Variant report

Variant	esv3436371
Chromosome Location	chr11:47291576-47292674
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:61)
Chromatin interactive
region (count:44)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:649 , 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	chr11:47292332-47292728	K562	blood:	n/a	n/a
2	ARID3A	chr11:47292479-47292675	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:47291463-47291694	K562	blood:	n/a	n/a
4	ARID3A	chr11:47291618-47291798	HepG2	liver:	n/a	n/a
5	ATF1	chr11:47292311-47293033	K562	blood:	n/a	n/a
6	ATF2	chr11:47290448-47291692	GM12878	blood:	n/a	n/a
7	ATF3	chr11:47291613-47291849	K562	blood:	n/a	n/a
8	BACH1	chr11:47289900-47291723	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:47292617-47292624	K562	blood:	n/a	n/a
10	BCL3	chr11:47291332-47291864	GM12878	blood:	n/a	chr11:47291742-47291755 chr11:47291743-47291756
11	BCL3	chr11:47290624-47291707	A549	lung:	n/a	chr11:47291220-47291233 chr11:47291201-47291214 chr11:47291224-47291237 chr11:47291254-47291267
12	BCLAF1	chr11:47291481-47291880	GM12878	blood:	n/a	chr11:47291742-47291755 chr11:47291743-47291756
13	BHLHE40	chr11:47290427-47291914	GM12878	blood:	n/a	chr11:47291200-47291216 chr11:47291737-47291753 chr11:47290951-47290972 chr11:47291629-47291645
14	BHLHE40	chr11:47292430-47292762	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:47290161-47291878	K562	blood:	n/a	chr11:47291200-47291216 chr11:47291737-47291753 chr11:47290951-47290972 chr11:47291629-47291645
16	BHLHE40	chr11:47292150-47292816	K562	blood:	n/a	n/a
17	BHLHE40	chr11:47290710-47291797	A549	lung:	n/a	chr11:47291200-47291216 chr11:47291737-47291753 chr11:47290951-47290972 chr11:47291629-47291645
18	BHLHE40	chr11:47290393-47291853	HepG2	liver:	n/a	chr11:47291200-47291216 chr11:47291737-47291753 chr11:47290951-47290972 chr11:47291629-47291645
19	BRCA1	chr11:47291422-47291695	HepG2	liver:	n/a	n/a
20	BRCA1	chr11:47290472-47291797	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr11:47292264-47292832	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr11:47292313-47292868	K562	blood:	n/a	n/a
23	CBX3	chr11:47290189-47291670	K562	blood:	n/a	n/a
24	CCNT2	chr11:47290451-47291878	K562	blood:	n/a	chr11:47291632-47291641 chr11:47290695-47290704 chr11:47291309-47291318
25	CCNT2	chr11:47292128-47292994	K562	blood:	n/a	chr11:47292348-47292357
26	CEBPB	chr11:47292306-47292676	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:47291371-47291645	Hela-S3	cervix:	n/a	n/a
28	CEBPD	chr11:47291334-47291853	HepG2	liver:	n/a	n/a
29	CEBPD	chr11:47290747-47291948	HepG2	liver:	n/a	n/a
30	CHD1	chr11:47290451-47291813	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD1	chr11:47290267-47291857	GM12878	blood:	n/a	n/a
32	CHD1	chr11:47290345-47292045	IMR90	lung:	n/a	n/a
33	CHD2	chr11:47290290-47291619	K562	blood:	n/a	n/a
34	CHD2	chr11:47290513-47291700	HepG2	liver:	n/a	n/a
35	CHD2	chr11:47290317-47291882	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr11:47290416-47291858	GM12878	blood:	n/a	n/a
37	CREB1	chr11:47290922-47291871	A549	lung:	n/a	n/a
38	CREB1	chr11:47290710-47291834	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr11:47290440-47291887	K562	blood:	n/a	n/a
40	CREB1	chr11:47290277-47292051	HepG2	liver:	n/a	n/a
41	CREB1	chr11:47291412-47291879	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr11:47290427-47291942	GM12878	blood:	n/a	n/a
43	CTCF	chr11:47292600-47292750	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr11:47292560-47292710	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:47292580-47292730	SAEC	small airway:	n/a	n/a
46	CTCF	chr11:47292540-47292690	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr11:47292540-47292690	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr11:47291480-47291630	GM12873	blood:	n/a	n/a
49	CTCF	chr11:47292560-47292710	HAc	cerebellar:	n/a	n/a
50	CTCF	chr11:47292500-47292650	NB4	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:47291846-47291896	SKMC	muscle:	n/a
2	chr11:47291846-47291896	SK-N-SH_RA	brain:	n/a
3	chr11:47291846-47291896	HPAEpiC	pulmonary alveolar:	n/a
4	chr11:47291846-47291896	AG10803	skin:	n/a
5	chr11:47291846-47291896	RPTEC	kidney:	n/a
6	chr11:47291846-47291896	HAEpiC	amniotic membrane:	n/a
7	chr11:47291846-47291896	SK-N-MC	brain:	n/a
8	chr11:47291846-47291896	U87	brain:	n/a
9	chr11:47291846-47291896	NB4	blood:	n/a
10	chr11:47291846-47291896	AG04450	lung:	fetal
11	chr11:47291846-47291896	A549	lung:	n/a
