Variant report

Variant	esv3353550
Chromosome Location	chr1:10853540-10857138
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:451)
CpG islands
(count:1223)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:10856711-10856837	K562	blood:	n/a	n/a
2	ARID3A	chr1:10856617-10856959	HepG2	liver:	n/a	n/a
3	ATF2	chr1:10856521-10856938	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr1:10856584-10856977	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr1:10856547-10856918	A549	lung:	n/a	n/a
6	BACH1	chr1:10853903-10854532	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:10856646-10856973	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr1:10856552-10857000	A549	lung:	n/a	chr1:10856780-10856793 chr1:10856690-10856703 chr1:10856590-10856599 chr1:10856585-10856598 chr1:10856593-10856602
9	BHLHE40	chr1:10853971-10854236	K562	blood:	n/a	n/a
10	BHLHE40	chr1:10854020-10854171	HepG2	liver:	n/a	n/a
11	BHLHE40	chr1:10854031-10854127	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:10853978-10854020	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr1:10856755-10856873	HepG2	liver:	n/a	n/a
14	BRCA1	chr1:10856661-10856883	H1-hESC	embryonic stem cell:	n/a	n/a
15	CBX3	chr1:10856631-10856918	K562	blood:	n/a	n/a
16	CCNT2	chr1:10853919-10854201	K562	blood:	n/a	chr1:10853946-10853955
17	CCNT2	chr1:10856670-10856938	K562	blood:	n/a	n/a
18	CEBPB	chr1:10856696-10856821	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:10856651-10857407	HepG2	liver:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
20	CEBPB	chr1:10856568-10857024	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr1:10853820-10854164	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:10853154-10853570	H1-hESC	embryonic stem cell:	n/a	chr1:10853340-10853351
23	CEBPB	chr1:10856627-10857350	IMR90	lung:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
24	CEBPB	chr1:10856646-10856864	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr1:10853841-10854239	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr1:10856659-10856913	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr1:10856784-10856824	HepG2	liver:	n/a	n/a
28	CREB1	chr1:10853856-10854391	H1-hESC	embryonic stem cell:	n/a	n/a
29	CREB1	chr1:10856548-10856958	A549	lung:	n/a	n/a
30	CTBP2	chr1:10853937-10854718	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTBP2	chr1:10855281-10855928	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTBP2	chr1:10856415-10857000	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr1:10853940-10854090	GM12874	blood:	n/a	chr1:10854070-10854083
34	CTCF	chr1:10856705-10856874	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr1:10854000-10854150	AG04449	skin:	n/a	chr1:10854070-10854083
36	CTCF	chr1:10854300-10854450	NHEK	skin:	n/a	n/a
37	CTCF	chr1:10853940-10854090	GM12866	blood:	n/a	chr1:10854070-10854083
38	CTCF	chr1:10854040-10854190	GM12875	blood:	n/a	chr1:10854070-10854083
39	CTCF	chr1:10854013-10854121	IMR90	lung:	n/a	chr1:10854070-10854083
40	CTCF	chr1:10854000-10854150	Caco-2	colon:	n/a	chr1:10854070-10854083
41	CTCF	chr1:10854000-10854150	WERI-Rb-1	eye:	n/a	chr1:10854070-10854083
42	CTCF	chr1:10853981-10854159	Gliobla	brain:	n/a	chr1:10854070-10854083
43	CTCF	chr1:10854076-10854082	K562	blood:	n/a	n/a
44	CTCF	chr1:10856240-10856390	SAEC	small airway:	n/a	n/a
