Variant report

Variant	esv3392512
Chromosome Location	chr20:25565052-25567300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:286)
CpG islands
(count:610)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:25565236-25565725	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:25565954-25566222	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:25566452-25566585	HepG2	liver:	n/a	n/a
4	BACH1	chr20:25565874-25566218	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr20:25565131-25566237	A549	lung:	n/a	chr20:25565815-25565824 chr20:25565704-25565717 chr20:25565700-25565713 chr20:25565668-25565681 chr20:25565884-25565893 chr20:25565855-25565868 chr20:25565861-25565869
6	BHLHE40	chr20:25565204-25565583	HepG2	liver:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
7	BHLHE40	chr20:25565120-25566722	HepG2	liver:	n/a	chr20:25565810-25565826 chr20:25565361-25565382 chr20:25566118-25566134 chr20:25565368-25565377 chr20:25565365-25565378
8	BHLHE40	chr20:25565181-25565563	A549	lung:	n/a	chr20:25565361-25565382 chr20:25565368-25565377 chr20:25565365-25565378
9	BRCA1	chr20:25565815-25566240	HepG2	liver:	n/a	n/a
10	BRCA1	chr20:25565272-25565601	HepG2	liver:	n/a	n/a
11	CEBPB	chr20:25566030-25566286	HepG2	liver:	n/a	n/a
12	CEBPB	chr20:25565788-25566252	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr20:25566088-25566202	Hela-S3	cervix:	n/a	n/a
14	CEBPD	chr20:25565968-25566430	HepG2	liver:	n/a	n/a
15	CEBPD	chr20:25565677-25566382	HepG2	liver:	n/a	n/a
16	CHD1	chr20:25565917-25566098	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr20:25566563-25566635	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr20:25565158-25565699	HepG2	liver:	n/a	n/a
19	CHD2	chr20:25565618-25566239	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr20:25565925-25566211	HepG2	liver:	n/a	n/a
21	CHD2	chr20:25565806-25566020	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr20:25566465-25566673	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr20:25565074-25566728	HepG2	liver:	n/a	n/a
24	CREB1	chr20:25565417-25566409	A549	lung:	n/a	n/a
25	CTCF	chr20:25566400-25566550	AG04449	skin:	n/a	n/a
26	CTCF	chr20:25566320-25566470	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr20:25566440-25566590	HCM	heart:	n/a	n/a
28	CTCF	chr20:25565060-25565210	HPAF	blood vessel:	n/a	n/a
29	CTCF	chr20:25566460-25566610	HMF	breast:	n/a	n/a
30	CTCF	chr20:25566440-25566590	HRE	kidney:	n/a	n/a
31	CTCF	chr20:25566380-25566530	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr20:25566471-25566518	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr20:25566080-25566230	AG04449	skin:	n/a	n/a
34	CTCF	chr20:25566400-25566550	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr20:25565860-25566010	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr20:25566460-25566610	HMEC	breast:	n/a	n/a
37	CTCF	chr20:25565100-25565250	HCM	heart:	n/a	n/a
38	CTCF	chr20:25566620-25566770	AG10803	skin:	n/a	n/a
39	CTCF	chr20:25566400-25566550	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr20:25565080-25565230	AG09319	gingival:	n/a	n/a
41	CTCF	chr20:25566300-25566450	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr20:25566340-25566490	HAc	cerebellar:	n/a	n/a
43	CTCF	chr20:25566420-25566570	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr20:25566380-25566530	HEK293	kidney:	n/a	n/a
45	CTCF	chr20:25566380-25566530	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr20:25566480-25566630	AG04450	lung:	n/a	n/a
47	CTCF	chr20:25565100-25565250	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr20:25566500-25566650	A549	lung:	n/a	n/a
49	CTCF	chr20:25565120-25565270	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr20:25566460-25566610	HPF	lung:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25566563-25566613	K562	blood:	n/a
2	chr20:25566336-25566386	AG04450	lung:	fetal
3	chr20:25565879-25565929	PFSK-1	brain:	n/a
4	chr20:25566336-25566386	HEK293	kidney:	embryo
5	chr20:25565879-25565929	Hela-S3	cervix:	n/a
6	chr20:25566336-25566386	RPTEC	kidney:	n/a
7	chr20:25565879-25565929	GM06990	blood:	n/a
8	chr20:25566180-25566230	GM19239	blood:	n/a
9	chr20:25566180-25566230	PrEC	prostate:	n/a
10	chr20:25566178-25566228	HNPCEpiC	eye:	n/a
11	chr20:25566180-25566230	NT2-D1	testis:	n/a
12	chr20:25566336-25566386	SK-N-SH	brain:	n/a
13	chr20:25566563-25566613	SK-N-SH_RA	brain:	n/a
14	chr20:25566513-25566563	GM12878	blood:	n/a
15	chr20:25566563-25566613	HAEpiC	amniotic membrane:	n/a
16	chr20:25566382-25566432	IMR90	lung:	fetal
17	chr20:25566178-25566228	HCPEpiC	choroid plexus:	n/a
18	chr20:25566178-25566228	CMK	blood:	n/a
19	chr20:25566180-25566230	GM06990	blood:	n/a
20	chr20:25566470-25566520	GM19239	blood:	n/a
21	chr20:25565667-25565717	HepG2	liver:	n/a
22	chr20:25566470-25566520	GM06990	blood:	n/a
23	chr20:25566382-25566432	T-47D	breast:	n/a
24	chr20:25566513-25566563	SK-N-SH	brain:	n/a
25	chr20:25566513-25566563	SKMC	muscle:	n/a
