Variant report

Variant	esv3393770
Chromosome Location	chr1:221051854-221054702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:421)
CpG islands
(count:1222)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:421 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:221051346-221051855	GM12878	blood:	n/a	n/a
2	BACH1	chr1:221052129-221052743	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:221054256-221054601	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:221053452-221053781	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:221051370-221051859	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:221053661-221053784	K562	blood:	n/a	n/a
7	BHLHE40	chr1:221053352-221053403	K562	blood:	n/a	n/a
8	BHLHE40	chr1:221052570-221052770	GM12878	blood:	n/a	n/a
9	CBX3	chr1:221052351-221052762	K562	blood:	n/a	n/a
10	CCNT2	chr1:221052822-221053769	K562	blood:	n/a	n/a
11	CEBPB	chr1:221054625-221054971	A549	lung:	n/a	n/a
12	CEBPB	chr1:221054577-221054961	K562	blood:	n/a	n/a
13	CEBPB	chr1:221054350-221054984	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr1:221054616-221054982	HepG2	liver:	n/a	n/a
15	CEBPB	chr1:221054505-221055085	A549	lung:	n/a	n/a
16	CEBPB	chr1:221053440-221053629	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr1:221054545-221055006	IMR90	lung:	n/a	n/a
18	CEBPB	chr1:221054602-221055030	MCF-7	breast:	n/a	n/a
19	CEBPB	chr1:221054589-221054902	A549	lung:	n/a	n/a
20	CEBPB	chr1:221054513-221055002	K562	blood:	n/a	n/a
21	CEBPB	chr1:221054639-221054969	Hela-S3	cervix:	n/a	n/a
22	CHD1	chr1:221054327-221054530	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr1:221052174-221052368	GM12878	blood:	n/a	n/a
24	CHD1	chr1:221052680-221053229	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD1	chr1:221053120-221053125	GM12878	blood:	n/a	n/a
26	CHD2	chr1:221052385-221052644	K562	blood:	n/a	n/a
27	CHD2	chr1:221052560-221053753	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr1:221053040-221053059	HepG2	liver:	n/a	n/a
29	CHD2	chr1:221052141-221052582	GM12878	blood:	n/a	n/a
30	CREB1	chr1:221052417-221053084	A549	lung:	n/a	n/a
31	CTBP2	chr1:221049806-221056533	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:221052311-221052363	A549	lung:	n/a	chr1:221052346-221052359 chr1:221052346-221052359
33	CTCF	chr1:221053420-221053570	AG10803	skin:	n/a	n/a
34	CTCF	chr1:221053440-221053590	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr1:221053440-221053590	AG04450	lung:	n/a	n/a
36	CTCF	chr1:221053340-221053490	Caco-2	colon:	n/a	n/a
37	CTCF	chr1:221053480-221053630	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr1:221053400-221053550	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr1:221053400-221053550	GM06990	blood:	n/a	n/a
40	CTCF	chr1:221053454-221053513	GM12891	blood:	n/a	n/a
41	CTCF	chr1:221053380-221053530	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr1:221052240-221052390	WERI-Rb-1	eye:	n/a	chr1:221052346-221052359 chr1:221052346-221052359
43	CTCF	chr1:221053420-221053570	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr1:221053332-221053655	GM12878	blood:	n/a	n/a
45	CTCF	chr1:221052260-221052410	GM12871	blood:	n/a	chr1:221052346-221052359 chr1:221052346-221052359
46	CTCF	chr1:221052340-221052490	NB4	blood:	n/a	chr1:221052346-221052359 chr1:221052346-221052359
47	CTCF	chr1:221052300-221052450	HCFaa	heart:	n/a	chr1:221052346-221052359 chr1:221052346-221052359
48	CTCF	chr1:221053220-221053370	GM12875	blood:	n/a	n/a
49	CTCF	chr1:221052982-221053066	GM19239	blood:	n/a	n/a
50	CTCF	chr1:221053000-221053150	NHDF-neo	bronchial:	n/a	n/a

