Variant report

Variant	nsv1050713
Chromosome Location	chr11:76147085-76267117
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1726)
CpG islands
(count:1344)
Chromatin interactive
region (count:119)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1726 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:76170417-76170695	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:76170444-76170716	K562	blood:	n/a	n/a
3	ARID3A	chr11:76155423-76156109	HepG2	liver:	n/a	chr11:76156005-76156013
4	ARID3A	chr11:76237845-76238331	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:76235073-76235758	HepG2	liver:	n/a	n/a
6	ATF1	chr11:76151321-76151403	K562	blood:	n/a	n/a
7	ATF1	chr11:76154648-76154944	K562	blood:	n/a	n/a
8	ATF1	chr11:76155442-76156143	K562	blood:	n/a	n/a
9	ATF1	chr11:76235636-76235763	K562	blood:	n/a	n/a
10	ATF2	chr11:76155371-76156229	GM12878	blood:	n/a	n/a
11	ATF2	chr11:76166330-76166898	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:76155172-76156214	GM12878	blood:	n/a	n/a
13	ATF2	chr11:76155234-76156040	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr11:76155269-76156077	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr11:76166298-76166952	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr11:76156698-76157173	H1-hESC	embryonic stem cell:	n/a	chr11:76156766-76156780
17	BACH1	chr11:76215563-76215651	K562	blood:	n/a	n/a
18	BACH1	chr11:76156633-76156723	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr11:76155276-76156124	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:76147120-76147367	K562	blood:	n/a	n/a
21	BATF	chr11:76147103-76147492	GM12878	blood:	n/a	chr11:76147294-76147305
22	BATF	chr11:76147213-76147402	GM12878	blood:	n/a	chr11:76147294-76147305
23	BCL11A	chr11:76166353-76166755	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL3	chr11:76155278-76156079	A549	lung:	n/a	chr11:76155437-76155446
25	BCLAF1	chr11:76155310-76156211	GM12878	blood:	n/a	chr11:76155437-76155446
26	BCLAF1	chr11:76155315-76156245	GM12878	blood:	n/a	chr11:76155437-76155446
27	BHLHE40	chr11:76154981-76155938	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:76155239-76156018	HepG2	liver:	n/a	n/a
29	BHLHE40	chr11:76155277-76156132	K562	blood:	n/a	chr11:76156036-76156052
30	BRCA1	chr11:76155307-76156382	HepG2	liver:	n/a	n/a
31	BRCA1	chr11:76155167-76156181	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr11:76155240-76156388	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr11:76155344-76156183	GM12878	blood:	n/a	n/a
34	CBX3	chr11:76156595-76157206	K562	blood:	n/a	n/a
35	CBX3	chr11:76155249-76156132	K562	blood:	n/a	n/a
36	CCNT2	chr11:76155574-76156953	K562	blood:	n/a	chr11:76156616-76156625 chr11:76156882-76156891
37	CCNT2	chr11:76263631-76263721	K562	blood:	n/a	n/a
38	CEBPB	chr11:76155318-76156101	K562	blood:	n/a	chr11:76155752-76155760
39	CEBPB	chr11:76181515-76181770	HepG2	liver:	n/a	chr11:76181663-76181674
40	CEBPB	chr11:76212863-76213181	HepG2	liver:	n/a	n/a
41	CEBPB	chr11:76181518-76181794	H1-hESC	embryonic stem cell:	n/a	chr11:76181663-76181674
42	CEBPB	chr11:76151684-76151933	K562	blood:	n/a	n/a
43	CEBPB	chr11:76212864-76213191	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:76155304-76156211	Hela-S3	cervix:	n/a	chr11:76155752-76155760
45	CEBPB	chr11:76212856-76213158	IMR90	lung:	n/a	n/a
46	CEBPB	chr11:76166381-76167051	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr11:76163118-76163275	HepG2	liver:	n/a	chr11:76163186-76163195 chr11:76163185-76163196 chr11:76163184-76163195
48	CEBPB	chr11:76153155-76153255	A549	lung:	n/a	n/a
49	CEBPB	chr11:76155290-76156112	IMR90	lung:	n/a	chr11:76155752-76155760
50	CEBPB	chr11:76155411-76156108	A549	lung:	n/a	chr11:76155752-76155760

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76156042-76156092	HEK293	kidney:	embryo
2	chr11:76156056-76156106	GM12878	blood:	n/a
3	chr11:76156042-76156092	HEK293	kidney:	embryo
4	chr11:76156056-76156106	GM12878	blood:	n/a
5	chr11:76155921-76155971	HCPEpiC	choroid plexus:	n/a
