Variant report

Variant	esv3420456
Chromosome Location	chr16:80837001-80839399
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr16:80837137-80837466	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr16:80838415-80838640	GM12878	blood:	n/a	n/a
3	BRCA1	chr16:80837217-80837371	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr16:80838097-80838323	IMR90	lung:	n/a	n/a
5	CEBPB	chr16:80838023-80838336	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr16:80837162-80837373	Hela-S3	cervix:	n/a	n/a
7	CHD2	chr16:80838188-80838190	HepG2	liver:	n/a	n/a
8	CHD2	chr16:80838303-80838853	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr16:80837220-80837790	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr16:80837174-80837480	GM19238	blood:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
11	CTCF	chr16:80837147-80837497	K562	blood:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
12	CTCF	chr16:80837180-80837330	GM12870	blood:	n/a	n/a
13	CTCF	chr16:80838403-80838476	LNCaP	prostate:	n/a	n/a
14	CTCF	chr16:80837020-80837170	NHLF	lung:	n/a	n/a
15	CTCF	chr16:80837287-80837337	Medullo	brain:	n/a	n/a
16	CTCF	chr16:80837240-80837390	SAEC	small airway:	n/a	chr16:80837328-80837344
17	CTCF	chr16:80838086-80838207	GM12891	blood:	n/a	n/a
18	CTCF	chr16:80837262-80837375	SK-N-SH_RA	brain:	n/a	chr16:80837328-80837344
19	CTCF	chr16:80838078-80838182	Fibrobl	skin:	n/a	n/a
20	CTCF	chr16:80837200-80837350	HRE	kidney:	n/a	chr16:80837328-80837344
21	CTCF	chr16:80838380-80838530	GM12872	blood:	n/a	n/a
22	CTCF	chr16:80837240-80837390	AoAF	blood vessel:	n/a	chr16:80837328-80837344
23	CTCF	chr16:80838358-80838510	IMR90	lung:	n/a	n/a
24	CTCF	chr16:80837261-80837443	GM13976	blood:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
25	CTCF	chr16:80837191-80837447	ProgFib	skin:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
26	CTCF	chr16:80838433-80838490	LNCaP	prostate:	n/a	n/a
27	CTCF	chr16:80838347-80838512	HepG2	liver:	n/a	n/a
28	CTCF	chr16:80837192-80837444	GM12878	blood:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
29	CTCF	chr16:80837037-80837596	MCF-7	breast:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
30	CTCF	chr16:80837220-80837370	HA-sp	spinal cord:	n/a	chr16:80837328-80837344
31	CTCF	chr16:80838111-80838187	GM19238	blood:	n/a	n/a
32	CTCF	chr16:80837254-80837430	LNCaP	prostate:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
33	CTCF	chr16:80837209-80837421	MCF-7	breast:	n/a	chr16:80837328-80837344
34	CTCF	chr16:80838415-80838444	Gliobla	brain:	n/a	n/a
35	CTCF	chr16:80837260-80837410	GM06990	blood:	n/a	chr16:80837328-80837344
36	CTCF	chr16:80837201-80837447	MCF-7	breast:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
37	CTCF	chr16:80838100-80838109	MCF-7	breast:	n/a	n/a
38	CTCF	chr16:80837129-80837501	A549	lung:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
39	CTCF	chr16:80837220-80837370	BE2_C	brain:	n/a	chr16:80837328-80837344
40	CTCF	chr16:80837240-80837390	HUVEC	blood vessel:	n/a	chr16:80837328-80837344
41	CTCF	chr16:80837260-80837410	AG09319	gingival:	n/a	chr16:80837328-80837344
42	CTCF	chr16:80838360-80838510	GM12875	blood:	n/a	n/a
43	CTCF	chr16:80838381-80838509	GM10248	blood:	n/a	n/a
44	CTCF	chr16:80837220-80837370	HVMF	connective:	n/a	chr16:80837328-80837344
45	CTCF	chr16:80837240-80837390	HPAF	blood vessel:	n/a	chr16:80837328-80837344
46	CTCF	chr16:80837280-80837430	AG04449	skin:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
47	CTCF	chr16:80837173-80837468	K562	blood:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
48	CTCF	chr16:80838141-80838146	MCF-7	breast:	n/a	n/a
49	CTCF	chr16:80837198-80837468	H1-hESC	embryonic stem cell:	n/a	chr16:80837328-80837344 chr16:80837415-80837428
50	CTCF	chr16:80837280-80837430	GM12865	blood:	n/a	chr16:80837328-80837344 chr16:80837415-80837428

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:80839183-80839233	AG04450	lung:	fetal
2	chr16:80838258-80838308	HCT-116	colon:	n/a
3	chr16:80838265-80838315	NHDF-neo	bronchial:	n/a
4	chr16:80838265-80838315	AG09319	gingival:	n/a
5	chr16:80839183-80839233	NHDF-neo	bronchial:	n/a
6	chr16:80839183-80839233	HEEpiC	esophagus:	n/a
7	chr16:80838738-80838788	ovcar-3	ovarian:	n/a
8	chr16:80838265-80838315	SKMC	muscle:	n/a
9	chr16:80838258-80838308	Hepatocyte	liver:	n/a
10	chr16:80838738-80838788	CMK	blood:	n/a
11	chr16:80838738-80838788	MCF10A-Er-Src	breast:	n/a
12	chr16:80838258-80838308	T-47D	breast:	n/a
13	chr16:80839183-80839233	GM12891	blood:	n/a
14	chr16:80839183-80839233	Jurkat	blood:	n/a
15	chr16:80839183-80839233	SK-N-MC	brain:	n/a
16	chr16:80838258-80838308	HEEpiC	esophagus:	n/a
17	chr16:80838265-80838315	Jurkat	blood:	n/a
18	chr16:80839183-80839233	HUVEC	blood vessel:	n/a
19	chr16:80839183-80839233	AG10803	skin:	n/a
20	chr16:80838258-80838308	BE2_C	brain:	n/a
21	chr16:80838738-80838788	Jurkat	blood:	n/a
22	chr16:80838738-80838788	GM06990	blood:	n/a
23	chr16:80838265-80838315	HCT-116	colon:	n/a
24	chr16:80839183-80839233	Hepatocyte	liver:	n/a
25	chr16:80839183-80839233	SK-N-SH	brain:	n/a
26	chr16:80838265-80838315	AoSMC	blood vessel:	n/a
