Variant report

Variant	esv3364090
Chromosome Location	chr11:119598267-119601315
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:119600051-119600221	HepG2	liver:	n/a	n/a
2	ATF2	chr11:119599846-119600105	GM12878	blood:	n/a	chr11:119599947-119599961
3	BACH1	chr11:119599960-119600558	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:119598253-119598534	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr11:119599682-119600369	GM12878	blood:	n/a	chr11:119599789-119599802 chr11:119599840-119599849 chr11:119599841-119599854 chr11:119599835-119599848 chr11:119600078-119600091 chr11:119600002-119600015
6	BHLHE40	chr11:119599364-119600490	GM12878	blood:	n/a	chr11:119600069-119600085 chr11:119599385-119599401 chr11:119599847-119599863
7	BHLHE40	chr11:119598579-119598839	GM12878	blood:	n/a	chr11:119598642-119598658
8	BHLHE40	chr11:119599872-119600308	K562	blood:	n/a	chr11:119600069-119600085
9	BHLHE40	chr11:119599815-119600370	HepG2	liver:	n/a	chr11:119600069-119600085 chr11:119599847-119599863
10	BHLHE40	chr11:119599078-119599083	GM12878	blood:	n/a	n/a
11	CCNT2	chr11:119599650-119600370	K562	blood:	n/a	chr11:119599964-119599973
12	CEBPB	chr11:119599828-119600079	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr11:119599882-119599934	HepG2	liver:	n/a	n/a
14	CEBPD	chr11:119599724-119600027	HepG2	liver:	n/a	n/a
15	CHD1	chr11:119599753-119600451	GM12878	blood:	n/a	chr11:119599801-119599811 chr11:119599940-119599950
16	CHD1	chr11:119598747-119599215	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr11:119599536-119599640	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr11:119598392-119599326	GM12878	blood:	n/a	n/a
19	CHD1	chr11:119599910-119600116	H1-hESC	embryonic stem cell:	n/a	chr11:119599940-119599950
20	CHD1	chr11:119599403-119601462	IMR90	lung:	n/a	chr11:119599801-119599811 chr11:119599940-119599950
21	CHD2	chr11:119599897-119600284	H1-hESC	embryonic stem cell:	n/a	chr11:119599940-119599950
22	CHD2	chr11:119600216-119600272	HepG2	liver:	n/a	n/a
23	CHD2	chr11:119598692-119598823	HepG2	liver:	n/a	n/a
24	CHD2	chr11:119599067-119599252	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr11:119600029-119600511	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr11:119600179-119600205	K562	blood:	n/a	n/a
27	CHD2	chr11:119599877-119600386	GM12878	blood:	n/a	chr11:119599940-119599950
28	CHD2	chr11:119599889-119599969	HepG2	liver:	n/a	chr11:119599940-119599950
29	CHD2	chr11:119600654-119601131	GM12878	blood:	n/a	n/a
30	CHD2	chr11:119598318-119598430	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr11:119598596-119598870	GM12878	blood:	n/a	n/a
32	CREB1	chr11:119599640-119600298	A549	lung:	n/a	n/a
33	CREB1	chr11:119599408-119600447	HepG2	liver:	n/a	n/a
34	CREB1	chr11:119599757-119600370	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr11:119599706-119600467	GM12878	blood:	n/a	n/a
36	CREB1	chr11:119599787-119600213	ECC-1	luminal epithelium:	n/a	n/a
37	CTCF	chr11:119600780-119600930	HBMEC	blood vessel:	n/a	chr11:119600881-119600890
38	CTCF	chr11:119598581-119598725	ProgFib	skin:	n/a	n/a
39	CTCF	chr11:119600120-119600270	GM12801	blood:	n/a	chr11:119600191-119600207 chr11:119600185-119600206
40	CTCF	chr11:119600120-119600270	HVMF	connective:	n/a	chr11:119600191-119600207 chr11:119600185-119600206
41	CTCF	chr11:119600040-119600190	A549	lung:	n/a	n/a
42	CTCF	chr11:119600140-119600290	GM12878	blood:	n/a	chr11:119600191-119600207 chr11:119600185-119600206
43	CTCF	chr11:119598588-119598741	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:119600360-119600510	A549	lung:	n/a	n/a
45	CTCF	chr11:119598544-119598813	GM19238	blood:	n/a	chr11:119598571-119598584
46	CTCF	chr11:119600140-119600290	RPTEC	kidney:	n/a	chr11:119600191-119600207 chr11:119600185-119600206
47	CTCF	chr11:119598580-119598730	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:119600820-119600970	AG04450	lung:	n/a	chr11:119600881-119600890
49	CTCF	chr11:119600100-119600250	BE2_C	brain:	n/a	chr11:119600191-119600207 chr11:119600185-119600206
50	CTCF	chr11:119600140-119600290	HMEC	breast:	n/a	chr11:119600191-119600207 chr11:119600185-119600206

