Variant report

Variant	nsv1035979
Chromosome Location	chr14:19438599-20420227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4849)
CpG islands
(count:4766)
Chromatin interactive
region (count:4)
LncRNA
region (count:252)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4849 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:19614565-19614964	K562	blood:	n/a	n/a
3	ARID3A	chr14:20346241-20346527	K562	blood:	n/a	n/a
4	ARID3A	chr14:20346227-20346537	HepG2	liver:	n/a	n/a
5	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
6	ATF1	chr14:19609027-19609227	K562	blood:	n/a	n/a
7	ATF1	chr14:19697695-19697910	K562	blood:	n/a	n/a
8	ATF1	chr14:20319622-20319703	K562	blood:	n/a	n/a
9	ATF1	chr14:19461425-19461537	K562	blood:	n/a	n/a
10	ATF1	chr14:19464826-19465023	K562	blood:	n/a	n/a
11	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
12	ATF1	chr14:19792967-19794009	K562	blood:	n/a	n/a
13	ATF1	chr14:19614523-19614771	K562	blood:	n/a	n/a
14	ATF1	chr14:19462190-19462538	K562	blood:	n/a	n/a
15	ATF1	chr14:19795048-19796237	K562	blood:	n/a	n/a
16	ATF1	chr14:20325048-20325100	K562	blood:	n/a	n/a
17	ATF1	chr14:19450073-19450214	K562	blood:	n/a	n/a
18	ATF1	chr14:19610591-19610826	K562	blood:	n/a	n/a
19	ATF1	chr14:19619825-19620010	K562	blood:	n/a	n/a
20	ATF3	chr14:19614578-19614850	K562	blood:	n/a	n/a
21	BACH1	chr14:19462184-19462510	K562	blood:	n/a	n/a
22	BACH1	chr14:19438368-19438886	K562	blood:	n/a	n/a
23	BACH1	chr14:19614506-19614753	K562	blood:	n/a	n/a
24	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
25	BACH1	chr14:19464051-19464239	K562	blood:	n/a	n/a
26	BACH1	chr14:19795663-19796213	K562	blood:	n/a	n/a
27	BACH1	chr14:19608951-19609223	K562	blood:	n/a	n/a
28	BATF	chr14:19541408-19541756	GM12878	blood:	n/a	n/a
29	BATF	chr14:19653590-19653843	GM12878	blood:	n/a	n/a
30	BATF	chr14:20085953-20086237	GM12878	blood:	n/a	n/a
31	BATF	chr14:19548118-19548363	GM12878	blood:	n/a	n/a
32	BATF	chr14:20131255-20131487	GM12878	blood:	n/a	n/a
33	BATF	chr14:19827024-19827305	GM12878	blood:	n/a	n/a
34	BATF	chr14:19541484-19541694	GM12878	blood:	n/a	n/a
35	BATF	chr14:19637495-19637851	GM12878	blood:	n/a	chr14:19637679-19637690
36	BATF	chr14:19921485-19921738	GM12878	blood:	n/a	n/a
37	BATF	chr14:20026256-20026650	GM12878	blood:	n/a	n/a
38	BATF	chr14:20025214-20025459	GM12878	blood:	n/a	n/a
39	BATF	chr14:19986920-19987123	GM12878	blood:	n/a	n/a
40	BATF	chr14:19637509-19637829	GM12878	blood:	n/a	chr14:19637679-19637690
41	BATF	chr14:19546952-19547321	GM12878	blood:	n/a	n/a
42	BATF	chr14:19937503-19937859	GM12878	blood:	n/a	chr14:19937698-19937709
43	BATF	chr14:19937525-19937845	GM12878	blood:	n/a	chr14:19937698-19937709
44	BATF	chr14:19487460-19487744	GM12878	blood:	n/a	n/a
45	BATF	chr14:19586478-19586681	GM12878	blood:	n/a	n/a
46	BATF	chr14:20031700-20032016	GM12878	blood:	n/a	n/a
47	BATF	chr14:19748478-19748726	GM12878	blood:	n/a	n/a
48	BATF	chr14:19548036-19548546	GM12878	blood:	n/a	n/a
49	BATF	chr14:20025031-20025541	GM12878	blood:	n/a	n/a
50	BCL11A	chr14:19821581-19821893	GM12878	blood:	n/a	n/a