6	chr11:76156134-76156184	SK-N-SH	brain:	n/a
7	chr11:76156056-76156106	BJ	skin:	n/a
8	chr11:76155921-76155971	GM12892	blood:	n/a
9	chr11:76156134-76156184	RPTEC	kidney:	n/a
10	chr11:76156044-76156094	HRCEpiC	kidney:	n/a
11	chr11:76155767-76155817	HCF	heart:	n/a
12	chr11:76166866-76166916	AG04450	lung:	fetal
13	chr11:76152669-76152719	Hela-S3	cervix:	n/a
14	chr11:76156096-76156146	BE2_C	brain:	n/a
15	chr11:76155921-76155971	LNCaP	prostate:	n/a
16	chr11:76152669-76152719	PrEC	prostate:	n/a
17	chr11:76156397-76156447	HAEpiC	amniotic membrane:	n/a
18	chr11:76156050-76156100	Hepatocyte	liver:	n/a
19	chr11:76156134-76156184	GM06990	blood:	n/a
20	chr11:76155379-76155429	CMK	blood:	n/a
21	chr11:76156922-76156972	HRCEpiC	kidney:	n/a
22	chr11:76156056-76156106	NB4	blood:	n/a
23	chr11:76155921-76155971	AG09309	skin:	n/a
24	chr11:76155379-76155429	BE2_C	brain:	n/a
25	chr11:76261997-76262047	NHBE	bronchial:	n/a
26	chr11:76265321-76265371	AG04450	lung:	fetal
27	chr11:76155379-76155429	HRCEpiC	kidney:	n/a
28	chr11:76156626-76156676	NB4	blood:	n/a
29	chr11:76156397-76156447	NB4	blood:	n/a
30	chr11:76155921-76155971	SK-N-SH	brain:	n/a
31	chr11:76166866-76166916	HL-60	blood:	n/a
32	chr11:76168949-76168999	PANC-1	pancreas:	n/a
33	chr11:76159160-76159210	SK-N-SH_RA	brain:	n/a
34	chr11:76156922-76156972	AG09319	gingival:	n/a
35	chr11:76156056-76156106	HIPEpiC	eye:	n/a
36	chr11:76155921-76155971	SKMC	muscle:	n/a
37	chr11:76156042-76156092	T-47D	breast:	n/a
38	chr11:76156050-76156100	HRPEpiC	eye:	n/a
39	chr11:76155767-76155817	Hela-S3	cervix:	n/a
40	chr11:76156050-76156100	IMR90	lung:	fetal
41	chr11:76156922-76156972	BJ	skin:	n/a
42	chr11:76156134-76156184	HIPEpiC	eye:	n/a
43	chr11:76168949-76168999	NB4	blood:	n/a
44	chr11:76222035-76222085	RPTEC	kidney:	n/a
45	chr11:76156050-76156100	ovcar-3	ovarian:	n/a
46	chr11:76155767-76155817	SK-N-SH	brain:	n/a
47	chr11:76156134-76156184	AoSMC	blood vessel:	n/a
48	chr11:76156040-76156090	GM12878	blood:	n/a
49	chr11:76156042-76156092	GM12892	blood:	n/a
50	chr11:76155487-76155537	HEK293	kidney:	embryo

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:76149871..76150715-chr13:27720328..27720828,2	HCT-116	colon:
2	chr11:76265177..76267818-chr11:76279245..76281186,2	K562	blood:
3	chr11:76234875..76236984-chr11:76240108..76241970,2	K562	blood:
4	chr11:76191502..76194293-chr11:76198687..76201522,2	MCF-7	breast:
5	chr11:76181244..76183930-chr11:76199565..76201178,2	K562	blood:
6	chr11:76156036..76156906-chr5:41904032..41904829,2	Hela-S3	cervix:
7	chr1:210546934..210547890-chr11:76154911..76155974,3	Hela-S3	cervix:
8	chr11:76090811..76092445-chr11:76176927..76179317,2	MCF-7	breast:
9	chr11:76262380..76263432-chr11:76391914..76393026,4	MCF-7	breast:
10	chr11:76155162..76155791-chr6:30711728..30712371,2	Hela-S3	cervix:
11	chr11:76155473..76156990-chr11:77788075..77790894,2	MCF-7	breast:
12	chr11:76159669..76162369-chr11:76163476..76167380,4	K562	blood:
13	chr11:76155242..76156014-chr18:48556195..48556733,2	Hela-S3	cervix:
14	chr11:76154138..76157007-chr17:62501424..62503777,2	MCF-7	breast:
15	chr11:16759751..16760339-chr11:76155088..76156401,3	Hela-S3	cervix:
16	chr11:76089758..76095735-chr11:76153234..76157826,15	MCF-7	breast:
17	chr11:76190688..76192947-chr11:76198433..76201383,2	K562	blood:
18	chr11:76206276..76208160-chr11:76208743..76210293,2	MCF-7	breast:
19	chr11:76155497..76156124-chr15:65596892..65597611,2	HCT-116	colon:
20	chr11:76155284..76156014-chr17:79481374..79482088,2	Hela-S3	cervix:
21	chr11:76261079..76263436-chr11:76264364..76265867,2	K562	blood:
22	chr11:76155227..76155947-chr7:39989290..39990183,2	Hela-S3	cervix:
23	chr11:76255778..76257554-chr11:76266242..76268584,2	MCF-7	breast:
24	chr11:76164027..76165933-chr11:76175646..76177507,2	MCF-7	breast:
25	chr11:76234875..76236984-chr11:76240108..76241970,2	K562	blood:
26	chr11:76210981..76212652-chr11:76215333..76217549,2	K562	blood:
27	chr11:76154597..76156492-chr11:76776948..76779266,2	K562	blood:
28	chr11:76152961..76155876-chr11:76158205..76163681,6	MCF-7	breast:
29	chr1:169862695..169863202-chr11:76155222..76156123,2	Hela-S3	cervix:
30	chr11:76157054..76159059-chr11:76166172..76168326,2	K562	blood:
31	chr11:76215740..76218864-chr11:76222952..76226299,3	K562	blood:
32	chr11:76154912..76157253-chr11:76299607..76302337,2	K562	blood:
33	chr11:76154330..76156315-chr11:76215728..76217827,2	MCF-7	breast:
34	chr11:76262469..76263152-chr11:76392001..76392517,2	K562	blood:
35	chr11:76157708..76159665-chr11:76175671..76178216,2	MCF-7	breast:
36	chr11:76154636..76157268-chr11:76209424..76211012,2	MCF-7	breast:
37	chr11:76231800..76233964-chr11:76234838..76236911,2	MCF-7	breast:
38	chr11:76262034..76262940-chr11:76309241..76310049,2	K562	blood:
39	chr11:76155250..76155837-chr2:55459276..55459949,2	Hela-S3	cervix:
40	chr11:76206276..76208160-chr11:76208743..76210293,2	MCF-7	breast:
41	chr11:76242469..76244011-chr11:76244453..76247142,2	MCF-7	breast:
42	chr11:76090615..76095251-chr11:76152894..76157527,10	K562	blood:
43	chr11:76090234..76093573-chr11:76154824..76158196,8	MCF-7	breast:
44	chr11:76182591..76185058-chr11:76186358..76187920,2	K562	blood:
45	chr11:76178422..76180245-chr11:76180873..76183428,2	K562	blood:
46	chr11:76217657..76219893-chr11:76220860..76223168,2	K562	blood:
47	chr11:76178745..76180889-chr11:76180922..76183428,2	K562	blood:
48	chr11:76250200..76253023-chr11:76260666..76263366,2	K562	blood:
49	chr11:76154094..76156954-chr11:76170479..76173196,2	MCF-7	breast:
50	chr11:76265376..76267987-chr11:76270130..76272636,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKRIR-1	chr11:76155322-76155618	ENSG00000255135.2
2	lnc-PRKRIR-1	chr11:76152382-76152683	ENSG00000255135.2
3	lnc-PRKRIR-1	chr11:76155322-76155704	XLOC_009507
4	lnc-PRKRIR-1	chr11:76154345-76154778	XLOC_009507
5	lnc-PRKRIR-1	chr11:76155249-76155700	ENSG00000255135.2
6	lnc-PRKRIR-1	chr11:76152384-76155841	NONHSAT023169
7	lnc-PRKRIR-1	chr11:76152398-76152683	ENSG00000255135.2
8	lnc-PRKRIR-1	chr11:76153117-76155724	ENSG00000255135.2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C11orf30	hsa-miR-26b-5p	chr11:76164698-76164718

Variant related genes	Relation type
ENSG00000255135	TF binding region
C11orf30	TF binding region
ENSG00000255135	CpG island
C11orf30	CpG island
ENSG00000108654	chromatin interactions
ENSG00000101150	chromatin interactions
ENSG00000205765	chromatin interactions
ENSG00000151366	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000166848	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000065883	chromatin interactions
ENSG00000100526	chromatin interactions
ENSG00000149260	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000137492	chromatin interactions
ENSG00000162994	chromatin interactions
ENSG00000254755	chromatin interactions
ENSG00000110696	chromatin interactions
ENSG00000173548	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000000457	chromatin interactions
ENSG00000167526	chromatin interactions
ENSG00000272301	chromatin interactions
ENSG00000117318	chromatin interactions
ENSG00000259112	chromatin interactions
ENSG00000106077	chromatin interactions
ENSG00000143947	chromatin interactions
ENSG00000133812	chromatin interactions
ENSG00000164070	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000259826	chromatin interactions
ENSG00000121060	chromatin interactions
ENSG00000141646	chromatin interactions
ENSG00000179240	chromatin interactions
ENSG00000110693	chromatin interactions
ENSG00000133739	chromatin interactions
ENSG00000198496	chromatin interactions
ENSG00000143321	chromatin interactions
ENSG00000012048	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000158636	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000136048	chromatin interactions
ARL5A	miRNA target sites
PHF14	miRNA target sites

Extended variants
