Variant report

Variant	nsv528423
Chromosome Location	chr16:47163874-47347780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2211)
CpG islands
(count:1344)
Chromatin interactive
region (count:80)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2211 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:47171892-47172010	K562	blood:	n/a	n/a
2	ARID3A	chr16:47216266-47216628	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:47175602-47176202	K562	blood:	n/a	n/a
4	ARID3A	chr16:47177086-47177176	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:47166225-47166502	K562	blood:	n/a	n/a
6	ARID3A	chr16:47180937-47181312	K562	blood:	n/a	n/a
7	ARID3A	chr16:47196782-47196800	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:47169900-47170121	K562	blood:	n/a	n/a
9	ARID3A	chr16:47175635-47176566	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:47178303-47178477	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:47176783-47176815	K562	blood:	n/a	n/a
12	ARID3A	chr16:47177441-47177480	K562	blood:	n/a	n/a
13	ATF1	chr16:47170098-47170312	K562	blood:	n/a	n/a
14	ATF1	chr16:47197545-47197587	K562	blood:	n/a	n/a
15	ATF1	chr16:47175658-47176054	K562	blood:	n/a	n/a
16	ATF2	chr16:47175531-47176062	GM12878	blood:	n/a	n/a
17	ATF2	chr16:47175571-47176087	GM12878	blood:	n/a	n/a
18	ATF2	chr16:47176142-47176695	GM12878	blood:	n/a	n/a
19	ATF2	chr16:47344576-47345243	GM12878	blood:	n/a	n/a
20	ATF2	chr16:47176226-47176738	GM12878	blood:	n/a	n/a
21	ATF3	chr16:47171874-47172117	K562	blood:	n/a	n/a
22	ATF3	chr16:47177260-47177528	K562	blood:	n/a	n/a
23	BACH1	chr16:47178178-47178180	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr16:47175631-47176087	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr16:47176731-47177908	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr16:47344674-47344855	GM12878	blood:	n/a	n/a
27	BATF	chr16:47175661-47175976	GM12878	blood:	n/a	n/a
28	BATF	chr16:47176399-47176669	GM12878	blood:	n/a	n/a
29	BATF	chr16:47176365-47176663	GM12878	blood:	n/a	n/a
30	BCL11A	chr16:47345681-47345863	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr16:47176367-47176707	GM12878	blood:	n/a	n/a
32	BCL11A	chr16:47344674-47344906	GM12878	blood:	n/a	n/a
33	BCLAF1	chr16:47175480-47176190	GM12878	blood:	n/a	n/a
34	BCLAF1	chr16:47176319-47176951	GM12878	blood:	n/a	n/a
35	BCLAF1	chr16:47177145-47177707	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
36	BCLAF1	chr16:47177271-47177669	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
37	BCLAF1	chr16:47175544-47176047	GM12878	blood:	n/a	n/a
38	BHLHE40	chr16:47176815-47178581	GM12878	blood:	n/a	chr16:47178152-47178168 chr16:47176993-47177009 chr16:47176944-47176960 chr16:47177449-47177465 chr16:47178004-47178020 chr16:47178144-47178160
39	BHLHE40	chr16:47177335-47177732	HepG2	liver:	n/a	chr16:47177449-47177465
40	BHLHE40	chr16:47177272-47178380	K562	blood:	n/a	chr16:47178152-47178168 chr16:47177449-47177465 chr16:47178004-47178020 chr16:47178144-47178160
41	BHLHE40	chr16:47175534-47176602	GM12878	blood:	n/a	n/a
42	BHLHE40	chr16:47175636-47176200	K562	blood:	n/a	n/a
43	BRCA1	chr16:47175537-47175997	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr16:47178424-47178462	GM12878	blood:	n/a	n/a
45	BRCA1	chr16:47178549-47178596	HepG2	liver:	n/a	n/a
46	BRCA1	chr16:47176374-47176777	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr16:47164027-47164063	GM12878	blood:	n/a	n/a
48	CBX3	chr16:47177298-47177690	K562	blood:	n/a	n/a
49	CBX3	chr16:47178273-47178641	K562	blood:	n/a	n/a
50	CBX3	chr16:47186439-47186720	K562	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47177603-47177653	HCPEpiC	choroid plexus:	n/a
2	chr16:47178359-47178409	HEEpiC	esophagus:	n/a
3	chr16:47177603-47177653	HCPEpiC	choroid plexus:	n/a
4	chr16:47178359-47178409	HEEpiC	esophagus:	n/a
5	chr16:47338451-47338501	HMEC	breast:	n/a
6	chr16:47344826-47344876	PANC-1	pancreas:	n/a
7	chr16:47178067-47178117	HCF	heart:	n/a
8	chr16:47178250-47178300	H1-hESC	embryonic stem cell:	embryo
9	chr16:47216988-47217038	CMK	blood:	n/a
10	chr16:47177480-47177530	HPAEpiC	pulmonary alveolar:	n/a
11	chr16:47177603-47177653	PrEC	prostate:	n/a
12	chr16:47164168-47164218	AG04449	skin:	fetal
13	chr16:47175842-47175892	PFSK-1	brain:	n/a
14	chr16:47175936-47175986	HCT-116	colon:	n/a
15	chr16:47216988-47217038	LNCaP	prostate:	n/a
16	chr16:47178070-47178120	HUVEC	blood vessel:	n/a
17	chr16:47178067-47178117	GM19239	blood:	n/a
18	chr16:47175936-47175986	MCF10A-Er-Src	breast:	n/a
19	chr16:47178359-47178409	HIPEpiC	eye:	n/a
20	chr16:47175842-47175892	GM12892	blood:	n/a
21	chr16:47338451-47338501	MCF-7	breast:	n/a
22	chr16:47178070-47178120	Hela-S3	cervix:	n/a
23	chr16:47164168-47164218	HRPEpiC	eye:	n/a
24	chr16:47178357-47178407	Jurkat	blood:	n/a
25	chr16:47175842-47175892	LNCaP	prostate:	n/a
26	chr16:47175912-47175962	HMEC	breast:	n/a
27	chr16:47177480-47177530	SK-N-MC	brain:	n/a
