Variant report

Variant	esv3440498
Chromosome Location	chr11:76090729-76093277
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:631)
CpG islands
(count:613)
Chromatin interactive
region (count:13)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:631 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:76092205-76092374	K562	blood:	n/a	n/a
2	ARID3A	chr11:76091313-76091471	K562	blood:	n/a	n/a
3	ARID3A	chr11:76092133-76093013	HepG2	liver:	n/a	n/a
4	ATF2	chr11:76091959-76092619	GM12878	blood:	n/a	n/a
5	ATF2	chr11:76092255-76092701	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr11:76092028-76092400	K562	blood:	n/a	chr11:76092308-76092317
7	BACH1	chr11:76091059-76091205	K562	blood:	n/a	n/a
8	BCL3	chr11:76092028-76092745	A549	lung:	n/a	chr11:76092312-76092321 chr11:76092111-76092120 chr11:76092219-76092228 chr11:76092114-76092123 chr11:76092117-76092126 chr11:76092313-76092326 chr11:76092268-76092281 chr11:76092112-76092125 chr11:76092111-76092124
9	BCLAF1	chr11:76091884-76092675	GM12878	blood:	n/a	chr11:76092312-76092321 chr11:76092111-76092120 chr11:76092219-76092228 chr11:76092114-76092123 chr11:76092117-76092126 chr11:76092313-76092326 chr11:76092268-76092281 chr11:76092112-76092125 chr11:76092111-76092124
10	BHLHE40	chr11:76091208-76091787	K562	blood:	n/a	n/a
11	BHLHE40	chr11:76092040-76092757	K562	blood:	n/a	chr11:76092112-76092128 chr11:76092307-76092323 chr11:76092115-76092131
12	BHLHE40	chr11:76091267-76092698	GM12878	blood:	n/a	chr11:76092112-76092128 chr11:76092307-76092323 chr11:76092115-76092131
13	BRCA1	chr11:76092285-76092577	HepG2	liver:	n/a	n/a
14	BRCA1	chr11:76092070-76092692	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr11:76091900-76092664	K562	blood:	n/a	n/a
16	CBX3	chr11:76090952-76091674	K562	blood:	n/a	n/a
17	CCNT2	chr11:76091562-76092618	K562	blood:	n/a	chr11:76092220-76092229
18	CEBPB	chr11:76092033-76092784	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr11:76092018-76092654	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:76092338-76092637	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr11:76092025-76092624	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr11:76092302-76092682	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:76092337-76092875	A549	lung:	n/a	n/a
24	CEBPB	chr11:76092291-76092659	K562	blood:	n/a	n/a
25	CEBPB	chr11:76092288-76092645	HepG2	liver:	n/a	n/a
26	CEBPD	chr11:76092032-76092405	HepG2	liver:	n/a	n/a
27	CHD1	chr11:76092029-76092246	GM12878	blood:	n/a	chr11:76092132-76092142
28	CHD2	chr11:76091425-76092215	K562	blood:	n/a	chr11:76092132-76092142
29	CHD2	chr11:76091626-76092584	HepG2	liver:	n/a	chr11:76092132-76092142
30	CHD2	chr11:76091154-76092616	Hela-S3	cervix:	n/a	chr11:76092132-76092142
31	CHD2	chr11:76091841-76092607	GM12878	blood:	n/a	chr11:76092132-76092142
32	CHD2	chr11:76092065-76092594	H1-hESC	embryonic stem cell:	n/a	chr11:76092132-76092142
33	CREB1	chr11:76091975-76092620	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr11:76091483-76092738	A549	lung:	n/a	n/a
35	CTCF	chr11:76092060-76092210	GM12869	blood:	n/a	n/a
36	CTCF	chr11:76092060-76092210	GM06990	blood:	n/a	n/a
37	CTCF	chr11:76092060-76092210	Caco-2	colon:	n/a	n/a
38	CTCF	chr11:76092100-76092250	GM12871	blood:	n/a	n/a
39	CTCF	chr11:76092040-76092190	BJ	skin:	n/a	n/a
40	CTCF	chr11:76091996-76092250	GM19238	blood:	n/a	n/a
41	CTCF	chr11:76091993-76092241	MCF-7	breast:	n/a	n/a
42	CTCF	chr11:76092120-76092270	K562	blood:	n/a	n/a
43	CTCF	chr11:76091540-76091690	GM12871	blood:	n/a	n/a
44	CTCF	chr11:76092060-76092210	GM12866	blood:	n/a	n/a
45	CTCF	chr11:76092000-76092150	GM12869	blood:	n/a	n/a
46	CTCF	chr11:76092020-76092170	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr11:76092013-76092255	GM12891	blood:	n/a	n/a
48	CTCF	chr11:76091980-76092130	GM12866	blood:	n/a	n/a
49	CTCF	chr11:76092005-76092234	MCF-7	breast:	n/a	n/a
50	CTCF	chr11:76092020-76092170	NHDF-neo	bronchial:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76092535-76092585	T-47D	breast:	n/a
2	chr11:76092535-76092585	AG09309	skin:	n/a
