Variant report

Variant	esv1801199
Chromosome Location	chr16:30376959-30382642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:812)
CpG islands
(count:855)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:812 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:30381841-30382730	K562	blood:	n/a	n/a
2	ARID3A	chr16:30381840-30382586	HepG2	liver:	n/a	n/a
3	ATF1	chr16:30381831-30382639	K562	blood:	n/a	n/a
4	ATF2	chr16:30381832-30382716	GM12878	blood:	n/a	n/a
5	BACH1	chr16:30382461-30382468	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr16:30381694-30381935	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr16:30382349-30382624	K562	blood:	n/a	n/a
8	BHLHE40	chr16:30381719-30382156	HepG2	liver:	n/a	n/a
9	BRCA1	chr16:30381780-30382566	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr16:30381901-30382711	K562	blood:	n/a	n/a
11	CCNT2	chr16:30381549-30381951	K562	blood:	n/a	n/a
12	CCNT2	chr16:30382322-30382618	K562	blood:	n/a	chr16:30382564-30382573
13	CEBPB	chr16:30379756-30380104	IMR90	lung:	n/a	n/a
14	CEBPB	chr16:30379804-30380044	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr16:30382167-30382189	A549	lung:	n/a	n/a
16	CEBPB	chr16:30379865-30380054	K562	blood:	n/a	n/a
17	CEBPB	chr16:30381031-30381038	HepG2	liver:	n/a	n/a
18	CEBPB	chr16:30379113-30379247	HepG2	liver:	n/a	n/a
19	CEBPD	chr16:30381558-30381826	HepG2	liver:	n/a	n/a
20	CEBPD	chr16:30381271-30381897	HepG2	liver:	n/a	n/a
21	CEBPZ	chr16:30381766-30382611	HepG2	liver:	n/a	n/a
22	CHD2	chr16:30381649-30382654	Hela-S3	cervix:	n/a	chr16:30381753-30381763
23	CHD2	chr16:30381686-30382634	H1-hESC	embryonic stem cell:	n/a	chr16:30381753-30381763
24	CHD2	chr16:30381761-30382633	K562	blood:	n/a	n/a
25	CHD2	chr16:30381713-30382691	GM12878	blood:	n/a	chr16:30381753-30381763
26	CHD2	chr16:30381693-30382498	HepG2	liver:	n/a	chr16:30381753-30381763
27	CREB1	chr16:30381152-30382878	HepG2	liver:	n/a	n/a
28	CREB1	chr16:30381792-30382679	ECC-1	luminal epithelium:	n/a	n/a
29	CREB1	chr16:30381657-30382628	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr16:30381728-30382582	A549	lung:	n/a	n/a
31	CREB1	chr16:30381548-30382813	GM12878	blood:	n/a	n/a
32	CREB1	chr16:30381319-30382840	HepG2	liver:	n/a	n/a
33	CREB1	chr16:30381691-30382668	ECC-1	luminal epithelium:	n/a	n/a
34	CREB1	chr16:30381562-30382977	GM12878	blood:	n/a	n/a
35	CREB1	chr16:30381780-30382672	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr16:30381650-30382752	K562	blood:	n/a	n/a
37	CREB1	chr16:30381479-30382694	A549	lung:	n/a	n/a
38	CTBP2	chr16:30382374-30382713	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr16:30382620-30382770	AoAF	blood vessel:	n/a	n/a
40	CTCF	chr16:30381420-30381570	AG04449	skin:	n/a	n/a
41	CTCF	chr16:30382406-30382566	MCF-7	breast:	n/a	chr16:30382478-30382491 chr16:30382475-30382493
42	CTCF	chr16:30382600-30382750	GM12871	blood:	n/a	n/a
43	CTCF	chr16:30382389-30382669	K562	blood:	n/a	chr16:30382478-30382491 chr16:30382475-30382493
44	CTCF	chr16:30382360-30382510	AG09309	skin:	n/a	chr16:30382478-30382491 chr16:30382475-30382493
45	CTCF	chr16:30382391-30382579	K562	blood:	n/a	chr16:30382478-30382491 chr16:30382475-30382493
46	CTCF	chr16:30382380-30382530	AG04450	lung:	n/a	chr16:30382478-30382491 chr16:30382475-30382493
47	CTCF	chr16:30382380-30382530	HFF	foreskin:	n/a	chr16:30382478-30382491 chr16:30382475-30382493
48	CTCF	chr16:30382072-30382225	Spleen_OC	spleen:	n/a	n/a
49	CTCF	chr16:30381355-30381600	K562	blood:	n/a	n/a
50	CTCF	chr16:30382360-30382510	HUVEC	blood vessel:	n/a	chr16:30382478-30382491 chr16:30382475-30382493

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:30381303-30381353	NHDF-neo	bronchial:	n/a
2	chr16:30381303-30381353	NHDF-neo	bronchial:	n/a
3	chr16:30382066-30382116	A549	lung:	n/a
4	chr16:30380794-30380844	NB4	blood:	n/a
5	chr16:30380794-30380844	NHBE	bronchial:	n/a
6	chr16:30381677-30381727	HL-60	blood:	n/a
7	chr16:30380600-30380650	HUVEC	blood vessel:	n/a
8	chr16:30381677-30381727	PANC-1	pancreas:	n/a
9	chr16:30382066-30382116	BE2_C	brain:	n/a
10	chr16:30380794-30380844	AoSMC	blood vessel:	n/a
11	chr16:30382569-30382619	HMEC	breast:	n/a
12	chr16:30380794-30380844	HAEpiC	amniotic membrane:	n/a
13	chr16:30381303-30381353	HRCEpiC	kidney:	n/a
14	chr16:30381303-30381353	H1-hESC	embryonic stem cell:	embryo
15	chr16:30379585-30379635	GM06990	blood:	n/a
16	chr16:30382517-30382567	K562	blood:	n/a
17	chr16:30381677-30381727	BJ	skin:	n/a
18	chr16:30381109-30381159	HNPCEpiC	eye:	n/a
19	chr16:30382517-30382567	CMK	blood:	n/a
20	chr16:30382569-30382619	HCM	heart:	n/a
21	chr16:30379391-30379441	Hela-S3	cervix:	n/a
22	chr16:30382517-30382567	Hela-S3	cervix:	n/a
23	chr16:30381887-30381937	HUVEC	blood vessel:	n/a
