Variant report

Variant	nsv998124
Chromosome Location	chr1:220132739-220189211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:566)
CpG islands
(count:123)
Chromatin interactive
region (count:54)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:566 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:220133296-220133448	K562	blood:	n/a	n/a
2	ARID3A	chr1:220136870-220137034	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:220164343-220164674	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:220164368-220164700	K562	blood:	n/a	n/a
5	ARID3A	chr1:220167031-220167220	HepG2	liver:	n/a	n/a
6	ATF1	chr1:220186287-220186339	K562	blood:	n/a	n/a
7	ATF1	chr1:220140136-220140189	K562	blood:	n/a	n/a
8	ATF1	chr1:220159572-220159639	K562	blood:	n/a	n/a
9	ATF2	chr1:220161520-220162244	GM12878	blood:	n/a	n/a
10	BACH1	chr1:220155654-220155669	K562	blood:	n/a	n/a
11	BACH1	chr1:220133179-220133482	K562	blood:	n/a	n/a
12	BACH1	chr1:220133249-220133472	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr1:220161821-220162147	GM12878	blood:	n/a	n/a
14	BCLAF1	chr1:220161550-220162282	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:220146543-220146775	K562	blood:	n/a	n/a
16	BHLHE40	chr1:220158687-220158770	GM12878	blood:	n/a	n/a
17	CBX3	chr1:220133132-220133547	K562	blood:	n/a	n/a
18	CCNT2	chr1:220145567-220145750	K562	blood:	n/a	n/a
19	CCNT2	chr1:220161065-220161211	K562	blood:	n/a	n/a
20	CCNT2	chr1:220165024-220165335	K562	blood:	n/a	n/a
21	CEBPB	chr1:220178881-220179152	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:220178817-220179155	K562	blood:	n/a	n/a
23	CEBPB	chr1:220178863-220179156	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:220178941-220179144	HepG2	liver:	n/a	n/a
25	CEBPB	chr1:220138393-220138502	A549	lung:	n/a	chr1:220138477-220138490
26	CEBPB	chr1:220163851-220163996	K562	blood:	n/a	n/a
27	CEBPB	chr1:220159572-220159724	A549	lung:	n/a	n/a
28	CEBPB	chr1:220138850-220138854	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:220138637-220139034	K562	blood:	n/a	chr1:220138845-220138856 chr1:220138845-220138856
30	CEBPB	chr1:220159606-220159651	K562	blood:	n/a	n/a
31	CEBPD	chr1:220138445-220138981	K562	blood:	n/a	n/a
32	CEBPD	chr1:220138544-220139041	K562	blood:	n/a	n/a
33	CTCF	chr1:220164420-220164570	GM06990	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
34	CTCF	chr1:220185860-220186010	HCT-116	colon:	n/a	n/a
35	CTCF	chr1:220185780-220185930	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr1:220185760-220185910	HMF	breast:	n/a	n/a
37	CTCF	chr1:220185680-220185830	HVMF	connective:	n/a	n/a
38	CTCF	chr1:220185760-220185910	GM12864	blood:	n/a	n/a
39	CTCF	chr1:220171760-220171910	AG09309	skin:	n/a	n/a
40	CTCF	chr1:220164397-220164658	K562	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
41	CTCF	chr1:220164196-220164281	GM10248	blood:	n/a	n/a
42	CTCF	chr1:220164480-220164630	GM12864	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
43	CTCF	chr1:220164460-220164610	HEEpiC	esophagus:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
44	CTCF	chr1:220185720-220185870	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr1:220164400-220164550	HMF	breast:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
46	CTCF	chr1:220164420-220164570	WI-38	lung:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542
47	CTCF	chr1:220185812-220185887	Lung_OC	lung:	n/a	n/a
48	CTCF	chr1:220185711-220185909	IMR90	lung:	n/a	n/a
49	CTCF	chr1:220164580-220164730	A549	lung:	n/a	n/a
50	CTCF	chr1:220164480-220164630	GM12871	blood:	n/a	chr1:220164526-220164547 chr1:220164529-220164537 chr1:220164524-220164542

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:220132728-220132778	NT2-D1	testis:	n/a
2	chr1:220132728-220132778	NT2-D1	testis:	n/a
3	chr1:220142138-220142188	HRE	kidney:	n/a
4	chr1:220142138-220142188	ovcar-3	ovarian:	n/a
5	chr1:220142138-220142188	MCF-7	breast:	n/a
6	chr1:220132728-220132778	BE2_C	brain:	n/a
7	chr1:220142138-220142188	HRPEpiC	eye:	n/a
8	chr1:220142138-220142188	Hepatocyte	liver:	n/a
9	chr1:220132728-220132778	NHDF-neo	bronchial:	n/a
10	chr1:220132728-220132778	LNCaP	prostate:	n/a
11	chr1:220142138-220142188	SK-N-SH	brain:	n/a
12	chr1:220132728-220132778	AG04450	lung:	fetal
13	chr1:220132728-220132778	GM19239	blood:	n/a
14	chr1:220132728-220132778	AG09319	gingival:	n/a
15	chr1:220132728-220132778	NB4	blood:	n/a
16	chr1:220142138-220142188	BJ	skin:	n/a
17	chr1:220142138-220142188	K562	blood:	n/a
18	chr1:220132728-220132778	PFSK-1	brain:	n/a
19	chr1:220142138-220142188	NH-A	brain:	n/a
20	chr1:220132728-220132778	HRCEpiC	kidney:	n/a
21	chr1:220142138-220142188	GM12891	blood:	n/a
