Variant report

Variant	nsv534182
Chromosome Location	chr14:35579022-35620232
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:956)
CpG islands
(count:915)
Chromatin interactive
region (count:73)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:956 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35591026-35591699	K562	blood:	n/a	chr14:35591480-35591488
3	ARID3A	chr14:35615869-35616033	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35590633-35592472	HepG2	liver:	n/a	chr14:35591480-35591488
5	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
6	ATF1	chr14:35590856-35592000	K562	blood:	n/a	n/a
7	ATF2	chr14:35590839-35591575	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr14:35591095-35591822	GM12878	blood:	n/a	n/a
9	ATF2	chr14:35590456-35592108	GM12878	blood:	n/a	n/a
10	ATF2	chr14:35590769-35591863	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr14:35591254-35591787	A549	lung:	n/a	chr14:35591484-35591504
12	ATF3	chr14:35591305-35591773	H1-hESC	embryonic stem cell:	n/a	chr14:35591484-35591504
13	ATF3	chr14:35591368-35591602	GM12878	blood:	n/a	chr14:35591484-35591504
14	ATF3	chr14:35591069-35591891	HepG2	liver:	n/a	chr14:35591484-35591504
15	ATF3	chr14:35590988-35592153	HepG2	liver:	n/a	chr14:35591484-35591504
16	ATF3	chr14:35591326-35591632	K562	blood:	n/a	chr14:35591484-35591504
17	ATF3	chr14:35591062-35591829	GM12878	blood:	n/a	chr14:35591484-35591504
18	BATF	chr14:35591663-35591964	GM12878	blood:	n/a	n/a
19	BCL3	chr14:35590950-35592103	A549	lung:	n/a	n/a
20	BCL3	chr14:35590607-35591936	A549	lung:	n/a	n/a
21	BCLAF1	chr14:35590870-35592203	GM12878	blood:	n/a	n/a
22	BCLAF1	chr14:35590896-35592186	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:35591280-35591665	A549	lung:	n/a	n/a
24	BHLHE40	chr14:35590781-35592288	GM12878	blood:	n/a	n/a
25	BHLHE40	chr14:35590665-35592190	K562	blood:	n/a	n/a
26	BHLHE40	chr14:35590749-35592231	HepG2	liver:	n/a	n/a
27	BRCA1	chr14:35591074-35592013	HepG2	liver:	n/a	n/a
28	BRCA1	chr14:35590603-35591644	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr14:35613335-35613393	GM12878	blood:	n/a	n/a
30	BRCA1	chr14:35590611-35592191	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr14:35602269-35602685	K562	blood:	n/a	n/a
32	CBX3	chr14:35602360-35602546	K562	blood:	n/a	n/a
33	CBX3	chr14:35580902-35581120	K562	blood:	n/a	n/a
34	CBX3	chr14:35580846-35581125	K562	blood:	n/a	n/a
35	CBX3	chr14:35590828-35591964	K562	blood:	n/a	n/a
36	CCNT2	chr14:35590784-35592019	K562	blood:	n/a	n/a
37	CEBPB	chr14:35590674-35592463	GM12878	blood:	n/a	chr14:35591541-35591552
38	CEBPB	chr14:35601915-35601965	HepG2	liver:	n/a	chr14:35601943-35601954
39	CEBPB	chr14:35612292-35612467	HepG2	liver:	n/a	chr14:35612414-35612425
40	CEBPB	chr14:35591210-35591766	K562	blood:	n/a	chr14:35591541-35591552
41	CEBPB	chr14:35590944-35591690	H1-hESC	embryonic stem cell:	n/a	chr14:35591541-35591552