12	chr11:47291846-47291896	LNCaP	prostate:	n/a
13	chr11:47291846-47291896	HNPCEpiC	eye:	n/a
14	chr11:47291846-47291896	BE2_C	brain:	n/a
15	chr11:47291846-47291896	NHDF-neo	bronchial:	n/a
16	chr11:47291846-47291896	PANC-1	pancreas:	n/a
17	chr11:47291846-47291896	GM12891	blood:	n/a
18	chr11:47291846-47291896	CMK	blood:	n/a
19	chr11:47291846-47291896	SAEC	small airway:	n/a
20	chr11:47291846-47291896	HRE	kidney:	n/a
21	chr11:47291846-47291896	ProgFib	skin:	n/a
22	chr11:47291846-47291896	GM06990	blood:	n/a
23	chr11:47291846-47291896	SK-N-SH	brain:	n/a
24	chr11:47291846-47291896	AoSMC	blood vessel:	n/a
25	chr11:47291846-47291896	H1-hESC	embryonic stem cell:	embryo
26	chr11:47291846-47291896	MCF10A-Er-Src	breast:	n/a
27	chr11:47291846-47291896	GM19239	blood:	n/a
28	chr11:47291846-47291896	PrEC	prostate:	n/a
29	chr11:47291846-47291896	HepG2	liver:	n/a
30	chr11:47291846-47291896	NT2-D1	testis:	n/a
31	chr11:47291846-47291896	ovcar-3	ovarian:	n/a
32	chr11:47291846-47291896	Hepatocyte	liver:	n/a
33	chr11:47291846-47291896	HMEC	breast:	n/a
34	chr11:47291846-47291896	MCF-7	breast:	n/a
35	chr11:47291846-47291896	GM12892	blood:	n/a
36	chr11:47291846-47291896	IMR90	lung:	fetal
37	chr11:47291846-47291896	ECC-1	luminal epithelium:	n/a
38	chr11:47291846-47291896	NHBE	bronchial:	n/a
39	chr11:47291846-47291896	HCPEpiC	choroid plexus:	n/a
40	chr11:47291846-47291896	HUVEC	blood vessel:	n/a
41	chr11:47291846-47291896	Caco-2	colon:	n/a
42	chr11:47291846-47291896	HEK293	kidney:	embryo
43	chr11:47291846-47291896	HRCEpiC	kidney:	n/a
44	chr11:47291846-47291896	K562	blood:	n/a
45	chr11:47291846-47291896	HIPEpiC	eye:	n/a
46	chr11:47291846-47291896	Hela-S3	cervix:	n/a
47	chr11:47291846-47291896	HL-60	blood:	n/a
48	chr11:47291846-47291896	T-47D	breast:	n/a
49	chr11:47291846-47291896	HCF	heart:	n/a
50	chr11:47291846-47291896	Jurkat	blood:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:46867608..46869466-chr11:47290892..47293495,3	MCF-7	breast:
2	chr11:47196068..47203526-chr11:47288943..47293025,13	MCF-7	breast:
3	chr11:47194502..47201735-chr11:47289181..47294156,14	K562	blood:
4	chr11:47270208..47270736-chr11:47291056..47291685,2	K562	blood:
5	chr11:47290951..47293321-chr11:47445782..47448016,2	K562	blood:
6	chr11:47291432..47292021-chr8:22462067..22462755,2	HCT-116	colon:
7	chr11:47263865..47272320-chr11:47288426..47294726,14	MCF-7	breast:
8	chr11:47291353..47293892-chr11:47343454..47345274,2	K562	blood:
9	chr11:47277979..47283267-chr11:47289057..47293509,9	K562	blood:
10	chr11:47279843..47284326-chr11:47288675..47293634,16	MCF-7	breast:
11	chr11:47292062..47293120-chr11:47376381..47377320,5	MCF-7	breast:
12	chr11:47268938..47272778-chr11:47288986..47293565,7	MCF-7	breast:
13	chr1:16173725..16174683-chr11:47291183..47291944,2	Hela-S3	cervix:
14	chr11:47290254..47293439-chr11:47374246..47378968,6	MCF-7	breast:
15	chr11:47267881..47272421-chr11:47288787..47294481,12	K562	blood:
16	chr11:47292004..47292682-chr11:47376539..47377229,2	MCF-7	breast:
17	chr11:47289567..47294786-chr11:47310778..47315538,7	MCF-7	breast:
18	chr11:47291467..47292011-chr20:43991703..43992344,2	Hela-S3	cervix:
19	chr11:47234552..47236757-chr11:47290593..47292750,2	MCF-7	breast:
20	chr11:47195231..47200543-chr11:47288487..47293127,12	MCF-7	breast:
21	chr11:47195816..47200318-chr11:47289518..47292814,8	K562	blood:
22	chr11:47290799..47291583-chr8:120867901..120868534,2	Hela-S3	cervix:
23	chr11:47291167..47293193-chr11:47345602..47348128,2	K562	blood:
24	chr11:47290429..47293321-chr11:47445782..47448351,3	K562	blood:
25	chr11:47290389..47294105-chr11:47428413..47432863,5	MCF-7	breast:
26	chr11:47290760..47291689-chr16:67694026..67694999,2	Hela-S3	cervix:
27	chr11:47206281..47210029-chr11:47290997..47292963,3	K562	blood:
28	chr11:47235321..47238553-chr11:47290387..47292949,4	K562	blood:
29	chr11:47277336..47279783-chr11:47290576..47292976,4	MCF-7	breast:
30	chr11:47289554..47292260-chr11:47397624..47400665,3	K562	blood:
31	chr11:47268303..47273264-chr11:47289525..47294481,12	K562	blood:
32	chr1:23885363..23886146-chr11:47291031..47291703,2	Hela-S3	cervix:
33	chr11:47292359..47292934-chr16:87551044..87551823,2	Hela-S3	cervix:
34	chr11:47264797..47267629-chr11:47289343..47292246,3	K562	blood:
35	chr11:47205837..47210171-chr11:47289770..47293955,7	MCF-7	breast:
36	chr11:47190024..47192945-chr11:47289457..47292109,2	MCF-7	breast:
37	chr11:47235395..47237642-chr11:47289103..47291887,3	K562	blood:
38	chr11:46401780..46403457-chr11:47290200..47292891,2	MCF-7	breast:
39	chr11:47207085..47210178-chr11:47288214..47292056,4	MCF-7	breast:
40	chr11:47292200..47292859-chr11:47429308..47429854,2	MCF-7	breast:
41	chr11:47290550..47292544-chr11:47348957..47351454,2	MCF-7	breast:
42	chr11:47291588..47294118-chr11:47313687..47316370,3	K562	blood:
43	chr11:47204494..47207545-chr11:47289955..47292546,3	K562	blood:
44	chr11:47235151..47238129-chr11:47286989..47291992,5	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACP2-2	chr11:47292630-47292692	ENSG00000256746.1
2	lnc-ACP2-2	chr11:47292208-47292531	ENSG00000256746.1
3	lnc-ACP2-2	chr11:47292630-47292692	ENSG00000256746.1
4	lnc-ACP2-2	chr11:47292217-47292531	ENSG00000256746.1

No data

Variant related genes	Relation type
MADD	TF binding region
MADD	CpG island
ENSG00000165912	chromatin interactions
ENSG00000254806	chromatin interactions
ENSG00000255197	chromatin interactions
ENSG00000149182	chromatin interactions
ENSG00000117318	chromatin interactions
ENSG00000270060	chromatin interactions
ENSG00000247675	chromatin interactions
ENSG00000165916	chromatin interactions
ENSG00000136982	chromatin interactions
ENSG00000102981	chromatin interactions
ENSG00000165915	chromatin interactions
ENSG00000134575	chromatin interactions
ENSG00000025434	chromatin interactions
ENSG00000110514	chromatin interactions
ENSG00000102977	chromatin interactions
ENSG00000134574	chromatin interactions
ENSG00000175216	chromatin interactions
ENSG00000179743	chromatin interactions
ENSG00000066336	chromatin interactions
ENSG00000204070	chromatin interactions
ENSG00000065526	chromatin interactions
ENSG00000158941	chromatin interactions
ENSG00000134571	chromatin interactions
ENSG00000110492	chromatin interactions

Extended variants
information (count: 35 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:35 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535108276	chr11:47291596-47291597	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
2	rs555436410	chr11:47291610-47291611	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
3	rs45489595	chr11:47291635-47291636	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	24 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs534724632	chr11:47291650-47291651	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
5	rs567720927	chr11:47291656-47291657	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
6	rs558022299	chr11:47291660-47291661	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
7	rs536659716	chr11:47291666-47291667	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
8	rs578230364	chr11:47291682-47291683	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	24 gene(s)	Overlapped CNVs	n/a
9	rs184636256	chr11:47291701-47291702	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	22 gene(s)	Overlapped CNVs	n/a
10	rs551975480	chr11:47291725-47291726	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
11	rs75960102	chr11:47291774-47291775	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
12	rs180879014	chr11:47291817-47291818	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
13	rs12800862	chr11:47291944-47291945	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	21 gene(s)	Overlapped CNVs	n/a
14	rs12800869	chr11:47291958-47291959	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
15	rs542703915	chr11:47291964-47291965	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	19 gene(s)	Overlapped CNVs	n/a
16	rs189006909	chr11:47292127-47292128	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
17	rs372058927	chr11:47292183-47292184	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
18	rs573825537	chr11:47292213-47292214	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
19	rs528539850	chr11:47292215-47292216	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
20	rs570279354	chr11:47292219-47292220	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
21	rs1055510	chr11:47292237-47292238	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs563901209	chr11:47292241-47292242	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	15 gene(s)	Overlapped CNVs	n/a
23	rs532992022	chr11:47292304-47292305	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
24	rs146103812	chr11:47292308-47292309	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
25	rs569660698	chr11:47292327-47292328	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