24	chr16:30381109-30381159	PFSK-1	brain:	n/a
25	chr16:30379391-30379441	HCF	heart:	n/a
26	chr16:30381109-30381159	MCF-7	breast:	n/a
27	chr16:30379585-30379635	GM19239	blood:	n/a
28	chr16:30382569-30382619	GM06990	blood:	n/a
29	chr16:30380794-30380844	SK-N-SH	brain:	n/a
30	chr16:30382569-30382619	MCF10A-Er-Src	breast:	n/a
31	chr16:30379391-30379441	HNPCEpiC	eye:	n/a
32	chr16:30379585-30379635	HCF	heart:	n/a
33	chr16:30380794-30380844	PFSK-1	brain:	n/a
34	chr16:30381109-30381159	SK-N-SH	brain:	n/a
35	chr16:30381109-30381159	BJ	skin:	n/a
36	chr16:30380794-30380844	SK-N-SH_RA	brain:	n/a
37	chr16:30380006-30380056	HRE	kidney:	n/a
38	chr16:30380183-30380233	Caco-2	colon:	n/a
39	chr16:30382569-30382619	NT2-D1	testis:	n/a
40	chr16:30382066-30382116	PANC-1	pancreas:	n/a
41	chr16:30380006-30380056	IMR90	lung:	fetal
42	chr16:30381303-30381353	GM12878	blood:	n/a
43	chr16:30379391-30379441	AG09319	gingival:	n/a
44	chr16:30381887-30381937	HEK293	kidney:	embryo
45	chr16:30382517-30382567	SK-N-SH_RA	brain:	n/a
46	chr16:30381109-30381159	ECC-1	luminal epithelium:	n/a
47	chr16:30378782-30378832	GM19239	blood:	n/a
48	chr16:30382066-30382116	GM12878	blood:	n/a
49	chr16:30381677-30381727	HRPEpiC	eye:	n/a
50	chr16:30382066-30382116	SK-N-SH	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:30376477..30383094-chr16:30415979..30420163,8	MCF-7	breast:
2	chr16:30381350..30382003-chr17:56708904..56709454,2	Hela-S3	cervix:
3	chr16:30381426..30383001-chr16:30455584..30457801,2	MCF-7	breast:
4	chr16:30374941..30377851-chr16:30378291..30382008,9	K562	blood:
5	chr16:30378764..30380971-chr16:30419142..30421108,2	K562	blood:
6	chr16:30374634..30377122-chr16:30405649..30407903,2	K562	blood:
7	chr16:30380765..30382933-chr16:30403703..30406768,3	K562	blood:
8	chr16:30346170..30348596-chr16:30376800..30378752,2	MCF-7	breast:
9	chr16:30196751..30201052-chr16:30379113..30382636,3	MCF-7	breast:
10	chr16:30376934..30383374-chr16:30417165..30421108,8	K562	blood:
11	chr16:30381512..30383944-chr16:30455828..30458052,2	K562	blood:
12	chr16:30378594..30387256-chr16:30387352..30391288,21	MCF-7	breast:
13	chr16:30381703..30382505-chr16:30456763..30457379,2	K562	blood:
14	chr16:30368801..30385970-chr16:30403825..30413311,30	MCF-7	breast:
15	chr16:30381749..30384813-chr16:30709284..30711839,3	MCF-7	breast:
16	chr16:30101858..30103931-chr16:30381450..30384176,2	K562	blood:
17	chr16:30379558..30384763-chr16:30404117..30407449,5	MCF-7	breast:
18	chr16:30380806..30383330-chr16:30405774..30407377,2	K562	blood:
19	chr16:30376626..30379434-chr16:30417426..30420453,4	MCF-7	breast:
20	chr16:30381262..30384231-chr16:30661276..30663868,2	MCF-7	breast:
21	chr16:30344696..30347636-chr16:30378058..30380333,2	MCF-7	breast:
22	chr16:30381117..30384208-chr16:30417593..30420362,3	MCF-7	breast:
23	chr16:30374941..30377851-chr16:30378291..30382008,9	K562	blood:
24	chr1:27718866..27719686-chr16:30381542..30382345,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
MYLPF	TF binding region
TBC1D10B	TF binding region
MYLPF	CpG island
TBC1D10B	CpG island
ENSG00000180096	chromatin interactions
ENSG00000102879	chromatin interactions
ENSG00000179965	chromatin interactions
ENSG00000179918	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000181773	chromatin interactions
ENSG00000080603	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000183604	chromatin interactions
ENSG00000180209	chromatin interactions
ENSG00000261840	chromatin interactions
ENSG00000149922	chromatin interactions
ENSG00000156858	chromatin interactions
ENSG00000169221	chromatin interactions

Extended variants
information (count: 167 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:167 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11646130	chr16:30376959-30376960	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs543130803	chr16:30376979-30376980	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs113429036	chr16:30377009-30377010	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs79962611	chr16:30377018-30377019	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs145829463	chr16:30377211-30377212	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs537608407	chr16:30377214-30377215	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs183086683	chr16:30377316-30377317	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs373650561	chr16:30377330-30377331	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs372745470	chr16:30377345-30377346	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs34873078	chr16:30377390-30377391	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs148136749	chr16:30377438-30377439	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs574444239	chr16:30377455-30377456	