Variant report

Variant	esv3446155
Chromosome Location	chr16:70471476-70474424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:642)
CpG islands
(count:549)
Chromatin interactive
region (count:21)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:642 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:70473092-70473348	K562	blood:	n/a	n/a
2	ARID3A	chr16:70473092-70473292	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:70473976-70474273	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:70470896-70471550	K562	blood:	n/a	n/a
5	ATF2	chr16:70473018-70473359	GM12878	blood:	n/a	n/a
6	ATF3	chr16:70473062-70473393	K562	blood:	n/a	n/a
7	ATF3	chr16:70473083-70473416	HepG2	liver:	n/a	n/a
8	ATF3	chr16:70473072-70473431	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr16:70473026-70473478	GM12878	blood:	n/a	n/a
10	BACH1	chr16:70473099-70473894	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr16:70473280-70473468	K562	blood:	n/a	n/a
12	BCL3	chr16:70473099-70473669	A549	lung:	n/a	chr16:70473155-70473164 chr16:70473484-70473497
13	BCLAF1	chr16:70473010-70473552	GM12878	blood:	n/a	chr16:70473155-70473164 chr16:70473484-70473497
14	BCLAF1	chr16:70472949-70473608	GM12878	blood:	n/a	chr16:70473155-70473164 chr16:70473484-70473497
15	BHLHE40	chr16:70473049-70473565	HepG2	liver:	n/a	n/a
16	BHLHE40	chr16:70473064-70473600	K562	blood:	n/a	chr16:70473578-70473594
17	BHLHE40	chr16:70470669-70472305	K562	blood:	n/a	n/a
18	BHLHE40	chr16:70473005-70473587	GM12878	blood:	n/a	n/a
19	BRCA1	chr16:70471867-70472055	HepG2	liver:	n/a	n/a
20	BRCA1	chr16:70473254-70473385	HepG2	liver:	n/a	n/a
21	BRCA1	chr16:70471751-70471918	GM12878	blood:	n/a	n/a
22	BRCA1	chr16:70473115-70473160	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr16:70472992-70473656	K562	blood:	n/a	n/a
24	CCNT2	chr16:70472194-70473665	K562	blood:	n/a	chr16:70473120-70473129 chr16:70472446-70472455
25	CEBPB	chr16:70471832-70472189	IMR90	lung:	n/a	n/a
26	CEBPB	chr16:70473797-70474359	HepG2	liver:	n/a	chr16:70473846-70473859
27	CEBPB	chr16:70473130-70473327	HepG2	liver:	n/a	n/a
28	CEBPB	chr16:70473139-70473355	Hela-S3	cervix:	n/a	n/a
29	CEBPD	chr16:70473859-70474225	HepG2	liver:	n/a	n/a
30	CEBPD	chr16:70472872-70473627	HepG2	liver:	n/a	n/a
31	CEBPD	chr16:70472944-70473488	HepG2	liver:	n/a	n/a
32	CHD1	chr16:70472194-70472398	GM12878	blood:	n/a	n/a
33	CHD1	chr16:70472703-70472797	GM12878	blood:	n/a	n/a
34	CHD1	chr16:70471269-70471570	GM12878	blood:	n/a	n/a
35	CHD2	chr16:70471676-70471839	GM12878	blood:	n/a	n/a
36	CHD2	chr16:70472998-70473632	HepG2	liver:	n/a	n/a
37	CHD2	chr16:70472961-70473675	K562	blood:	n/a	n/a
38	CHD2	chr16:70472286-70473518	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr16:70473003-70473610	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr16:70472922-70473700	GM12878	blood:	n/a	n/a
41	CREB1	chr16:70472562-70474425	HepG2	liver:	n/a	n/a
42	CREB1	chr16:70472824-70473672	GM12878	blood:	n/a	n/a
43	CREB1	chr16:70472803-70473698	K562	blood:	n/a	n/a
44	CREB1	chr16:70472909-70473545	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr16:70472948-70473377	A549	lung:	n/a	n/a
46	CREB1	chr16:70472907-70473628	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr16:70472883-70473684	A549	lung:	n/a	n/a
48	CTCF	chr16:70473100-70473250	NHEK	skin:	n/a	n/a
49	CTCF	chr16:70473100-70473250	HepG2	liver:	n/a	n/a
50	CTCF	chr16:70472620-70472770	GM12869	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:70472963-70473013	Jurkat	blood:	n/a
2	chr16:70472963-70473013	U87	brain:	n/a
3	chr16:70472477-70472527	HUVEC	blood vessel:	n/a
4	chr16:70472589-70472639	K562	blood:	n/a
5	chr16:70472589-70472639	HAEpiC	amniotic membrane:	n/a
6	chr16:70472993-70473043	HepG2	liver:	n/a
7	chr16:70472678-70472728	HIPEpiC	eye:	n/a
8	chr16:70472678-70472728	T-47D	breast:	n/a
9	chr16:70472589-70472639	SK-N-SH_RA	brain:	n/a
10	chr16:70472963-70473013	HRPEpiC	eye:	n/a
11	chr16:70472678-70472728	GM12892	blood:	n/a
12	chr16:70473841-70473891	LNCaP	prostate:	n/a
13	chr16:70472678-70472728	Jurkat	blood:	n/a
14	chr16:70472589-70472639	Hepatocyte	liver:	n/a
15	chr16:70472589-70472639	NT2-D1	testis:	n/a
16	chr16:70472678-70472728	HEK293	kidney:	embryo
17	chr16:70473648-70473698	HAEpiC	amniotic membrane:	n/a
18	chr16:70472477-70472527	HCT-116	colon:	n/a
19	chr16:70473648-70473698	CMK	blood:	n/a
20	chr16:70473316-70473366	HL-60	blood:	n/a
21	chr16:70473447-70473497	RPTEC	kidney:	n/a
22	chr16:70472589-70472639	MCF10A-Er-Src	breast:	n/a
23	chr16:70472993-70473043	NH-A	brain:	n/a
24	chr16:70473841-70473891	Caco-2	colon:	n/a
25	chr16:70472589-70472639	NHBE	bronchial:	n/a
26	chr16:70473316-70473366	ECC-1	luminal epithelium:	n/a
27	chr16:70472678-70472728	Caco-2	colon:	n/a
28	chr16:70473316-70473366	PrEC	prostate:	n/a
29	chr16:70473841-70473891	K562	blood:	n/a
30	chr16:70472678-70472728	GM12891	blood:	n/a
31	chr16:70473447-70473497	K562	blood:	n/a
32	chr16:70472993-70473043	NB4	blood:	n/a
33	chr16:70472993-70473043	ovcar-3	ovarian:	n/a
34	chr16:70472589-70472639	AG10803	skin:	n/a
35	chr16:70472963-70473013	BE2_C	brain:	n/a
36	chr16:70472589-70472639	MCF-7	breast:	n/a
37	chr16:70472963-70473013	HAEpiC	amniotic membrane:	n/a
38	chr16:70472993-70473043	HNPCEpiC	eye:	n/a
39	chr16:70472993-70473043	K562	blood:	n/a
40	chr16:70472963-70473013	T-47D	breast:	n/a
41	chr16:70472993-70473043	PANC-1	pancreas:	n/a
42	chr16:70472678-70472728	NHBE	bronchial:	n/a
