Variant report

Variant	nsv1032750
Chromosome Location	chr8:48877179-48924828
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1794)
CpG islands
(count:977)
Chromatin interactive
region (count:64)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1794 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48879708-48880140	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:48920792-48921191	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:48909809-48910128	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:48909808-48910086	K562	blood:	n/a	n/a
5	ARID3A	chr8:48905475-48905861	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:48909052-48909241	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:48895484-48895695	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:48915966-48916230	HepG2	liver:	n/a	n/a
9	ATF1	chr8:48920761-48921122	K562	blood:	n/a	n/a
10	ATF1	chr8:48911599-48911799	K562	blood:	n/a	n/a
11	ATF2	chr8:48920689-48921069	GM12878	blood:	n/a	n/a
12	ATF3	chr8:48920796-48921148	A549	lung:	n/a	n/a
13	ATF3	chr8:48920715-48921150	K562	blood:	n/a	n/a
14	ATF3	chr8:48920846-48921194	A549	lung:	n/a	n/a
15	BACH1	chr8:48892735-48892903	K562	blood:	n/a	n/a
16	BACH1	chr8:48920856-48921088	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr8:48886320-48886704	GM12878	blood:	n/a	n/a
18	BATF	chr8:48886372-48886721	GM12878	blood:	n/a	n/a
19	BCLAF1	chr8:48920662-48921584	K562	blood:	n/a	chr8:48920936-48920949 chr8:48920951-48920960
20	BCLAF1	chr8:48920710-48921420	GM12878	blood:	n/a	chr8:48920936-48920949 chr8:48920951-48920960
21	BHLHE40	chr8:48920764-48921043	A549	lung:	n/a	n/a
22	BHLHE40	chr8:48909901-48910101	K562	blood:	n/a	n/a
23	BHLHE40	chr8:48920343-48921461	HepG2	liver:	n/a	chr8:48921081-48921097 chr8:48921092-48921108
24	BHLHE40	chr8:48920643-48921428	GM12878	blood:	n/a	chr8:48921081-48921097 chr8:48921092-48921108
25	BHLHE40	chr8:48920260-48921514	K562	blood:	n/a	chr8:48921081-48921097 chr8:48921092-48921108
26	BHLHE40	chr8:48905552-48905822	HepG2	liver:	n/a	n/a
27	BHLHE40	chr8:48909820-48910026	GM12878	blood:	n/a	n/a
28	BHLHE40	chr8:48886509-48886614	GM12878	blood:	n/a	n/a
29	BHLHE40	chr8:48920268-48920421	GM12878	blood:	n/a	n/a
30	BHLHE40	chr8:48910592-48910762	K562	blood:	n/a	n/a
31	BRCA1	chr8:48920912-48921112	GM12878	blood:	n/a	n/a
32	BRCA1	chr8:48920817-48921113	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr8:48920883-48921083	HepG2	liver:	n/a	n/a
34	CBX3	chr8:48906327-48906746	K562	blood:	n/a	n/a
35	CBX3	chr8:48912148-48912502	K562	blood:	n/a	n/a
36	CBX3	chr8:48920250-48921766	K562	blood:	n/a	n/a
37	CBX3	chr8:48920321-48920964	K562	blood:	n/a	n/a
38	CBX3	chr8:48909806-48910168	K562	blood:	n/a	n/a
39	CBX3	chr8:48906403-48906593	K562	blood:	n/a	n/a
40	CCNT2	chr8:48920735-48921427	K562	blood:	n/a	n/a
41	CCNT2	chr8:48911716-48911926	K562	blood:	n/a	n/a
42	CEBPB	chr8:48912290-48912954	K562	blood:	n/a	chr8:48912782-48912793
43	CEBPB	chr8:48912605-48912960	K562	blood:	n/a	chr8:48912782-48912793
44	CEBPB	chr8:48895380-48895684	HepG2	liver:	n/a	chr8:48895587-48895598
45	CEBPB	chr8:48912329-48912538	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr8:48903291-48903603	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:48912398-48912972	IMR90	lung:	n/a	chr8:48912782-48912793
48	CEBPB	chr8:48895499-48895636	Hela-S3	cervix:	n/a	chr8:48895587-48895598
49	CEBPB	chr8:48920274-48921011	A549	lung:	n/a	n/a
50	CEBPB	chr8:48895437-48895759	HepG2	liver:	n/a	chr8:48895587-48895598

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:48920777-48920827	Hela-S3	cervix:	n/a
2	chr8:48920777-48920827	Hela-S3	cervix:	n/a
3	chr8:48920761-48920811	K562	blood:	n/a
4	chr8:48920761-48920811	HRCEpiC	kidney:	n/a
5	chr8:48920860-48920910	SK-N-SH_RA	brain:	n/a
6	chr8:48910636-48910686	HEEpiC	esophagus:	n/a
7	chr8:48920761-48920811	ProgFib	skin:	n/a
8	chr8:48921337-48921387	HRPEpiC	eye:	n/a
9	chr8:48921554-48921604	HRE	kidney:	n/a
10	chr8:48889520-48889570	AG10803	skin:	n/a
11	chr8:48920838-48920888	HRCEpiC	kidney:	n/a
12	chr8:48921337-48921387	HUVEC	blood vessel:	n/a
13	chr8:48920858-48920908	HNPCEpiC	eye:	n/a
14	chr8:48921062-48921112	RPTEC	kidney:	n/a
15	chr8:48921554-48921604	NT2-D1	testis:	n/a
16	chr8:48920460-48920510	Caco-2	colon:	n/a
17	chr8:48921554-48921604	HCF	heart:	n/a
18	chr8:48924348-48924398	HRE	kidney:	n/a
19	chr8:48920777-48920827	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:48920777-48920827	RPTEC	kidney:	n/a
21	chr8:48920838-48920888	PFSK-1	brain:	n/a
22	chr8:48877513-48877563	HCF	heart:	n/a
