Variant report

Variant	nsv914964
Chromosome Location	chr22:30081715-30150549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1369)
CpG islands
(count:1465)
Chromatin interactive
region (count:70)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1369 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:30097434-30097985	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:30100619-30100836	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:30112673-30113047	HepG2	liver:	n/a	n/a
4	ATF3	chr22:30123277-30123446	K562	blood:	n/a	n/a
5	BACH1	chr22:30117117-30117164	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL3	chr22:30101958-30102330	GM12878	blood:	n/a	n/a
7	BHLHE40	chr22:30128256-30128610	K562	blood:	n/a	n/a
8	BHLHE40	chr22:30129772-30130101	K562	blood:	n/a	n/a
9	BHLHE40	chr22:30123039-30123491	K562	blood:	n/a	chr22:30123301-30123317 chr22:30123298-30123314
10	BHLHE40	chr22:30122204-30122269	K562	blood:	n/a	n/a
11	BHLHE40	chr22:30112938-30112959	K562	blood:	n/a	n/a
12	BHLHE40	chr22:30129783-30130011	GM12878	blood:	n/a	n/a
13	BRCA1	chr22:30129764-30130130	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr22:30128277-30128548	K562	blood:	n/a	n/a
15	CBX3	chr22:30122729-30123043	K562	blood:	n/a	n/a
16	CCNT2	chr22:30122115-30122354	K562	blood:	n/a	n/a
17	CCNT2	chr22:30130069-30130217	K562	blood:	n/a	n/a
18	CEBPB	chr22:30087982-30088055	K562	blood:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
19	CEBPB	chr22:30112795-30113094	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr22:30129437-30129695	K562	blood:	n/a	n/a
21	CEBPB	chr22:30123286-30123530	A549	lung:	n/a	n/a
22	CEBPB	chr22:30087950-30088067	Hela-S3	cervix:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
23	CEBPB	chr22:30087842-30088200	H1-hESC	embryonic stem cell:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
24	CEBPB	chr22:30129409-30129687	K562	blood:	n/a	n/a
25	CEBPB	chr22:30120297-30120612	HepG2	liver:	n/a	chr22:30120448-30120459
26	CEBPB	chr22:30147153-30147508	K562	blood:	n/a	n/a
27	CEBPB	chr22:30123279-30123521	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr22:30129330-30129738	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr22:30112805-30112998	K562	blood:	n/a	n/a
30	CEBPB	chr22:30087998-30088064	IMR90	lung:	n/a	chr22:30088030-30088041 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088030-30088039 chr22:30088028-30088041
31	CEBPB	chr22:30120302-30120606	MCF-7	breast:	n/a	chr22:30120448-30120459
32	CEBPB	chr22:30112804-30113093	IMR90	lung:	n/a	n/a
33	CEBPB	chr22:30120413-30120592	Hela-S3	cervix:	n/a	chr22:30120448-30120459
34	CEBPB	chr22:30112775-30113097	HepG2	liver:	n/a	n/a
35	CEBPB	chr22:30112810-30112951	HepG2	liver:	n/a	n/a
36	CEBPB	chr22:30129294-30130046	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr22:30140848-30141119	IMR90	lung:	n/a	n/a
38	CEBPB	chr22:30106956-30107195	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr22:30129150-30130110	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr22:30120332-30120505	A549	lung:	n/a	chr22:30120448-30120459
41	CEBPB	chr22:30123245-30123541	IMR90	lung:	n/a	n/a
42	CEBPB	chr22:30147207-30147440	IMR90	lung:	n/a	n/a
43	CEBPB	chr22:30123247-30123550	HepG2	liver:	n/a	n/a
44	CEBPB	chr22:30123242-30123551	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr22:30123189-30123587	MCF-7	breast:	n/a	n/a
46	CEBPB	chr22:30123253-30123563	K562	blood:	n/a	n/a
47	CEBPB	chr22:30120445-30120468	IMR90	lung:	n/a	chr22:30120448-30120459
48	CEBPB	chr22:30099063-30099290	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr22:30147179-30147493	HepG2	liver:	n/a	n/a
50	CEBPD	chr22:30129823-30130320	K562	blood:	n/a	n/a

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:30116328-30116378	A549	lung:	n/a
2	chr22:30116328-30116378	A549	lung:	n/a
3	chr22:30107178-30107228	HCM	heart:	n/a
4	chr22:30119712-30119762	U87	brain:	n/a
5	chr22:30125642-30125692	PrEC	prostate:	n/a
6	chr22:30116319-30116369	HepG2	liver:	n/a
7	chr22:30117734-30117784	GM19239	blood:	n/a
8	chr22:30119712-30119762	HCPEpiC	choroid plexus:	n/a
9	chr22:30116037-30116087	SKMC	muscle:	n/a
10	chr22:30115154-30115204	HRCEpiC	kidney:	n/a
11	chr22:30122327-30122377	HEK293	kidney:	embryo
12	chr22:30116319-30116369	MCF10A-Er-Src	breast:	n/a
13	chr22:30117734-30117784	HEK293	kidney:	embryo
14	chr22:30116953-30117003	HUVEC	blood vessel:	n/a
15	chr22:30091734-30091784	K562	blood:	n/a
16	chr22:30117734-30117784	Caco-2	colon:	n/a
17	chr22:30107178-30107228	NHDF-neo	bronchial:	n/a
18	chr22:30125353-30125403	HAEpiC	amniotic membrane:	n/a
19	chr22:30125483-30125533	NT2-D1	testis:	n/a
20	chr22:30117148-30117198	HAEpiC	amniotic membrane:	n/a
21	chr22:30116037-30116087	MCF10A-Er-Src	breast:	n/a
22	chr22:30117734-30117784	T-47D	breast:	n/a
23	chr22:30119712-30119762	AG09319	gingival:	n/a
