Variant report

Variant	esv3414899
Chromosome Location	chr1:97187980-97211076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:97193528-97193710	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:97205907-97205957	K562	blood:	n/a	n/a
3	BACH1	chr1:97207568-97207587	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr1:97187063-97188238	K562	blood:	n/a	n/a
5	CEBPB	chr1:97205875-97206220	K562	blood:	n/a	chr1:97206051-97206062
6	CEBPB	chr1:97205887-97206183	HepG2	liver:	n/a	chr1:97206051-97206062
7	CEBPB	chr1:97205914-97206224	Hela-S3	cervix:	n/a	chr1:97206051-97206062
8	CEBPB	chr1:97205895-97206177	IMR90	lung:	n/a	chr1:97206051-97206062
9	CEBPB	chr1:97193517-97193755	K562	blood:	n/a	chr1:97193601-97193612
10	CEBPB	chr1:97209684-97209690	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr1:97205970-97206216	H1-hESC	embryonic stem cell:	n/a	chr1:97206051-97206062
12	CEBPB	chr1:97186960-97188485	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:97193435-97193769	HepG2	liver:	n/a	chr1:97193601-97193612
14	CEBPB	chr1:97205895-97206220	A549	lung:	n/a	chr1:97206051-97206062
15	CHD1	chr1:97188768-97188985	GM12878	blood:	n/a	n/a
16	CHD1	chr1:97187426-97188595	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD2	chr1:97187031-97188487	K562	blood:	n/a	chr1:97187163-97187170
18	CHD2	chr1:97186983-97188270	H1-hESC	embryonic stem cell:	n/a	chr1:97187163-97187170
19	CHD2	chr1:97186955-97188370	Hela-S3	cervix:	n/a	chr1:97187163-97187170
20	CHD2	chr1:97186940-97188352	GM12878	blood:	n/a	chr1:97187163-97187170
21	CTCF	chr1:97195312-97195384	Kidney_OC	kidney:	n/a	n/a
22	CTCF	chr1:97193614-97193703	Fibrobl	skin:	n/a	n/a
23	CUX1	chr1:97188398-97188466	GM12878	blood:	n/a	n/a
24	E2F1	chr1:97186996-97188046	Hela-S3	cervix:	n/a	chr1:97187161-97187175 chr1:97187165-97187176 chr1:97188013-97188025 chr1:97187163-97187170 chr1:97188011-97188021 chr1:97187344-97187359
25	E2F4	chr1:97188594-97188761	MCF10A-Er-Src	breast:	n/a	chr1:97188643-97188652
26	E2F4	chr1:97199304-97199376	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr1:97187076-97188240	MCF10A-Er-Src	breast:	n/a	chr1:97187161-97187175 chr1:97188013-97188025 chr1:97187163-97187170 chr1:97188011-97188021 chr1:97187344-97187359 chr1:97188076-97188088
28	E2F4	chr1:97199670-97199992	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr1:97201296-97201437	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr1:97190601-97190784	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F6	chr1:97187847-97188056	K562	blood:	n/a	chr1:97188013-97188025 chr1:97188011-97188021
32	E2F6	chr1:97186921-97188064	K562	blood:	n/a	chr1:97187161-97187175 chr1:97188013-97188025 chr1:97187163-97187170 chr1:97188011-97188021 chr1:97187344-97187359
33	EGR1	chr1:97187932-97188162	K562	blood:	n/a	chr1:97188074-97188084 chr1:97188071-97188084
34	EGR1	chr1:97187879-97188198	K562	blood:	n/a	chr1:97188074-97188084 chr1:97188071-97188084
35	ELK1	chr1:97187791-97187991	Hela-S3	cervix:	n/a	n/a
36	EP300	chr1:97199779-97199819	K562	blood:	n/a	n/a
37	EP300	chr1:97186769-97188405	K562	blood:	n/a	chr1:97187201-97187214
38	EP300	chr1:97188702-97188824	GM12878	blood:	n/a	n/a
39	FOXA1	chr1:97187960-97188330	HepG2	liver:	n/a	n/a
40	FOXA1	chr1:97187993-97188386	HepG2	liver:	n/a	n/a
41	FOXA1	chr1:97196135-97196473	HepG2	liver:	n/a	n/a
42	FOXA1	chr1:97188011-97188334	HepG2	liver:	n/a	n/a
43	FOXA2	chr1:97196097-97196456	HepG2	liver:	n/a	n/a
44	FOXA2	chr1:97188115-97188363	HepG2	liver:	n/a	n/a
45	GATA2	chr1:97198161-97198436	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr1:97192917-97192995	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr1:97198249-97198393	SH-SY5Y	brain:	n/a	n/a
48	HA-E2F1	chr1:97186694-97188257	MCF-7	breast:	n/a	chr1:97187161-97187175 chr1:97187165-97187176 chr1:97188013-97188025 chr1:97187163-97187170 chr1:97188011-97188021 chr1:97188076-97188088
49	HA-E2F1	chr1:97186981-97188024	Hela-S3	cervix:	n/a	chr1:97187161-97187175 chr1:97187165-97187176 chr1:97187163-97187170 chr1:97188011-97188021
50	HCFC1	chr1:97186670-97188073	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:97188168-97188218	HAEpiC	amniotic membrane:	n/a
