Variant report

Variant	esv34108
Chromosome Location	chr16:81469090-81510471
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1806)
CpG islands
(count:1164)
Chromatin interactive
region (count:66)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1806 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81496408-81496516	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:81491370-81491732	K562	blood:	n/a	n/a
3	ARID3A	chr16:81482255-81482609	K562	blood:	n/a	n/a
4	ARID3A	chr16:81483167-81483278	K562	blood:	n/a	n/a
5	ARID3A	chr16:81498971-81499400	HepG2	liver:	n/a	n/a
6	ARID3A	chr16:81490481-81491047	HepG2	liver:	n/a	n/a
7	ARID3A	chr16:81485540-81486378	HepG2	liver:	n/a	n/a
8	ARID3A	chr16:81476830-81476831	HepG2	liver:	n/a	n/a
9	ARID3A	chr16:81491479-81491749	HepG2	liver:	n/a	n/a
10	ARID3A	chr16:81481788-81482488	HepG2	liver:	n/a	n/a
11	ARID3A	chr16:81484523-81484840	K562	blood:	n/a	n/a
12	ARID3A	chr16:81485624-81486205	K562	blood:	n/a	n/a
13	ARID3A	chr16:81502815-81503782	K562	blood:	n/a	n/a
14	ATF1	chr16:81503034-81503848	K562	blood:	n/a	n/a
15	ATF1	chr16:81485410-81486105	K562	blood:	n/a	n/a
16	ATF1	chr16:81491437-81491830	K562	blood:	n/a	n/a
17	ATF1	chr16:81478183-81478360	K562	blood:	n/a	n/a
18	ATF2	chr16:81503435-81503802	GM12878	blood:	n/a	n/a
19	ATF3	chr16:81478131-81478500	HepG2	liver:	n/a	chr16:81478316-81478323 chr16:81478313-81478324 chr16:81478316-81478326 chr16:81478313-81478326 chr16:81478315-81478326 chr16:81478313-81478326 chr16:81478316-81478326
20	ATF3	chr16:81478170-81478463	K562	blood:	n/a	chr16:81478316-81478323 chr16:81478313-81478324 chr16:81478316-81478326 chr16:81478313-81478326 chr16:81478315-81478326 chr16:81478313-81478326 chr16:81478316-81478326
21	ATF3	chr16:81478217-81478415	GM12878	blood:	n/a	chr16:81478316-81478323 chr16:81478313-81478324 chr16:81478316-81478326 chr16:81478313-81478326 chr16:81478315-81478326 chr16:81478313-81478326 chr16:81478316-81478326
22	ATF3	chr16:81491377-81491851	K562	blood:	n/a	n/a
23	ATF3	chr16:81478207-81478457	H1-hESC	embryonic stem cell:	n/a	chr16:81478316-81478323 chr16:81478313-81478324 chr16:81478316-81478326 chr16:81478313-81478326 chr16:81478315-81478326 chr16:81478313-81478326 chr16:81478316-81478326
24	ATF3	chr16:81491253-81491762	A549	lung:	n/a	n/a
25	BACH1	chr16:81491444-81491701	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr16:81491548-81491726	K562	blood:	n/a	n/a
27	BACH1	chr16:81477569-81477632	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr16:81478209-81478481	H1-hESC	embryonic stem cell:	n/a	n/a
29	BATF	chr16:81470021-81470325	GM12878	blood:	n/a	n/a
30	BCL3	chr16:81479534-81480243	A549	lung:	n/a	n/a
31	BCL3	chr16:81481003-81481657	A549	lung:	n/a	chr16:81481557-81481566
32	BCL3	chr16:81479929-81480640	A549	lung:	n/a	n/a
33	BHLHE40	chr16:81503570-81504198	GM12878	blood:	n/a	n/a
34	BHLHE40	chr16:81485454-81486102	K562	blood:	n/a	n/a
35	BHLHE40	chr16:81502912-81504111	K562	blood:	n/a	n/a
36	BHLHE40	chr16:81482153-81482449	K562	blood:	n/a	n/a
37	BHLHE40	chr16:81478092-81478621	GM12878	blood:	n/a	chr16:81478288-81478304 chr16:81478289-81478305
38	BHLHE40	chr16:81481941-81482563	HepG2	liver:	n/a	n/a
39	BHLHE40	chr16:81478257-81478686	HepG2	liver:	n/a	chr16:81478288-81478304 chr16:81478289-81478305
40	BHLHE40	chr16:81478953-81479204	K562	blood:	n/a	n/a
41	BHLHE40	chr16:81479639-81479884	GM12878	blood:	n/a	n/a
42	BHLHE40	chr16:81491143-81491912	K562	blood:	n/a	n/a
43	BHLHE40	chr16:81478189-81478695	K562	blood:	n/a	chr16:81478288-81478304 chr16:81478289-81478305
44	BHLHE40	chr16:81490256-81491713	HepG2	liver:	n/a	n/a
45	BHLHE40	chr16:81502519-81502520	K562	blood:	n/a	n/a
46	BHLHE40	chr16:81480235-81480415	K562	blood:	n/a	n/a
47	BHLHE40	chr16:81476582-81476848	GM12878	blood:	n/a	n/a
48	BHLHE40	chr16:81477238-81477474	K562	blood:	n/a	n/a
49	BHLHE40	chr16:81471643-81471699	K562	blood:	n/a	n/a
50	BHLHE40	chr16:81485436-81486355	HepG2	liver:	n/a	n/a

(count:1164 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81477864-81477914	GM12892	blood:	n/a
2	chr16:81506476-81506526	SKMC	muscle:	n/a
3	chr16:81480610-81480660	Hela-S3	cervix:	n/a
4	chr16:81480610-81480660	Caco-2	colon:	n/a
5	chr16:81491312-81491362	K562	blood:	n/a
6	chr16:81477864-81477914	GM12892	blood:	n/a
7	chr16:81506476-81506526	SKMC	muscle:	n/a
8	chr16:81480610-81480660	Hela-S3	cervix:	n/a
9	chr16:81480610-81480660	Caco-2	colon:	n/a
10	chr16:81491312-81491362	K562	blood:	n/a
11	chr16:81480610-81480660	AG04450	lung:	fetal
12	chr16:81481448-81481498	SAEC	small airway:	n/a
13	chr16:81478765-81478815	GM19239	blood:	n/a
14	chr16:81478990-81479040	K562	blood:	n/a
