Variant report

Variant	nsv1066333
Chromosome Location	chr16:74228790-74323927
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:588)
CpG islands
(count:366)
Chromatin interactive
region (count:55)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:588 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:74308954-74309313	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:74308886-74309309	K562	blood:	n/a	n/a
3	ATF1	chr16:74286277-74286473	K562	blood:	n/a	n/a
4	ATF1	chr16:74314393-74314660	K562	blood:	n/a	n/a
5	ATF1	chr16:74307917-74307980	K562	blood:	n/a	n/a
6	BACH1	chr16:74260681-74260746	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr16:74266888-74267069	GM12878	blood:	n/a	n/a
8	BHLHE40	chr16:74314437-74314616	K562	blood:	n/a	n/a
9	BHLHE40	chr16:74291122-74291234	GM12878	blood:	n/a	n/a
10	CBX3	chr16:74313152-74313467	K562	blood:	n/a	n/a
11	CCNT2	chr16:74315269-74315543	K562	blood:	n/a	n/a
12	CCNT2	chr16:74314382-74314666	K562	blood:	n/a	n/a
13	CCNT2	chr16:74311832-74312183	K562	blood:	n/a	chr16:74312036-74312056
14	CEBPB	chr16:74250203-74250419	HepG2	liver:	n/a	chr16:74250281-74250294 chr16:74250281-74250292 chr16:74250281-74250294 chr16:74250282-74250293 chr16:74250283-74250292 chr16:74250281-74250294
15	CEBPB	chr16:74286332-74286582	H1-hESC	embryonic stem cell:	n/a	chr16:74286439-74286450
16	CEBPB	chr16:74286263-74286633	K562	blood:	n/a	chr16:74286439-74286450
17	CEBPB	chr16:74238706-74238796	IMR90	lung:	n/a	chr16:74238764-74238775
18	CEBPB	chr16:74286329-74286579	A549	lung:	n/a	chr16:74286439-74286450
19	CEBPB	chr16:74321894-74322022	K562	blood:	n/a	n/a
20	CEBPB	chr16:74238724-74238826	HepG2	liver:	n/a	chr16:74238764-74238775
21	CEBPB	chr16:74286262-74286631	HepG2	liver:	n/a	chr16:74286439-74286450
22	CEBPB	chr16:74286365-74286514	HepG2	liver:	n/a	chr16:74286439-74286450
23	CEBPB	chr16:74286272-74286542	K562	blood:	n/a	chr16:74286439-74286450
24	CEBPB	chr16:74250193-74250503	IMR90	lung:	n/a	chr16:74250281-74250294 chr16:74250281-74250292 chr16:74250281-74250294 chr16:74250282-74250293 chr16:74250283-74250292 chr16:74250281-74250294
25	CEBPB	chr16:74298624-74298723	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr16:74250204-74250323	K562	blood:	n/a	chr16:74250281-74250294 chr16:74250281-74250292 chr16:74250281-74250294 chr16:74250282-74250293 chr16:74250283-74250292 chr16:74250281-74250294
27	CEBPB	chr16:74321811-74322006	HepG2	liver:	n/a	n/a
28	CEBPB	chr16:74286293-74286506	K562	blood:	n/a	chr16:74286439-74286450
29	CEBPD	chr16:74314379-74314649	K562	blood:	n/a	n/a
30	CEBPD	chr16:74314359-74314758	K562	blood:	n/a	n/a
31	CTCF	chr16:74308980-74309130	HAc	cerebellar:	n/a	n/a
32	CTCF	chr16:74309380-74309530	AG09319	gingival:	n/a	n/a
33	CTCF	chr16:74309080-74309230	GM12867	blood:	n/a	chr16:74309126-74309147 chr16:74309131-74309149
34	CTCF	chr16:74260664-74260793	GM10248	blood:	n/a	chr16:74260703-74260721 chr16:74260698-74260719 chr16:74260705-74260718
35	CTCF	chr16:74260620-74260770	GM12866	blood:	n/a	chr16:74260703-74260721 chr16:74260698-74260719 chr16:74260705-74260718
36	CTCF	chr16:74309060-74309210	K562	blood:	n/a	chr16:74309126-74309147 chr16:74309131-74309149
37	CTCF	chr16:74260580-74260730	GM12864	blood:	n/a	chr16:74260703-74260721 chr16:74260698-74260719 chr16:74260705-74260718
38	CTCF	chr16:74260540-74260690	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr16:74317540-74317690	GM12873	blood:	n/a	n/a
40	CTCF	chr16:74308980-74309130	SAEC	small airway:	n/a	n/a
41	CTCF	chr16:74309320-74309470	AG10803	skin:	n/a	n/a
42	CTCF	chr16:74260620-74260770	GM12868	blood:	n/a	chr16:74260703-74260721 chr16:74260698-74260719 chr16:74260705-74260718
43	CTCF	chr16:74260640-74260790	MCF-7	breast:	n/a	chr16:74260703-74260721 chr16:74260698-74260719 chr16:74260705-74260718
44	CTCF	chr16:74260583-74260987	HCT-116	colon:	n/a	chr16:74260703-74260721 chr16:74260698-74260719 chr16:74260705-74260718
45	CTCF	chr16:74309040-74309190	HMF	breast:	n/a	chr16:74309126-74309147 chr16:74309131-74309149
46	CTCF	chr16:74309040-74309190	HRPEpiC	eye:	n/a	chr16:74309126-74309147 chr16:74309131-74309149