3	chr11:76091836-76091886	AG10803	skin:	n/a
4	chr11:76092535-76092585	T-47D	breast:	n/a
5	chr11:76092535-76092585	AG09309	skin:	n/a
6	chr11:76091836-76091886	AG10803	skin:	n/a
7	chr11:76091884-76091934	PrEC	prostate:	n/a
8	chr11:76093056-76093106	HRPEpiC	eye:	n/a
9	chr11:76091674-76091724	HCT-116	colon:	n/a
10	chr11:76091674-76091724	GM12878	blood:	n/a
11	chr11:76092429-76092479	PFSK-1	brain:	n/a
12	chr11:76091836-76091886	K562	blood:	n/a
13	chr11:76091836-76091886	HCT-116	colon:	n/a
14	chr11:76091884-76091934	ProgFib	skin:	n/a
15	chr11:76091881-76091931	NH-A	brain:	n/a
16	chr11:76091881-76091931	GM19239	blood:	n/a
17	chr11:76091884-76091934	HMEC	breast:	n/a
18	chr11:76092056-76092106	A549	lung:	n/a
19	chr11:76093056-76093106	H1-hESC	embryonic stem cell:	embryo
20	chr11:76092535-76092585	K562	blood:	n/a
21	chr11:76093056-76093106	MCF10A-Er-Src	breast:	n/a
22	chr11:76092429-76092479	GM12891	blood:	n/a
23	chr11:76091836-76091886	HCPEpiC	choroid plexus:	n/a
24	chr11:76092056-76092106	RPTEC	kidney:	n/a
25	chr11:76092056-76092106	HUVEC	blood vessel:	n/a
26	chr11:76092535-76092585	IMR90	lung:	fetal
27	chr11:76091836-76091886	HPAEpiC	pulmonary alveolar:	n/a
28	chr11:76092435-76092485	NH-A	brain:	n/a
29	chr11:76091674-76091724	HRPEpiC	eye:	n/a
30	chr11:76091884-76091934	AoSMC	blood vessel:	n/a
31	chr11:76092311-76092361	HEK293	kidney:	embryo
32	chr11:76092535-76092585	HIPEpiC	eye:	n/a
33	chr11:76091836-76091886	A549	lung:	n/a
34	chr11:76092311-76092361	AG09309	skin:	n/a
35	chr11:76092311-76092361	GM06990	blood:	n/a
36	chr11:76092435-76092485	Jurkat	blood:	n/a
37	chr11:76092311-76092361	ovcar-3	ovarian:	n/a
38	chr11:76091881-76091931	AG09309	skin:	n/a
39	chr11:76091884-76091934	NT2-D1	testis:	n/a
40	chr11:76092429-76092479	SK-N-SH_RA	brain:	n/a
41	chr11:76092535-76092585	GM12891	blood:	n/a
42	chr11:76091881-76091931	PFSK-1	brain:	n/a
43	chr11:76092535-76092585	H1-hESC	embryonic stem cell:	embryo
44	chr11:76091881-76091931	H1-hESC	embryonic stem cell:	embryo
45	chr11:76093056-76093106	HEEpiC	esophagus:	n/a
46	chr11:76092056-76092106	GM12891	blood:	n/a
47	chr11:76092056-76092106	HCT-116	colon:	n/a
48	chr11:76091674-76091724	GM12891	blood:	n/a
49	chr11:76091674-76091724	SKMC	muscle:	n/a
50	chr11:76092056-76092106	PFSK-1	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:75919700..75922037-chr11:76092044..76093720,2	MCF-7	breast:
2	chr11:76091836..76092375-chr5:137514081..137514947,2	Hela-S3	cervix:
3	chr11:76092719..76095251-chr11:76155129..76157307,4	K562	blood:
4	chr11:76090234..76093573-chr11:76154824..76158196,8	MCF-7	breast:
5	chr1:70686774..70687532-chr11:76091229..76092168,2	HCT-116	colon:
6	chr11:76071533..76073218-chr11:76090981..76092790,2	K562	blood:
7	chr11:76091642..76092465-chr11:76155561..76156248,2	Hela-S3	cervix:
8	chr11:76089758..76095735-chr11:76153234..76157826,15	MCF-7	breast:
9	chr11:76090615..76095251-chr11:76152894..76157527,10	K562	blood:
10	chr11:76079303..76082514-chr11:76090617..76092781,5	K562	blood:
11	chr11:76089990..76094695-chr11:76100568..76104844,7	MCF-7	breast:
12	chr11:76091181..76093702-chr11:76114020..76116665,2	K562	blood:
13	chr11:76092137..76092838-chr3:9834644..9835181,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-111M22.2.1-1	chr11:76092357-76092418	NONHSAT023165

No data

Variant related genes	Relation type
ENSG00000179240	TF binding region
PRKRIR	TF binding region
ENSG00000179240	CpG island
PRKRIR	CpG island
ENSG00000201756	chromatin interactions
ENSG00000112984	chromatin interactions
ENSG00000116754	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000272301	chromatin interactions
ENSG00000112983	chromatin interactions
ENSG00000085741	chromatin interactions
ENSG00000250151	chromatin interactions
ENSG00000171148	chromatin interactions
ENSG00000271757	chromatin interactions
ENSG00000158636	chromatin interactions
ENSG00000241553	chromatin interactions
ENSG00000137492	chromatin interactions

Extended variants
