Variant report

Variant	nsv891246
Chromosome Location	chr8:103928940-103967694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:553)
CpG islands
(count:246)
Chromatin interactive
region (count:37)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:103936915-103937705	K562	blood:	n/a	n/a
2	ATF1	chr8:103930999-103931202	K562	blood:	n/a	n/a
3	ATF2	chr8:103942028-103942511	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr8:103936977-103937537	GM12878	blood:	n/a	n/a
5	ATF2	chr8:103942193-103942771	GM12878	blood:	n/a	n/a
6	ATF2	chr8:103937145-103937485	GM12878	blood:	n/a	n/a
7	BACH1	chr8:103937109-103937266	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:103937084-103937325	K562	blood:	n/a	n/a
9	BATF	chr8:103937096-103937421	GM12878	blood:	n/a	n/a
10	BATF	chr8:103932181-103932571	GM12878	blood:	n/a	n/a
11	BATF	chr8:103932194-103932513	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:103952604-103952886	GM12878	blood:	n/a	n/a
13	BCL3	chr8:103936982-103937538	A549	lung:	n/a	n/a
14	BCL3	chr8:103936928-103937579	A549	lung:	n/a	n/a
15	BHLHE40	chr8:103943859-103944161	GM12878	blood:	n/a	n/a
16	BHLHE40	chr8:103942344-103942693	GM12878	blood:	n/a	n/a
17	BHLHE40	chr8:103945223-103945316	GM12878	blood:	n/a	n/a
18	BHLHE40	chr8:103952656-103952846	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:103950146-103950358	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:103937222-103937416	K562	blood:	n/a	n/a
21	BRCA1	chr8:103937125-103937358	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr8:103934053-103934399	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr8:103948301-103948639	K562	blood:	n/a	n/a
24	CBX3	chr8:103936891-103937738	K562	blood:	n/a	chr8:103936916-103936927
25	CBX3	chr8:103937876-103938296	K562	blood:	n/a	n/a
26	CCNT2	chr8:103937371-103937715	K562	blood:	n/a	n/a
27	CEBPB	chr8:103930405-103930738	K562	blood:	n/a	chr8:103930575-103930586
28	CEBPB	chr8:103930992-103931244	K562	blood:	n/a	n/a
29	CEBPB	chr8:103930474-103930723	A549	lung:	n/a	chr8:103930575-103930586
30	CEBPB	chr8:103930400-103930636	MCF-7	breast:	n/a	chr8:103930575-103930586
31	CEBPB	chr8:103930527-103930743	HepG2	liver:	n/a	chr8:103930575-103930586
32	CEBPB	chr8:103930457-103930659	H1-hESC	embryonic stem cell:	n/a	chr8:103930575-103930586
33	CEBPB	chr8:103930370-103931321	Hela-S3	cervix:	n/a	chr8:103930575-103930586
34	CEBPB	chr8:103934087-103934428	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr8:103942650-103942651	K562	blood:	n/a	n/a
36	CEBPB	chr8:103931005-103931222	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr8:103943700-103944044	GM12878	blood:	n/a	n/a
38	CHD2	chr8:103932069-103932208	GM12878	blood:	n/a	n/a
39	CHD2	chr8:103941830-103942653	GM12878	blood:	n/a	n/a
40	CHD2	chr8:103943627-103944005	GM12878	blood:	n/a	n/a
41	CHD2	chr8:103937216-103937459	GM12878	blood:	n/a	n/a
42	CHD2	chr8:103952256-103952715	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr8:103942096-103942462	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr8:103952578-103952883	GM12878	blood:	n/a	n/a
45	CTCF	chr8:103958120-103958270	A549	lung:	n/a	n/a
46	CTCF	chr8:103932800-103932950	HEK293	kidney:	n/a	n/a
47	CTCF	chr8:103932820-103932970	BE2_C	brain:	n/a	n/a
48	CTCF	chr8:103932748-103933031	K562	blood:	n/a	n/a
49	CTCF	chr8:103932800-103932950	GM12878	blood:	n/a	n/a
50	CTCF	chr8:103932740-103932890	HCM	heart:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103932076-103932126	MCF-7	breast:	n/a
2	chr8:103932076-103932126	MCF10A-Er-Src	breast:	n/a
3	chr8:103932076-103932126	MCF-7	breast:	n/a
4	chr8:103932076-103932126	MCF10A-Er-Src	breast:	n/a
5	chr8:103937374-103937424	ProgFib	skin:	n/a
6	chr8:103943308-103943358	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:103943308-103943358	BE2_C	brain:	n/a
8	chr8:103932076-103932126	NHDF-neo	bronchial:	n/a
9	chr8:103943308-103943358	H1-hESC	embryonic stem cell:	embryo
