Variant report

Variant	nsv897898
Chromosome Location	chr11:71103143-71211654
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2411)
CpG islands
(count:5133)
Chromatin interactive
region (count:122)
LncRNA
region (count:9)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:2411 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71144739-71144757	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:71158261-71158580	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:71161584-71161841	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:71160951-71161088	K562	blood:	n/a	n/a
5	ARID3A	chr11:71159395-71159730	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:71131580-71131838	K562	blood:	n/a	n/a
7	ARID3A	chr11:71159482-71159803	K562	blood:	n/a	n/a
8	ARID3A	chr11:71140352-71140466	HepG2	liver:	n/a	n/a
9	ATF1	chr11:71159298-71159956	K562	blood:	n/a	n/a
10	ATF1	chr11:71113918-71114253	K562	blood:	n/a	n/a
11	ATF1	chr11:71160559-71161136	K562	blood:	n/a	n/a
12	ATF1	chr11:71103739-71103878	K562	blood:	n/a	n/a
13	ATF1	chr11:71121445-71121846	K562	blood:	n/a	n/a
14	ATF2	chr11:71200262-71200721	GM12878	blood:	n/a	n/a
15	ATF2	chr11:71159258-71159690	GM12878	blood:	n/a	n/a
16	ATF2	chr11:71159204-71159548	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr11:71159221-71159697	GM12878	blood:	n/a	n/a
18	ATF2	chr11:71159188-71159850	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr11:71159564-71159941	K562	blood:	n/a	chr11:71159709-71159729
20	BACH1	chr11:71163899-71163977	K562	blood:	n/a	n/a
21	BACH1	chr11:71158921-71159910	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr11:71200324-71200707	GM12878	blood:	n/a	chr11:71200539-71200550
23	BCL11A	chr11:71129809-71130088	GM12878	blood:	n/a	n/a
24	BCL3	chr11:71195577-71196144	GM12878	blood:	n/a	n/a
25	BCL3	chr11:71164062-71164876	A549	lung:	n/a	chr11:71164307-71164320 chr11:71164436-71164445 chr11:71164439-71164448
26	BCL3	chr11:71195121-71195384	GM12878	blood:	n/a	n/a
27	BCL3	chr11:71195483-71196158	GM12878	blood:	n/a	n/a
28	BHLHE40	chr11:71144741-71144795	K562	blood:	n/a	n/a
29	BHLHE40	chr11:71163260-71165062	GM12878	blood:	n/a	n/a
30	BHLHE40	chr11:71131531-71131751	K562	blood:	n/a	n/a
31	BHLHE40	chr11:71158933-71159040	K562	blood:	n/a	chr11:71159014-71159030
32	BHLHE40	chr11:71199259-71199455	K562	blood:	n/a	n/a
33	BHLHE40	chr11:71164289-71165095	K562	blood:	n/a	n/a
34	BHLHE40	chr11:71162977-71163210	K562	blood:	n/a	n/a
35	BHLHE40	chr11:71159271-71160321	K562	blood:	n/a	chr11:71159577-71159593
36	BHLHE40	chr11:71200401-71200653	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:71129894-71130027	GM12878	blood:	n/a	n/a
38	BHLHE40	chr11:71159278-71159865	GM12878	blood:	n/a	chr11:71159577-71159593
39	BHLHE40	chr11:71163833-71164054	K562	blood:	n/a	n/a
40	BHLHE40	chr11:71159967-71160275	HepG2	liver:	n/a	n/a
41	BRCA1	chr11:71113975-71114145	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr11:71121368-71121550	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr11:71158929-71159086	GM12878	blood:	n/a	n/a
44	BRCA1	chr11:71159749-71159968	GM12878	blood:	n/a	n/a
45	BRCA1	chr11:71159358-71160464	Hela-S3	cervix:	n/a	n/a
46	CBX3	chr11:71180502-71180788	K562	blood:	n/a	n/a
47	CBX3	chr11:71164123-71164508	K562	blood:	n/a	n/a
48	CCNT2	chr11:71158894-71160252	K562	blood:	n/a	chr11:71159125-71159134 chr11:71159698-71159707 chr11:71159221-71159230
49	CCNT2	chr11:71163988-71164661	K562	blood:	n/a	chr11:71164233-71164242
50	CCNT2	chr11:71146414-71146869	K562	blood:	n/a	n/a

(count:5133 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71159708-71159758	GM12891	blood:	n/a
2	chr11:71159731-71159781	GM12892	blood:	n/a
3	chr11:71200489-71200539	Hepatocyte	liver:	n/a
4	chr11:71147213-71147263	HRPEpiC	eye:	n/a
5	chr11:71189490-71189540	NB4	blood:	n/a