47	CTCF	chr16:74309540-74309690	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr16:74308965-74309266	H1-hESC	embryonic stem cell:	n/a	chr16:74309126-74309147 chr16:74309131-74309149
49	CTCF	chr16:74309040-74309190	HEEpiC	esophagus:	n/a	chr16:74309126-74309147 chr16:74309131-74309149
50	CTCF	chr16:74260560-74260710	GM12865	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:74254113-74254163	HCT-116	colon:	n/a
2	chr16:74233200-74233250	SKMC	muscle:	n/a
3	chr16:74250313-74250363	NH-A	brain:	n/a
4	chr16:74249500-74249550	HNPCEpiC	eye:	n/a
5	chr16:74233200-74233250	ovcar-3	ovarian:	n/a
6	chr16:74310568-74310618	T-47D	breast:	n/a
7	chr16:74250313-74250363	BJ	skin:	n/a
8	chr16:74254113-74254163	U87	brain:	n/a
9	chr16:74254113-74254163	H1-hESC	embryonic stem cell:	embryo
10	chr16:74310568-74310618	RPTEC	kidney:	n/a
11	chr16:74249798-74249848	T-47D	breast:	n/a
12	chr16:74233200-74233250	HCPEpiC	choroid plexus:	n/a
13	chr16:74249500-74249550	BE2_C	brain:	n/a
14	chr16:74250313-74250363	AG09309	skin:	n/a
15	chr16:74254113-74254163	Caco-2	colon:	n/a
16	chr16:74249798-74249848	K562	blood:	n/a
17	chr16:74310568-74310618	HCPEpiC	choroid plexus:	n/a
18	chr16:74310568-74310618	NH-A	brain:	n/a
19	chr16:74310568-74310618	K562	blood:	n/a
20	chr16:74249798-74249848	HRPEpiC	eye:	n/a
21	chr16:74310568-74310618	IMR90	lung:	fetal
22	chr16:74233200-74233250	HUVEC	blood vessel:	n/a
23	chr16:74249500-74249550	HL-60	blood:	n/a
24	chr16:74249500-74249550	HUVEC	blood vessel:	n/a
25	chr16:74254113-74254163	K562	blood:	n/a
26	chr16:74310568-74310618	HNPCEpiC	eye:	n/a
27	chr16:74249500-74249550	NH-A	brain:	n/a
28	chr16:74254113-74254163	GM06990	blood:	n/a
29	chr16:74310568-74310618	AG04449	skin:	fetal
30	chr16:74249798-74249848	HNPCEpiC	eye:	n/a
31	chr16:74250313-74250363	HepG2	liver:	n/a
32	chr16:74310568-74310618	SK-N-MC	brain:	n/a
33	chr16:74250313-74250363	HL-60	blood:	n/a
34	chr16:74250313-74250363	H1-hESC	embryonic stem cell:	embryo
35	chr16:74233200-74233250	HAEpiC	amniotic membrane:	n/a
36	chr16:74310568-74310618	AG09319	gingival:	n/a
37	chr16:74249500-74249550	RPTEC	kidney:	n/a
38	chr16:74249500-74249550	HEK293	kidney:	embryo
39	chr16:74233200-74233250	Caco-2	colon:	n/a
40	chr16:74249798-74249848	Caco-2	colon:	n/a
41	chr16:74249798-74249848	ovcar-3	ovarian:	n/a
42	chr16:74249798-74249848	SAEC	small airway:	n/a
43	chr16:74233200-74233250	AoSMC	blood vessel:	n/a
44	chr16:74310568-74310618	BJ	skin:	n/a
45	chr16:74233200-74233250	AG04449	skin:	fetal
46	chr16:74310568-74310618	NB4	blood:	n/a
47	chr16:74254113-74254163	BE2_C	brain:	n/a
48	chr16:74250313-74250363	HCPEpiC	choroid plexus:	n/a
49	chr16:74310568-74310618	GM12892	blood:	n/a
50	chr16:74233200-74233250	PFSK-1	brain:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:74260260..74261155-chr16:74308724..74309531,4	MCF-7	breast:
2	chr16:74262699..74265375-chr16:74267614..74270176,2	K562	blood:
3	chr16:74252229..74253733-chr16:74255287..74256912,2	K562	blood:
4	chr16:74317863..74320560-chr16:74322294..74325340,4	K562	blood:
5	chr16:74226754..74228837-chr16:74233306..74235343,2	K562	blood:
6	chr16:74317938..74319871-chr16:74323515..74325442,2	MCF-7	breast:
7	chr16:74276279..74277864-chr16:74338868..74341244,2	K562	blood:
8	chr16:74315500..74319684-chr16:74320288..74324568,5	K562	blood:
9	chr16:73990566..73991128-chr16:74260572..74261318,2	MCF-7	breast:
10	chr16:74311355..74313701-chr16:74317287..74319712,2	K562	blood:
11	chr16:74097985..74098900-chr16:74260227..74261150,3	MCF-7	breast:
12	chr16:74252229..74253733-chr16:74255287..74256912,2	K562	blood:
13	chr16:74069423..74070583-chr16:74308622..74309589,7	MCF-7	breast:
14	chr16:74317863..74320560-chr16:74322294..74325340,4	K562	blood:
15	chr16:74312086..74314734-chr16:74330934..74333737,2	K562	blood:
16	chr16:74233694..74235922-chr16:74237408..74239169,2	MCF-7	breast:
17	chr16:74221595..74224496-chr16:74229302..74231293,2	K562	blood:
18	chr16:74316550..74318420-chr16:74320671..74323348,2	MCF-7	breast:
19	chr16:74309954..74311613-chr16:74330276..74331845,2	MCF-7	breast:
20	chr16:74256645..74258476-chr16:74262562..74264855,2	MCF-7	breast:
21	chr16:73912290..73912990-chr16:74308865..74309503,2	MCF-7	breast:
22	chr16:74226754..74228837-chr16:74233306..74235343,2	K562	blood:
23	chr16:74233694..74235922-chr16:74237408..74239169,2	MCF-7	breast:
24	chr16:74256645..74258476-chr16:74262562..74264855,2	MCF-7	breast:
25	chr16:74275836..74277816-chr16:74285028..74286684,2	MCF-7	breast:
26	chr16:74260260..74261155-chr16:74308724..74309531,4	MCF-7	breast:
27	chr16:74287123..74288772-chr16:74308292..74310923,2	MCF-7	breast:
28	chr16:74272355..74274259-chr16:74299813..74302391,2	MCF-7	breast:
29	chr16:74098007..74098865-chr16:74308598..74309538,5	MCF-7	breast:
30	chr16:74311605..74313575-chr16:74314428..74316245,2	K562	blood:
31	chr16:74258760..74260294-chr16:74328794..74331064,2	MCF-7	breast:
32	chr16:74311605..74313575-chr16:74314428..74316245,2	K562	blood:
33	chr16:74316224..74318585-chr16:74330462..74332814,2	K562	blood:
34	chr16:74311355..74313701-chr16:74317287..74319712,2	K562	blood:
35	chr16:74069689..74070330-chr16:74308730..74309631,3	MCF-7	breast:
36	chr16:74316550..74318420-chr16:74320671..74323348,2	MCF-7	breast:
37	chr16:74262699..74265375-chr16:74267614..74270176,2	K562	blood:
38	chr16:74272355..74274259-chr16:74299813..74302391,2	MCF-7	breast:
39	chr16:74098142..74098838-chr16:74260245..74261120,2	MCF-7	breast:
40	chr16:74317938..74319871-chr16:74323515..74325442,2	MCF-7	breast:
41	chr16:74287123..74288772-chr16:74308292..74310923,2	MCF-7	breast:
42	chr16:74315898..74319035-chr16:74328257..74331798,3	MCF-7	breast:
43	chr16:74286339..74287913-chr16:74291970..74293491,2	MCF-7	breast:
44	chr16:74302601..74304809-chr16:74308002..74310214,2	MCF-7	breast:
45	chr16:74069299..74070320-chr16:74260061..74261105,4	MCF-7	breast:
46	chr16:74286339..74287913-chr16:74291970..74293491,2	MCF-7	breast:
47	chr16:74255170..74257506-chr16:74284177..74286100,2	MCF-7	breast:
48	chr16:74068477..74070420-chr16:74260250..74261186,10	MCF-7	breast:
49	chr16:74275836..74277816-chr16:74285028..74286684,2	MCF-7	breast:
50	chr16:74255170..74257506-chr16:74284177..74286100,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC009120.10.1-2	chr16:74299393-74302493	NONHSAT143661
2	lnc-CLEC18B-3	chr16:74239804-74240064	NONHSAT143657
3	lnc-CLEC18B-3	chr16:74249733-74249779	NONHSAT143657
4	lnc-AC009120.10.1-2	chr16:74302754-74302955	NONHSAT143661
5	lnc-CLEC18B-3	chr16:74239804-74240064	XLOC_012007
6	lnc-CLEC18B-3	chr16:74239804-74240064	XLOC_012007
7	lnc-CLEC18B-3	chr16:74244205-74244404	ENSG00000249447
8	lnc-CLEC18B-3	chr16:74249251-74249420	ENSG00000249447
9	lnc-CLEC18B-3	chr16:74244205-74244404	XLOC_012007
10	lnc-CLEC18B-3	chr16:74239690-74240064	XLOC_012007
11	lnc-CLEC18B-3	chr16:74239804-74240064	ENSG00000249447
12	lnc-CLEC18B-3	chr16:74239994-74240064	ENSG00000261404.1
13	lnc-CLEC18B-3	chr16:74239804-74240064	ENSG00000261404.1
14	lnc-CLEC18B-3	chr16:74249733-74250474	XLOC_012007
15	lnc-CLEC18B-3	chr16:74249865-74249888	XLOC_012007
16	lnc-AC009120.10.1-1	chr16:74320967-74321417	ENSG00000261248.1
17	lnc-CLEC18B-3	chr16:74244205-74244452	XLOC_012007
18	lnc-CLEC18B-3	chr16:74244205-74244404	NONHSAT143657
19	lnc-CLEC18B-3	chr16:74239542-74240064	XLOC_012007
20	lnc-AC009120.10.1-2	chr16:74302755-74302955	XLOC_011789
21	lnc-AC009120.10.1-2	chr16:74299394-74302493	XLOC_011789
22	lnc-AC009120.10.1-1	chr16:74316313-74316336	ENSG00000261248.1

No data

Variant related genes	Relation type
ENSG00000260471	TF binding region
ENSG00000261248	TF binding region
ENSG00000261404	TF binding region
ENSG00000260471	CpG island
ENSG00000261248	CpG island
ENSG00000261404	CpG island
ENSG00000103035	chromatin interactions
ENSG00000261404	chromatin interactions
ENSG00000261248	chromatin interactions
TGFBR2	miRNA target sites
HMGA1	miRNA target sites
FAM54B	miRNA target sites
NME4	miRNA target sites

Extended variants