(count:4766 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19614829-19614879	AG09309	skin:	n/a
2	chr14:20012038-20012088	NHBE	bronchial:	n/a
3	chr14:20215980-20216030	AG04449	skin:	fetal
4	chr14:19746900-19746950	HNPCEpiC	eye:	n/a
5	chr14:19887082-19887132	SK-N-SH_RA	brain:	n/a
6	chr14:19855384-19855434	H1-hESC	embryonic stem cell:	embryo
7	chr14:20020024-20020074	NH-A	brain:	n/a
8	chr14:19625820-19625870	AG09319	gingival:	n/a
9	chr14:19614829-19614879	AG09309	skin:	n/a
10	chr14:20012038-20012088	NHBE	bronchial:	n/a
11	chr14:20215980-20216030	AG04449	skin:	fetal
12	chr14:19746900-19746950	HNPCEpiC	eye:	n/a
13	chr14:19887082-19887132	SK-N-SH_RA	brain:	n/a
14	chr14:19855384-19855434	H1-hESC	embryonic stem cell:	embryo
15	chr14:20020024-20020074	NH-A	brain:	n/a
16	chr14:19625820-19625870	AG09319	gingival:	n/a
17	chr14:19643599-19643649	AG04449	skin:	fetal
18	chr14:20137365-20137415	ProgFib	skin:	n/a
19	chr14:20295616-20295666	NB4	blood:	n/a
20	chr14:19625154-19625204	AG04450	lung:	fetal
21	chr14:20147652-20147702	BJ	skin:	n/a
22	chr14:19888327-19888377	BJ	skin:	n/a
23	chr14:20215980-20216030	Caco-2	colon:	n/a
24	chr14:20147652-20147702	MCF10A-Er-Src	breast:	n/a
25	chr14:20295005-20295055	HCF	heart:	n/a
26	chr14:19962440-19962490	AoSMC	blood vessel:	n/a
27	chr14:19925080-19925130	SK-N-MC	brain:	n/a
28	chr14:20148125-20148175	GM19239	blood:	n/a
29	chr14:19888327-19888377	A549	lung:	n/a
30	chr14:19626001-19626051	SK-N-SH_RA	brain:	n/a
31	chr14:20020762-20020812	Caco-2	colon:	n/a
32	chr14:19626001-19626051	AoSMC	blood vessel:	n/a
33	chr14:19950047-19950097	T-47D	breast:	n/a
34	chr14:19614541-19614591	HRE	kidney:	n/a
35	chr14:19719117-19719167	Hela-S3	cervix:	n/a
36	chr14:20136693-20136743	H1-hESC	embryonic stem cell:	embryo
37	chr14:20135228-20135278	ProgFib	skin:	n/a
38	chr14:19602855-19602905	MCF10A-Er-Src	breast:	n/a
39	chr14:20403239-20403289	SKMC	muscle:	n/a
40	chr14:19625154-19625204	SK-N-SH_RA	brain:	n/a
41	chr14:19625820-19625870	HepG2	liver:	n/a
42	chr14:19888327-19888377	HCPEpiC	choroid plexus:	n/a
43	chr14:19600442-19600492	AG04450	lung:	fetal
44	chr14:19597077-19597127	MCF10A-Er-Src	breast:	n/a
45	chr14:19890087-19890137	HEK293	kidney:	embryo
46	chr14:20403239-20403289	HNPCEpiC	eye:	n/a
47	chr14:19614829-19614879	HRE	kidney:	n/a
48	chr14:20403239-20403289	GM19239	blood:	n/a
49	chr14:19626001-19626051	ECC-1	luminal epithelium:	n/a
50	chr14:20136822-20136872	PFSK-1	brain:	n/a

