Variant report

Variant	esv1821100
Chromosome Location	chr16:47171333-47330244
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2011)
CpG islands
(count:1161)
Chromatin interactive
region (count:75)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2011 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

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	chr16:47177086-47177176	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:47196782-47196800	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:47180937-47181312	K562	blood:	n/a	n/a
5	ARID3A	chr16:47176783-47176815	K562	blood:	n/a	n/a
6	ARID3A	chr16:47175635-47176566	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:47177441-47177480	K562	blood:	n/a	n/a
8	ARID3A	chr16:47175602-47176202	K562	blood:	n/a	n/a
9	ARID3A	chr16:47178303-47178477	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:47216266-47216628	HepG2	liver:	n/a	n/a
11	ATF1	chr16:47175658-47176054	K562	blood:	n/a	n/a
12	ATF1	chr16:47197545-47197587	K562	blood:	n/a	n/a
13	ATF2	chr16:47176226-47176738	GM12878	blood:	n/a	n/a
14	ATF2	chr16:47175531-47176062	GM12878	blood:	n/a	n/a
15	ATF2	chr16:47175571-47176087	GM12878	blood:	n/a	n/a
16	ATF2	chr16:47176142-47176695	GM12878	blood:	n/a	n/a
17	ATF3	chr16:47171874-47172117	K562	blood:	n/a	n/a
18	ATF3	chr16:47177260-47177528	K562	blood:	n/a	n/a
19	BACH1	chr16:47175631-47176087	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr16:47176731-47177908	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr16:47178178-47178180	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr16:47176399-47176669	GM12878	blood:	n/a	n/a
23	BATF	chr16:47175661-47175976	GM12878	blood:	n/a	n/a
24	BATF	chr16:47176365-47176663	GM12878	blood:	n/a	n/a
25	BCL11A	chr16:47176367-47176707	GM12878	blood:	n/a	n/a
26	BCLAF1	chr16:47177145-47177707	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
27	BCLAF1	chr16:47175480-47176190	GM12878	blood:	n/a	n/a
28	BCLAF1	chr16:47175544-47176047	GM12878	blood:	n/a	n/a
29	BCLAF1	chr16:47177271-47177669	GM12878	blood:	n/a	chr16:47177425-47177438 chr16:47177593-47177602 chr16:47177563-47177572
30	BCLAF1	chr16:47176319-47176951	GM12878	blood:	n/a	n/a
31	BHLHE40	chr16:47177272-47178380	K562	blood:	n/a	chr16:47178152-47178168 chr16:47177449-47177465 chr16:47178004-47178020 chr16:47178144-47178160
32	BHLHE40	chr16:47177335-47177732	HepG2	liver:	n/a	chr16:47177449-47177465
33	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
34	BHLHE40	chr16:47175534-47176602	GM12878	blood:	n/a	n/a
35	BHLHE40	chr16:47175636-47176200	K562	blood:	n/a	n/a
36	BRCA1	chr16:47175537-47175997	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr16:47178549-47178596	HepG2	liver:	n/a	n/a
38	BRCA1	chr16:47178424-47178462	GM12878	blood:	n/a	n/a
39	BRCA1	chr16:47176374-47176777	Hela-S3	cervix:	n/a	n/a
40	CBX3	chr16:47178273-47178641	K562	blood:	n/a	n/a
41	CBX3	chr16:47186439-47186720	K562	blood:	n/a	n/a