information (count: 82 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:82 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535256253	chr11:76090782-76090783	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs148433135	chr11:76090799-76090800	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs143586030	chr11:76090818-76090819	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs534356618	chr11:76090836-76090837	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs7948288	chr11:76090843-76090844	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs577943332	chr11:76090913-76090914	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs537768212	chr11:76090938-76090939	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs557334050	chr11:76090957-76090958	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs147193133	chr11:76090965-76090966	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs542851107	chr11:76091093-76091094	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs559928158	chr11:76091103-76091104	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs573359783	chr11:76091127-76091128	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs545446185	chr11:76091233-76091234	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs565304047	chr11:76091235-76091236	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs139759147	chr11:76091289-76091290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs186096442	chr11:76091303-76091304	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs191813895	chr11:76091304-76091305	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs9645695	chr11:76091320-76091321	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs372987789	chr11:76091335-76091336	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs563391286	chr11:76091343-76091344	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs369230565	chr11:76091368-76091369	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs529131367	chr11:76091412-76091413	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs182439062	chr11:76091418-76091419	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs542238107	chr11:76091435-76091436	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs77019124	chr11:76091451-76091452	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs565469494	chr11:76091480-76091481	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs78757925	chr11:76091488-76091489	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs373772025	chr11:76091520-76091521	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs372964641	chr11:76091592-76091593	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs112052875	chr11:76091604-76091605	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs113365962	chr11:76091605-76091606	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs11607475	chr11:76091640-76091641	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs570925126	chr11:76091719-76091720	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs536601228	chr11:76091759-76091760	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs200581079	chr11:76091847-76091848	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs201541896	chr11:76091854-76091855	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs557635816	chr11:76091961-76091962	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs574243690	chr11:76091977-76091978	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs536884905	chr11:76092003-76092004	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs553583429	chr11:76092071-76092072	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
41	rs557523834	chr11:76092077-76092078	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
42	rs575797647	chr11:76092098-76092099	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
43	rs545536145	chr11:76092127-76092128	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
44	rs12804786	chr11:76092150-76092151	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs559055759	chr11:76092173-76092174	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
46	rs575599631	chr11:76092317-76092318	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