15	chr16:81480610-81480660	GM12891	blood:	n/a
16	chr16:81478765-81478815	AG04450	lung:	fetal
17	chr16:81484457-81484507	A549	lung:	n/a
18	chr16:81510145-81510195	BJ	skin:	n/a
19	chr16:81484457-81484507	H1-hESC	embryonic stem cell:	embryo
20	chr16:81474764-81474814	NB4	blood:	n/a
21	chr16:81506476-81506526	GM12892	blood:	n/a
22	chr16:81477864-81477914	MCF10A-Er-Src	breast:	n/a
23	chr16:81484457-81484507	BE2_C	brain:	n/a
24	chr16:81484457-81484507	HEEpiC	esophagus:	n/a
25	chr16:81478359-81478409	IMR90	lung:	fetal
26	chr16:81507328-81507378	HEEpiC	esophagus:	n/a
27	chr16:81478359-81478409	CMK	blood:	n/a
28	chr16:81477840-81477890	AG04449	skin:	fetal
29	chr16:81480551-81480601	NH-A	brain:	n/a
30	chr16:81477373-81477423	H1-hESC	embryonic stem cell:	embryo
31	chr16:81480610-81480660	SK-N-MC	brain:	n/a
32	chr16:81510145-81510195	GM19239	blood:	n/a
33	chr16:81474764-81474814	Caco-2	colon:	n/a
34	chr16:81507328-81507378	HUVEC	blood vessel:	n/a
35	chr16:81510145-81510195	AG04449	skin:	fetal
36	chr16:81480610-81480660	PFSK-1	brain:	n/a
37	chr16:81480551-81480601	IMR90	lung:	fetal
38	chr16:81479837-81479887	AG10803	skin:	n/a
39	chr16:81478990-81479040	ECC-1	luminal epithelium:	n/a
40	chr16:81506476-81506526	PANC-1	pancreas:	n/a
41	chr16:81479272-81479322	AoSMC	blood vessel:	n/a
42	chr16:81477840-81477890	HNPCEpiC	eye:	n/a
43	chr16:81478359-81478409	GM19239	blood:	n/a
44	chr16:81476518-81476568	LNCaP	prostate:	n/a
45	chr16:81478990-81479040	GM19239	blood:	n/a
46	chr16:81474764-81474814	AoSMC	blood vessel:	n/a
47	chr16:81484457-81484507	AG04449	skin:	fetal
48	chr16:81484457-81484507	HL-60	blood:	n/a
49	chr16:81477840-81477890	SKMC	muscle:	n/a
50	chr16:81507328-81507378	Hela-S3	cervix:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr16:81467736..81470910-chr16:81471366..81473360,3	MCF-7	breast:
2	chr16:81500553..81502385-chr16:81503708..81505589,2	MCF-7	breast:
3	chr16:81475858..81478568-chr16:81729319..81732099,2	K562	blood:
4	chr16:81490986..81492646-chr16:81531978..81534213,2	MCF-7	breast:
5	chr16:81476822..81479616-chr16:81528551..81531319,2	MCF-7	breast:
6	chr16:81482289..81484303-chr16:81490604..81493407,2	MCF-7	breast:
7	chr16:81067967..81070895-chr16:81477501..81479169,2	K562	blood:
8	chr16:81501153..81503002-chr16:81601427..81603985,2	K562	blood:
9	chr16:81422912..81425576-chr16:81496658..81498919,2	K562	blood:
10	chr16:81437645..81439695-chr16:81483087..81485039,2	MCF-7	breast:
11	chr16:81489735..81495358-chr16:81495824..81502529,7	MCF-7	breast:
12	chr16:81493353..81497487-chr16:81505659..81509589,4	MCF-7	breast:
13	chr16:81489735..81495358-chr16:81495824..81502529,7	MCF-7	breast:
14	chr16:81484368..81486187-chr16:81489220..81491535,2	MCF-7	breast:
15	chr16:81480768..81483026-chr16:81506735..81508794,2	MCF-7	breast:
16	chr16:81462213..81464618-chr16:81468888..81470732,2	MCF-7	breast:
17	chr16:81480285..81482687-chr16:81557234..81559498,2	K562	blood:
18	chr16:81490358..81492408-chr16:81493886..81495406,2	MCF-7	breast:
19	chr16:81347539..81350872-chr16:81478035..81482618,4	MCF-7	breast:
20	chr16:81479233..81481383-chr16:81669168..81671118,2	MCF-7	breast:
21	chr16:81490358..81492408-chr16:81493886..81495406,2	MCF-7	breast:
22	chr12:10554334..10554872-chr16:81477760..81478703,2	Hela-S3	cervix:
23	chr16:81477412..81480094-chr16:81509013..81511595,4	MCF-7	breast:
24	chr1:153939722..153940249-chr16:81477656..81478327,2	Hela-S3	cervix:
25	chr16:81486409..81487978-chr16:81548913..81551529,2	K562	blood:
26	chr16:81476183..81478436-chr16:81605516..81607162,2	K562	blood:
27	chr16:81480040..81482006-chr16:81671001..81673698,2	K562	blood:
28	chr16:81475472..81478406-chr16:81671837..81673759,2	MCF-7	breast:
29	chr16:81476563..81478400-chr16:81499399..81501663,2	MCF-7	breast:
30	chr16:81481928..81485099-chr16:81576354..81580756,4	K562	blood:
31	chr16:81465030..81467170-chr16:81468085..81470508,3	K562	blood:
32	chr16:81476956..81478649-chr16:81496180..81498094,2	MCF-7	breast:
33	chr16:81434018..81436498-chr16:81482154..81484633,2	K562	blood:
34	chr16:81273374..81275112-chr16:81481220..81483509,2	MCF-7	breast:
35	chr16:81498244..81500651-chr16:81691686..81694302,2	K562	blood:
36	chr16:81480566..81483421-chr16:81511394..81514320,4	MCF-7	breast:
37	chr16:81484666..81489373-chr16:81491892..81496112,4	MCF-7	breast:
38	chr16:81500553..81502385-chr16:81503708..81505589,2	MCF-7	breast:
39	chr16:81480210..81481743-chr16:81584414..81586701,2	K562	blood:
40	chr16:81490893..81492885-chr16:81614585..81616374,2	MCF-7	breast:
41	chr16:81476563..81478400-chr16:81499399..81501663,2	MCF-7	breast:
42	chr16:81480171..81484417-chr16:81492553..81495426,4	MCF-7	breast:
43	chr16:81506233..81509171-chr16:81529935..81531469,2	MCF-7	breast:
44	chr16:81504288..81507057-chr16:81508113..81511868,3	MCF-7	breast:
45	chr16:81488699..81490361-chr16:81495076..81496755,2	MCF-7	breast:
46	chr16:81482289..81484303-chr16:81490604..81493407,2	MCF-7	breast:
47	chr16:81484368..81486187-chr16:81489220..81491535,2	MCF-7	breast:
48	chr16:81493353..81497487-chr16:81505659..81509589,4	MCF-7	breast:
49	chr16:81486896..81488783-chr16:81605459..81607539,2	K562	blood:
50	chr16:81434998..81437971-chr16:81482154..81484687,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000260229	TF binding region
CMIP	TF binding region
ENSG00000260229	CpG island
CMIP	CpG island
ENSG00000153815	chromatin interactions
ENSG00000140043	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000197943	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000261609	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000064787	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000258653	chromatin interactions
ENSG00000260229	chromatin interactions

Extended variants
information (count: 2099 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2099 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11860316	chr16:81469090-81469091	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563411699	chr16:81469097-81469098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141817854	chr16:81469144-81469145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567503851	chr16:81469145-81469146	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs192414462	chr16:81469155-81469156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182090230	chr16:81469192-81469193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187222319	chr16:81469232-81469233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200472153	chr16:81469282-81469283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs28367160	chr16:81469306-81469307	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543349353	chr16:81469321-81469322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555171125	chr16:81469405-81469406	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147115144	chr16:81469490-81469491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556166300	chr16:81469519-81469520	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs138455430	chr16:81469554-81469555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532008126	chr16:81469594-81469595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs116728827	chr16:81469632-81469633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567025047	chr16:81469672-81469673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558932225	chr16:81469673-81469674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10468367	chr16:81469674-81469675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs5818335	chr16:81469675-81469676	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs142192854	chr16:81469676-81469677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs76266805	chr16:81469677-81469678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562406425	chr16:81469687-81469688	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs840116	chr16:81469690-81469691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569500357	chr16:81469716-81469717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559326401	chr16:81469729-81469730	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373947189	chr16:81469736-81469737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144010652	chr16:81469743-81469744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550005674	chr16:81469776-81469777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571754456	chr16:81469812-81469813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376065564	chr16:81469819-81469820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538768416	chr16:81469836-81469837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs554164580	chr16:81469839-81469840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191592996	chr16:81469840-81469841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558828371	chr16:81469875-81469876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182940281	chr16:81469900-81469901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370110474	chr16:81469912-81469913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs572278565	chr16:81469939-81469940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555334652	chr16:81469968-81469969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374319357	