Variant report

Variant	esv3404977
Chromosome Location	chr11:67055801-67058349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:852)
CpG islands
(count:428)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:67055761-67055959	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:67056262-67056458	HepG2	liver:	n/a	n/a
3	ATF2	chr11:67055600-67056492	GM12878	blood:	n/a	n/a
4	ATF2	chr11:67055236-67056699	GM12878	blood:	n/a	n/a
5	ATF3	chr11:67055429-67056028	A549	lung:	n/a	n/a
6	BACH1	chr11:67056083-67056711	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:67056354-67056379	K562	blood:	n/a	n/a
8	BCL11A	chr11:67055792-67056002	GM12878	blood:	n/a	chr11:67055795-67055804
9	BCL11A	chr11:67055739-67056286	GM12878	blood:	n/a	chr11:67055795-67055804
10	BCL3	chr11:67055267-67056401	A549	lung:	n/a	chr11:67055795-67055804 chr11:67055465-67055473
11	BCL3	chr11:67055344-67056717	GM12878	blood:	n/a	chr11:67055795-67055804 chr11:67055465-67055473 chr11:67056547-67056560
12	BCL3	chr11:67055403-67056543	A549	lung:	n/a	chr11:67055795-67055804 chr11:67055465-67055473
13	BCLAF1	chr11:67055459-67056725	GM12878	blood:	n/a	chr11:67055795-67055804 chr11:67055465-67055473 chr11:67056547-67056560
14	BCLAF1	chr11:67054908-67056693	GM12878	blood:	n/a	chr11:67055795-67055804 chr11:67055465-67055473 chr11:67056547-67056560
15	BHLHE40	chr11:67055665-67056713	GM12878	blood:	n/a	chr11:67056547-67056563 chr11:67056531-67056547 chr11:67056111-67056127
16	BHLHE40	chr11:67055855-67056605	HepG2	liver:	n/a	chr11:67056547-67056563 chr11:67056531-67056547 chr11:67056111-67056127
17	BHLHE40	chr11:67057225-67057267	K562	blood:	n/a	n/a
18	BHLHE40	chr11:67055599-67056613	K562	blood:	n/a	chr11:67056547-67056563 chr11:67056531-67056547 chr11:67056111-67056127
19	BRCA1	chr11:67055551-67056383	GM12878	blood:	n/a	n/a
20	BRCA1	chr11:67055818-67056319	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr11:67055525-67056547	K562	blood:	n/a	n/a
22	CCNT2	chr11:67055758-67057049	K562	blood:	n/a	n/a
23	CEBPB	chr11:67055827-67056128	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:67055803-67056195	A549	lung:	n/a	n/a
25	CEBPB	chr11:67055662-67056668	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:67055831-67056169	K562	blood:	n/a	n/a
27	CEBPB	chr11:67055459-67056626	A549	lung:	n/a	n/a
28	CEBPB	chr11:67055508-67056385	GM12878	blood:	n/a	n/a
29	CEBPB	chr11:67055273-67056639	HCT-116	colon:	n/a	n/a
30	CEBPB	chr11:67055787-67056378	K562	blood:	n/a	n/a
31	CEBPB	chr11:67055751-67056150	ECC-1	luminal epithelium:	n/a	n/a
32	CEBPB	chr11:67055592-67056495	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr11:67055734-67056252	A549	lung:	n/a	n/a
34	CEBPB	chr11:67055726-67056074	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:67055759-67056721	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:67055675-67056505	MCF-7	breast:	n/a	n/a
37	CEBPB	chr11:67055775-67056498	IMR90	lung:	n/a	n/a
38	CEBPB	chr11:67055816-67056186	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr11:67055623-67056422	MCF-7	breast:	n/a	n/a
40	CEBPB	chr11:67055633-67056371	K562	blood:	n/a	n/a
41	CEBPB	chr11:67055789-67056181	HepG2	liver:	n/a	n/a
42	CEBPD	chr11:67055511-67057041	HepG2	liver:	n/a	n/a
43	CEBPD	chr11:67055768-67056163	HepG2	liver:	n/a	n/a
44	CEBPD	chr11:67055726-67056330	K562	blood:	n/a	n/a
45	CEBPD	chr11:67056291-67056582	HepG2	liver:	n/a	n/a
46	CEBPD	chr11:67055638-67056779	K562	blood:	n/a	n/a
47	CHD1	chr11:67055413-67056670	GM12878	blood:	n/a	n/a
48	CHD2	chr11:67055579-67056646	GM12878	blood:	n/a	n/a
49	CHD2	chr11:67055642-67056188	K562	blood:	n/a	n/a
50	CHD2	chr11:67055646-67057005	Hela-S3	cervix:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67057304-67057354	HAEpiC	amniotic membrane:	n/a
2	chr11:67057304-67057354	HAEpiC	amniotic membrane:	n/a
3	chr11:67057248-67057298	HCPEpiC	choroid plexus:	n/a
4	chr11:67055946-67055996	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:67056238-67056288	BE2_C	brain:	n/a
6	chr11:67057304-67057354	HCM	heart:	n/a
7	chr11:67056238-67056288	CMK	blood:	n/a
8	chr11:67057304-67057354	PrEC	prostate:	n/a
9	chr11:67056918-67056968	Caco-2	colon:	n/a
10	chr11:67055946-67055996	HRE	kidney:	n/a
11	chr11:67057304-67057354	AG09319	gingival:	n/a
12	chr11:67055946-67055996	NH-A	brain:	n/a
13	chr11:67056918-67056968	NB4	blood:	n/a
14	chr11:67057003-67057053	LNCaP	prostate:	n/a