24	chr22:30115348-30115398	SKMC	muscle:	n/a
25	chr22:30116489-30116539	HRCEpiC	kidney:	n/a
26	chr22:30116953-30117003	NB4	blood:	n/a
27	chr22:30116319-30116369	SKMC	muscle:	n/a
28	chr22:30116319-30116369	AG04449	skin:	fetal
29	chr22:30117734-30117784	ovcar-3	ovarian:	n/a
30	chr22:30116489-30116539	HCF	heart:	n/a
31	chr22:30115348-30115398	HEEpiC	esophagus:	n/a
32	chr22:30129607-30129657	HCF	heart:	n/a
33	chr22:30116439-30116489	GM12891	blood:	n/a
34	chr22:30122327-30122377	GM12878	blood:	n/a
35	chr22:30115154-30115204	HEEpiC	esophagus:	n/a
36	chr22:30091734-30091784	H1-hESC	embryonic stem cell:	embryo
37	chr22:30116439-30116489	HCM	heart:	n/a
38	chr22:30125353-30125403	NH-A	brain:	n/a
39	chr22:30115348-30115398	HRE	kidney:	n/a
40	chr22:30115348-30115398	HRPEpiC	eye:	n/a
41	chr22:30116439-30116489	H1-hESC	embryonic stem cell:	embryo
42	chr22:30116489-30116539	AG09319	gingival:	n/a
43	chr22:30115348-30115398	GM06990	blood:	n/a
44	chr22:30107178-30107228	ProgFib	skin:	n/a
45	chr22:30127118-30127168	Hepatocyte	liver:	n/a
46	chr22:30115154-30115204	Caco-2	colon:	n/a
47	chr22:30129607-30129657	LNCaP	prostate:	n/a
48	chr22:30129607-30129657	T-47D	breast:	n/a
49	chr22:30107178-30107228	ECC-1	luminal epithelium:	n/a
50	chr22:30125642-30125692	MCF-7	breast:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:30130941..30133818-chr22:30144985..30147499,2	MCF-7	breast:
2	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:
3	chr22:30096098..30098972-chr22:30384609..30387065,2	MCF-7	breast:
4	chr22:30094321..30096563-chr22:30160914..30162763,2	MCF-7	breast:
5	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
6	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
7	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
8	chr22:30148345..30151530-chr22:30155464..30158156,3	MCF-7	breast:
9	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
10	chr22:30098089..30098947-chr22:30484640..30485526,4	MCF-7	breast:
11	chr22:30127476..30130014-chr22:30183535..30186061,2	MCF-7	breast:
12	chr22:30122754..30125379-chr22:30128810..30131334,3	MCF-7	breast:
13	chr22:30085941..30086486-chr22:30484564..30485178,2	K562	blood:
14	chr22:30096975..30100180-chr22:30101896..30105574,4	K562	blood:
15	chr22:30133945..30136337-chr22:30161656..30163853,2	MCF-7	breast:
16	chr22:30097362..30099278-chr22:30100636..30102663,2	K562	blood:
17	chr22:30086550..30091376-chr22:30091742..30099600,10	MCF-7	breast:
18	chr22:30082647..30084223-chr22:30084382..30086016,2	K562	blood:
19	chr22:30142692..30145269-chr22:30145289..30147345,2	K562	blood:
20	chr22:30091150..30094109-chr22:30098424..30101093,2	K562	blood:
21	chr22:30119899..30121884-chr22:30123778..30126684,2	MCF-7	breast:
22	chr22:30128408..30130433-chr22:30161291..30163799,2	MCF-7	breast:
23	chr22:30086357..30088684-chr22:30160929..30163029,2	MCF-7	breast:
24	chr22:30091841..30093848-chr22:30094919..30097302,3	MCF-7	breast:
25	chr22:30098350..30101826-chr22:30195223..30196896,3	MCF-7	breast:
26	chr22:30097300..30097855-chr22:30400940..30401466,2	K562	blood:
27	chr22:30091889..30092650-chr22:30194897..30195405,2	MCF-7	breast:
28	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
29	chr22:30136102..30138464-chr22:30143800..30146252,2	MCF-7	breast:
30	chr22:30085509..30086792-chr22:30400990..30401964,4	MCF-7	breast:
31	chr22:30139115..30141689-chr22:30143703..30146029,2	K562	blood:
32	chr22:30145045..30147687-chr22:30166151..30168873,2	MCF-7	breast:
33	chr22:30130941..30133818-chr22:30144985..30147499,2	MCF-7	breast:
34	chr22:30126344..30127866-chr22:30201046..30202629,2	K562	blood:
35	chr22:30139115..30141689-chr22:30143703..30146029,2	K562	blood:
36	chr22:30126165..30128637-chr22:30161660..30163491,2	MCF-7	breast:
37	chr22:30135111..30137455-chr22:30141470..30144208,2	K562	blood:
38	chr22:30114234..30116768-chr22:30120016..30122557,3	MCF-7	breast:
39	chr22:30086550..30091376-chr22:30091742..30099600,10	MCF-7	breast:
40	chr22:30101634..30103485-chr22:30110793..30113259,2	K562	blood:
41	chr22:30097693..30098380-chr22:30484799..30485447,2	MCF-7	breast:
42	chr22:30103672..30106590-chr22:30107402..30109092,2	MCF-7	breast:
43	chr22:30085928..30087473-chr22:30162751..30164903,2	MCF-7	breast:
44	chr22:30096968..30098760-chr22:30102459..30104662,3	MCF-7	breast:
45	chr22:30097244..30097815-chr22:30485015..30485549,2	MCF-7	breast:
46	chr22:30086150..30087724-chr22:30089523..30091656,2	K562	blood:
47	chr22:30142692..30145269-chr22:30145289..30147345,2	K562	blood:
48	chr22:30085533..30086077-chr22:30484646..30485170,2	MCF-7	breast:
49	chr22:30086150..30087724-chr22:30089523..30091656,2	K562	blood:
50	chr22:30123279..30125899-chr22:30126231..30128918,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZMAT5-1	chr22:30115558-30115703	XLOC_014338
2	lnc-ZMAT5-1	chr22:30107809-30107906	XLOC_014338
