Variant report

Variant	nsv898355
Chromosome Location	chr11:104730322-104897843
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1543)
CpG islands
(count:2015)
Chromatin interactive
region (count:6)
LncRNA
region (count:79)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104874651-104875141	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:104855516-104855852	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:104865690-104866388	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:104817646-104818039	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:104838864-104839516	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:104814360-104814630	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:104814897-104815170	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:104870648-104871335	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:104827306-104827643	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:104838331-104838340	HepG2	liver:	n/a	n/a
11	ATF2	chr11:104768528-104769091	GM12878	blood:	n/a	n/a
12	BATF	chr11:104753441-104753681	GM12878	blood:	n/a	n/a
13	BATF	chr11:104778610-104778889	GM12878	blood:	n/a	chr11:104778766-104778777
14	BCL3	chr11:104761233-104761516	GM12878	blood:	n/a	n/a
15	BCL3	chr11:104761069-104761606	GM12878	blood:	n/a	n/a
16	BHLHE40	chr11:104865796-104866149	HepG2	liver:	n/a	n/a
17	BHLHE40	chr11:104871511-104871851	GM12878	blood:	n/a	n/a
18	BHLHE40	chr11:104752556-104752567	GM12878	blood:	n/a	n/a
19	BHLHE40	chr11:104838963-104839549	GM12878	blood:	n/a	n/a
20	BHLHE40	chr11:104747879-104748167	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:104840122-104840539	HepG2	liver:	n/a	n/a
22	BHLHE40	chr11:104885004-104885054	GM12878	blood:	n/a	n/a
23	BRCA1	chr11:104838120-104838701	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr11:104839210-104839268	HepG2	liver:	n/a	n/a
25	BRCA1	chr11:104839197-104839617	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr11:104817608-104818133	HCT-116	colon:	n/a	n/a
27	CBX3	chr11:104843718-104843957	HCT-116	colon:	n/a	n/a
28	CBX3	chr11:104871491-104872014	HCT-116	colon:	n/a	n/a
29	CEBPB	chr11:104827178-104827731	Hela-S3	cervix:	n/a	chr11:104827468-104827479
30	CEBPB	chr11:104827300-104827618	K562	blood:	n/a	chr11:104827468-104827479
31	CEBPB	chr11:104814346-104815203	HepG2	liver:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
32	CEBPB	chr11:104827256-104827636	MCF-7	breast:	n/a	chr11:104827468-104827479
33	CEBPB	chr11:104827235-104827625	A549	lung:	n/a	chr11:104827468-104827479
34	CEBPB	chr11:104855556-104855922	HepG2	liver:	n/a	chr11:104855728-104855739
35	CEBPB	chr11:104840644-104840840	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:104814408-104814668	Hela-S3	cervix:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
37	CEBPB	chr11:104789758-104789850	A549	lung:	n/a	n/a
38	CEBPB	chr11:104874694-104875210	HepG2	liver:	n/a	chr11:104874861-104874874 chr11:104874861-104874872 chr11:104875128-104875139 chr11:104874862-104874873
39	CEBPB	chr11:104827272-104827658	H1-hESC	embryonic stem cell:	n/a	chr11:104827468-104827479
40	CEBPB	chr11:104827282-104827644	IMR90	lung:	n/a	chr11:104827468-104827479
41	CEBPB	chr11:104827216-104827712	HCT-116	colon:	n/a	chr11:104827468-104827479
42	CEBPB	chr11:104827256-104827673	HepG2	liver:	n/a	chr11:104827468-104827479
43	CEBPB	chr11:104763488-104764195	IMR90	lung:	n/a	n/a
44	CEBPB	chr11:104780576-104780776	HepG2	liver:	n/a	chr11:104780651-104780664 chr11:104780651-104780662
45	CEBPB	chr11:104839019-104839634	HCT-116	colon:	n/a	n/a
46	CEBPB	chr11:104839133-104839577	MCF-7	breast:	n/a	n/a
47	CEBPB	chr11:104827299-104827601	HepG2	liver:	n/a	chr11:104827468-104827479
48	CEBPB	chr11:104839183-104839555	HepG2	liver:	n/a	n/a
49	CEBPB	chr11:104839125-104839510	ECC-1	luminal epithelium:	n/a	n/a
50	CEBPB	chr11:104827194-104827678	MCF-7	breast:	n/a	chr11:104827468-104827479

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104769411-104769461	HCM	heart:	n/a
2	chr11:104789052-104789102	SKMC	muscle:	n/a
3	chr11:104769411-104769461	HCM	heart:	n/a
4	chr11:104789052-104789102	SKMC	muscle:	n/a
5	chr11:104789337-104789387	GM19239	blood:	n/a
6	chr11:104762787-104762837	AG10803	skin:	n/a
7	chr11:104778374-104778424	AG04450	lung:	fetal
8	chr11:104839343-104839393	K562	blood:	n/a
9	chr11:104887307-104887357	HNPCEpiC	eye:	n/a
10	chr11:104780712-104780762	HRCEpiC	kidney:	n/a
11	chr11:104780795-104780845	SKMC	muscle:	n/a
12	chr11:104865951-104866001	SK-N-MC	brain:	n/a
13	chr11:104828060-104828110	AG10803	skin:	n/a
14	chr11:104894216-104894266	HCF	heart:	n/a
