Variant report

Variant	esv3361899
Chromosome Location	chr11:67133576-67138574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:172)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:172 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:67136054-67136498	GM12878	blood:	n/a	n/a
2	ATF2	chr11:67136050-67136411	GM12878	blood:	n/a	n/a
3	BATF	chr11:67136107-67136354	GM12878	blood:	n/a	chr11:67136142-67136150
4	BCL11A	chr11:67136154-67136350	GM12878	blood:	n/a	n/a
5	BCL3	chr11:67136713-67137737	A549	lung:	n/a	chr11:67137479-67137492 chr11:67137449-67137458
6	BCL3	chr11:67135782-67136381	A549	lung:	n/a	n/a
7	BHLHE40	chr11:67137919-67138191	K562	blood:	n/a	chr11:67137965-67137978
8	BHLHE40	chr11:67136189-67136374	GM12878	blood:	n/a	n/a
9	CTCF	chr11:67136236-67136281	GM19238	blood:	n/a	n/a
10	CTCF	chr11:67138420-67138570	SAEC	small airway:	n/a	n/a
11	CTCF	chr11:67137280-67137430	AG04450	lung:	n/a	n/a
12	CTCF	chr11:67137240-67137390	HFF	foreskin:	n/a	n/a
13	CTCF	chr11:67138280-67138430	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr11:67137200-67137350	BJ	skin:	n/a	n/a
15	CTCF	chr11:67136229-67136306	GM12892	blood:	n/a	n/a
16	CTCF	chr11:67136185-67136324	GM19239	blood:	n/a	n/a
17	CTCF	chr11:67137220-67137370	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr11:67138358-67139875	A549	lung:	n/a	chr11:67139137-67139150
19	CTCF	chr11:67137280-67137430	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr11:67137280-67137430	BJ	skin:	n/a	n/a
21	CTCF	chr11:67137200-67137350	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr11:67138320-67138470	HPAF	blood vessel:	n/a	n/a
23	CTCF	chr11:67137240-67137390	HVMF	connective:	n/a	n/a
24	E2F6	chr11:67134480-67135012	A549	lung:	n/a	chr11:67134667-67134677 chr11:67134598-67134607
25	E2F6	chr11:67137596-67137757	K562	blood:	n/a	n/a
26	EBF1	chr11:67136689-67136975	GM12878	blood:	n/a	chr11:67136854-67136864 chr11:67136854-67136863 chr11:67136854-67136863 chr11:67136853-67136864 chr11:67136852-67136865
27	EBF1	chr11:67136155-67136332	GM12878	blood:	n/a	n/a
28	EBF1	chr11:67136742-67136965	GM12878	blood:	n/a	chr11:67136854-67136864 chr11:67136854-67136863 chr11:67136854-67136863 chr11:67136853-67136864 chr11:67136852-67136865
29	EBF1	chr11:67136112-67136338	GM12878	blood:	n/a	n/a
30	EBF1	chr11:67135977-67136386	GM12878	blood:	n/a	n/a
31	EGR1	chr11:67133542-67133781	K562	blood:	n/a	n/a
32	EGR1	chr11:67133500-67133796	K562	blood:	n/a	n/a
33	ELF1	chr11:67137930-67138169	K562	blood:	n/a	n/a
34	EP300	chr11:67136125-67136428	GM12878	blood:	n/a	n/a
35	FOS	chr11:67136711-67137385	HUVEC	blood vessel:	n/a	chr11:67136960-67136969 chr11:67136954-67136964
36	FOSL2	chr11:67138547-67139777	A549	lung:	n/a	n/a
37	FOXA2	chr11:67134333-67134751	A549	lung:	n/a	n/a
38	FOXA2	chr11:67134383-67134946	A549	lung:	n/a	n/a
39	FOXP2	chr11:67137744-67138274	PFSK-1	brain:	n/a	n/a
40	FOXP2	chr11:67137846-67138286	PFSK-1	brain:	n/a	n/a
41	GATA3	chr11:67138557-67145601	A549	lung:	n/a	n/a
42	IKZF1	chr11:67136060-67136523	GM12878	blood:	n/a	n/a
43	JUND	chr11:67134340-67135141	A549	lung:	n/a	chr11:67134661-67134670 chr11:67134665-67134674
44	JUND	chr11:67134958-67134982	HepG2	liver:	n/a	n/a
45	MAX	chr11:67137875-67138351	K562	blood:	n/a	chr11:67138167-67138177 chr11:67138019-67138029
46	MAX	chr11:67137569-67137837	K562	blood:	n/a	n/a
47	MAX	chr11:67138561-67140292	A549	lung:	n/a	chr11:67139214-67139223
48	MAX	chr11:67134437-67135039	A549	lung:	n/a	n/a
49	MAX	chr11:67134429-67134992	ECC-1	luminal epithelium:	n/a	n/a
50	MAX	chr11:67138076-67138332	NB4	blood:	n/a	chr11:67138167-67138177