3	lnc-ZMAT5-1	chr22:30114214-30114787	NONHSAT084729
4	lnc-ZMAT5-1	chr22:30107802-30107984	XLOC_014338
5	lnc-ZMAT5-1	chr22:30102120-30102223	XLOC_014338
6	lnc-ZMAT5-1	chr22:30115537-30115756	NONHSAT084729
7	lnc-ZMAT5-1	chr22:30101245-30101418	XLOC_014338
8	lnc-ZMAT5-1	chr22:30115537-30115848	XLOC_014338
9	lnc-ZMAT5-1	chr22:30115537-30115737	XLOC_014338

No data

Variant related genes	Relation type
ENSG00000200976	TF binding region
CABP7	TF binding region
ENSG00000232396	TF binding region
ENSG00000239446	TF binding region
ENSG00000200976	CpG island
CABP7	CpG island
ENSG00000232396	CpG island
ENSG00000239446	CpG island
ENSG00000200976	chromatin interactions
ENSG00000232396	chromatin interactions
ENSG00000100325	chromatin interactions
ENSG00000239446	chromatin interactions
ENSG00000100314	chromatin interactions
ENSG00000184076	chromatin interactions
ENSG00000100319	chromatin interactions
NID1	miRNA target sites
NHLRC3	miRNA target sites

Extended variants
information (count: 2692 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:2692 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2530678	chr22:30081715-30081716	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189710150	chr22:30081759-30081760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143026869	chr22:30081783-30081784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147759566	chr22:30081842-30081843	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549076229	chr22:30081847-30081848	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373984234	chr22:30081879-30081880	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560693315	chr22:30081924-30081925	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75765368	chr22:30081944-30081945	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79758160	chr22:30081945-30081946	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79609702	chr22:30081946-30081947	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551252887	chr22:30081955-30081956	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs557350169	chr22:30081956-30081957	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs569559008	chr22:30081957-30081958	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533714139	chr22:30081992-30081993	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551980490	chr22:30081993-30081994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs180783449	chr22:30082048-30082049	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368261472	chr22:30082052-30082053	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183765833	chr22:30082093-30082094	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374848138	chr22:30082102-30082103	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117943290	chr22:30082110-30082111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs28557267	chr22:30082120-30082121	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141869519	chr22:30082137-30082138	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537858755	chr22:30082165-30082166	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556179154	chr22:30082171-30082172	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs577515059	chr22:30082179-30082180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs147105522	chr22:30082182-30082183	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs138492946	chr22:30082225-30082226	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567521984	chr22:30082268-30082269	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542311046	chr22:30082275-30082276	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9625850	chr22:30082331-30082332	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs141934268	chr22:30082366-30082367	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543436855	chr22:30082384-30082385	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs5763418	chr22:30082434-30082435	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564899765	chr22:30082445-30082446	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533654007	chr22:30082457-30082458	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189310004	chr22:30082562-30082563	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2530679	chr22:30082569-30082570	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