information (count: 3992 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:3992 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550119429	chr11:76147089-76147090	ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs555915930	chr11:76147096-76147097	ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs541490275	chr11:76147111-76147112	ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs569068836	chr11:76147137-76147138	ZNF genes & repeats Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs12798475	chr11:76147170-76147171	ZNF genes & repeats Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs74237459	chr11:76147210-76147211	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs567894836	chr11:76147258-76147259	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188262867	chr11:76147304-76147305	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553466658	chr11:76147389-76147390	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576502148	chr11:76147408-76147409	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545485872	chr11:76147438-76147439	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs180673181	chr11:76147506-76147507	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576704195	chr11:76147580-76147581	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542506462	chr11:76147601-76147602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375638178	chr11:76147606-76147607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527869517	chr11:76147639-76147640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs74237460	chr11:76147659-76147660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534885763	chr11:76147692-76147693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs185347933	chr11:76147739-76147740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533417381	chr11:76147748-76147749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549950275	chr11:76147749-76147750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574847860	chr11:76147768-76147769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78893103	chr11:76147847-76147848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190497431	chr11:76147892-76147893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548452954	chr11:76147960-76147961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6592634	chr11:76147984-76147985	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs533761245	chr11:76148021-76148022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182204985	chr11:76148067-76148068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201088479	chr11:76148188-76148189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6592635	chr11:76148197-76148198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs112208880	chr11:76148200-76148201	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs539509966	chr11:76148212-76148213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs555931354	chr11:76148214-76148215	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs59691748	chr11:76148233-76148234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs186876187	chr11:76148278-76148279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs535806142	chr11:76148280-76148281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6592636	chr11:76148282-76148283	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs572746225	chr11:76148309-76148310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs191753300	chr11:76148319-76148320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147575615	chr11:76148334-76148335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578179396	chr11:76148348-76148349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142114690	chr11:76148354-76148355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529531189	chr11:76148375-76148376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs367921589	chr11:76148376-76148377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs529303976	chr11:76148459-76148460	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs566155465	chr11:76148487-76148488	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs75970982	chr11:76148500-76148501	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs182519340	chr11:76148673-76148674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558442766	chr11:76148706-76148707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570307729	chr11:76148712-76148713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3899 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76144000-76154000	Weak transcription	Left Ventricle	heart
