Variant report

Variant	esv1792701
Chromosome Location	chr16:46709686-46751452
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1231)
CpG islands
(count:1099)
Chromatin interactive
region (count:54)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1231 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

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	chr16:46724802-46724977	HepG2	liver:	n/a	n/a
3	ATF1	chr16:46722183-46722444	K562	blood:	n/a	n/a
4	ATF2	chr16:46722080-46722641	GM12878	blood:	n/a	n/a
5	ATF3	chr16:46722919-46723192	K562	blood:	n/a	chr16:46723144-46723153 chr16:46723102-46723111
6	ATF3	chr16:46722850-46723393	HepG2	liver:	n/a	chr16:46723144-46723153 chr16:46723102-46723111
7	BACH1	chr16:46722530-46722978	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr16:46723562-46723604	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCLAF1	chr16:46723413-46724657	GM12878	blood:	n/a	chr16:46723771-46723780
10	BCLAF1	chr16:46722382-46723167	GM12878	blood:	n/a	chr16:46723144-46723157
11	BHLHE40	chr16:46720967-46721036	GM12878	blood:	n/a	n/a
12	BHLHE40	chr16:46722889-46723497	HepG2	liver:	n/a	chr16:46723072-46723088
13	BHLHE40	chr16:46724848-46725107	HepG2	liver:	n/a	n/a
14	BHLHE40	chr16:46722436-46723601	K562	blood:	n/a	chr16:46723536-46723552 chr16:46723072-46723088
15	BHLHE40	chr16:46722292-46722408	GM12878	blood:	n/a	n/a
16	BHLHE40	chr16:46723952-46724113	K562	blood:	n/a	n/a
17	BHLHE40	chr16:46722644-46723649	GM12878	blood:	n/a	chr16:46723536-46723552 chr16:46723072-46723088
18	BHLHE40	chr16:46724868-46725048	K562	blood:	n/a	n/a
19	BRCA1	chr16:46723113-46723343	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr16:46723188-46723270	HepG2	liver:	n/a	n/a
21	BRCA1	chr16:46722507-46722707	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr16:46722970-46723593	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr16:46722218-46722764	K562	blood:	n/a	n/a
24	CBX3	chr16:46723892-46724289	K562	blood:	n/a	n/a
25	CBX3	chr16:46749087-46749498	K562	blood:	n/a	n/a
26	CCNT2	chr16:46722420-46723811	K562	blood:	n/a	chr16:46723519-46723528 chr16:46723144-46723153
27	CEBPB	chr16:46722499-46722692	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr16:46745063-46745615	HepG2	liver:	n/a	n/a
29	CEBPB	chr16:46724695-46725030	HepG2	liver:	n/a	n/a
30	CEBPB	chr16:46745148-46745275	K562	blood:	n/a	n/a
31	CEBPB	chr16:46725617-46725793	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr16:46722620-46722638	K562	blood:	n/a	n/a
33	CEBPB	chr16:46725618-46725782	HepG2	liver:	n/a	n/a
34	CEBPB	chr16:46745116-46745602	HepG2	liver:	n/a	n/a
35	CEBPB	chr16:46722610-46722660	HepG2	liver:	n/a	n/a
36	CEBPB	chr16:46723938-46724241	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr16:46745178-46745557	IMR90	lung:	n/a	n/a
38	CEBPB	chr16:46745374-46745551	HepG2	liver:	n/a	n/a
39	CEBPB	chr16:46745123-46745342	HepG2	liver:	n/a	n/a
40	CEBPB	chr16:46722429-46723652	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr16:46745054-46745636	HepG2	liver:	n/a	n/a
42	CEBPD	chr16:46722759-46723460	HepG2	liver:	n/a	n/a
43	CEBPD	chr16:46745118-46745356	HepG2	liver:	n/a	n/a
44	CEBPD	chr16:46723464-46723833	HepG2	liver:	n/a	n/a
45	CHD1	chr16:46723893-46724273	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr16:46723980-46724150	GM12878	blood:	n/a	n/a
47	CHD2	chr16:46722982-46723709	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr16:46722309-46722408	GM12878	blood:	n/a	n/a
49	CHD2	chr16:46722972-46723686	HepG2	liver:	n/a	n/a
50	CHD2	chr16:46723008-46723719	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:46724037-46724087	PANC-1	pancreas:	n/a
2	chr16:46724037-46724087	PANC-1	pancreas:	n/a
3	chr16:46722642-46722692	HEEpiC	esophagus:	n/a
4	chr16:46724152-46724202	HL-60	blood:	n/a
5	chr16:46723432-46723482	Hepatocyte	liver:	n/a
6	chr16:46724152-46724202	Hepatocyte	liver:	n/a
7	chr16:46724152-46724202	H1-hESC	embryonic stem cell:	embryo
8	chr16:46739767-46739817	NT2-D1	testis:	n/a
9	chr16:46723153-46723203	AG09309	skin:	n/a
10	chr16:46723518-46723568	K562	blood:	n/a
11	chr16:46722642-46722692	U87	brain:	n/a
12	chr16:46722642-46722692	T-47D	breast:	n/a
13	chr16:46723204-46723254	GM12892	blood:	n/a
14	chr16:46723088-46723138	CMK	blood:	n/a
15	chr16:46724096-46724146	ECC-1	luminal epithelium:	n/a
16	chr16:46723432-46723482	HCT-116	colon:	n/a
17	chr16:46723204-46723254	GM19239	blood:	n/a
18	chr16:46726887-46726937	GM06990	blood:	n/a
19	chr16:46728312-46728362	AoSMC	blood vessel:	n/a
20	chr16:46722642-46722692	NHDF-neo	bronchial:	n/a
21	chr16:46726887-46726937	AoSMC	blood vessel:	n/a
22	chr16:46723426-46723476	Caco-2	colon:	n/a
23	chr16:46726887-46726937	SK-N-SH_RA	brain:	n/a
24	chr16:46723166-46723216	ovcar-3	ovarian:	n/a
25	chr16:46723420-46723470	SKMC	muscle:	n/a
