Variant report

Variant	nsv832255
Chromosome Location	chr11:104674918-104846961
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1197)
CpG islands
(count:1467)
Chromatin interactive
region (count:8)
LncRNA
region (count:77)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1197 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104827306-104827643	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:104838864-104839516	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:104814360-104814630	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:104716018-104716072	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:104814897-104815170	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:104838331-104838340	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:104817646-104818039	HepG2	liver:	n/a	n/a
8	ATF2	chr11:104768528-104769091	GM12878	blood:	n/a	n/a
9	BATF	chr11:104690270-104690487	GM12878	blood:	n/a	n/a
10	BATF	chr11:104753441-104753681	GM12878	blood:	n/a	n/a
11	BATF	chr11:104778610-104778889	GM12878	blood:	n/a	chr11:104778766-104778777
12	BCL3	chr11:104761233-104761516	GM12878	blood:	n/a	n/a
13	BCL3	chr11:104761069-104761606	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:104838963-104839549	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:104840122-104840539	HepG2	liver:	n/a	n/a
16	BHLHE40	chr11:104747879-104748167	GM12878	blood:	n/a	n/a
17	BHLHE40	chr11:104752556-104752567	GM12878	blood:	n/a	n/a
18	BRCA1	chr11:104838120-104838701	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr11:104839210-104839268	HepG2	liver:	n/a	n/a
20	BRCA1	chr11:104839197-104839617	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr11:104817608-104818133	HCT-116	colon:	n/a	n/a
22	CBX3	chr11:104843718-104843957	HCT-116	colon:	n/a	n/a
23	CEBPB	chr11:104701685-104701820	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:104839158-104839571	MCF-7	breast:	n/a	n/a
25	CEBPB	chr11:104839183-104839555	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:104827200-104827640	ECC-1	luminal epithelium:	n/a	chr11:104827468-104827479
27	CEBPB	chr11:104827256-104827636	MCF-7	breast:	n/a	chr11:104827468-104827479
28	CEBPB	chr11:104827192-104827735	A549	lung:	n/a	chr11:104827468-104827479
29	CEBPB	chr11:104827300-104827618	K562	blood:	n/a	chr11:104827468-104827479
30	CEBPB	chr11:104789758-104789850	A549	lung:	n/a	n/a
31	CEBPB	chr11:104827282-104827644	IMR90	lung:	n/a	chr11:104827468-104827479
32	CEBPB	chr11:104827278-104827652	HepG2	liver:	n/a	chr11:104827468-104827479
33	CEBPB	chr11:104827256-104827673	HepG2	liver:	n/a	chr11:104827468-104827479
34	CEBPB	chr11:104839133-104839577	MCF-7	breast:	n/a	n/a
35	CEBPB	chr11:104827214-104827637	ECC-1	luminal epithelium:	n/a	chr11:104827468-104827479
36	CEBPB	chr11:104827278-104827653	A549	lung:	n/a	chr11:104827468-104827479
37	CEBPB	chr11:104827292-104827597	HepG2	liver:	n/a	chr11:104827468-104827479
38	CEBPB	chr11:104838936-104839546	A549	lung:	n/a	n/a
39	CEBPB	chr11:104712797-104713014	Hela-S3	cervix:	n/a	chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
40	CEBPB	chr11:104712733-104713048	K562	blood:	n/a	chr11:104712750-104712758 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
41	CEBPB	chr11:104712712-104713052	HepG2	liver:	n/a	chr11:104712750-104712758 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
42	CEBPB	chr11:104839264-104839441	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:104712719-104713038	A549	lung:	n/a	chr11:104712750-104712758 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
44	CEBPB	chr11:104827235-104827625	A549	lung:	n/a	chr11:104827468-104827479
45	CEBPB	chr11:104712754-104712944	H1-hESC	embryonic stem cell:	n/a	chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
46	CEBPB	chr11:104814346-104815203	HepG2	liver:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
47	CEBPB	chr11:104839090-104839625	A549	lung:	n/a	n/a
48	CEBPB	chr11:104784953-104785176	HepG2	liver:	n/a	chr11:104785067-104785078
49	CEBPB	chr11:104840644-104840840	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:104839203-104839562	ECC-1	luminal epithelium:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104839343-104839393	HCF	heart:	n/a
2	chr11:104840183-104840233	AG04449	skin:	fetal
3	chr11:104769411-104769461	CMK	blood:	n/a
4	chr11:104839343-104839393	HCF	heart:	n/a
5	chr11:104840183-104840233	AG04449	skin:	fetal
6	chr11:104769411-104769461	CMK	blood:	n/a
7	chr11:104758766-104758816	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:104778374-104778424	RPTEC	kidney:	n/a
9	chr11:104780712-104780762	SK-N-MC	brain:	n/a