(count:4 , 50 per page) page: 1

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

(count:252 , 50 per page) page: 1 2 3 4 5 6

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEG-4	chr14:19680591-19680685	ENSG00000225210
2	lnc-POTEG-4	chr14:19650061-19650126	ENSG00000225210
3	lnc-POTEM-2	chr14:19894700-19894794	ENSG00000244306
4	lnc-POTEG-4	chr14:19683692-19684834	ENSG00000225210
5	lnc-POTEG-4	chr14:19650060-19650126	ENSG00000225210
6	lnc-POTEM-2	chr14:19925240-19925300	ENSG00000244306
7	lnc-POTEG-4	chr14:19691355-19691701	ENSG00000225210
8	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT140152
9	lnc-POTEG-3	chr14:19639008-19639483	NONHSAT035465
10	lnc-POTEM-3	chr14:19858667-19861377	ENSG00000249549
11	lnc-POTEG-4	chr14:19691355-19692916	NR_110526
12	lnc-POTEM-8	chr14:19563712-19564808	NR_046571
13	lnc-POTEM-12	chr14:19806437-19807415	NONHSAT035495
14	lnc-POTEG-4	chr14:19650021-19650126	ENSG00000225210
15	lnc-OR4N2-4	chr14:19894369-19894691	ENSG00000215394
16	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
17	lnc-POTEM-2	chr14:19884775-19884897	ENSG00000244306
18	lnc-POTEM-2	chr14:19883543-19884029	ENSG00000244306
19	lnc-OR4N2-3	chr14:20008836-20010958	ENSG00000258276
20	lnc-POTEG-4	chr14:19680595-19681519	ENSG00000225210
21	lnc-POTEM-1	chr14:19955880-19955945	ENSG00000257931
22	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT035520
23	lnc-POTEG-4	chr14:19650055-19650126	ENSG00000225210
24	lnc-POTEM-6	chr14:19887445-19887497	ENSG00000257898.1
25	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT140152
26	lnc-POTEM-2	chr14:19872436-19872514	ENSG00000244306
27	lnc-POTEM-2	chr14:19925240-19925345	ENSG00000244306
28	lnc-POTEG-4	chr14:19650021-19650126	ENSG00000225210
29	lnc-POTEG-3	chr14:19630574-19630835	NONHSAT035465
30	lnc-OR4N2-3	chr14:20006913-20007358	NR_110505
31	lnc-POTEG-4	chr14:19652244-19652354	NR_110526
32	lnc-POTEM-2	chr14:19925240-19925332	ENSG00000244306
33	lnc-OR4N2-1	chr14:20150010-20150118	ENSG00000257395
34	lnc-POTEG-4	chr14:19653893-19654004	ENSG00000225210
35	lnc-POTEM-2	chr14:19925240-19925334	NR_110526
36	lnc-POTEG-4	chr14:19656089-19656224	ENSG00000225210
37	lnc-POTEM-1	chr14:19944559-19944820	ENSG00000257931
38	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
39	lnc-POTEG-7	chr14:19595933-19596023	NONHSAT035463
40	lnc-POTEM-2	chr14:19921591-19921705	NONHSAT035520
41	lnc-POTEM-2	chr14:19921359-19921390	NONHSAT035499
42	lnc-POTEM-2	chr14:19919492-19919629	NR_110526
43	lnc-POTEG-4	chr14:19650061-19650126	ENSG00000225210
44	lnc-POTEG-4	chr14:19650032-19650126	NR_110526
45	lnc-POTEG-4	chr14:19680595-19680685	ENSG00000225210
46	lnc-POTEG-4	chr14:19653893-19654004	NR_110526
47	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
48	lnc-POTEM-7	chr14:19670480-19671105	ENSG00000228294
49	lnc-POTEM-2	chr14:19880596-19880882	ENSG00000244306
50	lnc-POTEM-2	chr14:19912015-19913438	ENSG00000244306

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
ENSG00000257558	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
ENSG00000239200	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
ENSG00000257558	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
ENSG00000239200	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
ENSG00000176290	chromatin interactions

Extended variants
information (count: 10121 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:10121 , 50 per page) page: 1 2 3 4 5 6 7 ... 203

