Variant report

Variant	esv3326788
Chromosome Location	chr1:94701989-94704537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:416)
CpG islands
(count:916)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:416 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:94703115-94703411	HepG2	liver:	n/a	n/a
2	ATF3	chr1:94703191-94703418	K562	blood:	n/a	n/a
3	BACH1	chr1:94702412-94703480	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:94702792-94703439	HepG2	liver:	n/a	chr1:94703020-94703036
5	BRCA1	chr1:94702281-94702690	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr1:94703266-94703466	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr1:94702926-94703662	HCT-116	colon:	n/a	n/a
8	CCNT2	chr1:94703070-94703299	K562	blood:	n/a	n/a
9	CEBPB	chr1:94703179-94703407	Hela-S3	cervix:	n/a	n/a
10	CEBPD	chr1:94703007-94703432	HepG2	liver:	n/a	n/a
11	CHD2	chr1:94703159-94703549	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr1:94702519-94703480	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr1:94703052-94703520	HepG2	liver:	n/a	n/a
14	CREB1	chr1:94703041-94703685	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr1:94703057-94703562	K562	blood:	n/a	n/a
16	CREB1	chr1:94702943-94703626	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr1:94702378-94703584	HepG2	liver:	n/a	n/a
18	CREB1	chr1:94702908-94703446	A549	lung:	n/a	n/a
19	CTBP2	chr1:94702819-94703514	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr1:94703451-94703536	Medullo	brain:	n/a	n/a
21	CTCF	chr1:94703380-94703530	NHEK	skin:	n/a	n/a
22	CTCF	chr1:94702500-94702650	AG09309	skin:	n/a	n/a
23	CTCF	chr1:94702457-94702575	MCF-7	breast:	n/a	n/a
24	CTCF	chr1:94702440-94702590	HepG2	liver:	n/a	n/a
25	CTCF	chr1:94703420-94703570	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr1:94702540-94702690	HAc	cerebellar:	n/a	n/a
27	CTCF	chr1:94702420-94702570	HMEC	breast:	n/a	n/a
28	CTCF	chr1:94703420-94703570	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr1:94702440-94702590	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr1:94702500-94702650	BE2_C	brain:	n/a	n/a
31	CTCF	chr1:94702460-94702610	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr1:94702478-94702620	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr1:94703420-94703570	NHEK	skin:	n/a	n/a
34	CTCF	chr1:94702415-94702684	A549	lung:	n/a	n/a
35	CTCF	chr1:94702380-94702530	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr1:94702449-94702600	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:94702440-94702590	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr1:94702440-94702590	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr1:94702440-94702590	HRE	kidney:	n/a	n/a
40	CTCF	chr1:94702460-94702610	AG04450	lung:	n/a	n/a
41	CTCF	chr1:94702512-94702549	GM10266	blood:	n/a	n/a
42	CTCF	chr1:94703358-94703583	A549	lung:	n/a	n/a
43	CTCF	chr1:94703400-94703550	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr1:94702460-94702610	AG10803	skin:	n/a	n/a