27	chr16:80839183-80839233	ProgFib	skin:	n/a
28	chr16:80838265-80838315	SK-N-MC	brain:	n/a
29	chr16:80839183-80839233	K562	blood:	n/a
30	chr16:80839183-80839233	HPAEpiC	pulmonary alveolar:	n/a
31	chr16:80839183-80839233	GM12878	blood:	n/a
32	chr16:80838258-80838308	HRE	kidney:	n/a
33	chr16:80838738-80838788	AG10803	skin:	n/a
34	chr16:80838258-80838308	SKMC	muscle:	n/a
35	chr16:80838258-80838308	AG10803	skin:	n/a
36	chr16:80838258-80838308	HAEpiC	amniotic membrane:	n/a
37	chr16:80838738-80838788	SKMC	muscle:	n/a
38	chr16:80838738-80838788	BJ	skin:	n/a
39	chr16:80838258-80838308	HEK293	kidney:	embryo
40	chr16:80838738-80838788	GM12892	blood:	n/a
41	chr16:80838258-80838308	BJ	skin:	n/a
42	chr16:80838738-80838788	SAEC	small airway:	n/a
43	chr16:80838738-80838788	HPAEpiC	pulmonary alveolar:	n/a
44	chr16:80838265-80838315	HEK293	kidney:	embryo
45	chr16:80838258-80838308	NT2-D1	testis:	n/a
46	chr16:80838265-80838315	HL-60	blood:	n/a
47	chr16:80839183-80839233	ECC-1	luminal epithelium:	n/a
48	chr16:80838265-80838315	CMK	blood:	n/a
49	chr16:80839183-80839233	HCF	heart:	n/a
50	chr16:80838738-80838788	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:80745711..80747675-chr16:80834808..80837555,2	MCF-7	breast:
2	chr16:80836267..80838116-chr16:81067816..81069508,2	MCF-7	breast:
3	chr16:80742029..80744707-chr16:80834367..80837032,2	MCF-7	breast:
4	chr16:80839103..80839861-chr16:80858662..80859582,2	K562	blood:
5	chr16:80653224..80655610-chr16:80835327..80837663,2	MCF-7	breast:
6	chr16:80838427..80840322-chr16:80885425..80887354,2	MCF-7	breast:
7	chr16:80573487..80575142-chr16:80836688..80838672,2	MCF-7	breast:
8	chr16:80744840..80746889-chr16:80835828..80837978,2	MCF-7	breast:
9	chr16:80836730..80839628-chr16:80867393..80871297,3	MCF-7	breast:

Variant related genes	Relation type
CDYL2	TF binding region
CDYL2	CpG island
ENSG00000260213	chromatin interactions
ENSG00000259867	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000260896	chromatin interactions
ENSG00000168589	chromatin interactions

Extended variants
information (count: 60 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:60 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554180134	chr16:80837004-80837005	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs74030456	chr16:80837008-80837009	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs575693239	chr16:80837034-80837035	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs34592681	chr16:80837035-80837036	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs539637971	chr16:80837052-80837053	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs117035243	chr16:80837120-80837121	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs149234971	chr16:80837137-80837138	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs368135853	chr16:80837139-80837140	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs540902264	chr16:80837218-80837219	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs372059733	chr16:80837221-80837222	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs562385382	chr16:80837235-80837236	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs573517624	chr16:80837242-80837243	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs375073851	chr16:80837257-80837258	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs192357487	chr16:80837258-80837259	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs562361334	chr16:80837275-80837276	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs73583957	chr16:80837284-80837285	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs562440594	chr16:80837294-80837295	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs114094868	chr16:80837363-80837364	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs144502647	chr16:80837370-80837371	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs559943399	chr16:80837376-80837377	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs527502757	chr16:80837384-80837385	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs548829286	chr16:80837406-80837407	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs567230291	chr16:80837426-80837427	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs375945143	chr16:80837451-80837452	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs535432952	chr16:80837480-80837481	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs550995630	chr16:80837693-80837694	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs183660830	chr16:80837812-80837813	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs539952247	chr16:80837892-80837893	Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs558307416	chr16:80838001-80838002	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs573442059	chr16:80838005-80838006	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs534402864	chr16:80838022-80838023	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs556049311	chr16:80838116-80838117	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs574322904	chr16:80838125-80838126	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs543853720	chr16:80838195-80838196	