Variant report

Variant	esv3438070
Chromosome Location	chr1:10855190-10857938
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:230)
CpG islands
(count:793)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:230 , 50 per page) page: 1 2 3 4 5

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	chr1:10856584-10856977	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr1:10856521-10856938	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr1:10856547-10856918	A549	lung:	n/a	n/a
6	BACH1	chr1:10856646-10856973	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr1:10856552-10857000	A549	lung:	n/a	chr1:10856780-10856793 chr1:10856690-10856703 chr1:10856590-10856599 chr1:10856585-10856598 chr1:10856593-10856602
8	BRCA1	chr1:10856661-10856883	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr1:10856755-10856873	HepG2	liver:	n/a	n/a
10	CBX3	chr1:10856631-10856918	K562	blood:	n/a	n/a
11	CCNT2	chr1:10856670-10856938	K562	blood:	n/a	n/a
12	CEBPB	chr1:10856646-10856864	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:10857145-10857399	K562	blood:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
14	CEBPB	chr1:10856696-10856821	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:10856651-10857407	HepG2	liver:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
16	CEBPB	chr1:10857222-10857252	H1-hESC	embryonic stem cell:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
17	CEBPB	chr1:10856568-10857024	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr1:10856627-10857350	IMR90	lung:	n/a	chr1:10857237-10857250 chr1:10857238-10857249
19	CHD2	chr1:10856659-10856913	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr1:10856784-10856824	HepG2	liver:	n/a	n/a
21	CREB1	chr1:10856548-10856958	A549	lung:	n/a	n/a
22	CTBP2	chr1:10856415-10857000	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTBP2	chr1:10855281-10855928	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr1:10856705-10856874	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr1:10856716-10856866	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr1:10855240-10855390	SK-N-SH_RA	brain:	n/a	chr1:10855270-10855280
27	CTCF	chr1:10856240-10856390	SAEC	small airway:	n/a	n/a
28	CTCF	chr1:10856691-10856868	Lung_OC	lung:	n/a	n/a
29	CTCF	chr1:10855880-10856030	SAEC	small airway:	n/a	chr1:10855938-10855959 chr1:10855943-10855961
30	CTCF	chr1:10856665-10856767	Pancreas_OC	pancreas:	n/a	n/a
31	E2F4	chr1:10856651-10856916	MCF10A-Er-Src	breast:	n/a	chr1:10856700-10856709 chr1:10856655-10856669
32	E2F6	chr1:10856599-10856980	A549	lung:	n/a	chr1:10856700-10856709 chr1:10856655-10856669
33	E2F6	chr1:10856619-10856752	K562	blood:	n/a	chr1:10856700-10856709 chr1:10856655-10856669
34	EGR1	chr1:10856569-10857012	H1-hESC	embryonic stem cell:	n/a	chr1:10856586-10856596 chr1:10856700-10856709
35	EGR1	chr1:10856630-10856950	K562	blood:	n/a	chr1:10856700-10856709
36	EGR1	chr1:10856634-10856968	K562	blood:	n/a	chr1:10856700-10856709
37	EGR1	chr1:10856630-10857003	H1-hESC	embryonic stem cell:	n/a	chr1:10856700-10856709
38	ELF1	chr1:10856661-10856845	HepG2	liver:	n/a	n/a
39	ELF1	chr1:10854957-10855260	GM12878	blood:	n/a	n/a
40	ELF1	chr1:10856617-10856988	K562	blood:	n/a	chr1:10856834-10856846
41	EP300	chr1:10856472-10856969	A549	lung:	n/a	n/a
42	EP300	chr1:10856539-10856884	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr1:10856517-10857025	H1-hESC	embryonic stem cell:	n/a	n/a
44	EP300	chr1:10856565-10856948	T-47D	breast:	n/a	n/a
45	EP300	chr1:10856616-10856965	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr1:10856426-10857017	ECC-1	luminal epithelium:	n/a	n/a
47	EP300	chr1:10856644-10856871	HepG2	liver:	n/a	n/a
48	EP300	chr1:10856533-10857113	SK-N-SH	brain:	n/a	n/a
49	ETS1	chr1:10856662-10856832	K562	blood:	n/a	n/a
50	ETS1	chr1:10856521-10856856	A549	lung:	n/a	chr1:10856584-10856595

