Variant report

Variant	nsv1039478
Chromosome Location	chr14:19469508-20424926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4794)
CpG islands
(count:4765)
Chromatin interactive
region (count:5)
LncRNA
region (count:249)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4794 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20346227-20346537	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:20346241-20346527	K562	blood:	n/a	n/a
3	ARID3A	chr14:19614565-19614964	K562	blood:	n/a	n/a
4	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
5	ATF1	chr14:19619825-19620010	K562	blood:	n/a	n/a
6	ATF1	chr14:19610591-19610826	K562	blood:	n/a	n/a
7	ATF1	chr14:19792967-19794009	K562	blood:	n/a	n/a
8	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
9	ATF1	chr14:19697695-19697910	K562	blood:	n/a	n/a
10	ATF1	chr14:20325048-20325100	K562	blood:	n/a	n/a
11	ATF1	chr14:19614523-19614771	K562	blood:	n/a	n/a
12	ATF1	chr14:20319622-20319703	K562	blood:	n/a	n/a
13	ATF1	chr14:19609027-19609227	K562	blood:	n/a	n/a
14	ATF1	chr14:19795048-19796237	K562	blood:	n/a	n/a
15	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
16	ATF3	chr14:19614578-19614850	K562	blood:	n/a	n/a
17	BACH1	chr14:19795663-19796213	K562	blood:	n/a	n/a
18	BACH1	chr14:19614506-19614753	K562	blood:	n/a	n/a
19	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
20	BACH1	chr14:19608951-19609223	K562	blood:	n/a	n/a
21	BATF	chr14:19541484-19541694	GM12878	blood:	n/a	n/a
22	BATF	chr14:20026256-20026650	GM12878	blood:	n/a	n/a
23	BATF	chr14:19937503-19937859	GM12878	blood:	n/a	chr14:19937698-19937709
24	BATF	chr14:19653590-19653843	GM12878	blood:	n/a	n/a
25	BATF	chr14:19548036-19548546	GM12878	blood:	n/a	n/a
26	BATF	chr14:19748478-19748726	GM12878	blood:	n/a	n/a
27	BATF	chr14:19937525-19937845	GM12878	blood:	n/a	chr14:19937698-19937709
28	BATF	chr14:20085953-20086237	GM12878	blood:	n/a	n/a
29	BATF	chr14:20025031-20025541	GM12878	blood:	n/a	n/a
30	BATF	chr14:19637495-19637851	GM12878	blood:	n/a	chr14:19637679-19637690
31	BATF	chr14:19546952-19547321	GM12878	blood:	n/a	n/a
32	BATF	chr14:19487460-19487744	GM12878	blood:	n/a	n/a
33	BATF	chr14:19827024-19827305	GM12878	blood:	n/a	n/a
34	BATF	chr14:19637509-19637829	GM12878	blood:	n/a	chr14:19637679-19637690
35	BATF	chr14:19541408-19541756	GM12878	blood:	n/a	n/a
36	BATF	chr14:19921485-19921738	GM12878	blood:	n/a	n/a
37	BATF	chr14:20031700-20032016	GM12878	blood:	n/a	n/a
38	BATF	chr14:20025214-20025459	GM12878	blood:	n/a	n/a
39	BATF	chr14:19586478-19586681	GM12878	blood:	n/a	n/a
40	BATF	chr14:19548118-19548363	GM12878	blood:	n/a	n/a
41	BATF	chr14:20131255-20131487	GM12878	blood:	n/a	n/a
42	BATF	chr14:19986920-19987123	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:19654370-19654535	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:19748407-19748711	GM12878	blood:	n/a	n/a
45	BCL11A	chr14:19747489-19747677	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:20025076-20025493	GM12878	blood:	n/a	chr14:20025351-20025360
47	BCL11A	chr14:19826185-19826607	GM12878	blood:	n/a	n/a
48	BCL11A	chr14:19637542-19637751	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:19937603-19937812	GM12878	blood:	n/a	n/a
50	BCL11A	chr14:19824315-19824574	GM12878	blood:	n/a	n/a

(count:4765 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20404281-20404331	HEK293	kidney:	embryo
2	chr14:19890087-19890137	GM12892	blood:	n/a
3	chr14:20344083-20344133	PANC-1	pancreas:	n/a
4	chr14:19959522-19959572	HRE	kidney:	n/a
5	chr14:19932946-19932996	HCM	heart:	n/a
6	chr14:20146694-20146744	SK-N-SH_RA	brain:	n/a
7	chr14:19643599-19643649	NHBE	bronchial:	n/a
8	chr14:20404281-20404331	HEK293	kidney:	embryo
9	chr14:19890087-19890137	GM12892	blood:	n/a
10	chr14:20344083-20344133	PANC-1	pancreas:	n/a
11	chr14:19959522-19959572	HRE	kidney:	n/a
12	chr14:19932946-19932996	HCM	heart:	n/a
13	chr14:20146694-20146744	SK-N-SH_RA	brain:	n/a
14	chr14:19643599-19643649	NHBE	bronchial:	n/a
15	chr14:20106919-20106969	MCF-7	breast:	n/a
16	chr14:20148125-20148175	NH-A	brain:	n/a
17	chr14:20136822-20136872	HCPEpiC	choroid plexus:	n/a