15	chr11:67055946-67055996	H1-hESC	embryonic stem cell:	embryo
16	chr11:67057248-67057298	K562	blood:	n/a
17	chr11:67057248-67057298	GM12878	blood:	n/a
18	chr11:67056918-67056968	HEEpiC	esophagus:	n/a
19	chr11:67057304-67057354	GM12891	blood:	n/a
20	chr11:67056446-67056496	A549	lung:	n/a
21	chr11:67057003-67057053	HEK293	kidney:	embryo
22	chr11:67056446-67056496	HAEpiC	amniotic membrane:	n/a
23	chr11:67057248-67057298	GM06990	blood:	n/a
24	chr11:67057003-67057053	NB4	blood:	n/a
25	chr11:67057248-67057298	HCF	heart:	n/a
26	chr11:67057248-67057298	LNCaP	prostate:	n/a
27	chr11:67056918-67056968	Hela-S3	cervix:	n/a
28	chr11:67056446-67056496	AG09319	gingival:	n/a
29	chr11:67056238-67056288	Hepatocyte	liver:	n/a
30	chr11:67057003-67057053	Jurkat	blood:	n/a
31	chr11:67057248-67057298	HL-60	blood:	n/a
32	chr11:67055946-67055996	SK-N-SH	brain:	n/a
33	chr11:67057248-67057298	HEEpiC	esophagus:	n/a
34	chr11:67056446-67056496	PrEC	prostate:	n/a
35	chr11:67056238-67056288	MCF-7	breast:	n/a
36	chr11:67055946-67055996	AoSMC	blood vessel:	n/a
37	chr11:67056238-67056288	LNCaP	prostate:	n/a
38	chr11:67056446-67056496	HEK293	kidney:	embryo
39	chr11:67056238-67056288	HEK293	kidney:	embryo
40	chr11:67055946-67055996	BJ	skin:	n/a
41	chr11:67055946-67055996	HIPEpiC	eye:	n/a
42	chr11:67056238-67056288	PFSK-1	brain:	n/a
43	chr11:67056918-67056968	H1-hESC	embryonic stem cell:	embryo
44	chr11:67056918-67056968	Hepatocyte	liver:	n/a
45	chr11:67056918-67056968	MCF10A-Er-Src	breast:	n/a
46	chr11:67057304-67057354	Hepatocyte	liver:	n/a
47	chr11:67056918-67056968	AG09309	skin:	n/a
48	chr11:67057003-67057053	GM06990	blood:	n/a
49	chr11:67057248-67057298	HAEpiC	amniotic membrane:	n/a
50	chr11:67055946-67055996	GM12878	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67055723..67056241-chr13:98628294..98628801,2	NB4	blood:
2	chr11:67053008..67062318-chr11:67075341..67086484,24	K562	blood:
3	chr11:67056267..67057775-chr15:68549196..68551810,2	MCF-7	breast:
4	chr11:67054211..67056226-chr11:67160780..67163309,2	MCF-7	breast:
5	chr11:67056152..67057908-chr11:67157420..67159394,2	MCF-7	breast:
6	chr11:66821441..66825228-chr11:67054009..67057657,5	MCF-7	breast:
7	chr11:67055136..67057390-chr11:67140087..67141656,2	MCF-7	breast:
8	chr11:67056211..67059053-chr11:67235087..67237043,2	MCF-7	breast:
9	chr11:66885437..66888305-chr11:67055921..67058495,2	MCF-7	breast:
10	chr11:67033435..67034183-chr11:67056208..67056959,2	K562	blood:
11	chr11:67054455..67063331-chr11:67064649..67075279,24	K562	blood:
12	chr11:67055725..67056438-chr6:26199156..26199993,2	NB4	blood:
13	chr11:67055572..67057454-chr15:91474041..91476602,2	MCF-7	breast:
14	chr11:67053474..67057507-chr11:67138689..67143945,8	MCF-7	breast:
15	chr11:66793222..66795910-chr11:67054347..67057344,2	MCF-7	breast:
16	chr11:67054960..67058476-chr11:67120507..67123269,5	MCF-7	breast:
17	chr11:67033837..67034854-chr11:67056054..67056870,3	MCF-7	breast:
18	chr11:67055526..67056164-chr3:52231773..52232652,2	NB4	blood:
19	chr11:66610034..66612192-chr11:67054679..67057615,2	MCF-7	breast:
20	chr11:67055923..67056800-chr15:90744214..90744805,2	NB4	blood:
21	chr11:67054274..67056695-chr11:67119376..67121625,2	K562	blood:
22	chr11:67055858..67057082-chr3:73160101..73160609,3	Hela-S3	cervix:
23	chr11:67033464..67034256-chr11:67056090..67056695,3	MCF-7	breast:
24	chr11:67055669..67056641-chr17:72744389..72745314,2	NB4	blood:

No data

Variant related genes	Relation type
ANKRD13D	TF binding region
ANKRD13D	CpG island
ENSG00000109062	chromatin interactions
ENSG00000256514	chromatin interactions
ENSG00000172663	chromatin interactions
ENSG00000266036	chromatin interactions
ENSG00000173653	chromatin interactions
ENSG00000264624	chromatin interactions
ENSG00000185033	chromatin interactions
ENSG00000173156	chromatin interactions
ENSG00000128973	chromatin interactions
ENSG00000173227	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000172613	chromatin interactions
ENSG00000172830	chromatin interactions
ENSG00000253024	chromatin interactions
ENSG00000023330	chromatin interactions
ENSG00000172932	chromatin interactions
ENSG00000175482	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000065150	chromatin interactions
ENSG00000175505	chromatin interactions
ENSG00000173020	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000184508	chromatin interactions
