Variant report

Variant	nsv430370
Chromosome Location	chr11:33202614-33505494
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3292)
CpG islands
(count:2751)
Chromatin interactive
region (count:224)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:3292 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33204058-33204223	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:33288174-33288395	K562	blood:	n/a	n/a
3	ARID3A	chr11:33342559-33342940	K562	blood:	n/a	n/a
4	ARID3A	chr11:33280061-33280282	K562	blood:	n/a	n/a
5	ARID3A	chr11:33277822-33278022	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:33280804-33281150	K562	blood:	n/a	n/a
7	ARID3A	chr11:33383925-33384254	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:33229217-33229421	K562	blood:	n/a	n/a
9	ARID3A	chr11:33288039-33288460	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:33499524-33499864	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:33364523-33364723	K562	blood:	n/a	n/a
12	ARID3A	chr11:33351288-33351628	HepG2	liver:	n/a	n/a
13	ARID3A	chr11:33351286-33351649	K562	blood:	n/a	n/a
14	ARID3A	chr11:33383912-33384198	K562	blood:	n/a	n/a
15	ARID3A	chr11:33233161-33233450	HepG2	liver:	n/a	n/a
16	ARID3A	chr11:33467294-33467606	HepG2	liver:	n/a	n/a
17	ARID3A	chr11:33280884-33281018	HepG2	liver:	n/a	n/a
18	ARID3A	chr11:33394101-33394301	HepG2	liver:	n/a	n/a
19	ARID3A	chr11:33278760-33279150	HepG2	liver:	n/a	n/a
20	ARID3A	chr11:33279537-33280483	HepG2	liver:	n/a	n/a
21	ATF1	chr11:33342458-33342912	K562	blood:	n/a	n/a
22	ATF1	chr11:33329665-33330069	K562	blood:	n/a	n/a
23	ATF1	chr11:33351332-33351614	K562	blood:	n/a	n/a
24	ATF1	chr11:33275258-33275288	K562	blood:	n/a	n/a
25	ATF1	chr11:33394198-33394335	K562	blood:	n/a	n/a
26	ATF1	chr11:33249480-33249846	K562	blood:	n/a	n/a
27	ATF1	chr11:33341606-33341888	K562	blood:	n/a	n/a
28	ATF2	chr11:33409042-33410013	GM12878	blood:	n/a	n/a
29	ATF2	chr11:33404441-33405009	GM12878	blood:	n/a	n/a
30	ATF2	chr11:33279439-33280494	GM12878	blood:	n/a	n/a
31	ATF2	chr11:33411036-33411671	GM12878	blood:	n/a	n/a
32	ATF2	chr11:33279927-33280370	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr11:33409013-33410089	GM12878	blood:	n/a	n/a
34	ATF2	chr11:33404542-33405049	GM12878	blood:	n/a	n/a
35	ATF3	chr11:33382233-33382453	K562	blood:	n/a	chr11:33382358-33382372
36	ATF3	chr11:33342449-33342699	K562	blood:	n/a	n/a
37	ATF3	chr11:33279599-33280413	A549	lung:	n/a	n/a
38	ATF3	chr11:33249491-33249809	K562	blood:	n/a	n/a
39	ATF3	chr11:33279487-33279990	A549	lung:	n/a	n/a
40	BACH1	chr11:33364471-33364818	K562	blood:	n/a	n/a
41	BACH1	chr11:33279271-33279281	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr11:33279652-33280280	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr11:33397385-33398563	H1-hESC	embryonic stem cell:	n/a	n/a
44	BATF	chr11:33404575-33404911	GM12878	blood:	n/a	n/a
45	BATF	chr11:33411172-33411511	GM12878	blood:	n/a	n/a
46	BATF	chr11:33363521-33363808	GM12878	blood:	n/a	n/a
47	BATF	chr11:33408990-33409983	GM12878	blood:	n/a	n/a
48	BATF	chr11:33404521-33404947	GM12878	blood:	n/a	n/a
49	BATF	chr11:33363592-33363812	GM12878	blood:	n/a	n/a
50	BATF	chr11:33409566-33409855	GM12878	blood:	n/a	n/a

(count:2751 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33394273-33394323	IMR90	lung:	fetal
2	chr11:33279899-33279949	PrEC	prostate:	n/a
3	chr11:33346306-33346356	PFSK-1	brain:	n/a
4	chr11:33278679-33278729	GM19239	blood:	n/a
5	chr11:33317015-33317065	U87	brain:	n/a
6	chr11:33308269-33308319	HL-60	blood:	n/a
7	chr11:33394273-33394323	IMR90	lung:	fetal
8	chr11:33279899-33279949	PrEC	prostate:	n/a
9	chr11:33346306-33346356	PFSK-1	brain:	n/a
10	chr11:33278679-33278729	GM19239	blood:	n/a
11	chr11:33317015-33317065	U87	brain:	n/a
12	chr11:33308269-33308319	HL-60	blood:	n/a
13	chr11:33375412-33375462	ProgFib	skin:	n/a
14	chr11:33278752-33278802	HMEC	breast:	n/a
15	chr11:33278752-33278802	SK-N-SH_RA	brain:	n/a
16	chr11:33396983-33397033	HAEpiC	amniotic membrane:	n/a
17	chr11:33279091-33279141	AG09309	skin:	n/a
18	chr11:33279084-33279134	IMR90	lung:	fetal
