Variant report

Variant	nsv1060148
Chromosome Location	chr16:70896033-71039315
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2116)
CpG islands
(count:671)
Chromatin interactive
region (count:185)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2116 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70909125-70909126	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:70898638-70899114	K562	blood:	n/a	n/a
3	ARID3A	chr16:71021049-71021536	K562	blood:	n/a	n/a
4	ARID3A	chr16:70910409-70910772	K562	blood:	n/a	n/a
5	ARID3A	chr16:70961655-70961897	K562	blood:	n/a	n/a
6	ARID3A	chr16:70928843-70929353	K562	blood:	n/a	n/a
7	ARID3A	chr16:70956273-70956284	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:70971786-70971832	HepG2	liver:	n/a	n/a
9	ATF1	chr16:70990674-70991056	K562	blood:	n/a	n/a
10	ATF1	chr16:70919761-70920048	K562	blood:	n/a	n/a
11	ATF1	chr16:70921358-70921430	K562	blood:	n/a	n/a
12	ATF1	chr16:70980043-70980287	K562	blood:	n/a	n/a
13	ATF1	chr16:70898619-70899190	K562	blood:	n/a	n/a
14	ATF1	chr16:70992165-70992287	K562	blood:	n/a	n/a
15	ATF1	chr16:71021180-71021685	K562	blood:	n/a	n/a
16	ATF1	chr16:70987738-70988064	K562	blood:	n/a	n/a
17	ATF1	chr16:70977109-70977159	K562	blood:	n/a	n/a
18	ATF1	chr16:70928955-70929581	K562	blood:	n/a	n/a
19	ATF1	chr16:70903146-70903233	K562	blood:	n/a	n/a
20	ATF2	chr16:70987603-70988175	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr16:71021188-71021575	K562	blood:	n/a	n/a
22	ATF3	chr16:70898546-70898968	K562	blood:	n/a	n/a
23	ATF3	chr16:70914323-70914530	K562	blood:	n/a	n/a
24	BACH1	chr16:70969729-70969731	K562	blood:	n/a	n/a
25	BACH1	chr16:70937028-70937453	K562	blood:	n/a	n/a
26	BACH1	chr16:71020996-71021702	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr16:71021074-71021564	K562	blood:	n/a	n/a
28	BACH1	chr16:70895746-70896281	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr16:70896722-70896732	K562	blood:	n/a	n/a
30	BACH1	chr16:70898321-70899349	K562	blood:	n/a	n/a
31	BACH1	chr16:70897093-70897112	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr16:70908751-70908815	K562	blood:	n/a	n/a
33	BACH1	chr16:70916104-70916516	H1-hESC	embryonic stem cell:	n/a	n/a
34	BATF	chr16:70963263-70963562	GM12878	blood:	n/a	n/a
35	BATF	chr16:70898626-70898920	GM12878	blood:	n/a	chr16:70898733-70898744
36	BCL3	chr16:70983386-70983627	GM12878	blood:	n/a	n/a
37	BCL3	chr16:70973830-70974232	GM12878	blood:	n/a	chr16:70974079-70974088
38	BCL3	chr16:70976321-70976732	GM12878	blood:	n/a	n/a
39	BCL3	chr16:70976273-70976645	GM12878	blood:	n/a	n/a
40	BCL3	chr16:70973768-70974260	GM12878	blood:	n/a	chr16:70974079-70974088
41	BHLHE40	chr16:70997563-70997637	K562	blood:	n/a	n/a
42	BHLHE40	chr16:70956190-70956375	HepG2	liver:	n/a	n/a
43	BHLHE40	chr16:70899625-70900244	K562	blood:	n/a	n/a
44	BHLHE40	chr16:71002389-71002555	K562	blood:	n/a	n/a
45	BHLHE40	chr16:70934006-70934034	A549	lung:	n/a	n/a
46	BHLHE40	chr16:70898649-70899144	K562	blood:	n/a	n/a
47	BHLHE40	chr16:71019095-71019184	GM12878	blood:	n/a	n/a
48	BHLHE40	chr16:70976497-70976604	K562	blood:	n/a	n/a
49	BHLHE40	chr16:70896798-70896822	K562	blood:	n/a	n/a
50	BHLHE40	chr16:70928952-70929241	K562	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70955865-70955915	GM06990	blood:	n/a
2	chr16:71008454-71008504	BE2_C	brain:	n/a
3	chr16:71034828-71034878	Jurkat	blood:	n/a
4	chr16:70955879-70955929	AG09319	gingival:	n/a
5	chr16:71008732-71008782	Hepatocyte	liver:	n/a
6	chr16:71009778-71009828	AG09319	gingival:	n/a
7	chr16:70955879-70955929	GM12892	blood:	n/a
8	chr16:71011407-71011457	CMK	blood:	n/a
9	chr16:70955879-70955929	SK-N-SH_RA	brain:	n/a
10	chr16:71008050-71008100	HCM	heart:	n/a
11	chr16:71008732-71008782	HNPCEpiC	eye:	n/a
12	chr16:71008063-71008113	Hepatocyte	liver:	n/a
13	chr16:71008454-71008504	HRE	kidney:	n/a
14	chr16:71009778-71009828	GM19239	blood:	n/a
15	chr16:70955223-70955273	Caco-2	colon:	n/a
16	chr16:71009778-71009828	SAEC	small airway:	n/a
17	chr16:70955865-70955915	Hepatocyte	liver:	n/a
18	chr16:70955879-70955929	HRPEpiC	eye:	n/a
19	chr16:70967321-70967371	Caco-2	colon:	n/a
20	chr16:71008732-71008782	HCPEpiC	choroid plexus:	n/a
21	chr16:71011407-71011457	LNCaP	prostate:	n/a
22	chr16:71011407-71011457	AG09309	skin:	n/a
23	chr16:70967321-70967371	BJ	skin:	n/a
24	chr16:71008732-71008782	RPTEC	kidney:	n/a
25	chr16:70955865-70955915	SK-N-MC	brain:	n/a
26	chr16:71034828-71034878	HAEpiC	amniotic membrane:	n/a
27	chr16:71009778-71009828	HCM	heart:	n/a
28	chr16:70955223-70955273	AG04449	skin:	fetal
29	chr16:71008063-71008113	PrEC	prostate:	n/a