18	chr14:19960976-19961026	HEK293	kidney:	embryo
19	chr14:19626001-19626051	HCT-116	colon:	n/a
20	chr14:19959522-19959572	RPTEC	kidney:	n/a
21	chr14:19686155-19686205	HCPEpiC	choroid plexus:	n/a
22	chr14:19562827-19562877	SK-N-SH	brain:	n/a
23	chr14:19562827-19562877	BJ	skin:	n/a
24	chr14:19888327-19888377	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:19602149-19602199	GM06990	blood:	n/a
26	chr14:19747134-19747184	SK-N-MC	brain:	n/a
27	chr14:19828288-19828338	HAEpiC	amniotic membrane:	n/a
28	chr14:19855384-19855434	HIPEpiC	eye:	n/a
29	chr14:20147187-20147237	HCT-116	colon:	n/a
30	chr14:20020668-20020718	A549	lung:	n/a
31	chr14:20020657-20020707	MCF-7	breast:	n/a
32	chr14:19932946-19932996	GM06990	blood:	n/a
33	chr14:19746900-19746950	HEK293	kidney:	embryo
34	chr14:19747134-19747184	HNPCEpiC	eye:	n/a
35	chr14:19888434-19888484	NHBE	bronchial:	n/a
36	chr14:20136822-20136872	HepG2	liver:	n/a
37	chr14:20134518-20134568	A549	lung:	n/a
38	chr14:20389177-20389227	SK-N-SH	brain:	n/a
39	chr14:20136822-20136872	Jurkat	blood:	n/a
40	chr14:19925080-19925130	AG04450	lung:	fetal
41	chr14:20389177-20389227	AG09309	skin:	n/a
42	chr14:20403845-20403895	NHDF-neo	bronchial:	n/a
43	chr14:19614556-19614606	HMEC	breast:	n/a
44	chr14:20135228-20135278	NHBE	bronchial:	n/a
45	chr14:19614541-19614591	NB4	blood:	n/a
46	chr14:19614541-19614591	GM12891	blood:	n/a
47	chr14:20136693-20136743	HepG2	liver:	n/a
48	chr14:19562827-19562877	SKMC	muscle:	n/a
49	chr14:19600442-19600492	NHDF-neo	bronchial:	n/a
50	chr14:19626001-19626051	NB4	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20421291..20423829-chr14:20424473..20427279,2	MCF-7	breast:
2	chr14:20378405..20379102-chr22:33621834..33622612,2	MCF-7	breast:
3	chr14:20330082..20332945-chr14:20336237..20338891,2	K562	blood:
4	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:
5	chr14:20382435..20385861-chr14:20389212..20390807,3	K562	blood:

(count:249 , 50 per page) page: 1 2 3 4 5

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEM-2	chr14:19925240-19925300	ENSG00000244306
2	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
3	lnc-POTEG-6	chr14:19566012-19566082	NR_027480
4	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT035520
5	lnc-POTEG-6	chr14:19571348-19571418	NR_027480
6	lnc-POTEG-7	chr14:19597285-19597388	NONHSAT035463
7	lnc-POTEM-2	chr14:19925240-19925305	ENSG00000244306
8	lnc-OR4K14-1	chr14:20376255-20376808	NONHSAT035546
9	lnc-POTEG-4	chr14:19653908-19654004	ENSG00000225210
10	lnc-POTEG-3	chr14:19611695-19611964	ENSG00000258314
11	lnc-POTEG-3	chr14:19643174-19643316	NONHSAT035469
12	lnc-POTEM-2	chr14:19880209-19884029	NONHSAT035503
13	lnc-POTEG-2	chr14:19517501-19517607	ENSG00000257891.1
14	lnc-POTEM-2	chr14:19921648-19921738	NONHSAT035522
15	lnc-OR4N2-4	chr14:19894369-19894691	ENSG00000215394
16	lnc-POTEM-6	chr14:19837830-19837836	ENSG00000257898.1
17	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
18	lnc-POTEG-4	chr14:19691355-19691701	ENSG00000225210
19	lnc-POTEM-7	chr14:19680694-19681014	ENSG00000228294
20	lnc-POTEG-3	chr14:19606385-19606529	ENSG00000258314
21	lnc-POTEM-2	chr14:19921359-19921390	NONHSAT035499
22	lnc-POTEM-8	chr14:19566286-19566680	NR_046571
23	lnc-POTEG-7	chr14:19603204-19603279	NONHSAT035463
24	lnc-POTEG-3	chr14:19643072-19643377	ENSG00000258314.2
25	lnc-POTEM-2	chr14:19882464-19884029	ENSG00000244306
26	lnc-POTEG-6	chr14:19558991-19559164	NR_027480
27	lnc-POTEM-7	chr14:19670792-19671105	XLOC_010962
28	lnc-POTEM-1	chr14:19944559-19944820	ENSG00000257931
29	lnc-POTEG-4	chr14:19653625-19653772	NR_110526
30	lnc-POTEM-2	chr14:19921591-19921738	NR_110526
31	lnc-POTEG-3	chr14:19643072-19643377	ENSG00000258314
32	lnc-POTEM-2	chr14:19921591-19921705	NONHSAT035520
33	lnc-POTEG-4	chr14:19655734-19655871	ENSG00000225210
34	lnc-POTEM-7	chr14:19678513-19678600	ENSG00000228294
35	lnc-POTEM-2	chr14:19894700-19894790	ENSG00000244306
36	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
37	lnc-OR4N2-4	chr14:19896785-19896872	XLOC_010749
38	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT035503