26	chr16:46723088-46723138	PFSK-1	brain:	n/a
27	chr16:46724096-46724146	Hepatocyte	liver:	n/a
28	chr16:46723432-46723482	HNPCEpiC	eye:	n/a
29	chr16:46724096-46724146	HCT-116	colon:	n/a
30	chr16:46724037-46724087	K562	blood:	n/a
31	chr16:46728312-46728362	RPTEC	kidney:	n/a
32	chr16:46723545-46723595	HIPEpiC	eye:	n/a
33	chr16:46723518-46723568	MCF-7	breast:	n/a
34	chr16:46723545-46723595	PrEC	prostate:	n/a
35	chr16:46722505-46722555	GM19239	blood:	n/a
36	chr16:46723204-46723254	H1-hESC	embryonic stem cell:	embryo
37	chr16:46723048-46723098	AG10803	skin:	n/a
38	chr16:46724096-46724146	HCPEpiC	choroid plexus:	n/a
39	chr16:46723153-46723203	HRE	kidney:	n/a
40	chr16:46723420-46723470	HAEpiC	amniotic membrane:	n/a
41	chr16:46724096-46724146	CMK	blood:	n/a
42	chr16:46723420-46723470	NHDF-neo	bronchial:	n/a
43	chr16:46723426-46723476	AG09309	skin:	n/a
44	chr16:46723426-46723476	HCT-116	colon:	n/a
45	chr16:46723518-46723568	RPTEC	kidney:	n/a
46	chr16:46723420-46723470	PrEC	prostate:	n/a
47	chr16:46723204-46723254	SK-N-SH	brain:	n/a
48	chr16:46723420-46723470	HepG2	liver:	n/a
49	chr16:46723545-46723595	HPAEpiC	pulmonary alveolar:	n/a
50	chr16:46724152-46724202	AG10803	skin:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:46721631..46724836-chr16:46779909..46784170,7	K562	blood:
2	chr16:46729440..46732206-chr16:46768844..46771531,2	K562	blood:
3	chr1:153935466..153936188-chr16:46723180..46724080,2	Hela-S3	cervix:
4	chr16:46732635..46735109-chr16:46739940..46743405,3	K562	blood:
5	chr16:46734124..46735947-chr16:46738836..46740756,2	K562	blood:
6	chr16:46707772..46709754-chr16:46720793..46723011,2	MCF-7	breast:
7	chr16:46732635..46735109-chr16:46739940..46743405,3	K562	blood:
8	chr16:46734124..46735947-chr16:46738836..46740756,2	K562	blood:
9	chr16:46715468..46717180-chr16:46722050..46724165,2	MCF-7	breast:
10	chr16:46719470..46721064-chr16:46737912..46740527,2	MCF-7	breast:
11	chr16:46681844..46684169-chr16:46721518..46723822,2	K562	blood:
12	chr16:46720929..46723857-chr16:46796007..46798416,2	MCF-7	breast:
13	chr16:46721087..46725989-chr16:46862740..46865236,7	K562	blood:
14	chr16:46723337..46723856-chr16:67312562..67313464,2	Hela-S3	cervix:
15	chr16:46723417..46723944-chr17:74733002..74733817,2	Hela-S3	cervix:
16	chr16:46713745..46716784-chr16:46720254..46722290,4	K562	blood:
17	chr1:75198609..75199364-chr16:46723157..46724066,2	Hela-S3	cervix:
18	chr16:46722901..46723856-chr5:108083974..108084613,2	Hela-S3	cervix:
19	chr16:46723399..46726142-chr16:46727594..46729309,2	MCF-7	breast:
20	chr16:46717600..46719603-chr16:46859611..46862308,2	K562	blood:
21	chr16:46718438..46720564-chr16:46723434..46725231,2	K562	blood:
22	chr15:50646591..50647385-chr16:46723275..46723855,2	Hela-S3	cervix:
23	chr16:46723658..46727681-chr16:46823795..46826359,3	K562	blood:
24	chr16:46722783..46723664-chr19:49990885..49991440,2	Hela-S3	cervix:
25	chr16:46722548..46723423-chr16:87425505..87426277,2	Hela-S3	cervix:
26	chr16:46732778..46734710-chr16:46734762..46736460,2	K562	blood:
27	chr16:46723042..46725138-chr16:46863743..46865908,3	MCF-7	breast:
28	chr1:173836705..173837651-chr16:46723495..46724172,2	Hela-S3	cervix:
29	chr16:46653721..46656886-chr16:46721851..46724551,4	K562	blood:
30	chr16:46717563..46719531-chr16:46720868..46724407,3	MCF-7	breast:
31	chr16:46721630..46725552-chr16:46779076..46784170,6	K562	blood:
32	chr16:46715468..46717180-chr16:46722050..46724165,2	MCF-7	breast:
33	chr16:46723531..46724116-chr22:30233901..30234633,2	Hela-S3	cervix:
34	chr16:46707772..46709754-chr16:46720793..46723011,2	MCF-7	breast:
35	chr16:46732778..46734710-chr16:46734762..46736460,2	K562	blood:
36	chr16:46723133..46724018-chr9:139440419..139440966,2	NB4	blood:
37	chr16:46723399..46726142-chr16:46727594..46729309,2	MCF-7	breast:
38	chr16:46746554..46747352-chr17:77807630..77808493,2	MCF-7	breast:
39	chr16:46711146..46713693-chr16:46721499..46723929,2	K562	blood:
40	chr16:46711146..46713693-chr16:46721499..46723929,2	K562	blood:
41	chr1:180123484..180124292-chr16:46722902..46723601,2	HCT-116	colon:
42	chr16:46729513..46731801-chr16:46734128..46737979,3	K562	blood:
43	chr16:46741908..46744593-chr16:46750303..46752897,2	MCF-7	breast:
44	chr12:50135161..50135689-chr16:46722187..46722768,2	Hela-S3	cervix:
45	chr16:46721417..46725620-chr16:46861860..46865482,8	K562	blood:
46	chr16:46701863..46703903-chr16:46713521..46715933,2	K562	blood:
47	chr16:46723293..46723894-chr6:26020511..26021178,2	Hela-S3	cervix:
48	chr16:46723503..46724070-chr7:112090386..112091066,2	Hela-S3	cervix:
49	chr16:46731723..46733835-chr16:46735349..46737949,2	K562	blood:
50	chr16:46722609..46724172-chr16:46751390..46753908,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYLK3-1	chr16:46737281-46737937	ENSG00000261788.1

No data