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:119598909-119598959	HRPEpiC	eye:	n/a
2	chr11:119600292-119600342	GM06990	blood:	n/a
3	chr11:119600595-119600645	GM12892	blood:	n/a
4	chr11:119599620-119599670	HRCEpiC	kidney:	n/a
5	chr11:119599427-119599477	PFSK-1	brain:	n/a
6	chr11:119599427-119599477	HRE	kidney:	n/a
7	chr11:119599176-119599226	SAEC	small airway:	n/a
8	chr11:119599620-119599670	NH-A	brain:	n/a
9	chr11:119600292-119600342	PrEC	prostate:	n/a
10	chr11:119599617-119599667	AG04450	lung:	fetal
11	chr11:119599622-119599672	PFSK-1	brain:	n/a
12	chr11:119599620-119599670	H1-hESC	embryonic stem cell:	embryo
13	chr11:119599176-119599226	K562	blood:	n/a
14	chr11:119599176-119599226	HRPEpiC	eye:	n/a
15	chr11:119599617-119599667	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:119600595-119600645	HL-60	blood:	n/a
17	chr11:119599176-119599226	NT2-D1	testis:	n/a
18	chr11:119599176-119599226	HUVEC	blood vessel:	n/a
19	chr11:119599425-119599475	PANC-1	pancreas:	n/a
20	chr11:119600292-119600342	NHDF-neo	bronchial:	n/a
21	chr11:119598257-119598307	SK-N-SH_RA	brain:	n/a
22	chr11:119598725-119598775	ProgFib	skin:	n/a
23	chr11:119598497-119598547	NT2-D1	testis:	n/a
24	chr11:119599620-119599670	AG09309	skin:	n/a
25	chr11:119600595-119600645	NH-A	brain:	n/a
26	chr11:119599622-119599672	PrEC	prostate:	n/a
27	chr11:119599176-119599226	HCPEpiC	choroid plexus:	n/a
28	chr11:119598725-119598775	NH-A	brain:	n/a
29	chr11:119598725-119598775	HUVEC	blood vessel:	n/a
30	chr11:119598497-119598547	HCPEpiC	choroid plexus:	n/a
31	chr11:119599427-119599477	AG04449	skin:	fetal
32	chr11:119599620-119599670	HEK293	kidney:	embryo
33	chr11:119598909-119598959	PANC-1	pancreas:	n/a
34	chr11:119599176-119599226	GM12891	blood:	n/a
35	chr11:119598909-119598959	HEEpiC	esophagus:	n/a
36	chr11:119599620-119599670	HEEpiC	esophagus:	n/a
37	chr11:119599427-119599477	GM19239	blood:	n/a
38	chr11:119598497-119598547	K562	blood:	n/a
39	chr11:119598497-119598547	HUVEC	blood vessel:	n/a
40	chr11:119598497-119598547	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:119600292-119600342	HCM	heart:	n/a
42	chr11:119598497-119598547	SKMC	muscle:	n/a
43	chr11:119600090-119600140	AG09319	gingival:	n/a
44	chr11:119599617-119599667	RPTEC	kidney:	n/a
45	chr11:119600292-119600342	A549	lung:	n/a
46	chr11:119600292-119600342	U87	brain:	n/a
47	chr11:119598497-119598547	Hepatocyte	liver:	n/a
48	chr11:119599617-119599667	IMR90	lung:	fetal
49	chr11:119598257-119598307	HEK293	kidney:	embryo
50	chr11:119598909-119598959	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:119564818..119565650-chr11:119598208..119598847,2	MCF-7	breast:
2	chr11:119557449..119558968-chr11:119599043..119600568,2	MCF-7	breast:
3	chr11:119599752..119600308-chr21:34914463..34915203,2	NB4	blood:
4	chr11:119598280..119601010-chr11:119990751..119994590,4	MCF-7	breast:
5	chr11:119593045..119595193-chr11:119597284..119598893,2	K562	blood:
6	chr11:119600585..119602314-chr11:119925639..119927228,2	MCF-7	breast:
7	chr11:119537222..119537812-chr11:119598187..119599149,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2523D13.1.1-1	chr11:119600281-119600516	XLOC_009299
2	lnc-CTD-2523D13.1.1-1	chr11:119600510-119600516	XLOC_009299
3	lnc-CTD-2523D13.1.1-1	chr11:119600361-119600563	XLOC_009299
4	lnc-CTD-2523D13.1.1-1	chr11:119600356-119600563	XLOC_009299
5	lnc-CTD-2523D13.1.1-1	chr11:119600109-119600184	XLOC_009299

Variant related genes	Relation type
PVRL1	TF binding region
ENSG00000254854	TF binding region
PVRL1	CpG island
ENSG00000254854	CpG island
ENSG00000159140	chromatin interactions
ENSG00000159131	chromatin interactions
ENSG00000137699	chromatin interactions
ENSG00000110400	chromatin interactions
DICER1	miRNA target sites
SUV420H2	miRNA target sites

