Variant report

Variant	nsv528695
Chromosome Location	chr8:98960813-99022009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:564)
CpG islands
(count:367)
Chromatin interactive
region (count:47)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:564 , 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	ATF2	chr8:99017769-99018265	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr8:98983310-98983792	GM12878	blood:	n/a	n/a
3	ATF2	chr8:98983369-98983643	GM12878	blood:	n/a	n/a
4	ATF2	chr8:98992242-98992761	GM12878	blood:	n/a	n/a
5	BACH1	chr8:99017909-99018344	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:98993750-98993927	H1-hESC	embryonic stem cell:	n/a	chr8:98993765-98993779
7	BATF	chr8:98983441-98983734	GM12878	blood:	n/a	n/a
8	BATF	chr8:98964143-98964347	GM12878	blood:	n/a	chr8:98964231-98964241 chr8:98964230-98964241
9	BATF	chr8:98988040-98988296	GM12878	blood:	n/a	chr8:98988187-98988197 chr8:98988186-98988197
10	BATF	chr8:98983391-98983828	GM12878	blood:	n/a	n/a
11	BATF	chr8:98988039-98988276	GM12878	blood:	n/a	chr8:98988187-98988197 chr8:98988186-98988197
12	BATF	chr8:98992371-98992697	GM12878	blood:	n/a	n/a
13	BATF	chr8:98992292-98992729	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:98992389-98992674	GM12878	blood:	n/a	chr8:98992610-98992619
15	BCL11A	chr8:98992346-98992764	GM12878	blood:	n/a	chr8:98992610-98992619
16	BCL11A	chr8:99017904-99018110	H1-hESC	embryonic stem cell:	n/a	n/a
17	BHLHE40	chr8:98964147-98964347	K562	blood:	n/a	n/a
18	BHLHE40	chr8:98992306-98992738	GM12878	blood:	n/a	n/a
19	BHLHE40	chr8:99019713-99019830	K562	blood:	n/a	n/a
20	BHLHE40	chr8:98973889-98973920	K562	blood:	n/a	n/a
21	CEBPB	chr8:99004937-99005307	MCF-7	breast:	n/a	chr8:99005098-99005109
22	CEBPB	chr8:99010995-99011311	IMR90	lung:	n/a	chr8:99011144-99011155 chr8:99011005-99011016
23	CEBPB	chr8:99010995-99011195	HepG2	liver:	n/a	chr8:99011144-99011155 chr8:99011005-99011016
24	CEBPB	chr8:98993337-98993916	IMR90	lung:	n/a	n/a
25	CEBPB	chr8:99002276-99002879	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:99003289-99003549	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:99004877-99005208	IMR90	lung:	n/a	chr8:99005098-99005109
28	CEBPB	chr8:99014050-99014277	Hela-S3	cervix:	n/a	chr8:99014263-99014271
29	CEBPB	chr8:98983490-98983844	IMR90	lung:	n/a	n/a
30	CEBPB	chr8:98984979-98985512	A549	lung:	n/a	chr8:98985225-98985238 chr8:98985242-98985253 chr8:98985242-98985253
31	CEBPB	chr8:98985028-98985516	MCF-7	breast:	n/a	chr8:98985225-98985238 chr8:98985242-98985253 chr8:98985242-98985253
32	CEBPB	chr8:99007808-99008200	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:99005015-99005187	H1-hESC	embryonic stem cell:	n/a	chr8:99005098-99005109
34	CEBPB	chr8:98965078-98965244	K562	blood:	n/a	n/a
35	CEBPB	chr8:98993415-98993715	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr8:99014010-99014633	IMR90	lung:	n/a	chr8:99014263-99014271
37	CEBPB	chr8:98964101-98964536	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:98964128-98964593	IMR90	lung:	n/a	n/a
39	CEBPB	chr8:99004934-99005134	HepG2	liver:	n/a	chr8:99005098-99005109
40	CEBPB	chr8:99002513-99002897	MCF-7	breast:	n/a	n/a
41	CEBPB	chr8:99010997-99011202	K562	blood:	n/a	chr8:99011144-99011155 chr8:99011005-99011016
42	CEBPB	chr8:99004918-99005159	A549	lung:	n/a	chr8:99005098-99005109
43	CEBPB	chr8:99011006-99011312	A549	lung:	n/a	chr8:99011144-99011155
44	CHD2	chr8:98992491-98992639	GM12878	blood:	n/a	n/a
45	CHD2	chr8:99017849-99018338	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTBP2	chr8:99017502-99018449	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr8:99014380-99014530	BE2_C	brain:	n/a	chr8:99014444-99014462 chr8:99014439-99014460
48	CTCF	chr8:99014388-99014501	K562	blood:	n/a	chr8:99014444-99014462 chr8:99014439-99014460
49	CTCF	chr8:98963740-98963890	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr8:99014380-99014530	NHDF-neo	bronchial:	n/a	chr8:99014444-99014462 chr8:99014439-99014460

