Variant report

Variant	nsv572983
Chromosome Location	chr16:75539436-75575410
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1256)
CpG islands
(count:1344)
Chromatin interactive
region (count:88)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:75561718-75562303	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:75540441-75540853	K562	blood:	n/a	n/a
3	ARID3A	chr16:75551252-75551631	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:75551044-75551602	K562	blood:	n/a	n/a
5	ARID3A	chr16:75543367-75543781	K562	blood:	n/a	n/a
6	ARID3A	chr16:75540461-75540804	HepG2	liver:	n/a	n/a
7	ATF1	chr16:75543362-75543935	K562	blood:	n/a	n/a
8	ATF1	chr16:75540441-75540853	K562	blood:	n/a	n/a
9	ATF1	chr16:75551026-75551543	K562	blood:	n/a	n/a
10	ATF1	chr16:75539875-75540195	K562	blood:	n/a	n/a
11	ATF2	chr16:75551161-75551633	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr16:75550916-75551679	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr16:75551025-75551513	K562	blood:	n/a	chr16:75551099-75551107
14	ATF3	chr16:75543263-75543677	K562	blood:	n/a	n/a
15	BACH1	chr16:75550536-75551659	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr16:75549905-75550229	GM12878	blood:	n/a	n/a
17	BATF	chr16:75549927-75550130	GM12878	blood:	n/a	n/a
18	BCL3	chr16:75551134-75551652	A549	lung:	n/a	chr16:75551309-75551322
19	BCLAF1	chr16:75551137-75551633	GM12878	blood:	n/a	chr16:75551309-75551322
20	BHLHE40	chr16:75550976-75551669	K562	blood:	n/a	chr16:75551106-75551122 chr16:75551188-75551204 chr16:75551304-75551320
21	BHLHE40	chr16:75551111-75551605	GM12878	blood:	n/a	chr16:75551188-75551204 chr16:75551304-75551320
22	BHLHE40	chr16:75543277-75543975	K562	blood:	n/a	n/a
23	BHLHE40	chr16:75559972-75560220	K562	blood:	n/a	n/a
24	BHLHE40	chr16:75551026-75551554	HepG2	liver:	n/a	chr16:75551106-75551122 chr16:75551188-75551204 chr16:75551304-75551320
25	BHLHE40	chr16:75563977-75564136	K562	blood:	n/a	n/a
26	BRCA1	chr16:75551050-75551564	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr16:75540448-75540781	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr16:75551105-75551472	HepG2	liver:	n/a	n/a
29	BRCA1	chr16:75550999-75551543	H1-hESC	embryonic stem cell:	n/a	n/a
30	CBX3	chr16:75543145-75543731	K562	blood:	n/a	n/a
31	CBX3	chr16:75540292-75541038	HCT-116	colon:	n/a	n/a
32	CBX3	chr16:75540335-75541012	HCT-116	colon:	n/a	n/a
33	CBX3	chr16:75550890-75551727	K562	blood:	n/a	n/a
34	CBX3	chr16:75551286-75551594	K562	blood:	n/a	n/a
35	CCNT2	chr16:75550657-75551545	K562	blood:	n/a	n/a
36	CCNT2	chr16:75543308-75543999	K562	blood:	n/a	n/a
37	CEBPB	chr16:75540526-75540869	HepG2	liver:	n/a	chr16:75540740-75540753
38	CEBPB	chr16:75540344-75540947	Hela-S3	cervix:	n/a	chr16:75540397-75540410 chr16:75540740-75540753
39	CEBPB	chr16:75548039-75548460	K562	blood:	n/a	chr16:75548145-75548156 chr16:75548145-75548158 chr16:75548145-75548156
40	CEBPB	chr16:75540420-75540943	A549	lung:	n/a	chr16:75540740-75540753
41	CEBPB	chr16:75540223-75541088	HCT-116	colon:	n/a	chr16:75540397-75540410 chr16:75540740-75540753
42	CEBPB	chr16:75540413-75540869	K562	blood:	n/a	chr16:75540740-75540753
43	CEBPB	chr16:75543235-75543689	K562	blood:	n/a	n/a
44	CEBPB	chr16:75540403-75540915	ECC-1	luminal epithelium:	n/a	chr16:75540740-75540753
45	CEBPB	chr16:75540565-75540907	A549	lung:	n/a	chr16:75540740-75540753
46	CEBPB	chr16:75540415-75540882	K562	blood:	n/a	chr16:75540740-75540753
47	CEBPB	chr16:75551235-75551481	HepG2	liver:	n/a	n/a
48	CEBPB	chr16:75551163-75551617	HepG2	liver:	n/a	n/a
49	CEBPB	chr16:75551157-75551546	IMR90	lung:	n/a	n/a
50	CEBPB	chr16:75540508-75540916	MCF-7	breast:	n/a	chr16:75540740-75540753

