Variant report

Variant	nsv914992
Chromosome Location	chr22:34135007-34283144
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1055)
CpG islands
(count:61)
Chromatin interactive
region (count:44)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:34219541-34219836	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:34263027-34263505	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:34260707-34261720	HepG2	liver:	n/a	n/a
4	ATF2	chr22:34181226-34181686	GM12878	blood:	n/a	n/a
5	ATF2	chr22:34185755-34186363	GM12878	blood:	n/a	n/a
6	ATF2	chr22:34237683-34238915	GM12878	blood:	n/a	n/a
7	ATF2	chr22:34267833-34268333	GM12878	blood:	n/a	n/a
8	ATF2	chr22:34237716-34238353	GM12878	blood:	n/a	n/a
9	ATF2	chr22:34183601-34184137	GM12878	blood:	n/a	n/a
10	ATF2	chr22:34183459-34184387	GM12878	blood:	n/a	n/a
11	ATF2	chr22:34185841-34186312	GM12878	blood:	n/a	n/a
12	ATF2	chr22:34267904-34268303	GM12878	blood:	n/a	n/a
13	BACH1	chr22:34267545-34267589	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr22:34221773-34221807	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr22:34244328-34244642	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr22:34135101-34135251	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr22:34225564-34225840	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr22:34279594-34279893	GM12878	blood:	n/a	chr22:34279726-34279737
19	BATF	chr22:34185838-34186311	GM12878	blood:	n/a	n/a
20	BATF	chr22:34185847-34186124	GM12878	blood:	n/a	n/a
21	BATF	chr22:34244253-34244653	GM12878	blood:	n/a	chr22:34244450-34244461
22	BATF	chr22:34279533-34279901	GM12878	blood:	n/a	chr22:34279726-34279737
23	BATF	chr22:34183589-34183875	GM12878	blood:	n/a	n/a
24	BATF	chr22:34184057-34184349	GM12878	blood:	n/a	n/a
25	BATF	chr22:34237726-34237991	GM12878	blood:	n/a	n/a
26	BATF	chr22:34154766-34154993	GM12878	blood:	n/a	n/a
27	BCL11A	chr22:34279585-34279869	GM12878	blood:	n/a	n/a
28	BCL11A	chr22:34279521-34279833	GM12878	blood:	n/a	n/a
29	BCL11A	chr22:34183569-34183918	GM12878	blood:	n/a	n/a
30	BCL3	chr22:34185878-34186387	GM12878	blood:	n/a	n/a
31	BCL3	chr22:34139772-34140140	GM12878	blood:	n/a	n/a
32	BCL3	chr22:34153825-34154068	GM12878	blood:	n/a	n/a
33	BCL3	chr22:34279570-34279880	GM12878	blood:	n/a	n/a
34	BCLAF1	chr22:34183553-34184056	GM12878	blood:	n/a	n/a
35	BCLAF1	chr22:34185839-34186424	GM12878	blood:	n/a	n/a
36	BCLAF1	chr22:34237755-34238277	GM12878	blood:	n/a	n/a
37	BCLAF1	chr22:34181218-34181676	GM12878	blood:	n/a	n/a
38	BCLAF1	chr22:34183601-34183918	GM12878	blood:	n/a	n/a
39	BCLAF1	chr22:34238364-34238878	GM12878	blood:	n/a	n/a
40	BHLHE40	chr22:34185856-34186187	GM12878	blood:	n/a	n/a
41	BHLHE40	chr22:34202110-34202534	GM12878	blood:	n/a	n/a
42	BHLHE40	chr22:34168931-34169192	GM12878	blood:	n/a	n/a
43	CEBPB	chr22:34237675-34238915	GM12878	blood:	n/a	n/a
44	CEBPB	chr22:34142598-34142923	HepG2	liver:	n/a	chr22:34142745-34142756 chr22:34142744-34142757
45	CEBPB	chr22:34181187-34181655	IMR90	lung:	n/a	n/a
46	CEBPB	chr22:34194364-34194659	HepG2	liver:	n/a	chr22:34194414-34194427
47	CEBPB	chr22:34257515-34257838	MCF-7	breast:	n/a	chr22:34257719-34257730
48	CEBPB	chr22:34153833-34154197	HepG2	liver:	n/a	n/a
49	CEBPB	chr22:34260638-34261015	IMR90	lung:	n/a	chr22:34260820-34260831
50	CEBPB	chr22:34160038-34160378	HepG2	liver:	n/a	chr22:34160214-34160225 chr22:34160212-34160223

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34192387-34192437	HRE	kidney:	n/a
2	chr22:34192387-34192437	CMK	blood:	n/a
3	chr22:34192387-34192437	SAEC	small airway:	n/a
4	chr22:34192387-34192437	SK-N-SH_RA	brain:	n/a
5	chr22:34192387-34192437	IMR90	lung:	fetal
6	chr22:34192387-34192437	NB4	blood:	n/a
7	chr22:34192387-34192437	NT2-D1	testis:	n/a
8	chr22:34192387-34192437	PFSK-1	brain:	n/a
9	chr22:34192387-34192437	HL-60	blood:	n/a
10	chr22:34192387-34192437	U87	brain:	n/a
11	chr22:34192387-34192437	HCPEpiC	choroid plexus:	n/a
12	chr22:34192387-34192437	GM06990	blood:	n/a
13	chr22:34192387-34192437	HRPEpiC	eye:	n/a
14	chr22:34192387-34192437	RPTEC	kidney:	n/a
15	chr22:34192387-34192437	HRCEpiC	kidney:	n/a
16	chr22:34192387-34192437	HNPCEpiC	eye:	n/a
17	chr22:34192387-34192437	BE2_C	brain:	n/a
18	chr22:34192387-34192437	AG04449	skin:	fetal
19	chr22:34192387-34192437	A549	lung:	n/a
20	chr22:34192387-34192437	HCT-116	colon:	n/a
21	chr22:34192387-34192437	HEEpiC	esophagus:	n/a
22	chr22:34192387-34192437	BJ	skin:	n/a
23	chr22:34192387-34192437	MCF-7	breast:	n/a
24	chr22:34192387-34192437	MCF10A-Er-Src	breast:	n/a
25	chr22:34192387-34192437	SK-N-MC	brain:	n/a
26	chr22:34192387-34192437	NH-A	brain:	n/a
27	chr22:34192387-34192437	ovcar-3	ovarian:	n/a
28	chr22:34192387-34192437	Hela-S3	cervix:	n/a
29	chr22:34192387-34192437	ECC-1	luminal epithelium:	n/a
30	chr22:34192387-34192437	K562	blood:	n/a