15	chr11:104827790-104827840	K562	blood:	n/a
16	chr11:104840183-104840233	LNCaP	prostate:	n/a
17	chr11:104817914-104817964	SK-N-SH	brain:	n/a
18	chr11:104769543-104769593	GM06990	blood:	n/a
19	chr11:104778374-104778424	HEK293	kidney:	embryo
20	chr11:104827238-104827288	NH-A	brain:	n/a
21	chr11:104789052-104789102	K562	blood:	n/a
22	chr11:104839349-104839399	HAEpiC	amniotic membrane:	n/a
23	chr11:104769087-104769137	IMR90	lung:	fetal
24	chr11:104762787-104762837	GM12891	blood:	n/a
25	chr11:104817914-104817964	NHBE	bronchial:	n/a
26	chr11:104879683-104879733	GM06990	blood:	n/a
27	chr11:104894216-104894266	Caco-2	colon:	n/a
28	chr11:104896587-104896637	MCF-7	breast:	n/a
29	chr11:104839349-104839399	K562	blood:	n/a
30	chr11:104876060-104876110	HNPCEpiC	eye:	n/a
31	chr11:104894514-104894564	K562	blood:	n/a
32	chr11:104894216-104894266	PFSK-1	brain:	n/a
33	chr11:104865951-104866001	RPTEC	kidney:	n/a
34	chr11:104827790-104827840	BJ	skin:	n/a
35	chr11:104758766-104758816	AG09309	skin:	n/a
36	chr11:104865951-104866001	AoSMC	blood vessel:	n/a
37	chr11:104839281-104839331	IMR90	lung:	fetal
38	chr11:104896587-104896637	PFSK-1	brain:	n/a
39	chr11:104865951-104866001	HRCEpiC	kidney:	n/a
40	chr11:104839281-104839331	HAEpiC	amniotic membrane:	n/a
41	chr11:104789052-104789102	NHBE	bronchial:	n/a
42	chr11:104778374-104778424	GM12892	blood:	n/a
43	chr11:104814390-104814440	LNCaP	prostate:	n/a
44	chr11:104896587-104896637	AG04449	skin:	fetal
45	chr11:104879683-104879733	A549	lung:	n/a
46	chr11:104887371-104887421	GM12891	blood:	n/a
47	chr11:104896587-104896637	BJ	skin:	n/a
48	chr11:104769543-104769593	HCPEpiC	choroid plexus:	n/a
49	chr11:104781259-104781309	HCF	heart:	n/a
50	chr11:104769543-104769593	HMEC	breast:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:104894289..104896311-chr11:104901290..104902903,2	K562	blood:
2	chr1:151511788..151512678-chr11:104838165..104838828,2	Hela-S3	cervix:
3	chr11:104838939..104839536-chr7:127228342..127228894,2	Hela-S3	cervix:
4	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:
5	chr11:62420312..62421283-chr11:104838756..104839379,2	Hela-S3	cervix:
6	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:

(count:79 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-2	chr11:104769135-104769397	NR_034068
2	lnc-CASP12-2	chr11:104767944-104768195	NR_034061
3	lnc-CASP12-3	chr11:104774118-104774437	NONHSAT023942
4	lnc-CASP12-2	chr11:104769135-104769397	NR_034065
5	lnc-CASP12-2	chr11:104767944-104768195	NR_034067
6	lnc-CASP12-3	chr11:104772277-104772386	NONHSAT023942
7	lnc-CASP4-1	chr11:104813600-104813700	NONHSAT023946
8	lnc-CASP12-3	chr11:104779562-104779735	NR_034078
9	lnc-CASP12-2	chr11:104763058-104763230	NR_034064
10	lnc-CASP12-3	chr11:104779415-104779735	NONHSAT023944
11	lnc-CASP12-3	chr11:104788840-104788902	NR_034079
12	lnc-CASP12-2	chr11:104757923-104758028	NR_034061
13	lnc-CASP12-2	chr11:104763058-104763230	NR_034067
14	lnc-CASP12-3	chr11:104774118-104774278	NR_034078
15	lnc-CASP12-2	chr11:104757923-104758028	NR_034070
16	lnc-CASP12-3	chr11:104776175-104776284	NR_034079
17	lnc-CASP12-2	chr11:104761897-104762131	NR_034070
18	lnc-CASP12-2	chr11:104767944-104768195	NR_034063
19	lnc-CASP12-3	chr11:104789658-104789800	NONHSAT023943
20	lnc-CASP12-2	chr11:104757418-104757539	NR_034063
21	lnc-CASP12-2	chr11:104757418-104757539	NR_034065
22	lnc-CASP12-2	chr11:104763058-104763230	NR_034061
23	lnc-CASP12-2	chr11:104767944-104768195	NR_034064
24	lnc-CASP12-3	chr11:104772276-104772386	NR_034078
25	lnc-CASP12-2	chr11:104763624-104763718	NR_034070
26	lnc-CASP12-2	chr11:104761101-104761250	NR_034067
27	lnc-CASP12-2	chr11:104763058-104763230	NR_034065
28	lnc-CASP12-2	chr11:104769135-104769397	NR_034063
29	lnc-CASP12-2	chr11:104769135-104769397	NR_034067
30	lnc-CASP12-2	chr11:104761097-104761250	NR_034066
31	lnc-CASP12-2	chr11:104767944-104768195	NR_034070
32	lnc-CASP12-3	chr11:104776175-104776284	NR_034078
33	lnc-CASP12-2	chr11:104757923-104758028	NR_034065
34	lnc-CASP12-2	chr11:104769135-104769397	NR_034064
35	lnc-CASP12-3	chr11:104774118-104774278	NR_034079
36	lnc-CASP12-2	chr11:104763058-104763230	NR_034068
37	lnc-CASP12-3	chr11:104788840-104788870	NONHSAT023944
38	lnc-CASP4-1	chr11:104815475-104815578	NONHSAT023946
39	lnc-CASP12-2	chr11:104763058-104763230	NR_034066
40	lnc-CASP5-2	chr11:104896235-104896327	NONHSAT023949
41	lnc-CASP12-2	chr11:104769135-104769397	NR_034071
42	lnc-CASP12-2	chr11:104763058-104763230	NR_034071
43	lnc-CASP12-2	chr11:104757923-104758028	NR_034066
44	lnc-CASP12-2	chr11:104761897-104762131	NR_034061
45	lnc-CASP12-3	chr11:104772276-104772383	NR_034079