39	lnc-POTEM-8	chr14:19566286-19566731	ENSG00000258252
40	lnc-POTEM-2	chr14:19921591-19921738	ENSG00000244306
41	lnc-POTEM-7	chr14:19670480-19671105	ENSG00000228294
42	lnc-POTEG-4	chr14:19650055-19650126	ENSG00000225210
43	lnc-POTEG-4	chr14:19653893-19654004	ENSG00000225210
44	lnc-POTEG-7	chr14:19595933-19596023	NONHSAT035463
45	lnc-POTEM-2	chr14:19923013-19923123	NR_110526
46	lnc-POTEM-2	chr14:19893856-19894790	ENSG00000244306
47	lnc-POTEG-4	chr14:19653893-19654004	NONHSAT035478
48	lnc-POTEM-2	chr14:19884775-19884897	ENSG00000244306
49	lnc-POTEM-2	chr14:19923013-19923068	NONHSAT035522
50	lnc-POTEM-4	chr14:20146951-20147175	ENSG00000259069.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	POTEG	hsa-miR-26b-5p	chr14:19563442-19563464

Variant related genes	Relation type
ENSG00000259016	TF binding region
OR4K5	TF binding region
GRAMD4P3	TF binding region
ENSG00000244306	TF binding region
ENSG00000257142	TF binding region
ENSG00000258265	TF binding region
ENSG00000259069	TF binding region
OR4K4P	TF binding region
ENSG00000257884	TF binding region
ENSG00000258324	TF binding region
OR4K3	TF binding region
ARHGAP42P4	TF binding region
ENSG00000238492	TF binding region
OR4K16P	TF binding region
ENSG00000257573	TF binding region
ENSG00000257846	TF binding region
BMS1P18	TF binding region
OR11H2	TF binding region
ENSG00000257357	TF binding region
ENSG00000257868	TF binding region
OR4N2	TF binding region
ENSG00000258314	TF binding region
OR11H13P	TF binding region
ENSG00000258027	TF binding region
OR4K1	TF binding region
ENSG00000258198	TF binding region
MED15P6	TF binding region
RNU6-1239P	TF binding region
OR4M1	TF binding region
BMS1P17	TF binding region
ENSG00000258781	TF binding region
ENSG00000258252	TF binding region
NF1P4	TF binding region
OR11K2P	TF binding region
ENSG00000257891	TF binding region
ENSG00000257395	TF binding region
OR4N1P	TF binding region
ENSG00000257493	TF binding region
OR4Q3	TF binding region
ENSG00000258276	TF binding region
ENSG00000271632	TF binding region
MED15P1	TF binding region
OR4H12P	TF binding region
ENSG00000257931	TF binding region
ENSG00000257635	TF binding region
OR4K6P	TF binding region
ENSG00000225210	TF binding region
ENSG00000257310	TF binding region
GRAMD4P4	TF binding region
ENSG00000257224	TF binding region
ENSG00000257751	TF binding region
RNU6-1268P	TF binding region
ENSG00000257749	TF binding region
ENSG00000258188	TF binding region
ENSG00000257977	TF binding region
ENSG00000257432	TF binding region
POTEM	TF binding region
OR4K2	TF binding region
POTEG	TF binding region
DUXAP10	TF binding region
ENSG00000259016	CpG island
OR4K5	CpG island
GRAMD4P3	CpG island
ENSG00000244306	CpG island
ENSG00000257142	CpG island
ENSG00000258265	CpG island
ENSG00000259069	CpG island
OR4K4P	CpG island
ENSG00000257884	CpG island
ENSG00000258324	CpG island
OR4K3	CpG island
ARHGAP42P4	CpG island
ENSG00000238492	CpG island
OR4K16P	CpG island
ENSG00000257573	CpG island
ENSG00000257846	CpG island
BMS1P18	CpG island
OR11H2	CpG island
ENSG00000257357	CpG island
ENSG00000257868	CpG island
OR4N2	CpG island
ENSG00000258314	CpG island
OR11H13P	CpG island
ENSG00000258027	CpG island
OR4K1	CpG island
ENSG00000258198	CpG island
MED15P6	CpG island
RNU6-1239P	CpG island
OR4M1	CpG island
BMS1P17	CpG island
ENSG00000258781	CpG island
ENSG00000258252	CpG island
NF1P4	CpG island
OR11K2P	CpG island
ENSG00000257891	CpG island
ENSG00000257395	CpG island
OR4N1P	CpG island
ENSG00000257493	CpG island
OR4Q3	CpG island
ENSG00000258276	CpG island
ENSG00000271632	CpG island
MED15P1	CpG island
OR4H12P	CpG island
ENSG00000257931	CpG island
ENSG00000257635	CpG island
OR4K6P	CpG island
ENSG00000225210	CpG island
ENSG00000257310	CpG island
GRAMD4P4	CpG island
ENSG00000257224	CpG island
ENSG00000257751	CpG island
RNU6-1268P	CpG island
ENSG00000257749	CpG island
ENSG00000258188	CpG island
ENSG00000257977	CpG island
ENSG00000257432	CpG island
POTEM	CpG island
OR4K2	CpG island
POTEG	CpG island
DUXAP10	CpG island
ENSG00000258822	chromatin interactions
ENSG00000176290	chromatin interactions

Extended variants
