Variant report

Variant	esv3362620
Chromosome Location	chr1:215739954-215742502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:601)
CpG islands
(count:488)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:215740265-215740878	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:215740376-215740690	K562	blood:	n/a	n/a
3	BACH1	chr1:215740321-215740761	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:215740222-215740685	K562	blood:	n/a	n/a
5	BACH1	chr1:215741172-215741269	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr1:215740317-215740899	A549	lung:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215740885-215740894
7	BCLAF1	chr1:215740366-215741262	GM12878	blood:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215741130-215741143 chr1:215740885-215740894
8	BCLAF1	chr1:215740328-215740960	K562	blood:	n/a	chr1:215740719-215740732 chr1:215740865-215740878 chr1:215740885-215740894
9	BHLHE40	chr1:215740502-215741201	GM12878	blood:	n/a	chr1:215740964-215740980
10	BHLHE40	chr1:215740115-215741532	K562	blood:	n/a	chr1:215740964-215740980
11	BRCA1	chr1:215740383-215740558	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr1:215740073-215740146	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr1:215740296-215740719	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:215742181-215743187	K562	blood:	n/a	n/a
15	CBX3	chr1:215741077-215741619	K562	blood:	n/a	n/a
16	CBX3	chr1:215740281-215740949	K562	blood:	n/a	n/a
17	CCNT2	chr1:215740373-215741290	K562	blood:	n/a	n/a
18	CEBPB	chr1:215741018-215741094	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr1:215740060-215740887	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr1:215740527-215740802	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr1:215740158-215740868	MCF-7	breast:	n/a	n/a
22	CEBPB	chr1:215740197-215740562	A549	lung:	n/a	n/a
23	CEBPB	chr1:215741097-215741591	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:215741235-215741591	ECC-1	luminal epithelium:	n/a	n/a
25	CEBPB	chr1:215740367-215740700	K562	blood:	n/a	n/a
26	CEBPD	chr1:215740378-215741077	HepG2	liver:	n/a	n/a
27	CHD1	chr1:215739972-215741689	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD1	chr1:215741048-215741499	GM12878	blood:	n/a	n/a
29	CHD1	chr1:215742064-215742237	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr1:215740304-215740768	GM12878	blood:	n/a	n/a
31	CHD2	chr1:215740354-215741584	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr1:215741109-215741309	GM12878	blood:	n/a	n/a
33	CHD2	chr1:215740381-215740711	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr1:215741123-215741327	HepG2	liver:	n/a	n/a
35	CHD2	chr1:215741101-215741334	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr1:215740425-215740829	HepG2	liver:	n/a	n/a
37	CHD2	chr1:215740378-215741620	K562	blood:	n/a	n/a
38	CREB1	chr1:215740259-215741593	HepG2	liver:	n/a	n/a
39	CREB1	chr1:215740357-215741136	A549	lung:	n/a	n/a
40	CREB1	chr1:215740378-215740854	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr1:215740382-215741372	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr1:215741180-215741330	HPAF	blood vessel:	n/a	n/a
43	CTCF	chr1:215741220-215741370	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr1:215741100-215741250	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr1:215741180-215741330	BJ	skin:	n/a	n/a
