Variant report

Variant	esv3390466
Chromosome Location	chr11:94276729-94279277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:533)
CpG islands
(count:1102)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:94276902-94277397	K562	blood:	n/a	n/a
2	ATF2	chr11:94277254-94277635	GM12878	blood:	n/a	n/a
3	BACH1	chr11:94276790-94277173	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:94277614-94277988	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr11:94276793-94277277	GM12878	blood:	n/a	chr11:94277191-94277200
6	BHLHE40	chr11:94276681-94277746	GM12878	blood:	n/a	chr11:94276897-94276913
7	BHLHE40	chr11:94278560-94278564	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:94276557-94277735	K562	blood:	n/a	chr11:94276897-94276913
9	BRCA1	chr11:94277023-94277193	GM12878	blood:	n/a	n/a
10	BRCA1	chr11:94277431-94277575	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr11:94276750-94277712	K562	blood:	n/a	n/a
12	CCNT2	chr11:94278538-94278783	K562	blood:	n/a	n/a
13	CCNT2	chr11:94276792-94278206	K562	blood:	n/a	n/a
14	CEBPB	chr11:94278592-94278691	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr11:94277348-94277650	Hela-S3	cervix:	n/a	n/a
16	CHD1	chr11:94276815-94277263	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr11:94277940-94278154	GM12878	blood:	n/a	n/a
18	CHD1	chr11:94276766-94277340	GM12878	blood:	n/a	n/a
19	CHD2	chr11:94276881-94277723	K562	blood:	n/a	n/a
20	CHD2	chr11:94278382-94278413	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr11:94276744-94277725	GM12878	blood:	n/a	n/a
22	CHD2	chr11:94277717-94277758	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr11:94276863-94277197	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr11:94277405-94277488	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr11:94277965-94278274	GM12878	blood:	n/a	n/a
26	CHD2	chr11:94277333-94277643	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr11:94277432-94278019	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr11:94276848-94277940	A549	lung:	n/a	n/a
29	CTBP2	chr11:94276885-94278743	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr11:94277680-94277830	GM12870	blood:	n/a	n/a
31	CTCF	chr11:94277400-94277550	GM12871	blood:	n/a	n/a
32	CTCF	chr11:94276900-94277050	GM06990	blood:	n/a	n/a
33	CTCF	chr11:94277952-94277953	IMR90	lung:	n/a	n/a
34	CTCF	chr11:94276980-94277130	HMF	breast:	n/a	n/a
35	CTCF	chr11:94276840-94276990	HCM	heart:	n/a	n/a
36	CTCF	chr11:94276961-94277121	A549	lung:	n/a	n/a
37	CTCF	chr11:94276986-94277109	Fibrobl	skin:	n/a	n/a
38	CTCF	chr11:94276987-94277071	GM13976	blood:	n/a	n/a
39	CTCF	chr11:94276980-94277130	BJ	skin:	n/a	n/a
40	CTCF	chr11:94276980-94277130	HRE	kidney:	n/a	n/a
41	CTCF	chr11:94277060-94277210	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr11:94277780-94277930	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr11:94277440-94277590	GM12878	blood:	n/a	n/a
44	CTCF	chr11:94276860-94277010	SAEC	small airway:	n/a	n/a
45	CTCF	chr11:94277776-94277885	Fibrobl	skin:	n/a	n/a
46	CTCF	chr11:94277460-94277610	GM12867	blood:	n/a	n/a
47	CTCF	chr11:94276870-94277106	K562	blood:	n/a	n/a
48	CTCF	chr11:94276960-94277110	BJ	skin:	n/a	n/a
49	CTCF	chr11:94277760-94277910	GM12872	blood:	n/a	n/a
50	CTCF	chr11:94277820-94277970	GM12869	blood:	n/a	n/a

(count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:94278457-94278507	GM12892	blood:	n/a
2	chr11:94277138-94277188	AoSMC	blood vessel:	n/a
3	chr11:94279068-94279118	PrEC	prostate:	n/a
4	chr11:94276960-94277010	SKMC	muscle:	n/a
5	chr11:94278457-94278507	GM12892	blood:	n/a
6	chr11:94277138-94277188	AoSMC	blood vessel:	n/a
7	chr11:94279068-94279118	PrEC	prostate:	n/a
8	chr11:94276960-94277010	SKMC	muscle:	n/a
9	chr11:94278324-94278374	GM12891	blood:	n/a
10	chr11:94279068-94279118	HRE	kidney:	n/a
11	chr11:94278538-94278588	SAEC	small airway:	n/a
12	chr11:94278595-94278645	GM06990	blood:	n/a
13	chr11:94278324-94278374	HL-60	blood:	n/a
14	chr11:94277138-94277188	PFSK-1	brain:	n/a
15	chr11:94277138-94277188	AG04449	skin:	fetal
16	chr11:94278595-94278645	U87	brain:	n/a
17	chr11:94278595-94278645	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:94276960-94277010	U87	brain:	n/a
19	chr11:94278603-94278653	ovcar-3	ovarian:	n/a
20	chr11:94277826-94277876	GM12891	blood:	n/a
21	chr11:94279068-94279118	BJ	skin:	n/a
22	chr11:94279068-94279118	HUVEC	blood vessel:	n/a
23	chr11:94276903-94276953	AoSMC	blood vessel:	n/a
24	chr11:94277190-94277240	ECC-1	luminal epithelium:	n/a
25	chr11:94278407-94278457	HNPCEpiC	eye:	n/a
26	chr11:94278457-94278507	IMR90	lung:	fetal
27	chr11:94277138-94277188	GM19239	blood:	n/a
28	chr11:94277826-94277876	H1-hESC	embryonic stem cell:	embryo
29	chr11:94277190-94277240	HIPEpiC	eye:	n/a
30	chr11:94278407-94278457	HRE	kidney:	n/a
31	chr11:94279068-94279118	HRCEpiC	kidney:	n/a
32	chr11:94277451-94277501	HCT-116	colon:	n/a
33	chr11:94278324-94278374	RPTEC	kidney:	n/a
34	chr11:94278603-94278653	SKMC	muscle:	n/a
35	chr11:94277451-94277501	SKMC	muscle:	n/a
