Variant report

Variant	nsv572536
Chromosome Location	chr16:46694649-46727385
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1336)
CpG islands
(count:978)
Chromatin interactive
region (count:49)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1336 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:46723286-46723437	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:46707412-46707608	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:46724802-46724977	HepG2	liver:	n/a	n/a
4	ATF1	chr16:46722183-46722444	K562	blood:	n/a	n/a
5	ATF2	chr16:46722080-46722641	GM12878	blood:	n/a	n/a
6	ATF3	chr16:46722919-46723192	K562	blood:	n/a	chr16:46723144-46723153 chr16:46723102-46723111
7	ATF3	chr16:46722850-46723393	HepG2	liver:	n/a	chr16:46723144-46723153 chr16:46723102-46723111
8	BACH1	chr16:46723562-46723604	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr16:46722530-46722978	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr16:46708611-46708840	GM12878	blood:	n/a	n/a
11	BCLAF1	chr16:46722382-46723167	GM12878	blood:	n/a	chr16:46723144-46723157
12	BCLAF1	chr16:46723413-46724657	GM12878	blood:	n/a	chr16:46723771-46723780
13	BHLHE40	chr16:46724868-46725048	K562	blood:	n/a	n/a
14	BHLHE40	chr16:46722292-46722408	GM12878	blood:	n/a	n/a
15	BHLHE40	chr16:46707413-46707487	K562	blood:	n/a	n/a
16	BHLHE40	chr16:46720967-46721036	GM12878	blood:	n/a	n/a
17	BHLHE40	chr16:46722889-46723497	HepG2	liver:	n/a	chr16:46723072-46723088
18	BHLHE40	chr16:46722644-46723649	GM12878	blood:	n/a	chr16:46723536-46723552 chr16:46723072-46723088
19	BHLHE40	chr16:46707447-46707607	GM12878	blood:	n/a	n/a
20	BHLHE40	chr16:46724848-46725107	HepG2	liver:	n/a	n/a
21	BHLHE40	chr16:46723952-46724113	K562	blood:	n/a	n/a
22	BHLHE40	chr16:46722436-46723601	K562	blood:	n/a	chr16:46723536-46723552 chr16:46723072-46723088
23	BRCA1	chr16:46723188-46723270	HepG2	liver:	n/a	n/a
24	BRCA1	chr16:46723113-46723343	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr16:46722970-46723593	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr16:46722507-46722707	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr16:46723892-46724289	K562	blood:	n/a	n/a
28	CBX3	chr16:46722218-46722764	K562	blood:	n/a	n/a
29	CCNT2	chr16:46722420-46723811	K562	blood:	n/a	chr16:46723519-46723528 chr16:46723144-46723153
30	CEBPB	chr16:46725617-46725793	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr16:46722620-46722638	K562	blood:	n/a	n/a
32	CEBPB	chr16:46723938-46724241	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr16:46722499-46722692	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr16:46725618-46725782	HepG2	liver:	n/a	n/a
35	CEBPB	chr16:46722610-46722660	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:46722429-46723652	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr16:46724695-46725030	HepG2	liver:	n/a	n/a
38	CEBPD	chr16:46723464-46723833	HepG2	liver:	n/a	n/a
39	CEBPD	chr16:46722759-46723460	HepG2	liver:	n/a	n/a
40	CHD1	chr16:46723980-46724150	GM12878	blood:	n/a	n/a
41	CHD1	chr16:46707077-46707871	IMR90	lung:	n/a	n/a
42	CHD1	chr16:46723893-46724273	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr16:46722440-46722682	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr16:46722445-46722592	HepG2	liver:	n/a	n/a
45	CHD2	chr16:46722309-46722408	GM12878	blood:	n/a	n/a
46	CHD2	chr16:46723945-46724152	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr16:46722982-46723709	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr16:46722454-46724195	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr16:46722614-46723779	GM12878	blood:	n/a	n/a
50	CHD2	chr16:46723008-46723719	K562	blood:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46722642-46722692	ECC-1	luminal epithelium:	n/a
2	chr16:46723426-46723476	PFSK-1	brain:	n/a
3	chr16:46722642-46722692	ECC-1	luminal epithelium:	n/a
4	chr16:46723426-46723476	PFSK-1	brain:	n/a
5	chr16:46723204-46723254	HL-60	blood:	n/a
6	chr16:46723204-46723254	PrEC	prostate:	n/a
7	chr16:46724037-46724087	SKMC	muscle:	n/a
8	chr16:46722505-46722555	NH-A	brain:	n/a
9	chr16:46723432-46723482	GM06990	blood:	n/a
10	chr16:46726887-46726937	Jurkat	blood:	n/a
11	chr16:46723153-46723203	HCPEpiC	choroid plexus:	n/a
12	chr16:46723088-46723138	Hela-S3	cervix:	n/a
13	chr16:46724152-46724202	HCPEpiC	choroid plexus:	n/a
14	chr16:46723545-46723595	HRCEpiC	kidney:	n/a
15	chr16:46723088-46723138	HMEC	breast:	n/a
16	chr16:46723153-46723203	SK-N-SH_RA	brain:	n/a
17	chr16:46722642-46722692	Hela-S3	cervix:	n/a
18	chr16:46724152-46724202	GM12892	blood:	n/a
19	chr16:46726887-46726937	AG04449	skin:	fetal
20	chr16:46723204-46723254	BJ	skin:	n/a
21	chr16:46723166-46723216	GM12878	blood:	n/a
22	chr16:46723088-46723138	H1-hESC	embryonic stem cell:	embryo
23	chr16:46723204-46723254	U87	brain:	n/a
24	chr16:46724152-46724202	HCT-116	colon:	n/a