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:221052579-221052629	AG09319	gingival:	n/a
2	chr1:221052705-221052755	IMR90	lung:	fetal
3	chr1:221052579-221052629	AG09319	gingival:	n/a
4	chr1:221052705-221052755	IMR90	lung:	fetal
5	chr1:221052468-221052518	HEK293	kidney:	embryo
6	chr1:221052143-221052193	U87	brain:	n/a
7	chr1:221052558-221052608	GM06990	blood:	n/a
8	chr1:221053904-221053954	Hela-S3	cervix:	n/a
9	chr1:221052729-221052779	RPTEC	kidney:	n/a
10	chr1:221054273-221054323	HL-60	blood:	n/a
11	chr1:221052143-221052193	K562	blood:	n/a
12	chr1:221054273-221054323	HUVEC	blood vessel:	n/a
13	chr1:221052468-221052518	MCF-7	breast:	n/a
14	chr1:221052023-221052073	MCF-7	breast:	n/a
15	chr1:221052705-221052755	T-47D	breast:	n/a
16	chr1:221052579-221052629	ECC-1	luminal epithelium:	n/a
17	chr1:221052558-221052608	HNPCEpiC	eye:	n/a
18	chr1:221052729-221052779	NHDF-neo	bronchial:	n/a
19	chr1:221052729-221052779	AG04449	skin:	fetal
20	chr1:221053904-221053954	AG09309	skin:	n/a
21	chr1:221052886-221052936	AG09319	gingival:	n/a
22	chr1:221051907-221051957	HRCEpiC	kidney:	n/a
23	chr1:221052350-221052400	HNPCEpiC	eye:	n/a
24	chr1:221054201-221054251	HCM	heart:	n/a
25	chr1:221052579-221052629	GM06990	blood:	n/a
26	chr1:221054273-221054323	ECC-1	luminal epithelium:	n/a
27	chr1:221052350-221052400	HL-60	blood:	n/a
28	chr1:221054365-221054415	Jurkat	blood:	n/a
29	chr1:221052718-221052768	LNCaP	prostate:	n/a
30	chr1:221054273-221054323	HIPEpiC	eye:	n/a
31	chr1:221052729-221052779	Jurkat	blood:	n/a
32	chr1:221053841-221053891	HNPCEpiC	eye:	n/a
33	chr1:221051907-221051957	HL-60	blood:	n/a
34	chr1:221053128-221053178	BJ	skin:	n/a
35	chr1:221051907-221051957	SK-N-MC	brain:	n/a
36	chr1:221052718-221052768	ovcar-3	ovarian:	n/a
37	chr1:221052350-221052400	HEK293	kidney:	embryo
38	chr1:221052350-221052400	IMR90	lung:	fetal
39	chr1:221052023-221052073	AG09309	skin:	n/a
40	chr1:221052705-221052755	NHDF-neo	bronchial:	n/a
41	chr1:221052350-221052400	SK-N-MC	brain:	n/a
42	chr1:221052579-221052629	HRE	kidney:	n/a
43	chr1:221054273-221054323	HNPCEpiC	eye:	n/a
44	chr1:221053904-221053954	GM12892	blood:	n/a
45	chr1:221052350-221052400	SK-N-SH	brain:	n/a
46	chr1:221053409-221053459	PANC-1	pancreas:	n/a
47	chr1:221054273-221054323	IMR90	lung:	fetal
48	chr1:221053409-221053459	GM12892	blood:	n/a
49	chr1:221052886-221052936	ProgFib	skin:	n/a
50	chr1:221052558-221052608	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:221052748..221053427-chr3:5024866..5025606,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
HLA-AS1	TF binding region
HLX	TF binding region
HLA-AS1	CpG island
HLX	CpG island

Extended variants
information (count: 130 )
Associated
traits (count: 94 )

