Variant report

Variant	esv3344806
Chromosome Location	chr1:166807953-166810501
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:790)
CpG islands
(count:550)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:790 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:166809459-166810194	K562	blood:	n/a	n/a
2	ARID3A	chr1:166808596-166808750	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:166808438-166808588	K562	blood:	n/a	n/a
4	ATF1	chr1:166809787-166810214	K562	blood:	n/a	n/a
5	ATF2	chr1:166808190-166808825	GM12878	blood:	n/a	n/a
6	ATF3	chr1:166808317-166808843	K562	blood:	n/a	chr1:166808510-166808519 chr1:166808637-166808650 chr1:166808802-166808822 chr1:166808814-166808823
7	BACH1	chr1:166808342-166808769	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr1:166808201-166808826	GM12878	blood:	n/a	n/a
9	BCLAF1	chr1:166808230-166808792	GM12878	blood:	n/a	n/a
10	BHLHE40	chr1:166808346-166808854	HepG2	liver:	n/a	n/a
11	BHLHE40	chr1:166808200-166808882	K562	blood:	n/a	n/a
12	BHLHE40	chr1:166809322-166810227	K562	blood:	n/a	n/a
13	BHLHE40	chr1:166808215-166809270	GM12878	blood:	n/a	chr1:166809049-166809065 chr1:166808996-166809012
14	BRCA1	chr1:166807917-166808761	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr1:166810105-166810206	GM12878	blood:	n/a	n/a
16	CBX3	chr1:166808008-166808896	K562	blood:	n/a	n/a
17	CBX3	chr1:166808152-166808719	K562	blood:	n/a	n/a
18	CBX3	chr1:166809303-166810287	K562	blood:	n/a	n/a
19	CCNT2	chr1:166808154-166810295	K562	blood:	n/a	n/a
20	CEBPB	chr1:166809028-166809299	HepG2	liver:	n/a	n/a
21	CEBPB	chr1:166808191-166808720	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr1:166808040-166808730	HepG2	liver:	n/a	chr1:166808183-166808194
23	CEBPB	chr1:166809050-166809315	IMR90	lung:	n/a	n/a
24	CEBPB	chr1:166807984-166809815	Hela-S3	cervix:	n/a	chr1:166808183-166808194 chr1:166809668-166809680
25	CEBPB	chr1:166809054-166809301	A549	lung:	n/a	n/a
26	CEBPB	chr1:166807906-166808505	A549	lung:	n/a	chr1:166808183-166808194
27	CEBPB	chr1:166807999-166808785	IMR90	lung:	n/a	chr1:166808183-166808194
28	CEBPB	chr1:166807960-166808385	K562	blood:	n/a	chr1:166808183-166808194
29	CEBPB	chr1:166808006-166808416	A549	lung:	n/a	chr1:166808183-166808194
30	CEBPB	chr1:166807997-166808464	K562	blood:	n/a	chr1:166808183-166808194
31	CEBPB	chr1:166809125-166809378	K562	blood:	n/a	n/a
32	CEBPD	chr1:166808288-166808890	HepG2	liver:	n/a	n/a
33	CEBPD	chr1:166809567-166810281	K562	blood:	n/a	n/a
34	CEBPD	chr1:166809702-166810273	K562	blood:	n/a	n/a
35	CHD1	chr1:166808422-166808821	GM12878	blood:	n/a	n/a
36	CHD2	chr1:166808263-166808853	GM12878	blood:	n/a	n/a
37	CHD2	chr1:166809166-166809466	K562	blood:	n/a	n/a
38	CHD2	chr1:166808195-166809580	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr1:166808257-166808789	K562	blood:	n/a	n/a
40	CHD2	chr1:166808367-166808765	HepG2	liver:	n/a	n/a
41	CHD2	chr1:166808391-166808771	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr1:166809206-166809506	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr1:166808159-166808946	HepG2	liver:	n/a	n/a
44	CREB1	chr1:166808271-166808852	A549	lung:	n/a	n/a
45	CREB1	chr1:166808192-166808880	K562	blood:	n/a	n/a
46	CREB1	chr1:166808335-166808788	A549	lung:	n/a	n/a
47	CREB1	chr1:166808233-166808854	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:166809460-166809610	A549	lung:	n/a	n/a
49	CTCF	chr1:166808719-166808723	GM10266	blood:	n/a	n/a
50	CTCF	chr1:166808620-166808770	SK-N-SH_RA	brain:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:166808417-166808467	HRPEpiC	eye:	n/a
2	chr1:166808417-166808467	HRPEpiC	eye:	n/a
3	chr1:166808266-166808316	SK-N-MC	brain:	n/a
4	chr1:166808266-166808316	NH-A	brain:	n/a
5	chr1:166808266-166808316	Jurkat	blood:	n/a
6	chr1:166809144-166809194	HMEC	breast:	n/a
7	chr1:166808351-166808401	ProgFib	skin:	n/a
8	chr1:166809144-166809194	SK-N-SH_RA	brain:	n/a
9	chr1:166808417-166808467	ProgFib	skin:	n/a
10	chr1:166809306-166809356	HepG2	liver:	n/a
11	chr1:166809343-166809393	ProgFib	skin:	n/a
12	chr1:166809407-166809457	BJ	skin:	n/a
13	chr1:166808266-166808316	HepG2	liver:	n/a
14	chr1:166808417-166808467	PrEC	prostate:	n/a
15	chr1:166809384-166809434	MCF-7	breast:	n/a
16	chr1:166808266-166808316	PFSK-1	brain:	n/a
17	chr1:166809384-166809434	H1-hESC	embryonic stem cell:	embryo
18	chr1:166809407-166809457	HCM	heart:	n/a
19	chr1:166808428-166808478	HL-60	blood:	n/a
20	chr1:166809343-166809393	HRCEpiC	kidney:	n/a
21	chr1:166809306-166809356	ECC-1	luminal epithelium:	n/a
22	chr1:166809407-166809457	Hela-S3	cervix:	n/a
23	chr1:166809343-166809393	GM12892	blood:	n/a
24	chr1:166809306-166809356	NB4	blood:	n/a
25	chr1:166809407-166809457	ovcar-3	ovarian:	n/a
26	chr1:166809407-166809457	NHDF-neo	bronchial:	n/a
27	chr1:166809384-166809434	AG04449	skin:	fetal
28	chr1:166808417-166808467	Jurkat	blood:	n/a
29	chr1:166809384-166809434	AG10803	skin:	n/a
30	chr1:166809384-166809434	GM12891	blood:	n/a
31	chr1:166809343-166809393	PFSK-1	brain:	n/a
32	chr1:166808351-166808401	SKMC	muscle:	n/a
33	chr1:166809144-166809194	HEK293	kidney:	embryo
34	chr1:166809144-166809194	ProgFib	skin:	n/a
35	chr1:166809306-166809356	K562	blood:	n/a
36	chr1:166809144-166809194	SAEC	small airway:	n/a