10	chr8:103932076-103932126	GM12891	blood:	n/a
11	chr8:103952396-103952446	AG10803	skin:	n/a
12	chr8:103952396-103952446	RPTEC	kidney:	n/a
13	chr8:103932076-103932126	NH-A	brain:	n/a
14	chr8:103932076-103932126	HCF	heart:	n/a
15	chr8:103952396-103952446	HUVEC	blood vessel:	n/a
16	chr8:103952396-103952446	SK-N-MC	brain:	n/a
17	chr8:103943308-103943358	AG04450	lung:	fetal
18	chr8:103937374-103937424	GM12878	blood:	n/a
19	chr8:103932076-103932126	ECC-1	luminal epithelium:	n/a
20	chr8:103952396-103952446	GM19239	blood:	n/a
21	chr8:103943308-103943358	MCF10A-Er-Src	breast:	n/a
22	chr8:103937374-103937424	GM12892	blood:	n/a
23	chr8:103943308-103943358	PFSK-1	brain:	n/a
24	chr8:103952396-103952446	AG04450	lung:	fetal
25	chr8:103932076-103932126	Jurkat	blood:	n/a
26	chr8:103943308-103943358	HCF	heart:	n/a
27	chr8:103943308-103943358	K562	blood:	n/a
28	chr8:103937374-103937424	AG09309	skin:	n/a
29	chr8:103932076-103932126	HCT-116	colon:	n/a
30	chr8:103937374-103937424	HAEpiC	amniotic membrane:	n/a
31	chr8:103952396-103952446	CMK	blood:	n/a
32	chr8:103952396-103952446	HMEC	breast:	n/a
33	chr8:103952396-103952446	ovcar-3	ovarian:	n/a
34	chr8:103952396-103952446	HNPCEpiC	eye:	n/a
35	chr8:103952396-103952446	Hepatocyte	liver:	n/a
36	chr8:103952396-103952446	HCT-116	colon:	n/a
37	chr8:103932076-103932126	PANC-1	pancreas:	n/a
38	chr8:103952396-103952446	PrEC	prostate:	n/a
39	chr8:103952396-103952446	T-47D	breast:	n/a
40	chr8:103937374-103937424	HepG2	liver:	n/a
41	chr8:103943308-103943358	HCT-116	colon:	n/a
42	chr8:103952396-103952446	HIPEpiC	eye:	n/a
43	chr8:103932076-103932126	SK-N-SH	brain:	n/a
44	chr8:103952396-103952446	PFSK-1	brain:	n/a
45	chr8:103932076-103932126	U87	brain:	n/a
46	chr8:103932076-103932126	HCM	heart:	n/a
47	chr8:103952396-103952446	SK-N-SH	brain:	n/a
48	chr8:103937374-103937424	Hepatocyte	liver:	n/a
49	chr8:103943308-103943358	HAEpiC	amniotic membrane:	n/a
50	chr8:103937374-103937424	RPTEC	kidney:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:103875112..103878223-chr8:103936319..103939684,4	K562	blood:
2	chr8:103874736..103877340-chr8:103957475..103959172,2	MCF-7	breast:
3	chr8:103936331..103939322-chr8:103948640..103950158,2	K562	blood:
4	chr8:103874816..103877664-chr8:103936329..103938732,4	MCF-7	breast:
5	chr8:103944911..103946439-chr8:103949626..103952620,2	K562	blood:
6	chr8:103926652..103929593-chr8:103930931..103933539,2	K562	blood:
7	chr8:103875028..103877482-chr8:103931087..103934755,3	MCF-7	breast:
8	chr8:103936608..103938218-chr8:104032062..104033919,2	MCF-7	breast:
9	chr8:103964753..103967650-chr8:104045838..104047640,2	K562	blood:
10	chr8:103876310..103878750-chr8:103935739..103937868,3	MCF-7	breast:
11	chr8:103943378..103945919-chr8:103945978..103949181,3	MCF-7	breast:
12	chr8:103875385..103877214-chr8:103958627..103960858,2	MCF-7	breast:
13	chr8:103941652..103943631-chr8:103947233..103949355,2	K562	blood:
14	chr14:101754945..101755657-chr8:103930953..103931581,2	MCF-7	breast:
15	chr8:103936331..103939322-chr8:103948640..103950158,2	K562	blood:
16	chr8:103875189..103878093-chr8:103942369..103944654,3	K562	blood:
17	chr8:103941652..103943631-chr8:103947233..103949355,2	K562	blood:
18	chr8:103926652..103929593-chr8:103930931..103933539,2	K562	blood:
19	chr8:103961586..103965372-chr8:103965644..103968506,3	MCF-7	breast:
20	chr8:103962535..103965315-chr8:103967073..103968689,2	MCF-7	breast:
21	chr8:103875368..103877553-chr8:103967686..103969276,3	MCF-7	breast:
22	chr8:103874643..103877584-chr8:103931125..103934060,5	MCF-7	breast:
23	chr8:103937650..103939410-chr8:103943379..103945768,2	MCF-7	breast:
24	chr8:103937650..103939410-chr8:103943379..103945768,2	MCF-7	breast:
25	chr8:103875189..103877224-chr8:103941864..103944592,2	K562	blood:
26	chr8:103951762..103954440-chr8:103965375..103967122,2	MCF-7	breast:
27	chr8:103939891..103942069-chr8:103943605..103945175,2	K562	blood:
28	chr8:103931524..103933304-chr8:104018085..104019856,2	K562	blood:
29	chr8:103913695..103915719-chr8:103927933..103930318,2	MCF-7	breast:
30	chr8:103874124..103877156-chr8:103929505..103932868,5	K562	blood:
31	chr8:103937164..103938846-chr8:103972423..103974367,2	MCF-7	breast:
32	chr8:103875533..103877919-chr8:103950749..103952905,2	K562	blood:
33	chr8:103874124..103876322-chr8:103930861..103932524,2	K562	blood:
34	chr8:103939891..103942069-chr8:103943605..103945175,2	K562	blood:
35	chr8:103884385..103886058-chr8:103926996..103929208,2	MCF-7	breast:
36	chr17:79368009..79368821-chr8:103942711..103943225,2	MCF-7	breast:
37	chr8:103876583..103878231-chr8:103928522..103930334,3	MCF-7	breast:

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KB-1507C5.2.1-4	chr8:103961299-103961462	l_3661_chr8:103945582-103948344_thyroid
2	lnc-KB-1507C5.2.1-4	chr8:103949910-103949985	NONHSAT128139
3	lnc-KB-1507C5.2.1-4	chr8:103949852-103949985	NONHSAT128134
4	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128134
5	lnc-AZIN1-1	chr8:103966207-103967946	ncRnaDb_ncrna_FR151132_1
6	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128141
7	lnc-KB-1507C5.2.1-4	chr8:103949964-103949985	NONHSAT128140
8	lnc-AZIN1-2	chr8:103961693-103962042	NONHSAT128138
9	lnc-KB-1507C5.2.1-4	chr8:103953851-103953926	NONHSAT147657
10	lnc-KB-1507C5.2.1-4	chr8:103953774-103953926	NONHSAT128141
11	lnc-AZIN1-2	chr8:103949852-103949985	NONHSAT128138
12	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT147657
13	lnc-KB-1507C5.2.1-4	chr8:103949852-103949989	NONHSAT128135
14	lnc-KB-1507C5.2.1-4	chr8:103942460-103942746	NONHSAT128135
15	lnc-KB-1507C5.2.1-4	chr8:103949852-103949985	NONHSAT128132
16	lnc-KB-1507C5.2.1-4	chr8:103942545-103942746	NONHSAT128136
17	lnc-KB-1507C5.2.1-4	chr8:103954149-103954193	NONHSAT128119
18	lnc-KB-1507C5.2.1-4	chr8:103953767-103953805	NONHSAT128136
19	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128140
20	lnc-KB-1507C5.2.1-4	chr8:103937260-103937351	NONHSAT128132
21	lnc-KB-1507C5.2.1-4	chr8:103948223-103948358	NONHSAT128137
22	lnc-KB-1507C5.2.1-4	chr8:103953799-103953926	NONHSAT128140
23	lnc-AZIN1-2	chr8:103953851-103953926	NONHSAT128138
24	lnc-KB-1507C5.2.1-4	chr8:103942410-103942746	NONHSAT128134
25	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128132
26	lnc-KB-1507C5.2.1-4	chr8:103949852-103949985	NONHSAT128133
27	lnc-KB-1507C5.2.1-4	chr8:103945583-103946031	l_3661_chr8:103945582-103948344_thyroid
28	lnc-KB-1507C5.2.1-4	chr8:103949661-103949946	NONHSAT128137
29	lnc-KB-1507C5.2.1-4	chr8:103954149-103955587	NONHSAT128133
30	lnc-KB-1507C5.2.1-4	chr8:103954149-103954281	NONHSAT128139
31	lnc-KB-1507C5.2.1-4	chr8:103941606-103942746	NONHSAT128133
32	lnc-AZIN1-2	chr8:103954149-103954281	NONHSAT128138
33	lnc-KB-1507C5.2.1-4	chr8:103946913-103948344	l_3661_chr8:103945582-103948344_thyroid
34	lnc-KB-1507C5.2.1-4	chr8:103949852-103949985	NONHSAT128119
35	lnc-KB-1507C5.2.1-4	chr8:103946507-103946902	l_3661_chr8:103945582-103948344_thyroid

No data

Variant related genes	Relation type
ENSG00000201216	TF binding region
ENSG00000253320	TF binding region
RPL5P24	TF binding region
ENSG00000201216	CpG island
ENSG00000253320	CpG island
RPL5P24	CpG island
ENSG00000155097	chromatin interactions
ENSG00000265898	chromatin interactions
ENSG00000244052	chromatin interactions
ENSG00000201216	chromatin interactions
ENSG00000254236	chromatin interactions
ENSG00000253320	chromatin interactions
ENSG00000155096	chromatin interactions

Extended variants