31	chr22:34192387-34192437	PANC-1	pancreas:	n/a
32	chr22:34192387-34192437	Hepatocyte	liver:	n/a
33	chr22:34192387-34192437	GM12878	blood:	n/a
34	chr22:34192387-34192437	T-47D	breast:	n/a
35	chr22:34192387-34192437	AG09309	skin:	n/a
36	chr22:34192387-34192437	LNCaP	prostate:	n/a
37	chr22:34192387-34192437	GM19239	blood:	n/a
38	chr22:34192387-34192437	GM12892	blood:	n/a
39	chr22:34192387-34192437	Jurkat	blood:	n/a
40	chr22:34192387-34192437	HCF	heart:	n/a
41	chr22:34192387-34192437	AG10803	skin:	n/a
42	chr22:34192387-34192437	HMEC	breast:	n/a
43	chr22:34192387-34192437	GM12891	blood:	n/a
44	chr22:34192387-34192437	AG09319	gingival:	n/a
45	chr22:34192387-34192437	SKMC	muscle:	n/a
46	chr22:34192387-34192437	PrEC	prostate:	n/a
47	chr22:34192387-34192437	HCM	heart:	n/a
48	chr22:34192387-34192437	HEK293	kidney:	embryo
49	chr22:34192387-34192437	HUVEC	blood vessel:	n/a
50	chr22:34192387-34192437	HepG2	liver:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:34255181..34259842-chr22:34260995..34265736,9	MCF-7	breast:
2	chr22:34259639..34261419-chr22:34267116..34269181,2	MCF-7	breast:
3	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
4	chr22:34255630..34257426-chr22:34307549..34309607,2	MCF-7	breast:
5	chr22:34261522..34263199-chr22:34316447..34319258,2	MCF-7	breast:
6	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
7	chr22:34181411..34183196-chr22:34314966..34317332,2	MCF-7	breast:
8	chr22:34265653..34267240-chr22:34270322..34272194,2	MCF-7	breast:
9	chr22:34262180..34264985-chr22:34291444..34294296,2	MCF-7	breast:
10	chr22:34261283..34264105-chr22:34285527..34288136,2	MCF-7	breast:
11	chr22:34269817..34272444-chr22:34314882..34316654,2	MCF-7	breast:
12	chr22:34265653..34267240-chr22:34270322..34272194,2	MCF-7	breast:
13	chr22:34243203..34243910-chr9:5087187..5087998,2	MCF-7	breast:
14	chr22:34259639..34261419-chr22:34267116..34269181,2	MCF-7	breast:
15	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
16	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
17	chr22:34255666..34258346-chr22:34316396..34318049,2	MCF-7	breast:
18	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
19	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
20	chr22:34248231..34249994-chr22:34261049..34263874,2	MCF-7	breast:
21	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
22	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
23	chr22:34247996..34248570-chr22:34261032..34261815,2	MCF-7	breast:
24	chr22:34248231..34249994-chr22:34261049..34263874,2	MCF-7	breast:
25	chr22:34247996..34248570-chr22:34261032..34261815,2	MCF-7	breast:
26	chr22:34226044..34229431-chr22:34231299..34234951,3	MCF-7	breast:
27	chr22:34260736..34263686-chr22:34313890..34318281,7	MCF-7	breast:
28	chr22:34270428..34272649-chr22:34273804..34275941,2	MCF-7	breast:
29	chr22:34270457..34273179-chr22:34316799..34318425,2	MCF-7	breast:
30	chr22:34277917..34281628-chr22:34285820..34288664,3	MCF-7	breast:
31	chr22:34247616..34248584-chr22:34315645..34316533,2	MCF-7	breast:
32	chr22:34264153..34267717-chr22:34273021..34274940,3	MCF-7	breast:
33	chr22:34143232..34145432-chr22:34315745..34318657,2	MCF-7	breast:
34	chr22:34276961..34279522-chr22:34313897..34317110,3	MCF-7	breast:
35	chr22:34270428..34272649-chr22:34273804..34275941,2	MCF-7	breast:
36	chr22:34246562..34250566-chr22:34253925..34258689,11	MCF-7	breast:
37	chr22:34264153..34267717-chr22:34273021..34274940,3	MCF-7	breast:
38	chr22:34248240..34252170-chr22:34315347..34319641,4	MCF-7	breast:
39	chr22:34279207..34280839-chr22:34295025..34297477,2	MCF-7	breast:
40	chr22:34188517..34191299-chr22:34192329..34196152,3	MCF-7	breast:
41	chr22:34167046..34169223-chr22:34170241..34173338,3	MCF-7	breast:
42	chr22:34210266..34212147-chr22:34215786..34217625,2	MCF-7	breast:
43	chr22:34172664..34173221-chr22:34313368..34314036,2	MCF-7	breast:
44	chr22:34245347..34248923-chr22:34315491..34319689,7	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TIMP3-6	chr22:34146591-34146670	ENSG00000224973.1
2	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085011
3	lnc-TIMP3-6	chr22:34139996-34140315	ENSG00000224973.1
4	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085014
5	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
6	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085015
7	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085018
8	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085012
9	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
10	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085015
11	lnc-TIMP3-6	chr22:34146591-34146729	ENSG00000224973.1
12	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
13	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085014
14	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085011
