Variant report

Variant	nsv3340
Chromosome Location	chr20:25160137-25190540
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:946)
CpG islands
(count:1160)
Chromatin interactive
region (count:55)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:946 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25176013-25176425	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:25159569-25160219	HepG2	liver:	n/a	n/a
3	ATF2	chr20:25176192-25176491	GM12878	blood:	n/a	n/a
4	ATF3	chr20:25176044-25176392	K562	blood:	n/a	chr20:25176044-25176053
5	ATF3	chr20:25176095-25176474	GM12878	blood:	n/a	n/a
6	ATF3	chr20:25176202-25176391	GM12878	blood:	n/a	n/a
7	ATF3	chr20:25176091-25176405	K562	blood:	n/a	n/a
8	ATF3	chr20:25175972-25176540	A549	lung:	n/a	chr20:25176044-25176053
9	ATF3	chr20:25175898-25176470	A549	lung:	n/a	chr20:25176044-25176053
10	ATF3	chr20:25175968-25176619	HepG2	liver:	n/a	chr20:25176044-25176053
11	BACH1	chr20:25175999-25177550	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr20:25184569-25184887	GM12878	blood:	n/a	n/a
13	BATF	chr20:25184490-25184951	GM12878	blood:	n/a	n/a
14	BCL3	chr20:25175885-25176526	A549	lung:	n/a	chr20:25176345-25176354 chr20:25176313-25176326 chr20:25176043-25176052 chr20:25176040-25176049
15	BHLHE40	chr20:25184777-25184885	GM12878	blood:	n/a	n/a
16	BHLHE40	chr20:25175995-25176922	GM12878	blood:	n/a	n/a
17	BHLHE40	chr20:25175961-25177007	HepG2	liver:	n/a	n/a
18	BHLHE40	chr20:25183968-25184085	GM12878	blood:	n/a	n/a
19	BHLHE40	chr20:25176032-25176867	K562	blood:	n/a	n/a
20	BHLHE40	chr20:25176219-25176411	HepG2	liver:	n/a	n/a
21	BRCA1	chr20:25178624-25178632	HepG2	liver:	n/a	n/a
22	BRCA1	chr20:25176010-25176459	HepG2	liver:	n/a	n/a
23	BRCA1	chr20:25176897-25177213	HepG2	liver:	n/a	n/a
24	CBX3	chr20:25173713-25174013	K562	blood:	n/a	n/a
25	CCNT2	chr20:25176096-25176737	K562	blood:	n/a	chr20:25176265-25176274
26	CEBPB	chr20:25176206-25176427	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr20:25165149-25165346	A549	lung:	n/a	n/a
28	CEBPB	chr20:25159426-25160198	A549	lung:	n/a	n/a
29	CEBPB	chr20:25159323-25160257	HCT-116	colon:	n/a	n/a
30	CEBPB	chr20:25159322-25160261	A549	lung:	n/a	n/a
31	CEBPB	chr20:25159390-25160172	HCT-116	colon:	n/a	n/a
32	CEBPB	chr20:25165049-25165353	HepG2	liver:	n/a	n/a
33	CEBPB	chr20:25176158-25176388	HepG2	liver:	n/a	n/a
34	CEBPB	chr20:25178311-25178544	HepG2	liver:	n/a	n/a
35	CEBPB	chr20:25175816-25176562	A549	lung:	n/a	n/a
36	CEBPB	chr20:25165142-25165235	IMR90	lung:	n/a	n/a
37	CEBPB	chr20:25175966-25176457	K562	blood:	n/a	n/a
38	CEBPB	chr20:25176161-25176482	HepG2	liver:	n/a	n/a
39	CEBPD	chr20:25176038-25176530	HepG2	liver:	n/a	n/a
40	CEBPD	chr20:25175921-25176790	HepG2	liver:	n/a	n/a
41	CHD1	chr20:25177863-25178019	GM12878	blood:	n/a	n/a
42	CHD1	chr20:25175990-25176614	GM12878	blood:	n/a	n/a
43	CHD1	chr20:25175823-25177112	IMR90	lung:	n/a	n/a
44	CHD2	chr20:25175965-25176641	GM12878	blood:	n/a	n/a
45	CHD2	chr20:25184764-25184766	GM12878	blood:	n/a	n/a
46	CHD2	chr20:25176167-25176408	K562	blood:	n/a	n/a
47	CHD2	chr20:25176007-25176448	HepG2	liver:	n/a	n/a
48	CHD2	chr20:25176777-25176868	HepG2	liver:	n/a	n/a
49	CHD2	chr20:25176202-25176374	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr20:25176087-25176745	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25176806-25176856	HUVEC	blood vessel:	n/a
2	chr20:25176806-25176856	HUVEC	blood vessel:	n/a
3	chr20:25176178-25176228	Jurkat	blood:	n/a
4	chr20:25176907-25176957	NH-A	brain:	n/a
5	chr20:25180223-25180273	SKMC	muscle:	n/a
6	chr20:25176220-25176270	HRE	kidney:	n/a
7	chr20:25176907-25176957	HCT-116	colon:	n/a
8	chr20:25176127-25176177	NB4	blood:	n/a
9	chr20:25176379-25176429	HRE	kidney:	n/a
10	chr20:25177027-25177077	GM12891	blood:	n/a
11	chr20:25176157-25176207	HUVEC	blood vessel:	n/a
12	chr20:25176127-25176177	NH-A	brain:	n/a
13	chr20:25180223-25180273	HPAEpiC	pulmonary alveolar:	n/a
14	chr20:25176806-25176856	NB4	blood:	n/a
15	chr20:25177340-25177390	MCF-7	breast:	n/a
16	chr20:25174319-25174369	AG04449	skin:	fetal
17	chr20:25177389-25177439	AG09309	skin:	n/a
18	chr20:25176907-25176957	HL-60	blood:	n/a
19	chr20:25176214-25176264	AG04449	skin:	fetal
20	chr20:25176214-25176264	HMEC	breast:	n/a
21	chr20:25176806-25176856	HMEC	breast:	n/a
22	chr20:25176146-25176196	GM12891	blood:	n/a
23	chr20:25172755-25172805	Hela-S3	cervix:	n/a
24	chr20:25176220-25176270	GM19239	blood:	n/a
25	chr20:25177340-25177390	H1-hESC	embryonic stem cell:	embryo
26	chr20:25177389-25177439	AG09319	gingival:	n/a
