Variant report

Variant	nsv902117
Chromosome Location	chr14:81643800-81682392
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:326)
CpG islands
(count:122)
Chromatin interactive
region (count:47)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:326 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81663352-81663382	K562	blood:	n/a	n/a
2	ARID3A	chr14:81678314-81678544	HepG2	liver:	n/a	n/a
3	ATF2	chr14:81675515-81675881	GM12878	blood:	n/a	n/a
4	BACH1	chr14:81665493-81665770	K562	blood:	n/a	n/a
5	BACH1	chr14:81665513-81665708	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:81675489-81675838	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:81675531-81675906	GM12878	blood:	n/a	n/a
8	BCL11A	chr14:81675563-81675915	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:81675486-81675944	GM12878	blood:	n/a	n/a
10	BHLHE40	chr14:81675584-81675627	K562	blood:	n/a	n/a
11	BRCA1	chr14:81647457-81647497	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr14:81661345-81661480	K562	blood:	n/a	n/a
13	CEBPB	chr14:81678332-81678623	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:81661413-81661440	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:81675026-81675141	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:81674920-81675188	HepG2	liver:	n/a	n/a
17	CHD2	chr14:81675493-81675860	GM12878	blood:	n/a	n/a
18	CHD2	chr14:81675526-81675727	K562	blood:	n/a	n/a
19	CTCF	chr14:81678280-81678430	HMEC	breast:	n/a	n/a
20	CTCF	chr14:81678300-81678450	GM12866	blood:	n/a	n/a
21	CTCF	chr14:81678300-81678450	HCFaa	heart:	n/a	n/a
22	CTCF	chr14:81678280-81678430	HAc	cerebellar:	n/a	n/a
23	CTCF	chr14:81678280-81678430	GM12874	blood:	n/a	n/a
24	CTCF	chr14:81678260-81678410	HCT-116	colon:	n/a	n/a
25	CTCF	chr14:81682281-81682301	Fibrobl	skin:	n/a	n/a
26	CTCF	chr14:81678281-81678410	MCF-7	breast:	n/a	n/a
27	CTCF	chr14:81678280-81678430	GM06990	blood:	n/a	n/a
28	CTCF	chr14:81678255-81678504	MCF-7	breast:	n/a	n/a
29	CTCF	chr14:81678240-81678390	GM12870	blood:	n/a	n/a
30	CTCF	chr14:81678280-81678430	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr14:81678360-81678510	HFF	foreskin:	n/a	n/a
32	CTCF	chr14:81678280-81678430	GM12864	blood:	n/a	n/a
33	CTCF	chr14:81678300-81678450	GM12871	blood:	n/a	n/a
34	CTCF	chr14:81678260-81678410	GM12866	blood:	n/a	n/a
35	CTCF	chr14:81678300-81678450	GM12873	blood:	n/a	n/a
36	CTCF	chr14:81678300-81678450	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr14:81678300-81678450	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr14:81678280-81678430	Caco-2	colon:	n/a	n/a
39	CTCF	chr14:81678300-81678450	AG09319	gingival:	n/a	n/a
40	CTCF	chr14:81678300-81678450	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr14:81678300-81678450	AG09309	skin:	n/a	n/a
42	CTCF	chr14:81678300-81678450	HMEC	breast:	n/a	n/a
43	CTCF	chr14:81678280-81678430	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr14:81678300-81678450	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr14:81670293-81670330	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:81678242-81678437	A549	lung:	n/a	n/a
47	CTCF	chr14:81678300-81678450	GM12867	blood:	n/a	n/a
48	CTCF	chr14:81678284-81678475	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr14:81678340-81678490	HEK293	kidney:	n/a	n/a
50	CTCF	chr14:81678280-81678440	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81649681-81649731	NH-A	brain:	n/a
2	chr14:81670281-81670331	HepG2	liver:	n/a
3	chr14:81670281-81670331	A549	lung:	n/a
4	chr14:81649681-81649731	HNPCEpiC	eye:	n/a
5	chr14:81670281-81670331	HMEC	breast:	n/a
6	chr14:81670281-81670331	PFSK-1	brain:	n/a
7	chr14:81649681-81649731	IMR90	lung:	fetal
8	chr14:81649681-81649731	Caco-2	colon:	n/a
9	chr14:81670281-81670331	K562	blood:	n/a
10	chr14:81649681-81649731	SKMC	muscle:	n/a
11	chr14:81649681-81649731	NHBE	bronchial:	n/a
12	chr14:81670281-81670331	AG09309	skin:	n/a
13	chr14:81670281-81670331	BJ	skin:	n/a
14	chr14:81649681-81649731	K562	blood:	n/a
15	chr14:81670281-81670331	NT2-D1	testis:	n/a
16	chr14:81649681-81649731	MCF-7	breast:	n/a
17	chr14:81649681-81649731	BE2_C	brain:	n/a
18	chr14:81649681-81649731	AG10803	skin:	n/a
19	chr14:81649681-81649731	HEEpiC	esophagus:	n/a
20	chr14:81649681-81649731	GM12891	blood:	n/a
21	chr14:81670281-81670331	HUVEC	blood vessel:	n/a
22	chr14:81670281-81670331	AG04449	skin:	fetal
23	chr14:81649681-81649731	AG09309	skin:	n/a