information (count: 1449 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1449 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs608236	chr8:103928940-103928941	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs370938177	chr8:103928985-103928986	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs184225314	chr8:103928988-103928989	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148737083	chr8:103928993-103928994	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs35322900	chr8:103929047-103929048	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs67499452	chr8:103929048-103929049	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs564167179	chr8:103929070-103929071	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs538550819	chr8:103929087-103929088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs531388366	chr8:103929091-103929092	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs187953233	chr8:103929105-103929106	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568530239	chr8:103929117-103929118	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs56353970	chr8:103929142-103929143	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529615523	chr8:103929181-103929182	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547753625	chr8:103929192-103929193	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367984331	chr8:103929193-103929194	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs6999525	chr8:103929196-103929197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs192347807	chr8:103929297-103929298	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs557874182	chr8:103929303-103929304	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs143127829	chr8:103929311-103929312	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs540624226	chr8:103929335-103929336	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112472767	chr8:103929344-103929345	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556337545	chr8:103929375-103929376	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs113202408	chr8:103929383-103929384	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368206129	chr8:103929449-103929450	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs62526533	chr8:103929462-103929463	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542141974	chr8:103929537-103929538	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs538922858	chr8:103929547-103929548	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs147182650	chr8:103929560-103929561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs368895776	chr8:103929565-103929566	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs563467989	chr8:103929590-103929591	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs367630078	chr8:103929603-103929604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs545817615	chr8:103929618-103929619	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs564033409	chr8:103929619-103929620	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs140554031	chr8:103929670-103929671	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543517728	chr8:103929681-103929682	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs114769541	chr8:103929701-103929702	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs368662848	chr8:103929708-103929709	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs144504497	chr8:103929709-103929710	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs35895233	chr8:103929733-103929734	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs657000	chr8:103929742-103929743	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs533397333	chr8:103929743-103929744	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs117680841	chr8:103929757-103929758	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569680981	chr8:103929764-103929765	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs369616695	chr8:103929782-103929783	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541563792	chr8:103929798-103929799	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs117070810	chr8:103929820-103929821	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs375028079	chr8:103929825-103929826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555556266	chr8:103929950-103929951	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs568287100	chr8:103929957-103929958	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192767870	chr8:103929979-103929980	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Bladder cancer	21909424	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103913400-103929800	Weak transcription	Psoas Muscle	Psoas