27	chr20:25176806-25176856	SAEC	small airway:	n/a
28	chr20:25176220-25176270	HL-60	blood:	n/a
29	chr20:25176407-25176457	H1-hESC	embryonic stem cell:	embryo
30	chr20:25176127-25176177	SK-N-SH_RA	brain:	n/a
31	chr20:25176806-25176856	SK-N-SH_RA	brain:	n/a
32	chr20:25177027-25177077	HNPCEpiC	eye:	n/a
33	chr20:25174319-25174369	NHBE	bronchial:	n/a
34	chr20:25175138-25175188	LNCaP	prostate:	n/a
35	chr20:25176157-25176207	NB4	blood:	n/a
36	chr20:25175138-25175188	SK-N-SH_RA	brain:	n/a
37	chr20:25180223-25180273	Jurkat	blood:	n/a
38	chr20:25176907-25176957	HIPEpiC	eye:	n/a
39	chr20:25176437-25176487	PrEC	prostate:	n/a
40	chr20:25176157-25176207	NH-A	brain:	n/a
41	chr20:25176178-25176228	HCT-116	colon:	n/a
42	chr20:25176806-25176856	SK-N-MC	brain:	n/a
43	chr20:25176146-25176196	HRE	kidney:	n/a
44	chr20:25175138-25175188	AoSMC	blood vessel:	n/a
45	chr20:25174319-25174369	GM12878	blood:	n/a
46	chr20:25180223-25180273	NB4	blood:	n/a
47	chr20:25177340-25177390	NHDF-neo	bronchial:	n/a
48	chr20:25176379-25176429	Jurkat	blood:	n/a
49	chr20:25172755-25172805	NHBE	bronchial:	n/a
50	chr20:25172755-25172805	NHDF-neo	bronchial:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:25188229..25190332-chr20:25200782..25202362,2	K562	blood:
2	chr20:25167222..25169276-chr20:25170020..25172814,2	MCF-7	breast:
3	chr20:24972059..24974449-chr20:25176101..25177683,2	MCF-7	breast:
4	chr20:25177563..25180784-chr20:25185797..25188604,4	MCF-7	breast:
5	chr20:25188229..25190723-chr20:25206277..25208127,2	MCF-7	breast:
6	chr20:25176534..25179250-chr20:25179296..25181376,2	MCF-7	breast:
7	chr20:25175979..25179968-chr20:25200206..25203711,4	MCF-7	breast:
8	chr20:25183250..25185573-chr20:25216058..25218999,2	K562	blood:
9	chr20:25175724..25177464-chr6:157799912..157802892,2	MCF-7	breast:
10	chr20:24975144..24976098-chr20:25159512..25160449,4	MCF-7	breast:
11	chr20:25183254..25185690-chr20:25227240..25230153,3	MCF-7	breast:
12	chr20:25119381..25120481-chr20:25159221..25160482,27	MCF-7	breast:
13	chr20:25174010..25179528-chr20:25225802..25231331,13	MCF-7	breast:
14	chr20:25185632..25187734-chr20:25204064..25206266,3	MCF-7	breast:
15	chr20:24974051..24974784-chr20:25159865..25160396,2	MCF-7	breast:
16	chr20:25189131..25190922-chr20:25228814..25231748,2	MCF-7	breast:
17	chr20:25182714..25185445-chr20:25216908..25218844,2	MCF-7	breast:
18	chr20:24972851..24974876-chr20:25158706..25161889,3	MCF-7	breast:
19	chr20:24972385..24977147-chr20:25157333..25161116,4	MCF-7	breast:
20	chr20:25140270..25141974-chr20:25158745..25161206,2	MCF-7	breast:
21	chr20:25175993..25177808-chr20:25179457..25181859,3	K562	blood:
22	chr20:25176141..25177768-chr20:25206257..25208862,2	MCF-7	breast:
23	chr20:25166380..25169258-chr20:25173266..25174773,2	K562	blood:
24	chr20:25167996..25170885-chr20:25176013..25177980,3	K562	blood:
25	chr20:24971936..24974944-chr20:25175039..25178381,3	MCF-7	breast:
26	chr20:25189324..25193219-chr20:25201165..25204097,4	MCF-7	breast:
27	chr20:25184070..25187780-chr20:25226267..25231211,5	MCF-7	breast:
28	chr20:25176534..25179250-chr20:25179296..25181376,2	MCF-7	breast:
29	chr20:25166380..25169258-chr20:25173266..25174773,2	K562	blood:
30	chr20:25178198..25180990-chr20:25188876..25192724,4	MCF-7	breast:
31	chr20:25183731..25186136-chr20:25238166..25239977,2	MCF-7	breast:
32	chr20:24980779..24981584-chr20:25159554..25160358,4	MCF-7	breast:
33	chr20:25159426..25161850-chr20:25175828..25177766,2	K562	blood:
34	chr20:25176590..25179411-chr20:25196913..25199010,2	MCF-7	breast:
35	chr20:25176013..25179017-chr20:25181894..25184717,4	K562	blood:
36	chr20:25046140..25046670-chr20:25159575..25160213,2	MCF-7	breast:
37	chr20:25174902..25179249-chr20:25225017..25231959,9	MCF-7	breast:
38	chr20:25062967..25063590-chr20:25159722..25160459,2	MCF-7	breast:
39	chr10:103577667..103578508-chr20:25176215..25176933,2	NB4	blood:
40	chr20:25173813..25179807-chr20:25203379..25207002,9	MCF-7	breast:
41	chr20:25185473..25187365-chr20:25194994..25197584,2	K562	blood:
42	chr20:25056370..25059250-chr20:25174569..25177571,3	MCF-7	breast:
43	chr20:25180225..25182029-chr20:25219353..25221557,2	MCF-7	breast:
44	chr20:25046117..25046996-chr20:25159492..25160465,5	MCF-7	breast:
45	chr20:25171254..25173860-chr20:25228240..25230126,2	MCF-7	breast:
46	chr20:25174588..25176232-chr20:25268673..25270382,2	MCF-7	breast:
47	chr20:25167222..25169276-chr20:25170020..25172814,2	MCF-7	breast:
48	chr20:25177243..25179011-chr20:25246862..25248615,2	K562	blood:
49	chr20:25180384..25184358-chr20:25185233..25189796,6	K562	blood:
50	chr20:25178198..25180990-chr20:25188876..25192724,4	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABHD12-4	chr20:25168489-25168583	NR_109994
2	lnc-ABHD12-4	chr20:25167178-25167335	NR_109994
3	lnc-ABHD12-4	chr20:25167533-25167615	NONHSAT079137
4	lnc-ABHD12-4	chr20:25177259-25177508	NONHSAT079137
5	lnc-ABHD12-4	chr20:25165308-25166796	NR_109994
6	lnc-ABHD12-4	chr20:25170854-25170938	NR_109994
7	lnc-ABHD12-4	chr20:25167178-25167335	NONHSAT079137
8	lnc-ABHD12-4	chr20:25165310-25166796	NONHSAT079137
9	lnc-ABHD12-4	chr20:25177259-25177528	NR_109994
10	lnc-ABHD12-4	chr20:25170854-25170938	NONHSAT079137
11	lnc-ABHD12-4	chr20:25167533-25167615	NR_109994
12	lnc-ABHD12-4	chr20:25168489-25168583	NONHSAT079137

No data

Variant related genes	Relation type
ENSG00000202414	TF binding region
ENTPD6	TF binding region
ENSG00000202414	CpG island
ENTPD6	CpG island
ENSG00000198408	chromatin interactions
ENSG00000202414	chromatin interactions
ENSG00000197586	chromatin interactions
ENSG00000100987	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000175048	chromatin interactions
ENSG00000101474	chromatin interactions
ENSG00000268302	chromatin interactions
ENSG00000100997	chromatin interactions

Extended variants
information (count: 1151 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1151 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75816152	chr20:25160185-25160186	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs80274994	chr20:25160239-25160240	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs534916666	chr20:25160251-25160252	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs138195695	chr20:25160252-25160253	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs577687305	chr20:25160271-25160272	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs183533838	chr20:25160308-25160309	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs563034873	chr20:25160309-25160310	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs201898909	chr20:25160325-25160326	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs6138530	chr20:25160341-25160342	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs542167538	chr20:25160363-25160364	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs143688149	chr20:25160389-25160390	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs57359365	chr20:25160510-25160511	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551306540	chr20:25160535-25160536	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs531623954	chr20:25160557-25160558	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs565114223	chr20:25160569-25160570	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs150615463	chr20:25160570-25160571	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550340499	chr20:25160572-25160573	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs570162080	chr20:25160580-25160581	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs139676249	chr20:25160613-25160614	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs573139265	chr20:25160614-25160615	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs149380694	chr20:25160624-25160625	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs551787072	chr20:25160636-25160637	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs535299333	chr20:25160643-25160644	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs373969281	chr20:25160652-25160653	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs6076323	chr20:25160671-25160672	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558151134	chr20:25160693-25160694	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs578154084	chr20:25160731-25160732	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs2038182	chr20:25160760-25160761	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs189342205	chr20:25160761-25160762	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573360117	chr20:25160806-25160807	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs566849684	chr20:25160809-25160810	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs181758782	chr20:25160826-25160827	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs58134777	chr20:25160855-25160856	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs572726508	chr20:25160869-25160870	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs116571861	chr20:25160923-25160924	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs565027351	