24	chr14:81649681-81649731	A549	lung:	n/a
25	chr14:81670281-81670331	HEK293	kidney:	embryo
26	chr14:81670281-81670331	SK-N-MC	brain:	n/a
27	chr14:81670281-81670331	BE2_C	brain:	n/a
28	chr14:81670281-81670331	HRCEpiC	kidney:	n/a
29	chr14:81649681-81649731	SK-N-SH	brain:	n/a
30	chr14:81670281-81670331	HL-60	blood:	n/a
31	chr14:81670281-81670331	PANC-1	pancreas:	n/a
32	chr14:81649681-81649731	HCT-116	colon:	n/a
33	chr14:81649681-81649731	Hela-S3	cervix:	n/a
34	chr14:81649681-81649731	HPAEpiC	pulmonary alveolar:	n/a
35	chr14:81649681-81649731	GM19239	blood:	n/a
36	chr14:81670281-81670331	IMR90	lung:	fetal
37	chr14:81670281-81670331	AG10803	skin:	n/a
38	chr14:81649681-81649731	HRE	kidney:	n/a
39	chr14:81670281-81670331	AG09319	gingival:	n/a
40	chr14:81670281-81670331	ECC-1	luminal epithelium:	n/a
41	chr14:81670281-81670331	GM06990	blood:	n/a
42	chr14:81670281-81670331	T-47D	breast:	n/a
43	chr14:81670281-81670331	HIPEpiC	eye:	n/a
44	chr14:81649681-81649731	HAEpiC	amniotic membrane:	n/a
45	chr14:81670281-81670331	AG04450	lung:	fetal
46	chr14:81670281-81670331	ProgFib	skin:	n/a
47	chr14:81649681-81649731	HL-60	blood:	n/a
48	chr14:81649681-81649731	HCF	heart:	n/a
49	chr14:81649681-81649731	AoSMC	blood vessel:	n/a
50	chr14:81649681-81649731	HepG2	liver:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:81630975..81634065-chr14:81679806..81681376,3	K562	blood:
2	chr14:81682072..81683582-chr14:81925884..81928192,2	MCF-7	breast:
3	chr14:81656769..81659084-chr14:81679590..81681923,2	K562	blood:
4	chr14:81405868..81408101-chr14:81681556..81683750,2	K562	blood:
5	chr14:81645137..81647091-chr14:81650122..81652233,2	K562	blood:
6	chr14:81656858..81657712-chr8:102572368..102573072,2	MCF-7	breast:
7	chr14:81636684..81637247-chr14:81677958..81678593,2	MCF-7	breast:
8	chr14:81637815..81640374-chr14:81649220..81650814,2	K562	blood:
9	chr14:81649550..81651536-chr14:81676600..81679545,2	K562	blood:
10	chr14:81654146..81656422-chr14:81667896..81670751,2	MCF-7	breast:
11	chr14:81655881..81668737-chr14:81683092..81689639,25	K562	blood:
12	chr14:81668782..81673405-chr14:81676338..81680193,5	K562	blood:
13	chr14:81642022..81644044-chr14:81645949..81648164,2	MCF-7	breast:
14	chr14:81644812..81647166-chr14:81685708..81688180,2	MCF-7	breast:
15	chr14:81671482..81674302-chr14:81674927..81677251,2	MCF-7	breast:
16	chr14:81656769..81659084-chr14:81679590..81681923,2	K562	blood:
17	chr14:81643246..81655314-chr14:81683241..81689401,24	K562	blood:
18	chr14:81647686..81650322-chr14:81684054..81687029,2	MCF-7	breast:
19	chr14:81649550..81651536-chr14:81676600..81679545,2	K562	blood:
20	chr14:81642022..81644044-chr14:81645949..81648164,2	MCF-7	breast:
21	chr14:81682255..81691444-chr14:81709014..81722196,43	MCF-7	breast:
22	chr14:81420309..81422917-chr14:81682384..81684780,2	MCF-7	breast:
23	chr14:81656301..81665753-chr14:81684174..81688927,14	MCF-7	breast:
24	chr14:81657573..81659438-chr14:81663408..81665237,2	MCF-7	breast:
25	chr14:81645018..81646752-chr14:81685163..81687318,3	MCF-7	breast:
26	chr14:81649228..81655392-chr14:81682762..81688409,10	K562	blood:
27	chr14:81653722..81660939-chr14:81683638..81690429,10	MCF-7	breast:
28	chr14:81634706..81637472-chr14:81662917..81664868,3	MCF-7	breast:
29	chr14:81647401..81650665-chr14:81685451..81688014,6	MCF-7	breast:
30	chr14:81639700..81642191-chr14:81644635..81646691,2	K562	blood:
31	chr14:81647751..81650741-chr14:81651817..81654403,2	K562	blood:
32	chr14:81644106..81646643-chr14:81658404..81660204,2	MCF-7	breast:
33	chr14:81651257..81653411-chr14:81683481..81686410,2	MCF-7	breast:
34	chr14:81645137..81647091-chr14:81650122..81652233,2	K562	blood:
35	chr14:81638146..81640079-chr14:81645451..81648200,3	MCF-7	breast:
36	chr14:81635572..81638228-chr14:81643135..81644647,2	K562	blood:
37	chr14:81664368..81667115-chr14:81668581..81672072,3	K562	blood:
38	chr14:81643515..81648900-chr14:81684307..81689030,7	K562	blood:
39	chr14:81665997..81674006-chr14:81683759..81689461,17	MCF-7	breast:
40	chr14:81641589..81644244-chr14:81683359..81688610,5	MCF-7	breast:
41	chr14:81657573..81659438-chr14:81663408..81665237,2	MCF-7	breast:
42	chr14:81644138..81645856-chr14:81700213..81702978,2	K562	blood:
43	chr14:81671482..81674302-chr14:81674927..81677251,2	MCF-7	breast:
44	chr14:81663416..81665215-chr14:81667787..81670212,2	MCF-7	breast:
45	chr14:81635464..81641822-chr14:81682247..81689009,10	K562	blood:
46	chr14:81647751..81650741-chr14:81651817..81654403,2	K562	blood:
47	chr14:81644106..81646643-chr14:81658404..81660204,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STON2-5	chr14:81641799-81645528	NONHSAT038052

No data

Variant related genes	Relation type
SNORA79	TF binding region
SNORA79	CpG island
ENSG00000205579	chromatin interactions
ENSG00000100629	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000165409	chromatin interactions
ENSG00000258999	chromatin interactions
ENSG00000221303	chromatin interactions

Extended variants
information (count: 1429 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4899786	chr14:81643800-81643801	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533389126	chr14:81643810-81643811	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs377251836	chr14:81643852-81643853	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs191489963	chr14:81643998-81643999	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs554290037	chr14:81644070-81644071	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs549165251	chr14:81644074-81644075	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs184105757	chr14:81644094-81644095	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs370679118	chr14:81644098-81644099	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs188785304	chr14:81644099-81644100	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs557055750	chr14:81644117-81644118	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs181587984	chr14:81644146-81644147	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs116495522	chr14:81644149-81644150	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs539463383	chr14:81644152-81644153	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs558051581	chr14:81644162-81644163	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs370857330	chr14:81644174-81644175	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs568033560	chr14:81644192-81644193	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs186935621	chr14:81644193-81644194	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs536984747	chr14:81644215-81644216	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs573046745	chr14:81644217-81644218	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs554839378	chr14:81644274-81644275	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs190268702	chr14:81644319-81644320	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs149399520	chr14:81644330-81644331	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs563021138	chr14:81644333-81644334	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs181920300	chr14:81644488-81644489	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs187502804	chr14:81644506-81644507	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs545008570	chr14:81644511-81644512	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs560365462	chr14:81644572-81644573	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs116368250	chr14:81644598-81644599	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs189568115	chr14:81644606-81644607	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs144861232	chr14:81644673-81644674	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs60733595	chr14:81644712-81644713	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs531962241	chr14:81644746-81644747	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs117060001	chr14:81644779-81644780	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs180958728	chr14:81644789-81644790	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs185469018	chr14:81644910-81644911	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs201018932	chr14:81644938-81644939	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs539399394	chr14:81644945-81644946	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs557789820	chr14:81644947-81644948	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs200845641	chr14:81644948-81644949	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs61651620	chr14:81644988-81644989	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs61451161	chr14:81645026-81645027	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs534071623	chr14:81645089-81645090	