37	chr1:166809343-166809393	GM19239	blood:	n/a
38	chr1:166808417-166808467	GM12891	blood:	n/a
39	chr1:166808266-166808316	AG09309	skin:	n/a
40	chr1:166808428-166808478	AG10803	skin:	n/a
41	chr1:166808266-166808316	HCT-116	colon:	n/a
42	chr1:166809306-166809356	LNCaP	prostate:	n/a
43	chr1:166809384-166809434	BJ	skin:	n/a
44	chr1:166808428-166808478	HAEpiC	amniotic membrane:	n/a
45	chr1:166809343-166809393	NH-A	brain:	n/a
46	chr1:166809306-166809356	GM12878	blood:	n/a
47	chr1:166808351-166808401	Jurkat	blood:	n/a
48	chr1:166808417-166808467	AoSMC	blood vessel:	n/a
49	chr1:166809384-166809434	ProgFib	skin:	n/a
50	chr1:166809343-166809393	A549	lung:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:166807390..166809881-chr1:167187703..167190795,4	MCF-7	breast:
2	chr1:166806593..166810261-chr1:166844073..166846866,6	K562	blood:
3	chr1:165795265..165796893-chr1:166808551..166810494,2	K562	blood:
4	chr1:166806409..166808484-chr1:167002328..167004286,2	K562	blood:
5	chr1:166649643..166651708-chr1:166806859..166808634,2	MCF-7	breast:
6	chr1:166808183..166808891-chr2:88315947..88316502,2	Hela-S3	cervix:
7	chr1:166805232..166812474-chr1:166842359..166847542,11	MCF-7	breast:
8	chr1:166808599..166809122-chr15:59396935..59397740,2	Hela-S3	cervix:
9	chr1:166808391..166808920-chr1:202858119..202858926,2	Hela-S3	cervix:
10	chr1:166810016..166811525-chr1:166822714..166824801,2	MCF-7	breast:
11	chr1:166794651..166797041-chr1:166805983..166808109,2	K562	blood:
12	chr1:166808206..166809091-chr15:72523170..72524154,2	Hela-S3	cervix:
13	chr1:166808293..166809161-chr19:2050789..2051603,2	Hela-S3	cervix:
14	chr1:166805959..166811139-chr1:166841080..166848642,15	MCF-7	breast:
15	chr1:166808237..166810193-chr1:166835815..166838073,2	MCF-7	breast:
16	chr1:166810319..166812756-chr20:58636526..58639447,2	MCF-7	breast:
17	chr1:166808283..166808793-chr18:9137108..9137608,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
POGK	TF binding region
POGK	CpG island
ENSG00000183155	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000099875	chromatin interactions
ENSG00000272205	chromatin interactions
ENSG00000143190	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000143179	chromatin interactions
ENSG00000101745	chromatin interactions
ENSG00000157456	chromatin interactions
ENSG00000225171	chromatin interactions
ENSG00000152382	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376004616	chr1:166808064-166808065	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs55675362	chr1:166808083-166808084	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533737355	chr1:166808085-166808086	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs532078076	chr1:166808119-166808120	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs555566804	chr1:166808138-166808139	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs547731490	chr1:166808144-166808145	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs573840434	chr1:166808166-166808167	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs544513361	chr1:166808177-166808178	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs556256311	chr1:166808189-166808190	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs578072526	chr1:166808223-166808224	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs7548191	chr1:166808253-166808254	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs374264702	chr1:166808290-166808291	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs376578291	chr1:166808307-166808308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs369093581	chr1:166808314-166808315	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs185798799	chr1:166808317-166808318	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs534536885	chr1:166808354-166808355	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs542830570	chr1:166808357-166808358	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs568008895	chr1:166808367-166808368	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs536844483	chr1:166808418-166808419	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs551540319	chr1:166808483-166808484	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs561563862	chr1:166808497-166808498	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs149964546	chr1:166808532-166808533	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs113315804	chr1:166808602-166808603	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
24	rs550470411	chr1:166808620-166808621	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
25	rs562094405	chr1:166808634-166808635	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
26	rs532772147	chr1:166808646-166808647	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
27	rs551010792	chr1:166808691-166808692	Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
28	rs12749440	chr1:166808809-166808810	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