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:10856739-10856789	HAEpiC	amniotic membrane:	n/a
2	chr1:10856609-10856659	MCF-7	breast:	n/a
3	chr1:10856466-10856516	NHBE	bronchial:	n/a
4	chr1:10855226-10855276	ProgFib	skin:	n/a
5	chr1:10856202-10856252	HL-60	blood:	n/a
6	chr1:10856609-10856659	HPAEpiC	pulmonary alveolar:	n/a
7	chr1:10856202-10856252	HCM	heart:	n/a
8	chr1:10856943-10856993	MCF10A-Er-Src	breast:	n/a
9	chr1:10856707-10856757	PFSK-1	brain:	n/a
10	chr1:10856609-10856659	ovcar-3	ovarian:	n/a
11	chr1:10856466-10856516	HUVEC	blood vessel:	n/a
12	chr1:10856657-10856707	LNCaP	prostate:	n/a
13	chr1:10856707-10856757	HCF	heart:	n/a
14	chr1:10855226-10855276	BE2_C	brain:	n/a
15	chr1:10856466-10856516	HL-60	blood:	n/a
16	chr1:10856657-10856707	AG04450	lung:	fetal
17	chr1:10857436-10857486	Caco-2	colon:	n/a
18	chr1:10857110-10857160	AG09319	gingival:	n/a
19	chr1:10856609-10856659	MCF10A-Er-Src	breast:	n/a
20	chr1:10856466-10856516	SK-N-SH	brain:	n/a
21	chr1:10857091-10857141	HUVEC	blood vessel:	n/a
22	chr1:10856466-10856516	MCF-7	breast:	n/a
23	chr1:10856943-10856993	H1-hESC	embryonic stem cell:	embryo
24	chr1:10855226-10855276	NHBE	bronchial:	n/a
25	chr1:10857110-10857160	PFSK-1	brain:	n/a
26	chr1:10856707-10856757	GM12891	blood:	n/a
27	chr1:10855806-10855856	MCF10A-Er-Src	breast:	n/a
28	chr1:10855553-10855603	GM06990	blood:	n/a
29	chr1:10855226-10855276	IMR90	lung:	fetal
30	chr1:10856739-10856789	U87	brain:	n/a
31	chr1:10857436-10857486	MCF-7	breast:	n/a
32	chr1:10857110-10857160	BJ	skin:	n/a
33	chr1:10857110-10857160	Hela-S3	cervix:	n/a
34	chr1:10855553-10855603	HCPEpiC	choroid plexus:	n/a
35	chr1:10856202-10856252	Hepatocyte	liver:	n/a
36	chr1:10856707-10856757	SK-N-MC	brain:	n/a
37	chr1:10855553-10855603	BE2_C	brain:	n/a
38	chr1:10856609-10856659	SK-N-SH_RA	brain:	n/a
39	chr1:10857110-10857160	HRE	kidney:	n/a
40	chr1:10855226-10855276	GM12878	blood:	n/a
41	chr1:10856739-10856789	AG10803	skin:	n/a
42	chr1:10855553-10855603	PrEC	prostate:	n/a
43	chr1:10855806-10855856	BJ	skin:	n/a
44	chr1:10857110-10857160	NHBE	bronchial:	n/a
45	chr1:10857110-10857160	AG04449	skin:	fetal
46	chr1:10856739-10856789	RPTEC	kidney:	n/a
47	chr1:10856202-10856252	HNPCEpiC	eye:	n/a
48	chr1:10856609-10856659	AG04450	lung:	fetal
49	chr1:10856739-10856789	CMK	blood:	n/a
50	chr1:10856657-10856707	Jurkat	blood:	n/a