28	chr16:47173093-47173143	BJ	skin:	n/a
29	chr16:47178070-47178120	K562	blood:	n/a
30	chr16:47178067-47178117	AG04450	lung:	fetal
31	chr16:47175936-47175986	AG09319	gingival:	n/a
32	chr16:47164168-47164218	ECC-1	luminal epithelium:	n/a
33	chr16:47344826-47344876	Hepatocyte	liver:	n/a
34	chr16:47178208-47178258	HEEpiC	esophagus:	n/a
35	chr16:47181961-47182011	PANC-1	pancreas:	n/a
36	chr16:47164168-47164218	SK-N-SH	brain:	n/a
37	chr16:47164168-47164218	Hepatocyte	liver:	n/a
38	chr16:47178067-47178117	MCF10A-Er-Src	breast:	n/a
39	chr16:47344826-47344876	NB4	blood:	n/a
40	chr16:47178078-47178128	AG10803	skin:	n/a
41	chr16:47178723-47178773	SK-N-SH	brain:	n/a
42	chr16:47177175-47177225	GM12892	blood:	n/a
43	chr16:47178250-47178300	SK-N-SH_RA	brain:	n/a
44	chr16:47175842-47175892	HRE	kidney:	n/a
45	chr16:47164168-47164218	NT2-D1	testis:	n/a
46	chr16:47178359-47178409	HCM	heart:	n/a
47	chr16:47177175-47177225	GM06990	blood:	n/a
48	chr16:47177603-47177653	HAEpiC	amniotic membrane:	n/a
49	chr16:47214942-47214992	CMK	blood:	n/a
50	chr16:47178208-47178258	Jurkat	blood:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
2	chr16:47203225..47205164-chr16:47207074..47209665,2	K562	blood:
3	chr16:47311388..47314338-chr16:47314364..47316020,2	K562	blood:
4	chr16:47233470..47235990-chr16:47244208..47246996,2	K562	blood:
5	chr16:47177500..47180441-chr16:47180510..47182693,2	K562	blood:
6	chr16:47176370..47177924-chr16:47205584..47208161,2	MCF-7	breast:
7	chr16:47005815..47008447-chr16:47177298..47179122,2	K562	blood:
8	chr16:47337967..47339829-chr16:47344000..47345924,2	K562	blood:
9	chr16:47282712..47286365-chr16:47287931..47291615,3	K562	blood:
10	chr16:47184664..47186977-chr16:47194583..47196786,2	K562	blood:
11	chr16:47290498..47293236-chr16:47492799..47495777,2	MCF-7	breast:
12	chr16:47175296..47177509-chr16:48190040..48191217,7	MCF-7	breast:
13	chr16:47269900..47272616-chr16:47277828..47281996,3	K562	blood:
14	chr16:47298562..47302472-chr16:47302634..47305844,3	K562	blood:
15	chr16:47201430..47205164-chr16:47207074..47210552,4	K562	blood:
16	chr16:47184664..47186977-chr16:47194583..47196786,2	K562	blood:
17	chr16:47175627..47176240-chr16:48199483..48200032,2	MCF-7	breast:
18	chr16:47178986..47180526-chr16:47182698..47184295,2	K562	blood:
19	chr16:47281267..47281944-chr3:111725286..111725871,2	MCF-7	breast:
20	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
21	chr16:47177997..47179501-chr16:47190203..47192834,2	K562	blood:
22	chr16:47071376..47072506-chr16:47175620..47176296,3	K562	blood:
23	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
24	chr16:47176885..47177462-chr16:47479483..47480444,2	K562	blood:
25	chr16:47263413..47265450-chr16:47271876..47274264,2	K562	blood:
26	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
27	chr16:47175322..47176299-chr16:48190360..48191104,3	K562	blood:
28	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
29	chr16:47173268..47175899-chr16:48024944..48027276,2	K562	blood:
30	chr16:47174837..47177337-chr16:47189035..47191316,2	K562	blood:
31	chr16:47175994..47177897-chr16:48278487..48280949,2	MCF-7	breast:
32	chr16:47259812..47262289-chr16:47267299..47269084,2	K562	blood:
33	chr16:47305590..47308851-chr16:47316493..47319236,3	K562	blood:
34	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
35	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
36	chr16:47259812..47262289-chr16:47267299..47269084,2	K562	blood:
37	chr16:47009479..47012393-chr16:47173213..47175154,2	K562	blood:
38	chr16:47311388..47314338-chr16:47314364..47316020,2	K562	blood:
39	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
40	chr16:47177383..47180950-chr16:47184423..47188537,5	K562	blood:
41	chr16:47264762..47266642-chr16:47266702..47269300,2	K562	blood:
42	chr16:47174837..47177337-chr16:47189035..47191316,2	K562	blood:
43	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
44	chr16:47238697..47239501-chr16:48151319..48151975,2	MCF-7	breast:
45	chr16:47298562..47302472-chr16:47302634..47305844,3	K562	blood:
46	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
47	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
48	chr16:47305590..47308851-chr16:47316493..47319236,3	K562	blood:
49	chr16:47174790..47177797-chr16:47493413..47496816,5	K562	blood:
50	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPT2-11	chr16:47213203-47213513	l_1316_chr16:47211651-47213507_testes
2	lnc-GPT2-3	chr16:47191466-47191515	NONHSAT142282
3	lnc-GPT2-3	chr16:47216667-47217006	NONHSAT142282
4	lnc-GPT2-3	chr16:47195460-47195501	NONHSAT142282
5	lnc-GPT2-3	chr16:47187543-47187707	NONHSAT142282
6	lnc-GPT2-3	chr16:47177999-47178405	NONHSAT142282
7	lnc-PHKB-1	chr16:47333358-47333859	ENSG00000261369.1
8	lnc-NETO2-2	chr16:47296678-47296925	NONHSAT142288
9	lnc-GPT2-11	chr16:47211652-47211793	l_1316_chr16:47211651-47213507_testes
10	lnc-PHKB-1	chr16:47346550-47346651	ENSG00000261369.1
