Variant report

Variant	nsv897203
Chromosome Location	chr11:33236644-33339593
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1464)
CpG islands
(count:1344)
Chromatin interactive
region (count:108)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33280884-33281018	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33288039-33288460	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:33280804-33281150	K562	blood:	n/a	n/a
4	ARID3A	chr11:33277822-33278022	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:33279537-33280483	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:33280061-33280282	K562	blood:	n/a	n/a
7	ARID3A	chr11:33288174-33288395	K562	blood:	n/a	n/a
8	ARID3A	chr11:33278760-33279150	HepG2	liver:	n/a	n/a
9	ATF1	chr11:33249480-33249846	K562	blood:	n/a	n/a
10	ATF1	chr11:33275258-33275288	K562	blood:	n/a	n/a
11	ATF1	chr11:33329665-33330069	K562	blood:	n/a	n/a
12	ATF2	chr11:33279439-33280494	GM12878	blood:	n/a	n/a
13	ATF2	chr11:33279927-33280370	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr11:33279487-33279990	A549	lung:	n/a	n/a
15	ATF3	chr11:33279599-33280413	A549	lung:	n/a	n/a
16	ATF3	chr11:33249491-33249809	K562	blood:	n/a	n/a
17	BACH1	chr11:33279652-33280280	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr11:33279271-33279281	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr11:33262786-33263061	GM12878	blood:	n/a	n/a
20	BCL3	chr11:33278860-33279547	A549	lung:	n/a	chr11:33279283-33279296 chr11:33279375-33279384
21	BCL3	chr11:33279580-33280476	A549	lung:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
22	BCL3	chr11:33279715-33280657	A549	lung:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
23	BCLAF1	chr11:33278387-33279453	GM12878	blood:	n/a	chr11:33278749-33278762 chr11:33279283-33279296 chr11:33278715-33278728 chr11:33279375-33279384
24	BCLAF1	chr11:33280280-33280701	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:33279496-33280164	GM12878	blood:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
26	BCLAF1	chr11:33279706-33280419	GM12878	blood:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
27	BCLAF1	chr11:33279558-33280680	K562	blood:	n/a	chr11:33280069-33280078 chr11:33280094-33280107 chr11:33280065-33280078 chr11:33280086-33280099 chr11:33280095-33280108
28	BHLHE40	chr11:33278549-33279227	HepG2	liver:	n/a	chr11:33278914-33278930 chr11:33278754-33278770 chr11:33279027-33279043
29	BHLHE40	chr11:33279326-33280463	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:33278211-33279049	GM12878	blood:	n/a	chr11:33278914-33278930 chr11:33278754-33278770 chr11:33279027-33279043
31	BHLHE40	chr11:33308243-33308452	K562	blood:	n/a	n/a
32	BHLHE40	chr11:33278538-33280495	K562	blood:	n/a	chr11:33278914-33278930 chr11:33278754-33278770 chr11:33279027-33279043
33	BHLHE40	chr11:33313026-33313370	GM12878	blood:	n/a	n/a
34	BRCA1	chr11:33249532-33249862	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr11:33279640-33280018	GM12878	blood:	n/a	n/a
36	BRCA1	chr11:33277747-33278995	Hela-S3	cervix:	n/a	chr11:33278211-33278218
37	BRCA1	chr11:33337746-33337909	HepG2	liver:	n/a	n/a
38	BRCA1	chr11:33279762-33280748	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr11:33288182-33288633	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr11:33281913-33282019	GM12878	blood:	n/a	n/a
41	BRCA1	chr11:33278927-33278994	HepG2	liver:	n/a	n/a
42	BRCA1	chr11:33295193-33295271	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr11:33279874-33280054	HepG2	liver:	n/a	n/a
44	BRCA1	chr11:33279391-33279392	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr11:33238357-33238527	K562	blood:	n/a	n/a
46	CBX3	chr11:33279435-33280496	K562	blood:	n/a	n/a
47	CBX3	chr11:33278780-33279168	K562	blood:	n/a	n/a
48	CBX3	chr11:33279871-33280090	K562	blood:	n/a	n/a
49	CCNT2	chr11:33306514-33306664	K562	blood:	n/a	n/a
50	CCNT2	chr11:33278594-33280253	K562	blood:	n/a	chr11:33279153-33279162

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33278186-33278236	Jurkat	blood:	n/a
2	chr11:33317093-33317143	HCT-116	colon:	n/a
3	chr11:33278186-33278236	Jurkat	blood:	n/a
4	chr11:33317093-33317143	HCT-116	colon:	n/a
5	chr11:33278679-33278729	HCT-116	colon:	n/a
6	chr11:33308345-33308395	HIPEpiC	eye:	n/a
7	chr11:33317015-33317065	BE2_C	brain:	n/a
8	chr11:33280348-33280398	HEK293	kidney:	embryo
9	chr11:33279091-33279141	NH-A	brain:	n/a
10	chr11:33264842-33264892	HEEpiC	esophagus:	n/a
11	chr11:33279084-33279134	HRCEpiC	kidney:	n/a
12	chr11:33265440-33265490	GM12891	blood:	n/a
13	chr11:33279087-33279137	HUVEC	blood vessel:	n/a
14	chr11:33280012-33280062	GM12878	blood:	n/a
15	chr11:33317039-33317089	HRCEpiC	kidney:	n/a
16	chr11:33278752-33278802	ProgFib	skin:	n/a
17	chr11:33280012-33280062	HepG2	liver:	n/a
18	chr11:33278679-33278729	NHDF-neo	bronchial:	n/a