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:98993142-98993192	GM12878	blood:	n/a
2	chr8:98993142-98993192	GM12878	blood:	n/a
3	chr8:98963918-98963968	HMEC	breast:	n/a
4	chr8:98963918-98963968	GM12891	blood:	n/a
5	chr8:99017690-99017740	RPTEC	kidney:	n/a
6	chr8:99015178-99015228	HAEpiC	amniotic membrane:	n/a
7	chr8:98993142-98993192	HAEpiC	amniotic membrane:	n/a
8	chr8:99007318-99007368	AG09319	gingival:	n/a
9	chr8:99017690-99017740	NH-A	brain:	n/a
10	chr8:99007318-99007368	ECC-1	luminal epithelium:	n/a
11	chr8:98963918-98963968	RPTEC	kidney:	n/a
12	chr8:99007318-99007368	PFSK-1	brain:	n/a
13	chr8:99017690-99017740	AG04450	lung:	fetal
14	chr8:98969923-98969973	AG10803	skin:	n/a
15	chr8:98963918-98963968	AG09319	gingival:	n/a
16	chr8:98963918-98963968	NHBE	bronchial:	n/a
17	chr8:99007318-99007368	SAEC	small airway:	n/a
18	chr8:99015178-99015228	K562	blood:	n/a
19	chr8:98969923-98969973	LNCaP	prostate:	n/a
20	chr8:98969923-98969973	HPAEpiC	pulmonary alveolar:	n/a
21	chr8:98963918-98963968	HepG2	liver:	n/a
22	chr8:98963918-98963968	AG10803	skin:	n/a
23	chr8:98969923-98969973	HRCEpiC	kidney:	n/a
24	chr8:98963918-98963968	NHDF-neo	bronchial:	n/a
25	chr8:98963918-98963968	Caco-2	colon:	n/a
26	chr8:99015178-99015228	Hepatocyte	liver:	n/a
27	chr8:99017690-99017740	GM12892	blood:	n/a
28	chr8:99007318-99007368	HCPEpiC	choroid plexus:	n/a
29	chr8:99017690-99017740	NB4	blood:	n/a
30	chr8:98969923-98969973	RPTEC	kidney:	n/a
31	chr8:98969923-98969973	SKMC	muscle:	n/a
32	chr8:99017690-99017740	PFSK-1	brain:	n/a
33	chr8:99007318-99007368	AG10803	skin:	n/a
34	chr8:98963918-98963968	ProgFib	skin:	n/a
35	chr8:99017690-99017740	MCF-7	breast:	n/a
36	chr8:98963918-98963968	HRE	kidney:	n/a
37	chr8:98993142-98993192	HRCEpiC	kidney:	n/a
38	chr8:98963918-98963968	CMK	blood:	n/a
39	chr8:98963918-98963968	HAEpiC	amniotic membrane:	n/a
40	chr8:99007318-99007368	HCM	heart:	n/a
41	chr8:98963918-98963968	SK-N-SH_RA	brain:	n/a
42	chr8:99015178-99015228	Hela-S3	cervix:	n/a
43	chr8:98969923-98969973	HCM	heart:	n/a
44	chr8:99017690-99017740	HL-60	blood:	n/a
45	chr8:99015178-99015228	IMR90	lung:	fetal
46	chr8:98969923-98969973	HRPEpiC	eye:	n/a
47	chr8:98963918-98963968	NT2-D1	testis:	n/a
48	chr8:99015178-99015228	GM12892	blood:	n/a
49	chr8:98993142-98993192	HRPEpiC	eye:	n/a
50	chr8:99017690-99017740	IMR90	lung:	fetal