11	lnc-PHKB-3	chr16:47235986-47236340	ENSG00000260744.1
12	lnc-NETO2-3	chr16:47310408-47311851	NONHSAT142289
13	lnc-NETO2-2	chr16:47294571-47294606	NONHSAT142288
14	lnc-GPT2-10	chr16:47185464-47185705	NONHSAT142284
15	lnc-PHKB-3	chr16:47230222-47230630	ENSG00000260744.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ITFG1	hsa-miR-23b-3p	chr16:47189629-47189649

Variant related genes	Relation type
ENSG00000261369	TF binding region
ENSG00000260281	TF binding region
NETO2	TF binding region
ENSG00000222767	TF binding region
RPL23AP72	TF binding region
ITFG1	TF binding region
ENSG00000260012	TF binding region
ENSG00000260744	TF binding region
ENSG00000261369	CpG island
ENSG00000260281	CpG island
NETO2	CpG island
ENSG00000222767	CpG island
RPL23AP72	CpG island
ITFG1	CpG island
ENSG00000260012	CpG island
ENSG00000260744	CpG island
ENSG00000102893	chromatin interactions
ENSG00000171208	chromatin interactions
ENSG00000069345	chromatin interactions
ENSG00000239840	chromatin interactions
ENSG00000260281	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000121270	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000261173	chromatin interactions

Extended variants
information (count: 5625 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5625 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7200954	chr16:47163874-47163875	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184646900	chr16:47163875-47163876	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs549805733	chr16:47163889-47163890	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs561616758	chr16:47163896-47163897	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs528926534	chr16:47163897-47163898	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs140190889	chr16:47164010-47164011	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs563387457	chr16:47164040-47164041	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs189429959	chr16:47164054-47164055	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs181563356	chr16:47164073-47164074	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs150307191	chr16:47164111-47164112	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs560370437	chr16:47164194-47164195	Weak transcription Enhancers Strong transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs570977071	chr16:47164222-47164223	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs538046867	chr16:47164254-47164255	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556666485	chr16:47164297-47164298	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs73536870	chr16:47164328-47164329	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187033878	chr16:47164335-47164336	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs150943898	chr16:47164367-47164368	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs11860720	chr16:47164380-47164381	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs535886682	chr16:47164407-47164408	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs554176955	chr16:47164445-47164446	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs189415849	chr16:47164500-47164501	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs572395073	chr16:47164579-47164580	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs137887060	chr16:47164581-47164582	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs74510064	chr16:47164585-47164586	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542714743	chr16:47164648-47164649	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs368634859	chr16:47164731-47164732	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs557680118	chr16:47164766-47164767	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs576224141	chr16:47164809-47164810	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs543247570	chr16:47164843-47164844	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs561845200	chr16:47164849-47164850	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs528962957	chr16:47164856-47164857	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372123288	chr16:47164905-47164906	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs149225568	chr16:47164910-47164911	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540641290	chr16:47164923-47164924	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs113170007	chr16:47164978-47164979	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs74349516	chr16:47164998-47164999	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs79449397	chr16:47165000-47165001	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs118011245	chr16:47165003-47165004	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs35542273	chr16:47165007-47165008	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527980456	chr16:47165114-47165115	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs552412725	