Variant report

Variant	esv3368553
Chromosome Location	chr2:11294376-11296624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:672)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:11295473-11295878	A549	lung:	n/a	n/a
2	ATF3	chr2:11295556-11295753	K562	blood:	n/a	n/a
3	BACH1	chr2:11295585-11296168	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr2:11294746-11295201	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL3	chr2:11295474-11295933	A549	lung:	n/a	chr2:11295601-11295614 chr2:11295827-11295840
6	BCL3	chr2:11294412-11295322	A549	lung:	n/a	n/a
7	BCLAF1	chr2:11295486-11295895	GM12878	blood:	n/a	chr2:11295601-11295614 chr2:11295827-11295840
8	BHLHE40	chr2:11295541-11296183	K562	blood:	n/a	chr2:11295824-11295840 chr2:11295848-11295864 chr2:11295859-11295875
9	BHLHE40	chr2:11295590-11295787	GM12878	blood:	n/a	n/a
10	BRCA1	chr2:11294665-11294689	GM12878	blood:	n/a	n/a
11	CBX3	chr2:11294535-11295165	K562	blood:	n/a	n/a
12	CBX3	chr2:11295488-11296311	K562	blood:	n/a	n/a
13	CCNT2	chr2:11295392-11296114	K562	blood:	n/a	n/a
14	CCNT2	chr2:11294847-11295167	K562	blood:	n/a	n/a
15	CEBPB	chr2:11295626-11295790	Hela-S3	cervix:	n/a	n/a
16	CEBPD	chr2:11295014-11295279	HepG2	liver:	n/a	n/a
17	CEBPD	chr2:11294921-11295267	HepG2	liver:	n/a	n/a
18	CEBPD	chr2:11295511-11295831	HepG2	liver:	n/a	n/a
19	CHD1	chr2:11295652-11295890	GM12878	blood:	n/a	n/a
20	CHD1	chr2:11295794-11295898	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr2:11295620-11295667	K562	blood:	n/a	n/a
22	CHD2	chr2:11296017-11296151	K562	blood:	n/a	n/a
23	CHD2	chr2:11295590-11295831	HepG2	liver:	n/a	n/a
24	CHD2	chr2:11295165-11295314	GM12878	blood:	n/a	n/a
25	CHD2	chr2:11294942-11294998	HepG2	liver:	n/a	n/a
26	CHD2	chr2:11295636-11295758	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr2:11295566-11295837	GM12878	blood:	n/a	n/a
28	CHD2	chr2:11294919-11295995	Hela-S3	cervix:	n/a	n/a
29	CREB1	chr2:11295429-11295894	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr2:11294717-11295962	A549	lung:	n/a	n/a
31	CTBP2	chr2:11295567-11296038	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr2:11295624-11295688	GM10266	blood:	n/a	n/a
33	CTCF	chr2:11295640-11295790	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr2:11295540-11295690	HVMF	connective:	n/a	n/a
35	CTCF	chr2:11295534-11295840	K562	blood:	n/a	n/a
36	CTCF	chr2:11295580-11295730	K562	blood:	n/a	n/a
37	CTCF	chr2:11294860-11295010	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:11295560-11295710	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr2:11294920-11295070	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr2:11295567-11295754	K562	blood:	n/a	n/a
41	CTCF	chr2:11294780-11294930	K562	blood:	n/a	n/a
42	CTCF	chr2:11295571-11295744	NHEK	skin:	n/a	n/a
43	CTCF	chr2:11294780-11294930	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr2:11295600-11295750	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr2:11295600-11295750	Caco-2	colon:	n/a	n/a
46	CTCF	chr2:11295700-11295850	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr2:11295609-11295724	GM12891	blood:	n/a	n/a
48	CTCF	chr2:11295590-11295755	GM19240	blood:	n/a	n/a
49	CTCF	chr2:11294740-11294890	HCFaa	heart:	n/a	n/a
50	CTCF	chr2:11295620-11295770	WERI-Rb-1	eye:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:11295222-11295272	GM12878	blood:	n/a
2	chr2:11295222-11295272	GM12878	blood:	n/a
3	chr2:11295833-11295883	SKMC	muscle:	n/a
4	chr2:11295416-11295466	HL-60	blood:	n/a
5	chr2:11294738-11294788	HRPEpiC	eye:	n/a
6	chr2:11295416-11295466	GM12878	blood:	n/a
7	chr2:11294585-11294635	SK-N-SH_RA	brain:	n/a
8	chr2:11294585-11294635	K562	blood:	n/a
9	chr2:11295383-11295433	AG04450	lung:	fetal
10	chr2:11295383-11295433	HRPEpiC	eye:	n/a
11	chr2:11295313-11295363	Hepatocyte	liver:	n/a
12	chr2:11295416-11295466	NB4	blood:	n/a
13	chr2:11295394-11295444	HRCEpiC	kidney:	n/a
14	chr2:11295919-11295969	HRCEpiC	kidney:	n/a
15	chr2:11295394-11295444	HAEpiC	amniotic membrane:	n/a
16	chr2:11295313-11295363	NHDF-neo	bronchial:	n/a
17	chr2:11294585-11294635	Hepatocyte	liver:	n/a
18	chr2:11295222-11295272	NB4	blood:	n/a
19	chr2:11295416-11295466	HAEpiC	amniotic membrane:	n/a
20	chr2:11295717-11295767	GM12878	blood:	n/a
21	chr2:11294738-11294788	A549	lung:	n/a
22	chr2:11295313-11295363	ECC-1	luminal epithelium:	n/a
23	chr2:11294738-11294788	NB4	blood:	n/a
24	chr2:11295833-11295883	HRE	kidney:	n/a
25	chr2:11295833-11295883	GM12891	blood:	n/a
26	chr2:11295222-11295272	BJ	skin:	n/a
27	chr2:11294738-11294788	ECC-1	luminal epithelium:	n/a
28	chr2:11295416-11295466	HepG2	liver:	n/a
29	chr2:11295416-11295466	T-47D	breast:	n/a
30	chr2:11295394-11295444	HepG2	liver:	n/a
31	chr2:11295919-11295969	SK-N-SH	brain:	n/a
32	chr2:11295833-11295883	HCM	heart:	n/a
33	chr2:11295416-11295466	ovcar-3	ovarian:	n/a
34	chr2:11295383-11295433	HUVEC	blood vessel:	n/a
35	chr2:11295416-11295466	SK-N-SH	brain:	n/a
36	chr2:11295717-11295767	A549	lung:	n/a
37	chr2:11295416-11295466	PFSK-1	brain:	n/a
38	chr2:11295313-11295363	AG09309	skin:	n/a
39	chr2:11295833-11295883	U87	brain:	n/a
