Variant report

Variant	nsv873728
Chromosome Location	chr2:21250914-21460786
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1920)
CpG islands
(count:1892)
Chromatin interactive
region (count:58)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1920 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:21451017-21451718	K562	blood:	n/a	n/a
2	ARID3A	chr2:21279332-21279476	K562	blood:	n/a	n/a
3	ARID3A	chr2:21327252-21327458	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:21295439-21295634	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:21274904-21275191	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:21315238-21315825	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:21292755-21294059	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:21266739-21267203	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:21264476-21266439	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:21378501-21379250	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:21320226-21320577	HepG2	liver:	n/a	n/a
12	ARID3A	chr2:21279096-21280158	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:21319206-21319794	HepG2	liver:	n/a	n/a
14	ARID3A	chr2:21341174-21341527	HepG2	liver:	n/a	n/a
15	ARID3A	chr2:21261474-21262426	HepG2	liver:	n/a	n/a
16	ARID3A	chr2:21254102-21254422	HepG2	liver:	n/a	n/a
17	ARID3A	chr2:21269907-21270388	HepG2	liver:	n/a	n/a
18	ARID3A	chr2:21289715-21290538	HepG2	liver:	n/a	n/a
19	ATF1	chr2:21341235-21341624	K562	blood:	n/a	n/a
20	ATF1	chr2:21451093-21451775	K562	blood:	n/a	n/a
21	ATF3	chr2:21451385-21451728	K562	blood:	n/a	n/a
22	BACH1	chr2:21322163-21322433	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCLAF1	chr2:21451237-21451714	K562	blood:	n/a	n/a
24	BHLHE40	chr2:21265710-21267533	HepG2	liver:	n/a	chr2:21266821-21266837
25	BHLHE40	chr2:21451390-21451775	K562	blood:	n/a	n/a
26	BHLHE40	chr2:21265872-21265984	K562	blood:	n/a	n/a
27	BHLHE40	chr2:21261526-21262419	HepG2	liver:	n/a	n/a
28	BHLHE40	chr2:21269857-21270787	HepG2	liver:	n/a	n/a
29	BHLHE40	chr2:21270037-21270337	HepG2	liver:	n/a	n/a
30	BHLHE40	chr2:21445953-21446030	K562	blood:	n/a	n/a
31	BHLHE40	chr2:21262750-21262980	HepG2	liver:	n/a	n/a
32	BHLHE40	chr2:21293239-21293741	HepG2	liver:	n/a	n/a
33	BHLHE40	chr2:21264675-21265371	HepG2	liver:	n/a	n/a
34	BHLHE40	chr2:21279223-21279609	HepG2	liver:	n/a	n/a
35	BHLHE40	chr2:21269908-21270348	HepG2	liver:	n/a	n/a
36	BRCA1	chr2:21256327-21256827	HepG2	liver:	n/a	n/a
37	BRCA1	chr2:21270160-21270305	HepG2	liver:	n/a	n/a
38	BRCA1	chr2:21265766-21266387	HepG2	liver:	n/a	n/a
39	BRCA1	chr2:21341220-21341503	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr2:21265876-21266325	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr2:21266770-21267220	HepG2	liver:	n/a	n/a
42	BRCA1	chr2:21319473-21319557	HepG2	liver:	n/a	n/a
43	BRCA1	chr2:21257399-21257690	HepG2	liver:	n/a	n/a
44	BRCA1	chr2:21259139-21259309	HepG2	liver:	n/a	n/a
45	BRCA1	chr2:21264845-21265354	HepG2	liver:	n/a	n/a
46	CBX3	chr2:21451269-21451772	K562	blood:	n/a	n/a
47	CBX3	chr2:21442812-21443130	K562	blood:	n/a	n/a
48	CBX3	chr2:21447076-21447477	K562	blood:	n/a	n/a
49	CBX3	chr2:21451090-21451866	K562	blood:	n/a	n/a
50	CCNT2	chr2:21279347-21279521	K562	blood:	n/a	n/a

(count:1892 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:21291088-21291138	SAEC	small airway:	n/a
2	chr2:21291088-21291138	SAEC	small airway:	n/a
3	chr2:21346326-21346376	GM12878	blood:	n/a
4	chr2:21346738-21346788	SK-N-SH_RA	brain:	n/a
5	chr2:21265912-21265962	HIPEpiC	eye:	n/a
6	chr2:21267212-21267262	HRCEpiC	kidney:	n/a
7	chr2:21276681-21276731	HL-60	blood:	n/a
8	chr2:21265912-21265962	HCPEpiC	choroid plexus:	n/a
9	chr2:21265939-21265989	AoSMC	blood vessel:	n/a
10	chr2:21266956-21267006	HCT-116	colon:	n/a
11	chr2:21269910-21269960	NHDF-neo	bronchial:	n/a