22	chr1:220142138-220142188	SK-N-MC	brain:	n/a
23	chr1:220142138-220142188	HEK293	kidney:	embryo
24	chr1:220132728-220132778	PANC-1	pancreas:	n/a
25	chr1:220132728-220132778	NHBE	bronchial:	n/a
26	chr1:220142138-220142188	HCT-116	colon:	n/a
27	chr1:220142138-220142188	LNCaP	prostate:	n/a
28	chr1:220132728-220132778	SAEC	small airway:	n/a
29	chr1:220132728-220132778	HRPEpiC	eye:	n/a
30	chr1:220142138-220142188	HCPEpiC	choroid plexus:	n/a
31	chr1:220132728-220132778	T-47D	breast:	n/a
32	chr1:220132728-220132778	SK-N-MC	brain:	n/a
33	chr1:220142138-220142188	PANC-1	pancreas:	n/a
34	chr1:220142138-220142188	ProgFib	skin:	n/a
35	chr1:220142138-220142188	GM19239	blood:	n/a
36	chr1:220132728-220132778	Hepatocyte	liver:	n/a
37	chr1:220142138-220142188	NHBE	bronchial:	n/a
38	chr1:220142138-220142188	CMK	blood:	n/a
39	chr1:220132728-220132778	MCF-7	breast:	n/a
40	chr1:220132728-220132778	HCPEpiC	choroid plexus:	n/a
41	chr1:220142138-220142188	Caco-2	colon:	n/a
42	chr1:220142138-220142188	BE2_C	brain:	n/a
43	chr1:220132728-220132778	HAEpiC	amniotic membrane:	n/a
44	chr1:220132728-220132778	CMK	blood:	n/a
45	chr1:220132728-220132778	ECC-1	luminal epithelium:	n/a
46	chr1:220132728-220132778	MCF10A-Er-Src	breast:	n/a
47	chr1:220142138-220142188	HNPCEpiC	eye:	n/a
48	chr1:220132728-220132778	HUVEC	blood vessel:	n/a
49	chr1:220132728-220132778	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:220142138-220142188	AG09309	skin:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:220173071..220175187-chr1:220185418..220188228,2	K562	blood:
2	chr1:220163102..220165191-chr1:220201695..220204471,2	K562	blood:
3	chr1:220164810..220167759-chr1:220168424..220170636,2	K562	blood:
4	chr1:220164112..220164967-chr1:220297177..220297836,2	MCF-7	breast:
5	chr1:220140733..220143631-chr1:220153944..220155522,2	K562	blood:
6	chr1:220153591..220159773-chr1:220159981..220165102,9	K562	blood:
7	chr1:220153591..220159773-chr1:220159981..220165102,9	K562	blood:
8	chr1:220150167..220154916-chr1:220176228..220180180,4	K562	blood:
9	chr1:220183779..220186037-chr1:220201298..220203530,2	K562	blood:
10	chr1:220178050..220179958-chr1:220184112..220186105,3	K562	blood:
11	chr1:220178050..220179958-chr1:220184112..220186105,3	K562	blood:
12	chr1:220163484..220165362-chr1:220165481..220167153,2	K562	blood:
13	chr1:220147760..220150265-chr1:220156237..220158449,2	K562	blood:
14	chr1:220011035..220013766-chr1:220162762..220165197,2	K562	blood:
15	chr1:220170479..220172595-chr1:220177659..220180264,2	K562	blood:
16	chr1:220177307..220179895-chr1:220184539..220186379,2	K562	blood:
17	chr1:220163484..220165362-chr1:220165481..220167153,2	K562	blood:
18	chr1:220186799..220188990-chr1:220192313..220195142,2	K562	blood:
19	chr1:220139066..220142338-chr1:220143870..220147751,4	K562	blood:
20	chr1:220186134..220187962-chr1:220260106..220262494,2	K562	blood:
21	chr1:220165101..220168556-chr1:220168858..220170933,3	K562	blood:
22	chr1:220170067..220172994-chr1:220191581..220193107,2	K562	blood:
23	chr1:220009813..220011470-chr1:220168662..220170226,2	K562	blood:
24	chr1:220171119..220172994-chr1:220190101..220193081,2	K562	blood:
25	chr1:220177307..220179895-chr1:220184539..220186379,2	K562	blood:
26	chr1:220164810..220167759-chr1:220168424..220170636,2	K562	blood:
27	chr1:220138957..220140569-chr1:220217050..220219686,2	K562	blood:
28	chr1:220168435..220171336-chr1:220322060..220324695,2	K562	blood:
29	chr1:220163115..220165079-chr1:220292412..220294107,2	K562	blood:
30	chr1:220049633..220050383-chr1:220164327..220165162,2	MCF-7	breast:
31	chr1:220177032..220178609-chr1:220180305..220182071,2	K562	blood:
32	chr1:220152386..220154432-chr1:220156720..220158691,2	K562	blood:
33	chr1:220166855..220169233-chr1:220184126..220185704,2	K562	blood:
34	chr1:220155862..220157451-chr1:220170241..220172026,2	K562	blood:
35	chr1:220183714..220185388-chr1:220190799..220194584,3	K562	blood:
36	chr1:220144163..220148221-chr1:220163054..220166012,3	K562	blood:
37	chr1:220166855..220169233-chr1:220184126..220185704,2	K562	blood:
38	chr1:220139066..220142338-chr1:220143870..220147751,4	K562	blood:
39	chr1:220170479..220172595-chr1:220177659..220180264,2	K562	blood:
40	chr1:220072242..220074837-chr1:220162775..220165302,2	K562	blood:
41	chr1:220147044..220149200-chr1:220160027..220162362,2	K562	blood:
42	chr1:220176489..220178483-chr1:220194555..220197465,2	MCF-7	breast:
43	chr1:220148652..220150555-chr1:220203564..220205134,2	K562	blood:
44	chr1:220152386..220154865-chr1:220156720..220158835,3	K562	blood:
45	chr1:220150167..220154916-chr1:220176228..220180180,4	K562	blood:
46	chr1:220146642..220149260-chr1:220156237..220158114,2	K562	blood:
47	chr1:220161264..220163445-chr1:220234115..220237098,2	K562	blood:
48	chr1:220155862..220157451-chr1:220170241..220172026,2	K562	blood:
49	chr1:220165101..220168556-chr1:220168858..220170933,3	K562	blood:
50	chr1:220144163..220148221-chr1:220163054..220166012,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPRS-1	chr1:220158557-220158677	NONHSAT009569
2	lnc-EPRS-1	chr1:220153727-220153823	NONHSAT009569
3	lnc-EPRS-1	chr1:220158557-220158677	NONHSAT009572
4	lnc-EPRS-1	chr1:220154388-220154496	NONHSAT009569
5	lnc-EPRS-1	chr1:220154388-220154496	NONHSAT009572
6	lnc-EPRS-1	chr1:220153613-220153823	NONHSAT009572

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EPRS	hsa-miR-155-5p	chr1:220142097-220142122

Variant related genes	Relation type
SLC30A10	TF binding region
ENSG00000221673	TF binding region
ENSG00000238798	TF binding region
EPRS	TF binding region
SLC30A10	CpG island
ENSG00000221673	CpG island
ENSG00000238798	CpG island
EPRS	CpG island
ENSG00000136628	chromatin interactions
ENSG00000238798	chromatin interactions
ENSG00000196660	chromatin interactions

Extended variants
information (count: 2321 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4846608	chr1:220132739-220132740	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs76055036	chr1:220132743-220132744	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
3	rs147115478	chr1:220132750-220132751	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
4	rs563308186	chr1:220132788-220132789	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs147764698	chr1:220132790-220132791	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs542549206	chr1:220132812-220132813	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs189411715	chr1:220132822-220132823	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs528124661	chr1:220132898-220132899	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs6663868	chr1:220132906-220132907	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs543797766	chr1:220132931-220132932	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs181988403	chr1:220132935-220132936	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs11118471	chr1:220132961-220132962	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs577389955	chr1:220132973-220132974	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs367590551	chr1:220132999-220133000	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs375652229	chr1:220133048-220133049	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs570117136	chr1:220133068-220133069	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs77720185	chr1:220133080-220133081	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs185995386	chr1:220133104-220133105	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs566366755	chr1:220133106-220133107	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs6663947	chr1:220133115-220133116	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs6699954	chr1:220133129-220133130	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs578062755	chr1:220133144-220133145	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs6663964	chr1:220133150-220133151	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs190957918	chr1:220133156-220133157	Weak transcription Enhancers Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs370826143	chr1:220133219-220133220	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs141145921	chr1:220133230-220133231	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs367940539	chr1:220133279-220133280	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs542412221	chr1:220133281-220133282	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs77685442	chr1:220133306-220133307	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs572761000	chr1:220133324-220133325	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs11118472	chr1:220133340-220133341	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs564699786	chr1:220133345-220133346	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs181265624	chr1:220133357-220133358	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs13375889	chr1:220133364-220133365	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550614500	chr1:220133368-220133369	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs560960993	chr1:220133370-220133371	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs570597689	chr1:220133391-220133392	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs186374282	chr1:220133400-220133401	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs529551811	chr1:220133418-220133419	