29	rs567551584	chr1:166808934-166808935	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs879654	chr1:166808982-166808983	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs182163474	chr1:166809086-166809087	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs145062492	chr1:166809213-166809214	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs548873605	chr1:166809233-166809234	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs140816181	chr1:166809291-166809292	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs537704069	chr1:166809292-166809293	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs369690735	chr1:166809303-166809304	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs556431503	chr1:166809356-166809357	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs578029742	chr1:166809407-166809408	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs539031167	chr1:166809428-166809429	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs186755565	chr1:166809434-166809435	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs554235987	chr1:166809438-166809439	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs572554643	chr1:166809448-166809449	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs570278128	chr1:166809453-166809454	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs6683488	chr1:166809602-166809603	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs376534018	chr1:166809687-166809688	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs561294068	chr1:166809719-166809720	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs576579352	chr1:166809762-166809763	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs543715124	chr1:166809784-166809785	Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs565227625	chr1:166809852-166809853	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs532696182	chr1:166809860-166809861	Transcr. at gene 5' and 3' Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:166803400-166808200	Weak transcription	Lung	lung
2	chr1:166806200-166808200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:166807200-166808200	Enhancers	Placenta Amnion	Placenta Amnion
4	chr1:166807400-166808000	Enhancers	Primary T cells fromperipheralblood	blood
5	chr1:166807400-166808000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:166807400-166808200	Enhancers	Pancreas	Pancrea
7	chr1:166807400-166808400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:166807400-166808400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
9	chr1:166807400-166808400	Flanking Active TSS	K562	blood
10	chr1:166807400-166808600	Flanking Active TSS	Dnd41	blood
11	chr1:166807600-166808000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr1:166807600-166808000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr1:166807600-166808000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:166807600-166808000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
15	chr1:166807600-166808000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr1:166807600-166808000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:166807600-166808000	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr1:166807600-166808000	Enhancers	Primary B cells from cord blood	blood
19	chr1:166807600-166808000	Enhancers	Primary B cells from peripheral blood	blood
20	chr1:166807600-166808000	Enhancers	Primary hematopoietic stem cells	blood
21	chr1:166807600-166808000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr1:166807600-166808000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr1:166807600-166808000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr1:166807600-166808000	Flanking Active TSS	Brain Cingulate Gyrus	brain
25	chr1:166807600-166808000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr1:166807600-166808000	Flanking Active TSS	Fetal Brain Female	brain
27	chr1:166807600-166808000	Enhancers	Fetal Stomach	stomach
28	chr1:166807600-166808000	Enhancers	Fetal Thymus	thymus
29	chr1:166807600-166808000	Enhancers	Left Ventricle	heart
30	chr1:166807600-166808000	Enhancers	Ovary	ovary
31	chr1:166807600-166808000	Flanking Active TSS	Rectal Smooth Muscle	rectum
32	chr1:166807600-166808000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr1:166807600-166808000	Enhancers	Small Intestine	intestine
34	chr1:166807600-166808000	Active TSS	GM12878-XiMat	blood
35	chr1:166807600-166808000	Enhancers	NHDF-Ad	bronchial
36	chr1:166807600-166808200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr1:166807600-166808200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:166807600-166808200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:166807600-166808200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr1:166807600-166808200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:166807600-166808200	Flanking Active TSS	Brain Substantia Nigra	brain
42	chr1:166807600-166808200	Flanking Active TSS	Colon Smooth Muscle	Colon
43	chr1:166807600-166808200	Enhancers	Placenta	Placenta
44	chr1:166807600-166808200	Enhancers	Spleen	Spleen
45	chr1:166807600-166808400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr1:166807600-166808400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr1:166807600-166808400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr1:166807600-166808400	Flanking Active TSS	Fetal Lung	lung
49	chr1:166807600-166808400	Flanking Active TSS	Stomach Smooth Muscle	stomach
50	chr1:166807600-166808600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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