36	chr11:94278581-94278631	SK-N-SH	brain:	n/a
37	chr11:94276903-94276953	HNPCEpiC	eye:	n/a
38	chr11:94278324-94278374	MCF-7	breast:	n/a
39	chr11:94276898-94276948	HCF	heart:	n/a
40	chr11:94276898-94276948	GM12892	blood:	n/a
41	chr11:94278603-94278653	AG04450	lung:	fetal
42	chr11:94277826-94277876	AoSMC	blood vessel:	n/a
43	chr11:94276903-94276953	AG04449	skin:	fetal
44	chr11:94278538-94278588	HUVEC	blood vessel:	n/a
45	chr11:94278581-94278631	AG09309	skin:	n/a
46	chr11:94278538-94278588	NH-A	brain:	n/a
47	chr11:94278324-94278374	NHBE	bronchial:	n/a
48	chr11:94276898-94276948	NHBE	bronchial:	n/a
49	chr11:94278595-94278645	HNPCEpiC	eye:	n/a
50	chr11:94276898-94276948	HIPEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:94279156..94280673-chr11:94309932..94312809,2	K562	blood:
2	chr11:94279228..94280782-chr11:94283741..94285745,2	MCF-7	breast:
3	chr11:94277201..94277899-chr3:150421042..150421878,2	NB4	blood:
4	chr11:94225466..94228271-chr11:94275709..94278301,3	K562	blood:
5	chr11:94226771..94229140-chr11:94275887..94279295,4	K562	blood:
6	chr11:94277458..94279077-chr11:94299379..94301250,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRE11A-3	chr11:94276131-94277949	NONHSAT023724
2	lnc-MRE11A-3	chr11:94275325-94277016	NONHSAT023723

No data

Variant related genes	Relation type
PIWIL4	TF binding region
FUT4	TF binding region
PIWIL4	CpG island
FUT4	CpG island
ENSG00000020922	chromatin interactions
ENSG00000163645	chromatin interactions
ENSG00000134627	chromatin interactions
ENSG00000168876	chromatin interactions
ENSG00000240137	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551811257	chr11:94276762-94276763	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
2	rs371838750	chr11:94276782-94276783	Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
3	rs563646855	chr11:94276849-94276850	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
4	rs141458597	chr11:94276857-94276858	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
5	rs549738057	chr11:94276867-94276868	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs185465809	chr11:94276870-94276871	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs190272940	chr11:94276917-94276918	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs181240567	chr11:94276918-94276919	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs376495240	chr11:94276933-94276934	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs543690557	chr11:94276935-94276936	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs11574856	chr11:94276983-94276984	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs573600293	chr11:94277002-94277003	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs12280950	chr11:94277033-94277034	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs114789869	chr11:94277055-94277056	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs5793688	chr11:94277080-94277081	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs185907530	chr11:94277121-94277122	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs150833829	chr11:94277126-94277127	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs555722992	chr11:94277137-94277138	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs574382685	chr11:94277138-94277139	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs541698537	chr11:94277165-94277166	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs560097265	chr11:94277175-94277176	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs578046235	chr11:94277203-94277204	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
23	rs34512155	chr11:94277219-94277220	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs563781662	chr11:94277274-94277275	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
25	rs530942667	chr11:94277341-94277342	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
26	rs369136885	chr11:94277389-94277390	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
27	rs543595914	chr11:94277390-94277391	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
28	rs561596556	chr11:94277403-94277404	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
29	rs539435556	chr11:94277424-94277425	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
30	rs529058869	chr11:94277451-94277452	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
31	rs190868751	chr11:94277461-94277462	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
32	rs80318628	chr11:94277515-94277516	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
33	rs373252364	chr11:94277570-94277571	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
34	rs532915818	chr11:94277587-94277588	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
35	rs113253321	chr11:94277592-94277593	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
36	rs562924697	chr11:94277681-94277682	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs569720539	chr11:94277698-94277699	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs34365654	chr11:94277730-94277731	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