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs555660868	chr14:81645104-81645105	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs111954559	chr14:81645107-81645108	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs573726318	chr14:81645131-81645132	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs544411509	chr14:81645135-81645136	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs556339904	chr14:81645155-81645156	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs552661412	chr14:81645159-81645160	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs577173310	chr14:81645166-81645167	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs560103101	chr14:81645174-81645175	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81637000-81646400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr14:81637000-81647000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr14:81637000-81652200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr14:81637000-81659000	Weak transcription	Esophagus	oesophagus
5	chr14:81637000-81683800	Weak transcription	Small Intestine	intestine
6	chr14:81637200-81643800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr14:81637200-81644800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:81637200-81645000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr14:81637200-81645600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr14:81637200-81646200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr14:81637200-81646800	Weak transcription	Fetal Intestine Small	intestine
12	chr14:81637200-81648400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr14:81637200-81650000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr14:81637200-81650200	Weak transcription	Fetal Lung	lung
15	chr14:81637200-81651400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr14:81637200-81651800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr14:81637200-81652400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr14:81637200-81652600	Weak transcription	NHEK	skin
19	chr14:81637200-81652800	Weak transcription	Fetal Stomach	stomach
20	chr14:81637200-81653000	Weak transcription	Fetal Muscle Leg	muscle
21	chr14:81637200-81658200	Weak transcription	HSMMtube	muscle
22	chr14:81637200-81658800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr14:81637200-81658800	Weak transcription	Colonic Mucosa	Colon
24	chr14:81637200-81658800	Weak transcription	Left Ventricle	heart
25	chr14:81637400-81644200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr14:81637400-81644600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr14:81637400-81645600	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr14:81637400-81646000	Weak transcription	K562	blood
29	chr14:81637400-81646200	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr14:81637400-81646200	Weak transcription	Fetal Thymus	thymus
31	chr14:81637400-81646400	Weak transcription	Fetal Intestine Large	intestine
32	chr14:81637400-81646400	Weak transcription	Thymus	Thymus
33	chr14:81637400-81646600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr14:81637400-81646800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr14:81637400-81648200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr14:81637400-81649800	Weak transcription	HepG2	liver
37	chr14:81637400-81650000	Weak transcription	Adipose Nuclei	Adipose
38	chr14:81637400-81650000	Weak transcription	Fetal Kidney	kidney
39	chr14:81637400-81651600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr14:81637400-81651800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:81637400-81652200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr14:81637400-81653000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:81637400-81653000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr14:81637400-81656800	Weak transcription	HMEC	breast
45	chr14:81637400-81658800	Weak transcription	Fetal Brain Male	brain
46	chr14:81637400-81659000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr14:81637600-81643800	Weak transcription	Brain Anterior Caudate	brain
48	chr14:81637600-81643800	Weak transcription	Stomach Mucosa	stomach
49	chr14:81637600-81646600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr14:81637600-81646800	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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