30	chr16:70955879-70955929	A549	lung:	n/a
31	chr16:70955223-70955273	PrEC	prostate:	n/a
32	chr16:70967321-70967371	RPTEC	kidney:	n/a
33	chr16:71034828-71034878	GM06990	blood:	n/a
34	chr16:70955223-70955273	NHBE	bronchial:	n/a
35	chr16:71008063-71008113	SKMC	muscle:	n/a
36	chr16:71009778-71009828	Jurkat	blood:	n/a
37	chr16:71008732-71008782	NH-A	brain:	n/a
38	chr16:71034828-71034878	GM19239	blood:	n/a
39	chr16:71034828-71034878	HUVEC	blood vessel:	n/a
40	chr16:71011407-71011457	HEEpiC	esophagus:	n/a
41	chr16:70955223-70955273	GM12891	blood:	n/a
42	chr16:71008050-71008100	HEEpiC	esophagus:	n/a
43	chr16:70955879-70955929	ECC-1	luminal epithelium:	n/a
44	chr16:71008050-71008100	AG04449	skin:	fetal
45	chr16:70967321-70967371	HRPEpiC	eye:	n/a
46	chr16:71034828-71034878	AG10803	skin:	n/a
47	chr16:71008063-71008113	ProgFib	skin:	n/a
48	chr16:71008732-71008782	HEK293	kidney:	embryo
49	chr16:71008050-71008100	Caco-2	colon:	n/a
50	chr16:71009778-71009828	Hepatocyte	liver:	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr16:70953024..70955680-chr16:71392998..71394958,2	K562	blood:
2	chr16:71016847..71019528-chr16:71019803..71022593,2	K562	blood:
3	chr16:71022061..71023931-chr16:71025665..71027702,2	K562	blood:
4	chr16:71009810..71011533-chr16:71011886..71014440,2	K562	blood:
5	chr1:147726655..147727787-chr16:71033535..71034576,7	MCF-7	breast:
6	chr16:70917671..70920310-chr16:70923586..70926212,2	MCF-7	breast:
7	chr16:71018662..71021748-chr16:71021953..71025067,5	MCF-7	breast:
8	chr16:70988936..70990480-chr16:71001097..71003483,2	MCF-7	breast:
9	chr16:71034368..71036024-chr16:71392122..71393042,7	MCF-7	breast:
10	chr1:146555062..146557093-chr16:71013791..71016169,2	K562	blood:
11	chr16:71001861..71002521-chr4:43883310..43883810,2	MCF-7	breast:
12	chr16:70932562..70934508-chr16:70936479..70938187,2	K562	blood:
13	chr16:71021462..71023279-chr16:71026554..71028512,2	MCF-7	breast:
14	chr16:70984290..70985826-chr16:70990032..70992588,2	K562	blood:
15	chr16:70955002..70955523-chr16:70975950..70976822,2	MCF-7	breast:
16	chr1:146712973..146714848-chr16:71024751..71027232,2	K562	blood:
17	chr16:70901149..70903044-chr16:70910466..70912413,2	K562	blood:
18	chr16:70952046..70954043-chr16:70969052..70971934,2	K562	blood:
19	chr16:70913032..70914937-chr16:70919869..70924288,3	MCF-7	breast:
20	chr16:70917851..70921517-chr16:70926732..70930037,3	MCF-7	breast:
21	chr16:71001935..71005265-chr16:71019285..71021480,3	MCF-7	breast:
22	chr16:70910703..70912215-chr16:70925552..70928004,2	K562	blood:
23	chr16:70989001..70991561-chr16:71001327..71004060,2	K562	blood:
24	chr16:71033432..71034748-chr16:71345163..71346194,8	MCF-7	breast:
25	chr16:70897651..70899575-chr16:70902607..70905321,2	K562	blood:
26	chr16:71018662..71021748-chr16:71021953..71025067,5	MCF-7	breast:
27	chr16:71018902..71020683-chr16:71024263..71026975,2	K562	blood:
28	chr16:70902244..70904397-chr16:70906076..70908681,2	MCF-7	breast:
29	chr1:146553932..146556565-chr16:70965325..70968195,2	K562	blood:
30	chr16:70909112..70910995-chr16:70914381..70916223,2	K562	blood:
31	chr16:70924358..70925904-chr16:70930765..70932621,2	MCF-7	breast:
32	chr16:71026324..71028568-chr16:71031839..71034810,3	K562	blood:
33	chr1:147726394..147729051-chr16:71032449..71035209,3	MCF-7	breast:
34	chr16:70932562..70934508-chr16:70936479..70938187,2	K562	blood:
35	chr16:70973640..70974283-chr16:71001999..71002517,2	MCF-7	breast:
36	chr16:70998731..71000452-chr16:71002285..71005126,2	K562	blood:
37	chr16:70917671..70920310-chr16:70923586..70926212,2	MCF-7	breast:
38	chr16:71004902..71006542-chr16:71008221..71010075,2	MCF-7	breast:
39	chr16:70910703..70912215-chr16:70925552..70928004,2	K562	blood:
40	chr16:70975629..70978329-chr16:70983065..70987137,4	MCF-7	breast:
41	chr16:70921030..70924111-chr16:70924173..70927727,3	K562	blood:
42	chr16:71004948..71009172-chr16:71010296..71014045,4	MCF-7	breast:
43	chr16:70993038..70996024-chr16:70999635..71003501,3	MCF-7	breast:
44	chr16:70961723..70963824-chr16:70975853..70978413,2	K562	blood:
45	chr16:70926767..70929774-chr16:70940233..70943239,3	K562	blood:
46	chr16:70988681..70989466-chr16:71391903..71392654,2	MCF-7	breast:
47	chr1:146551738..146553728-chr16:71003126..71004713,2	K562	blood:
48	chr16:71034869..71035905-chr16:71345260..71345928,3	MCF-7	breast:
49	chr16:70899947..70901471-chr9:136214163..136216466,2	MCF-7	breast:
50	chr1:149221974..149225327-chr16:71033119..71035749,8	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL34-4	chr16:71017348-71020288	ucscGeneNc_uc002fch_1
2	lnc-CALB2-4	chr16:71020753-71021463	ucscGeneNc_uc002fci_1

No data