12	chr2:21267175-21267225	HRE	kidney:	n/a
13	chr2:21266960-21267010	AG10803	skin:	n/a
14	chr2:21251355-21251405	SAEC	small airway:	n/a
15	chr2:21451686-21451736	Caco-2	colon:	n/a
16	chr2:21267113-21267163	AG09309	skin:	n/a
17	chr2:21266500-21266550	AG09309	skin:	n/a
18	chr2:21266947-21266997	HCPEpiC	choroid plexus:	n/a
19	chr2:21451686-21451736	GM12878	blood:	n/a
20	chr2:21267212-21267262	RPTEC	kidney:	n/a
21	chr2:21266727-21266777	CMK	blood:	n/a
22	chr2:21346738-21346788	SK-N-SH	brain:	n/a
23	chr2:21266568-21266618	HUVEC	blood vessel:	n/a
24	chr2:21266568-21266618	Hela-S3	cervix:	n/a
25	chr2:21324804-21324854	SAEC	small airway:	n/a
26	chr2:21255279-21255329	GM06990	blood:	n/a
27	chr2:21266727-21266777	HUVEC	blood vessel:	n/a
28	chr2:21266953-21267003	GM19239	blood:	n/a
29	chr2:21255298-21255348	PANC-1	pancreas:	n/a
30	chr2:21267212-21267262	SK-N-SH_RA	brain:	n/a
31	chr2:21266960-21267010	AG09319	gingival:	n/a
32	chr2:21251355-21251405	AG09309	skin:	n/a
33	chr2:21267212-21267262	NHDF-neo	bronchial:	n/a
34	chr2:21266500-21266550	AG04450	lung:	fetal
35	chr2:21320297-21320347	ProgFib	skin:	n/a
36	chr2:21267113-21267163	NB4	blood:	n/a
37	chr2:21266960-21267010	AG09309	skin:	n/a
38	chr2:21255279-21255329	HMEC	breast:	n/a
39	chr2:21266995-21267045	IMR90	lung:	fetal
40	chr2:21265912-21265962	LNCaP	prostate:	n/a
41	chr2:21266568-21266618	SAEC	small airway:	n/a
42	chr2:21269910-21269960	HRE	kidney:	n/a
43	chr2:21266953-21267003	SK-N-SH_RA	brain:	n/a
44	chr2:21451686-21451736	SKMC	muscle:	n/a
45	chr2:21346738-21346788	SAEC	small airway:	n/a
46	chr2:21267113-21267163	HCM	heart:	n/a
47	chr2:21267113-21267163	T-47D	breast:	n/a
48	chr2:21267113-21267163	HIPEpiC	eye:	n/a
49	chr2:21266947-21266997	HRCEpiC	kidney:	n/a
50	chr2:21265939-21265989	HCPEpiC	choroid plexus:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:21364410..21366730-chr2:21369104..21371071,2	K562	blood:
2	chr2:21260491..21263046-chr2:21265697..21267958,2	MCF-7	breast:
3	chr2:21265489..21266445-chr2:23574136..23574916,2	K562	blood:
4	chr2:21376708..21379043-chr2:21381243..21383355,2	K562	blood:
5	chr2:21348742..21351585-chr2:21351799..21353530,2	MCF-7	breast:
6	chr2:21444080..21447303-chr2:21449844..21452884,4	K562	blood:
7	chr2:20861361..20861889-chr2:21250078..21250989,2	K562	blood:
8	chr2:21265474..21266321-chr2:21340848..21341823,6	K562	blood:
9	chr2:21247697..21249209-chr2:21263867..21265752,2	MCF-7	breast:
10	chr2:21418535..21420316-chr2:21426531..21428200,2	K562	blood:
11	chr2:21418535..21420316-chr2:21426531..21428200,2	K562	blood:
12	chr2:21321831..21323587-chr2:21325099..21327379,2	K562	blood:
13	chr2:21265425..21266383-chr2:21340846..21341842,5	MCF-7	breast:
14	chr2:21265474..21266321-chr2:21340848..21341823,6	K562	blood:
15	chr2:21265398..21266438-chr2:21388039..21388919,4	MCF-7	breast:
16	chr2:20861026..20861895-chr2:21387713..21388571,3	MCF-7	breast:
17	chr2:21259349..21261938-chr2:21262179..21264854,2	K562	blood:
18	chr2:21265408..21266174-chr2:21276468..21277419,3	K562	blood:
19	chr2:21363957..21366730-chr2:21369571..21371543,2	K562	blood:
20	chr2:21259349..21261938-chr2:21262179..21264854,2	K562	blood:
21	chr2:21376708..21379043-chr2:21381243..21383355,2	K562	blood:
22	chr2:21444986..21447643-chr2:21451279..21452884,2	K562	blood:
23	chr2:21294169..21296510-chr2:21313708..21315944,2	MCF-7	breast:
24	chr2:20981301..20981947-chr2:21340955..21341754,2	MCF-7	breast:
25	chr2:21265670..21266461-chr2:21292907..21293760,2	MCF-7	breast:
26	chr2:21265514..21266581-chr2:21387973..21389226,4	MCF-7	breast:
27	chr2:21265434..21266455-chr2:21539160..21540754,7	K562	blood:
28	chr2:21398404..21399245-chr2:21539754..21540781,4	MCF-7	breast:
29	chr2:21348742..21351585-chr2:21351799..21353530,2	MCF-7	breast:
30	chr2:20852272..20854551-chr2:21285830..21287375,2	MCF-7	breast:
31	chr2:21274973..21277054-chr2:21293701..21295645,2	MCF-7	breast:
32	chr2:20841906..20842864-chr2:21340988..21341488,2	K562	blood:
33	chr2:21265425..21266383-chr2:21340846..21341842,5	MCF-7	breast:
34	chr2:20881708..20882267-chr2:21250302..21250996,2	MCF-7	breast:
35	chr2:21265408..21266174-chr2:21276468..21277419,3	K562	blood:
36	chr2:21265338..21266452-chr2:21340549..21342036,14	MCF-7	breast:
37	chr2:21265514..21266581-chr2:21387973..21389226,4	MCF-7	breast:
38	chr2:21398441..21399385-chr2:21539677..21540629,3	MCF-7	breast:
39	chr2:21363957..21366730-chr2:21369571..21371543,2	K562	blood:
40	chr2:21020725..21022503-chr2:21444417..21447318,2	K562	blood:
41	chr2:21444986..21447643-chr2:21451279..21452884,2	K562	blood:
42	chr2:21273537..21275484-chr2:21337666..21339362,2	MCF-7	breast:
43	chr2:21265670..21266461-chr2:21292907..21293760,2	MCF-7	breast:
44	chr2:21283850..21285927-chr2:21290254..21292144,2	MCF-7	breast:
45	chr2:21265241..21266102-chr2:21539688..21540633,3	MCF-7	breast:
46	chr2:21454261..21455870-chr2:21482924..21484730,2	K562	blood:
47	chr2:21283850..21285927-chr2:21290254..21292144,2	MCF-7	breast:
48	chr2:21444080..21447303-chr2:21449844..21452884,4	K562	blood:
49	chr19:28456998..28457870-chr2:21351809..21352309,2	MCF-7	breast:
50	chr2:21265398..21266438-chr2:21388039..21388919,4	MCF-7	breast:

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC010872.2.1-2	chr2:21267790-21268484	NONHSAT069474
2	lnc-AC010872.2.1-1	chr2:21309876-21309901	NONHSAT069479
3	lnc-AC010872.2.1-6	chr2:21297552-21297671	NONHSAT069477
4	lnc-APOB-3	chr2:21321870-21322019	XLOC_002013
5	lnc-AC010872.2.1-2	chr2:21267101-21267138	NONHSAT069474
6	lnc-AC010872.2.1-1	chr2:21316445-21317719	NONHSAT069479
7	lnc-APOB-3	chr2:21320551-21320771	XLOC_002013
8	lnc-AC010872.2.1-8	chr2:21394037-21394190	NONHSAT069484
9	lnc-AC010872.2.1-2	chr2:21267790-21268881	XLOC_001386
10	lnc-AC010872.2.1-4	chr2:21444057-21444166	ENSG00000233005
11	lnc-AC010872.2.1-6	chr2:21297562-21297671	NONHSAT069478
12	lnc-APOB-2	chr2:21316935-21317683	XLOC_002012
13	lnc-AC010872.2.1-1	chr2:21319248-21319427	XLOC_001387
14	lnc-APOB-11	chr2:21421390-21421768	NONHSAT069485
15	lnc-APOB-10	chr2:21385443-21385646	NONHSAT069483
16	lnc-APOB-10	chr2:21376215-21376270	NONHSAT069483
17	lnc-AC010872.2.1-1	chr2:21319126-21319151	XLOC_001387
18	lnc-AC010872.2.1-8	chr2:21396780-21396871	NONHSAT069484
19	lnc-AC010872.2.1-6	chr2:21340070-21340463	NONHSAT069478
20	lnc-APOB-2	chr2:21319226-21319427	XLOC_002012
21	lnc-AC010872.2.1-4	chr2:21444047-21444166	ENSG00000233005
22	lnc-APOB-2	chr2:21316951-21317683	NONHSAT069480
23	lnc-APOB-2	chr2:21319226-21319473	NONHSAT069480
24	lnc-AC010872.2.1-1	chr2:21318785-21319683	NONHSAT069479
25	lnc-AC010872.2.1-2	chr2:21267101-21267489	XLOC_001386

No data

Variant related genes	Relation type
APOB	TF binding region
TDRD15	TF binding region
ENSG00000233005	TF binding region
ENSG00000271629	TF binding region
APOB	CpG island
TDRD15	CpG island
ENSG00000233005	CpG island
ENSG00000271629	CpG island
ENSG00000084674	chromatin interactions
ENSG00000231204	chromatin interactions
CYP26B1	miRNA target sites
LRIG3	miRNA target sites
CYP24A1	miRNA target sites

Extended variants
information (count: 6183 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6183 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs679899	chr2:21250914-21250915	Strong transcription Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549861013	chr2:21250969-21250970	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569621676	chr2:21250970-21250971	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374000835	chr2:21250984-21250985	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535509756	chr2:21251000-21251001	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184298864	