25	chr16:46723048-46723098	IMR90	lung:	fetal
26	chr16:46724096-46724146	NHDF-neo	bronchial:	n/a
27	chr16:46724152-46724202	GM12891	blood:	n/a
28	chr16:46723088-46723138	HCF	heart:	n/a
29	chr16:46723426-46723476	HUVEC	blood vessel:	n/a
30	chr16:46723166-46723216	GM19239	blood:	n/a
31	chr16:46722642-46722692	HNPCEpiC	eye:	n/a
32	chr16:46723518-46723568	HAEpiC	amniotic membrane:	n/a
33	chr16:46722505-46722555	AG09309	skin:	n/a
34	chr16:46723048-46723098	HPAEpiC	pulmonary alveolar:	n/a
35	chr16:46723166-46723216	NH-A	brain:	n/a
36	chr16:46723426-46723476	SK-N-SH	brain:	n/a
37	chr16:46723048-46723098	AG04449	skin:	fetal
38	chr16:46723426-46723476	AG09319	gingival:	n/a
39	chr16:46722505-46722555	RPTEC	kidney:	n/a
40	chr16:46723518-46723568	RPTEC	kidney:	n/a
41	chr16:46724152-46724202	ProgFib	skin:	n/a
42	chr16:46723166-46723216	BJ	skin:	n/a
43	chr16:46724037-46724087	HAEpiC	amniotic membrane:	n/a
44	chr16:46723088-46723138	SK-N-SH_RA	brain:	n/a
45	chr16:46722505-46722555	GM12892	blood:	n/a
46	chr16:46723420-46723470	A549	lung:	n/a
47	chr16:46724096-46724146	HCF	heart:	n/a
48	chr16:46724037-46724087	BJ	skin:	n/a
49	chr16:46723153-46723203	Hela-S3	cervix:	n/a
50	chr16:46723088-46723138	HEK293	kidney:	embryo

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153935466..153936188-chr16:46723180..46724080,2	Hela-S3	cervix:
2	chr16:46681844..46684169-chr16:46721518..46723822,2	K562	blood:
3	chr16:46713745..46716784-chr16:46720254..46722290,3	K562	blood:
4	chr16:46705954..46707514-chr16:46711367..46713742,2	K562	blood:
5	chr1:210547382..210548026-chr16:46722608..46723579,2	Hela-S3	cervix:
6	chr16:46722901..46723856-chr5:108083974..108084613,2	Hela-S3	cervix:
7	chr16:46723133..46724018-chr9:139440419..139440966,2	NB4	blood:
8	chr16:46707772..46709754-chr16:46720793..46723011,2	MCF-7	breast:
9	chr16:46721087..46725989-chr16:46862740..46865236,7	K562	blood:
10	chr16:46722783..46723664-chr19:49990885..49991440,2	Hela-S3	cervix:
11	chr16:46690502..46692806-chr16:46719055..46720847,2	MCF-7	breast:
12	chr16:46707001..46707974-chr16:46963384..46964655,3	K562	blood:
13	chr16:46701863..46703903-chr16:46713521..46715933,2	K562	blood:
14	chr16:46723042..46725138-chr16:46863743..46865908,3	MCF-7	breast:
15	chr16:46707772..46709754-chr16:46720793..46723011,2	MCF-7	breast:
16	chr16:46722548..46723423-chr16:87425505..87426277,2	Hela-S3	cervix:
17	chr16:46707953..46708653-chr16:46887447..46888372,2	K562	blood:
18	chr16:46715468..46717180-chr16:46722050..46724165,2	MCF-7	breast:
19	chr16:46723417..46723944-chr17:74733002..74733817,2	Hela-S3	cervix:
20	chr1:173836705..173837651-chr16:46723495..46724172,2	Hela-S3	cervix:
21	chr16:46723337..46723856-chr16:67312562..67313464,2	Hela-S3	cervix:
22	chr16:46719470..46721064-chr16:46737912..46740527,2	MCF-7	breast:
23	chr1:180123484..180124292-chr16:46722902..46723601,2	HCT-116	colon:
24	chr16:46721631..46724836-chr16:46779909..46784170,7	K562	blood:
25	chr16:46718438..46720564-chr16:46723434..46725231,2	K562	blood:
26	chr16:46723658..46727681-chr16:46823795..46826359,3	K562	blood:
27	chr16:46711146..46713693-chr16:46721499..46723929,2	K562	blood:
28	chr16:46653721..46656886-chr16:46721851..46724551,4	K562	blood:
29	chr16:46717563..46719531-chr16:46720868..46724407,3	MCF-7	breast:
30	chr16:46707389..46708210-chr16:46835449..46836029,2	MCF-7	breast:
31	chr16:46723399..46726142-chr16:46727594..46729309,2	MCF-7	breast:
32	chr16:46689494..46691834-chr16:46696786..46698368,2	K562	blood:
33	chr16:46721630..46725552-chr16:46779076..46784170,6	K562	blood:
34	chr16:46717600..46719603-chr16:46859611..46862308,2	K562	blood:
35	chr16:46704847..46706863-chr16:46794204..46795904,2	MCF-7	breast:
36	chr16:46723503..46724070-chr7:112090386..112091066,2	Hela-S3	cervix:
37	chr16:46701863..46703903-chr16:46713521..46715933,2	K562	blood:
38	chr16:46682731..46685856-chr16:46692484..46695135,3	K562	blood:
39	chr16:46720929..46723857-chr16:46796007..46798416,2	MCF-7	breast:
40	chr16:46713745..46716784-chr16:46720254..46722290,4	K562	blood:
41	chr16:46723531..46724116-chr22:30233901..30234633,2	Hela-S3	cervix:
42	chr1:75198609..75199364-chr16:46723157..46724066,2	Hela-S3	cervix:
43	chr16:46706996..46707945-chr16:46942502..46943366,7	K562	blood:
44	chr16:46715468..46717180-chr16:46722050..46724165,2	MCF-7	breast:
45	chr12:50135161..50135689-chr16:46722187..46722768,2	Hela-S3	cervix:
46	chr16:46711146..46713693-chr16:46721499..46723929,2	K562	blood:
47	chr16:46723293..46723894-chr6:26020511..26021178,2	Hela-S3	cervix:
48	chr16:46721417..46725620-chr16:46861860..46865482,8	K562	blood:
49	chr15:50646591..50647385-chr16:46723275..46723855,2	Hela-S3	cervix:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYLK3-5	chr16:46707358-46707839	NONHSAT142259
2	lnc-SHCBP1-2	chr16:46695441-46695503	ENSG00000261131.1