Variant related genes	Relation type
VPS35	TF binding region
MYLK3	TF binding region
ORC6	TF binding region
ENSG00000261788	TF binding region
VPS35	CpG island
MYLK3	CpG island
ORC6	CpG island
ENSG00000261788	CpG island
ENSG00000100325	chromatin interactions
ENSG00000162623	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000091651	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000140795	chromatin interactions
ENSG00000265181	chromatin interactions
ENSG00000196155	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000116260	chromatin interactions
ENSG00000104064	chromatin interactions
ENSG00000198366	chromatin interactions
ENSG00000261788	chromatin interactions
ENSG00000142541	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000151422	chromatin interactions
ENSG00000260909	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000103264	chromatin interactions
ENSG00000260782	chromatin interactions
ENSG00000116791	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000069329	chromatin interactions
ENSG00000237886	chromatin interactions
ENSG00000155330	chromatin interactions
ENSG00000171241	chromatin interactions

Extended variants
information (count: 1350 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1350 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs250420	chr16:46709686-46709687	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569154774	chr16:46709690-46709691	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs570599883	chr16:46709716-46709717	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142807358	chr16:46709717-46709718	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs202008963	chr16:46709731-46709732	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548040319	chr16:46709751-46709752	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs153259	chr16:46709752-46709753	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs141462266	chr16:46709822-46709823	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190457919	chr16:46709871-46709872	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570655077	chr16:46709941-46709942	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369452932	chr16:46709977-46709978	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1209760	chr16:46710000-46710001	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs71158882	chr16:46710001-46710002	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs369580318	chr16:46710006-46710007	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372543180	chr16:46710011-46710012	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537541040	chr16:46710101-46710102	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs180895450	chr16:46710116-46710117	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574314379	chr16:46710124-46710125	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1641118	chr16:46710198-46710199	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376332931	chr16:46710273-46710274	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555275589	chr16:46710284-46710285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112581516	chr16:46710399-46710400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs540959584	chr16:46710423-46710424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186652215	chr16:46710457-46710458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371218680	chr16:46710495-46710496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs148572750	chr16:46710575-46710576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368227261	chr16:46710626-46710627	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372416237	chr16:46710635-46710636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199882439	chr16:46710643-46710644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs529995457	chr16:46710653-46710654	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148918317	chr16:46710687-46710688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147624833	chr16:46710737-46710738	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181200771	chr16:46710773-46710774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111405329	chr16:46710829-46710830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34738934	chr16:46710869-46710870	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs552100339	chr16:46710894-46710895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570546023	chr16:46710926-46710927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs538056979	chr16:46710938-46710939	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186249883	chr16:46710954-46710955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568171721	chr16:46710965-46710966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535409310	