2	chr11:76145600-76153600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:76146000-76152400	Weak transcription	Fetal Intestine Small	intestine
4	chr11:76147000-76147600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:76147200-76148600	Enhancers	K562	blood
6	chr11:76147600-76150800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:76147600-76154400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr11:76148000-76154400	Weak transcription	HSMM	muscle
9	chr11:76148200-76154600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:76148400-76148600	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr11:76148400-76148600	Enhancers	Fetal Heart	heart
12	chr11:76148400-76148600	Enhancers	Right Ventricle	heart
13	chr11:76148400-76148600	Active TSS	Stomach Smooth Muscle	stomach
14	chr11:76148600-76151000	Weak transcription	K562	blood
15	chr11:76148600-76152800	Weak transcription	Fetal Heart	heart
16	chr11:76148600-76154000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:76148600-76154200	Weak transcription	Stomach Smooth Muscle	stomach
18	chr11:76148600-76154400	Weak transcription	Right Ventricle	heart
19	chr11:76149200-76150800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:76149200-76154400	Weak transcription	Spleen	Spleen
21	chr11:76149600-76152800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:76149600-76153600	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr11:76149600-76153800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr11:76149600-76154000	Weak transcription	Fetal Thymus	thymus
25	chr11:76150000-76154200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr11:76150000-76154400	Weak transcription	Fetal Muscle Leg	muscle
27	chr11:76150200-76152600	Weak transcription	NHEK	skin
28	chr11:76150400-76153200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr11:76150600-76152600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr11:76150800-76151000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr11:76150800-76153400	Weak transcription	HepG2	liver
32	chr11:76150800-76153800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:76150800-76153800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:76150800-76154400	Weak transcription	Fetal Kidney	kidney
35	chr11:76151000-76151200	ZNF genes & repeats	Brain Angular Gyrus	brain
36	chr11:76151000-76151600	Enhancers	K562	blood
37	chr11:76151000-76152600	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr11:76151000-76154000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr11:76151000-76154200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr11:76151000-76154400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:76151200-76152000	Enhancers	Psoas Muscle	Psoas
42	chr11:76151200-76152800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr11:76151200-76154200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr11:76151200-76154200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:76151200-76154200	Weak transcription	Brain Angular Gyrus	brain
46	chr11:76151200-76154200	Weak transcription	HUVEC	blood vessel
47	chr11:76151400-76153400	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr11:76151400-76154200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:76151400-76154400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr11:76151400-76154400	Weak transcription	Primary B cells from cord blood	blood

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