43	chr16:70473447-70473497	BJ	skin:	n/a
44	chr16:70472963-70473013	HUVEC	blood vessel:	n/a
45	chr16:70473841-70473891	AG04449	skin:	fetal
46	chr16:70473841-70473891	GM12892	blood:	n/a
47	chr16:70472963-70473013	LNCaP	prostate:	n/a
48	chr16:70473447-70473497	AG10803	skin:	n/a
49	chr16:70472477-70472527	HepG2	liver:	n/a
50	chr16:70472589-70472639	HL-60	blood:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:70472362..70474949-chr16:70478691..70481186,3	K562	blood:
2	chr16:70470847..70473025-chr16:70556099..70558287,2	K562	blood:
3	chr16:70471110..70472642-chr16:70476908..70478527,2	K562	blood:
4	chr16:70432075..70434927-chr16:70469206..70471536,2	K562	blood:
5	chr16:70471134..70474092-chr16:70555921..70560516,5	K562	blood:
6	chr16:70472717..70474630-chr16:70487093..70489671,2	MCF-7	breast:
7	chr16:70427347..70429652-chr16:70469861..70473258,4	K562	blood:
8	chr16:70414149..70416279-chr16:70469419..70471972,3	MCF-7	breast:
9	chr16:70431049..70433575-chr16:70469316..70471536,2	K562	blood:
10	chr16:70469678..70473680-chr16:70486697..70489592,5	K562	blood:
11	chr16:70321413..70324290-chr16:70473557..70475529,2	K562	blood:
12	chr16:70425305..70429574-chr16:70469861..70473545,6	K562	blood:
13	chr16:70470745..70475630-chr16:70476191..70481668,5	MCF-7	breast:
14	chr16:70384661..70386503-chr16:70470352..70471994,2	K562	blood:
15	chr16:70473375..70475549-chr16:70479370..70482339,3	MCF-7	breast:
16	chr16:70379526..70383319-chr16:70470652..70474068,4	K562	blood:
17	chr16:70470349..70472713-chr17:58712894..58714465,2	MCF-7	breast:
18	chr16:70472361..70474333-chr16:70486789..70489619,2	MCF-7	breast:
19	chr16:70470174..70475385-chr16:70486021..70489021,8	K562	blood:
20	chr16:70455430..70458238-chr16:70472208..70474351,2	MCF-7	breast:
21	chr16:70455763..70457596-chr16:70471554..70474518,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST3GAL2-1	chr16:70472852-70473140	NONHSAT143426

No data

Variant related genes	Relation type
ST3GAL2	TF binding region
ST3GAL2	CpG island
ENSG00000240043	chromatin interactions
ENSG00000189091	chromatin interactions
ENSG00000157350	chromatin interactions
ENSG00000157349	chromatin interactions
ENSG00000200153	chromatin interactions
ENSG00000261777	chromatin interactions
ENSG00000090861	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000157353	chromatin interactions
ENSG00000168872	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184176804	chr16:70471602-70471603	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs567778614	chr16:70471608-70471609	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs557553034	chr16:70471626-70471627	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs532656014	chr16:70471708-70471709	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs575782534	chr16:70471717-70471718	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs187289655	chr16:70471748-70471749	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs555081752	chr16:70471753-70471754	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs191960340	chr16:70471778-70471779	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs184386406	chr16:70471780-70471781	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs371149141	chr16:70471790-70471791	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs11863943	chr16:70471827-70471828	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs559054785	chr16:70471840-70471841	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs578215139	chr16:70471850-70471851	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs113163337	chr16:70471858-70471859	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs374208352	chr16:70471968-70471969	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs545333934	chr16:70471969-70471970	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs563882305	chr16:70471996-70471997	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs531169863	chr16:70472072-70472073	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs188381388	chr16:70472087-70472088	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs565711437	chr16:70472134-70472135	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs374212370	chr16:70472187-70472188	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs116840827	chr16:70472197-70472198	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs546987573	chr16:70472223-70472224	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs571522013	chr16:70472227-70472228	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs539722862	chr16:70472239-70472240	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs374476720	chr16:70472265-70472266	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs138210796	chr16:70472322-70472323	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs74658410	chr16:70472364-70472365	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs536069440	chr16:70472378-70472379	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs192918244	chr16:70472412-70472413	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs555118904	chr16:70472427-70472428	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs567372843	chr16:70472475-70472476	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs535270119	chr16:70472489-70472490	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs116127924	chr16:70472569-70472570	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs184338363	chr16:70472575-70472576	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs556315159	chr16:70472579-70472580	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs544979640	chr16:70472637-70472638	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs62049031	chr16:70472713-70472714	Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs113413800	chr16:70472829-70472830	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs575986555	chr16:70472883-70472884	Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	8 gene(s)	Overlapped CNVs	n/a