42	CEBPB	chr14:35590954-35591859	HepG2	liver:	n/a	chr14:35591541-35591552
43	CEBPB	chr14:35591272-35591915	A549	lung:	n/a	chr14:35591541-35591552
44	CEBPB	chr14:35581914-35582023	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr14:35583289-35583522	A549	lung:	n/a	n/a
46	CEBPB	chr14:35615956-35615976	IMR90	lung:	n/a	n/a
47	CEBPB	chr14:35612279-35612564	HepG2	liver:	n/a	chr14:35612414-35612425
48	CEBPB	chr14:35619064-35619239	HepG2	liver:	n/a	chr14:35619155-35619166
49	CEBPB	chr14:35588289-35588318	HepG2	liver:	n/a	n/a
50	CEBPB	chr14:35605476-35605702	HepG2	liver:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35583718-35583768	PrEC	prostate:	n/a
2	chr14:35591951-35592001	HEEpiC	esophagus:	n/a
3	chr14:35591781-35591831	HepG2	liver:	n/a
4	chr14:35587750-35587800	BE2_C	brain:	n/a
5	chr14:35591695-35591745	HUVEC	blood vessel:	n/a
6	chr14:35591695-35591745	SK-N-SH	brain:	n/a
7	chr14:35591951-35592001	IMR90	lung:	fetal
8	chr14:35592116-35592166	HRCEpiC	kidney:	n/a
9	chr14:35591473-35591523	RPTEC	kidney:	n/a
10	chr14:35591840-35591890	T-47D	breast:	n/a
11	chr14:35591625-35591675	Hela-S3	cervix:	n/a
12	chr14:35591951-35592001	AG09319	gingival:	n/a
13	chr14:35589334-35589384	GM19239	blood:	n/a
14	chr14:35591781-35591831	HMEC	breast:	n/a
15	chr14:35591840-35591890	Hela-S3	cervix:	n/a
16	chr14:35591625-35591675	MCF-7	breast:	n/a
17	chr14:35594356-35594406	HUVEC	blood vessel:	n/a
18	chr14:35591779-35591829	ovcar-3	ovarian:	n/a
19	chr14:35583718-35583768	PFSK-1	brain:	n/a
20	chr14:35583718-35583768	HL-60	blood:	n/a
21	chr14:35592116-35592166	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:35591779-35591829	HRPEpiC	eye:	n/a
23	chr14:35591572-35591622	HUVEC	blood vessel:	n/a
24	chr14:35591840-35591890	BE2_C	brain:	n/a
25	chr14:35591473-35591523	HRCEpiC	kidney:	n/a
26	chr14:35591781-35591831	GM06990	blood:	n/a
27	chr14:35589334-35589384	U87	brain:	n/a
28	chr14:35591473-35591523	NT2-D1	testis:	n/a
29	chr14:35591252-35591302	HIPEpiC	eye:	n/a
30	chr14:35591523-35591573	HCF	heart:	n/a
31	chr14:35587750-35587800	HCF	heart:	n/a
32	chr14:35591473-35591523	ovcar-3	ovarian:	n/a
33	chr14:35591572-35591622	ovcar-3	ovarian:	n/a
34	chr14:35591951-35592001	HAEpiC	amniotic membrane:	n/a
35	chr14:35591781-35591831	NT2-D1	testis:	n/a
36	chr14:35591252-35591302	HCM	heart:	n/a
37	chr14:35591840-35591890	U87	brain:	n/a
38	chr14:35587750-35587800	MCF-7	breast:	n/a
39	chr14:35591951-35592001	BE2_C	brain:	n/a
40	chr14:35583718-35583768	CMK	blood:	n/a
41	chr14:35587750-35587800	HCPEpiC	choroid plexus:	n/a
42	chr14:35591779-35591829	BJ	skin:	n/a
43	chr14:35592116-35592166	GM06990	blood:	n/a
44	chr14:35591951-35592001	SKMC	muscle:	n/a
45	chr14:35591951-35592001	NB4	blood:	n/a
46	chr14:35591951-35592001	GM12878	blood:	n/a
47	chr14:35591840-35591890	AG10803	skin:	n/a
48	chr14:35591572-35591622	AG10803	skin:	n/a
49	chr14:35594356-35594406	ECC-1	luminal epithelium:	n/a
50	chr14:35583718-35583768	HIPEpiC	eye:	n/a