Extended variants
information (count: 103 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:103 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370933894	chr11:119598319-119598320	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs188649891	chr11:119598331-119598332	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552859212	chr11:119598376-119598377	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs36088567	chr11:119598404-119598405	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs535751914	chr11:119598419-119598420	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577558698	chr11:119598442-119598443	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs544900288	chr11:119598446-119598447	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs563172504	chr11:119598501-119598502	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530716373	chr11:119598526-119598527	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs542771299	chr11:119598557-119598558	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs561405817	chr11:119598571-119598572	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs2048246	chr11:119598653-119598654	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576993312	chr11:119598687-119598688	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546974700	chr11:119598726-119598727	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs571657834	chr11:119598727-119598728	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs3829260	chr11:119598729-119598730	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs181762112	chr11:119598743-119598744	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs569382244	chr11:119598846-119598847	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs529427162	chr11:119598858-119598859	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs564652891	chr11:119598871-119598872	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs77630867	chr11:119598971-119598972	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs186021028	chr11:119598976-119598977	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs190761597	chr11:119598984-119598985	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs552597520	chr11:119599009-119599010	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs577197872	chr11:119599063-119599064	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs538581430	chr11:119599072-119599073	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs557186830	chr11:119599098-119599099	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs575370590	chr11:119599111-119599112	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs542760632	chr11:119599181-119599182	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs561234624	chr11:119599199-119599200	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs199772536	chr11:119599212-119599213	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs540724557	chr11:119599267-119599268	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs565306004	chr11:119599269-119599270	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs532532784	chr11:119599277-119599278	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs376092672	chr11:119599297-119599298	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs551309974	chr11:119599316-119599317	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs563153149	chr11:119599317-119599318	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs181960402	chr11:119599337-119599338	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs548806010	chr11:119599500-119599501	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs566951383	chr11:119599530-119599531	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs138907015	chr11:119599641-119599642	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs546275711	chr11:119599677-119599678	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs570926917	chr11:119599756-119599757	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs538220313	chr11:119599779-119599780	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs556978215	chr11:119599833-119599834	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs372461320	chr11:119599839-119599840	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs536145336	chr11:119599864-119599865	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs554795502	chr11:119599972-119599973	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs573051500	chr11:119600029-119600030	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs146307925	chr11:119600049-119600050	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	17142309	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119596000-119598400	Flanking Active TSS	Brain Angular Gyrus	brain
2	chr11:119596400-119598400	Flanking Active TSS	Duodenum Mucosa	Duodenum
3	chr11:119596600-119598800	Flanking Active TSS	Brain Hippocampus Middle	brain
4	chr11:119596600-119600400	Active TSS	Esophagus	oesophagus
5	chr11:119597000-119598600	Flanking Active TSS	Fetal Brain Male	brain
6	chr11:119597000-119599200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
7	chr11:119597000-119599200	Flanking Active TSS	GM12878-XiMat	blood
8	chr11:119597200-119598800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
9	chr11:119597200-119599200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr11:119597200-119599200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr11:119597200-119599200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
12	chr11:119597200-119599600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr11:119597200-119600400	Active TSS	H1 Cell Line	embryonic stem cell
14	chr11:119597200-119600400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:119597200-119600400	Active TSS	iPS-15b Cell Line	embryonic stem cell
16	chr11:119597200-119600800	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr11:119597200-119601000	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr11:119597200-119601000	Active TSS	H9 Cell Line	embryonic stem cell
19	chr11:119597400-119598400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr11:119597400-119598400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr11:119597400-119598400	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
22	chr11:119597400-119598800	Flanking Active TSS	Stomach Smooth Muscle	stomach
23	chr11:119597400-119599200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
24	chr11:119597400-119600600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr11:119597400-119600800	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr11:119597400-119601000	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr11:119597400-119601000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:119597600-119598400	Flanking Bivalent TSS/Enh	Placenta	Placenta
29	chr11:119597600-119598400	Enhancers	Placenta Amnion	Placenta Amnion
30	chr11:119597600-119598400	Flanking Active TSS	Rectal Smooth Muscle	rectum
31	chr11:119597600-119598600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:119597600-119598600	Flanking Active TSS	Fetal Intestine Large	intestine
33	chr11:119597600-119598600	Flanking Active TSS	NH-A	brain
34	chr11:119597600-119598800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
35	chr11:119597600-119598800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
36	chr11:119597600-119598800	Flanking Active TSS	Right Ventricle	heart
37	chr11:119597600-119598800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
38	chr11:119597600-119599000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr11:119597600-119599000	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
40	chr11:119597600-119599200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:119597600-119599400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr11:119597600-119599400	Flanking Active TSS	Adipose Nuclei	Adipose
43	chr11:119597600-119599400	Flanking Active TSS	Colonic Mucosa	Colon
44	chr11:119597600-119601000	Active TSS	Fetal Kidney	kidney
45	chr11:119597800-119598400	Flanking Active TSS	HepG2	liver
46	chr11:119597800-119598400	Flanking Bivalent TSS/Enh	Osteobl	bone
47	chr11:119597800-119598600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr11:119597800-119598600	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr11:119597800-119598600	Flanking Active TSS	Stomach Mucosa	stomach
50	chr11:119597800-119598600	Flanking Active TSS	NHLF	lung

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