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:98929668..98932562-chr8:98996810..98999331,2	K562	blood:
2	chr8:99014119..99017352-chr8:99021059..99024142,3	MCF-7	breast:
3	chr8:98880331..98882636-chr8:99012826..99014648,3	MCF-7	breast:
4	chr8:99000977..99004318-chr8:99007120..99009154,3	K562	blood:
5	chr8:99015593..99019656-chr8:99049212..99053715,4	MCF-7	breast:
6	chr8:98981599..98983583-chr8:98984099..98986745,2	MCF-7	breast:
7	chr8:98852045..98852568-chr8:99013936..99014703,2	MCF-7	breast:
8	chr8:98992573..98995424-chr8:98996000..98998679,2	MCF-7	breast:
9	chr8:98973467..98975670-chr8:98979919..98982620,2	MCF-7	breast:
10	chr17:57915257..57916823-chr8:98971519..98974188,2	MCF-7	breast:
11	chr8:98981599..98983583-chr8:98984099..98986745,2	MCF-7	breast:
12	chr8:98994617..98996981-chr8:99019389..99021453,2	MCF-7	breast:
13	chr8:99006609..99009034-chr8:99014356..99016713,2	MCF-7	breast:
14	chr8:98961024..98963389-chr8:99054505..99057436,2	MCF-7	breast:
15	chr8:98991788..98993846-chr8:99008923..99010508,2	MCF-7	breast:
16	chr8:98964671..98967862-chr8:98969521..98972694,3	MCF-7	breast:
17	chr8:98974372..98976072-chr8:99045013..99046832,2	K562	blood:
18	chr8:98991788..98993846-chr8:99008923..99010508,2	MCF-7	breast:
19	chr8:98973539..98975203-chr8:98975943..98977611,2	K562	blood:
20	chr8:99005306..99006937-chr8:99007959..99009953,2	MCF-7	breast:
21	chr8:98966806..98971038-chr8:98972037..98974632,4	K562	blood:
22	chr8:98994950..98998234-chr8:99001793..99004607,3	K562	blood:
23	chr8:99014119..99017352-chr8:99021059..99024142,3	MCF-7	breast:
24	chr8:98983972..98985766-chr8:98995097..98997700,2	MCF-7	breast:
25	chr8:99020262..99022328-chr8:99024233..99025913,2	K562	blood:
26	chr8:98985735..98990217-chr8:98991050..98995817,5	K562	blood:
27	chr8:98964671..98967862-chr8:98969521..98972694,3	MCF-7	breast:
28	chr8:99006609..99009034-chr8:99014356..99016713,2	MCF-7	breast:
29	chr8:98969704..98971901-chr8:98988416..98991010,2	MCF-7	breast:
30	chr8:98880636..98882554-chr8:98986565..98988277,2	MCF-7	breast:
31	chr8:98992573..98995424-chr8:98996000..98998679,2	MCF-7	breast:
32	chr8:98969704..98971901-chr8:98988416..98991010,2	MCF-7	breast:
33	chr8:99011784..99014375-chr8:99051357..99053193,2	MCF-7	breast:
34	chr8:98994950..98998234-chr8:99001793..99004607,3	K562	blood:
35	chr8:98968508..98970567-chr8:98972102..98974220,2	K562	blood:
36	chr8:98786769..98788995-chr8:98993109..98995354,2	MCF-7	breast:
37	chr8:98958651..98961201-chr8:98961711..98963303,2	MCF-7	breast:
38	chr8:98881106..98881826-chr8:98970641..98971277,2	MCF-7	breast:
39	chr8:98985735..98990217-chr8:98991050..98995817,5	K562	blood:
40	chr8:98963788..98966015-chr8:99056664..99058893,2	MCF-7	breast:
41	chr8:98983972..98985766-chr8:98995097..98997700,2	MCF-7	breast:
42	chr8:99000977..99004318-chr8:99007120..99009154,3	K562	blood:
43	chr8:98985817..98987615-chr8:98987755..98989901,2	MCF-7	breast:
44	chr8:98985817..98987615-chr8:98987755..98989901,2	MCF-7	breast:
45	chr8:99005306..99006937-chr8:99007959..99009953,2	MCF-7	breast:
46	chr8:99009762..99011272-chr8:99018097..99019778,2	MCF-7	breast:
47	chr8:98880171..98881728-chr8:99021126..99023057,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LAPTM4B-4	chr8:98963047-98963126	NONHSAT127890
2	lnc-LAPTM4B-4	chr8:98964212-98964530	NONHSAT127890

No data

Variant related genes	Relation type
MATN2	TF binding region
MATN2	CpG island
ENSG00000156482	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000132561	chromatin interactions
ENSG00000104341	chromatin interactions