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:75550118-75550168	GM12878	blood:	n/a
2	chr16:75572883-75572933	AG09319	gingival:	n/a
3	chr16:75550118-75550168	GM12878	blood:	n/a
4	chr16:75572883-75572933	AG09319	gingival:	n/a
5	chr16:75554060-75554110	HCT-116	colon:	n/a
6	chr16:75563280-75563330	SK-N-SH_RA	brain:	n/a
7	chr16:75563280-75563330	Caco-2	colon:	n/a
8	chr16:75551627-75551677	AG10803	skin:	n/a
9	chr16:75564221-75564271	GM12878	blood:	n/a
10	chr16:75568999-75569049	SAEC	small airway:	n/a
11	chr16:75550118-75550168	HCT-116	colon:	n/a
12	chr16:75554060-75554110	ProgFib	skin:	n/a
13	chr16:75551144-75551194	A549	lung:	n/a
14	chr16:75550118-75550168	ECC-1	luminal epithelium:	n/a
15	chr16:75564221-75564271	NT2-D1	testis:	n/a
16	chr16:75550927-75550977	NHBE	bronchial:	n/a
17	chr16:75551481-75551531	H1-hESC	embryonic stem cell:	embryo
18	chr16:75563009-75563059	IMR90	lung:	fetal
19	chr16:75563280-75563330	NB4	blood:	n/a
20	chr16:75551481-75551531	Hela-S3	cervix:	n/a
21	chr16:75554060-75554110	HepG2	liver:	n/a
22	chr16:75548557-75548607	NB4	blood:	n/a
23	chr16:75550927-75550977	HMEC	breast:	n/a
24	chr16:75550118-75550168	AG09319	gingival:	n/a
25	chr16:75568999-75569049	H1-hESC	embryonic stem cell:	embryo
26	chr16:75563489-75563539	PrEC	prostate:	n/a
27	chr16:75569164-75569214	Jurkat	blood:	n/a
28	chr16:75566465-75566515	Caco-2	colon:	n/a
29	chr16:75563280-75563330	K562	blood:	n/a
30	chr16:75572883-75572933	GM12892	blood:	n/a
31	chr16:75564221-75564271	SK-N-SH_RA	brain:	n/a
32	chr16:75550676-75550726	BJ	skin:	n/a
33	chr16:75563114-75563164	CMK	blood:	n/a
34	chr16:75572883-75572933	H1-hESC	embryonic stem cell:	embryo
35	chr16:75563901-75563951	LNCaP	prostate:	n/a
36	chr16:75564221-75564271	HUVEC	blood vessel:	n/a
37	chr16:75566465-75566515	AG09319	gingival:	n/a
38	chr16:75568999-75569049	SK-N-SH_RA	brain:	n/a
39	chr16:75569459-75569509	U87	brain:	n/a
40	chr16:75551481-75551531	LNCaP	prostate:	n/a
41	chr16:75563489-75563539	HCPEpiC	choroid plexus:	n/a
42	chr16:75563489-75563539	SAEC	small airway:	n/a
43	chr16:75550927-75550977	GM12891	blood:	n/a
44	chr16:75569852-75569902	AG09319	gingival:	n/a
45	chr16:75551481-75551531	GM06990	blood:	n/a
46	chr16:75550927-75550977	GM12878	blood:	n/a
47	chr16:75569164-75569214	MCF10A-Er-Src	breast:	n/a
48	chr16:75551144-75551194	SK-N-SH_RA	brain:	n/a
49	chr16:75563280-75563330	SK-N-MC	brain:	n/a
50	chr16:75563009-75563059	AG10803	skin:	n/a