10	chr11:104814390-104814440	PANC-1	pancreas:	n/a
11	chr11:104839281-104839331	ECC-1	luminal epithelium:	n/a
12	chr11:104839074-104839124	SK-N-SH_RA	brain:	n/a
13	chr11:104769087-104769137	AG09319	gingival:	n/a
14	chr11:104839858-104839908	ECC-1	luminal epithelium:	n/a
15	chr11:104789052-104789102	Hela-S3	cervix:	n/a
16	chr11:104758259-104758309	HIPEpiC	eye:	n/a
17	chr11:104827238-104827288	A549	lung:	n/a
18	chr11:104780795-104780845	PANC-1	pancreas:	n/a
19	chr11:104769543-104769593	AG09319	gingival:	n/a
20	chr11:104839074-104839124	NH-A	brain:	n/a
21	chr11:104769411-104769461	K562	blood:	n/a
22	chr11:104814390-104814440	ECC-1	luminal epithelium:	n/a
23	chr11:104827790-104827840	SK-N-SH	brain:	n/a
24	chr11:104827790-104827840	BE2_C	brain:	n/a
25	chr11:104840183-104840233	HCT-116	colon:	n/a
26	chr11:104839349-104839399	K562	blood:	n/a
27	chr11:104840183-104840233	HRCEpiC	kidney:	n/a
28	chr11:104758766-104758816	NHDF-neo	bronchial:	n/a
29	chr11:104781259-104781309	RPTEC	kidney:	n/a
30	chr11:104839074-104839124	HIPEpiC	eye:	n/a
31	chr11:104769543-104769593	HAEpiC	amniotic membrane:	n/a
32	chr11:104780712-104780762	SK-N-SH_RA	brain:	n/a
33	chr11:104780795-104780845	AG04450	lung:	fetal
34	chr11:104839858-104839908	H1-hESC	embryonic stem cell:	embryo
35	chr11:104762787-104762837	AG10803	skin:	n/a
36	chr11:104839281-104839331	AG04449	skin:	fetal
37	chr11:104769087-104769137	PANC-1	pancreas:	n/a
38	chr11:104827238-104827288	HCF	heart:	n/a
39	chr11:104780795-104780845	GM12892	blood:	n/a
40	chr11:104839349-104839399	AG09319	gingival:	n/a
41	chr11:104758766-104758816	NH-A	brain:	n/a
42	chr11:104839349-104839399	HAEpiC	amniotic membrane:	n/a
43	chr11:104817914-104817964	HMEC	breast:	n/a
44	chr11:104781259-104781309	AG09319	gingival:	n/a
45	chr11:104758766-104758816	BJ	skin:	n/a
46	chr11:104789337-104789387	Jurkat	blood:	n/a
47	chr11:104758766-104758816	K562	blood:	n/a
48	chr11:104839343-104839393	GM12892	blood:	n/a
49	chr11:104789052-104789102	PFSK-1	brain:	n/a
50	chr11:104762787-104762837	HPAEpiC	pulmonary alveolar:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:104715402..104717976-chr11:104720645..104722717,2	K562	blood:
2	chr11:104838939..104839536-chr7:127228342..127228894,2	Hela-S3	cervix:
3	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:
4	chr11:62420312..62421283-chr11:104838756..104839379,2	Hela-S3	cervix:
5	chr1:151511788..151512678-chr11:104838165..104838828,2	Hela-S3	cervix:
6	chr11:104715402..104717976-chr11:104720645..104722717,2	K562	blood:
7	chr11:104702644..104703296-chr17:57832337..57832880,2	MCF-7	breast:
8	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:

(count:77 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-2	chr11:104761097-104761250	NR_034071
2	lnc-CASP12-3	chr11:104776175-104776284	NONHSAT023943
3	lnc-CASP12-2	chr11:104761097-104761250	NR_034061
4	lnc-CASP12-2	chr11:104761897-104762131	NR_034070
5	lnc-CASP4-1	chr11:104813600-104813700	NONHSAT023946
6	lnc-CASP12-3	chr11:104779415-104779735	NONHSAT023944
7	lnc-CASP12-2	chr11:104769135-104769397	NR_034067
8	lnc-CASP12-2	chr11:104769135-104769397	NR_034063
9	lnc-CASP12-2	chr11:104763058-104763230	NR_034070
10	lnc-CASP12-2	chr11:104761097-104761250	NR_034070
11	lnc-CASP12-2	chr11:104761101-104761250	NR_034067
12	lnc-CASP12-2	chr11:104769135-104769397	NR_034061
13	lnc-CASP12-3	chr11:104776175-104776284	NR_034078
14	lnc-CASP12-2	chr11:104763058-104763230	NR_034065
15	lnc-CASP4-1	chr11:104815475-104815578	NONHSAT023946
16	lnc-CASP12-2	chr11:104769135-104769397	NR_034070
17	lnc-CASP12-2	chr11:104761101-104761250	NR_034068
18	lnc-CASP12-2	chr11:104761101-104761250	NR_034063
19	lnc-CASP12-2	chr11:104757418-104757539	NR_034066
20	lnc-CASP12-3	chr11:104779562-104779735	NR_034078
21	lnc-CASP12-2	chr11:104761101-104761250	NR_034064
22	lnc-CASP12-3	chr11:104774118-104774278	NONHSAT023943
23	lnc-CASP12-2	chr11:104767944-104768195	NR_034061
24	lnc-CASP12-2	chr11:104763058-104763230	NR_034071
25	lnc-CASP12-2	chr11:104769135-104769397	NR_034068
26	lnc-CASP12-2	chr11:104761097-104761250	NR_034065
27	lnc-CASP12-2	chr11:104757418-104757539	NR_034067
28	lnc-CASP12-2	chr11:104769135-104769397	NR_034065
29	lnc-CASP12-2	chr11:104761925-104762131	NR_034064
30	lnc-CASP12-2	chr11:104767944-104768195	NR_034070
31	lnc-CASP4-1	chr11:104817351-104817919	NONHSAT023947
32	lnc-CASP12-3	chr11:104788840-104788870	NONHSAT023944
33	lnc-CASP12-2	chr11:104763624-104763718	NR_034070
34	lnc-CASP12-2	chr11:104757923-104758028	NR_034061
35	lnc-CASP12-3	chr11:104772277-104772386	NONHSAT023942
36	lnc-CASP12-2	chr11:104763058-104763230	NR_034066