47	rs78586198	chr11:76092337-76092338	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
48	rs12788555	chr11:76092361-76092362	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs558006982	chr11:76092367-76092368	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
50	rs542438777	chr11:76092383-76092384	Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Melanoma	18172304	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
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76067600-76091000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:76082400-76091000	Weak transcription	Aorta	Aorta
3	chr11:76085600-76090800	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr11:76085800-76091000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr11:76087200-76091000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr11:76087600-76091000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
7	chr11:76089200-76091000	Enhancers	Primary T cells fromperipheralblood	blood
8	chr11:76089200-76091000	Enhancers	Ovary	ovary
9	chr11:76089600-76090800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:76089600-76091000	Enhancers	Fetal Thymus	thymus
11	chr11:76089600-76091200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:76089600-76091200	Flanking Active TSS	Dnd41	blood
13	chr11:76089800-76090800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr11:76089800-76091000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr11:76089800-76091000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr11:76089800-76091000	Enhancers	Left Ventricle	heart
17	chr11:76090000-76090800	Enhancers	Fetal Intestine Large	intestine
18	chr11:76090000-76090800	Enhancers	Fetal Intestine Small	intestine
19	chr11:76090000-76090800	Enhancers	Placenta	Placenta
20	chr11:76090000-76090800	Enhancers	Sigmoid Colon	Sigmoid Colon
21	chr11:76090000-76091000	Enhancers	Primary B cells from peripheral blood	blood
22	chr11:76090000-76091000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr11:76090000-76091000	Enhancers	Small Intestine	intestine
24	chr11:76090200-76090800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr11:76090200-76090800	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr11:76090200-76090800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr11:76090200-76090800	Weak transcription	Fetal Muscle Trunk	muscle
28	chr11:76090200-76090800	Flanking Active TSS	HMEC	breast
29	chr11:76090200-76091000	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr11:76090200-76091000	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr11:76090200-76091000	Enhancers	Primary T killer memory cells from peripheral blood	blood
32	chr11:76090200-76091200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
33	chr11:76090200-76091200	Flanking Active TSS	Fetal Brain Female	brain
34	chr11:76090200-76091200	Flanking Active TSS	Hela-S3	cervix
35	chr11:76090200-76091400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr11:76090200-76091600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:76090200-76091600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:76090200-76093400	Active TSS	HUES48 Cell Line	embryonic stem cell
39	chr11:76090400-76090800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:76090400-76090800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr11:76090400-76090800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr11:76090400-76090800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:76090400-76090800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:76090400-76090800	Flanking Active TSS	Brain Anterior Caudate	brain
45	chr11:76090400-76090800	Flanking Active TSS	Brain Germinal Matrix	brain
46	chr11:76090400-76090800	Flanking Active TSS	Brain Hippocampus Middle	brain
47	chr11:76090400-76090800	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
48	chr11:76090400-76090800	Enhancers	Fetal Muscle Leg	muscle
49	chr11:76090400-76090800	Flanking Active TSS	Right Ventricle	heart
50	chr11:76090400-76090800	Flanking Active TSS	A549	lung

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