information (count: 2942 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2942 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570724139	chr16:74228808-74228809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539394491	chr16:74228836-74228837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556504784	chr16:74228847-74228848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112158365	chr16:74228863-74228864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs150781777	chr16:74228903-74228904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370794744	chr16:74228910-74228911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183555223	chr16:74228915-74228916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541566027	chr16:74228921-74228922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540700221	chr16:74228944-74228945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs60876698	chr16:74228949-74228950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs560499865	chr16:74229035-74229036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372785994	chr16:74229042-74229043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529288374	chr16:74229098-74229099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200281	chr16:74229153-74229154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs187267385	chr16:74229169-74229170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74030831	chr16:74229175-74229176	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs548217623	chr16:74229185-74229186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561830242	chr16:74229192-74229193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139150639	chr16:74229229-74229230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113512684	chr16:74229254-74229255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149917970	chr16:74229257-74229258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533231565	chr16:74229290-74229291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549776773	chr16:74229353-74229354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146036698	chr16:74229354-74229355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139953411	chr16:74229415-74229416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555344157	chr16:74229424-74229425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565831894	chr16:74229429-74229430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538016731	chr16:74229469-74229470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117330054	chr16:74229506-74229507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200280	chr16:74229529-74229530	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs143625454	chr16:74229557-74229558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557648397	chr16:74229577-74229578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35106694	chr16:74229584-74229585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574389963	chr16:74229595-74229596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs375272727	chr16:74229600-74229601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541845943	chr16:74229645-74229646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183933217	chr16:74229651-74229652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527366741	chr16:74229667-74229668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188264810	chr16:74229668-74229669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564226417	chr16:74229685-74229686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532946937	chr16:74229687-74229688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113551569	chr16:74229696-74229697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569567727	chr16:74229735-74229736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529197460	chr16:74229736-74229737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192516195	chr16:74229822-74229823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565770287	chr16:74229827-74229828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185602147	chr16:74229849-74229850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368125432	chr16:74229851-74229852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs172060	chr16:74229882-74229883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs571724100	chr16:74229883-74229884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Breast cancer	17603634	CNVD