chr20:25160947-25160948	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs139732366	chr20:25160973-25160974	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs77932872	chr20:25160974-25160975	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs370316754	chr20:25160979-25160980	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs6050406	chr20:25161020-25161021	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs186016045	chr20:25161025-25161026	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189968029	chr20:25161040-25161041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs6050407	chr20:25161060-25161061	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs566093159	chr20:25161065-25161066	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs71312679	chr20:25161090-25161091	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs398039876	chr20:25161100-25161101	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs62212112	chr20:25161102-25161103	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs534699947	chr20:25161109-25161110	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs552098526	chr20:25161119-25161120	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs369271414	chr20:25161120-25161121	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25155800-25161600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:25157000-25160200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr20:25158000-25160600	Enhancers	NHEK	skin
4	chr20:25158000-25160800	Enhancers	HMEC	breast
5	chr20:25158200-25160200	Enhancers	Hela-S3	cervix
6	chr20:25158200-25160400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:25158200-25160400	Enhancers	NH-A	brain
8	chr20:25158200-25160400	Enhancers	Osteobl	bone
9	chr20:25158200-25160600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr20:25158200-25160800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr20:25158400-25160200	Enhancers	Colon Smooth Muscle	Colon
12	chr20:25158400-25160400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr20:25158600-25160400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr20:25158600-25160600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr20:25158600-25160600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr20:25158600-25160800	Enhancers	NHLF	lung
17	chr20:25158800-25160600	Enhancers	NHDF-Ad	bronchial
18	chr20:25158800-25160800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr20:25158800-25160800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr20:25159200-25160600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr20:25159200-25160800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr20:25159400-25160200	Enhancers	Adipose Nuclei	Adipose
23	chr20:25159400-25160200	Enhancers	Fetal Heart	heart
24	chr20:25159400-25160200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr20:25159400-25160800	Enhancers	HepG2	liver
26	chr20:25159600-25160400	Weak transcription	Esophagus	oesophagus
27	chr20:25159600-25160400	Weak transcription	Lung	lung
28	chr20:25159600-25160800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr20:25159600-25162000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr20:25159800-25160200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr20:25159800-25160400	Weak transcription	HSMM	muscle
32	chr20:25159800-25160800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr20:25160000-25160200	Enhancers	A549	lung
34	chr20:25160200-25160600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr20:25160400-25160600	Enhancers	Esophagus	oesophagus
36	chr20:25160400-25160600	Enhancers	Lung	lung
37	chr20:25160400-25160600	Enhancers	HSMM	muscle
38	chr20:25160400-25163000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr20:25163000-25163200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr20:25164800-25168000	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr20:25166800-25169400	Enhancers	Thymus	Thymus
42	chr20:25167400-25169400	Enhancers	Fetal Heart	heart
43	chr20:25167600-25169400	Enhancers	Dnd41	blood
44	chr20:25167800-25169400	Enhancers	Lung	lung
45	chr20:25167800-25169400	Enhancers	Ovary	ovary
46	chr20:25167800-25169600	Enhancers	Fetal Thymus	thymus
47	chr20:25168000-25168200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr20:25168000-25168600	Enhancers	Placenta	Placenta
49	chr20:25168200-25168600	Enhancers	Left Ventricle	heart
50	chr20:25168200-25169400	Enhancers	Right Atrium	heart

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