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552553173	chr14:19438615-19438616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs577005789	chr14:19438636-19438637	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs537884600	chr14:19438645-19438646	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs555955661	chr14:19438674-19438675	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs568161254	chr14:19438752-19438753	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs28655231	chr14:19438771-19438772	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs536405526	chr14:19438791-19438792	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs28628467	chr14:19438793-19438794	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs368846410	chr14:19438795-19438796	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs28605984	chr14:19438800-19438801	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs554744091	chr14:19438836-19438837	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs573147680	chr14:19438843-19438844	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs540513942	chr14:19438900-19438901	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs28540056	chr14:19438914-19438915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs559236001	chr14:19438922-19438923	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs112894871	chr14:19438980-19438981	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs28583759	chr14:19439006-19439007	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs189395682	chr14:19439029-19439030	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs28706434	chr14:19439030-19439031	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs544617438	chr14:19439046-19439047	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs28737273	chr14:19439067-19439068	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs562808026	chr14:19439068-19439069	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs530228849	chr14:19439086-19439087	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs368279398	chr14:19439109-19439110	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs181387232	chr14:19439124-19439125	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs560388560	chr14:19439134-19439135	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs112965624	chr14:19439149-19439150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs527524341	chr14:19439153-19439154	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs552487887	chr14:19439154-19439155	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs570753921	chr14:19439191-19439192	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs372157774	chr14:19439512-19439513	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs537810213	chr14:19439530-19439531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs556525481	chr14:19439531-19439532	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs574934629	chr14:19439646-19439647	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs542335962	chr14:19439647-19439648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs112350946	chr14:19439684-19439685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs371308971	chr14:19439699-19439700	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs560606571	chr14:19439733-19439734	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs142845257	chr14:19439756-19439757	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs200978278	chr14:19439787-19439788	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs28562403	chr14:19441681-19441682	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200270610	chr14:19441689-19441690	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568721806	chr14:19441737-19441738	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs374780898	chr14:19441781-19441782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs117187404	chr14:19441831-19441832	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs201363031	chr14:19441834-19441835	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs115800344	chr14:19441847-19441848	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs60801548	chr14:19441848-19441849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs376433001	chr14:19441849-19441850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs371143192	chr14:19441850-19441851	Inactive region	TF binding region	1 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
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	21293372	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
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

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19435400-19439200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr14:19444400-19444800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr14:19444400-19445200	ZNF genes & repeats	Fetal Lung	lung
4	chr14:19444400-19445800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr14:19444400-19446000	Active TSS	Fetal Heart	heart
6	chr14:19445000-19445200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr14:19462400-19462800	ZNF genes & repeats	Fetal Kidney	kidney
8	chr14:19500000-19500200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:19597000-19597600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:19597200-19597600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:19607400-19609600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr14:19608600-19609200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr14:19610800-19612800	Weak transcription	Fetal Lung	lung
14	chr14:19611000-19611200	Enhancers	Lung	lung
15	chr14:19611200-19612800	Weak transcription	Lung	lung
16	chr14:19612600-19615200	Weak transcription	Right Atrium	heart
17	chr14:19612800-19613400	ZNF genes & repeats	Fetal Kidney	kidney
18	chr14:19612800-19613400	ZNF genes & repeats	Fetal Lung	lung
19	chr14:19612800-19613400	ZNF genes & repeats	Lung	lung
20	chr14:19613000-19613200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr14:19613000-19613200	ZNF genes & repeats	Gastric	stomach
22	chr14:19613000-19613200	Bivalent Enhancer	K562	blood
23	chr14:19613000-19613400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr14:19613000-19613400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
25	chr14:19613000-19613400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr14:19613000-19613400	ZNF genes & repeats	Fetal Brain Male	brain
27	chr14:19613000-19613400	ZNF genes & repeats	Pancreas	Pancrea
28	chr14:19613000-19615000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr14:19613400-19614200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr14:19613400-19614400	Weak transcription	Pancreas	Pancrea
31	chr14:19613400-19614600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr14:19613400-19616200	Weak transcription	Fetal Lung	lung
33	chr14:19613600-19614200	Weak transcription	Lung	lung
34	chr14:19614200-19614800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr14:19614200-19614800	Active TSS	K562	blood
36	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr14:19614400-19614800	Bivalent Enhancer	Lung	lung
39	chr14:19614400-19614800	ZNF genes & repeats	Pancreas	Pancrea
40	chr14:19614400-19615000	Bivalent/Poised TSS	A549	lung
41	chr14:19614600-19614800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr14:19614600-19614800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
43	chr14:19614600-19614800	Bivalent Enhancer	Right Ventricle	heart
44	chr14:19614800-19616000	Weak transcription	Pancreas	Pancrea
45	chr14:19619800-19620000	Bivalent Enhancer	A549	lung
46	chr14:19641200-19641400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr14:19641200-19641400	Enhancers	K562	blood
48	chr14:19641200-19641600	Active TSS	A549	lung
49	chr14:19641200-19641600	Active TSS	HepG2	liver
50	chr14:19641600-19642800	Weak transcription	HepG2	liver

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