2	chr1:97188168-97188218	Caco-2	colon:	n/a
3	chr1:97188168-97188218	RPTEC	kidney:	n/a
4	chr1:97188168-97188218	NHBE	bronchial:	n/a
5	chr1:97188168-97188218	Hela-S3	cervix:	n/a
6	chr1:97188168-97188218	AG10803	skin:	n/a
7	chr1:97191447-97191497	NH-A	brain:	n/a
8	chr1:97191447-97191497	NT2-D1	testis:	n/a
9	chr1:97188168-97188218	HRPEpiC	eye:	n/a
10	chr1:97191447-97191497	HCT-116	colon:	n/a
11	chr1:97188168-97188218	GM12891	blood:	n/a
12	chr1:97188168-97188218	HIPEpiC	eye:	n/a
13	chr1:97191447-97191497	HPAEpiC	pulmonary alveolar:	n/a
14	chr1:97191447-97191497	T-47D	breast:	n/a
15	chr1:97188168-97188218	AG09309	skin:	n/a
16	chr1:97191447-97191497	GM06990	blood:	n/a
17	chr1:97188168-97188218	HCPEpiC	choroid plexus:	n/a
18	chr1:97188168-97188218	HEEpiC	esophagus:	n/a
19	chr1:97188168-97188218	AoSMC	blood vessel:	n/a
20	chr1:97191447-97191497	HMEC	breast:	n/a
21	chr1:97188168-97188218	GM06990	blood:	n/a
22	chr1:97191447-97191497	PFSK-1	brain:	n/a
23	chr1:97191447-97191497	AG09309	skin:	n/a
24	chr1:97191447-97191497	ProgFib	skin:	n/a
25	chr1:97191447-97191497	AG10803	skin:	n/a
26	chr1:97191447-97191497	AG04449	skin:	fetal
27	chr1:97188168-97188218	AG04450	lung:	fetal
28	chr1:97188168-97188218	CMK	blood:	n/a
29	chr1:97188168-97188218	AG04449	skin:	fetal
30	chr1:97191447-97191497	SKMC	muscle:	n/a
31	chr1:97191447-97191497	A549	lung:	n/a
32	chr1:97188168-97188218	HCF	heart:	n/a
33	chr1:97191447-97191497	RPTEC	kidney:	n/a
34	chr1:97188168-97188218	HNPCEpiC	eye:	n/a
35	chr1:97188168-97188218	GM12892	blood:	n/a
36	chr1:97191447-97191497	H1-hESC	embryonic stem cell:	embryo
37	chr1:97191447-97191497	HUVEC	blood vessel:	n/a
38	chr1:97188168-97188218	HCT-116	colon:	n/a
39	chr1:97191447-97191497	HIPEpiC	eye:	n/a
40	chr1:97188168-97188218	NT2-D1	testis:	n/a
41	chr1:97188168-97188218	MCF-7	breast:	n/a
42	chr1:97191447-97191497	SK-N-SH	brain:	n/a
43	chr1:97191447-97191497	SAEC	small airway:	n/a
44	chr1:97191447-97191497	ECC-1	luminal epithelium:	n/a
45	chr1:97191447-97191497	GM12878	blood:	n/a
46	chr1:97191447-97191497	HRE	kidney:	n/a
47	chr1:97188168-97188218	HPAEpiC	pulmonary alveolar:	n/a
48	chr1:97191447-97191497	HEEpiC	esophagus:	n/a
49	chr1:97191447-97191497	HCF	heart:	n/a
50	chr1:97191447-97191497	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr1:97197101..97199084-chr1:97207944..97210511,3	K562	blood:
2	chr1:97208833..97210812-chr1:97213392..97216325,3	K562	blood:
3	chr1:97192682..97195496-chr1:97195725..97198522,3	K562	blood:
4	chr1:97186109..97190198-chr1:97195662..97200448,7	K562	blood:
5	chr1:97186905..97188651-chr1:97192849..97194502,2	K562	blood:
6	chr1:97194900..97197490-chr1:97200989..97203029,2	K562	blood:
7	chr1:97194900..97197490-chr1:97200989..97203029,2	K562	blood:
8	chr1:97190427..97193323-chr1:97215149..97216990,2	K562	blood:
9	chr1:97191200..97196400-chr1:97196525..97203029,7	K562	blood:
10	chr1:97198539..97201059-chr1:97203019..97206054,3	K562	blood:
11	chr1:97185922..97188883-chr1:97189602..97191671,2	MCF-7	breast:
12	chr1:97197101..97199084-chr1:97207944..97210511,3	K562	blood:
13	chr1:97197858..97199535-chr1:97199584..97201298,2	K562	blood:
14	chr1:97191200..97196400-chr1:97196525..97203029,7	K562	blood:
15	chr1:97186433..97189424-chr1:97201467..97203616,2	K562	blood:
16	chr1:97183615..97185204-chr1:97188330..97190541,2	K562	blood:
17	chr1:97192682..97195496-chr1:97195725..97198522,3	K562	blood:
18	chr1:97196400..97201176-chr1:97201528..97207021,6	K562	blood:
19	chr1:97202628..97206379-chr1:97208567..97211407,3	MCF-7	breast:
20	chr1:97187688..97188569-chr12:6643781..6644363,2	Hela-S3	cervix:
21	chr1:97202628..97206379-chr1:97208567..97211407,3	MCF-7	breast:
22	chr1:97197858..97199535-chr1:97199584..97201298,2	K562	blood:
23	chr1:97198539..97201059-chr1:97203019..97206054,3	K562	blood:
24	chr1:97187532..97188205-chr11:46264654..46265306,2	Hela-S3	cervix:
25	chr1:97184820..97186357-chr1:97189356..97191096,2	MCF-7	breast:
26	chr1:97185840..97188668-chr1:97188930..97190541,2	K562	blood:
27	chr1:97196400..97201176-chr1:97201528..97207021,6	K562	blood:
28	chr1:97186163..97189722-chr1:97192382..97194410,3	MCF-7	breast:

Variant related genes	Relation type
PTBP2	TF binding region
PTBP2	CpG island
ENSG00000111640	chromatin interactions
ENSG00000117569	chromatin interactions

Extended variants
information (count: 924 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:924 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185810457	chr1:97188003-97188004	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs368403832	chr1:97188011-97188012	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566656101	chr1:97188049-97188050	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191359054	chr1:97188082-97188083	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs375895314	chr1:97188097-97188098	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs371079943	chr1:97188098-97188099	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372140226	chr1:97188122-97188123	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561637320	chr1:97188166-97188167	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs568638566	chr1:97188213-97188214	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs537422143	chr1:97188308-97188309	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs557348477	chr1:97188358-97188359	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs578158673	chr1:97188376-97188377	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7552545	chr1:97188394-97188395	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs543821155	chr1:97188422-97188423	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs182761756	chr1:97188447-97188448	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs563501462	chr1:97188456-97188457	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111233830	chr1:97188484-97188485	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs78093879	chr1:97188495-97188496	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs7531045	chr1:97188559-97188560	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs546779971	chr1:97188588-97188589	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs112795189	chr1:97188599-97188600	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs565282768	chr1:97188621-97188622	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559635759	chr1:97188675-97188676	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372816437	chr1:97188713-97188714	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs367996059	chr1:97188773-97188774	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527728218	chr1:97188778-97188779	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75019551	chr1:97188783-97188784	Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566687543	chr1:97188805-97188806	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529030750	chr1:97188808-97188809	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548788509	chr1:97188856-97188857	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528288453	chr1:97188890-97188891	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs568579753	chr1:97188945-97188946	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs553569838	chr1:97188986-97188987	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148386635	chr1:97189006-97189007	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142226500	chr1:97189007-97189008	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs571221800	chr1:97189019-97189020	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533594922	chr1:97189020-97189021	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554433762	chr1:97189065-97189066	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs187691653	chr1:97189075-97189076	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs3762411	chr1:97189091-97189092	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs373728182	chr1:97189126-97189127	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201223963	chr1:97189154-97189155	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs568363561	chr1:97189163-97189164	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370809577	chr1:97189164-97189165	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs202229496	chr1:97189172-97189173	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535866203	chr1:97189217-97189218	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545513184	chr1:97189219-97189220	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs193109791	chr1:97189236-97189237	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs572388144	chr1:97189240-97189241	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111625719	chr1:97189260-97189261	Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