26	chr20:25566382-25566432	GM12892	blood:	n/a
27	chr20:25566336-25566386	PrEC	prostate:	n/a
28	chr20:25566470-25566520	Hela-S3	cervix:	n/a
29	chr20:25565667-25565717	U87	brain:	n/a
30	chr20:25566336-25566386	SKMC	muscle:	n/a
31	chr20:25565460-25565510	HCF	heart:	n/a
32	chr20:25566470-25566520	NT2-D1	testis:	n/a
33	chr20:25566563-25566613	MCF10A-Er-Src	breast:	n/a
34	chr20:25566513-25566563	GM06990	blood:	n/a
35	chr20:25565879-25565929	NHDF-neo	bronchial:	n/a
36	chr20:25565667-25565717	SK-N-SH	brain:	n/a
37	chr20:25566470-25566520	NHBE	bronchial:	n/a
38	chr20:25566336-25566386	AG09319	gingival:	n/a
39	chr20:25566382-25566432	HRCEpiC	kidney:	n/a
40	chr20:25566336-25566386	PFSK-1	brain:	n/a
41	chr20:25566180-25566230	AG04449	skin:	fetal
42	chr20:25565879-25565929	LNCaP	prostate:	n/a
43	chr20:25566382-25566432	SK-N-SH_RA	brain:	n/a
44	chr20:25566563-25566613	ovcar-3	ovarian:	n/a
45	chr20:25566470-25566520	HL-60	blood:	n/a
46	chr20:25566513-25566563	SAEC	small airway:	n/a
47	chr20:25565879-25565929	GM12878	blood:	n/a
48	chr20:25565879-25565929	Caco-2	colon:	n/a
49	chr20:25566382-25566432	HCM	heart:	n/a
50	chr20:25565667-25565717	HPAEpiC	pulmonary alveolar:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:25476655..25479810-chr20:25563858..25567519,3	MCF-7	breast:
2	chr20:25564265..25567754-chr20:25602950..25606854,10	MCF-7	breast:
3	chr20:25565180..25567156-chr20:25676091..25678288,2	MCF-7	breast:
4	chr20:25566937..25569724-chr20:25600095..25602685,2	K562	blood:
5	chr20:25563758..25567670-chr20:25600746..25606260,10	MCF-7	breast:

No data

Variant related genes	Relation type
NINL	TF binding region
NINL	CpG island
ENSG00000213742	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000101004	chromatin interactions
ENSG00000130684	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7274550	chr20:25565052-25565053	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs150209811	chr20:25565117-25565118	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs138903570	chr20:25565168-25565169	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs569531719	chr20:25565183-25565184	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs369834781	chr20:25565210-25565211	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs376862172	chr20:25565224-25565225	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs371646504	chr20:25565228-25565229	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs6050690	chr20:25565239-25565240	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs555038049	chr20:25565256-25565257	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs377067771	chr20:25565285-25565286	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs571809090	chr20:25565299-25565300	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs534084701	chr20:25565324-25565325	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs13044596	chr20:25565328-25565329	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs113455160	chr20:25565329-25565330	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs56791487	chr20:25565394-25565395	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs376439833	chr20:25565402-25565403	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs546158584	chr20:25565418-25565419	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs149397804	chr20:25565438-25565439	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs576496373	chr20:25565450-25565451	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs375138158	chr20:25565463-25565464	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs542290917	chr20:25565468-25565469	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs562118075	chr20:25565482-25565483	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs527797215	chr20:25565485-25565486	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs547581597	chr20:25565487-25565488	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs117495226	chr20:25565515-25565516	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs560941504	chr20:25565519-25565520	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs533183196	chr20:25565546-25565547	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs6050691	chr20:25565552-25565553	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191187571	chr20:25565561-25565562	Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs560250611	chr20:25565617-25565618	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs535034537	chr20:25565650-25565651	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs142751587	chr20:25565671-25565672	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs113775785	chr20:25565730-25565731	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs372642972	chr20:25565736-25565737	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs534432757	chr20:25565768-25565769	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs182332054	