2	chr8:103922200-103929600	Weak transcription	Fetal Intestine Small	intestine
3	chr8:103922800-103929800	Weak transcription	Fetal Brain Male	brain
4	chr8:103922800-103930600	Weak transcription	Ovary	ovary
5	chr8:103923000-103929400	Weak transcription	Left Ventricle	heart
6	chr8:103923000-103929600	Weak transcription	Placenta	Placenta
7	chr8:103923000-103931000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:103923000-103931000	Weak transcription	Brain Substantia Nigra	brain
9	chr8:103923000-103931600	Weak transcription	Fetal Stomach	stomach
10	chr8:103923000-103932000	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr8:103923200-103929800	Weak transcription	Brain Anterior Caudate	brain
12	chr8:103923200-103931000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr8:103923200-103935800	Weak transcription	Fetal Lung	lung
14	chr8:103923400-103931200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr8:103923400-103932000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:103923600-103929200	Weak transcription	Fetal Heart	heart
17	chr8:103923600-103931200	Weak transcription	HMEC	breast
18	chr8:103923600-103931600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr8:103926000-103931800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:103926000-103932000	Weak transcription	Small Intestine	intestine
21	chr8:103926000-103932600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:103926200-103929600	Weak transcription	Brain Hippocampus Middle	brain
23	chr8:103926200-103930800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr8:103926200-103931000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr8:103926400-103930000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr8:103926400-103931000	Weak transcription	Aorta	Aorta
27	chr8:103926400-103931400	Weak transcription	Right Ventricle	heart
28	chr8:103926400-103932600	Weak transcription	Fetal Muscle Leg	muscle
29	chr8:103926400-103937400	Weak transcription	Lung	lung
30	chr8:103926600-103929800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr8:103926600-103931000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr8:103926600-103931000	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr8:103926600-103936600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr8:103926800-103931000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr8:103926800-103931200	Weak transcription	Osteobl	bone
36	chr8:103926800-103931800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:103926800-103932600	Weak transcription	NHDF-Ad	bronchial
38	chr8:103927000-103931800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:103927200-103931000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr8:103927200-103931000	Weak transcription	Colon Smooth Muscle	Colon
41	chr8:103927800-103929400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr8:103927800-103929400	Weak transcription	Pancreas	Pancrea
43	chr8:103927800-103930200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr8:103927800-103930600	Weak transcription	Right Atrium	heart
45	chr8:103927800-103939800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr8:103927800-103941600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr8:103928800-103929000	Enhancers	Adipose Nuclei	Adipose
48	chr8:103928800-103933400	Enhancers	A549	lung
49	chr8:103929000-103929400	Weak transcription	Adipose Nuclei	Adipose
50	chr8:103929200-103933600	Enhancers	Fetal Heart	heart

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