Variant report

Variant	nsv1058368
Chromosome Location	chr16:82029516-82152788
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1633)
CpG islands
(count:1649)
Chromatin interactive
region (count:104)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1633 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:82030746-82031028	K562	blood:	n/a	n/a
2	ARID3A	chr16:82115933-82117726	HepG2	liver:	n/a	n/a
3	ARID3A	chr16:82093606-82093975	HepG2	liver:	n/a	n/a
4	ARID3A	chr16:82089583-82090359	HepG2	liver:	n/a	n/a
5	ARID3A	chr16:82078193-82078428	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:82095460-82096457	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:82084411-82084959	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:82101178-82101501	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:82067492-82067597	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:82113187-82113930	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:82068380-82069032	HepG2	liver:	n/a	n/a
12	ATF1	chr16:82062715-82062915	K562	blood:	n/a	n/a
13	ATF1	chr16:82030720-82031082	K562	blood:	n/a	n/a
14	ATF1	chr16:82114661-82114765	K562	blood:	n/a	n/a
15	ATF1	chr16:82096406-82096697	K562	blood:	n/a	n/a
16	ATF1	chr16:82104326-82104461	K562	blood:	n/a	n/a
17	ATF1	chr16:82112112-82112365	K562	blood:	n/a	n/a
18	ATF1	chr16:82065155-82065355	K562	blood:	n/a	n/a
19	ATF1	chr16:82138925-82138954	K562	blood:	n/a	n/a
20	ATF3	chr16:82030806-82031006	K562	blood:	n/a	n/a
21	ATF3	chr16:82030756-82031066	K562	blood:	n/a	n/a
22	BACH1	chr16:82137189-82137191	K562	blood:	n/a	n/a
23	BACH1	chr16:82104509-82105032	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr16:82142916-82143193	GM12878	blood:	n/a	n/a
25	BATF	chr16:82116362-82116724	GM12878	blood:	n/a	chr16:82116546-82116557
26	BATF	chr16:82116361-82116774	GM12878	blood:	n/a	chr16:82116546-82116557
27	BCL3	chr16:82062723-82062977	GM12878	blood:	n/a	n/a
28	BCL3	chr16:82062677-82063053	GM12878	blood:	n/a	n/a
29	BCLAF1	chr16:82044862-82045288	GM12878	blood:	n/a	chr16:82045106-82045115
30	BCLAF1	chr16:82044872-82045285	GM12878	blood:	n/a	chr16:82045106-82045115
31	BCLAF1	chr16:82116435-82116713	GM12878	blood:	n/a	n/a
32	BHLHE40	chr16:82113873-82113886	HepG2	liver:	n/a	n/a
33	BHLHE40	chr16:82030649-82030962	K562	blood:	n/a	n/a
34	BHLHE40	chr16:82115821-82115866	K562	blood:	n/a	n/a
35	BHLHE40	chr16:82116388-82116902	HepG2	liver:	n/a	n/a
36	BRCA1	chr16:82030662-82030803	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr16:82080899-82081012	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr16:82044941-82045184	K562	blood:	n/a	n/a
39	CBX3	chr16:82042640-82042841	K562	blood:	n/a	n/a
40	CBX3	chr16:82042563-82042946	K562	blood:	n/a	n/a
41	CEBPB	chr16:82113635-82114071	HepG2	liver:	n/a	n/a
42	CEBPB	chr16:82096280-82096396	K562	blood:	n/a	n/a
43	CEBPB	chr16:82093688-82093868	HepG2	liver:	n/a	chr16:82093779-82093796
44	CEBPB	chr16:82122122-82122287	HepG2	liver:	n/a	n/a
45	CEBPB	chr16:82145685-82146347	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr16:82095229-82095863	IMR90	lung:	n/a	chr16:82095329-82095342 chr16:82095715-82095728 chr16:82095717-82095726 chr16:82095329-82095342 chr16:82095329-82095342 chr16:82095717-82095728 chr16:82095329-82095340 chr16:82095329-82095340
47	CEBPB	chr16:82095538-82095898	H1-hESC	embryonic stem cell:	n/a	chr16:82095715-82095728 chr16:82095717-82095726 chr16:82095717-82095728
48	CEBPB	chr16:82080999-82081187	IMR90	lung:	n/a	n/a
49	CEBPB	chr16:82031205-82031673	A549	lung:	n/a	n/a
50	CEBPB	chr16:82080316-82080319	HepG2	liver:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:82044788-82044838	HIPEpiC	eye:	n/a
2	chr16:82045183-82045233	ovcar-3	ovarian:	n/a
3	chr16:82044788-82044838	HIPEpiC	eye:	n/a
4	chr16:82045183-82045233	ovcar-3	ovarian:	n/a
5	chr16:82041595-82041645	HMEC	breast:	n/a
6	chr16:82044788-82044838	Jurkat	blood:	n/a
7	chr16:82132065-82132115	ECC-1	luminal epithelium:	n/a
8	chr16:82033681-82033731	CMK	blood:	n/a
9	chr16:82117013-82117063	HEEpiC	esophagus:	n/a
10	chr16:82045758-82045808	AG10803	skin:	n/a
11	chr16:82068803-82068853	IMR90	lung:	fetal
12	chr16:82048758-82048808	AG04450	lung:	fetal
13	chr16:82104638-82104688	HRPEpiC	eye:	n/a
14	chr16:82031434-82031484	LNCaP	prostate:	n/a
15	chr16:82045758-82045808	NHDF-neo	bronchial:	n/a
16	chr16:82078460-82078510	CMK	blood:	n/a
17	chr16:82068803-82068853	MCF-7	breast:	n/a
18	chr16:82045078-82045128	MCF-7	breast:	n/a
19	chr16:82031434-82031484	HL-60	blood:	n/a
20	chr16:82045758-82045808	PANC-1	pancreas:	n/a
21	chr16:82048758-82048808	AoSMC	blood vessel:	n/a
22	chr16:82031434-82031484	BE2_C	brain:	n/a
23	chr16:82044788-82044838	ovcar-3	ovarian:	n/a
