Variant report

Variant	nsv428249
Chromosome Location	chr11:8068594-8216369
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2285)
CpG islands
(count:2562)
Chromatin interactive
region (count:58)
LncRNA
region (count:26)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:2285 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:8214207-8214365	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:8112471-8112689	K562	blood:	n/a	n/a
3	ARID3A	chr11:8090219-8090439	HepG2	liver:	n/a	n/a
4	ATF2	chr11:8189910-8190353	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr11:8090199-8090453	K562	blood:	n/a	n/a
6	ATF3	chr11:8214232-8214372	K562	blood:	n/a	n/a
7	BACH1	chr11:8189998-8190845	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:8088616-8088947	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:8103306-8103389	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr11:8102356-8102660	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr11:8149288-8149520	GM12878	blood:	n/a	n/a
12	BCL3	chr11:8183779-8184029	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:8214228-8214485	K562	blood:	n/a	n/a
14	BHLHE40	chr11:8114180-8114514	K562	blood:	n/a	n/a
15	BHLHE40	chr11:8189913-8190856	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:8112478-8112599	K562	blood:	n/a	n/a
17	BHLHE40	chr11:8090210-8090834	K562	blood:	n/a	n/a
18	BRCA1	chr11:8214147-8214471	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr11:8090240-8090988	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr11:8183031-8184006	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr11:8204707-8205096	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr11:8114108-8114554	K562	blood:	n/a	n/a
23	CCNT2	chr11:8090343-8090745	K562	blood:	n/a	n/a
24	CEBPB	chr11:8175856-8176056	HepG2	liver:	n/a	chr11:8175946-8175957
25	CEBPB	chr11:8078549-8078949	HepG2	liver:	n/a	chr11:8078740-8078751
26	CEBPB	chr11:8078543-8078860	HepG2	liver:	n/a	chr11:8078740-8078751
27	CEBPB	chr11:8078444-8078955	IMR90	lung:	n/a	chr11:8078740-8078751
28	CEBPB	chr11:8119108-8119305	IMR90	lung:	n/a	n/a
29	CEBPB	chr11:8154977-8155258	A549	lung:	n/a	chr11:8155023-8155034
30	CEBPB	chr11:8078514-8078939	MCF-7	breast:	n/a	chr11:8078740-8078751
31	CEBPB	chr11:8078632-8078863	HepG2	liver:	n/a	chr11:8078740-8078751
32	CEBPB	chr11:8078429-8078954	K562	blood:	n/a	chr11:8078740-8078751
33	CEBPB	chr11:8174208-8174228	HepG2	liver:	n/a	chr11:8174211-8174222
34	CEBPB	chr11:8169255-8169264	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr11:8183122-8184080	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr11:8187380-8187399	A549	lung:	n/a	n/a
37	CEBPB	chr11:8187394-8187411	K562	blood:	n/a	n/a
38	CEBPB	chr11:8078386-8078929	HCT-116	colon:	n/a	chr11:8078740-8078751
39	CEBPB	chr11:8204636-8205160	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr11:8078484-8078961	ECC-1	luminal epithelium:	n/a	chr11:8078740-8078751
41	CEBPB	chr11:8078557-8078939	H1-hESC	embryonic stem cell:	n/a	chr11:8078740-8078751
42	CEBPB	chr11:8190037-8190693	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr11:8186408-8186564	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:8082191-8082712	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:8078603-8078812	K562	blood:	n/a	chr11:8078740-8078751
46	CEBPB	chr11:8155035-8155235	HepG2	liver:	n/a	n/a
47	CEBPB	chr11:8078484-8078918	K562	blood:	n/a	chr11:8078740-8078751
48	CEBPB	chr11:8078336-8079119	A549	lung:	n/a	chr11:8078740-8078751
49	CEBPB	chr11:8187297-8187450	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr11:8155018-8155173	IMR90	lung:	n/a	chr11:8155023-8155034

(count:2562 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:8102450-8102500	MCF10A-Er-Src	breast:	n/a
2	chr11:8128361-8128411	NT2-D1	testis:	n/a
3	chr11:8080975-8081025	HL-60	blood:	n/a
4	chr11:8101907-8101957	NH-A	brain:	n/a
5	chr11:8123205-8123255	IMR90	lung:	fetal