Extended variants
information (count: 2244 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:2244 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2512028	chr8:98960813-98960814	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs35447815	chr8:98960874-98960875	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs533373654	chr8:98960892-98960893	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs2444883	chr8:98960906-98960907	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559780362	chr8:98960909-98960910	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs369927496	chr8:98960915-98960916	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs528999015	chr8:98960951-98960952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs541806266	chr8:98960960-98960961	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568802341	chr8:98961025-98961026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373382552	chr8:98961068-98961069	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537457214	chr8:98961075-98961076	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200332283	chr8:98961094-98961095	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs201468631	chr8:98961095-98961096	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs140768830	chr8:98961098-98961099	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs200417945	chr8:98961103-98961104	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs531632851	chr8:98961150-98961151	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs551730806	chr8:98961188-98961189	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192204654	chr8:98961269-98961270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557740506	chr8:98961274-98961275	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533940889	chr8:98961281-98961282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554032250	chr8:98961302-98961303	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs566912348	chr8:98961305-98961306	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149162119	chr8:98961342-98961343	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs71271175	chr8:98961399-98961400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs398008960	chr8:98961415-98961416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555722544	chr8:98961432-98961433	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577709718	chr8:98961461-98961462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575596370	chr8:98961542-98961543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376365375	chr8:98961543-98961544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs11774615	chr8:98961599-98961600	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534122235	chr8:98961651-98961652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143267427	chr8:98961735-98961736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs554093216	chr8:98961771-98961772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs558060737	chr8:98961781-98961782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573784996	chr8:98961939-98961940	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs184636721	chr8:98962004-98962005	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs542782902	chr8:98962008-98962009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561875332	chr8:98962012-98962013	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs528975846	chr8:98962017-98962018	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs138868443	chr8:98962022-98962023	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs370211458	chr8:98962105-98962106	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531244964	chr8:98962129-98962130	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs189372348	chr8:98962152-98962153	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs571538727	chr8:98962243-98962244	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562859244	chr8:98962252-98962253	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs372962099	chr8:98962340-98962341	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141928414	chr8:98962380-98962381	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530907113	chr8:98962419-98962420	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs118097681	chr8:98962426-98962427	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs180737855	chr8:98962434-98962435	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	22341455	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD

Chromatin state (count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:98938200-98969200	Weak transcription	Colonic Mucosa	Colon
2	chr8:98941000-98968000	Weak transcription	Esophagus	oesophagus
3	chr8:98945600-98970200	Weak transcription	Spleen	Spleen
4	chr8:98950400-98964600	Weak transcription	Pancreas	Pancrea
5	chr8:98952200-98962200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr8:98955600-98962200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr8:98955600-98962400	Weak transcription	Fetal Kidney	kidney
8	chr8:98956600-98962400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr8:98956600-98968800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr8:98956600-98973600	Weak transcription	Duodenum Mucosa	Duodenum
11	chr8:98957000-98961800	Weak transcription	Brain Angular Gyrus	brain
12	chr8:98957000-98962000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:98957000-98962000	Weak transcription	Brain Substantia Nigra	brain
14	chr8:98957000-98962400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr8:98957000-98962600	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr8:98957000-98962800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr8:98957000-98963200	Weak transcription	NH-A	brain
18	chr8:98957200-98962400	Weak transcription	NHLF	lung
19	chr8:98957200-98962400	Weak transcription	Osteobl	bone
20	chr8:98957200-98962600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:98957200-98962600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr8:98957200-98963000	Weak transcription	Fetal Muscle Trunk	muscle
23	chr8:98957200-98963200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr8:98957200-98970800	Weak transcription	Colon Smooth Muscle	Colon
25	chr8:98957200-98973600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr8:98957400-98963000	Weak transcription	Fetal Heart	heart
27	chr8:98957600-98961800	Weak transcription	Brain Hippocampus Middle	brain
28	chr8:98957600-98962000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr8:98957600-98962600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr8:98957600-98962800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr8:98957600-98963000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr8:98957600-98963000	Weak transcription	Adipose Nuclei	Adipose
33	chr8:98957600-98963000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr8:98957600-98963200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr8:98957800-98963000	Weak transcription	Right Atrium	heart
36	chr8:98957800-98963000	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr8:98957800-98969200	Weak transcription	Left Ventricle	heart
38	chr8:98958200-98962600	Weak transcription	Fetal Muscle Leg	muscle
39	chr8:98958600-98962200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr8:98958800-98962800	Weak transcription	Fetal Lung	lung
41	chr8:98959400-98962000	Weak transcription	Fetal Stomach	stomach
42	chr8:98959600-98961400	Weak transcription	Ovary	ovary
43	chr8:98960200-98961800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
44	chr8:98960400-98961000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr8:98960800-98962000	Weak transcription	NHDF-Ad	bronchial
46	chr8:98961000-98962200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr8:98961400-98964400	Enhancers	Ovary	ovary
48	chr8:98961800-98962200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr8:98961800-98963200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr8:98961800-98963800	Enhancers	Brain Angular Gyrus	brain

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