chr16:46710971-46710972	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553785091	chr16:46710973-46710974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190622480	chr16:46711008-46711009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182864023	chr16:46711101-46711102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs559239994	chr16:46711105-46711106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs150127053	chr16:46711180-46711181	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs567967692	chr16:46711196-46711197	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs535490916	chr16:46711199-46711200	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs575279246	chr16:46711200-46711201	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs371814413	chr16:46711209-46711210	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 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:1392 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:46689000-46713600	Strong transcription	Fetal Muscle Trunk	muscle
2	chr16:46689200-46715800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr16:46689800-46716200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr16:46690400-46716200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr16:46691000-46714800	Strong transcription	Skeletal Muscle Female	skeletal muscle
6	chr16:46691000-46715000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr16:46691000-46715600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr16:46691000-46716200	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr16:46691000-46716800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr16:46691000-46718000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr16:46691200-46714800	Strong transcription	Liver	Liver
12	chr16:46691200-46716200	Strong transcription	Adipose Nuclei	Adipose
13	chr16:46691200-46716400	Strong transcription	Primary T cells fromperipheralblood	blood
14	chr16:46691200-46716800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr16:46691200-46717000	Strong transcription	Dnd41	blood
16	chr16:46691200-46717400	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr16:46692400-46716800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
18	chr16:46692600-46716200	Strong transcription	HUES6 Cell Line	embryonic stem cell
19	chr16:46692600-46717000	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr16:46692800-46717400	Strong transcription	Rectal Mucosa Donor 29	rectum
21	chr16:46693000-46713200	Strong transcription	Fetal Intestine Large	intestine
22	chr16:46693000-46715200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr16:46693000-46716800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr16:46694000-46716600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr16:46694000-46717600	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr16:46694200-46716600	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr16:46694200-46716800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr16:46694600-46716800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr16:46695000-46716400	Weak transcription	Stomach Mucosa	stomach
30	chr16:46697000-46711400	Weak transcription	Esophagus	oesophagus
31	chr16:46697000-46713000	Strong transcription	Primary neutrophils fromperipheralblood	blood
32	chr16:46697000-46716200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr16:46698600-46717800	Strong transcription	Primary B cells from peripheral blood	blood
34	chr16:46698800-46715600	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr16:46699000-46715600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
36	chr16:46700000-46713600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr16:46700600-46711200	Strong transcription	HepG2	liver
38	chr16:46700800-46714800	Strong transcription	Stomach Smooth Muscle	stomach
39	chr16:46701200-46713200	Strong transcription	Fetal Kidney	kidney
40	chr16:46702000-46713600	Strong transcription	Sigmoid Colon	Sigmoid Colon
41	chr16:46702400-46713600	Strong transcription	Fetal Brain Female	brain
42	chr16:46702400-46717600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr16:46702600-46715600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr16:46702600-46716400	Weak transcription	Fetal Heart	heart
45	chr16:46702600-46716800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr16:46702600-46722200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr16:46702800-46712800	Weak transcription	NHLF	lung
48	chr16:46703000-46712200	Weak transcription	Psoas Muscle	Psoas
49	chr16:46703400-46716200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
50	chr16:46704200-46715600	Strong transcription	Fetal Lung	lung

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