Variant related genes	Relation type
HYDIN	TF binding region
ENSG00000223316	TF binding region
ENSG00000251700	TF binding region
HYDIN	CpG island
ENSG00000223316	CpG island
ENSG00000251700	CpG island
ENSG00000206737	chromatin interactions
ENSG00000131778	chromatin interactions
ENSG00000260593	chromatin interactions
ENSG00000223316	chromatin interactions
ENSG00000140832	chromatin interactions
ENSG00000148303	chromatin interactions
ENSG00000131781	chromatin interactions
ENSG00000103043	chromatin interactions
ENSG00000148297	chromatin interactions
ENSG00000251700	chromatin interactions
ENSG00000272426	chromatin interactions
ENSG00000172137	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000206611	chromatin interactions
ENSG00000157423	chromatin interactions
ENSG00000167553	chromatin interactions
ENSG00000259798	chromatin interactions
ENSG00000230832	chromatin interactions

Extended variants
information (count: 5513 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5513 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1626593	chr16:70896033-70896034	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs372684458	chr16:70896064-70896065	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376951268	chr16:70896073-70896074	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs547639554	chr16:70896079-70896080	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs199690569	chr16:70896090-70896091	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs533388473	chr16:70896092-70896093	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs1774421	chr16:70896118-70896119	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs7192347	chr16:70896122-70896123	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs552045085	chr16:70896126-70896127	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs12050964	chr16:70896144-70896145	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs374528893	chr16:70896174-70896175	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs570400127	chr16:70896186-70896187	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs537003560	chr16:70896247-70896248	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs555402499	chr16:70896250-70896251	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567336889	chr16:70896251-70896252	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs12102979	chr16:70896353-70896354	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs534701729	chr16:70896354-70896355	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552823454	chr16:70896367-70896368	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577767256	chr16:70896395-70896396	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs528115361	chr16:70896397-70896398	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs576486047	chr16:70896404-70896405	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs7193376	chr16:70896405-70896406	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs9936165	chr16:70896537-70896538	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537590849	chr16:70896546-70896547	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368241287	chr16:70896561-70896562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs577380833	chr16:70896590-70896591	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs12102532	chr16:70896626-70896627	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs544915740	chr16:70896633-70896634	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556796923	chr16:70896722-70896723	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199615121	chr16:70896756-70896757	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs59147110	chr16:70896757-70896758	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541416975	chr16:70896774-70896775	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs1798322	chr16:70896776-70896777	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs575182065	chr16:70896801-70896802	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs1798323	chr16:70896818-70896819	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7199747	chr16:70896876-70896877	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543385054	chr16:70896890-70896891	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370627693	chr16:70896941-70896942	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs74024475	chr16:70896954-70896955	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374063246	chr16:70896956-70896957	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368143224	chr16:70896963-70896964	