23	chr8:48920858-48920908	SK-N-SH_RA	brain:	n/a
24	chr8:48920818-48920868	SKMC	muscle:	n/a
25	chr8:48889520-48889570	AG04449	skin:	fetal
26	chr8:48921407-48921457	HCPEpiC	choroid plexus:	n/a
27	chr8:48910778-48910828	GM06990	blood:	n/a
28	chr8:48920860-48920910	RPTEC	kidney:	n/a
29	chr8:48920860-48920910	LNCaP	prostate:	n/a
30	chr8:48921407-48921457	Hela-S3	cervix:	n/a
31	chr8:48924348-48924398	ovcar-3	ovarian:	n/a
32	chr8:48920460-48920510	ovcar-3	ovarian:	n/a
33	chr8:48920777-48920827	ECC-1	luminal epithelium:	n/a
34	chr8:48920858-48920908	HUVEC	blood vessel:	n/a
35	chr8:48889520-48889570	BJ	skin:	n/a
36	chr8:48920838-48920888	H1-hESC	embryonic stem cell:	embryo
37	chr8:48920777-48920827	HEEpiC	esophagus:	n/a
38	chr8:48921062-48921112	NH-A	brain:	n/a
39	chr8:48920460-48920510	SK-N-SH	brain:	n/a
40	chr8:48920858-48920908	HIPEpiC	eye:	n/a
41	chr8:48921337-48921387	RPTEC	kidney:	n/a
42	chr8:48921407-48921457	ECC-1	luminal epithelium:	n/a
43	chr8:48924348-48924398	HEEpiC	esophagus:	n/a
44	chr8:48889520-48889570	HUVEC	blood vessel:	n/a
45	chr8:48924348-48924398	AoSMC	blood vessel:	n/a
46	chr8:48920838-48920888	Hela-S3	cervix:	n/a
47	chr8:48920838-48920888	A549	lung:	n/a
48	chr8:48877513-48877563	K562	blood:	n/a
49	chr8:48924348-48924398	K562	blood:	n/a
50	chr8:48920838-48920888	SKMC	muscle:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:48871383..48875366-chr8:48919489..48922712,6	MCF-7	breast:
2	chr8:48871080..48872628-chr8:48898193..48900084,2	K562	blood:
3	chr8:48900431..48902138-chr8:48907383..48908901,2	MCF-7	breast:
4	chr8:48881678..48884216-chr8:48908511..48910413,2	K562	blood:
5	chr8:48869236..48871124-chr8:48909959..48911972,2	K562	blood:
6	chr8:48906937..48908708-chr8:48918974..48921656,2	K562	blood:
7	chr8:48900497..48902093-chr8:48902216..48905127,2	MCF-7	breast:
8	chr8:48900431..48902138-chr8:48907383..48908901,2	MCF-7	breast:
9	chr8:48923287..48925205-chr8:48959755..48962369,2	K562	blood:
10	chr8:48919638..48923031-chr8:48924229..48928095,7	MCF-7	breast:
11	chr8:48912051..48914601-chr8:48916476..48918963,2	K562	blood:
12	chr8:48896074..48898394-chr8:48900447..48902848,3	K562	blood:
13	chr8:48854376..48857161-chr8:48889369..48891262,2	MCF-7	breast:
14	chr8:48878812..48881751-chr8:48883436..48885898,2	MCF-7	breast:
15	chr8:48908935..48911744-chr8:48919435..48922520,3	K562	blood:
16	chr8:48872720..48874508-chr8:48901078..48903958,2	K562	blood:
17	chr8:48898201..48900058-chr8:48903051..48905001,2	K562	blood:
18	chr8:48907169..48911737-chr8:48918914..48922421,4	K562	blood:
19	chr8:48923260..48926236-chr8:48933537..48935762,2	K562	blood:
20	chr8:48870802..48875414-chr8:48919446..48923770,8	MCF-7	breast:
21	chr8:48909455..48910993-chr8:49046960..49049925,2	K562	blood:
22	chr8:48900497..48902093-chr8:48902216..48905127,2	MCF-7	breast:
23	chr8:48924792..48926393-chr8:48927338..48929721,2	K562	blood:
24	chr8:48878378..48881135-chr8:48887828..48890847,3	MCF-7	breast:
25	chr8:48871178..48874087-chr8:48899526..48903049,3	MCF-7	breast:
26	chr8:48879303..48881040-chr8:48891932..48894237,2	MCF-7	breast:
27	chr8:48885569..48887967-chr8:48920138..48922569,2	K562	blood:
28	chr8:48870843..48877121-chr8:48919292..48922738,10	K562	blood:
29	chr8:48878812..48881751-chr8:48883436..48885898,2	MCF-7	breast:
30	chr8:48912051..48914601-chr8:48916476..48918963,2	K562	blood:
31	chr8:48873301..48875713-chr8:48914847..48916375,2	K562	blood:
32	chr8:48880651..48882181-chr8:48887317..48888822,2	MCF-7	breast:
33	chr8:48896074..48898394-chr8:48900447..48902848,3	K562	blood:
34	chr8:48872465..48875841-chr8:48908901..48912776,4	MCF-7	breast:
35	chr19:50879673..50880251-chr8:48920915..48921687,2	Hela-S3	cervix:
36	chr8:48873884..48879338-chr8:48885468..48891171,6	MCF-7	breast:
37	chr1:28974788..28975451-chr8:48920936..48921691,2	Hela-S3	cervix:
38	chr8:48886822..48888941-chr8:48919839..48922442,3	MCF-7	breast:
39	chr8:48870534..48872766-chr8:48885611..48888462,2	MCF-7	breast:
40	chr8:48880651..48882181-chr8:48887317..48888822,2	MCF-7	breast:
41	chr8:48885569..48887967-chr8:48920138..48922569,2	K562	blood:
42	chr8:48871876..48875068-chr8:48914519..48916969,3	MCF-7	breast:
43	chr8:48920860..48923835-chr8:48924077..48926728,4	MCF-7	breast:
44	chr8:48871246..48875685-chr8:48919504..48923066,10	K562	blood:
45	chr15:60770926..60771435-chr8:48920467..48921398,2	Hela-S3	cervix:
46	chr8:48872462..48875713-chr8:48912843..48916347,3	K562	blood:
47	chr8:48871644..48875335-chr8:48903503..48906313,3	MCF-7	breast:
48	chr8:48873449..48876076-chr8:48887828..48890421,3	MCF-7	breast:
49	chr8:48909845..48912339-chr8:48920798..48922536,2	MCF-7	breast:
50	chr8:48878989..48881250-chr8:48961083..48963468,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MCM4	hsa-miR-183-5p	chr8:48889872-48889892

Variant related genes	Relation type
PRKDC	TF binding region
MCM4	TF binding region
UBE2V2	TF binding region
RNU6-519P	TF binding region
PRKDC	CpG island
MCM4	CpG island
UBE2V2	CpG island
RNU6-519P	CpG island
ENSG00000131408	chromatin interactions
ENSG00000143633	chromatin interactions
ENSG00000253729	chromatin interactions
ENSG00000101213	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000222522	chromatin interactions
ENSG00000245534	chromatin interactions
ENSG00000169139	chromatin interactions
ENSG00000104738	chromatin interactions
ENSG00000128915	chromatin interactions

Extended variants
information (count: 1853 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1853 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549554177	chr8:48877179-48877180	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs146842638	chr8:48877183-48877184	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs373114613	chr8:48877197-48877198	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs145966797	chr8:48877227-48877228	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs368142326	chr8:48877232-48877233	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs80302822	chr8:48877234-48877235	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372063762	chr8:48877235-48877236	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs202237323	chr8:48877259-48877260	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs374693496	chr8:48877288-48877289	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs367749655	chr8:48877290-48877291	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs372213371	chr8:48877291-48877292	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs577078382	chr8:48877321-48877322	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs373846910	chr8:48877324-48877325	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs568105615	chr8:48877342-48877343	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs544466530	chr8:48877346-48877347	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs34606779	chr8:48877347-48877348	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs562675122	chr8:48877356-48877357	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs529873742	chr8:48877402-48877403	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs548393506	chr8:48877407-48877408	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs186077340	chr8:48877513-48877514	Strong transcription Weak transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs17287591	chr8:48877514-48877515	Strong transcription Weak transcription Genic enhancers	CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs368327272	chr8:48877520-48877521	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs552306368	chr8:48877535-48877536	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs570799816	chr8:48877545-48877546	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs538161676	chr8:48877550-48877551	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs550022987	chr8:48877611-48877612	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs568405864	chr8:48877640-48877641	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs375472960	chr8:48877645-48877646	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs553926316	chr8:48877658-48877659	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs17287598	chr8:48877705-48877706	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs191935637	chr8:48877758-48877759	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs148671693	chr8:48877774-48877775	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs113918401	chr8:48877775-48877776	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs533849524	chr8:48877888-48877889	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558289918	chr8:48877892-48877893	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs576723931	chr8:48877905-48877906	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs369707274	chr8:48877921-48877922	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs35096709	chr8:48877929-48877930	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs553541311	chr8:48877989-48877990	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544187745	chr8:48878035-48878036	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs570485318	