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:62608635..62609543-chr16:75550660..75551562,3	Hela-S3	cervix:
2	chr16:75525799..75526656-chr16:75550606..75551571,3	MCF-7	breast:
3	chr16:75554986..75555868-chr16:75797911..75798528,2	MCF-7	breast:
4	chr16:75535711..75537222-chr16:75539478..75542235,2	MCF-7	breast:
5	chr16:75564501..75567219-chr16:75571368..75573194,2	K562	blood:
6	chr16:75551190..75551731-chr16:75654745..75655449,2	K562	blood:
7	chr16:75546074..75547889-chr16:75549218..75551422,3	K562	blood:
8	chr16:75549705..75551956-chr16:75553998..75556744,2	K562	blood:
9	chr16:75566186..75568910-chr16:75569034..75571524,2	MCF-7	breast:
10	chr16:75550007..75552554-chr16:75597669..75600323,2	MCF-7	breast:
11	chr16:75553671..75555315-chr16:75557566..75560051,2	K562	blood:
12	chr16:75539405..75541198-chr16:75546430..75548650,2	K562	blood:
13	chr16:75543492..75545467-chr16:75573221..75576000,2	K562	blood:
14	chr16:75568229..75570112-chr16:75587872..75589519,2	K562	blood:
15	chr16:75520122..75522617-chr16:75545167..75547600,2	MCF-7	breast:
16	chr16:75549910..75552098-chr16:75575318..75577076,2	MCF-7	breast:
17	chr16:75539405..75540962-chr16:75572342..75574110,2	K562	blood:
18	chr11:65271441..65272209-chr16:75551020..75551636,2	Hela-S3	cervix:
19	chr16:75505099..75506340-chr16:75550615..75551890,14	MCF-7	breast:
20	chr16:75496257..75499246-chr16:75542255..75545311,3	MCF-7	breast:
21	chr16:75542394..75545244-chr16:75549898..75552701,3	K562	blood:
22	chr16:75539387..75542121-chr16:75553084..75554957,2	MCF-7	breast:
23	chr16:75523790..75524565-chr16:75542425..75543396,2	K562	blood:
24	chr16:75536938..75540823-chr16:75549516..75552807,4	MCF-7	breast:
25	chr16:75497125..75499382-chr16:75564750..75566395,2	MCF-7	breast:
26	chr16:75554663..75556998-chr16:75557661..75561177,3	MCF-7	breast:
27	chr16:75553671..75555315-chr16:75557566..75560051,2	K562	blood:
28	chr16:75496257..75500180-chr16:75546505..75548984,3	MCF-7	breast:
29	chr16:75505348..75506153-chr16:75551055..75551869,3	MCF-7	breast:
30	chr16:75497752..75498618-chr16:75550411..75551452,5	Hela-S3	cervix:
31	chr16:75539405..75541198-chr16:75546430..75548650,2	K562	blood:
32	chr16:75549686..75552508-chr16:75588605..75590350,2	MCF-7	breast:
33	chr16:75536938..75540823-chr16:75549516..75552807,4	MCF-7	breast:
34	chr16:75539405..75540962-chr16:75572342..75574110,2	K562	blood:
35	chr16:75570762..75572723-chr16:75573865..75576124,2	K562	blood:
36	chr16:75550796..75551693-chr7:5569576..5570412,2	Hela-S3	cervix:
37	chr16:75550465..75552637-chr16:75558863..75560839,2	K562	blood:
38	chr16:75550671..75551452-chr22:50247463..50248018,2	HCT-116	colon:
39	chr16:75538464..75540762-chr16:75575477..75578098,2	MCF-7	breast:
40	chr16:75538570..75543222-chr16:75547718..75552328,5	MCF-7	breast:
41	chr16:75555083..75558060-chr16:75589292..75591957,2	MCF-7	breast:
42	chr16:75529289..75531150-chr16:75543079..75544974,2	K562	blood:
43	chr16:75548080..75552218-chr16:75679936..75683385,4	K562	blood:
44	chr16:75465566..75468619-chr16:75548282..75552307,4	MCF-7	breast:
45	chr1:154155243..154155810-chr16:75550915..75551583,2	Hela-S3	cervix:
46	chr16:75496672..75499382-chr16:75549463..75551344,4	MCF-7	breast:
47	chr16:75550675..75551536-chr2:122288289..122288930,2	Hela-S3	cervix:
48	chr16:75498381..75499126-chr16:75550587..75551534,2	K562	blood:
49	chr16:75541323..75546353-chr16:75547690..75552176,10	MCF-7	breast:
50	chr16:75574262..75576234-chr16:75588612..75590836,2	MCF-7	breast:

No data

Variant related genes	Relation type
CHST5	TF binding region
ENSG00000262583	TF binding region
CHST5	CpG island
ENSG00000262583	CpG island
ENSG00000153774	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000166848	chromatin interactions
ENSG00000050820	chromatin interactions
ENSG00000090432	chromatin interactions
ENSG00000262583	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000065427	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000135702	chromatin interactions
ENSG00000034713	chromatin interactions
ENSG00000166822	chromatin interactions
ENSG00000261717	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000075624	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000183196	chromatin interactions
ENSG00000100426	chromatin interactions
ENSG00000205084	chromatin interactions