3	lnc-SHCBP1-2	chr16:46694608-46694865	ENSG00000261131.1

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	VPS35	hsa-miR-24-3p	chr16:46694780-46694801
2	VPS35	hsa-miR-590-3p	chr16:46695074-46695094
3	VPS35	hsa-miR-590-3p	chr16:46695671-46695691

Variant related genes	Relation type
ENSG00000261131	TF binding region
VPS35	TF binding region
ORC6	TF binding region
ENSG00000261131	CpG island
VPS35	CpG island
ORC6	CpG island
ENSG00000103264	chromatin interactions
ENSG00000265181	chromatin interactions
ENSG00000100325	chromatin interactions
ENSG00000171241	chromatin interactions
ENSG00000091651	chromatin interactions
ENSG00000260782	chromatin interactions
ENSG00000140795	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000069329	chromatin interactions
ENSG00000260909	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000196155	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000261788	chromatin interactions
ENSG00000142541	chromatin interactions
ENSG00000155330	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000237886	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000116791	chromatin interactions
ENSG00000162623	chromatin interactions
ENSG00000198366	chromatin interactions

Extended variants
information (count: 1060 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1645943	chr16:46694649-46694650	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
2	rs568023547	chr16:46694672-46694673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs186258822	chr16:46694695-46694696	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs200622483	chr16:46694719-46694720	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs372099857	chr16:46694732-46694733	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
6	rs565732396	chr16:46694746-46694747	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
7	rs557977102	chr16:46694750-46694751	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
8	rs59019355	chr16:46694751-46694752	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs202068466	chr16:46694752-46694753	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs190723691	chr16:46694781-46694782	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region lncRNA miRNA target site	2 gene(s)	Overlapped CNVs	n/a
11	rs141712678	chr16:46694893-46694894	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576101446	chr16:46694928-46694929	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs369400643	chr16:46694958-46694959	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543480796	chr16:46694984-46694985	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs797016	chr16:46695049-46695050	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs200838578	chr16:46695102-46695103	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529618823	chr16:46695130-46695131	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150566564	chr16:46695171-46695172	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139500607	chr16:46695208-46695209	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs8045759	chr16:46695244-46695245	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377058699	chr16:46695245-46695246	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs8045760	chr16:46695249-46695250	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113299301	chr16:46695282-46695283	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527915941	chr16:46695286-46695287	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs566537780	chr16:46695298-46695299	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111681844	chr16:46695300-46695301	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549766600	chr16:46695326-46695327	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375588134	chr16:46695353-46695354	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533439925	chr16:46695399-46695400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376854281	chr16:46695497-46695498	Weak transcription Strong transcription Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs180891154	chr16:46695536-46695537	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547702686	chr16:46695539-46695540	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116282128	chr16:46695557-46695558	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs374061684	chr16:46695579-46695580	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539664511	chr16:46695586-46695587	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs371343319	chr16:46695611-46695612	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375273548	chr16:46695619-46695620	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557875371	chr16:46695632-46695633	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369831560	chr16:46695660-46695661	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184960717	