information (count: 10013 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:10013 , 50 per page) page: 1 2 3 4 5 6 7 ... 201

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs60680698	chr14:19476460-19476461	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs547626676	chr14:19476467-19476468	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs566030963	chr14:19476468-19476469	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs533475528	chr14:19476476-19476477	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs551348310	chr14:19476478-19476479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs570051873	chr14:19476479-19476480	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs537103157	chr14:19476488-19476489	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs555839611	chr14:19476492-19476493	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567695184	chr14:19476493-19476494	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs370833453	chr14:19476510-19476511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs553230362	chr14:19476541-19476542	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs577985855	chr14:19476555-19476556	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs545335764	chr14:19476560-19476561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs374915854	chr14:19476563-19476564	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs556971329	chr14:19476570-19476571	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs192908730	chr14:19476577-19476578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs368121435	chr14:19476587-19476588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs149606088	chr14:19476588-19476589	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs561032738	chr14:19476590-19476591	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528220884	chr14:19476594-19476595	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs113322333	chr14:19476605-19476606	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs185326022	chr14:19476607-19476608	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs201328679	chr14:19476614-19476615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs367821392	chr14:19476647-19476648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs533414217	chr14:19476664-19476665	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs551659813	chr14:19476665-19476666	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs61969336	chr14:19476670-19476671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs569908775	chr14:19476687-19476688	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs200883530	chr14:19476700-19476701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs369469831	chr14:19476705-19476706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533600643	chr14:19478648-19478649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs558220011	chr14:19478673-19478674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs576575796	chr14:19478691-19478692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372308991	chr14:19478713-19478714	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs545558863	chr14:19478715-19478716	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs61969343	chr14:19478716-19478717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563763755	chr14:19478718-19478719	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs375526431	chr14:19478768-19478769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs575859611	chr14:19478777-19478778	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs542971823	chr14:19478784-19478785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs369942107	chr14:19478785-19478786	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs561221949	chr14:19478801-19478802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs371643622	chr14:19478920-19478921	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs528506141	chr14:19479114-19479115	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs547057328	chr14:19479120-19479121	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs565375510	chr14:19479127-19479128	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs532684758	chr14:19479129-19479130	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs550739186	chr14:19479163-19479164	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs111370249	chr14:19479358-19479359	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs376329375	chr14:19479389-19479390	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Schizophrenia	20967226	CNVD