19	chr11:33397679-33397729	HRPEpiC	eye:	n/a
20	chr11:33264842-33264892	ECC-1	luminal epithelium:	n/a
21	chr11:33280012-33280062	AoSMC	blood vessel:	n/a
22	chr11:33474484-33474534	HCM	heart:	n/a
23	chr11:33442321-33442371	SK-N-MC	brain:	n/a
24	chr11:33279252-33279302	HRE	kidney:	n/a
25	chr11:33397387-33397437	CMK	blood:	n/a
26	chr11:33279136-33279186	GM06990	blood:	n/a
27	chr11:33265440-33265490	HCM	heart:	n/a
28	chr11:33279087-33279137	PrEC	prostate:	n/a
29	chr11:33214297-33214347	MCF10A-Er-Src	breast:	n/a
30	chr11:33279087-33279137	HEEpiC	esophagus:	n/a
31	chr11:33280157-33280207	Hela-S3	cervix:	n/a
32	chr11:33282841-33282891	AG09309	skin:	n/a
33	chr11:33317015-33317065	NHDF-neo	bronchial:	n/a
34	chr11:33398366-33398416	PFSK-1	brain:	n/a
35	chr11:33214297-33214347	NHBE	bronchial:	n/a
36	chr11:33394273-33394323	NH-A	brain:	n/a
37	chr11:33209645-33209695	NB4	blood:	n/a
38	chr11:33317015-33317065	HEEpiC	esophagus:	n/a
39	chr11:33346306-33346356	HAEpiC	amniotic membrane:	n/a
40	chr11:33278679-33278729	SK-N-SH	brain:	n/a
41	chr11:33399978-33400028	RPTEC	kidney:	n/a
42	chr11:33264842-33264892	GM12892	blood:	n/a
43	chr11:33214297-33214347	RPTEC	kidney:	n/a
44	chr11:33211414-33211464	SAEC	small airway:	n/a
45	chr11:33396983-33397033	AG09309	skin:	n/a
46	chr11:33308345-33308395	T-47D	breast:	n/a
47	chr11:33308345-33308395	ProgFib	skin:	n/a
48	chr11:33334443-33334493	AG10803	skin:	n/a
49	chr11:33317039-33317089	NB4	blood:	n/a
50	chr11:33276523-33276573	GM12878	blood:	n/a

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr11:33308929..33311681-chr11:33352469..33354383,2	MCF-7	breast:
2	chr11:33404576..33406306-chr11:33408202..33410856,2	MCF-7	breast:
3	chr11:33377235..33380179-chr11:33384228..33387621,3	K562	blood:
4	chr11:33421417..33423758-chr11:33435787..33437817,2	K562	blood:
5	chr11:33192932..33194844-chr11:33338349..33340157,2	K562	blood:
6	chr11:33319935..33321547-chr11:33324870..33327830,2	K562	blood:
7	chr11:33279524..33280025-chr3:9437578..9438488,2	Hela-S3	cervix:
8	chr11:33366273..33368343-chr11:33370196..33371959,2	K562	blood:
9	chr11:33308929..33311681-chr11:33352469..33354383,2	MCF-7	breast:
10	chr11:33264545..33268685-chr11:33272682..33276323,4	MCF-7	breast:
11	chr11:33383304..33384229-chr11:33708679..33709748,3	MCF-7	breast:
12	chr11:33187604..33188364-chr11:33351039..33351579,2	MCF-7	breast:
13	chr11:33347446..33349133-chr11:33352606..33354562,2	K562	blood:
14	chr11:33300069..33303546-chr11:33304515..33307878,3	K562	blood:
15	chr11:33277741..33279641-chr11:33288313..33289989,2	MCF-7	breast:
16	chr11:33278311..33281091-chr22:19157790..19160697,2	MCF-7	breast:
17	chr11:33279409..33279923-chr13:52026765..52027551,2	Hela-S3	cervix:
18	chr11:33181707..33184014-chr11:33222885..33224416,2	K562	blood:
19	chr11:33290160..33295323-chr11:33296264..33299611,6	K562	blood:
20	chr11:33279534..33280463-chr2:39351094..39351986,2	Hela-S3	cervix:
21	chr11:33396319..33398155-chr11:33401081..33403706,2	MCF-7	breast:
22	chr11:33246835..33249604-chr11:33278881..33281547,2	K562	blood:
23	chr11:33450480..33453431-chr11:33470843..33473158,2	MCF-7	breast:
24	chr11:33278564..33280833-chr11:33295728..33298096,2	K562	blood:
25	chr11:33340003..33342699-chr11:33347574..33349225,2	K562	blood:
26	chr11:33315778..33318693-chr11:33329241..33331442,2	K562	blood:
27	chr11:33392077..33394205-chr11:33397342..33400084,3	K562	blood:
28	chr11:33279345..33279976-chr6:27861115..27861730,2	Hela-S3	cervix:
29	chr11:33278126..33279710-chr11:33347501..33349004,2	MCF-7	breast:
30	chr11:33345288..33347427-chr11:33347864..33349944,2	MCF-7	breast:
31	chr11:33413545..33415997-chr11:33484077..33486158,2	K562	blood:
32	chr11:33392077..33394205-chr11:33397342..33400084,3	K562	blood:
33	chr11:33279068..33280061-chr11:67195914..67196832,2	Hela-S3	cervix:
34	chr11:33426996..33428983-chr11:33431666..33434178,3	K562	blood:
35	chr11:33181310..33183473-chr11:33251484..33253503,2	K562	blood:
36	chr11:33300641..33303261-chr11:33311159..33314863,3	K562	blood:
37	chr11:33475872..33478381-chr11:33480677..33482697,2	MCF-7	breast:
38	chr11:33187513..33188468-chr11:33351019..33351906,6	K562	blood:
39	chr11:33360581..33362754-chr11:33365388..33367285,2	K562	blood:
40	chr11:33433824..33436288-chr11:33439074..33441301,2	K562	blood:
41	chr11:33279061..33281281-chr11:34073248..34075291,2	K562	blood:
42	chr11:33277371..33280516-chr11:33349638..33353162,5	MCF-7	breast:
43	chr11:33395838..33399105-chr11:33400150..33402846,3	MCF-7	breast:
44	chr11:33372537..33375934-chr11:33378619..33381344,3	MCF-7	breast:
45	chr11:33278050..33279877-chr11:33311339..33315045,4	MCF-7	breast:
46	chr11:33278602..33279305-chr15:65588261..65588946,2	Hela-S3	cervix:
47	chr11:33399022..33400859-chr11:33402110..33404984,2	K562	blood:
48	chr11:33277788..33280266-chr11:33314208..33316157,2	K562	blood:
49	chr11:33372537..33375934-chr11:33378619..33381344,3	MCF-7	breast:
50	chr11:33278310..33280237-chr11:33303017..33305023,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TCP11L1-3	chr11:33333205-33333598	expReg_chr11_2971_+
2	lnc-HIPK3-2	chr11:33424762-33425151	NONHSAT018700
3	lnc-TCP11L1-1	chr11:33210316-33210396	ENSG00000247151
4	lnc-TCP11L1-1	chr11:33210914-33211103	ENSG00000247151
5	lnc-CSTF3-4	chr11:33212346-33212446	NONHSAT018694
6	lnc-TCP11L1-1	chr11:33211479-33213142	NONHSAT018691
7	lnc-CSTF3-3	chr11:33211608-33212049	NONHSAT018693
8	lnc-TCP11L1-1	chr11:33210914-33211103	NONHSAT018691
9	lnc-TCP11L1-1	chr11:33211479-33213144	ENSG00000247151
10	lnc-TCP11L1-1	chr11:33211479-33211840	ENSG00000247151
11	lnc-TCP11L1-1	chr11:33210316-33210396	ENSG00000247151
12	lnc-TCP11L1-1	chr11:33210316-33210396	NONHSAT018691
13	lnc-C11orf41-5	chr11:33472192-33472489	NONHSAT018701
14	lnc-CSTF3-5	chr11:33222131-33222464	NONHSAT018696
15	lnc-TCP11L1-4	chr11:33334713-33335041	expReg_chr11_2985_+
16	lnc-CSTF3-4	chr11:33212459-33213144	NONHSAT018694

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HIPK3	hsa-miR-20b-5p	chr11:33375709-33375730
2	HIPK3	hsa-miR-19b-3p	chr11:33375260-33375282
3	HIPK3	hsa-miR-19b-3p	chr11:33375275-33375282
4	HIPK3	hsa-miR-124-3p	chr11:33375651-33375670
5	HIPK3	hsa-miR-19b-3p	chr11:33358682-33358704
6	HIPK3	hsa-miR-106a-5p	chr11:33375245-33375267
7	HIPK3	hsa-miR-92a-3p	chr11:33375214-33375235
8	HIPK3	hsa-miR-124-3p	chr11:33375376-33375395
9	HIPK3	hsa-miR-92a-3p	chr11:33375228-33375234
10	HIPK3	hsa-miR-20b-5p	chr11:33375245-33375267
11	HIPK3	hsa-miR-335-5p	chr11:33375589-33375614
12	HIPK3	hsa-miR-106a-5p	chr11:33375709-33375730
13	HIPK3	hsa-miR-92a-3p	chr11:33375388-33375409
14	HIPK3	hsa-miR-124-3p	chr11:33375663-33375670

Variant related genes	Relation type
ENSG00000200485	TF binding region
HIPK3	TF binding region
RPL29P23	TF binding region
ENSG00000241255	TF binding region
ENSG00000255207	TF binding region
ENSG00000254537	TF binding region
ENSG00000223134	TF binding region
ENSG00000200485	CpG island
HIPK3	CpG island
RPL29P23	CpG island
ENSG00000241255	CpG island
ENSG00000255207	CpG island
ENSG00000254537	CpG island
ENSG00000223134	CpG island
ENSG00000199568	chromatin interactions
ENSG00000176102	chromatin interactions
ENSG00000175634	chromatin interactions
ENSG00000105479	chromatin interactions
ENSG00000247151	chromatin interactions
ENSG00000107745	chromatin interactions
ENSG00000115904	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000254718	chromatin interactions
ENSG00000255207	chromatin interactions
ENSG00000223134	chromatin interactions
ENSG00000079805	chromatin interactions
ENSG00000117335	chromatin interactions
ENSG00000128595	chromatin interactions
ENSG00000206808	chromatin interactions
ENSG00000263004	chromatin interactions
ENSG00000206573	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000130066	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000254537	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000200485	chromatin interactions
ENSG00000060749	chromatin interactions
ENSG00000110422	chromatin interactions
ENSG00000135387	chromatin interactions
ENSG00000196331	chromatin interactions
ENSG00000132570	chromatin interactions
ENSG00000207972	chromatin interactions