6	chr11:8190227-8190277	AoSMC	blood vessel:	n/a
7	chr11:8101793-8101843	MCF-7	breast:	n/a
8	chr11:8102311-8102361	MCF10A-Er-Src	breast:	n/a
9	chr11:8190448-8190498	HMEC	breast:	n/a
10	chr11:8190670-8190720	GM19239	blood:	n/a
11	chr11:8160625-8160675	HCT-116	colon:	n/a
12	chr11:8102450-8102500	HMEC	breast:	n/a
13	chr11:8133258-8133308	RPTEC	kidney:	n/a
14	chr11:8133258-8133308	HCM	heart:	n/a
15	chr11:8104458-8104508	SK-N-SH	brain:	n/a
16	chr11:8103101-8103151	HEK293	kidney:	embryo
17	chr11:8120396-8120446	ovcar-3	ovarian:	n/a
18	chr11:8103017-8103067	HAEpiC	amniotic membrane:	n/a
19	chr11:8102016-8102066	NHDF-neo	bronchial:	n/a
20	chr11:8190565-8190615	ovcar-3	ovarian:	n/a
21	chr11:8120396-8120446	LNCaP	prostate:	n/a
22	chr11:8103101-8103151	NB4	blood:	n/a
23	chr11:8187428-8187478	BJ	skin:	n/a
24	chr11:8187428-8187478	CMK	blood:	n/a
25	chr11:8102510-8102560	PFSK-1	brain:	n/a
26	chr11:8101907-8101957	AG04449	skin:	fetal
27	chr11:8102475-8102525	HCPEpiC	choroid plexus:	n/a
28	chr11:8187428-8187478	Hepatocyte	liver:	n/a
29	chr11:8128361-8128411	HUVEC	blood vessel:	n/a
30	chr11:8102450-8102500	GM12892	blood:	n/a
31	chr11:8123205-8123255	HMEC	breast:	n/a
32	chr11:8108498-8108548	NHBE	bronchial:	n/a
33	chr11:8190834-8190884	MCF-7	breast:	n/a
34	chr11:8190565-8190615	Hela-S3	cervix:	n/a
35	chr11:8102510-8102560	ProgFib	skin:	n/a
36	chr11:8103101-8103151	LNCaP	prostate:	n/a
37	chr11:8102510-8102560	AG09309	skin:	n/a
38	chr11:8190670-8190720	NHBE	bronchial:	n/a
39	chr11:8102475-8102525	PANC-1	pancreas:	n/a
40	chr11:8090206-8090256	NH-A	brain:	n/a
41	chr11:8190448-8190498	HL-60	blood:	n/a
42	chr11:8190572-8190622	AG04449	skin:	fetal
43	chr11:8077914-8077964	SK-N-SH	brain:	n/a
44	chr11:8101907-8101957	BE2_C	brain:	n/a
45	chr11:8160625-8160675	HUVEC	blood vessel:	n/a
46	chr11:8102510-8102560	AG04450	lung:	fetal
47	chr11:8190690-8190740	HAEpiC	amniotic membrane:	n/a
48	chr11:8102311-8102361	HIPEpiC	eye:	n/a
49	chr11:8160625-8160675	GM06990	blood:	n/a
50	chr11:8199971-8200021	HCT-116	colon:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:8054647..8055179-chr11:8112054..8112947,2	MCF-7	breast:
2	chr11:8067813..8069958-chr11:8075333..8077266,2	K562	blood:
3	chr11:8054438..8054991-chr11:8113935..8114446,2	K562	blood:
4	chr11:8121814..8124790-chr11:8126729..8128996,2	K562	blood:
5	chr11:8214233..8214925-chr11:8331212..8332019,2	MCF-7	breast:
6	chr11:8054475..8055081-chr11:8091864..8092628,2	MCF-7	breast:
7	chr11:8027654..8028564-chr11:8092088..8092653,2	K562	blood:
8	chr11:8061407..8063255-chr11:8084785..8086285,2	K562	blood:
9	chr11:8054438..8055155-chr11:8108441..8109253,4	MCF-7	breast:
10	chr11:8216194..8218883-chr11:8223154..8225386,2	K562	blood:
11	chr11:8150897..8153800-chr11:8158200..8159860,2	K562	blood:
12	chr11:8214526..8217689-chr11:8218013..8220798,3	K562	blood:
13	chr11:8054286..8054971-chr11:8112084..8112598,2	MCF-7	breast:
14	chr11:8067813..8069958-chr11:8075333..8077266,2	K562	blood:
15	chr11:8213913..8214737-chr11:8588214..8589161,2	K562	blood:
16	chr11:8074268..8076681-chr11:8112066..8114315,2	K562	blood:
17	chr11:8084754..8086469-chr11:8088768..8090631,2	K562	blood:
18	chr11:8106988..8108641-chr11:8110297..8112155,2	K562	blood:
19	chr11:8106988..8108641-chr11:8110297..8112155,2	K562	blood:
20	chr11:8027644..8028318-chr11:8112467..8113028,2	K562	blood:
21	chr11:8191876..8193485-chr11:8198068..8201621,3	K562	blood:
22	chr11:8027374..8028529-chr11:8120567..8121508,8	MCF-7	breast:
23	chr11:8126548..8128280-chr11:8129234..8131719,2	K562	blood:
24	chr11:8099105..8101607-chr11:8105342..8108244,2	MCF-7	breast:
25	chr11:7914034..7914945-chr11:8120637..8121875,4	K562	blood:
26	chr11:8051850..8054508-chr11:8112523..8114559,2	K562	blood:
27	chr11:8027612..8028573-chr11:8120562..8121429,4	K562	blood:
28	chr11:8092152..8092656-chr11:8100417..8101188,2	K562	blood:
29	chr11:8084754..8086469-chr11:8088768..8090631,2	K562	blood:
30	chr11:8074268..8076681-chr11:8112066..8114315,2	K562	blood:
31	chr11:8027342..8028618-chr11:8108548..8109930,5	MCF-7	breast:
32	chr11:8207451..8210232-chr11:8343773..8345724,2	K562	blood:
33	chr11:8126548..8128280-chr11:8129234..8131719,2	K562	blood:
34	chr11:8091175..8092761-chr11:8098490..8100768,2	K562	blood:
35	chr11:8028058..8028581-chr11:8112068..8112740,2	MCF-7	breast:
36	chr11:8191876..8193485-chr11:8198068..8201621,3	K562	blood:
37	chr11:8016616..8019167-chr11:8111283..8114167,2	MCF-7	breast:
38	chr11:8008779..8010283-chr11:8115133..8117124,2	MCF-7	breast:
39	chr11:8027630..8028590-chr11:8113864..8114843,6	MCF-7	breast:
40	chr11:8177939..8178854-chr16:67389082..67389881,2	MCF-7	breast:
41	chr11:8114581..8116309-chr11:8116337..8119171,2	MCF-7	breast:
42	chr11:8213784..8214547-chr11:8246894..8247601,2	K562	blood:
43	chr11:8054420..8055367-chr11:8120731..8121254,3	K562	blood:
44	chr11:8085796..8088311-chr11:8090818..8094631,3	K562	blood:
45	chr11:8092152..8092656-chr11:8100417..8101188,2	K562	blood:
46	chr11:8027965..8028589-chr11:8091639..8092221,2	MCF-7	breast:
47	chr11:8054442..8055441-chr11:8091763..8092397,3	K562	blood:
48	chr11:8027583..8028679-chr11:8120621..8121441,4	MCF-7	breast:
49	chr11:8213801..8214811-chr11:8255818..8256741,4	MCF-7	breast:
50	chr11:8027737..8028781-chr11:8112023..8112656,3	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF3F-1	chr11:8089157-8090920	ENSG00000248332
2	lnc-EIF3F-1	chr11:8089157-8089487	ENSG00000248332
3	lnc-TUB-3	chr11:8156447-8156628	l_429_chr11:8147179-8156628_testes
4	lnc-TUB-1	chr11:8196844-8200450	ENSG00000246820
5	lnc-EIF3F-1	chr11:8083620-8083778	ENSG00000248332
6	lnc-TUB-3	chr11:8156276-8156350	l_429_chr11:8147179-8156628_testes
7	lnc-TUB-1	chr11:8191432-8191535	NONHSAT017844
8	lnc-TUB-1	chr11:8190963-8190987	NONHSAT017844
9	lnc-TUB-3	chr11:8153420-8153489	l_429_chr11:8147179-8156628_testes
10	lnc-TUB-1	chr11:8201638-8201790	NONHSAT017844
11	lnc-TUB-3	chr11:8147180-8147367	l_429_chr11:8147179-8156628_testes
12	lnc-TUB-1	chr11:8191431-8191535	NONHSAT017845
13	lnc-TUB-1	chr11:8190714-8190736	ENSG00000246820
14	lnc-TUB-1	chr11:8191432-8191535	ENSG00000246820
15	lnc-TUB-1	chr11:8196844-8200450	NONHSAT017845
16	lnc-TUB-1	chr11:8199700-8199734	NONHSAT017844
17	lnc-TUB-1	chr11:8196844-8196913	NONHSAT017844
18	lnc-EIF3F-1	chr11:8082267-8082693	NONHSAT017822
19	lnc-TUB-3	chr11:8158214-8158337	l_429_chr11:8147179-8156628_testes
20	lnc-EIF3F-1	chr11:8088970-8089026	ENSG00000248332
21	lnc-EIF3F-1	chr11:8081509-8081625	NONHSAT017822
22	lnc-EIF3F-1	chr11:8081585-8081625	ENSG00000248332
23	lnc-TUB-3	chr11:8148008-8148111	l_429_chr11:8147179-8156628_testes
24	lnc-EIF3F-1	chr11:8081585-8081625	ENSG00000248332
25	lnc-RIC3-2	chr11:8097088-8099328	NONHSAT017825
26	lnc-EIF3F-1	chr11:8083620-8083778	ENSG00000248332

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	TUB	hsa-miR-221-3p	chr11:8123622-8123646
2	TUB	hsa-miR-181c-5p	chr11:8126303-8126309
3	TUB	hsa-miR-128-3p	chr11:8127263-8127283
4	TUB	hsa-miR-124-3p	chr11:8126308-8126315
5	TUB	hsa-miR-124-3p	chr11:8126296-8126315
6	TUB	hsa-miR-124-3p	chr11:8127280-8127286
7	TUB	hsa-miR-128-3p	chr11:8127276-8127282
8	TUB	hsa-miR-124-3p	chr11:8127267-8127287

Variant related genes	Relation type
RIC3	TF binding region
TUB	TF binding region
ENSG00000248332	TF binding region
ENSG00000246820	TF binding region
RIC3	CpG island
TUB	CpG island
ENSG00000248332	CpG island
ENSG00000246820	CpG island
ENSG00000175390	chromatin interactions
ENSG00000166407	chromatin interactions
RUNX2	miRNA target sites
SSH2	miRNA target sites
GNAI2	miRNA target sites
MCL1	miRNA target sites
SUSD5	miRNA target sites
TXNL1	miRNA target sites
OLA1	miRNA target sites
RPUSD4	miRNA target sites
GRTP1	miRNA target sites

Extended variants