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs549558056	chr1:220133446-220133447	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs566376962	chr1:220133456-220133457	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs535305231	chr1:220133462-220133463	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs551766382	chr1:220133487-220133488	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs190448581	chr1:220133508-220133509	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs571585417	chr1:220133516-220133517	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs375430929	chr1:220133602-220133603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200208175	chr1:220133609-220133610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183097972	chr1:220133611-220133612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs71169418	chr1:220133637-220133638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12145500	chr1:220133643-220133644	Weak transcription	n/a	n/a	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
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
Pleomorphic liposarcoma	18784837	CNVD
Autism	14699429	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220129200-220145800	Weak transcription	HepG2	liver
2	chr1:220129400-220133000	Weak transcription	Small Intestine	intestine
3	chr1:220132000-220133400	Enhancers	Rectal Mucosa Donor 29	rectum
4	chr1:220132000-220138800	Weak transcription	Aorta	Aorta
5	chr1:220132200-220132800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
6	chr1:220132200-220132800	ZNF genes & repeats	K562	blood
7	chr1:220132200-220144200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr1:220132400-220133000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:220132400-220133400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr1:220132400-220133600	Enhancers	Fetal Intestine Large	intestine
11	chr1:220132400-220143200	Weak transcription	Colonic Mucosa	Colon
12	chr1:220132600-220132800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:220132600-220132800	Flanking Active TSS	Duodenum Mucosa	Duodenum
14	chr1:220132600-220133600	Enhancers	Fetal Intestine Small	intestine
15	chr1:220132800-220133000	Enhancers	Duodenum Mucosa	Duodenum
16	chr1:220132800-220133000	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr1:220132800-220133000	Weak transcription	K562	blood
18	chr1:220132800-220141000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr1:220132800-220177000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr1:220133000-220133200	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
21	chr1:220133000-220133400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr1:220133000-220133600	Enhancers	Small Intestine	intestine
23	chr1:220133000-220133600	Enhancers	K562	blood
24	chr1:220133000-220141200	Weak transcription	Duodenum Mucosa	Duodenum
25	chr1:220133400-220133600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:220133400-220138600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr1:220133600-220134600	Weak transcription	K562	blood
28	chr1:220133600-220140800	Weak transcription	Fetal Intestine Large	intestine
29	chr1:220133600-220141000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr1:220133600-220142200	Weak transcription	Small Intestine	intestine
31	chr1:220134600-220135000	Enhancers	K562	blood
32	chr1:220135000-220135200	Flanking Active TSS	K562	blood
33	chr1:220135200-220135400	Enhancers	K562	blood
34	chr1:220135400-220137800	Weak transcription	K562	blood
35	chr1:220136400-220138000	Enhancers	Liver	Liver
36	chr1:220137000-220137400	Enhancers	Pancreas	Pancrea
37	chr1:220137200-220145800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr1:220137400-220140800	Weak transcription	Lung	lung
39	chr1:220137400-220142000	Weak transcription	Pancreas	Pancrea
40	chr1:220137600-220142200	Weak transcription	Primary B cells from cord blood	blood
41	chr1:220137800-220140200	Enhancers	K562	blood
42	chr1:220138000-220139200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr1:220138000-220140800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:220138000-220141000	Weak transcription	Liver	Liver
45	chr1:220138000-220141400	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr1:220138000-220141400	Weak transcription	HUVEC	blood vessel
47	chr1:220138200-220140800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:220138200-220140800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr1:220138400-220141000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:220138400-220141000	Weak transcription	Fetal Muscle Leg	muscle

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