ENSG00000260924	chromatin interactions
ARID2	miRNA target sites
YWHAZ	miRNA target sites
PSME3	miRNA target sites
MICALL1	miRNA target sites

Extended variants
information (count: 10901 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:10901 , 50 per page) page: 1 2 3 4 5 6 7 ... 219

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16924000	chr11:33202614-33202615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs145887367	chr11:33202635-33202636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10836036	chr11:33202683-33202684	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs193279268	chr11:33202703-33202704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11032195	chr11:33202807-33202808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185099163	chr11:33202817-33202818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536518604	chr11:33202837-33202838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530741392	chr11:33202854-33202855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs550473855	chr11:33202858-33202859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs570640685	chr11:33202861-33202862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs57808474	chr11:33202923-33202924	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs547072352	chr11:33202950-33202951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs71034658	chr11:33202959-33202960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563773600	chr11:33202961-33202962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398075841	chr11:33202967-33202968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs398115245	chr11:33202968-33202969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548781657	chr11:33202985-33202986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190290832	chr11:33202988-33202989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560985405	chr11:33203008-33203009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs11032196	chr11:33203009-33203010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535837920	chr11:33203024-33203025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs555830304	chr11:33203073-33203074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7482352	chr11:33203082-33203083	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs552143742	chr11:33203083-33203084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs548016460	chr11:33203084-33203085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs192547184	chr11:33203103-33203104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558036449	chr11:33203105-33203106	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs551547569	chr11:33203146-33203147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112981592	chr11:33203194-33203195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369770138	chr11:33203213-33203214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs117607382	chr11:33203362-33203363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7482452	chr11:33203401-33203402	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs559022062	chr11:33203468-33203469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112362107	chr11:33203479-33203480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572642496	chr11:33203487-33203488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs184029296	chr11:33203634-33203635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561367786	chr11:33203685-33203686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552088581	chr11:33203693-33203694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75910351	chr11:33203705-33203706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34891459	chr11:33203801-33203802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs398075842	chr11:33203807-33203808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564078969	chr11:33203808-33203809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376251732	chr11:33203881-33203882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs79487336	