19	chr11:33282841-33282891	BE2_C	brain:	n/a
20	chr11:33279252-33279302	NT2-D1	testis:	n/a
21	chr11:33280012-33280062	K562	blood:	n/a
22	chr11:33279136-33279186	MCF10A-Er-Src	breast:	n/a
23	chr11:33264842-33264892	GM12891	blood:	n/a
24	chr11:33278679-33278729	GM12891	blood:	n/a
25	chr11:33278752-33278802	HIPEpiC	eye:	n/a
26	chr11:33278752-33278802	HCPEpiC	choroid plexus:	n/a
27	chr11:33280157-33280207	SK-N-SH	brain:	n/a
28	chr11:33279084-33279134	GM19239	blood:	n/a
29	chr11:33265440-33265490	SKMC	muscle:	n/a
30	chr11:33280348-33280398	HRE	kidney:	n/a
31	chr11:33280348-33280398	MCF-7	breast:	n/a
32	chr11:33265440-33265490	ProgFib	skin:	n/a
33	chr11:33308269-33308319	HIPEpiC	eye:	n/a
34	chr11:33280157-33280207	GM12878	blood:	n/a
35	chr11:33278186-33278236	HepG2	liver:	n/a
36	chr11:33279091-33279141	HCPEpiC	choroid plexus:	n/a
37	chr11:33279087-33279137	NH-A	brain:	n/a
38	chr11:33278752-33278802	NH-A	brain:	n/a
39	chr11:33280012-33280062	SK-N-MC	brain:	n/a
40	chr11:33317093-33317143	AG10803	skin:	n/a
41	chr11:33279136-33279186	Caco-2	colon:	n/a
42	chr11:33279136-33279186	HL-60	blood:	n/a
43	chr11:33280012-33280062	PANC-1	pancreas:	n/a
44	chr11:33279136-33279186	HCM	heart:	n/a
45	chr11:33279136-33279186	HCPEpiC	choroid plexus:	n/a
46	chr11:33282841-33282891	HepG2	liver:	n/a
47	chr11:33308345-33308395	HMEC	breast:	n/a
48	chr11:33308269-33308319	SKMC	muscle:	n/a
49	chr11:33334443-33334493	GM06990	blood:	n/a
50	chr11:33280012-33280062	SK-N-SH	brain:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:74385851..74386629-chr11:33278605..33279285,2	Hela-S3	cervix:
2	chr11:33278726..33280450-chr11:33281351..33283602,2	MCF-7	breast:
3	chr11:33279534..33280463-chr2:39351094..39351986,2	Hela-S3	cervix:
4	chr11:33279409..33279923-chr13:52026765..52027551,2	Hela-S3	cervix:
5	chr11:33319935..33321547-chr11:33324870..33327830,2	K562	blood:
6	chr11:33277971..33280504-chr11:33330975..33332742,2	MCF-7	breast:
7	chr11:33323694..33328844-chr11:33341332..33344470,4	K562	blood:
8	chr11:33303628..33306131-chr11:33323858..33326842,2	MCF-7	breast:
9	chr11:33278311..33281091-chr22:19157790..19160697,2	MCF-7	breast:
10	chr11:33181310..33183473-chr11:33251484..33253503,2	K562	blood:
11	chr11:33315778..33318693-chr11:33329241..33331442,2	K562	blood:
12	chr11:33278153..33279017-chr7:128379096..128379858,2	Hela-S3	cervix:
13	chr11:33277681..33279194-chr11:33330254..33333182,2	MCF-7	breast:
14	chr11:33180418..33183694-chr11:33278346..33281012,5	MCF-7	breast:
15	chr11:33287096..33288603-chr11:33295589..33298178,2	K562	blood:
16	chr11:33279524..33280025-chr3:9437578..9438488,2	Hela-S3	cervix:
17	chr11:33192932..33194844-chr11:33338349..33340157,2	K562	blood:
18	chr11:33290160..33295323-chr11:33296264..33299611,6	K562	blood:
19	chr11:33277967..33280794-chr11:33331091..33333165,2	K562	blood:
20	chr11:33279747..33280263-chrX:23801172..23801824,2	Hela-S3	cervix:
21	chr11:33278310..33280237-chr11:33303017..33305023,2	MCF-7	breast:
22	chr11:33313913..33316207-chr11:33316446..33318411,2	MCF-7	breast:
23	chr11:33181657..33184341-chr11:33279051..33282180,3	MCF-7	breast:
24	chr11:33267480..33271185-chr11:33277468..33280694,5	MCF-7	breast:
25	chr11:33262756..33265436-chr11:33277701..33280558,4	MCF-7	breast:
26	chr11:33330031..33332498-chr11:33332591..33335075,2	MCF-7	breast:
27	chr11:33278564..33280833-chr11:33295728..33298096,2	K562	blood:
28	chr11:33246835..33249604-chr11:33278881..33281547,2	K562	blood:
29	chr11:33241181..33243191-chr11:33245641..33247862,2	MCF-7	breast:
30	chr11:33281647..33283954-chr11:33310623..33313368,2	MCF-7	breast:
31	chr11:33279271..33281260-chr11:33331405..33333879,2	MCF-7	breast:
32	chr11:33315778..33318693-chr11:33329241..33331442,2	K562	blood:
33	chr11:33292487..33295323-chr11:33297832..33299611,2	K562	blood:
34	chr11:33279432..33280386-chr19:10828430..10829287,2	NB4	blood:
35	chr11:33326071..33328703-chr11:33331126..33332666,2	K562	blood:
36	chr11:33327923..33330739-chr11:33334207..33336221,2	K562	blood:
37	chr11:33267892..33269409-chr11:33276644..33279476,3	MCF-7	breast:
38	chr11:33278197..33279052-chr5:134240296..134240970,2	Hela-S3	cervix:
39	chr11:33283955..33286219-chr11:33326919..33329577,2	K562	blood:
40	chr11:33277797..33278342-chr14:60715056..60715739,2	Hela-S3	cervix:
41	chr11:33277785..33280697-chr11:33298696..33301567,3	K562	blood:
42	chr11:33281647..33283954-chr11:33310623..33313368,2	MCF-7	breast:
43	chr11:33278516..33280068-chr11:33740390..33742827,2	MCF-7	breast:
44	chr11:33279561..33280411-chr17:55161648..55162447,2	Hela-S3	cervix:
45	chr11:33278384..33280021-chr11:33301631..33304072,2	MCF-7	breast:
46	chr11:33246053..33247762-chr11:33248545..33250079,2	K562	blood:
47	chr11:33308929..33311681-chr11:33352469..33354383,2	MCF-7	breast:
48	chr11:33272062..33275695-chr11:33277620..33281399,4	MCF-7	breast:
49	chr11:33319935..33321547-chr11:33324870..33327830,2	K562	blood:
50	chr11:33277741..33279641-chr11:33288313..33289989,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11L1-4	chr11:33334713-33335041	expReg_chr11_2985_+
2	lnc-TCP11L1-3	chr11:33333205-33333598	expReg_chr11_2971_+

No data

Variant related genes	Relation type
ENSG00000241255	TF binding region
HIPK3	TF binding region
ENSG00000241255	CpG island
HIPK3	CpG island
ENSG00000206808	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000260924	chromatin interactions
ENSG00000117335	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000132570	chromatin interactions
ENSG00000079805	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000199568	chromatin interactions
ENSG00000115904	chromatin interactions
ENSG00000263004	chromatin interactions
ENSG00000130066	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000206573	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000135387	chromatin interactions
ENSG00000207972	chromatin interactions
ENSG00000254718	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000128595	chromatin interactions
ENSG00000175634	chromatin interactions
ENSG00000107745	chromatin interactions
ENSG00000134294	chromatin interactions

Extended variants
information (count: 3575 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3575 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12797532	chr11:33236644-33236645	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533904026	chr11:33236772-33236773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111276820	chr11:33236774-33236775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs553751441	chr11:33236849-33236850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34636405	chr11:33236853-33236854	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs536205670	chr11:33236866-33236867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs57917382	chr11:33236875-33236876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs192368624	chr11:33236905-33236906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556628623	chr11:33236921-33236922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs540393040	chr11:33236922-33236923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576554668	chr11:33236959-33236960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545305070	chr11:33236968-33236969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554596131	chr11:33236992-33236993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs36048716	chr11:33237037-33237038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564172379	chr11:33237046-33237047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533065102	chr11:33237095-33237096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572785848	chr11:33237164-33237165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184951682	chr11:33237194-33237195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528945505	chr11:33237217-33237218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558391472	chr11:33237243-33237244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578099790	chr11:33237307-33237308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs71479199	chr11:33237354-33237355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs373888619	chr11:33237388-33237389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569091493	chr11:33237400-33237401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112607374	chr11:33237419-33237420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531500402	chr11:33237546-33237547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112557025	chr11:33237591-33237592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs551310450	chr11:33237596-33237597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563595108	chr11:33237597-33237598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575531530	chr11:33237599-33237600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553887871	chr11:33237603-33237604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567318283	chr11:33237611-33237612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367858131	chr11:33237636-33237637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs536272863	chr11:33237697-33237698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556797430	chr11:33237742-33237743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576677789	chr11:33237751-33237752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545552888	chr11:33237829-33237830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141176358	chr11:33237887-33237888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369069142	chr11:33237898-33237899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372487209	