Extended variants
information (count: 1750 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1750 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2550893	chr16:75539436-75539437	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545874273	chr16:75539461-75539462	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs117605261	chr16:75539480-75539481	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs149156452	chr16:75539493-75539494	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs56791151	chr16:75539517-75539518	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs34852438	chr16:75539518-75539519	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs12596528	chr16:75539550-75539551	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs147323651	chr16:75539599-75539600	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs190323	chr16:75539632-75539633	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs368805347	chr16:75539648-75539649	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs561034227	chr16:75539655-75539656	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs200699152	chr16:75539672-75539673	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs529826066	chr16:75539684-75539685	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs138114700	chr16:75539691-75539692	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs376551646	chr16:75539707-75539708	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs566653466	chr16:75539747-75539748	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs532442185	chr16:75539784-75539785	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs532557913	chr16:75539798-75539799	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs568530773	chr16:75539839-75539840	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs57829605	chr16:75539847-75539848	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs532590489	chr16:75539880-75539881	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs2550892	chr16:75539885-75539886	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs182115555	chr16:75539935-75539936	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs58986524	chr16:75540038-75540039	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs372632832	chr16:75540084-75540085	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs554391214	chr16:75540121-75540122	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs577416576	chr16:75540132-75540133	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs547765441	chr16:75540202-75540203	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs556561085	chr16:75540206-75540207	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs576524708	chr16:75540207-75540208	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs542268704	chr16:75540215-75540216	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs542072272	chr16:75540256-75540257	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs111398868	chr16:75540347-75540348	Flanking Active TSS Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs530014388	chr16:75540413-75540414	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs572549624	chr16:75540434-75540435	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs540010363	chr16:75540437-75540438	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs560306456	chr16:75540458-75540459	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs532274718	chr16:75540473-75540474	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs552076288	chr16:75540507-75540508	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113544502	chr16:75540567-75540568	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs77115465	chr16:75540605-75540606	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs531192337	chr16:75540611-75540612	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs547822786	chr16:75540626-75540627	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs187534263	chr16:75540636-75540637	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs549794569	chr16:75540681-75540682	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs191181480	chr16:75540692-75540693	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs375875674	chr16:75540698-75540699	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs547633553	chr16:75540719-75540720	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs571040257	chr16:75540764-75540765	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs540108002	chr16:75540765-75540766	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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	21806811	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Melanoma	22183965	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	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
Bipolar disorder	19114987	CNVD

Chromatin state (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:75529400-75550000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr16:75529600-75541800	Weak transcription	Right Atrium	heart
3	chr16:75529800-75550200	Weak transcription	Spleen	Spleen
4	chr16:75532600-75540000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr16:75532600-75549800	Weak transcription	Brain Anterior Caudate	brain
6	chr16:75532800-75550400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr16:75533800-75550200	Weak transcription	Small Intestine	intestine
8	chr16:75534200-75550400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr16:75534400-75550600	Weak transcription	Aorta	Aorta
10	chr16:75534600-75547400	Weak transcription	Fetal Intestine Small	intestine
11	chr16:75535600-75550200	Weak transcription	Brain Hippocampus Middle	brain
12	chr16:75535800-75543400	Weak transcription	HSMMtube	muscle
13	chr16:75536000-75550200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr16:75536200-75540000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr16:75536200-75540000	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr16:75536200-75550000	Weak transcription	Colon Smooth Muscle	Colon
17	chr16:75536400-75539800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr16:75536400-75549800	Weak transcription	Stomach Smooth Muscle	stomach
19	chr16:75536400-75550000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr16:75536400-75550000	Weak transcription	Brain Substantia Nigra	brain
21	chr16:75536600-75539600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr16:75536800-75540400	Weak transcription	Fetal Muscle Leg	muscle
23	chr16:75537200-75539800	Weak transcription	NHEK	skin
24	chr16:75537200-75540000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr16:75537600-75539800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr16:75538000-75539800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr16:75538000-75539800	Weak transcription	HMEC	breast
28	chr16:75538000-75540200	Weak transcription	A549	lung
29	chr16:75538000-75550000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr16:75538200-75541800	Weak transcription	Fetal Muscle Trunk	muscle
31	chr16:75538400-75546000	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr16:75538400-75550200	Weak transcription	Duodenum Mucosa	Duodenum
33	chr16:75539200-75541200	Enhancers	HepG2	liver
34	chr16:75539200-75543400	Enhancers	Hela-S3	cervix
35	chr16:75539400-75541200	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr16:75539600-75540000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr16:75539600-75540200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr16:75539600-75540800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr16:75539600-75541000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr16:75539800-75540200	Enhancers	Muscle Satellite Cultured Cells	--
41	chr16:75539800-75540400	Enhancers	Osteobl	bone
42	chr16:75539800-75541000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr16:75539800-75541000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr16:75539800-75541000	Enhancers	HMEC	breast
45	chr16:75539800-75541000	Enhancers	NHEK	skin
46	chr16:75540000-75540200	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr16:75540000-75540400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr16:75540000-75540400	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr16:75540000-75540400	Enhancers	Colonic Mucosa	Colon
50	chr16:75540000-75540600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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