ENSG00000173120	chromatin interactions

Extended variants
information (count: 81 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:81 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559132135	chr11:67055858-67055859	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
2	rs61763979	chr11:67055884-67055885	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs544951373	chr11:67055900-67055901	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
4	rs563336098	chr11:67055937-67055938	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
5	rs369390716	chr11:67055941-67055942	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
6	rs530849361	chr11:67056013-67056014	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
7	rs61763980	chr11:67056025-67056026	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
8	rs61763981	chr11:67056107-67056108	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
9	rs561195857	chr11:67056130-67056131	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
10	rs528599898	chr11:67056273-67056274	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
11	rs554988344	chr11:67056315-67056316	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
12	rs546835024	chr11:67056329-67056330	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
13	rs115593094	chr11:67056369-67056370	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
14	rs145635841	chr11:67056396-67056397	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	TF binding region Chromatin interactive region	23 gene(s)	Overlapped CNVs	n/a
15	rs551334823	chr11:67056447-67056448	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
16	rs373106878	chr11:67056493-67056494	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
17	rs536615067	chr11:67056576-67056577	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
18	rs555996331	chr11:67056601-67056602	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
19	rs112895629	chr11:67056640-67056641	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	20 gene(s)	Overlapped CNVs	n/a
20	rs545058578	chr11:67056710-67056711	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
21	rs534720385	chr11:67056711-67056712	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
22	rs552748613	chr11:67056712-67056713	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
23	rs530673733	chr11:67056748-67056749	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
24	rs577457623	chr11:67056779-67056780	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
25	rs549149064	chr11:67056795-67056796	Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	17 gene(s)	Overlapped CNVs	n/a
26	rs544890068	chr11:67056807-67056808	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
27	rs563273856	chr11:67056904-67056905	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
28	rs553569575	chr11:67056907-67056908	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
29	rs575513371	chr11:67057003-67057004	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs368498130	chr11:67057093-67057094	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs71462369	chr11:67057103-67057104	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs11227758	chr11:67057104-67057105	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs111935356	chr11:67057109-67057110	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs542618241	chr11:67057167-67057168	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs561342525	chr11:67057179-67057180	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs190522530	chr11:67057184-67057185	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs547117441	chr11:67057214-67057215	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs565467958	chr11:67057232-67057233	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs114522764	chr11:67057262-67057263	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs182751905	chr11:67057268-67057269	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
41	rs569538493	chr11:67057276-67057277	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
42	rs530432253	chr11:67057463-67057464	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs186933117	chr11:67057475-67057476	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs370552873	chr11:67057490-67057491	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