37	lnc-CASP12-2	chr11:104769135-104769397	NR_034066
38	lnc-CASP12-3	chr11:104772276-104772386	NR_034078
39	lnc-CASP12-3	chr11:104774118-104774278	NR_034078
40	lnc-CASP12-2	chr11:104757418-104757539	NR_034071
41	lnc-CASP12-3	chr11:104779562-104779735	NR_034079
42	lnc-CASP12-2	chr11:104757923-104758028	NR_034065
43	lnc-CASP12-2	chr11:104767944-104768195	NR_034064
44	lnc-CASP12-2	chr11:104761097-104761250	NR_034066
45	lnc-CASP12-2	chr11:104769135-104769397	NR_034071
46	lnc-CASP12-2	chr11:104757923-104758028	NR_034071
47	lnc-CASP12-2	chr11:104757923-104758028	NR_034066
48	lnc-CASP12-2	chr11:104761897-104762131	NR_034063
49	lnc-CASP4-1	chr11:104819260-104819461	NONHSAT023947
50	lnc-CASP12-3	chr11:104788840-104788902	NR_034079

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	chr11:104822275-104822295
2	CASP4	hsa-miR-26b-5p	chr11:104822249-104822272

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

Extended variants
information (count: 5697 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:5697 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10895730	chr11:104674935-104674936	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs541283783	chr11:104674958-104674959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183974909	chr11:104674973-104674974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs7131137	chr11:104674982-104674983	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs543982148	chr11:104675001-104675002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148586736	chr11:104675003-104675004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12272284	chr11:104675014-104675015	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144464955	chr11:104675054-104675055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146128127	chr11:104675059-104675060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs6591097	chr11:104675102-104675103	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs555432471	chr11:104675141-104675142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7924865	chr11:104675153-104675154	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189250169	chr11:104675202-104675203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550715033	chr11:104675229-104675230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11445553	chr11:104675231-104675232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs67555513	chr11:104675232-104675233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12273743	chr11:104675311-104675312	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572934948	chr11:104675324-104675325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536297996	chr11:104675328-104675329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs184240478	chr11:104675349-104675350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190832040	chr11:104675416-104675417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181854035	chr11:104675476-104675477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558066620	chr11:104675495-104675496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs185914760	chr11:104675501-104675502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140115918	chr11:104675512-104675513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563861298	chr11:104675527-104675528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs143778392	chr11:104675597-104675598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188337316	chr11:104682823-104682824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs536818490	chr11:104682826-104682827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553536713	chr11:104682837-104682838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150881541	chr11:104682865-104682866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs573219386	chr11:104682869-104682870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376597359	chr11:104682898-104682899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539042691	chr11:104682903-104682904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs564934195	chr11:104682913-104682914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575503213	chr11:104682935-104682936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527499835	chr11:104682937-104682938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180988172	chr11:104682967-104682968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368777260	chr11:104682970-104682971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200445740	