chr11:33237901-33237902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542952502	chr11:33237946-33237947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561318420	chr11:33237955-33237956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189620323	chr11:33237962-33237963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528502261	chr11:33237963-33237964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540693328	chr11:33237981-33237982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565249471	chr11:33237990-33237991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572720056	chr11:33238053-33238054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11032206	chr11:33238067-33238068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560319338	chr11:33238191-33238192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs375526055	chr11:33238252-33238253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
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
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2754 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33233600-33237000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:33233600-33237000	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr11:33236400-33237000	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr11:33236600-33241200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr11:33237000-33243400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr11:33237000-33243400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr11:33241200-33242600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:33241600-33242200	Enhancers	Adipose Nuclei	Adipose
9	chr11:33242200-33249000	Weak transcription	Adipose Nuclei	Adipose
10	chr11:33242600-33245000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr11:33243400-33243800	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr11:33243400-33244400	Enhancers	Stomach Mucosa	stomach
13	chr11:33243400-33244800	Enhancers	Primary B cells from cord blood	blood
14	chr11:33243400-33245600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr11:33243800-33244600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
16	chr11:33243800-33244800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr11:33244400-33244800	Enhancers	Primary B cells from peripheral blood	blood
18	chr11:33244400-33244800	Enhancers	Primary hematopoietic stem cells	blood
19	chr11:33244600-33246000	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr11:33244800-33245000	Weak transcription	Primary B cells from cord blood	blood
21	chr11:33244800-33249000	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr11:33244800-33255800	Weak transcription	Primary hematopoietic stem cells	blood
23	chr11:33245000-33246200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:33245600-33246800	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr11:33246000-33248400	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr11:33246200-33248600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:33246800-33250600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr11:33248400-33249000	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr11:33248600-33249000	Enhancers	Right Atrium	heart
30	chr11:33248600-33250200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr11:33248800-33250000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:33249000-33249800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr11:33249000-33249800	Enhancers	Psoas Muscle	Psoas
34	chr11:33249000-33249800	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr11:33249000-33250000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:33249000-33250000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr11:33249000-33250000	Enhancers	HSMMtube	muscle
38	chr11:33249000-33250200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr11:33249000-33250200	Enhancers	Adipose Nuclei	Adipose
40	chr11:33249000-33250200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr11:33249000-33250400	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr11:33249000-33250400	Enhancers	Hela-S3	cervix
43	chr11:33249800-33255000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:33250200-33250400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:33250400-33255200	Weak transcription	Monocytes-CD14+_RO01746	blood
46	chr11:33250600-33255400	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr11:33255000-33255200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr11:33255000-33257200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr11:33255200-33256000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr11:33255200-33256200	Enhancers	Monocytes-CD14+_RO01746	blood

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