chr8:48878047-48878048	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs75819385	chr8:48878140-48878141	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs146935350	chr8:48878143-48878144	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs560370426	chr8:48878150-48878151	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs147581897	chr8:48878151-48878152	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs17287604	chr8:48878156-48878157	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531773301	chr8:48878157-48878158	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549763258	chr8:48878159-48878160	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs181536105	chr8:48878174-48878175	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs186877367	chr8:48878190-48878191	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
22q11 deletion syndrome	20357662	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48874200-48877800	Weak transcription	Aorta	Aorta
2	chr8:48874400-48877200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr8:48874400-48877200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr8:48874400-48877200	Weak transcription	Stomach Smooth Muscle	stomach
5	chr8:48874400-48877400	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr8:48874400-48877600	Weak transcription	Brain Hippocampus Middle	brain
7	chr8:48874400-48877600	Weak transcription	Pancreas	Pancrea
8	chr8:48874400-48877800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr8:48874400-48877800	Weak transcription	Ovary	ovary
10	chr8:48874400-48878000	Weak transcription	Colonic Mucosa	Colon
11	chr8:48874400-48878000	Weak transcription	Psoas Muscle	Psoas
12	chr8:48874400-48878600	Weak transcription	HSMMtube	muscle
13	chr8:48874400-48881600	Weak transcription	Right Atrium	heart
14	chr8:48874400-48888800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr8:48874600-48877200	Weak transcription	Brain Angular Gyrus	brain
16	chr8:48874600-48877200	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr8:48874600-48877600	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr8:48874600-48877800	Weak transcription	Primary B cells from cord blood	blood
19	chr8:48874600-48878000	Weak transcription	Brain Substantia Nigra	brain
20	chr8:48874600-48878200	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:48874600-48879600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr8:48874600-48888800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr8:48874600-48891600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr8:48874600-48891800	Weak transcription	Colon Smooth Muscle	Colon
25	chr8:48874800-48877200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr8:48874800-48877200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr8:48874800-48877600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:48874800-48877600	Weak transcription	Lung	lung
29	chr8:48874800-48877600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr8:48874800-48877600	Weak transcription	Thymus	Thymus
31	chr8:48874800-48877800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr8:48874800-48877800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr8:48874800-48877800	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr8:48874800-48877800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr8:48874800-48877800	Weak transcription	Duodenum Mucosa	Duodenum
36	chr8:48874800-48877800	Weak transcription	Esophagus	oesophagus
37	chr8:48874800-48877800	Weak transcription	Fetal Brain Female	brain
38	chr8:48874800-48877800	Weak transcription	Gastric	stomach
39	chr8:48874800-48877800	Weak transcription	Right Ventricle	heart
40	chr8:48874800-48877800	Weak transcription	Spleen	Spleen
41	chr8:48874800-48878000	Weak transcription	Primary T cells from cord blood	blood
42	chr8:48874800-48878000	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr8:48874800-48878200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr8:48874800-48878400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr8:48874800-48890000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr8:48874800-48890400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr8:48874800-48890800	Strong transcription	ES-I3 Cell Line	embryonic stem cell
48	chr8:48874800-48890800	Strong transcription	Placenta	Placenta
49	chr8:48874800-48905800	Weak transcription	Stomach Mucosa	stomach
50	chr8:48875000-48877200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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