45	rs111345048	chr11:67057535-67057536	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs5792410	chr11:67057537-67057538	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs183188841	chr11:67057574-67057575	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs1574103	chr11:67057599-67057600	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs571090503	chr11:67057620-67057621	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs538420825	chr11:67057650-67057651	Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD

Chromatin state (count:564 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67050800-67056000	Weak transcription	Psoas Muscle	Psoas
2	chr11:67053400-67056000	Weak transcription	Ovary	ovary
3	chr11:67053600-67056000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr11:67053600-67056400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
5	chr11:67054400-67056000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
6	chr11:67054400-67056400	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr11:67054400-67056400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
8	chr11:67054400-67056400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr11:67054600-67056000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr11:67054600-67056000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
11	chr11:67054600-67056000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
12	chr11:67054600-67056000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
13	chr11:67054600-67056000	Enhancers	Left Ventricle	heart
14	chr11:67054600-67056400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr11:67054800-67056000	Flanking Active TSS	Brain Anterior Caudate	brain
16	chr11:67054800-67056400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr11:67054800-67056400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr11:67055000-67056000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
19	chr11:67055000-67056000	Flanking Active TSS	Primary T cells from cord blood	blood
20	chr11:67055000-67056000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:67055000-67056000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
22	chr11:67055000-67056000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr11:67055000-67056000	Flanking Active TSS	Duodenum Mucosa	Duodenum
24	chr11:67055000-67056000	Flanking Active TSS	Rectal Smooth Muscle	rectum
25	chr11:67055000-67056000	Flanking Active TSS	HepG2	liver
26	chr11:67055000-67056400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr11:67055000-67056400	Flanking Active TSS	Colonic Mucosa	Colon
28	chr11:67055200-67056000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr11:67055200-67056000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr11:67055200-67056000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
31	chr11:67055200-67056000	Flanking Active TSS	Thymus	Thymus
32	chr11:67055200-67056000	Flanking Active TSS	K562	blood
33	chr11:67055200-67056200	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr11:67055200-67056400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:67055200-67056400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:67055200-67056400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr11:67055400-67056000	Flanking Active TSS	H9 Cell Line	embryonic stem cell
38	chr11:67055400-67056000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr11:67055400-67056000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
40	chr11:67055400-67056000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr11:67055400-67056000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:67055400-67056000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
43	chr11:67055400-67056000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr11:67055400-67056000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr11:67055400-67056000	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr11:67055400-67056000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
47	chr11:67055400-67056000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr11:67055400-67056000	Flanking Active TSS	Fetal Brain Female	brain
49	chr11:67055400-67056000	Enhancers	Gastric	stomach
50	chr11:67055400-67056000	Flanking Active TSS	GM12878-XiMat	blood

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