skin:	fetal
27	chr8:92130025-92130075	Jurkat	blood:	n/a
28	chr8:92130454-92130504	NHDF-neo	bronchial:	n/a
29	chr8:92177481-92177531	PFSK-1	brain:	n/a
30	chr8:92130454-92130504	Hepatocyte	liver:	n/a
31	chr8:92130454-92130504	HNPCEpiC	eye:	n/a
32	chr8:92130454-92130504	LNCaP	prostate:	n/a
33	chr8:92129661-92129711	HL-60	blood:	n/a
34	chr8:92177481-92177531	HMEC	breast:	n/a
35	chr8:92130454-92130504	HCM	heart:	n/a
36	chr8:92130454-92130504	AG09319	gingival:	n/a
37	chr8:92130025-92130075	SK-N-MC	brain:	n/a
38	chr8:92129661-92129711	RPTEC	kidney:	n/a
39	chr8:92130454-92130504	PFSK-1	brain:	n/a
40	chr8:92177481-92177531	HCF	heart:	n/a
41	chr8:92130025-92130075	HEK293	kidney:	embryo
42	chr8:92177481-92177531	T-47D	breast:	n/a
43	chr8:92177481-92177531	NH-A	brain:	n/a
44	chr8:92129661-92129711	NT2-D1	testis:	n/a
45	chr8:92129661-92129711	LNCaP	prostate:	n/a
46	chr8:92129661-92129711	HNPCEpiC	eye:	n/a
47	chr8:92177481-92177531	AoSMC	blood vessel:	n/a
48	chr8:92177481-92177531	RPTEC	kidney:	n/a
49	chr8:92130454-92130504	NB4	blood:	n/a
50	chr8:92177481-92177531	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:92154407..92157062-chr8:92186719..92188314,2	K562	blood:
2	chr8:92120884..92123342-chr8:92135640..92137332,2	K562	blood:
3	chr8:92144011..92145737-chr8:92157940..92159530,2	K562	blood:
4	chr8:92132436..92135251-chr8:92135477..92137033,2	K562	blood:
5	chr8:92120884..92123955-chr8:92135517..92137332,3	K562	blood:
6	chr8:92134168..92136932-chr8:92139678..92141512,2	MCF-7	breast:
7	chr8:92185616..92187449-chr8:92210169..92211682,2	K562	blood:
8	chr8:92120884..92123342-chr8:92135640..92137332,2	K562	blood:
9	chr8:92134168..92136932-chr8:92139678..92141512,2	MCF-7	breast:
10	chr8:92119859..92121552-chr8:92126272..92127780,2	K562	blood:
11	chr8:92148959..92151184-chr8:92158932..92161122,2	K562	blood:
12	chr8:92120202..92121198-chr8:92265328..92266332,4	MCF-7	breast:
13	chr8:92119859..92121552-chr8:92126272..92127780,2	K562	blood:
14	chr8:92110691..92113252-chr8:92118062..92119956,2	K562	blood:
15	chr8:92117994..92121552-chr8:92125286..92129221,4	K562	blood:
16	chr8:92117994..92121552-chr8:92125286..92129221,4	K562	blood:
17	chr8:92052048..92053750-chr8:92131275..92133087,2	K562	blood:
18	chr8:92155872..92157525-chr8:92209191..92211411,2	K562	blood:
19	chr8:92144011..92145737-chr8:92157940..92159530,2	K562	blood:
20	chr8:92120884..92123955-chr8:92135517..92137332,3	K562	blood:
21	chr8:92132436..92135251-chr8:92135477..92137033,2	K562	blood:
22	chr8:92098468..92101361-chr8:92119773..92121850,2	K562	blood:
23	chr8:92110951..92113555-chr8:92117926..92119500,2	MCF-7	breast:
24	chr8:92120160..92121035-chr8:92355245..92356052,2	MCF-7	breast:
25	chr8:92081085..92084002-chr8:92118821..92120627,2	MCF-7	breast:
26	chr8:92148959..92151184-chr8:92158932..92161122,2	K562	blood:
27	chr8:92120448..92121074-chr8:92405403..92406245,2	MCF-7	breast:
28	chr8:92150726..92152514-chr8:92154521..92157433,2	MCF-7	breast:
29	chr8:92119728..92121505-chr8:92405339..92406291,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM55A-4	chr8:92149320-92151226	ucscGeneNc_uc003yet_1
2	lnc-OTUD6B-4	chr8:92142582-92142645	NONHSAT127672
3	lnc-TMEM55A-4	chr8:92151335-92151500	ucscGeneNc_uc003yet_1
4	lnc-OTUD6B-5	chr8:92150995-92151423	NONHSAT127673
5	lnc-OTUD6B-6	chr8:92151489-92151751	NONHSAT127674
6	lnc-OTUD6B-3	chr8:92136721-92137011	NONHSAT127671
7	lnc-OTUD6B-4	chr8:92142987-92143064	NONHSAT127672
8	lnc-OTUD6B-4	chr8:92145338-92145592	NONHSAT127672
9	lnc-OTUD6B-5	chr8:92147909-92147967	NONHSAT127673