40	chr2:11295919-11295969	Hepatocyte	liver:	n/a
41	chr2:11295226-11295276	SK-N-MC	brain:	n/a
42	chr2:11295222-11295272	GM19239	blood:	n/a
43	chr2:11294585-11294635	ovcar-3	ovarian:	n/a
44	chr2:11294738-11294788	AG04449	skin:	fetal
45	chr2:11295416-11295466	ECC-1	luminal epithelium:	n/a
46	chr2:11295313-11295363	AG09319	gingival:	n/a
47	chr2:11294585-11294635	AG10803	skin:	n/a
48	chr2:11295394-11295444	HNPCEpiC	eye:	n/a
49	chr2:11295222-11295272	SK-N-MC	brain:	n/a
50	chr2:11295833-11295883	NHDF-neo	bronchial:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:11296019..11298621-chr2:11300609..11302864,3	K562	blood:
2	chr2:11273055..11275301-chr2:11293268..11296881,3	MCF-7	breast:
3	chr2:11294400..11297941-chr2:11298345..11302243,10	MCF-7	breast:
4	chr2:11292941..11297094-chr2:11480820..11486254,6	MCF-7	breast:
5	chr12:92538292..92539809-chr2:11295819..11297319,2	K562	blood:
6	chr2:11292794..11295094-chr2:11339407..11341727,2	MCF-7	breast:
7	chr2:11294308..11297184-chr2:11482767..11485221,3	K562	blood:
8	chr2:11273067..11276077-chr2:11294167..11297061,3	K562	blood:
9	chr2:11293490..11296297-chr2:11680693..11684323,3	MCF-7	breast:
10	chr2:11294716..11295342-chr7:26239803..26240689,2	Hela-S3	cervix:
11	chr2:11284657..11286652-chr2:11293189..11295227,2	K562	blood:
12	chr2:11295159..11297169-chr2:11486526..11488952,2	K562	blood:
13	chr2:11292916..11295580-chr2:11604494..11607840,3	MCF-7	breast:
14	chr2:11295929..11299678-chr2:11300609..11303606,5	K562	blood:
15	chr2:11271098..11275692-chr2:11293512..11297101,4	MCF-7	breast:

No data

Variant related genes	Relation type
PQLC3	TF binding region
PQLC3	CpG island
ENSG00000150873	chromatin interactions
ENSG00000196208	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000169016	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000145063	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000162976	chromatin interactions
ENSG00000264010	chromatin interactions
ENSG00000134318	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114389093	chr2:11294379-11294380	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs577239647	chr2:11294459-11294460	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs544853748	chr2:11294475-11294476	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs563606404	chr2:11294494-11294495	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs530609341	chr2:11294518-11294519	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs542854516	chr2:11294528-11294529	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs561202233	chr2:11294542-11294543	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs73175632	chr2:11294618-11294619	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs547913600	chr2:11294670-11294671	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs547138515	chr2:11294745-11294746	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs368671447	chr2:11294747-11294748	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs190363522	chr2:11294825-11294826	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs532560207	chr2:11294833-11294834	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs73175633	chr2:11294849-11294850	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs12615623	chr2:11294890-11294891	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs558700492	chr2:11294922-11294923	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs555181105	chr2:11294925-11294926	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs192610296	chr2:11294950-11294951	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs534383984	chr2:11294956-11294957	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs139366835	chr2:11294958-11294959	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs183572902	chr2:11294994-11294995	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs188222651	chr2:11295099-11295100	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs577175294	chr2:11295132-11295133	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs181099942	chr2:11295133-11295134	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs556972139	chr2:11295144-11295145	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs575521836	chr2:11295153-11295154	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs542441660	chr2:11295169-11295170	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs554308010	chr2:11295186-11295187	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs148805827	chr2:11295226-11295227	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs368293631	chr2:11295247-11295248	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs184793019	chr2:11295253-11295254	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs190080066	chr2:11295266-11295267	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs528299062	chr2:11295318-11295319	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs540690262	chr2:11295356-11295357	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs565420290	chr2:11295371-11295372	