15	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085015
16	lnc-TIMP3-6	chr22:34146591-34146803	NONHSAT085011
17	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085012
18	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
19	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085018
20	lnc-TIMP3-6	chr22:34142402-34142444	NONHSAT085015
21	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085011
22	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
23	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
24	lnc-TIMP3-6	chr22:34140116-34140315	NONHSAT085012
25	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085018
26	lnc-TIMP3-6	chr22:34146591-34146715	NONHSAT085014
27	lnc-TIMP3-6	chr22:34142402-34142444	ENSG00000224973.1
28	lnc-TIMP3-6	chr22:34146591-34146830	ENSG00000224973.1
29	lnc-TIMP3-6	chr22:34140116-34140315	ENSG00000224973.1
30	lnc-TIMP3-6	chr22:34143657-34143811	ENSG00000224973.1
31	lnc-TIMP3-6	chr22:34143657-34143811	NONHSAT085014
32	lnc-TIMP3-6	chr22:34146591-34146644	ENSG00000224973.1
33	lnc-TIMP3-6	chr22:34139122-34139185	ENSG00000224973.1
34	lnc-TIMP3-6	chr22:34140116-34140179	ENSG00000224973.1

No data

Variant related genes	Relation type
LARGE-AS1	TF binding region
LARGE	TF binding region
LARGE-AS1	CpG island
LARGE	CpG island
ENSG00000133424	chromatin interactions
ENSG00000273082	chromatin interactions

Extended variants
information (count: 6527 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:6527 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs239330	chr22:34135007-34135008	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555638951	chr22:34135036-34135037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2283936	chr22:34135043-34135044	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs537998912	chr22:34135044-34135045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557576203	chr22:34135065-34135066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189669882	chr22:34135093-34135094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539870423	chr22:34135098-34135099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552479548	chr22:34135099-34135100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567725602	chr22:34135104-34135105	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs183472858	chr22:34135121-34135122	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs574036827	chr22:34135136-34135137	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs531384597	chr22:34135161-34135162	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs8137559	chr22:34135162-34135163	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs563152915	chr22:34135173-34135174	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141949960	chr22:34135174-34135175	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568174051	chr22:34135236-34135237	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs531824648	chr22:34135266-34135267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146343081	chr22:34135292-34135293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536810887	chr22:34135294-34135295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536696487	chr22:34135311-34135312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372729219	chr22:34135315-34135316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77720435	chr22:34135318-34135319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527761739	chr22:34135326-34135327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138202524	chr22:34135334-34135335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567653803	chr22:34135354-34135355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112466332	chr22:34135389-34135390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs56288740	chr22:34135413-34135414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs55662114	chr22:34135415-34135416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76672817	chr22:34135416-34135417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2283937	chr22:34135432-34135433	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs557913687	chr22:34135439-34135440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571044113	chr22:34135446-34135447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540723284	chr22:34135462-34135463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs239331	chr22:34135472-34135473	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs536294580	chr22:34135473-34135474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78133244	chr22:34135508-34135509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542177617	chr22:34135538-34135539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556598307	