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs556158830	chr16:80838198-80838199	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs546535613	chr16:80838291-80838292	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs559992090	chr16:80838297-80838298	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs528498874	chr16:80838299-80838300	Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs569785346	chr16:80838491-80838492	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs187975120	chr16:80838577-80838578	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs544675651	chr16:80838622-80838623	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs559829057	chr16:80838716-80838717	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550112426	chr16:80838743-80838744	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs192609100	chr16:80838761-80838762	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs560843405	chr16:80838769-80838770	Bivalent/Poised TSS Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs560607378	chr16:80838864-80838865	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531668504	chr16:80838940-80838941	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550681457	chr16:80838941-80838942	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs374639170	chr16:80838942-80838943	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs184856496	chr16:80838954-80838955	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80822600-80837200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr16:80832400-80838800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr16:80836000-80837200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr16:80836400-80837200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr16:80836400-80837200	Enhancers	Gastric	stomach
6	chr16:80836400-80837600	Enhancers	Esophagus	oesophagus
7	chr16:80836400-80838200	Active TSS	Brain Angular Gyrus	brain
8	chr16:80836600-80837200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr16:80836600-80837400	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr16:80836600-80837400	Flanking Active TSS	HUVEC	blood vessel
11	chr16:80836600-80839000	Active TSS	HSMM	muscle
12	chr16:80836800-80837200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr16:80836800-80837200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr16:80836800-80837200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
15	chr16:80836800-80837200	Weak transcription	Fetal Intestine Small	intestine
16	chr16:80836800-80837200	Enhancers	Pancreas	Pancrea
17	chr16:80836800-80837200	Enhancers	Small Intestine	intestine
18	chr16:80836800-80837400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr16:80836800-80838600	Active TSS	Primary hematopoietic stem cells	blood
20	chr16:80836800-80838600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
21	chr16:80836800-80838800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
22	chr16:80836800-80838800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr16:80836800-80838800	Active TSS	NH-A	brain
24	chr16:80836800-80838800	Active TSS	NHEK	skin
25	chr16:80836800-80839000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr16:80836800-80839000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
27	chr16:80837000-80837200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr16:80837000-80837200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
29	chr16:80837000-80837200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr16:80837000-80837200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
31	chr16:80837000-80837200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
32	chr16:80837000-80837200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
33	chr16:80837000-80837200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr16:80837000-80837200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr16:80837000-80837200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
36	chr16:80837000-80837200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr16:80837000-80837200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr16:80837000-80837200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr16:80837000-80837200	Enhancers	Liver	Liver
40	chr16:80837000-80837200	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
41	chr16:80837000-80837200	Bivalent Enhancer	Brain Hippocampus Middle	brain
42	chr16:80837000-80837200	Bivalent/Poised TSS	Fetal Brain Female	brain
43	chr16:80837000-80837200	Flanking Active TSS	Placenta	Placenta
44	chr16:80837000-80837200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
45	chr16:80837000-80837200	Enhancers	Spleen	Spleen
46	chr16:80837000-80837200	Flanking Active TSS	Hela-S3	cervix
47	chr16:80837000-80837200	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
48	chr16:80837000-80837400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr16:80837000-80837400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
50	chr16:80837000-80837400	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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