38	rs527891708	chr22:30082621-30082622	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181888230	chr22:30082624-30082625	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567739803	chr22:30082633-30082634	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537998421	chr22:30082663-30082664	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556117634	chr22:30082735-30082736	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138794521	chr22:30082763-30082764	Weak transcription Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs185700835	chr22:30082839-30082840	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539854061	chr22:30082859-30082860	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs191935800	chr22:30082887-30082888	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529852861	chr22:30082916-30082917	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs5763419	chr22:30082921-30082922	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs554512444	chr22:30082956-30082957	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs527974654	chr22:30082962-30082963	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
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
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	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
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	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
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2480 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30014400-30085800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr22:30020800-30097000	Weak transcription	Stomach Mucosa	stomach
3	chr22:30050200-30084800	Strong transcription	Primary T helper cells fromperipheralblood	blood
4	chr22:30050400-30084400	Strong transcription	Left Ventricle	heart
5	chr22:30050400-30093000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr22:30050800-30084800	Strong transcription	Thymus	Thymus
7	chr22:30051000-30083600	Strong transcription	Fetal Muscle Leg	muscle
8	chr22:30051000-30085400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr22:30051400-30082600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr22:30053400-30084400	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr22:30053400-30087400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr22:30053800-30084600	Strong transcription	Fetal Stomach	stomach
13	chr22:30054000-30094800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr22:30055400-30095200	Strong transcription	Fetal Intestine Small	intestine
15	chr22:30056000-30094800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr22:30056200-30084600	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr22:30056200-30084800	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr22:30056400-30084600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr22:30057800-30085600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr22:30057800-30086000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr22:30058200-30084200	Strong transcription	Muscle Satellite Cultured Cells	--
22	chr22:30059600-30081800	Strong transcription	NHLF	lung
23	chr22:30060000-30084800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr22:30060200-30093600	Strong transcription	Fetal Thymus	thymus
25	chr22:30061000-30083600	Strong transcription	NH-A	brain
26	chr22:30061000-30084400	Strong transcription	Osteobl	bone
27	chr22:30062000-30084600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr22:30063000-30083400	Strong transcription	Primary B cells from peripheral blood	blood
29	chr22:30063200-30084000	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr22:30063200-30084400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr22:30063200-30084400	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr22:30063200-30084600	Strong transcription	Sigmoid Colon	Sigmoid Colon
33	chr22:30063400-30084400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr22:30063400-30084400	Strong transcription	Fetal Muscle Trunk	muscle
35	chr22:30063400-30084600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr22:30063400-30084800	Strong transcription	Dnd41	blood
37	chr22:30063400-30085000	Strong transcription	Duodenum Mucosa	Duodenum
38	chr22:30063400-30094600	Strong transcription	Primary T cells from cord blood	blood
39	chr22:30063600-30084600	Strong transcription	Liver	Liver
40	chr22:30063800-30084200	Strong transcription	HSMM	muscle
41	chr22:30063800-30084400	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr22:30063800-30084400	Strong transcription	NHEK	skin
43	chr22:30064000-30082000	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr22:30064000-30083800	Strong transcription	Ovary	ovary
45	chr22:30064000-30084600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr22:30064200-30082000	Strong transcription	Fetal Brain Female	brain
47	chr22:30065200-30085200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr22:30066400-30083800	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr22:30067000-30082000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr22:30067600-30082600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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