chr11:33203890-33203891	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75734812	chr11:33203891-33203892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188715264	chr11:33203939-33203940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538154476	chr11:33203949-33203950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369470782	chr11:33203958-33203959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546516154	chr11:33204000-33204001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144413723	chr11:33204032-33204033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5339 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33183600-33203400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:33200200-33209400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr11:33200400-33202800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr11:33200600-33202800	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:33201400-33202800	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr11:33201600-33202800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr11:33201600-33213400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr11:33202000-33211400	Weak transcription	Dnd41	blood
9	chr11:33202400-33202800	Enhancers	Duodenum Mucosa	Duodenum
10	chr11:33202400-33202800	Enhancers	Placenta	Placenta
11	chr11:33202400-33202800	Enhancers	A549	lung
12	chr11:33202400-33203000	Enhancers	Stomach Mucosa	stomach
13	chr11:33202400-33205000	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr11:33202400-33205200	Enhancers	Fetal Intestine Large	intestine
15	chr11:33202600-33202800	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr11:33202600-33203400	Weak transcription	Gastric	stomach
17	chr11:33202600-33205200	Enhancers	Fetal Intestine Small	intestine
18	chr11:33202800-33203400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr11:33202800-33203800	Weak transcription	A549	lung
20	chr11:33202800-33209400	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr11:33203000-33203400	Weak transcription	Stomach Mucosa	stomach
22	chr11:33203000-33209000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr11:33203200-33205200	Enhancers	HepG2	liver
24	chr11:33203400-33203600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:33203400-33204200	Enhancers	Gastric	stomach
26	chr11:33203400-33205200	Enhancers	Duodenum Mucosa	Duodenum
27	chr11:33203400-33205200	Enhancers	Pancreas	Pancrea
28	chr11:33203400-33205200	Enhancers	Stomach Mucosa	stomach
29	chr11:33203600-33210000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:33203800-33204000	Enhancers	Colonic Mucosa	Colon
31	chr11:33203800-33204400	Enhancers	Fetal Muscle Leg	muscle
32	chr11:33203800-33204400	Enhancers	A549	lung
33	chr11:33204200-33205000	Weak transcription	Gastric	stomach
34	chr11:33204200-33209600	Weak transcription	Colonic Mucosa	Colon
35	chr11:33204400-33206200	Weak transcription	Fetal Muscle Leg	muscle
36	chr11:33205000-33205200	Enhancers	Gastric	stomach
37	chr11:33205000-33209200	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr11:33205200-33209200	Weak transcription	Duodenum Mucosa	Duodenum
39	chr11:33205200-33209400	Weak transcription	Fetal Intestine Large	intestine
40	chr11:33205200-33209400	Weak transcription	Fetal Intestine Small	intestine
41	chr11:33206200-33206800	Enhancers	Fetal Muscle Leg	muscle
42	chr11:33206400-33206600	Weak transcription	Fetal Muscle Trunk	muscle
43	chr11:33206600-33206800	Enhancers	Fetal Muscle Trunk	muscle
44	chr11:33206800-33208000	Weak transcription	Fetal Muscle Leg	muscle
45	chr11:33206800-33211400	Weak transcription	Fetal Muscle Trunk	muscle
46	chr11:33207000-33207600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:33207600-33209600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr11:33208000-33211000	Enhancers	Fetal Muscle Leg	muscle
49	chr11:33208800-33209600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr11:33209000-33209200	Enhancers	HSMMtube	muscle

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