(count:73 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:45196086..45196947-chr14:35590878..35591536,2	Hela-S3	cervix:
2	chr14:35580705..35582732-chr14:35589834..35592713,2	K562	blood:
3	chr10:134144877..134145604-chr14:35591124..35591775,2	Hela-S3	cervix:
4	chr14:35575108..35577004-chr14:35580748..35582498,2	MCF-7	breast:
5	chr14:35592944..35595456-chr14:35809160..35811582,2	K562	blood:
6	chr14:35450019..35452754-chr14:35591061..35594828,4	K562	blood:
7	chr14:35610009..35610550-chr14:36156270..36157192,2	K562	blood:
8	chr14:35617849..35620759-chr14:35622945..35624771,2	K562	blood:
9	chr14:35568810..35572401-chr14:35587846..35592624,4	MCF-7	breast:
10	chr14:35519480..35523190-chr14:35588742..35592990,5	MCF-7	breast:
11	chr14:35583281..35585103-chr14:35589464..35591782,2	K562	blood:
12	chr14:35450042..35454830-chr14:35589505..35593708,8	K562	blood:
13	chr14:35583719..35588379-chr14:35588655..35591956,6	MCF-7	breast:
14	chr14:35577086..35580056-chr14:35580213..35583818,4	MCF-7	breast:
15	chr14:35593883..35596766-chr14:35627445..35630133,2	MCF-7	breast:
16	chr14:35591208..35595473-chr14:35600554..35604133,4	K562	blood:
17	chr14:35342738..35344659-chr14:35589687..35591484,2	K562	blood:
18	chr14:35579453..35581651-chr14:35585942..35587733,2	K562	blood:
19	chr14:35450245..35452169-chr14:35590215..35593362,3	MCF-7	breast:
20	chr14:35590512..35592667-chr14:35626960..35629855,2	MCF-7	breast:
21	chr14:35591519..35595247-chr14:35614813..35617284,3	MCF-7	breast:
22	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
23	chr14:35585231..35589339-chr14:35589469..35593386,5	K562	blood:
24	chr14:35618961..35620951-chr14:35872636..35874969,2	K562	blood:
25	chr14:35589606..35593451-chr14:35594804..35598522,5	K562	blood:
26	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
27	chr14:35578569..35580087-chr14:35582011..35583731,2	K562	blood:
28	chr14:35450146..35454994-chr14:35588530..35593322,8	MCF-7	breast:
29	chr14:35342567..35345567-chr14:35590904..35592504,3	MCF-7	breast:
30	chr14:35576972..35579105-chr14:35589747..35591526,2	MCF-7	breast:
31	chr1:1709416..1709919-chr14:35590889..35591481,2	Hela-S3	cervix:
32	chr14:35341168..35344675-chr14:35590606..35593872,6	MCF-7	breast:
33	chr14:35579884..35582908-chr14:35589580..35593400,4	MCF-7	breast:
34	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
35	chr14:35514347..35518167-chr14:35589018..35591815,3	K562	blood:
36	chr14:35590804..35592605-chr14:35605460..35607939,2	K562	blood:
37	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
38	chr14:35342813..35344956-chr14:35595359..35597712,2	K562	blood:
39	chr14:35610882..35612765-chr14:35874078..35876845,2	MCF-7	breast:
40	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
41	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
42	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
43	chr14:35571820..35573660-chr14:35580909..35583356,2	MCF-7	breast:
44	chr14:35591181..35592726-chr14:35595848..35598610,3	MCF-7	breast:
45	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
46	chr14:35583308..35588876-chr14:35589178..35593731,8	MCF-7	breast:
47	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:
48	chr14:35607146..35612253-chr14:35870483..35876264,6	MCF-7	breast:
49	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
50	chr14:35591775..35593424-chr14:35873275..35875126,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-173D9.3.1-1	chr14:35579776-35579932	ENSG00000247658
2	lnc-BAZ1A-3	chr14:35591108-35591185	NONHSAT036363
3	lnc-RP11-173D9.3.1-1	chr14:35579101-35579166	ENSG00000247658
4	lnc-BAZ1A-3	chr14:35579129-35579835	NONHSAT036363
5	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366
6	lnc-BAZ1A-3	chr14:35585816-35585943	NONHSAT036363