6	chr11:71159853-71159903	BJ	skin:	n/a
7	chr11:71149985-71150035	ovcar-3	ovarian:	n/a
8	chr11:71135283-71135333	HEK293	kidney:	embryo
9	chr11:71189582-71189632	BJ	skin:	n/a
10	chr11:71159708-71159758	GM12891	blood:	n/a
11	chr11:71159731-71159781	GM12892	blood:	n/a
12	chr11:71200489-71200539	Hepatocyte	liver:	n/a
13	chr11:71147213-71147263	HRPEpiC	eye:	n/a
14	chr11:71189490-71189540	NB4	blood:	n/a
15	chr11:71159853-71159903	BJ	skin:	n/a
16	chr11:71149985-71150035	ovcar-3	ovarian:	n/a
17	chr11:71135283-71135333	HEK293	kidney:	embryo
18	chr11:71189582-71189632	BJ	skin:	n/a
19	chr11:71163907-71163957	HCPEpiC	choroid plexus:	n/a
20	chr11:71164601-71164651	Caco-2	colon:	n/a
21	chr11:71145665-71145715	NHDF-neo	bronchial:	n/a
22	chr11:71202368-71202418	BJ	skin:	n/a
23	chr11:71175039-71175089	ProgFib	skin:	n/a
24	chr11:71163555-71163605	AG04449	skin:	fetal
25	chr11:71155081-71155131	MCF-7	breast:	n/a
26	chr11:71188535-71188585	HL-60	blood:	n/a
27	chr11:71164601-71164651	AG09309	skin:	n/a
28	chr11:71163853-71163903	GM12878	blood:	n/a
29	chr11:71188535-71188585	AG10803	skin:	n/a
30	chr11:71164098-71164148	GM12878	blood:	n/a
31	chr11:71164265-71164315	NB4	blood:	n/a
32	chr11:71193499-71193549	PFSK-1	brain:	n/a
33	chr11:71187890-71187940	PrEC	prostate:	n/a
34	chr11:71117679-71117729	Hela-S3	cervix:	n/a
35	chr11:71189490-71189540	SK-N-SH_RA	brain:	n/a
36	chr11:71164098-71164148	HCT-116	colon:	n/a
37	chr11:71159392-71159442	HCM	heart:	n/a
38	chr11:71155081-71155131	HepG2	liver:	n/a
39	chr11:71196642-71196692	HRCEpiC	kidney:	n/a
40	chr11:71188535-71188585	T-47D	breast:	n/a
41	chr11:71164601-71164651	AG04450	lung:	fetal
42	chr11:71159218-71159268	HPAEpiC	pulmonary alveolar:	n/a
43	chr11:71185649-71185699	HRPEpiC	eye:	n/a
44	chr11:71164283-71164333	NHBE	bronchial:	n/a
45	chr11:71167505-71167555	HEEpiC	esophagus:	n/a
46	chr11:71202794-71202844	AG09319	gingival:	n/a
47	chr11:71159708-71159758	HCM	heart:	n/a
48	chr11:71200489-71200539	AG09319	gingival:	n/a
49	chr11:71202612-71202662	SKMC	muscle:	n/a
50	chr11:71183180-71183230	AG09319	gingival:	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:71122603..71125509-chr11:71135103..71137138,2	K562	blood:
2	chr11:71101438..71103370-chr11:71105330..71106999,2	MCF-7	breast:
3	chr11:71083691..71084429-chr11:71131113..71131671,2	MCF-7	breast:
4	chr11:71118859..71120385-chr11:71125434..71128124,2	MCF-7	breast:
5	chr11:71124869..71127186-chr11:71130587..71132175,2	K562	blood:
6	chr11:71173517..71174399-chr11:71192570..71193116,2	MCF-7	breast:
7	chr11:71164184..71164815-chr17:58469519..58470423,2	MCF-7	breast:
8	chr11:71157940..71161417-chr11:71161465..71165970,9	K562	blood:
9	chr11:71159116..71165503-chr11:71274687..71279227,9	MCF-7	breast:
10	chr11:71166959..71169196-chr11:71181524..71183295,2	MCF-7	breast:
11	chr11:71198500..71200702-chr11:71204795..71207728,3	MCF-7	breast:
12	chr11:71173517..71174399-chr11:71192570..71193116,2	MCF-7	breast:
13	chr11:70651550..70653868-chr11:71190955..71193136,3	MCF-7	breast:
14	chr11:71139536..71142433-chr11:71147657..71149469,2	K562	blood:
15	chr11:71170457..71172341-chr11:71179212..71180985,2	K562	blood:
16	chr11:71182002..71184181-chr11:71185465..71188579,3	K562	blood:
17	chr11:71113585..71115621-chr11:71119782..71121639,2	K562	blood:
18	chr11:71083987..71085496-chr11:71108216..71110305,2	MCF-7	breast:
19	chr11:71124009..71126373-chr11:71135133..71137138,2	K562	blood:
20	chr11:71163622..71164449-chr15:73075829..73076683,2	NB4	blood:
21	chr11:70651651..70652560-chr11:71192231..71193089,5	MCF-7	breast:
22	chr11:71133834..71136520-chr11:71167902..71170100,2	K562	blood:
23	chr11:71144398..71146962-chr11:71155881..71158329,2	K562	blood:
24	chr11:71156500..71159446-chr11:71168763..71171365,2	MCF-7	breast:
25	chr11:71205951..71209347-chr11:71211780..71215363,4	MCF-7	breast:
26	chr11:71186512..71188685-chr11:71191239..71193061,2	K562	blood:
27	chr11:71166687..71169492-chr11:71189793..71191469,2	MCF-7	breast:
28	chr11:71113585..71115621-chr11:71119782..71121639,2	K562	blood:
29	chr11:71154436..71156970-chr11:71198755..71201662,2	MCF-7	breast:
30	chr11:71177769..71179272-chr11:71180854..71183536,2	K562	blood:
31	chr11:71142709..71145080-chr11:71152155..71155719,3	K562	blood:
32	chr11:71197542..71205760-chr11:71207868..71214040,12	MCF-7	breast:
33	chr11:71138911..71140880-chr11:71154532..71157322,2	K562	blood:
34	chr11:71124009..71126373-chr11:71135133..71137138,2	K562	blood:
35	chr11:71146059..71148297-chr11:71153188..71155860,2	K562	blood:
36	chr11:71144398..71146962-chr11:71155881..71158329,2	K562	blood:
37	chr11:71176676..71180057-chr11:71180223..71183173,4	MCF-7	breast:
38	chr11:71209374..71211618-chr11:71213015..71214853,2	K562	blood:
39	chr11:71155911..71156698-chr3:193498553..193499213,2	MCF-7	breast:
40	chr11:70962836..70963538-chr11:71192225..71192780,2	MCF-7	breast:
41	chr11:71137158..71140424-chr11:71155885..71157748,3	K562	blood:
42	chr11:71138540..71142714-chr11:71144455..71147360,4	K562	blood:
43	chr11:71170457..71172341-chr11:71179212..71180985,2	K562	blood:
44	chr11:71164397..71166418-chr11:71178596..71181231,2	K562	blood:
45	chr11:71138911..71140880-chr11:71154532..71157322,2	K562	blood:
46	chr11:71101438..71103370-chr11:71105330..71106999,2	MCF-7	breast:
47	chr11:71122603..71125509-chr11:71135103..71137138,2	K562	blood:
48	chr11:71118859..71120385-chr11:71125434..71128124,2	MCF-7	breast:
49	chr11:70982645..70985292-chr11:71142311..71143975,2	MCF-7	breast:
50	chr11:71197776..71200724-chr11:71214372..71216917,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NADSYN1-1	chr11:71159587-71159931	NONHSAT022678
2	lnc-DHCR7-3	chr11:71134380-71134469	NONHSAT022677
3	lnc-DHCR7-3	chr11:71132847-71132950	NONHSAT022677
4	lnc-NADSYN1-1	chr11:71162736-71164062	NONHSAT022678
5	lnc-NADSYN1-1	chr11:71159586-71159931	XLOC_009199
6	lnc-NADSYN1-1	chr11:71162736-71163182	XLOC_009199
7	lnc-DHCR7-3	chr11:71125206-71125471	NONHSAT022677
8	lnc-NADSYN1-1	chr11:71159720-71159931	ENSG00000254682.1
9	lnc-NADSYN1-1	chr11:71162736-71163203	ENSG00000254682.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6754-3p	chr11:71184592-71184613	MIMAT0027409
hsa-miR-6754-5p	chr11:71184554-71184575	MIMAT0027408

No data

Variant related genes	Relation type
ENSG00000172900	TF binding region
ENSG00000254682	TF binding region
NADSYN1	TF binding region
DHCR7	TF binding region
ENSG00000172900	CpG island
ENSG00000254682	CpG island
NADSYN1	CpG island
DHCR7	CpG island
ENSG00000162105	chromatin interactions
ENSG00000249387	chromatin interactions
ENSG00000172890	chromatin interactions
ENSG00000159322	chromatin interactions
ENSG00000170832	chromatin interactions
ENSG00000204572	chromatin interactions
ENSG00000172893	chromatin interactions
ENSG00000254924	chromatin interactions
ENSG00000254682	chromatin interactions
ENSG00000141371	chromatin interactions
ENSG00000105669	chromatin interactions
ENSG00000196497	chromatin interactions
ENSG00000225362	chromatin interactions
ENSG00000172900	chromatin interactions

Extended variants