24	chr16:82068803-82068853	ProgFib	skin:	n/a
25	chr16:82068702-82068752	AG09319	gingival:	n/a
26	chr16:82041595-82041645	HEK293	kidney:	embryo
27	chr16:82044788-82044838	NHDF-neo	bronchial:	n/a
28	chr16:82129088-82129138	HAEpiC	amniotic membrane:	n/a
29	chr16:82129088-82129138	Caco-2	colon:	n/a
30	chr16:82048758-82048808	Hepatocyte	liver:	n/a
31	chr16:82117013-82117063	GM19239	blood:	n/a
32	chr16:82045203-82045253	RPTEC	kidney:	n/a
33	chr16:82096597-82096647	GM12892	blood:	n/a
34	chr16:82068702-82068752	NH-A	brain:	n/a
35	chr16:82104638-82104688	NHDF-neo	bronchial:	n/a
36	chr16:82044960-82045010	HRCEpiC	kidney:	n/a
37	chr16:82041595-82041645	HepG2	liver:	n/a
38	chr16:82067445-82067495	AG04449	skin:	fetal
39	chr16:82031434-82031484	A549	lung:	n/a
40	chr16:82044788-82044838	Caco-2	colon:	n/a
41	chr16:82045222-82045272	NB4	blood:	n/a
42	chr16:82048758-82048808	HEEpiC	esophagus:	n/a
43	chr16:82068702-82068752	MCF10A-Er-Src	breast:	n/a
44	chr16:82068702-82068752	GM12892	blood:	n/a
45	chr16:82031434-82031484	NT2-D1	testis:	n/a
46	chr16:82126267-82126317	GM12878	blood:	n/a
47	chr16:82045078-82045128	NHBE	bronchial:	n/a
48	chr16:82068980-82069030	SK-N-SH_RA	brain:	n/a
49	chr16:82048758-82048808	GM19239	blood:	n/a
50	chr16:82044957-82045007	NH-A	brain:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:82035415..82037702-chr16:82043551..82045082,2	MCF-7	breast:
2	chr16:81972632..81975511-chr16:82029375..82034440,5	MCF-7	breast:
3	chr16:82111015..82113316-chr16:82120148..82122366,2	MCF-7	breast:
4	chr16:82104751..82105655-chr16:82170497..82171564,4	MCF-7	breast:
5	chr16:82051682..82053515-chr16:82055462..82057301,2	MCF-7	breast:
6	chr16:82093387..82094131-chr16:82117369..82118164,3	MCF-7	breast:
7	chr16:64240204..64240760-chr16:82095477..82096225,2	MCF-7	breast:
8	chr16:82119460..82121680-chr16:82123785..82126010,2	MCF-7	breast:
9	chr16:82123378..82125016-chr16:82127857..82130334,2	K562	blood:
10	chr16:82094565..82097297-chr16:82099404..82102388,2	K562	blood:
11	chr16:82117593..82118221-chr16:82186289..82186795,2	MCF-7	breast:
12	chr16:81974029..81975094-chr16:82030141..82031465,7	MCF-7	breast:
13	chr16:82123385..82125267-chr16:82203354..82206097,2	K562	blood:
14	chr16:82123378..82125016-chr16:82127857..82130334,2	K562	blood:
15	chr16:82119460..82121680-chr16:82123785..82126010,2	MCF-7	breast:
16	chr16:82031950..82034782-chr16:82038461..82041370,3	K562	blood:
17	chr16:82095196..82096036-chr16:82263712..82264246,2	MCF-7	breast:
18	chr16:82044521..82045314-chr3:149470159..149470736,2	HCT-116	colon:
19	chr16:82117219..82118195-chr16:82138911..82139841,2	MCF-7	breast:
20	chr16:82029300..82030846-chr16:82035555..82037101,2	MCF-7	breast:
21	chr16:82030016..82033170-chr16:82033184..82036470,3	K562	blood:
22	chr16:82117219..82118195-chr16:82138911..82139841,3	MCF-7	breast:
23	chr16:82031112..82032708-chr16:82039797..82042760,2	MCF-7	breast:
24	chr16:81972807..81973396-chr16:82117292..82117826,2	MCF-7	breast:
25	chr16:82117283..82118187-chr16:82171594..82172375,3	MCF-7	breast:
26	chr16:82064842..82065598-chr16:82095362..82096218,4	MCF-7	breast:
27	chr16:82064842..82065598-chr16:82095362..82096218,4	MCF-7	breast:
28	chr16:82039216..82042021-chr16:82043959..82047046,3	MCF-7	breast:
29	chr1:45186606..45187940-chr16:82044607..82045675,4	HCT-116	colon:
30	chr16:82081727..82084645-chr16:82085577..82088514,2	MCF-7	breast:
31	chr16:82081727..82084645-chr16:82085577..82088514,2	MCF-7	breast:
32	chr16:82020585..82022664-chr16:82031489..82033612,2	MCF-7	breast:
33	chr16:82065223..82067133-chr16:82262887..82264649,2	MCF-7	breast:
34	chr16:82127698..82130155-chr16:82130878..82132469,2	MCF-7	breast:
35	chr16:82030016..82033170-chr16:82033184..82035673,3	K562	blood:
36	chr16:82030016..82033170-chr16:82033184..82035673,3	K562	blood:
37	chr16:81972421..81973396-chr16:82117292..82118076,5	MCF-7	breast:
38	chr16:82087347..82089906-chr16:82091633..82093166,2	K562	blood:
39	chr16:82043593..82046286-chr16:82047903..82050151,2	MCF-7	breast:
40	chr16:82094565..82097297-chr16:82099404..82102388,2	K562	blood:
41	chr16:82104757..82105690-chr16:82117301..82118203,5	MCF-7	breast:
42	chr16:82111015..82113316-chr16:82120148..82122366,2	MCF-7	breast:
43	chr16:82031112..82032708-chr16:82039797..82042760,2	MCF-7	breast:
44	chr16:82082499..82084016-chr16:82084295..82086029,2	K562	blood:
45	chr16:82069797..82071329-chr16:82092897..82095086,2	MCF-7	breast:
46	chr16:81974148..81975083-chr16:82064743..82066000,4	MCF-7	breast:
47	chr16:82064738..82065659-chr16:82263372..82264240,11	MCF-7	breast:
48	chr16:82031950..82034782-chr16:82038461..82041370,3	K562	blood:
49	chr16:82148823..82151078-chr16:82169723..82171440,2	K562	blood:
50	chr16:82117334..82118246-chr16:82170586..82171478,6	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SDR42E1-1	chr16:82096698-82096858	ENSG00000261235.1
2	lnc-SDR42E1-1	chr16:82077976-82078213	ENSG00000261235.1
3	lnc-SDR42E1-1	chr16:82077941-82078210	ENSG00000261235.1
4	lnc-SDR42E1-1	chr16:82085898-82086063	ENSG00000261235.1
5	lnc-SDR42E1-1	chr16:82096698-82096827	ENSG00000261235.1
6	lnc-SDR42E1-1	chr16:82104408-82104794	ENSG00000261235.1

No data

Variant related genes	Relation type
SDR42E1	TF binding region
HSD17B2	TF binding region
ENSG00000263636	TF binding region
ENSG00000261235	TF binding region
SDR42E1	CpG island
HSD17B2	CpG island
ENSG00000263636	CpG island
ENSG00000261235	CpG island
ENSG00000199377	chromatin interactions
ENSG00000263636	chromatin interactions
ENSG00000184860	chromatin interactions
ENSG00000114744	chromatin interactions
ENSG00000261235	chromatin interactions
ENSG00000261029	chromatin interactions
ENSG00000086696	chromatin interactions
ENSG00000135698	chromatin interactions
ENSG00000260682	chromatin interactions

Extended variants
information (count: 6654 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:6654 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536969270	chr16:82029552-82029553	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558503072	chr16:82029553-82029554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150760433	chr16:82029562-82029563	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139167820	chr16:82029580-82029581	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552696039	chr16:82029610-82029611	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs113949737	chr16:82029612-82029613	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs543164709	chr16:82029615-82029616	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs550954210	chr16:82029640-82029641	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs576645113	chr16:82029663-82029664	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs149903290	chr16:82029698-82029699	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs569278421	chr16:82029711-82029712	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs144960678	chr16:82029719-82029720	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs140284224	chr16:82029745-82029746	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs192335121	chr16:82029746-82029747	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs34143728	chr16:82029762-82029763	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs562999965	chr16:82029768-82029769	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs144169893	chr16:82029788-82029789	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs376608493	chr16:82029837-82029838	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs147777771	chr16:82029939-82029940	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs548337344	chr16:82029957-82029958	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs569779372	chr16:82029962-82029963	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs530818471	chr16:82030015-82030016	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs576457628	chr16:82030024-82030025	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs114985549	chr16:82030034-82030035	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs539402429	chr16:82030054-82030055	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs534272767	chr16:82030076-82030077	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs369241602	chr16:82030134-82030135	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs567778780	chr16:82030145-82030146	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs141809887	chr16:82030169-82030170	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs540110097	chr16:82030171-82030172	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs572694658	chr16:82030225-82030226	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs79139084	chr16:82030243-82030244	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs576603115	chr16:82030293-82030294	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs544094341	chr16:82030299-82030300	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76707329	chr16:82030319-82030320	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs577621825	chr16:82030324-82030325	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs74029333	chr16:82030352-82030353	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185515936	chr16:82030375-82030376	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs543905440	chr16:82030410-82030411	