chr2:21251022-21251023	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570877	chr2:21251040-21251041	Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs570075101	chr2:21251041-21251042	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557583766	chr2:21251047-21251048	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs577783818	chr2:21251072-21251073	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376935548	chr2:21251173-21251174	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs370598632	chr2:21251185-21251186	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199646491	chr2:21251199-21251200	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76135035	chr2:21251225-21251226	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138309196	chr2:21251228-21251229	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543224958	chr2:21251234-21251235	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139864087	chr2:21251243-21251244	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs140101603	chr2:21251275-21251276	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149835778	chr2:21251366-21251367	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12714214	chr2:21251367-21251368	Strong transcription Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs145862664	chr2:21251380-21251381	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139176904	chr2:21251388-21251389	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs555178793	chr2:21251394-21251395	Strong transcription Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs367788462	chr2:21251402-21251403	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373251374	chr2:21251412-21251413	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs187405118	chr2:21251414-21251415	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564732342	chr2:21251424-21251425	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371735411	chr2:21251465-21251466	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148994238	chr2:21251488-21251489	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570213681	chr2:21251507-21251508	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12714215	chr2:21251528-21251529	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs12714216	chr2:21251530-21251531	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548663377	chr2:21251531-21251532	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112749774	chr2:21251575-21251576	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574781032	chr2:21251587-21251588	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565339723	chr2:21251592-21251593	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372121495	chr2:21251603-21251604	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376754670	chr2:21251676-21251677	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571480825	chr2:21251679-21251680	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537417858	chr2:21251685-21251686	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192256910	chr2:21251712-21251713	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10208524	chr2:21251713-21251714	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs573778355	chr2:21251775-21251776	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12714221	chr2:21251800-21251801	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs555859240	chr2:21251818-21251819	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs532376840	chr2:21251820-21251821	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12714222	chr2:21251851-21251852	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545854945	chr2:21251863-21251864	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184739263	chr2:21251901-21251902	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189514419	chr2:21251903-21251904	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Medulloblastoma	22160402	CNVD