information (count: 5264 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5264 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1790315	chr11:71103143-71103144	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529709586	chr11:71103167-71103168	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs181315422	chr11:71103189-71103190	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs541406667	chr11:71103195-71103196	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs560054479	chr11:71103212-71103213	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186162610	chr11:71103228-71103229	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148085058	chr11:71103248-71103249	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116685746	chr11:71103249-71103250	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532514453	chr11:71103270-71103271	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548264970	chr11:71103312-71103313	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75358194	chr11:71103340-71103341	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569231087	chr11:71103345-71103346	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189880707	chr11:71103368-71103369	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116992543	chr11:71103380-71103381	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs116556744	chr11:71103382-71103383	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534449731	chr11:71103403-71103404	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369008582	chr11:71103408-71103409	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558897048	chr11:71103425-71103426	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs577336162	chr11:71103433-71103434	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538030372	chr11:71103482-71103483	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556255758	chr11:71103513-71103514	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10898079	chr11:71103564-71103565	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs541469814	chr11:71103568-71103569	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553303289	chr11:71103582-71103583	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs76108191	chr11:71103583-71103584	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141863104	chr11:71103585-71103586	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533136782	chr11:71103593-71103594	Bivalent Enhancer Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564148860	chr11:71103620-71103621	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531562871	chr11:71103625-71103626	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77782896	chr11:71103649-71103650	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75179314	chr11:71103687-71103688	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530216651	chr11:71103707-71103708	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548607569	chr11:71103712-71103713	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150369739	chr11:71103847-71103848	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116088531	chr11:71103881-71103882	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181518358	chr11:71103906-71103907	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571038111	chr11:71103910-71103911	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111985700	chr11:71103923-71103924	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538445538	chr11:71103926-71103927	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185946963	chr11:71103931-71103932	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567862725	chr11:71103967-71103968	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs535168819	chr11:71103972-71103973	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs138105015	chr11:71103979-71103980	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571685861	chr11:71104052-71104053	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114850159	chr11:71104086-71104087	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs558047323	chr11:71104096-71104097	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576216279	chr11:71104111-71104112	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs117153470	chr11:71104116-71104117	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs561859413	chr11:71104128-71104129	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs530256028	chr11:71104143-71104144	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Lung cancer	18438408	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