(count:6 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 115 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574632598	chr1:10855204-10855205	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs368220330	chr1:10855233-10855234	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs545273919	chr1:10855234-10855235	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs192914468	chr1:10855249-10855250	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs59253427	chr1:10855310-10855311	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs11577258	chr1:10855315-10855316	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs545486351	chr1:10855407-10855408	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs185235815	chr1:10855437-10855438	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs528177202	chr1:10855463-10855464	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs541187637	chr1:10855471-10855472	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs114528694	chr1:10855510-10855511	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs74052506	chr1:10855550-10855551	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs565187388	chr1:10855552-10855553	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs558296148	chr1:10855577-10855578	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs548628992	chr1:10855629-10855630	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11577305	chr1:10855638-10855639	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs376667795	chr1:10855668-10855669	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11588609	chr1:10855753-10855754	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74052507	chr1:10855778-10855779	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535140702	chr1:10855803-10855804	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs199635199	chr1:10855804-10855805	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552699099	chr1:10855839-10855840	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397863573	chr1:10855855-10855856	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs570910061	chr1:10855975-10855976	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535129429	chr1:10855996-10855997	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs553167130	chr1:10856001-10856002	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs761124	chr1:10856053-10856054	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs556792204	chr1:10856112-10856113	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535726936	chr1:10856236-10856237	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557016904	chr1:10856248-10856249	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs60558358	chr1:10856315-10856316	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs568988917	chr1:10856445-10856446	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61645034	chr1:10856462-10856463	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs557342465	chr1:10856502-10856503	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572570164	chr1:10856508-10856509	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539303659	chr1:10856513-10856514	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539962914	chr1:10856514-10856515	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2387418	chr1:10856516-10856517	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs1107018	chr1:10856517-10856518	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs3059010	chr1:10856521-10856522	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs377499242	chr1:10856586-10856587	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148108123	chr1:10856649-10856650	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76231909	chr1:10856661-10856662	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542500355	chr1:10856662-10856663	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11121627	chr1:10856692-10856693	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531231135	chr1:10856699-10856700	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113979795	chr1:10856708-10856709	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs574536244	chr1:10856723-10856724	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs552563055	chr1:10856773-10856774	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs373670381	chr1:10856778-10856779	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island	1 gene(s)	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:391 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10853000-10857200	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr1:10853200-10856200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
3	chr1:10853200-10856200	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
4	chr1:10853200-10857000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
5	chr1:10853200-10857000	Active TSS	Duodenum Mucosa	Duodenum
6	chr1:10853200-10857000	Active TSS	Psoas Muscle	Psoas
7	chr1:10853200-10857200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
8	chr1:10853200-10857200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:10853400-10855200	Active TSS	Colon Smooth Muscle	Colon
10	chr1:10853400-10855600	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr1:10853400-10856000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
12	chr1:10853400-10856000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr1:10853400-10856400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
14	chr1:10853400-10856600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
15	chr1:10853400-10856800	Active TSS	Esophagus	oesophagus
16	chr1:10853400-10856800	Active TSS	Left Ventricle	heart
17	chr1:10853400-10856800	Active TSS	Right Atrium	heart
18	chr1:10853400-10857000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
19	chr1:10853400-10857200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
20	chr1:10853600-10855400	Active TSS	Fetal Kidney	kidney
21	chr1:10853600-10856800	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr1:10853600-10856800	Active TSS	Aorta	Aorta
23	chr1:10853600-10856800	Active TSS	HSMMtube	muscle
24	chr1:10853600-10857000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:10853600-10857000	Active TSS	Rectal Mucosa Donor 31	rectum
26	chr1:10853600-10857000	Bivalent/Poised TSS	Thymus	Thymus
27	chr1:10853600-10857200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
28	chr1:10853600-10857200	Bivalent Enhancer	Fetal Brain Male	brain
29	chr1:10853800-10855400	Bivalent/Poised TSS	Small Intestine	intestine
30	chr1:10853800-10855400	Bivalent/Poised TSS	HepG2	liver
31	chr1:10853800-10855600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:10853800-10855600	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
33	chr1:10853800-10855800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
34	chr1:10853800-10856000	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
35	chr1:10853800-10856000	Flanking Active TSS	Liver	Liver
36	chr1:10853800-10856400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:10853800-10856600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr1:10853800-10856800	Active TSS	Lung	lung
39	chr1:10853800-10857000	Enhancers	Primary B cells from cord blood	blood
40	chr1:10853800-10857000	Active TSS	Gastric	stomach
41	chr1:10853800-10857200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr1:10854000-10855400	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:10854000-10855600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
44	chr1:10854000-10855600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
45	chr1:10854000-10855800	Bivalent/Poised TSS	Fetal Intestine Small	intestine
46	chr1:10854000-10856000	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:10854200-10855200	Enhancers	Primary B cells from peripheral blood	blood
48	chr1:10854200-10856000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr1:10854200-10856200	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:10854400-10855200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--

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