Autism	19287141	CNVD
early-passage human iPS cells	21368824	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	17142309	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	20369283	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Incontinentia Pigmenti	22033527	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Williams Syndrome	20824207	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21509527	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19500000-19500200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:19597000-19597600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr14:19597200-19597600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:19607400-19609600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr14:19608600-19609200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr14:19610800-19612800	Weak transcription	Fetal Lung	lung
7	chr14:19611000-19611200	Enhancers	Lung	lung
8	chr14:19611200-19612800	Weak transcription	Lung	lung
9	chr14:19612600-19615200	Weak transcription	Right Atrium	heart
10	chr14:19612800-19613400	ZNF genes & repeats	Fetal Kidney	kidney
11	chr14:19612800-19613400	ZNF genes & repeats	Fetal Lung	lung
12	chr14:19612800-19613400	ZNF genes & repeats	Lung	lung
13	chr14:19613000-19613200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:19613000-19613200	ZNF genes & repeats	Gastric	stomach
15	chr14:19613000-19613200	Bivalent Enhancer	K562	blood
16	chr14:19613000-19613400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:19613000-19613400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
18	chr14:19613000-19613400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr14:19613000-19613400	ZNF genes & repeats	Fetal Brain Male	brain
20	chr14:19613000-19613400	ZNF genes & repeats	Pancreas	Pancrea
21	chr14:19613000-19615000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr14:19613400-19614200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr14:19613400-19614400	Weak transcription	Pancreas	Pancrea
24	chr14:19613400-19614600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr14:19613400-19616200	Weak transcription	Fetal Lung	lung
26	chr14:19613600-19614200	Weak transcription	Lung	lung
27	chr14:19614200-19614800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr14:19614200-19614800	Active TSS	K562	blood
29	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr14:19614400-19614800	Bivalent Enhancer	Lung	lung
32	chr14:19614400-19614800	ZNF genes & repeats	Pancreas	Pancrea
33	chr14:19614400-19615000	Bivalent/Poised TSS	A549	lung
34	chr14:19614600-19614800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:19614600-19614800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
36	chr14:19614600-19614800	Bivalent Enhancer	Right Ventricle	heart
37	chr14:19614800-19616000	Weak transcription	Pancreas	Pancrea
38	chr14:19619800-19620000	Bivalent Enhancer	A549	lung
39	chr14:19641200-19641400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr14:19641200-19641400	Enhancers	K562	blood
41	chr14:19641200-19641600	Active TSS	A549	lung
42	chr14:19641200-19641600	Active TSS	HepG2	liver
43	chr14:19641600-19642800	Weak transcription	HepG2	liver
44	chr14:19641600-19643000	Weak transcription	A549	lung
45	chr14:19642800-19643200	Enhancers	HepG2	liver
46	chr14:19643000-19643200	Enhancers	K562	blood
47	chr14:19643000-19643400	Enhancers	A549	lung
48	chr14:19649600-19650000	Active TSS	A549	lung
49	chr14:19686600-19686800	Enhancers	Placenta	Placenta
50	chr14:19761400-19761600	Enhancers	Dnd41	blood

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