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs541960300	chr16:30377547-30377548	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs188006082	chr16:30377592-30377593	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs558321896	chr16:30377718-30377719	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs546113344	chr16:30377721-30377722	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs193085888	chr16:30377751-30377752	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs141928643	chr16:30377787-30377788	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs112855426	chr16:30377824-30377825	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs576900028	chr16:30377826-30377827	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs185346591	chr16:30377832-30377833	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs537731251	chr16:30377833-30377834	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs79979430	chr16:30377837-30377838	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs74623897	chr16:30377838-30377839	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs190542671	chr16:30378009-30378010	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs533065633	chr16:30378028-30378029	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs529332336	chr16:30378081-30378082	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs150751503	chr16:30378134-30378135	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs376848910	chr16:30378227-30378228	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs192619938	chr16:30378274-30378275	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs370723533	chr16:30378308-30378309	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs551492817	chr16:30378329-30378330	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs570281007	chr16:30378408-30378409	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs537363787	chr16:30378494-30378495	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs9926923	chr16:30378521-30378522	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs567890307	chr16:30378531-30378532	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs535543704	chr16:30378551-30378552	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs74826977	chr16:30378589-30378590	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs367606326	chr16:30378590-30378591	Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs572183942	chr16:30378631-30378632	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs541099116	chr16:30378681-30378682	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs143426022	chr16:30378700-30378701	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs559157427	chr16:30378728-30378729	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs557490799	chr16:30378752-30378753	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs527374195	chr16:30378781-30378782	Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs543388473	chr16:30378859-30378860	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs561898934	chr16:30378949-30378950	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs573545381	chr16:30378978-30378979	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs541118092	chr16:30379018-30379019	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs184970889	chr16:30379035-30379036	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Hodgkin''s lymphoma	20651079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Autism	22566537	CNVD
Intellectual disability	22566537	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
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
Lung cancer	18438408	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	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
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Mental retardation	19951919	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21990379	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	22499536	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22513405	CNVD
Autism	22958593	CNVD
Autism	18184952	CNVD
Autism	19966786	CNVD
Autism	21394203	CNVD
Autism	21969575	CNVD
Autism	22241247	CNVD
Autism	20970697	CNVD
Autism	20942916	CNVD
Epilepsy	20970697	CNVD
Intellectual disability	22045946	CNVD
Mental retardation	19966786	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	18923514	CNVD
Obesity	21881559	CNVD
Obesity	21956041	CNVD
Autism	20659124	CNVD
Mental retardation	21062444	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	22885689	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	20970697	CNVD
Schizophrenia	20433910	CNVD
Schizophrenia	22241247	CNVD