45	CTCF	chr1:94702500-94702650	NHEK	skin:	n/a	n/a
46	CTCF	chr1:94702580-94702730	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr1:94703320-94703470	RPTEC	kidney:	n/a	n/a
48	CTCF	chr1:94702500-94702650	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr1:94703400-94703550	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr1:94702454-94702648	MCF-7	breast:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:94703167-94703217	HMEC	breast:	n/a
2	chr1:94703167-94703217	HMEC	breast:	n/a
3	chr1:94704048-94704098	HCPEpiC	choroid plexus:	n/a
4	chr1:94702435-94702485	BJ	skin:	n/a
5	chr1:94703343-94703393	HRE	kidney:	n/a
6	chr1:94703098-94703148	PrEC	prostate:	n/a
7	chr1:94703098-94703148	HEK293	kidney:	embryo
8	chr1:94703463-94703513	U87	brain:	n/a
9	chr1:94704048-94704098	HUVEC	blood vessel:	n/a
10	chr1:94703463-94703513	Jurkat	blood:	n/a
11	chr1:94702583-94702633	HRPEpiC	eye:	n/a
12	chr1:94703411-94703461	HCT-116	colon:	n/a
13	chr1:94703411-94703461	Hepatocyte	liver:	n/a
14	chr1:94702724-94702774	NHDF-neo	bronchial:	n/a
15	chr1:94702724-94702774	NB4	blood:	n/a
16	chr1:94703378-94703428	HepG2	liver:	n/a
17	chr1:94702435-94702485	ProgFib	skin:	n/a
18	chr1:94703098-94703148	HAEpiC	amniotic membrane:	n/a
19	chr1:94703343-94703393	AG04450	lung:	fetal
20	chr1:94704048-94704098	GM12891	blood:	n/a
21	chr1:94703167-94703217	HRCEpiC	kidney:	n/a
22	chr1:94702583-94702633	BJ	skin:	n/a
23	chr1:94704178-94704228	T-47D	breast:	n/a
24	chr1:94703507-94703557	HL-60	blood:	n/a
25	chr1:94703378-94703428	NT2-D1	testis:	n/a
26	chr1:94704178-94704228	HEEpiC	esophagus:	n/a
27	chr1:94703343-94703393	SK-N-MC	brain:	n/a
28	chr1:94703343-94703393	HUVEC	blood vessel:	n/a
29	chr1:94703079-94703129	AG04450	lung:	fetal
30	chr1:94703079-94703129	BE2_C	brain:	n/a
31	chr1:94703172-94703222	LNCaP	prostate:	n/a
32	chr1:94704048-94704098	HNPCEpiC	eye:	n/a
33	chr1:94703378-94703428	AG09319	gingival:	n/a
34	chr1:94703411-94703461	HMEC	breast:	n/a
35	chr1:94703172-94703222	AG09319	gingival:	n/a
36	chr1:94703343-94703393	HCM	heart:	n/a
37	chr1:94703098-94703148	NHBE	bronchial:	n/a
38	chr1:94703176-94703226	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:94703172-94703222	GM12878	blood:	n/a
40	chr1:94704178-94704228	HRE	kidney:	n/a
41	chr1:94702435-94702485	LNCaP	prostate:	n/a
42	chr1:94702435-94702485	HCT-116	colon:	n/a
43	chr1:94703463-94703513	AG09319	gingival:	n/a
44	chr1:94703507-94703557	Jurkat	blood:	n/a
45	chr1:94703463-94703513	T-47D	breast:	n/a
46	chr1:94703079-94703129	PrEC	prostate:	n/a
47	chr1:94704178-94704228	AoSMC	blood vessel:	n/a
48	chr1:94703378-94703428	AG10803	skin:	n/a
49	chr1:94704048-94704098	MCF10A-Er-Src	breast:	n/a
50	chr1:94703167-94703217	Jurkat	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:94526735..94527649-chr1:94702636..94703585,3	MCF-7	breast:
2	chr1:94702062..94702972-chr11:62608352..62609217,2	Hela-S3	cervix:
3	chr1:94702688..94703242-chr17:73775493..73776017,2	HCT-116	colon:
4	chr1:94699487..94702162-chr1:94703136..94705781,2	MCF-7	breast:

No data

Variant related genes	Relation type
ARHGAP29	TF binding region
ARHGAP29	CpG island
ENSG00000198691	chromatin interactions
ENSG00000132475	chromatin interactions
ENSG00000137962	chromatin interactions

Extended variants
information (count: 75 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:75 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576282625	chr1:94702027-94702028	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs375883975	chr1:94702058-94702059	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs545316576	chr1:94702086-94702087	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564075586	chr1:94702103-94702104	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532775920	chr1:94702232-94702233	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs201927528	chr1:94702233-94702234	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs540252113	chr1:94702234-94702235	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs559990489	chr1:94702238-94702239	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529041379	chr1:94702239-94702240	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs11165099	chr1:94702240-94702241	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs569080033	chr1:94702241-94702242	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs531599429	chr1:94702260-94702261	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs551683259	chr1:94702278-94702279	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs571543889	chr1:94702282-94702283	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs533935394	chr1:94702284-94702285	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs573987122	chr1:94702340-94702341	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs547809323	chr1:94702393-94702394	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs189007653	chr1:94702407-94702408	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs370398920	chr1:94702441-94702442	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs17111243	chr1:94702449-94702450	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs556310018	chr1:94702478-94702479	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs576245749	chr1:94702544-94702545	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs538881967	chr1:94702655-94702656	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs115058767	chr1:94702677-94702678	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116443370	chr1:94702703-94702704	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562496856	chr1:94702714-94702715	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539840632	chr1:94702716-94702717	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs113278683	chr1:94702755-94702756	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs560105913	chr1:94702789-94702790	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573734059	chr1:94702790-94702791	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs542769647	chr1:94702831-94702832	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs576408012	chr1:94702860-94702861	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs531509146	chr1:94702898-94702899	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551596570	chr1:94702909-94702910	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565023187	chr1:94703012-94703013	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs527591281	chr1:94703030-94703031	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs373789567	chr1:94703126-94703127	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs199828867	chr1:94703127-94703128	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs536312082	chr1:94703192-94703193	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs549847817	chr1:94703262-94703263	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs569844073	chr1:94703279-94703280	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538846230	chr1:94703291-94703292	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs1411692	chr1:94703441-94703442	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs1360363	chr1:94703517-94703518	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140139073	chr1:94703533-94703534	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs572612292	chr1:94703550-94703551	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs535331434	chr1:94703614-94703615	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs71717670	chr1:94703635-94703636	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs145671411	chr1:94703680-94703681	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs147755123	chr1:94703695-94703696	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Autism	17483303	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Intestinal disease	21956041	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Glioblastoma multiforme	21510904	CNVD
Breast cancer	22522925	CNVD
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD

Chromatin state (count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94698200-94702800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:94699200-94703600	Active TSS	Breast Myoepithelial Primary Cells	Breast
3	chr1:94699600-94702200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:94699600-94703800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr1:94699800-94702400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr1:94699800-94702600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:94699800-94703200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:94699800-94703400	Active TSS	HMEC	breast
9	chr1:94700200-94703600	Active TSS	Skeletal Muscle Male	skeletal muscle
10	chr1:94700400-94702600	Bivalent/Poised TSS	Fetal Kidney	kidney
11	chr1:94700400-94703200	Active TSS	Skeletal Muscle Female	skeletal muscle
12	chr1:94700600-94702800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:94700600-94703400	Active TSS	Muscle Satellite Cultured Cells	--
14	chr1:94700600-94703800	Active TSS	Right Atrium	heart
15	chr1:94700800-94702000	Active TSS	Fetal Muscle Leg	muscle
16	chr1:94700800-94702200	Bivalent/Poised TSS	Fetal Intestine Large	intestine
17	chr1:94700800-94702400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
18	chr1:94700800-94702800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
19	chr1:94700800-94703200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
20	chr1:94700800-94703400	Active TSS	Stomach Smooth Muscle	stomach
21	chr1:94700800-94703600	Active TSS	NHLF	lung
22	chr1:94700800-94703800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr1:94701000-94702200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr1:94701000-94703400	Active TSS	Fetal Muscle Trunk	muscle
25	chr1:94701000-94703400	Active TSS	NHEK	skin
26	chr1:94701000-94703600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:94701000-94703600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:94701000-94703600	Active TSS	NHDF-Ad	bronchial
29	chr1:94701000-94703800	Active TSS	Psoas Muscle	Psoas
30	chr1:94701000-94703800	Active TSS	Right Ventricle	heart
31	chr1:94701000-94704000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
32	chr1:94701200-94702200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
33	chr1:94701200-94702200	Flanking Active TSS	Fetal Lung	lung
34	chr1:94701200-94702400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr1:94701200-94703000	Active TSS	Aorta	Aorta
36	chr1:94701200-94703200	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
37	chr1:94701200-94703400	Active TSS	Fetal Heart	heart
38	chr1:94701200-94703600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr1:94701200-94703600	Active TSS	HSMM	muscle
40	chr1:94701200-94703600	Active TSS	HSMMtube	muscle
41	chr1:94701200-94703800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:94701200-94703800	Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr1:94701200-94703800	Active TSS	Left Ventricle	heart
44	chr1:94701400-94702200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
45	chr1:94701400-94702200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
46	chr1:94701400-94702200	Active TSS	Duodenum Smooth Muscle	Duodenum
47	chr1:94701400-94702200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
48	chr1:94701400-94702400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
49	chr1:94701400-94702400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr1:94701400-94702400	Bivalent/Poised TSS	Brain Angular Gyrus	brain

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