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs532550001	chr2:11295392-11295393	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs550983371	chr2:11295464-11295465	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs563026461	chr2:11295564-11295565	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs530386504	chr2:11295574-11295575	Active TSS Bivalent/Poised TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs548620891	chr2:11295632-11295633	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs566675100	chr2:11295642-11295643	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs553468503	chr2:11295645-11295646	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs534131759	chr2:11295646-11295647	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs546277809	chr2:11295650-11295651	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs571056241	chr2:11295673-11295674	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs370912254	chr2:11295685-11295686	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs372049512	chr2:11295694-11295695	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs200593382	chr2:11295716-11295717	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs575146395	chr2:11295776-11295777	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs376938810	chr2:11295798-11295799	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:542 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11273600-11294400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr2:11274000-11294600	Weak transcription	Right Atrium	heart
3	chr2:11284600-11294600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:11288200-11294400	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr2:11288200-11294600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:11289600-11294600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:11289800-11294400	Weak transcription	Pancreas	Pancrea
8	chr2:11291600-11294400	Weak transcription	Adipose Nuclei	Adipose
9	chr2:11291800-11294800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:11292800-11294600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr2:11294200-11294400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr2:11294200-11294400	Active TSS	Primary T helper cells fromperipheralblood	blood
13	chr2:11294200-11294400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
14	chr2:11294200-11294400	Flanking Active TSS	Spleen	Spleen
15	chr2:11294200-11294400	Enhancers	Hela-S3	cervix
16	chr2:11294200-11294600	Enhancers	Primary B cells from cord blood	blood
17	chr2:11294200-11294600	Enhancers	Primary B cells from peripheral blood	blood
18	chr2:11294200-11294600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr2:11294200-11294600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr2:11294200-11294600	Bivalent Enhancer	Fetal Intestine Small	intestine
21	chr2:11294200-11294600	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr2:11294200-11294600	Enhancers	Placenta	Placenta
23	chr2:11294200-11294600	Enhancers	Rectal Mucosa Donor 29	rectum
24	chr2:11294200-11294800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr2:11294400-11294600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr2:11294400-11294600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr2:11294400-11294600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr2:11294400-11294600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr2:11294400-11294600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
30	chr2:11294400-11294600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr2:11294400-11294600	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr2:11294400-11294600	Enhancers	Primary T cells from cord blood	blood
33	chr2:11294400-11294600	Enhancers	Primary T cells fromperipheralblood	blood
34	chr2:11294400-11294600	Enhancers	Primary hematopoietic stem cells	blood
35	chr2:11294400-11294600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr2:11294400-11294600	Enhancers	Primary T helper naive cells from peripheral blood	blood
37	chr2:11294400-11294600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr2:11294400-11294600	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr2:11294400-11294600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr2:11294400-11294600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr2:11294400-11294600	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr2:11294400-11294600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr2:11294400-11294600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:11294400-11294600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
45	chr2:11294400-11294600	Enhancers	Liver	Liver
46	chr2:11294400-11294600	Enhancers	Brain Angular Gyrus	brain
47	chr2:11294400-11294600	Enhancers	Brain Cingulate Gyrus	brain
48	chr2:11294400-11294600	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr2:11294400-11294600	Active TSS	Colonic Mucosa	Colon
50	chr2:11294400-11294600	Active TSS	Colon Smooth Muscle	Colon

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