chr16:81469974-81469975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs576537105	chr16:81469978-81469979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs541079906	chr16:81470007-81470008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9927153	chr16:81470018-81470019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs187236665	chr16:81470058-81470059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576831896	chr16:81470060-81470061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78264268	chr16:81470077-81470078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529625671	chr16:81470111-81470112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558889298	chr16:81470156-81470157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200894758	chr16:81470183-81470184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529675659	chr16:81470199-81470200	Weak transcription Enhancers	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
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	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

Chromatin state (count:2694 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81463200-81469400	Weak transcription	Pancreas	Pancrea
2	chr16:81463200-81471600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr16:81466000-81469400	Weak transcription	NH-A	brain
4	chr16:81466000-81471600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr16:81466200-81469600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr16:81466200-81471400	Weak transcription	Osteobl	bone
7	chr16:81466800-81471400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr16:81466800-81471600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr16:81467200-81471600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr16:81467200-81471800	Weak transcription	A549	lung
11	chr16:81467400-81471000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr16:81467400-81471400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr16:81467600-81471000	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr16:81467600-81471400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr16:81467800-81470400	Weak transcription	Dnd41	blood
16	chr16:81467800-81471400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr16:81468400-81469800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr16:81468600-81469200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr16:81468600-81469400	Enhancers	Fetal Muscle Leg	muscle
20	chr16:81469000-81469200	Enhancers	Fetal Lung	lung
21	chr16:81469000-81469600	Enhancers	K562	blood
22	chr16:81469200-81470200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr16:81469400-81469600	Enhancers	NH-A	brain
24	chr16:81469600-81470600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr16:81469800-81473600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr16:81470200-81470400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr16:81470400-81470600	Enhancers	Dnd41	blood
28	chr16:81470600-81471000	Weak transcription	Dnd41	blood
29	chr16:81471000-81471800	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr16:81471000-81472400	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr16:81471000-81473000	Enhancers	Dnd41	blood
32	chr16:81471400-81471600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr16:81471400-81471600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr16:81471400-81471600	Bivalent Enhancer	HepG2	liver
35	chr16:81471400-81471800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr16:81471400-81472000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr16:81471400-81472000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr16:81471400-81472200	Enhancers	Primary hematopoietic stem cells	blood
39	chr16:81471400-81472200	Enhancers	HUVEC	blood vessel
40	chr16:81471400-81472200	Bivalent Enhancer	K562	blood
41	chr16:81471400-81472200	Enhancers	Osteobl	bone
42	chr16:81471600-81471800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr16:81471600-81471800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr16:81471600-81472200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr16:81471600-81472200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
46	chr16:81471600-81472200	Enhancers	NHEK	skin
47	chr16:81471600-81472400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr16:81471600-81472400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr16:81471600-81472800	Enhancers	Primary T cells fromperipheralblood	blood
50	chr16:81471600-81473000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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