42	CBX3	chr16:47177298-47177690	K562	blood:	n/a	n/a
43	CCNT2	chr16:47173695-47173896	K562	blood:	n/a	n/a
44	CCNT2	chr16:47176712-47178516	K562	blood:	n/a	chr16:47177471-47177480
45	CEBPB	chr16:47289349-47289645	IMR90	lung:	n/a	n/a
46	CEBPB	chr16:47200686-47201114	K562	blood:	n/a	chr16:47200944-47200955
47	CEBPB	chr16:47231474-47231853	K562	blood:	n/a	chr16:47231609-47231620
48	CEBPB	chr16:47274841-47274874	K562	blood:	n/a	n/a
49	CEBPB	chr16:47279181-47279381	K562	blood:	n/a	chr16:47279302-47279311
50	CEBPB	chr16:47268376-47268555	K562	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:47216988-47217038	HRCEpiC	kidney:	n/a
2	chr16:47177175-47177225	Hela-S3	cervix:	n/a
3	chr16:47216988-47217038	HRCEpiC	kidney:	n/a
4	chr16:47177175-47177225	Hela-S3	cervix:	n/a
5	chr16:47178723-47178773	LNCaP	prostate:	n/a
6	chr16:47175912-47175962	GM12892	blood:	n/a
7	chr16:47177480-47177530	BE2_C	brain:	n/a
8	chr16:47216988-47217038	GM12892	blood:	n/a
9	chr16:47177175-47177225	HUVEC	blood vessel:	n/a
10	chr16:47181961-47182011	Jurkat	blood:	n/a
11	chr16:47178359-47178409	PrEC	prostate:	n/a
12	chr16:47173093-47173143	HCT-116	colon:	n/a
13	chr16:47173093-47173143	GM12892	blood:	n/a
14	chr16:47175912-47175962	Hela-S3	cervix:	n/a
15	chr16:47175842-47175892	SAEC	small airway:	n/a
16	chr16:47173093-47173143	Hepatocyte	liver:	n/a
17	chr16:47175842-47175892	HRPEpiC	eye:	n/a
18	chr16:47178078-47178128	HepG2	liver:	n/a
19	chr16:47177603-47177653	NHBE	bronchial:	n/a
20	chr16:47175912-47175962	HNPCEpiC	eye:	n/a
21	chr16:47173093-47173143	GM06990	blood:	n/a
22	chr16:47177603-47177653	NT2-D1	testis:	n/a
23	chr16:47178357-47178407	HCM	heart:	n/a
24	chr16:47176710-47176760	AG09309	skin:	n/a
25	chr16:47178723-47178773	CMK	blood:	n/a
26	chr16:47178357-47178407	AG09309	skin:	n/a
27	chr16:47178357-47178407	AG04450	lung:	fetal
28	chr16:47216988-47217038	HCF	heart:	n/a
29	chr16:47178359-47178409	ovcar-3	ovarian:	n/a
30	chr16:47178078-47178128	MCF-7	breast:	n/a
31	chr16:47214942-47214992	GM12891	blood:	n/a
32	chr16:47178208-47178258	AG04449	skin:	fetal
33	chr16:47181961-47182011	AG09319	gingival:	n/a
34	chr16:47173093-47173143	NB4	blood:	n/a
35	chr16:47175936-47175986	Jurkat	blood:	n/a
36	chr16:47178208-47178258	SK-N-SH	brain:	n/a
37	chr16:47178070-47178120	HCT-116	colon:	n/a
38	chr16:47178250-47178300	GM06990	blood:	n/a
39	chr16:47177603-47177653	GM06990	blood:	n/a
40	chr16:47178070-47178120	Hepatocyte	liver:	n/a
41	chr16:47216988-47217038	AG09319	gingival:	n/a
42	chr16:47178723-47178773	HEK293	kidney:	embryo
43	chr16:47177175-47177225	BE2_C	brain:	n/a
44	chr16:47177603-47177653	HCF	heart:	n/a
45	chr16:47178067-47178117	NH-A	brain:	n/a
46	chr16:47177603-47177653	HCT-116	colon:	n/a
47	chr16:47178067-47178117	HPAEpiC	pulmonary alveolar:	n/a
48	chr16:47177175-47177225	AG04449	skin:	fetal
49	chr16:47176710-47176760	SKMC	muscle:	n/a
50	chr16:47175912-47175962	HMEC	breast:	n/a