46	lnc-CASP12-2	chr11:104757418-104757539	NR_034070
47	lnc-CASP12-3	chr11:104779562-104779735	NONHSAT023943
48	lnc-CASP12-3	chr11:104788840-104788902	NR_034078
49	lnc-CASP12-2	chr11:104769135-104769397	NR_034061
50	lnc-CASP12-3	chr11:104776175-104776284	NONHSAT023943

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CASP4	hsa-miR-26b-5p	chr11:104822249-104822272
2	CASP4	hsa-miR-26b-5p	chr11:104822275-104822295

Variant related genes	Relation type
CASP5	TF binding region
CASP4	TF binding region
ENSG00000235505	TF binding region
CASP12	TF binding region
ENSG00000254569	TF binding region
CASP5	CpG island
CASP4	CpG island
ENSG00000235505	CpG island
CASP12	CpG island
ENSG00000254569	CpG island
ENSG00000185085	chromatin interactions
ENSG00000004059	chromatin interactions

Extended variants
information (count: 5490 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5490 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6591101	chr11:104730322-104730323	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185617337	chr11:104730346-104730347	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs116139943	chr11:104730393-104730394	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs78308455	chr11:104730399-104730400	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs142191156	chr11:104730403-104730404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116908560	chr11:104730421-104730422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150410234	chr11:104730444-104730445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533443798	chr11:104730528-104730529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75867171	chr11:104730556-104730557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs77208279	chr11:104730557-104730558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372987763	chr11:104730571-104730572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11272525	chr11:104730573-104730574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs386757099	chr11:104730574-104730575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs56161920	chr11:104730575-104730576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142476407	chr11:104730576-104730577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs150984500	chr11:104730577-104730578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs55813600	chr11:104730580-104730581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs529159792	chr11:104730611-104730612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548817064	chr11:104730631-104730632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs367733786	chr11:104730632-104730633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375247783	chr11:104730638-104730639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs190012102	chr11:104730704-104730705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs481367	chr11:104730739-104730740	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs200373747	chr11:104730749-104730750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551143530	chr11:104730782-104730783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs151192795	chr11:104730807-104730808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181048748	chr11:104730845-104730846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116898087	chr11:104730876-104730877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567208830	chr11:104730895-104730896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369032028	chr11:104730947-104730948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563911559	chr11:104730956-104730957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs140629152	chr11:104730970-104730971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs186040123	chr11:104731005-104731006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191987863	chr11:104731041-104731042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183865612	chr11:104731049-104731050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs187589047	chr11:104731093-104731094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376725794	chr11:104731199-104731200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144268151	chr11:104731200-104731201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs501149	chr11:104737405-104737406	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs563098218	chr11:104737500-104737501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558267971	chr11:104737541-104737542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs477995	