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	rs147644821	chr1:221051869-221051870	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs547839793	chr1:221051899-221051900	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142241450	chr1:221051900-221051901	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs3806324	chr1:221051924-221051925	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186364569	chr1:221051948-221051949	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs369618023	chr1:221052012-221052013	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs535349565	chr1:221052086-221052087	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs2484692	chr1:221052101-221052102	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs535599092	chr1:221052170-221052171	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs568828297	chr1:221052185-221052186	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs3820355	chr1:221052205-221052206	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs565741824	chr1:221052225-221052226	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs117561904	chr1:221052249-221052250	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs113785694	chr1:221052270-221052271	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557142505	chr1:221052314-221052315	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs577210662	chr1:221052385-221052386	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs190603357	chr1:221052391-221052392	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs576752559	chr1:221052400-221052401	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs41441946	chr1:221052403-221052404	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs552951190	chr1:221052454-221052455	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs2184658	chr1:221052457-221052458	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs374813123	chr1:221052491-221052492	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs533125250	chr1:221052527-221052528	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs542380197	chr1:221052542-221052543	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs562118482	chr1:221052549-221052550	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs572605266	chr1:221052592-221052593	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs541526530	chr1:221052598-221052599	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs147865388	chr1:221052619-221052620	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs533315729	chr1:221052631-221052632	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs2807857	chr1:221052640-221052641	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs563567393	chr1:221052646-221052647	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs561534597	chr1:221052650-221052651	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs529101333	chr1:221052656-221052657	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs57695351	chr1:221052659-221052660	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs370590582	chr1:221052673-221052674	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs111613032	chr1:221052680-221052681	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs534453280	chr1:221052715-221052716	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs575141143	chr1:221052732-221052733	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs570914522	chr1:221052739-221052740	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
40	rs2738752	chr1:221052765-221052766	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs12730158	chr1:221052770-221052771	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs148346751	chr1:221052771-221052772	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs199553841	chr1:221052789-221052790	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs556600577	chr1:221052790-221052791	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs377063056	chr1:221052793-221052794	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs35462307	chr1:221052794-221052795	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs201873114	chr1:221052801-221052802	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs200566716	chr1:221052802-221052803	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs112618703	chr1:221052803-221052804	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs563665490	chr1:221052834-221052835	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	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
Breast cancer	21858162	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Acute myeloid leukemia	17268525	CNVD
Lung cancer	16740712	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17053054	CNVD
Developmental delay	21147756	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221048000-221052000	Weak transcription	A549	lung
2	chr1:221048400-221052000	Weak transcription	HSMMtube	muscle
3	chr1:221049000-221053800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr1:221049400-221052600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
5	chr1:221049600-221052600	Flanking Active TSS	Primary hematopoietic stem cells	blood
6	chr1:221049600-221052800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:221049600-221052800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr1:221049600-221055600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr1:221049800-221052600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
10	chr1:221049800-221055400	Active TSS	Right Atrium	heart
11	chr1:221049800-221055800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
12	chr1:221050000-221055400	Active TSS	Left Ventricle	heart
13	chr1:221050200-221052000	Active TSS	Brain Hippocampus Middle	brain
14	chr1:221050200-221053800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr1:221050400-221052200	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr1:221050400-221053600	Bivalent Enhancer	Fetal Brain Male	brain
17	chr1:221050400-221055200	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr1:221050600-221052000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
19	chr1:221050600-221052600	Enhancers	Spleen	Spleen
20	chr1:221050800-221052200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr1:221050800-221052600	Flanking Active TSS	Adipose Nuclei	Adipose
22	chr1:221051000-221052000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
23	chr1:221051000-221052000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:221051000-221052000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:221051000-221052000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
26	chr1:221051000-221052200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
27	chr1:221051000-221052200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:221051200-221052200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
29	chr1:221051200-221052200	Bivalent Enhancer	Stomach Mucosa	stomach
30	chr1:221051200-221052400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr1:221051200-221052600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
32	chr1:221051200-221053800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
33	chr1:221051200-221054400	Active TSS	Lung	lung
34	chr1:221051200-221055000	Active TSS	Rectal Smooth Muscle	rectum
35	chr1:221051200-221055600	Active TSS	Right Ventricle	heart
36	chr1:221051400-221052000	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood
37	chr1:221051400-221052200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
38	chr1:221051400-221052800	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
39	chr1:221051400-221054000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
40	chr1:221051400-221056000	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
41	chr1:221051600-221052000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr1:221051600-221052000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
43	chr1:221051600-221052000	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr1:221051600-221052000	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
45	chr1:221051600-221052000	Flanking Bivalent TSS/Enh	Fetal Lung	lung
46	chr1:221051600-221052000	Bivalent Enhancer	Fetal Thymus	thymus
47	chr1:221051600-221052000	Flanking Active TSS	NHDF-Ad	bronchial
48	chr1:221051600-221052200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:221051600-221052200	Flanking Active TSS	Osteobl	bone
50	chr1:221051600-221052400	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood

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