chr22:34135539-34135540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576649998	chr22:34135586-34135587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545298734	chr22:34135607-34135608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565458226	chr22:34135621-34135622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527825729	chr22:34135704-34135705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs16992923	chr22:34135756-34135757	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs561317811	chr22:34135776-34135777	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs187829709	chr22:34135783-34135784	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs550115281	chr22:34135789-34135790	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569085372	chr22:34135790-34135791	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs531620191	chr22:34135826-34135827	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs551329010	chr22:34135828-34135829	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs554609139	chr22:34135845-34135846	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:3221 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34111200-34146200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr22:34111800-34142800	Weak transcription	Fetal Intestine Small	intestine
3	chr22:34116400-34135800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr22:34120200-34135600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr22:34120400-34135800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr22:34121600-34136800	Weak transcription	Primary B cells from peripheral blood	blood
7	chr22:34123200-34152000	Weak transcription	Aorta	Aorta
8	chr22:34123800-34140800	Weak transcription	Fetal Stomach	stomach
9	chr22:34124800-34171000	Weak transcription	Ovary	ovary
10	chr22:34126000-34135400	Weak transcription	Right Ventricle	heart
11	chr22:34126000-34137600	Weak transcription	Psoas Muscle	Psoas
12	chr22:34126200-34176200	Weak transcription	Spleen	Spleen
13	chr22:34128600-34143200	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr22:34131000-34154200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr22:34133000-34136200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr22:34133000-34137200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr22:34133000-34138000	Enhancers	H1 Cell Line	embryonic stem cell
18	chr22:34133200-34136600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr22:34133200-34137600	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr22:34133400-34136200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr22:34133400-34136400	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr22:34133400-34136600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr22:34133400-34136800	Enhancers	H9 Cell Line	embryonic stem cell
24	chr22:34133400-34137200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr22:34133600-34140400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr22:34133800-34136200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr22:34133800-34138000	Enhancers	Fetal Heart	heart
28	chr22:34133800-34147600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr22:34134000-34135600	Enhancers	Fetal Brain Female	brain
30	chr22:34134000-34140400	Weak transcription	Lung	lung
31	chr22:34134200-34135400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr22:34134400-34164800	Weak transcription	Brain Anterior Caudate	brain
33	chr22:34134600-34135800	Weak transcription	Fetal Brain Male	brain
34	chr22:34134600-34138000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr22:34134800-34138000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr22:34135000-34135200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr22:34135000-34135800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr22:34135000-34139200	Enhancers	Left Ventricle	heart
39	chr22:34135200-34136000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr22:34135400-34136000	Enhancers	Right Ventricle	heart
41	chr22:34135400-34136200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr22:34135600-34136200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr22:34135600-34141000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr22:34135800-34136000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr22:34135800-34136000	Enhancers	Fetal Brain Male	brain
46	chr22:34135800-34136200	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr22:34135800-34137600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr22:34136000-34136400	Weak transcription	Fetal Brain Male	brain
49	chr22:34136000-34136800	Weak transcription	Right Ventricle	heart
50	chr22:34136000-34140200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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