45	CTCF	chr1:10854027-10854131	GM12878	blood:	n/a	chr1:10854070-10854083
46	CTCF	chr1:10853940-10854090	GM12878	blood:	n/a	chr1:10854070-10854083
47	CTCF	chr1:10854000-10854150	HCT-116	colon:	n/a	chr1:10854070-10854083
48	CTCF	chr1:10854020-10854170	HBMEC	blood vessel:	n/a	chr1:10854070-10854083
49	CTCF	chr1:10854045-10854113	HUVEC	blood vessel:	n/a	chr1:10854070-10854083
50	CTCF	chr1:10856665-10856767	Pancreas_OC	pancreas:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10855553-10855603	HCT-116	colon:	n/a
2	chr1:10856943-10856993	PFSK-1	brain:	n/a
3	chr1:10855062-10855112	AG09309	skin:	n/a
4	chr1:10855553-10855603	HCT-116	colon:	n/a
5	chr1:10856943-10856993	PFSK-1	brain:	n/a
6	chr1:10855062-10855112	AG09309	skin:	n/a
7	chr1:10856466-10856516	AG09319	gingival:	n/a
8	chr1:10855553-10855603	ProgFib	skin:	n/a
9	chr1:10857091-10857141	PANC-1	pancreas:	n/a
10	chr1:10853918-10853968	AoSMC	blood vessel:	n/a
11	chr1:10853793-10853843	ProgFib	skin:	n/a
12	chr1:10856466-10856516	HEK293	kidney:	embryo
13	chr1:10855062-10855112	AG04449	skin:	fetal
14	chr1:10854499-10854549	T-47D	breast:	n/a
15	chr1:10854205-10854255	NT2-D1	testis:	n/a
16	chr1:10854445-10854495	K562	blood:	n/a
17	chr1:10854205-10854255	ovcar-3	ovarian:	n/a
18	chr1:10856202-10856252	SK-N-SH_RA	brain:	n/a
19	chr1:10856943-10856993	U87	brain:	n/a
20	chr1:10855553-10855603	LNCaP	prostate:	n/a
21	chr1:10855226-10855276	HRPEpiC	eye:	n/a
22	chr1:10854445-10854495	HEK293	kidney:	embryo
23	chr1:10856609-10856659	MCF-7	breast:	n/a
24	chr1:10856707-10856757	RPTEC	kidney:	n/a
25	chr1:10855553-10855603	HCM	heart:	n/a
26	chr1:10856707-10856757	ECC-1	luminal epithelium:	n/a
27	chr1:10855806-10855856	PrEC	prostate:	n/a
28	chr1:10856943-10856993	AG10803	skin:	n/a
29	chr1:10853793-10853843	BE2_C	brain:	n/a
30	chr1:10855062-10855112	NHBE	bronchial:	n/a
31	chr1:10856609-10856659	Caco-2	colon:	n/a
32	chr1:10855806-10855856	ProgFib	skin:	n/a
33	chr1:10856943-10856993	HUVEC	blood vessel:	n/a
34	chr1:10854205-10854255	AG10803	skin:	n/a
35	chr1:10855806-10855856	HCF	heart:	n/a
36	chr1:10854445-10854495	A549	lung:	n/a
37	chr1:10856466-10856516	ProgFib	skin:	n/a
38	chr1:10856609-10856659	AoSMC	blood vessel:	n/a
39	chr1:10856202-10856252	NHDF-neo	bronchial:	n/a
40	chr1:10853918-10853968	SKMC	muscle:	n/a
41	chr1:10855806-10855856	NHBE	bronchial:	n/a
42	chr1:10857091-10857141	IMR90	lung:	fetal
43	chr1:10854205-10854255	AG04450	lung:	fetal
44	chr1:10855062-10855112	Caco-2	colon:	n/a
45	chr1:10854307-10854357	AG10803	skin:	n/a
46	chr1:10856202-10856252	HNPCEpiC	eye:	n/a
47	chr1:10856466-10856516	A549	lung:	n/a
48	chr1:10856202-10856252	GM12891	blood:	n/a
49	chr1:10856609-10856659	GM12878	blood:	n/a
50	chr1:10855553-10855603	HMEC	breast:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:10739929..10741898-chr1:10854079..10856532,2	MCF-7	breast:
2	chr1:10852601..10855720-chr1:10959417..10961902,3	MCF-7	breast:
3	chr1:10750259..10753196-chr1:10853460..10855878,3	MCF-7	breast:
4	chr1:10838788..10840629-chr1:10854389..10855939,2	MCF-7	breast:
5	chr1:10841137..10843114-chr1:10851742..10854578,2	MCF-7	breast:
6	chr1:10854264..10855791-chr1:10891105..10892781,2	MCF-7	breast:
7	chr1:10842014..10843891-chr1:10851096..10853809,2	K562	blood:
8	chr1:10712004..10714801-chr1:10852157..10855382,3	MCF-7	breast:

No data

Variant related genes	Relation type
CASZ1	TF binding region
CASZ1	CpG island

Extended variants
information (count: 130 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139354661	chr1:10853742-10853743	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs543557243	chr1:10853783-10853784	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs183473540	chr1:10853787-10853788	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs554222744	chr1:10853788-10853789	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs188164889	chr1:10853791-10853792	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs114130828	chr1:10853863-10853864	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191748896	chr1:10853969-10853970	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs61777360	chr1:10853981-10853982	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs529725653	chr1:10853990-10853991	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372822082	chr1:10854020-10854021	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75438587	chr1:10854046-10854047	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12728592	chr1:10854073-10854074	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs182424962	chr1:10854114-10854115	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376235656	chr1:10854128-10854129	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538926995	chr1:10854129-10854130	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546691614	chr1:10854138-10854139	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541981197	chr1:10854194-10854195	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145479984	chr1:10854201-10854202	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs565727779	chr1:10854203-10854204	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs75774820	chr1:10854220-10854221	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs571598254	chr1:10854225-10854226	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs554669546	chr1:10854227-10854228	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs563865279	chr1:10854234-10854235	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs531014319	chr1:10854236-10854237	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552830982	chr1:10854238-10854239	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs201970475	chr1:10854247-10854248	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs571097108	chr1:10854249-10854250	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369744993	chr1:10854255-10854256	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs538785126	chr1:10854257-10854258	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs558756948	chr1:10854345-10854346	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs117360158	chr1:10854389-10854390	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs541316124	chr1:10854399-10854400	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs559723102	chr1:10854411-10854412	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115175285	chr1:10854419-10854420	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115894232	chr1:10854446-10854447	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563145261	chr1:10854466-10854467	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2387416	chr1:10854473-10854474	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs117927896	chr1:10854478-10854479	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146474475	chr1:10854509-10854510	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs70997268	chr1:10854532-10854533	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201585850	chr1:10854534-10854535	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2387417	chr1:10854575-10854576	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs372089730	chr1:10854587-10854588	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547683447	chr1:10854599-10854600	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566318090	chr1:10854613-10854614	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536553955	chr1:10854647-10854648	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186707786	chr1:10854649-10854650	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368522720	chr1:10854657-10854658	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191325098	chr1:10854737-10854738	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141259286	chr1:10854776-10854777	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	22429812	CNVD
Epilepsy	22118685	CNVD
Schizophrenia	22118685	CNVD
Ovarian cancer	21720365	CNVD
Developmental delay	19490664	CNVD
Ewing''s sarcoma	21437220	CNVD
Prader-willi syndrome	18797701	CNVD
periventricular nodular heterotopia	20648244	CNVD
1p36 deletion syndrome	22283845	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Neuroblastoma	18923524	CNVD
Retinoblastoma	22278416	CNVD
Mental retardation	20152051	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Astrocytoma	17934521	CNVD
Glioblastoma	20031968	CNVD
Acute myeloid leukemia	18000384	CNVD
Glioblastoma multiforme	16951158	CNVD
Neuroblastoma	18574593	CNVD
Glioblastoma multiforme	17369134	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Myoepithelioma	18604193	CNVD
Wilms tumour	19047088	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	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
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	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
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Neuroblastoma	18923191	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21138945	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian neoplasms	16753589	CNVD
Neuroblastoma	19287153	CNVD
Hepatocellular carcinoma	18929564	CNVD
Melanoma	17363583	CNVD
renal disease	17924346	CNVD
Uveal melanoma	20484589	CNVD
Multiple myeloma	16616336	CNVD
Glioblastoma multiforme	22286061	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	20808228	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD

Chromatin state (count:563 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10850400-10853800	Weak transcription	Gastric	stomach
2	chr1:10851600-10853800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:10852000-10853600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:10852200-10853600	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr1:10852200-10853600	Weak transcription	HSMMtube	muscle
6	chr1:10852800-10853800	Enhancers	Fetal Heart	heart
7	chr1:10853000-10853600	Bivalent Enhancer	Dnd41	blood
8	chr1:10853000-10857200	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr1:10853200-10853600	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:10853200-10853600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
11	chr1:10853200-10853600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
12	chr1:10853200-10853600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
13	chr1:10853200-10853800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
14	chr1:10853200-10853800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
15	chr1:10853200-10853800	Enhancers	Liver	Liver
16	chr1:10853200-10853800	Flanking Active TSS	Fetal Intestine Small	intestine
17	chr1:10853200-10853800	Flanking Active TSS	NHEK	skin
18	chr1:10853200-10854000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
19	chr1:10853200-10854000	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr1:10853200-10854200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
21	chr1:10853200-10854200	Active TSS	Right Ventricle	heart
22	chr1:10853200-10854200	Active TSS	Stomach Smooth Muscle	stomach
23	chr1:10853200-10854400	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
24	chr1:10853200-10854400	Active TSS	Skeletal Muscle Female	skeletal muscle
25	chr1:10853200-10856200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
26	chr1:10853200-10856200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
27	chr1:10853200-10857000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
28	chr1:10853200-10857000	Active TSS	Duodenum Mucosa	Duodenum
29	chr1:10853200-10857000	Active TSS	Psoas Muscle	Psoas
30	chr1:10853200-10857200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
31	chr1:10853200-10857200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
33	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr1:10853400-10853600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:10853400-10853600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr1:10853400-10853600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
39	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
41	chr1:10853400-10853600	Bivalent Enhancer	Brain Inferior Temporal Lobe	brain
42	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
43	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	Fetal Kidney	kidney
44	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	Fetal Lung	lung
45	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
46	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
47	chr1:10853400-10853600	Enhancers	Stomach Mucosa	stomach
48	chr1:10853400-10853600	Flanking Bivalent TSS/Enh	A549	lung
49	chr1:10853400-10853600	Flanking Active TSS	HMEC	breast
50	chr1:10853400-10853600	Bivalent Enhancer	HSMM	muscle

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