46	CTCF	chr1:215740900-215741050	GM12868	blood:	n/a	n/a
47	CTCF	chr1:215740480-215740630	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr1:215740985-215741321	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:215740589-215740680	MCF-7	breast:	n/a	n/a
50	CTCF	chr1:215740517-215740737	MCF-7	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:215740071-215740121	SK-N-MC	brain:	n/a
2	chr1:215741182-215741232	K562	blood:	n/a
3	chr1:215741843-215741893	U87	brain:	n/a
4	chr1:215741258-215741308	Hela-S3	cervix:	n/a
5	chr1:215740697-215740747	PFSK-1	brain:	n/a
6	chr1:215741182-215741232	HUVEC	blood vessel:	n/a
7	chr1:215740424-215740474	HRE	kidney:	n/a
8	chr1:215741843-215741893	HIPEpiC	eye:	n/a
9	chr1:215740697-215740747	ECC-1	luminal epithelium:	n/a
10	chr1:215741843-215741893	HL-60	blood:	n/a
11	chr1:215740071-215740121	Jurkat	blood:	n/a
12	chr1:215741258-215741308	HEEpiC	esophagus:	n/a
13	chr1:215740424-215740474	AG10803	skin:	n/a
14	chr1:215741258-215741308	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:215741258-215741308	LNCaP	prostate:	n/a
16	chr1:215741843-215741893	PANC-1	pancreas:	n/a
17	chr1:215740424-215740474	HCF	heart:	n/a
18	chr1:215741843-215741893	IMR90	lung:	fetal
19	chr1:215741258-215741308	AG09319	gingival:	n/a
20	chr1:215741258-215741308	SK-N-MC	brain:	n/a
21	chr1:215740697-215740747	PANC-1	pancreas:	n/a
22	chr1:215741182-215741232	HIPEpiC	eye:	n/a
23	chr1:215740697-215740747	ovcar-3	ovarian:	n/a
24	chr1:215741258-215741308	BJ	skin:	n/a
25	chr1:215740697-215740747	LNCaP	prostate:	n/a
26	chr1:215741318-215741368	CMK	blood:	n/a
27	chr1:215741258-215741308	HUVEC	blood vessel:	n/a
28	chr1:215740697-215740747	AG09319	gingival:	n/a
29	chr1:215740701-215740751	NH-A	brain:	n/a
30	chr1:215741843-215741893	NT2-D1	testis:	n/a
31	chr1:215740701-215740751	U87	brain:	n/a
32	chr1:215741318-215741368	U87	brain:	n/a
33	chr1:215741258-215741308	BE2_C	brain:	n/a
34	chr1:215740697-215740747	BE2_C	brain:	n/a
35	chr1:215740697-215740747	NH-A	brain:	n/a
36	chr1:215741182-215741232	PrEC	prostate:	n/a
37	chr1:215741258-215741308	ovcar-3	ovarian:	n/a
38	chr1:215741318-215741368	ProgFib	skin:	n/a
39	chr1:215741182-215741232	MCF-7	breast:	n/a
40	chr1:215740701-215740751	SAEC	small airway:	n/a
41	chr1:215740071-215740121	HEEpiC	esophagus:	n/a
42	chr1:215740701-215740751	SK-N-MC	brain:	n/a
43	chr1:215740071-215740121	HAEpiC	amniotic membrane:	n/a
44	chr1:215740071-215740121	AG09309	skin:	n/a
45	chr1:215740701-215740751	HCM	heart:	n/a
46	chr1:215740697-215740747	MCF10A-Er-Src	breast:	n/a
47	chr1:215740701-215740751	RPTEC	kidney:	n/a
48	chr1:215741182-215741232	A549	lung:	n/a
49	chr1:215740697-215740747	NHBE	bronchial:	n/a
50	chr1:215740071-215740121	NH-A	brain:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:215740857..215741766-chr12:7052939..7053914,2	Hela-S3	cervix:
2	chr1:215740294..215741084-chr19:3985081..3985884,2	Hela-S3	cervix:
3	chr1:215740395..215741072-chr11:62608879..62609640,2	Hela-S3	cervix:
4	chr1:215741634..215744285-chr1:215769987..215771958,3	K562	blood:
5	chr1:215742124..215744108-chr1:215859791..215861523,2	K562	blood:
6	chr1:215727802..215730014-chr1:215737556..215740283,2	K562	blood:
7	chr1:215739388..215743068-chr1:215745972..215749293,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-USH2A-1	chr1:215740146-215740734	NONHSAT009473