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67136752-67136802	HUVEC	blood vessel:	n/a
2	chr11:67134607-67134657	HRE	kidney:	n/a
3	chr11:67136752-67136802	HL-60	blood:	n/a
4	chr11:67134607-67134657	SK-N-SH_RA	brain:	n/a
5	chr11:67134607-67134657	MCF-7	breast:	n/a
6	chr11:67136752-67136802	Hela-S3	cervix:	n/a
7	chr11:67134607-67134657	HEEpiC	esophagus:	n/a
8	chr11:67134607-67134657	AG10803	skin:	n/a
9	chr11:67134607-67134657	HNPCEpiC	eye:	n/a
10	chr11:67135897-67135947	HepG2	liver:	n/a
11	chr11:67136752-67136802	HIPEpiC	eye:	n/a
12	chr11:67136752-67136802	GM12892	blood:	n/a
13	chr11:67135897-67135947	GM19239	blood:	n/a
14	chr11:67134607-67134657	ECC-1	luminal epithelium:	n/a
15	chr11:67135897-67135947	PANC-1	pancreas:	n/a
16	chr11:67134607-67134657	LNCaP	prostate:	n/a
17	chr11:67135897-67135947	LNCaP	prostate:	n/a
18	chr11:67134607-67134657	ProgFib	skin:	n/a
19	chr11:67135897-67135947	HIPEpiC	eye:	n/a
20	chr11:67135897-67135947	Jurkat	blood:	n/a
21	chr11:67136752-67136802	ECC-1	luminal epithelium:	n/a
22	chr11:67135897-67135947	IMR90	lung:	fetal
23	chr11:67135897-67135947	NHBE	bronchial:	n/a
24	chr11:67134607-67134657	MCF10A-Er-Src	breast:	n/a
25	chr11:67135897-67135947	GM12892	blood:	n/a
26	chr11:67135897-67135947	ProgFib	skin:	n/a
27	chr11:67134607-67134657	SAEC	small airway:	n/a
28	chr11:67134607-67134657	Jurkat	blood:	n/a
29	chr11:67135897-67135947	AG09319	gingival:	n/a
30	chr11:67136752-67136802	NHBE	bronchial:	n/a
31	chr11:67136752-67136802	HCT-116	colon:	n/a
32	chr11:67135897-67135947	MCF-7	breast:	n/a
33	chr11:67135897-67135947	A549	lung:	n/a
34	chr11:67135897-67135947	AG09309	skin:	n/a
35	chr11:67135897-67135947	HRE	kidney:	n/a
36	chr11:67136752-67136802	IMR90	lung:	fetal
37	chr11:67135897-67135947	Caco-2	colon:	n/a
38	chr11:67135897-67135947	AG04449	skin:	fetal
39	chr11:67134607-67134657	AoSMC	blood vessel:	n/a
40	chr11:67135897-67135947	NT2-D1	testis:	n/a
41	chr11:67134607-67134657	HEK293	kidney:	embryo
42	chr11:67135897-67135947	SKMC	muscle:	n/a
43	chr11:67136752-67136802	SK-N-SH	brain:	n/a
44	chr11:67135897-67135947	ovcar-3	ovarian:	n/a
45	chr11:67135897-67135947	SK-N-SH_RA	brain:	n/a
46	chr11:67136752-67136802	BJ	skin:	n/a
47	chr11:67134607-67134657	Hepatocyte	liver:	n/a
48	chr11:67134607-67134657	AG09309	skin:	n/a
49	chr11:67134607-67134657	NHDF-neo	bronchial:	n/a
50	chr11:67134607-67134657	HRCEpiC	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67030856..67037366-chr11:67138319..67144892,13	MCF-7	breast:
2	chr11:67119765..67126816-chr11:67129168..67134805,10	K562	blood:
3	chr11:67138430..67143112-chr11:67157518..67161987,7	K562	blood:
4	chr11:67082881..67085755-chr11:67132076..67134677,2	K562	blood:
5	chr11:67138235..67140028-chr11:67271265..67273106,2	MCF-7	breast:
6	chr11:67078307..67080022-chr11:67137493..67139530,2	MCF-7	breast:
7	chr11:67116951..67127260-chr11:67135118..67146037,42	K562	blood:
8	chr11:66886882..66888512-chr11:67137835..67140678,2	MCF-7	breast:
9	chr11:67085099..67087143-chr11:67137966..67139875,2	K562	blood:
10	chr11:67118624..67119311-chr11:67137860..67138596,2	K562	blood:
11	chr11:67138426..67140382-chr11:67217472..67219205,2	K562	blood:
12	chr11:67133399..67135942-chr11:67204970..67207093,2	K562	blood:
13	chr11:67137032..67142528-chr11:67234580..67238729,6	MCF-7	breast:
14	chr11:67138420..67140492-chr11:67271610..67274474,2	K562	blood:
15	chr11:67088208..67091047-chr11:67138396..67140194,2	MCF-7	breast:

No data

Variant related genes	Relation type
CLCF1	TF binding region
CLCF1	CpG island
ENSG00000172613	chromatin interactions
ENSG00000213402	chromatin interactions
ENSG00000172830	chromatin interactions
ENSG00000110697	chromatin interactions
ENSG00000173120	chromatin interactions
ENSG00000175482	chromatin interactions
ENSG00000173020	chromatin interactions
ENSG00000172663	chromatin interactions