information (count: 6542 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:6542 , 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	rs562772498	chr11:8068599-8068600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73396713	chr11:8068601-8068602	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs182823256	chr11:8068602-8068603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185199081	chr11:8068677-8068678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs527383915	chr11:8068700-8068701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547106154	chr11:8068701-8068702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149733079	chr11:8068706-8068707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147826686	chr11:8068709-8068710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs571346972	chr11:8068772-8068773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111680357	chr11:8068786-8068787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs533623331	chr11:8068885-8068886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570242732	chr11:8068887-8068888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75094147	chr11:8068919-8068920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553366384	chr11:8068964-8068965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566099189	chr11:8069013-8069014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141382915	chr11:8069017-8069018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189625053	chr11:8069030-8069031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371040212	chr11:8069049-8069050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183439985	chr11:8069067-8069068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536458023	chr11:8069117-8069118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79687021	chr11:8069126-8069127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146977838	chr11:8069128-8069129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs138046639	chr11:8069144-8069145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79885788	chr11:8069190-8069191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117265780	chr11:8069231-8069232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149049883	chr11:8069236-8069237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76988047	chr11:8069264-8069265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529781605	chr11:8069292-8069293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556079033	chr11:8069458-8069459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187728047	chr11:8069470-8069471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs563934730	chr11:8069505-8069506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532679126	chr11:8069517-8069518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs193018869	chr11:8069523-8069524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552847328	chr11:8069579-8069580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565904904	chr11:8069624-8069625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541722667	chr11:8069635-8069636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528495579	chr11:8069673-8069674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73396716	chr11:8069699-8069700	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs568567029	chr11:8069731-8069732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117125550	chr11:8069744-8069745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571722539	chr11:8069746-8069747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556072124	chr11:8069772-8069773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183695498	chr11:8069814-8069815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34618577	chr11:8069834-8069835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369440752	chr11:8069877-8069878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs61449161	chr11:8069909-8069910	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188265601	chr11:8069924-8069925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs571667550	chr11:8069938-8069939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376060470	chr11:8069970-8069971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576242305	chr11:8069993-8069994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	17440070	CNVD