39	rs536791974	chr11:94277829-94277830	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
40	rs148605037	chr11:94277852-94277853	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
41	rs113641402	chr11:94277873-94277874	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
42	rs567818935	chr11:94277895-94277896	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
43	rs201519706	chr11:94277897-94277898	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
44	rs553674609	chr11:94277900-94277901	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs576786819	chr11:94277905-94277906	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs578256926	chr11:94277920-94277921	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs545371409	chr11:94277952-94277953	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs199688248	chr11:94277959-94277960	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs200974716	chr11:94278025-94278026	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs201063400	chr11:94278029-94278030	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:94271200-94276800	Weak transcription	HMEC	breast
2	chr11:94272600-94276800	Weak transcription	Small Intestine	intestine
3	chr11:94275400-94276800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr11:94276200-94276800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr11:94276200-94276800	Enhancers	Primary B cells from peripheral blood	blood
6	chr11:94276200-94277000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
7	chr11:94276200-94277000	Flanking Active TSS	Dnd41	blood
8	chr11:94276200-94277000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
9	chr11:94276200-94277200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
10	chr11:94276200-94277800	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr11:94276400-94276800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:94276400-94276800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:94276400-94276800	Flanking Active TSS	Brain Anterior Caudate	brain
14	chr11:94276400-94276800	Flanking Active TSS	Brain Cingulate Gyrus	brain
15	chr11:94276400-94276800	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr11:94276400-94276800	Flanking Active TSS	Colon Smooth Muscle	Colon
17	chr11:94276400-94276800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
18	chr11:94276400-94276800	Flanking Active TSS	Fetal Intestine Large	intestine
19	chr11:94276400-94276800	Flanking Active TSS	Fetal Intestine Small	intestine
20	chr11:94276400-94276800	Flanking Active TSS	Fetal Kidney	kidney
21	chr11:94276400-94276800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr11:94276400-94276800	Flanking Active TSS	Fetal Lung	lung
23	chr11:94276400-94276800	Flanking Active TSS	Stomach Smooth Muscle	stomach
24	chr11:94276400-94277000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr11:94276400-94277000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
26	chr11:94276400-94277000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr11:94276400-94277000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
28	chr11:94276400-94277000	Flanking Active TSS	Primary T cells from cord blood	blood
29	chr11:94276400-94277000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:94276400-94277000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr11:94276400-94277000	Flanking Active TSS	Adipose Nuclei	Adipose
32	chr11:94276400-94277000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr11:94276400-94277000	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr11:94276400-94277000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
35	chr11:94276400-94277000	Flanking Active TSS	GM12878-XiMat	blood
36	chr11:94276400-94277200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr11:94276400-94277200	Flanking Active TSS	Colonic Mucosa	Colon
38	chr11:94276400-94277600	Flanking Active TSS	Primary B cells from cord blood	blood
39	chr11:94276400-94279200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
40	chr11:94276400-94279200	Active TSS	Brain Substantia Nigra	brain
41	chr11:94276400-94279600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr11:94276400-94280000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr11:94276600-94276800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr11:94276600-94276800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr11:94276600-94276800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr11:94276600-94276800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr11:94276600-94276800	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
48	chr11:94276600-94276800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr11:94276600-94276800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:94276600-94276800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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