chr16:46695692-46695693	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145033509	chr16:46695696-46695697	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs375501847	chr16:46695718-46695719	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199940967	chr16:46695719-46695720	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs573618693	chr16:46695756-46695757	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs542139125	chr16:46695768-46695769	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150494360	chr16:46695773-46695774	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369864421	chr16:46695791-46695792	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372790222	chr16:46695818-46695819	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs191544365	chr16:46695821-46695822	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs377580366	chr16:46695822-46695823	Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Autism	19955444	CNVD
Schizophrenia	19955444	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:1554 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46683200-46696000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr16:46683200-46696600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr16:46684000-46695600	Weak transcription	K562	blood
4	chr16:46684000-46695800	Weak transcription	Colon Smooth Muscle	Colon
5	chr16:46684200-46695800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr16:46684200-46701800	Weak transcription	Psoas Muscle	Psoas
7	chr16:46684400-46695800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr16:46684600-46695600	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr16:46686000-46695600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr16:46686600-46701800	Weak transcription	Fetal Heart	heart
11	chr16:46688600-46695600	Weak transcription	Fetal Brain Male	brain
12	chr16:46689000-46713600	Strong transcription	Fetal Muscle Trunk	muscle
13	chr16:46689200-46696200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:46689200-46715800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr16:46689600-46697200	Strong transcription	Fetal Muscle Leg	muscle
16	chr16:46689800-46695600	Weak transcription	Fetal Kidney	kidney
17	chr16:46689800-46705400	Weak transcription	Small Intestine	intestine
18	chr16:46689800-46716200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr16:46690000-46695800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr16:46690000-46701200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr16:46690400-46716200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr16:46690600-46697200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr16:46690600-46700600	Strong transcription	Fetal Stomach	stomach
24	chr16:46691000-46695000	Strong transcription	Left Ventricle	heart
25	chr16:46691000-46697200	Strong transcription	Primary T cells from cord blood	blood
26	chr16:46691000-46697200	Strong transcription	A549	lung
27	chr16:46691000-46701600	Strong transcription	Fetal Brain Female	brain
28	chr16:46691000-46701800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr16:46691000-46702000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr16:46691000-46704000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr16:46691000-46705800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr16:46691000-46714800	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr16:46691000-46715000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr16:46691000-46715600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr16:46691000-46716200	Strong transcription	Primary T helper cells fromperipheralblood	blood
36	chr16:46691000-46716800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr16:46691000-46718000	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr16:46691200-46694800	Strong transcription	Muscle Satellite Cultured Cells	--
39	chr16:46691200-46698400	Strong transcription	Osteobl	bone
40	chr16:46691200-46699200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr16:46691200-46699600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr16:46691200-46701800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr16:46691200-46705800	Strong transcription	Duodenum Mucosa	Duodenum
44	chr16:46691200-46714800	Strong transcription	Liver	Liver
45	chr16:46691200-46716200	Strong transcription	Adipose Nuclei	Adipose
46	chr16:46691200-46716400	Strong transcription	Primary T cells fromperipheralblood	blood
47	chr16:46691200-46716800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr16:46691200-46717000	Strong transcription	Dnd41	blood
49	chr16:46691200-46717400	Strong transcription	HUES48 Cell Line	embryonic stem cell
50	chr16:46691400-46697000	Strong transcription	HUVEC	blood vessel

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