Autism	19242545	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Intracranial ependymoma	16609018	CNVD
Schizophrenia	21399695	CNVD
Autism	21956041	CNVD
Disorders of sex development	21048976	CNVD
Autism	22067053	CNVD
Autism	18156158	CNVD
Mental retardation	20152051	CNVD
Autism	19218893	CNVD
Autism	21289514	CNVD
Schizophrenia	19855392	CNVD
neurodevelopmental Syndrome	20503337	CNVD
Benign familial neonatal-infantile seizures	21060786	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Cancer	21183584	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	21045282	CNVD
Neuroblastoma	20406844	CNVD
Autism	19050728	CNVD
Epilepsy	20923578	CNVD
Psychiatric disorder	19050728	CNVD
Schizophrenia	19348701	CNVD
Attention deficit hyperactivity disorder	19097825	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Breast cancer	20409316	CNVD
Severe combined immunodeficiency	19097825	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Autism	18522746	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:30367400-30377200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr16:30367400-30377200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr16:30367600-30378600	Weak transcription	Fetal Kidney	kidney
4	chr16:30367600-30378600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr16:30367600-30378800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr16:30367800-30378000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr16:30368000-30378600	Strong transcription	Fetal Stomach	stomach
8	chr16:30368200-30377200	Strong transcription	Sigmoid Colon	Sigmoid Colon
9	chr16:30368200-30377600	Strong transcription	Duodenum Smooth Muscle	Duodenum
10	chr16:30368200-30378000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr16:30368200-30378200	Strong transcription	Lung	lung
12	chr16:30368200-30378600	Strong transcription	Fetal Intestine Small	intestine
13	chr16:30368200-30379000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr16:30368400-30377200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr16:30368400-30377200	Strong transcription	Colon Smooth Muscle	Colon
16	chr16:30368400-30377400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr16:30368400-30377800	Strong transcription	Thymus	Thymus
18	chr16:30368400-30378000	Strong transcription	Fetal Muscle Leg	muscle
19	chr16:30368400-30378000	Strong transcription	Fetal Thymus	thymus
20	chr16:30368400-30378200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr16:30368400-30378800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr16:30368400-30378800	Weak transcription	HSMMtube	muscle
23	chr16:30368600-30377200	Strong transcription	Duodenum Mucosa	Duodenum
24	chr16:30368600-30377600	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr16:30368600-30377800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr16:30368600-30378000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr16:30368600-30378000	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr16:30368600-30378400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr16:30368800-30377000	Strong transcription	Primary B cells from peripheral blood	blood
30	chr16:30368800-30377000	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr16:30368800-30377200	Strong transcription	Osteobl	bone
32	chr16:30368800-30378600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr16:30369000-30377200	Strong transcription	Adipose Nuclei	Adipose
34	chr16:30369000-30377400	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr16:30369000-30378200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
36	chr16:30369000-30378200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr16:30369200-30377600	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr16:30369200-30378000	Strong transcription	Primary monocytes fromperipheralblood	blood
39	chr16:30369200-30378000	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr16:30369200-30378400	Strong transcription	Fetal Intestine Large	intestine
41	chr16:30369400-30377200	Strong transcription	Liver	Liver
42	chr16:30369400-30380000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr16:30370000-30378000	Weak transcription	Psoas Muscle	Psoas
44	chr16:30370400-30378000	Weak transcription	Stomach Mucosa	stomach
45	chr16:30370600-30378800	Weak transcription	H9 Cell Line	embryonic stem cell
46	chr16:30370800-30379000	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr16:30371000-30379200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr16:30371400-30377200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr16:30371600-30378800	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr16:30371800-30378800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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