chr16:47165115-47165116	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs571055513	chr16:47165134-47165135	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs114835059	chr16:47165143-47165144	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs181380574	chr16:47165151-47165152	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs568556150	chr16:47165169-47165170	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186528686	chr16:47165181-47165182	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs561446975	chr16:47165190-47165191	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529049120	chr16:47165196-47165197	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs560868789	chr16:47165243-47165244	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs189820362	chr16:47165256-47165257	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Wilms tumour	21544195	CNVD
Cancer	20164920	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	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
Renal cell carcinoma	18765545	CNVD
Sudden cardiac death	19188705	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Colorectal cancer	19359472	CNVD
Olfactory neuroblastoma	18408657	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2574 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47117600-47170200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr16:47118400-47165000	Weak transcription	Fetal Brain Male	brain
3	chr16:47135400-47164000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr16:47140000-47166200	Weak transcription	K562	blood
5	chr16:47140400-47168600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr16:47143800-47170200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr16:47148000-47175400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr16:47148200-47166400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr16:47153400-47164000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr16:47155600-47173000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr16:47156200-47167800	Weak transcription	Brain Germinal Matrix	brain
12	chr16:47156200-47175800	Weak transcription	Psoas Muscle	Psoas
13	chr16:47156800-47170000	Weak transcription	NH-A	brain
14	chr16:47157400-47175600	Weak transcription	HSMM	muscle
15	chr16:47159600-47165200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr16:47159600-47169000	Weak transcription	HUVEC	blood vessel
17	chr16:47159800-47170600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr16:47160200-47164600	Weak transcription	HepG2	liver
19	chr16:47160800-47167000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr16:47161200-47169000	Weak transcription	A549	lung
21	chr16:47161600-47169000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr16:47161600-47175800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr16:47161800-47168600	Weak transcription	Fetal Brain Female	brain
24	chr16:47161800-47168800	Weak transcription	Hela-S3	cervix
25	chr16:47161800-47172600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr16:47162400-47167800	Weak transcription	NHEK	skin
27	chr16:47162400-47170000	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr16:47162600-47168800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr16:47162600-47170000	Weak transcription	Monocytes-CD14+_RO01746	blood
30	chr16:47163000-47169200	Weak transcription	HMEC	breast
31	chr16:47163200-47164000	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr16:47163200-47164000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr16:47163200-47164200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr16:47163200-47169200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr16:47163400-47164000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr16:47163400-47164200	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr16:47163400-47164200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr16:47163400-47172400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr16:47163600-47164200	Enhancers	GM12878-XiMat	blood
40	chr16:47163800-47164200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr16:47163800-47164200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr16:47163800-47164600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr16:47163800-47166600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr16:47164000-47164200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr16:47164000-47164200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr16:47164000-47164200	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr16:47164000-47166000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr16:47164000-47175600	Weak transcription	NHLF	lung
49	chr16:47164200-47168800	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr16:47164200-47169400	Weak transcription	GM12878-XiMat	blood

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