(count:75 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
2	chr16:47305590..47308851-chr16:47316493..47319236,3	K562	blood:
3	chr16:47171642..47174584-chr16:47493767..47496687,2	K562	blood:
4	chr16:47177383..47180950-chr16:47184423..47188537,5	K562	blood:
5	chr16:47005815..47008447-chr16:47177298..47179122,2	K562	blood:
6	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
7	chr16:47175322..47176299-chr16:48190360..48191104,3	K562	blood:
8	chr16:47173268..47175899-chr16:48024944..48027276,2	K562	blood:
9	chr16:47259812..47262289-chr16:47267299..47269084,2	K562	blood:
10	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
11	chr16:47175627..47176240-chr16:48199483..48200032,2	MCF-7	breast:
12	chr16:47263413..47265450-chr16:47271876..47274264,2	K562	blood:
13	chr16:47178385..47180317-chr16:47705518..47707688,2	K562	blood:
14	chr16:47245162..47247780-chr16:47248160..47249782,2	K562	blood:
15	chr16:47155510..47158192-chr16:47174850..47176528,2	K562	blood:
16	chr16:47311388..47314338-chr16:47314364..47316020,2	K562	blood:
17	chr16:47264762..47266642-chr16:47266702..47269300,2	K562	blood:
18	chr16:47288247..47290542-chr16:47297549..47300017,2	K562	blood:
19	chr16:47246745..47249247-chr16:47253084..47254713,2	K562	blood:
20	chr16:47264762..47266642-chr16:47266702..47269300,2	K562	blood:
21	chr16:47259812..47262289-chr16:47267299..47269084,2	K562	blood:
22	chr16:47305590..47308851-chr16:47316493..47319236,3	K562	blood:
23	chr16:47201430..47205164-chr16:47207074..47210552,4	K562	blood:
24	chr16:47189381..47191014-chr16:47191815..47193762,2	K562	blood:
25	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
26	chr16:47315203..47316940-chr16:47529898..47531487,2	K562	blood:
27	chr16:47177500..47180441-chr16:47180510..47182693,2	K562	blood:
28	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:
29	chr16:47284043..47286034-chr16:47297265..47300260,2	K562	blood:
30	chr16:47257065..47259254-chr16:47293834..47296356,2	K562	blood:
31	chr16:47269900..47272616-chr16:47277828..47281996,3	K562	blood:
32	chr16:47310628..47312888-chr16:47313901..47316020,2	K562	blood:
33	chr16:47281267..47281944-chr3:111725286..111725871,2	MCF-7	breast:
34	chr16:47175524..47179141-chr16:47493736..47496005,3	MCF-7	breast:
35	chr16:47005665..47009288-chr16:47176479..47179650,5	K562	blood:
36	chr16:47174005..47175581-chr16:47176201..47178952,2	MCF-7	breast:
37	chr16:47174837..47177337-chr16:47189035..47191316,2	K562	blood:
38	chr16:47178986..47180526-chr16:47182698..47184295,2	K562	blood:
39	chr16:47298562..47302472-chr16:47302634..47305844,3	K562	blood:
40	chr16:47310628..47312888-chr16:47313901..47316020,2	K562	blood:
41	chr16:47175296..47177509-chr16:48190040..48191217,7	MCF-7	breast:
42	chr16:47233470..47235990-chr16:47244208..47246996,2	K562	blood:
43	chr16:47178986..47180526-chr16:47182698..47184295,2	K562	blood:
44	chr16:47282712..47286365-chr16:47287931..47291615,3	K562	blood:
45	chr1:8938804..8939443-chr16:47177378..47177897,2	Hela-S3	cervix:
46	chr16:47247078..47250065-chr16:47259080..47261996,2	K562	blood:
47	chr16:47201430..47205164-chr16:47207074..47210552,4	K562	blood:
48	chr16:47177997..47179501-chr16:47190203..47192834,2	K562	blood:
49	chr16:47247078..47250065-chr16:47259080..47261996,2	K562	blood:
50	chr16:47233614..47236128-chr16:47259100..47261091,2	K562	blood:

(count:13 , 50 per page) page: 1

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

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
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
RPL23AP72	CpG island
ITFG1	CpG island
ENSG00000260012	CpG island
ENSG00000260744	CpG island
ENSG00000121270	chromatin interactions
ENSG00000239840	chromatin interactions
ENSG00000069345	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000261173	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000102893	chromatin interactions
ENSG00000129636	chromatin interactions
ENSG00000171208	chromatin interactions
ENSG00000260281	chromatin interactions

Extended variants
information (count: 4844 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:4844 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3095622	chr16:47171333-47171334	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184026263	chr16:47171353-47171354	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs187376106	chr16:47171356-47171357	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs542068582	chr16:47171402-47171403	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs560343420	chr16:47171413-47171414	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs545246794	chr16:47171414-47171415	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs527392934	chr16:47171466-47171467	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs565938370	chr16:47171519-47171520	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs191772870	chr16:47171551-47171552	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs563646364	chr16:47171555-47171556	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs531366576	chr16:47171596-47171597	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs549498325	chr16:47171610-47171611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530269481	chr16:47171678-47171679	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs139994356	chr16:47171703-47171704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs548370239	chr16:47171704-47171705	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530299722	chr16:47171724-47171725	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548374494	chr16:47171774-47171775	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs566681270	chr16:47171865-47171866	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs73536876	chr16:47171930-47171931	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs559053528	chr16:47171935-47171936	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs183554842	chr16:47171950-47171951	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs373579528	chr16:47171981-47171982	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs538272339	chr16:47171985-47171986	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs376968216	chr16:47172002-47172003	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186898173	chr16:47172039-47172040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs191742808	chr16:47172085-47172086	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs182075859	chr16:47172087-47172088	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543028512	chr16:47172088-47172089	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs542105581	chr16:47172095-47172096	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs141837196	chr16:47172103-47172104	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186669860	chr16:47172167-47172168	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs146251803	chr16:47172168-47172169	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs139133273	chr16:47172183-47172184	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs370296134	chr16:47172194-47172195	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs373713120	chr16:47172225-47172226	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149909171	chr16:47172235-47172236	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs192510674	chr16:47172297-47172298	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs543430846	chr16:47172392-47172393	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs144926534	chr16:47172430-47172431	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs530333371	chr16:47172463-47172464	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs548509836	chr16:47172489-47172490	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs566819586	chr16:47172502-47172503	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs376459176	chr16:47172528-47172529	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs12447010	chr16:47172550-47172551	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs527913913	chr16:47172552-47172553	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs552480198	chr16:47172575-47172576	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs558694469	chr16:47172602-47172603	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570940191	chr16:47172647-47172648	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs4386162	chr16:47172661-47172662	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs185652972	chr16:47172674-47172675	Enhancers Strong transcription Weak transcription Active TSS Genic 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:2084 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47148000-47175400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr16:47155600-47173000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr16:47156200-47175800	Weak transcription	Psoas Muscle	Psoas
4	chr16:47157400-47175600	Weak transcription	HSMM	muscle
5	chr16:47161600-47175800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr16:47161800-47172600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr16:47163400-47172400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr16:47164000-47175600	Weak transcription	NHLF	lung
9	chr16:47164200-47172400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr16:47168200-47171800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr16:47168600-47172600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr16:47169000-47172400	Enhancers	A549	lung
13	chr16:47169200-47171800	Weak transcription	Fetal Brain Female	brain
14	chr16:47169200-47173600	Enhancers	NHEK	skin
15	chr16:47169200-47173800	Enhancers	HMEC	breast
16	chr16:47169200-47174600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:47169400-47171400	Enhancers	GM12878-XiMat	blood
18	chr16:47169400-47172600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr16:47169400-47172800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr16:47169400-47173600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr16:47170000-47172000	Enhancers	NH-A	brain
22	chr16:47170000-47173600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:47170000-47175400	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr16:47170200-47172800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr16:47170400-47175800	Weak transcription	Gastric	stomach
26	chr16:47170600-47171800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr16:47170600-47171800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr16:47170600-47171800	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr16:47170600-47172200	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr16:47170600-47172800	Enhancers	HUVEC	blood vessel
31	chr16:47170600-47175400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr16:47170600-47175600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr16:47171000-47175000	Enhancers	Fetal Brain Male	brain
34	chr16:47171000-47175600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr16:47171200-47171400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr16:47171200-47171400	Enhancers	Brain Angular Gyrus	brain
37	chr16:47171200-47171400	Enhancers	Left Ventricle	heart
38	chr16:47171200-47171400	Flanking Active TSS	Hela-S3	cervix
39	chr16:47171200-47171800	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr16:47171200-47171800	Enhancers	Brain Germinal Matrix	brain
41	chr16:47171200-47173200	Enhancers	K562	blood
42	chr16:47171400-47171600	Flanking Active TSS	GM12878-XiMat	blood
43	chr16:47171400-47173400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr16:47171400-47175400	Enhancers	Hela-S3	cervix
45	chr16:47171400-47175600	Weak transcription	Brain Angular Gyrus	brain
46	chr16:47171400-47175800	Weak transcription	Left Ventricle	heart
47	chr16:47171400-47175800	Weak transcription	Spleen	Spleen
48	chr16:47171600-47171800	Enhancers	GM12878-XiMat	blood
49	chr16:47171800-47172000	Flanking Active TSS	Brain Germinal Matrix	brain
50	chr16:47171800-47172200	Enhancers	Muscle Satellite Cultured Cells	--

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