chr11:104682975-104682976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs146952249	chr11:104682976-104682977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530038157	chr11:104682978-104682979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574327985	chr11:104683000-104683001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs34591112	chr11:104683017-104683018	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs185220407	chr11:104683053-104683054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532064445	chr11:104683057-104683058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552162170	chr11:104683068-104683069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs139342837	chr11:104683094-104683095	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs531331279	chr11:104683161-104683162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs191202332	chr11:104683228-104683229	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1989 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104674400-104675000	Enhancers	GM12878-XiMat	blood
2	chr11:104674600-104675000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:104674800-104675600	Enhancers	Dnd41	blood
4	chr11:104682800-104683000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr11:104682800-104683200	Enhancers	Brain Cingulate Gyrus	brain
6	chr11:104682800-104683400	Enhancers	Brain Hippocampus Middle	brain
7	chr11:104682800-104685400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr11:104683000-104683200	Enhancers	Fetal Brain Female	brain
9	chr11:104683000-104683400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr11:104683000-104683400	Enhancers	Brain Substantia Nigra	brain
11	chr11:104683000-104683400	Enhancers	Fetal Lung	lung
12	chr11:104683000-104683600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr11:104683000-104684000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr11:104683000-104684600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr11:104683000-104684800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr11:104683000-104684800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr11:104683200-104683400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr11:104683400-104684800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr11:104683800-104684000	Enhancers	Fetal Brain Female	brain
20	chr11:104684000-104684800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr11:104684000-104684800	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr11:104684000-104685000	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr11:104684600-104685200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr11:104685000-104688200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr11:104685200-104685400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr11:104689000-104690000	Enhancers	Fetal Stomach	stomach
27	chr11:104689200-104691600	Enhancers	Fetal Brain Male	brain
28	chr11:104690000-104690400	Enhancers	Rectal Smooth Muscle	rectum
29	chr11:104690400-104690600	Enhancers	GM12878-XiMat	blood
30	chr11:104691600-104707600	Weak transcription	Fetal Brain Male	brain
31	chr11:104694400-104694800	Enhancers	Brain Hippocampus Middle	brain
32	chr11:104694600-104694800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr11:104694600-104695000	Enhancers	Brain Substantia Nigra	brain
34	chr11:104694800-104695400	Enhancers	HUVEC	blood vessel
35	chr11:104696400-104696600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:104696600-104697800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:104697800-104698600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:104698400-104699200	Enhancers	Ovary	ovary
39	chr11:104698600-104699800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:104699000-104699200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:104699000-104701600	Enhancers	Muscle Satellite Cultured Cells	--
42	chr11:104699200-104699400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr11:104699200-104699600	Weak transcription	Ovary	ovary
44	chr11:104699400-104700600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr11:104699600-104700600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:104699600-104701000	Enhancers	Ovary	ovary
47	chr11:104699800-104701000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr11:104700600-104701400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:104700600-104701600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:104700800-104701400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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