Extended variants
information (count: 217 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:217 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183729786	chr11:67133599-67133600	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs72932730	chr11:67133600-67133601	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs565061836	chr11:67133606-67133607	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373238005	chr11:67133669-67133670	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs188103767	chr11:67133685-67133686	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550532313	chr11:67133695-67133696	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs544941575	chr11:67133718-67133719	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369497841	chr11:67133772-67133773	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs568915059	chr11:67133773-67133774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs536305737	chr11:67133794-67133795	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs118152485	chr11:67133837-67133838	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs543587383	chr11:67133910-67133911	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs567048162	chr11:67133957-67133958	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534154946	chr11:67133967-67133968	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs76708013	chr11:67133973-67133974	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530298904	chr11:67133977-67133978	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs558772793	chr11:67134049-67134050	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs577432671	chr11:67134050-67134051	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538563340	chr11:67134067-67134068	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs577112448	chr11:67134099-67134100	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs141011378	chr11:67134119-67134120	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs575321548	chr11:67134139-67134140	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542735118	chr11:67134187-67134188	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs885764	chr11:67134224-67134225	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs885763	chr11:67134227-67134228	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs181941982	chr11:67134281-67134282	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs572972100	chr11:67134283-67134284	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs144974763	chr11:67134402-67134403	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs200686212	chr11:67134408-67134409	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs565110108	chr11:67134446-67134447	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs532226933	chr11:67134448-67134449	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs35983106	chr11:67134457-67134458	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs550470989	chr11:67134490-67134491	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562529931	chr11:67134495-67134496	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs374092097	chr11:67134536-67134537	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs530079384	chr11:67134550-67134551	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559848521	chr11:67134605-67134606	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566885035	chr11:67134651-67134652	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs550669012	chr11:67134667-67134668	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs552469936	chr11:67134668-67134669	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs571062739	chr11:67134673-67134674	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs538503336	chr11:67134708-67134709	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs527304924	chr11:67134714-67134715	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs575309212	chr11:67134715-67134716	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs542325196	chr11:67134760-67134761	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149088194	chr11:67134761-67134762	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554634393	chr11:67134775-67134776	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs572821354	chr11:67134808-67134809	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540324450	chr11:67134862-67134863	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558426361	chr11:67134863-67134864	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Myelofibrosis	22110671	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
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:438 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67125000-67137600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:67125200-67133600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:67125200-67138200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:67125200-67139200	Weak transcription	Small Intestine	intestine
5	chr11:67125600-67133600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr11:67125600-67136600	Weak transcription	HUVEC	blood vessel
7	chr11:67125800-67133600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:67125800-67133800	Weak transcription	K562	blood
9	chr11:67126000-67133600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:67126000-67133800	Weak transcription	HSMMtube	muscle
11	chr11:67126200-67134200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr11:67127000-67134200	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr11:67128800-67133600	Strong transcription	Muscle Satellite Cultured Cells	--
14	chr11:67129000-67133800	Strong transcription	Osteobl	bone
15	chr11:67130600-67134800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr11:67130800-67133800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:67131200-67137400	Genic enhancers	Primary B cells from peripheral blood	blood
18	chr11:67131200-67139400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr11:67131400-67133600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:67131400-67133800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:67131400-67133800	Strong transcription	HMEC	breast
22	chr11:67131400-67134000	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr11:67131400-67134000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr11:67131400-67134400	Enhancers	Primary hematopoietic stem cells	blood
25	chr11:67131400-67134400	Genic enhancers	A549	lung
26	chr11:67131400-67138800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr11:67131400-67138800	Enhancers	Primary B cells from cord blood	blood
28	chr11:67131600-67133600	Strong transcription	Hela-S3	cervix
29	chr11:67131800-67134000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:67131800-67134000	Genic enhancers	Placenta	Placenta
31	chr11:67132000-67133600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:67132000-67134000	Genic enhancers	Esophagus	oesophagus
33	chr11:67132000-67134200	Genic enhancers	Fetal Stomach	stomach
34	chr11:67132000-67135600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:67132200-67133600	Enhancers	Colonic Mucosa	Colon
36	chr11:67132200-67133600	Strong transcription	Gastric	stomach
37	chr11:67132200-67134000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr11:67132200-67134200	Genic enhancers	Placenta Amnion	Placenta Amnion
39	chr11:67132400-67133600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr11:67132400-67134800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
41	chr11:67132400-67137800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr11:67132400-67139200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:67132600-67133800	Weak transcription	Fetal Thymus	thymus
44	chr11:67132600-67134000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr11:67132600-67134000	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr11:67132600-67134800	Enhancers	Fetal Brain Female	brain
47	chr11:67132600-67136000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr11:67132600-67136000	Enhancers	Ovary	ovary
49	chr11:67132600-67136000	Enhancers	Right Atrium	heart
50	chr11:67132800-67133600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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