No data

Variant related genes	Relation type
KCTD3	TF binding region
KCTD3	CpG island
ENSG00000238923	chromatin interactions
ENSG00000167658	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000111678	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000136636	chromatin interactions

Extended variants
information (count: 77 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:77 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185811331	chr1:215739976-215739977	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs148839444	chr1:215739989-215739990	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs570457012	chr1:215740097-215740098	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs186899217	chr1:215740108-215740109	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs562767570	chr1:215740116-215740117	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs540162556	chr1:215740119-215740120	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531518184	chr1:215740149-215740150	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs76551420	chr1:215740319-215740320	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs561586826	chr1:215740359-215740360	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs190479700	chr1:215740366-215740367	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs527762822	chr1:215740386-215740387	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs371623164	chr1:215740418-215740419	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs80018194	chr1:215740419-215740420	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs570633071	chr1:215740457-215740458	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs536029832	chr1:215740508-215740509	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs141037534	chr1:215740512-215740513	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs73085412	chr1:215740525-215740526	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549915544	chr1:215740539-215740540	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs570281143	chr1:215740574-215740575	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs73085413	chr1:215740585-215740586	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs555921302	chr1:215740587-215740588	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs137954975	chr1:215740628-215740629	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs368806320	chr1:215740644-215740645	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs533853732	chr1:215740656-215740657	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs368217640	chr1:215740658-215740659	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs371879570	chr1:215740754-215740755	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs553875033	chr1:215740766-215740767	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs540761081	chr1:215740806-215740807	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs545744888	chr1:215740825-215740826	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs375096968	chr1:215740836-215740837	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs562348854	chr1:215740939-215740940	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs561919637	chr1:215740949-215740950	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs148547642	chr1:215740979-215740980	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs2275768	chr1:215741053-215741054	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs201239948	chr1:215741123-215741124	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs375009609	chr1:215741156-215741157	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs527455539	chr1:215741162-215741163	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs547202405	chr1:215741183-215741184	Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs564198004	chr1:215741234-215741235	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs112682035	chr1:215741295-215741296	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs550143960	chr1:215741351-215741352	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs141935194	chr1:215741370-215741371	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs536132545	chr1:215741374-215741375	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs147122424	chr1:215741418-215741419	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs566401304	chr1:215741428-215741429	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs544685017	chr1:215741430-215741431	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs535195811	chr1:215741449-215741450	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs368081174	chr1:215741490-215741491	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs186134870	chr1:215741506-215741507	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs375223389	chr1:215741561-215741562	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	Chromatin interactive region	4 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
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
Ovarian cancer	21720365	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215730800-215740200	Weak transcription	Pancreas	Pancrea
2	chr1:215732000-215740200	Weak transcription	Stomach Mucosa	stomach
3	chr1:215739000-215740000	Enhancers	Fetal Intestine Large	intestine
4	chr1:215739200-215740000	Enhancers	Fetal Lung	lung
5	chr1:215739200-215740000	Enhancers	Hela-S3	cervix
6	chr1:215739400-215742200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:215739600-215740200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:215739600-215742000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:215739800-215740000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr1:215739800-215740000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:215739800-215740000	Enhancers	Primary T cells from cord blood	blood
12	chr1:215739800-215740000	Enhancers	Primary hematopoietic stem cells	blood
13	chr1:215739800-215740000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:215739800-215740000	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr1:215739800-215740000	Enhancers	Adipose Nuclei	Adipose
16	chr1:215739800-215740000	Enhancers	Brain Angular Gyrus	brain
17	chr1:215739800-215740000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr1:215739800-215740000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr1:215739800-215740000	Enhancers	Dnd41	blood
20	chr1:215739800-215740000	Flanking Active TSS	HepG2	liver
21	chr1:215739800-215740000	Enhancers	NH-A	brain
22	chr1:215739800-215740200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr1:215739800-215740200	Active TSS	K562	blood
24	chr1:215739800-215740400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr1:215739800-215740400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr1:215739800-215740400	Flanking Active TSS	Duodenum Mucosa	Duodenum
27	chr1:215739800-215740400	Flanking Active TSS	HUVEC	blood vessel
28	chr1:215739800-215740600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr1:215739800-215742000	Active TSS	HUES64 Cell Line	embryonic stem cell
30	chr1:215739800-215742200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:215739800-215742200	Active TSS	Osteobl	bone
32	chr1:215739800-215742400	Active TSS	Muscle Satellite Cultured Cells	--
33	chr1:215739800-215742400	Active TSS	Brain Anterior Caudate	brain
34	chr1:215739800-215742600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr1:215739800-215742800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr1:215739800-215743200	Active TSS	A549	lung
37	chr1:215739800-215743200	Active TSS	NHDF-Ad	bronchial
38	chr1:215739800-215743400	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr1:215739800-215743400	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr1:215739800-215743600	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr1:215739800-215744400	Active TSS	NHLF	lung
42	chr1:215740000-215740200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr1:215740000-215740200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
44	chr1:215740000-215740200	Flanking Active TSS	Fetal Lung	lung
45	chr1:215740000-215740200	Flanking Active TSS	Rectal Smooth Muscle	rectum
46	chr1:215740000-215740200	Flanking Active TSS	Hela-S3	cervix
47	chr1:215740000-215740200	Active TSS	Monocytes-CD14+_RO01746	blood
48	chr1:215740000-215740400	Flanking Active TSS	Primary T cells from cord blood	blood
49	chr1:215740000-215740400	Flanking Active TSS	Primary hematopoietic stem cells	blood
50	chr1:215740000-215740400	Enhancers	Primary T helper naive cells from peripheral blood	blood

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