No data

Variant related genes	Relation type
KIAA0391	TF binding region
ENSG00000258790	TF binding region
PPP2R3C	TF binding region
ENSG00000241052	TF binding region
KIAA0391	CpG island
ENSG00000258790	CpG island
PPP2R3C	CpG island
ENSG00000241052	CpG island
ENSG00000151327	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000008130	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000174851	chromatin interactions
C2CD4A	miRNA target sites
NEFM	miRNA target sites

Extended variants
information (count: 1582 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1582 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544964267	chr14:35579030-35579031	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs75803663	chr14:35579048-35579049	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs149892552	chr14:35579068-35579069	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs376027395	chr14:35579069-35579070	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs369037088	chr14:35579098-35579099	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs369499237	chr14:35579101-35579102	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs144955472	chr14:35579105-35579106	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs547182743	chr14:35579151-35579152	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs565605614	chr14:35579195-35579196	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs528211658	chr14:35579209-35579210	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs144725443	chr14:35579229-35579230	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs373149562	chr14:35579232-35579233	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs547855434	chr14:35579234-35579235	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs567757926	chr14:35579246-35579247	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs187749256	chr14:35579257-35579258	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs373540227	chr14:35579298-35579299	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs139068345	chr14:35579319-35579320	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs570423395	chr14:35579391-35579392	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs539222259	chr14:35579404-35579405	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs569103245	chr14:35579426-35579427	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs149907608	chr14:35579465-35579466	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs373182426	chr14:35579535-35579536	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs573233436	chr14:35579543-35579544	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs542345425	chr14:35579599-35579600	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs11625939	chr14:35579614-35579615	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
26	rs555791469	chr14:35579624-35579625	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs575758447	chr14:35579634-35579635	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs201403377	chr14:35579746-35579747	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs554791537	chr14:35579760-35579761	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs34776163	chr14:35579811-35579812	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs144888404	chr14:35579846-35579847	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs375356716	chr14:35579854-35579855	Strong transcription Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs576240252	chr14:35579918-35579919	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs111631627	chr14:35579922-35579923	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs2295104	chr14:35579927-35579928	Strong transcription Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs537749457	chr14:35579963-35579964	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs76932844	chr14:35579968-35579969	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs576735889	chr14:35579970-35579971	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs540444861	chr14:35579991-35579992	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs73234490	chr14:35580002-35580003	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs528164269	chr14:35580050-35580051	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs547928153	chr14:35580119-35580120	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs192109792	chr14:35580174-35580175	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs112697442	chr14:35580186-35580187	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
45	rs558975367	chr14:35580187-35580188	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs184203342	chr14:35580210-35580211	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs570382353	chr14:35580212-35580213	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs377187261	chr14:35580215-35580216	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs375086207	chr14:35580266-35580267	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs12889019	chr14:35580276-35580277	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:61)

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
Acute lymphoblastic leukemia	20067559	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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:1673 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35529400-35590200	Weak transcription	Esophagus	oesophagus
2	chr14:35530600-35590000	Weak transcription	Fetal Heart	heart
3	chr14:35538200-35581000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr14:35542000-35589600	Weak transcription	Fetal Brain Male	brain
5	chr14:35543200-35580800	Weak transcription	K562	blood
6	chr14:35545600-35580800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:35545600-35582800	Strong transcription	Primary T helper cells fromperipheralblood	blood
8	chr14:35545600-35590000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:35546000-35581200	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr14:35546000-35585800	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr14:35546000-35587200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr14:35546200-35585000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr14:35547000-35580800	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr14:35547400-35580600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr14:35548000-35581000	Strong transcription	HepG2	liver
16	chr14:35548200-35580800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr14:35550200-35586000	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr14:35550800-35581000	Strong transcription	Dnd41	blood
19	chr14:35551600-35579400	Weak transcription	NHEK	skin
20	chr14:35552000-35586600	Strong transcription	Fetal Thymus	thymus
21	chr14:35553400-35589800	Weak transcription	Pancreas	Pancrea
22	chr14:35555000-35581200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr14:35560200-35581200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr14:35560600-35580600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:35560600-35580600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr14:35564200-35589400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr14:35564400-35579200	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr14:35564400-35580000	Weak transcription	Colonic Mucosa	Colon
29	chr14:35564800-35589800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr14:35565200-35582000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr14:35567800-35579400	Weak transcription	Gastric	stomach
32	chr14:35568000-35580800	Weak transcription	Spleen	Spleen
33	chr14:35569400-35585800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr14:35571000-35580800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr14:35571600-35581000	Strong transcription	Duodenum Mucosa	Duodenum
36	chr14:35571600-35585200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr14:35571600-35585200	Strong transcription	Liver	Liver
38	chr14:35571800-35583600	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr14:35572400-35580800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr14:35573400-35583400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr14:35573600-35579200	Weak transcription	NHLF	lung
42	chr14:35573600-35584800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr14:35573600-35584800	Strong transcription	Fetal Muscle Trunk	muscle
44	chr14:35573600-35586400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr14:35574000-35580800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr14:35574200-35580600	Weak transcription	Psoas Muscle	Psoas
47	chr14:35574800-35580800	Strong transcription	HUES64 Cell Line	embryonic stem cell
48	chr14:35574800-35584800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr14:35575000-35581000	Strong transcription	Primary B cells from cord blood	blood
50	chr14:35575200-35582800	Strong transcription	Fetal Lung	lung

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