No data

Variant related genes	Relation type
RN7SL777P	TF binding region
ENSG00000253525	TF binding region
LRRC69	TF binding region
RN7SL777P	CpG island
ENSG00000253525	CpG island
LRRC69	CpG island
ENSG00000155100	chromatin interactions
ENSG00000147606	chromatin interactions
ENSG00000155099	chromatin interactions
ENSG00000263888	chromatin interactions
ENSG00000253738	chromatin interactions

Extended variants
information (count: 1841 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1841 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142553015	chr8:92119027-92119028	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs191539001	chr8:92119032-92119033	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs115402859	chr8:92119049-92119050	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563251115	chr8:92119128-92119129	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs530846651	chr8:92119160-92119161	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs552461644	chr8:92119166-92119167	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs570666151	chr8:92119170-92119171	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs528325681	chr8:92119178-92119179	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs371199890	chr8:92119184-92119185	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546766920	chr8:92119196-92119197	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs57987672	chr8:92119197-92119198	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs60166362	chr8:92119198-92119199	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548200831	chr8:92119212-92119213	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs569681344	chr8:92119219-92119220	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs554233137	chr8:92119357-92119358	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs540958695	chr8:92119424-92119425	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs7816107	chr8:92119488-92119489	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs577462363	chr8:92119502-92119503	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs76036724	chr8:92119536-92119537	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs77762840	chr8:92119537-92119538	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs78423585	chr8:92119540-92119541	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs76991382	chr8:92119544-92119545	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs75172896	chr8:92119545-92119546	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs75881465	chr8:92119563-92119564	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs77815962	chr8:92119564-92119565	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs78325204	chr8:92119571-92119572	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs79059114	chr8:92119602-92119603	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs74632207	chr8:92119629-92119630	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs79573920	chr8:92119634-92119635	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs534944726	chr8:92119643-92119644	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs77544188	chr8:92119644-92119645	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs75816691	chr8:92119645-92119646	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs76445444	chr8:92119655-92119656	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs375280358	chr8:92119692-92119693	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs562933384	chr8:92119702-92119703	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs537221005	chr8:92119742-92119743	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574473936	chr8:92119880-92119881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs541917273	chr8:92119889-92119890	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs117303689	chr8:92119902-92119903	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs377721935	chr8:92119905-92119906	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs112468898	chr8:92119968-92119969	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs545814080	chr8:92120022-92120023	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs564267554	chr8:92120046-92120047	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560833350	chr8:92120211-92120212	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs116998479	chr8:92120215-92120216	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs182568536	chr8:92120252-92120253	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs561894803	chr8:92120272-92120273	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs530081505	chr8:92120283-92120284	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs185497690	chr8:92120290-92120291	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs569717723	chr8:92120331-92120332	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

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
Autism	22495311	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
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
Acute lymphoblastic leukemia	18458336	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
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	22014070	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:92083000-92147800	Weak transcription	Spleen	Spleen
2	chr8:92083400-92124400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:92083600-92150800	Weak transcription	Pancreas	Pancrea
4	chr8:92084000-92124600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr8:92085000-92125800	Weak transcription	Small Intestine	intestine
6	chr8:92091200-92133800	Weak transcription	NHLF	lung
7	chr8:92091800-92137800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr8:92092600-92147800	Weak transcription	Right Ventricle	heart
9	chr8:92092800-92124400	Weak transcription	Brain Cingulate Gyrus	brain
10	chr8:92094200-92125200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr8:92095200-92124400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr8:92095200-92130800	Weak transcription	HSMMtube	muscle
13	chr8:92095800-92126600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr8:92096800-92135000	Weak transcription	Hela-S3	cervix
15	chr8:92097200-92127000	Weak transcription	Colon Smooth Muscle	Colon
16	chr8:92097400-92126400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr8:92097400-92130800	Weak transcription	Osteobl	bone
18	chr8:92097400-92146200	Weak transcription	Psoas Muscle	Psoas
19	chr8:92098200-92124600	Weak transcription	HUVEC	blood vessel
20	chr8:92098600-92122800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr8:92100800-92130800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr8:92104400-92124400	Weak transcription	Gastric	stomach
23	chr8:92104600-92126000	Weak transcription	Fetal Intestine Large	intestine
24	chr8:92104600-92129600	Weak transcription	Brain Anterior Caudate	brain
25	chr8:92104800-92124400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr8:92104800-92124400	Weak transcription	Ovary	ovary
27	chr8:92104800-92125400	Weak transcription	Fetal Muscle Trunk	muscle
28	chr8:92104800-92126200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr8:92104800-92130600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:92104800-92134200	Weak transcription	Thymus	Thymus
31	chr8:92104800-92148000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr8:92105000-92119800	Weak transcription	Placenta	Placenta
33	chr8:92105800-92125800	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr8:92106000-92120000	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr8:92106000-92125800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr8:92106000-92126400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:92106800-92127400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr8:92107200-92141000	Weak transcription	HMEC	breast
39	chr8:92107400-92119800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr8:92107400-92123200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr8:92108400-92124400	Weak transcription	GM12878-XiMat	blood
42	chr8:92109200-92120000	Weak transcription	K562	blood
43	chr8:92109200-92147600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr8:92109600-92124400	Weak transcription	NHDF-Ad	bronchial
45	chr8:92110000-92120800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr8:92110000-92124600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:92110000-92124800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr8:92110000-92127400	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr8:92110200-92120400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr8:92110200-92128000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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