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1798324	chr16:70896975-70896976	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561761630	chr16:70897005-70897006	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs12149154	chr16:70897033-70897034	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372047627	chr16:70897035-70897036	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs1798325	chr16:70897039-70897040	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7198721	chr16:70897062-70897063	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs201571332	chr16:70897063-70897064	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541492994	chr16:70897080-70897081	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559637459	chr16:70897081-70897082	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	18923524	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:1559 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70880800-70906600	Weak transcription	Fetal Kidney	kidney
2	chr16:70883800-70902200	Weak transcription	Fetal Brain Male	brain
3	chr16:70883800-70904200	Weak transcription	Pancreas	Pancrea
4	chr16:70883800-70906400	Weak transcription	Brain Substantia Nigra	brain
5	chr16:70884400-70898800	Weak transcription	Brain Anterior Caudate	brain
6	chr16:70884400-70898800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr16:70884400-70899800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr16:70884600-70902000	Weak transcription	Brain Angular Gyrus	brain
9	chr16:70893600-70896400	Strong transcription	Fetal Brain Female	brain
10	chr16:70894200-70902400	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr16:70895200-70897000	Strong transcription	Brain Cingulate Gyrus	brain
12	chr16:70895200-70897000	Strong transcription	Brain Hippocampus Middle	brain
13	chr16:70895200-70899000	Weak transcription	Right Atrium	heart
14	chr16:70895400-70897200	Strong transcription	Brain Germinal Matrix	brain
15	chr16:70895800-70896800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr16:70896000-70896600	Weak transcription	Fetal Intestine Small	intestine
17	chr16:70896200-70904200	Weak transcription	Fetal Stomach	stomach
18	chr16:70896400-70899000	Weak transcription	Fetal Brain Female	brain
19	chr16:70896800-70897000	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr16:70896800-70897200	ZNF genes & repeats	Fetal Intestine Small	intestine
21	chr16:70896800-70904400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr16:70897000-70899600	Weak transcription	Brain Hippocampus Middle	brain
23	chr16:70897000-70899800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr16:70897000-70905000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr16:70897200-70899400	Weak transcription	Brain Germinal Matrix	brain
26	chr16:70897200-70904200	Weak transcription	Fetal Intestine Small	intestine
27	chr16:70897400-70906600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr16:70897800-70898600	Enhancers	K562	blood
29	chr16:70898400-70899400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr16:70898400-70899400	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr16:70898400-70899400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr16:70898400-70900000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr16:70898600-70899000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr16:70898600-70899400	Flanking Active TSS	K562	blood
35	chr16:70898600-70899800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr16:70898600-70905400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr16:70898800-70899200	Genic enhancers	Brain Inferior Temporal Lobe	brain
38	chr16:70898800-70899200	Enhancers	NH-A	brain
39	chr16:70898800-70900600	Strong transcription	Brain Anterior Caudate	brain
40	chr16:70899000-70899400	Enhancers	Right Atrium	heart
41	chr16:70899000-70899600	Enhancers	Fetal Heart	heart
42	chr16:70899000-70900000	Strong transcription	Fetal Brain Female	brain
43	chr16:70899200-70900200	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr16:70899400-70901600	Enhancers	K562	blood
45	chr16:70899400-70902800	Weak transcription	Right Atrium	heart
46	chr16:70899400-70904200	Strong transcription	Brain Germinal Matrix	brain
47	chr16:70899600-70900200	Strong transcription	Brain Hippocampus Middle	brain
48	chr16:70899800-70900400	Strong transcription	Brain Cingulate Gyrus	brain
49	chr16:70899800-70900600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr16:70900000-70900200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived

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