Chromatin state (count:2533 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8061200-8076200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:8067800-8070600	Weak transcription	Left Ventricle	heart
3	chr11:8070600-8071000	Enhancers	Left Ventricle	heart
4	chr11:8070600-8071000	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr11:8070600-8071000	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr11:8075800-8090000	Weak transcription	Spleen	Spleen
7	chr11:8076000-8076200	Enhancers	HMEC	breast
8	chr11:8076000-8076400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:8076000-8076400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr11:8076000-8076400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:8076200-8076400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:8076200-8076400	Enhancers	Brain Anterior Caudate	brain
13	chr11:8076200-8076400	Enhancers	Brain Substantia Nigra	brain
14	chr11:8076200-8076800	Bivalent Enhancer	Brain Cingulate Gyrus	brain
15	chr11:8076200-8078800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr11:8076200-8078800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr11:8076400-8076600	Enhancers	Brain Angular Gyrus	brain
18	chr11:8076400-8077600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr11:8076400-8077800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr11:8076400-8078200	Enhancers	Fetal Brain Male	brain
21	chr11:8076600-8077400	Weak transcription	Brain Angular Gyrus	brain
22	chr11:8076600-8077600	Weak transcription	Brain Anterior Caudate	brain
23	chr11:8076600-8078200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:8076800-8077000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr11:8076800-8078600	Enhancers	Brain Cingulate Gyrus	brain
26	chr11:8076800-8078800	Enhancers	Right Ventricle	heart
27	chr11:8076800-8079400	Enhancers	Fetal Stomach	stomach
28	chr11:8077000-8078600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:8077200-8077400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr11:8077400-8077600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:8077400-8077800	Enhancers	Placenta	Placenta
32	chr11:8077400-8078800	Enhancers	Brain Angular Gyrus	brain
33	chr11:8077400-8079200	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr11:8077600-8077800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:8077600-8078200	Enhancers	Brain Anterior Caudate	brain
36	chr11:8077600-8078600	Enhancers	Left Ventricle	heart
37	chr11:8077800-8078000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:8077800-8078000	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr11:8077800-8078000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:8077800-8078200	Weak transcription	Placenta	Placenta
41	chr11:8077800-8078600	Enhancers	Right Atrium	heart
42	chr11:8077800-8078600	Enhancers	Skeletal Muscle Female	skeletal muscle
43	chr11:8078000-8078200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:8078000-8078400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr11:8078000-8078400	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr11:8078000-8078600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr11:8078000-8079000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr11:8078000-8080000	Enhancers	Colon Smooth Muscle	Colon
49	chr11:8078200-8078400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:8078200-8078400	Enhancers	Brain Hippocampus Middle	brain

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