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19812545	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3399 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71102400-71103200	Enhancers	Duodenum Mucosa	Duodenum
2	chr11:71102400-71103200	Bivalent Enhancer	HepG2	liver
3	chr11:71102400-71104200	Bivalent Enhancer	Fetal Muscle Leg	muscle
4	chr11:71102600-71104200	Enhancers	Fetal Stomach	stomach
5	chr11:71102600-71104800	Bivalent Enhancer	Fetal Lung	lung
6	chr11:71102800-71114000	Weak transcription	Pancreas	Pancrea
7	chr11:71103000-71103200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr11:71103000-71103200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
9	chr11:71103000-71103200	Bivalent Enhancer	Fetal Heart	heart
10	chr11:71103000-71103400	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr11:71103000-71103400	Flanking Active TSS	HSMM	muscle
12	chr11:71103000-71103400	Flanking Active TSS	HSMMtube	muscle
13	chr11:71103000-71103600	Bivalent Enhancer	Fetal Intestine Small	intestine
14	chr11:71103000-71103600	Enhancers	Fetal Kidney	kidney
15	chr11:71103000-71103800	Enhancers	Ovary	ovary
16	chr11:71103200-71103400	Flanking Active TSS	Duodenum Mucosa	Duodenum
17	chr11:71103200-71104000	Bivalent Enhancer	Placenta	Placenta
18	chr11:71103400-71103600	Enhancers	Gastric	stomach
19	chr11:71103400-71103600	Enhancers	HSMM	muscle
20	chr11:71103400-71103800	Enhancers	HSMMtube	muscle
21	chr11:71103600-71104400	Weak transcription	Fetal Kidney	kidney
22	chr11:71103600-71104400	Weak transcription	Gastric	stomach
23	chr11:71104400-71104600	ZNF genes & repeats	Fetal Kidney	kidney
24	chr11:71104400-71105200	Enhancers	Gastric	stomach
25	chr11:71104600-71105000	Weak transcription	Fetal Kidney	kidney
26	chr11:71104600-71105000	Bivalent Enhancer	HepG2	liver
27	chr11:71104800-71105000	Enhancers	Spleen	Spleen
28	chr11:71105000-71106800	Enhancers	HepG2	liver
29	chr11:71105000-71111400	Weak transcription	Spleen	Spleen
30	chr11:71105600-71106200	Enhancers	Fetal Lung	lung
31	chr11:71105600-71106400	Bivalent Enhancer	Fetal Stomach	stomach
32	chr11:71105800-71106000	Enhancers	Fetal Muscle Trunk	muscle
33	chr11:71105800-71106400	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr11:71106000-71106600	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr11:71106000-71107000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr11:71107200-71107800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr11:71107200-71107800	Enhancers	Dnd41	blood
38	chr11:71107200-71108600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:71107600-71108000	Bivalent Enhancer	Fetal Muscle Leg	muscle
40	chr11:71107600-71109200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr11:71108000-71109000	Enhancers	Fetal Muscle Leg	muscle
42	chr11:71108200-71108400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr11:71108200-71108600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr11:71108600-71109000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:71109000-71109200	Bivalent Enhancer	Right Ventricle	heart
46	chr11:71109000-71110000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr11:71110000-71110600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr11:71110600-71113800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr11:71110800-71111400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:71112400-71113200	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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