41	rs567688682	chr16:70472925-70472926	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
42	rs543275979	chr16:70472949-70472950	Weak transcription Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
43	rs561431742	chr16:70473088-70473089	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
44	rs528607823	chr16:70473101-70473102	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
45	rs545302385	chr16:70473121-70473122	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
46	rs540321223	chr16:70473138-70473139	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
47	rs558620184	chr16:70473146-70473147	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs572086458	chr16:70473172-70473173	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs565287317	chr16:70473237-70473238	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs532439027	chr16:70473294-70473295	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute myeloid leukemia	16864856	CNVD
Infiltrating lobular breast cancer	19191266	CNVD
T-cell lymphomas	19863542	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	21909424	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21806811	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20841430	CNVD
Ependymoma	20639864	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70465400-70471600	Weak transcription	Pancreas	Pancrea
2	chr16:70468600-70471600	Weak transcription	Aorta	Aorta
3	chr16:70469000-70471600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr16:70470000-70471600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr16:70470200-70471600	Enhancers	Placenta	Placenta
6	chr16:70470400-70471600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr16:70470400-70471600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr16:70470400-70471600	Enhancers	Ovary	ovary
9	chr16:70470400-70471800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
10	chr16:70470400-70471800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chr16:70470400-70472000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr16:70470400-70472000	Flanking Active TSS	NH-A	brain
13	chr16:70470400-70472400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr16:70470400-70472400	Flanking Active TSS	Hela-S3	cervix
15	chr16:70470600-70471600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr16:70470600-70471600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr16:70470600-70471600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr16:70470600-70471600	Flanking Active TSS	Fetal Lung	lung
19	chr16:70470600-70471600	Enhancers	Psoas Muscle	Psoas
20	chr16:70470600-70471600	Enhancers	Right Atrium	heart
21	chr16:70470600-70471600	Enhancers	HMEC	breast
22	chr16:70470600-70471800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr16:70470600-70471800	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr16:70470600-70472200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr16:70470600-70472200	Enhancers	Spleen	Spleen
26	chr16:70470600-70472200	Flanking Active TSS	A549	lung
27	chr16:70470600-70472400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr16:70470600-70472400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
29	chr16:70470600-70472400	Flanking Active TSS	HUVEC	blood vessel
30	chr16:70470600-70472600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
31	chr16:70470600-70472600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr16:70470800-70471600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr16:70470800-70471600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr16:70470800-70471600	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr16:70470800-70471600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr16:70470800-70471600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr16:70470800-70471600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr16:70470800-70471600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr16:70470800-70471600	Enhancers	Liver	Liver
40	chr16:70470800-70471600	Enhancers	Brain Angular Gyrus	brain
41	chr16:70470800-70471600	Enhancers	Left Ventricle	heart
42	chr16:70470800-70471600	Flanking Active TSS	HepG2	liver
43	chr16:70470800-70471600	Flanking Active TSS	K562	blood
44	chr16:70470800-70471800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
45	chr16:70470800-70471800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr16:70470800-70471800	Flanking Active TSS	NHDF-Ad	bronchial
47	chr16:70470800-70472000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr16:70470800-70472000	Flanking Active TSS	Colon Smooth Muscle	Colon
49	chr16:70470800-70472200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr16:70470800-70472400	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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