Schizophrenia	22118685	CNVD
Epilepsy	22118685	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	17908972	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	18765546	CNVD
Neuroblastoma	18281664	CNVD
Neuroblastoma	17289879	CNVD
Neuroblastoma	19738985	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	21364760	CNVD
Obesity	20950786	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:786 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21234800-21262200	Weak transcription	Ovary	ovary
2	chr2:21235000-21261800	Strong transcription	Fetal Intestine Large	intestine
3	chr2:21242800-21251000	Weak transcription	Left Ventricle	heart
4	chr2:21247000-21252600	Strong transcription	Fetal Intestine Small	intestine
5	chr2:21247600-21254000	Genic enhancers	HepG2	liver
6	chr2:21248600-21252600	Strong transcription	Duodenum Mucosa	Duodenum
7	chr2:21249800-21251000	Strong transcription	Liver	Liver
8	chr2:21250600-21251400	Strong transcription	Adipose Nuclei	Adipose
9	chr2:21250600-21252800	Strong transcription	Aorta	Aorta
10	chr2:21251000-21251400	Genic enhancers	Liver	Liver
11	chr2:21251000-21252000	Strong transcription	Left Ventricle	heart
12	chr2:21251400-21252400	Strong transcription	Liver	Liver
13	chr2:21251400-21254000	Weak transcription	Adipose Nuclei	Adipose
14	chr2:21252000-21256200	Weak transcription	Left Ventricle	heart
15	chr2:21252400-21254200	Genic enhancers	Liver	Liver
16	chr2:21252600-21254400	Weak transcription	Fetal Intestine Small	intestine
17	chr2:21252600-21255200	Weak transcription	Duodenum Mucosa	Duodenum
18	chr2:21252800-21255200	Weak transcription	Aorta	Aorta
19	chr2:21254000-21254400	Transcr. at gene 5' and 3'	HepG2	liver
20	chr2:21254000-21256200	Strong transcription	Adipose Nuclei	Adipose
21	chr2:21254200-21255200	Strong transcription	Liver	Liver
22	chr2:21254400-21255000	Genic enhancers	HepG2	liver
23	chr2:21254400-21262000	Strong transcription	Fetal Intestine Small	intestine
24	chr2:21255000-21255400	Transcr. at gene 5' and 3'	HepG2	liver
25	chr2:21255200-21255400	Enhancers	Right Atrium	heart
26	chr2:21255200-21256400	Strong transcription	Aorta	Aorta
27	chr2:21255200-21258200	Genic enhancers	Liver	Liver
28	chr2:21255200-21260600	Strong transcription	Duodenum Mucosa	Duodenum
29	chr2:21255400-21256600	Genic enhancers	HepG2	liver
30	chr2:21255400-21262800	Weak transcription	Right Atrium	heart
31	chr2:21256200-21257200	Strong transcription	Left Ventricle	heart
32	chr2:21256200-21261400	Weak transcription	Adipose Nuclei	Adipose
33	chr2:21256400-21258400	Weak transcription	Aorta	Aorta
34	chr2:21256600-21266400	Transcr. at gene 5' and 3'	HepG2	liver
35	chr2:21257200-21260600	Weak transcription	Left Ventricle	heart
36	chr2:21258200-21258600	Transcr. at gene 5' and 3'	Liver	Liver
37	chr2:21258400-21259800	Genic enhancers	Aorta	Aorta
38	chr2:21258600-21261800	Genic enhancers	Liver	Liver
39	chr2:21259200-21259400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr2:21259400-21259800	Enhancers	Lung	lung
41	chr2:21259800-21260200	Weak transcription	Lung	lung
42	chr2:21259800-21262800	Weak transcription	Aorta	Aorta
43	chr2:21260200-21260400	Enhancers	Lung	lung
44	chr2:21260200-21260800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr2:21260400-21266000	Weak transcription	Lung	lung
46	chr2:21260600-21260800	Enhancers	Pancreas	Pancrea
47	chr2:21260600-21261600	Enhancers	Left Ventricle	heart
48	chr2:21260600-21261600	Enhancers	Right Ventricle	heart
49	chr2:21260600-21261600	Enhancers	Stomach Smooth Muscle	stomach
50	chr2:21260600-21262200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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