chr20:25565823-25565824	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs55823215	chr20:25565828-25565829	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs577349464	chr20:25565860-25565861	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs542836053	chr20:25565886-25565887	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs540065935	chr20:25565970-25565971	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs571834239	chr20:25565973-25565974	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs35378951	chr20:25565994-25565995	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs562036836	chr20:25565997-25565998	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs556576107	chr20:25566014-25566015	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs576812171	chr20:25566058-25566059	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs542205669	chr20:25566080-25566081	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs370580106	chr20:25566085-25566086	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs35218603	chr20:25566091-25566092	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs555814365	chr20:25566121-25566122	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs60663806	chr20:25566146-25566147	Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25548800-25565200	Weak transcription	Esophagus	oesophagus
2	chr20:25558200-25565200	Weak transcription	Spleen	Spleen
3	chr20:25560400-25565200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr20:25560400-25565200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:25560600-25565200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr20:25561800-25565200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr20:25561800-25565200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr20:25561800-25565200	Weak transcription	Placenta	Placenta
9	chr20:25561800-25565200	Weak transcription	Gastric	stomach
10	chr20:25561800-25565200	Weak transcription	Lung	lung
11	chr20:25561800-25565200	Weak transcription	HMEC	breast
12	chr20:25563800-25566400	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr20:25564200-25566600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr20:25564600-25565200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr20:25564600-25566600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr20:25564800-25565200	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr20:25564800-25565200	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr20:25564800-25565200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr20:25564800-25565200	Flanking Active TSS	Fetal Stomach	stomach
20	chr20:25564800-25565600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr20:25564800-25566600	Active TSS	H9 Cell Line	embryonic stem cell
22	chr20:25564800-25566800	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr20:25565000-25565200	Flanking Active TSS	H1 Cell Line	embryonic stem cell
24	chr20:25565000-25565200	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr20:25565000-25565200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
26	chr20:25565000-25565200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr20:25565000-25565200	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr20:25565000-25565200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr20:25565000-25565200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr20:25565000-25565200	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr20:25565000-25565200	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr20:25565000-25565200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr20:25565000-25565200	Enhancers	Primary T killer memory cells from peripheral blood	blood
34	chr20:25565000-25565200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr20:25565000-25565200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr20:25565000-25565200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr20:25565000-25565200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr20:25565000-25565200	Enhancers	Adipose Nuclei	Adipose
39	chr20:25565000-25565200	Enhancers	Aorta	Aorta
40	chr20:25565000-25565200	Enhancers	Brain Substantia Nigra	brain
41	chr20:25565000-25565200	Active TSS	Colon Smooth Muscle	Colon
42	chr20:25565000-25565200	Enhancers	Duodenum Mucosa	Duodenum
43	chr20:25565000-25565200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
44	chr20:25565000-25565200	Enhancers	Fetal Heart	heart
45	chr20:25565000-25565200	Enhancers	Fetal Thymus	thymus
46	chr20:25565000-25565200	Enhancers	Pancreas	Pancrea
47	chr20:25565000-25565200	Enhancers	Placenta Amnion	Placenta Amnion
48	chr20:25565000-25565200	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr20:25565000-25565200	Active TSS	Right Atrium	heart
50	chr20:25565000-25565200	Enhancers	Right Ventricle	heart

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