26	rs528848366	chr11:47292353-47292354	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
27	rs548660316	chr11:47292396-47292397	Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
28	rs79093948	chr11:47292411-47292412	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
29	rs539300372	chr11:47292452-47292453	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
30	rs547678148	chr11:47292454-47292455	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
31	rs148743147	chr11:47292522-47292523	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a
32	rs142180904	chr11:47292583-47292584	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs151191463	chr11:47292584-47292585	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs1133880	chr11:47292655-47292656	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs557685582	chr11:47292659-47292660	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	14 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47290400-47292400	Active TSS	Right Atrium	heart
2	chr11:47290400-47292800	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr11:47290600-47291800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr11:47290600-47292200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:47290600-47292200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:47290600-47292200	Active TSS	Colonic Mucosa	Colon
7	chr11:47290600-47292200	Active TSS	Duodenum Mucosa	Duodenum
8	chr11:47290600-47292200	Active TSS	Fetal Brain Male	brain
9	chr11:47290600-47292200	Active TSS	Fetal Intestine Small	intestine
10	chr11:47290600-47292200	Active TSS	Psoas Muscle	Psoas
11	chr11:47290600-47292200	Active TSS	K562	blood
12	chr11:47290600-47292400	Active TSS	H1 Cell Line	embryonic stem cell
13	chr11:47290600-47292400	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr11:47290600-47292400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:47290600-47292400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
16	chr11:47290600-47292400	Active TSS	Esophagus	oesophagus
17	chr11:47290600-47292400	Active TSS	Fetal Kidney	kidney
18	chr11:47290600-47292400	Active TSS	Sigmoid Colon	Sigmoid Colon
19	chr11:47290600-47292600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:47290600-47292600	Active TSS	Ovary	ovary
21	chr11:47290600-47292800	Active TSS	H9 Cell Line	embryonic stem cell
22	chr11:47290600-47292800	Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr11:47290600-47292800	Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr11:47290600-47294000	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr11:47290800-47292200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr11:47290800-47292200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr11:47290800-47292200	Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr11:47290800-47292200	Active TSS	Brain Anterior Caudate	brain
29	chr11:47290800-47292200	Active TSS	Placenta Amnion	Placenta Amnion
30	chr11:47290800-47292200	Active TSS	Thymus	Thymus
31	chr11:47290800-47292400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr11:47290800-47292400	Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr11:47290800-47292400	Active TSS	Brain Inferior Temporal Lobe	brain
34	chr11:47290800-47292400	Active TSS	Brain Substantia Nigra	brain
35	chr11:47290800-47292400	Active TSS	Duodenum Smooth Muscle	Duodenum
36	chr11:47290800-47292400	Active TSS	Gastric	stomach
37	chr11:47290800-47292400	Active TSS	Spleen	Spleen
38	chr11:47290800-47292600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr11:47290800-47292600	Active TSS	Aorta	Aorta
40	chr11:47290800-47292600	Active TSS	Small Intestine	intestine
41	chr11:47291000-47291800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:47291000-47291800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr11:47291000-47292000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:47291000-47292000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:47291000-47292200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr11:47291000-47292200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:47291000-47292200	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr11:47291000-47292200	Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr11:47291000-47292200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr11:47291000-47292200	Active TSS	Primary monocytes fromperipheralblood	blood

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