Gastric cancer	16891809	CNVD
Schizophrenia	17879154	CNVD
Mental retardation	17124404	CNVD
Intestinal disease	17828263	CNVD
Malignant melanoma	17260012	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:1155 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:97186400-97188200	Active TSS	Duodenum Mucosa	Duodenum
2	chr1:97186400-97188600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr1:97186400-97188600	Active TSS	Duodenum Smooth Muscle	Duodenum
4	chr1:97186400-97189600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:97186400-97189600	Active TSS	NHDF-Ad	bronchial
6	chr1:97186400-97190000	Active TSS	Breast Myoepithelial Primary Cells	Breast
7	chr1:97186600-97188200	Active TSS	Skeletal Muscle Male	skeletal muscle
8	chr1:97186600-97188200	Active TSS	HSMMtube	muscle
9	chr1:97186600-97188400	Active TSS	Primary T killer memory cells from peripheral blood	blood
10	chr1:97186600-97188400	Active TSS	Pancreas	Pancrea
11	chr1:97186600-97188600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
12	chr1:97186600-97188600	Active TSS	Placenta	Placenta
13	chr1:97186600-97188800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr1:97186600-97188800	Active TSS	Rectal Smooth Muscle	rectum
15	chr1:97186600-97189000	Active TSS	Fetal Intestine Large	intestine
16	chr1:97186600-97189000	Active TSS	Fetal Thymus	thymus
17	chr1:97186600-97189000	Active TSS	Psoas Muscle	Psoas
18	chr1:97186600-97189200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:97186600-97189200	Active TSS	Colonic Mucosa	Colon
20	chr1:97186600-97189200	Active TSS	Colon Smooth Muscle	Colon
21	chr1:97186600-97189200	Active TSS	Fetal Brain Male	brain
22	chr1:97186600-97189200	Active TSS	Fetal Muscle Trunk	muscle
23	chr1:97186600-97189200	Active TSS	Fetal Muscle Leg	muscle
24	chr1:97186600-97189200	Active TSS	Ovary	ovary
25	chr1:97186600-97189200	Active TSS	Thymus	Thymus
26	chr1:97186600-97189400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:97186600-97189600	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr1:97186600-97189800	Active TSS	NHLF	lung
29	chr1:97186600-97190200	Active TSS	Stomach Smooth Muscle	stomach
30	chr1:97186800-97188400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:97186800-97188400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr1:97186800-97188400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr1:97186800-97188400	Active TSS	Cortex derived primary cultured neurospheres	brain
34	chr1:97186800-97188400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
35	chr1:97186800-97188400	Active TSS	Gastric	stomach
36	chr1:97186800-97188400	Active TSS	Left Ventricle	heart
37	chr1:97186800-97188400	Active TSS	Lung	lung
38	chr1:97186800-97188600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr1:97186800-97188600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:97186800-97188600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr1:97186800-97188600	Active TSS	Esophagus	oesophagus
42	chr1:97186800-97188600	Active TSS	Placenta Amnion	Placenta Amnion
43	chr1:97186800-97188600	Active TSS	HepG2	liver
44	chr1:97186800-97188800	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr1:97186800-97188800	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr1:97186800-97188800	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr1:97186800-97188800	Active TSS	Brain Substantia Nigra	brain
48	chr1:97186800-97188800	Active TSS	Fetal Kidney	kidney
49	chr1:97186800-97188800	Active TSS	A549	lung
50	chr1:97186800-97189000	Active TSS	Right Ventricle	heart

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