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs554596823	chr16:82030415-82030416	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs141069470	chr16:82030419-82030420	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs150213645	chr16:82030429-82030430	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs552069654	chr16:82030464-82030465	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs530663051	chr16:82030477-82030478	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs574603044	chr16:82030484-82030485	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs570371405	chr16:82030491-82030492	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs528383778	chr16:82030501-82030502	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs546158177	chr16:82030536-82030537	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs567743533	chr16:82030538-82030539	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs145465357	chr16:82030539-82030540	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16461572	CNVD

Chromatin state (count:1613 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82021600-82029600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr16:82021800-82030000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr16:82022000-82030000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr16:82023000-82031800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr16:82023600-82036600	Weak transcription	Fetal Kidney	kidney
6	chr16:82024400-82030400	Weak transcription	Small Intestine	intestine
7	chr16:82024600-82030000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr16:82024800-82032800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr16:82025200-82030000	Weak transcription	Fetal Intestine Large	intestine
10	chr16:82026400-82030000	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr16:82026600-82030200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr16:82026600-82031000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr16:82027000-82031200	Weak transcription	Fetal Lung	lung
14	chr16:82027400-82031400	Weak transcription	Primary B cells from peripheral blood	blood
15	chr16:82027400-82044200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr16:82027600-82030000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr16:82027600-82030200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr16:82027600-82033200	Weak transcription	Primary B cells from cord blood	blood
19	chr16:82027800-82041600	Strong transcription	Primary T cells from cord blood	blood
20	chr16:82028000-82029600	Enhancers	HUVEC	blood vessel
21	chr16:82028200-82029600	Weak transcription	NHEK	skin
22	chr16:82028200-82029800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr16:82028200-82030000	Weak transcription	Thymus	Thymus
24	chr16:82028200-82030400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr16:82028200-82031800	Enhancers	Placenta	Placenta
26	chr16:82028400-82030200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr16:82028400-82030200	Weak transcription	Liver	Liver
28	chr16:82028400-82031000	Weak transcription	Pancreas	Pancrea
29	chr16:82028400-82031600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr16:82028600-82030200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr16:82028600-82032000	Enhancers	Colon Smooth Muscle	Colon
32	chr16:82028800-82031000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr16:82028800-82031400	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr16:82028800-82031800	Enhancers	Stomach Smooth Muscle	stomach
35	chr16:82029000-82030000	Weak transcription	Colonic Mucosa	Colon
36	chr16:82029000-82030200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr16:82029000-82030200	Weak transcription	HMEC	breast
38	chr16:82029000-82030800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr16:82029000-82031000	Weak transcription	Fetal Intestine Small	intestine
40	chr16:82029000-82031600	Weak transcription	Gastric	stomach
41	chr16:82029000-82031800	Enhancers	Fetal Stomach	stomach
42	chr16:82029200-82031200	Enhancers	Stomach Mucosa	stomach
43	chr16:82029200-82031400	Weak transcription	Fetal Thymus	thymus
44	chr16:82029200-82032200	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr16:82029400-82030000	Weak transcription	A549	lung
46	chr16:82029400-82041400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr16:82029600-82029800	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr16:82029600-82030000	Strong transcription	NHEK	skin
49	chr16:82029600-82030400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr16:82029600-82031400	Flanking Active TSS	HUVEC	blood vessel

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