Prostate cancer	16573809	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 lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Poland''s syndrome	22110015	CNVD
Neuroblastoma	21899760	CNVD
Liver carcinoma	19366792	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	19156837	CNVD
Acute myeloid leukemia	17377590	CNVD
Breast cancer	20409316	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:74227200-74230000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr16:74231600-74231800	Enhancers	Rectal Smooth Muscle	rectum
3	chr16:74231800-74239600	Weak transcription	Rectal Smooth Muscle	rectum
4	chr16:74232000-74234600	Enhancers	Liver	Liver
5	chr16:74232800-74234400	Enhancers	Fetal Lung	lung
6	chr16:74232800-74234600	Enhancers	Stomach Mucosa	stomach
7	chr16:74233800-74234200	Enhancers	NHLF	lung
8	chr16:74233800-74235000	Enhancers	Gastric	stomach
9	chr16:74233800-74236400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr16:74234000-74234200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr16:74234400-74235600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr16:74235200-74236000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr16:74235600-74236400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr16:74239600-74240200	Enhancers	Rectal Smooth Muscle	rectum
15	chr16:74247200-74247400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr16:74250000-74250600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr16:74250200-74250600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr16:74253200-74254000	Enhancers	Fetal Lung	lung
19	chr16:74254000-74257400	Weak transcription	Fetal Lung	lung
20	chr16:74257400-74258000	Enhancers	Fetal Lung	lung
21	chr16:74257600-74257800	Enhancers	Fetal Stomach	stomach
22	chr16:74257800-74258800	Weak transcription	Fetal Stomach	stomach
23	chr16:74258000-74258400	Weak transcription	Fetal Lung	lung
24	chr16:74258400-74259000	Enhancers	Fetal Lung	lung
25	chr16:74258600-74258800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr16:74258800-74260000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr16:74258800-74260600	Enhancers	Fetal Stomach	stomach
28	chr16:74259000-74259200	Active TSS	Psoas Muscle	Psoas
29	chr16:74259000-74259600	Flanking Active TSS	Fetal Lung	lung
30	chr16:74259200-74259400	Enhancers	Fetal Muscle Leg	muscle
31	chr16:74259200-74259400	Flanking Active TSS	Psoas Muscle	Psoas
32	chr16:74259200-74260400	Enhancers	Fetal Brain Male	brain
33	chr16:74259200-74260400	Enhancers	Dnd41	blood
34	chr16:74259200-74260600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr16:74259400-74260000	Weak transcription	Colon Smooth Muscle	Colon
36	chr16:74259600-74260600	Enhancers	Fetal Lung	lung
37	chr16:74260000-74260200	Enhancers	Fetal Muscle Leg	muscle
38	chr16:74260000-74260400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr16:74260000-74260400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr16:74260000-74260400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr16:74260000-74260600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr16:74260000-74260600	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr16:74260000-74260600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr16:74260000-74260800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr16:74260000-74260800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr16:74260000-74261000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr16:74260000-74261000	Enhancers	Colon Smooth Muscle	Colon
48	chr16:74260200-74260400	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr16:74260200-74260600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr16:74260200-74260600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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