chr11:104737590-104737591	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs531471978	chr11:104737598-104737599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566519618	chr11:104737599-104737600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543456586	chr11:104737670-104737671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563331861	chr11:104737689-104737690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs573605424	chr11:104737707-104737708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542465047	chr11:104737745-104737746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146847494	chr11:104737822-104737823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528254897	chr11:104737851-104737852	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2091 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104728000-104731000	Enhancers	Dnd41	blood
2	chr11:104728800-104730600	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr11:104729000-104730400	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr11:104729000-104730600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr11:104729000-104730800	Enhancers	Primary B cells from peripheral blood	blood
6	chr11:104729400-104730400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr11:104729400-104730400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:104729400-104730600	Enhancers	Primary T cells from cord blood	blood
9	chr11:104729800-104730400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr11:104729800-104730400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr11:104730000-104730400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr11:104730000-104730600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr11:104730000-104730600	Enhancers	Fetal Thymus	thymus
14	chr11:104730000-104730800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr11:104730000-104731200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:104730200-104730400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr11:104730200-104730400	Flanking Active TSS	Primary B cells from cord blood	blood
18	chr11:104730200-104730400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr11:104730200-104730600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr11:104730200-104730600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr11:104730400-104730600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr11:104730400-104731000	Enhancers	Primary B cells from cord blood	blood
23	chr11:104730400-104731000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr11:104737400-104737800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr11:104737600-104738200	Enhancers	NHEK	skin
26	chr11:104737600-104738400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:104741200-104742000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr11:104741200-104742000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:104741200-104742000	Enhancers	Primary B cells from peripheral blood	blood
30	chr11:104741200-104742200	Enhancers	Dnd41	blood
31	chr11:104741400-104741800	Enhancers	GM12878-XiMat	blood
32	chr11:104741400-104742000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr11:104741400-104742400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr11:104741600-104742000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr11:104741600-104742200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr11:104742000-104746600	Weak transcription	Primary B cells from peripheral blood	blood
37	chr11:104742200-104746000	Weak transcription	Dnd41	blood
38	chr11:104744000-104744200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr11:104744000-104744200	ZNF genes & repeats	Aorta	Aorta
40	chr11:104744200-104761000	Weak transcription	Aorta	Aorta
41	chr11:104744600-104744800	Enhancers	Primary T killer memory cells from peripheral blood	blood
42	chr11:104744800-104746000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr11:104745400-104749200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr11:104745600-104768600	Weak transcription	Left Ventricle	heart
45	chr11:104746000-104746400	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr11:104746000-104746800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr11:104746000-104747000	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr11:104746000-104747000	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr11:104746000-104747000	Enhancers	Dnd41	blood
50	chr11:104746000-104747600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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