Variant report

Variant	nsv1040007
Chromosome Location	chr14:19602662-20420227
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4216)
CpG islands
(count:4335)
Chromatin interactive
region (count:4)
LncRNA
region (count:224)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4216 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:20346241-20346527	K562	blood:	n/a	n/a
2	ARID3A	chr14:19614565-19614964	K562	blood:	n/a	n/a
3	ARID3A	chr14:20387153-20387455	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:20346227-20346537	HepG2	liver:	n/a	n/a
5	ATF1	chr14:19697695-19697910	K562	blood:	n/a	n/a
6	ATF1	chr14:19792967-19794009	K562	blood:	n/a	n/a
7	ATF1	chr14:19795048-19796237	K562	blood:	n/a	n/a
8	ATF1	chr14:20325048-20325100	K562	blood:	n/a	n/a
9	ATF1	chr14:20388271-20388560	K562	blood:	n/a	n/a
10	ATF1	chr14:19609027-19609227	K562	blood:	n/a	n/a
11	ATF1	chr14:19610591-19610826	K562	blood:	n/a	n/a
12	ATF1	chr14:19614523-19614771	K562	blood:	n/a	n/a
13	ATF1	chr14:20374096-20374405	K562	blood:	n/a	n/a
14	ATF1	chr14:19619825-19620010	K562	blood:	n/a	n/a
15	ATF1	chr14:20319622-20319703	K562	blood:	n/a	n/a
16	ATF3	chr14:19614578-19614850	K562	blood:	n/a	n/a
17	BACH1	chr14:19614506-19614753	K562	blood:	n/a	n/a
18	BACH1	chr14:20348120-20348235	K562	blood:	n/a	n/a
19	BACH1	chr14:19795663-19796213	K562	blood:	n/a	n/a
20	BACH1	chr14:19608951-19609223	K562	blood:	n/a	n/a
21	BATF	chr14:19827024-19827305	GM12878	blood:	n/a	n/a
22	BATF	chr14:20031700-20032016	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	chr14:19937525-19937845	GM12878	blood:	n/a	chr14:19937698-19937709
26	BATF	chr14:19637509-19637829	GM12878	blood:	n/a	chr14:19637679-19637690
27	BATF	chr14:19986920-19987123	GM12878	blood:	n/a	n/a
28	BATF	chr14:19921485-19921738	GM12878	blood:	n/a	n/a
29	BATF	chr14:20026256-20026650	GM12878	blood:	n/a	n/a
30	BATF	chr14:20025031-20025541	GM12878	blood:	n/a	n/a
31	BATF	chr14:20131255-20131487	GM12878	blood:	n/a	n/a
32	BATF	chr14:19748478-19748726	GM12878	blood:	n/a	n/a
33	BATF	chr14:19637495-19637851	GM12878	blood:	n/a	chr14:19637679-19637690
34	BATF	chr14:20025214-20025459	GM12878	blood:	n/a	n/a
35	BATF	chr14:20085953-20086237	GM12878	blood:	n/a	n/a
36	BCL11A	chr14:19653966-19654150	GM12878	blood:	n/a	n/a
37	BCL11A	chr14:19826185-19826607	GM12878	blood:	n/a	n/a
38	BCL11A	chr14:19921178-19921362	GM12878	blood:	n/a	n/a
39	BCL11A	chr14:19748843-19749025	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:19826657-19827003	GM12878	blood:	n/a	n/a
41	BCL11A	chr14:19827491-19827723	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:19819837-19820033	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:19637542-19637751	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:19937603-19937812	GM12878	blood:	n/a	n/a
45	BCL11A	chr14:19821581-19821893	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:19827039-19827376	GM12878	blood:	n/a	n/a
47	BCL11A	chr14:19637480-19637880	GM12878	blood:	n/a	n/a
48	BCL11A	chr14:19829015-19829207	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:19920793-19920958	GM12878	blood:	n/a	n/a
50	BCL11A	chr14:20084307-20084477	GM12878	blood:	n/a	n/a

(count:4335 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20404281-20404331	NH-A	brain:	n/a
2	chr14:19949555-19949605	PFSK-1	brain:	n/a
3	chr14:20020024-20020074	HNPCEpiC	eye:	n/a
4	chr14:19626001-19626051	HMEC	breast:	n/a
5	chr14:20404281-20404331	NH-A	brain:	n/a
6	chr14:19949555-19949605	PFSK-1	brain:	n/a
7	chr14:20020024-20020074	HNPCEpiC	eye:	n/a
8	chr14:19626001-19626051	HMEC	breast:	n/a
9	chr14:20148103-20148153	HepG2	liver:	n/a
10	chr14:19686670-19686720	HCPEpiC	choroid plexus:	n/a
11	chr14:19959522-19959572	HCT-116	colon:	n/a
12	chr14:19858845-19858895	AG04450	lung:	fetal
13	chr14:20020657-20020707	CMK	blood:	n/a
14	chr14:20137365-20137415	RPTEC	kidney:	n/a
15	chr14:20247697-20247747	GM12892	blood:	n/a
16	chr14:20403845-20403895	HPAEpiC	pulmonary alveolar:	n/a
17	chr14:19829406-19829456	SK-N-SH_RA	brain:	n/a
18	chr14:20344083-20344133	HRPEpiC	eye:	n/a
19	chr14:19719117-19719167	SK-N-MC	brain:	n/a
20	chr14:19964024-19964074	HAEpiC	amniotic membrane:	n/a
21	chr14:19855384-19855434	GM12891	blood:	n/a
22	chr14:19959522-19959572	SK-N-SH	brain:	n/a
23	chr14:19686672-19686722	MCF-7	breast:	n/a
24	chr14:20137365-20137415	HPAEpiC	pulmonary alveolar:	n/a
25	chr14:20136693-20136743	SK-N-SH	brain:	n/a
26	chr14:19960976-19961026	PANC-1	pancreas:	n/a
27	chr14:19614541-19614591	HRPEpiC	eye:	n/a
28	chr14:20012038-20012088	MCF10A-Er-Src	breast:	n/a
29	chr14:20148125-20148175	AG04450	lung:	fetal
30	chr14:19602855-19602905	Jurkat	blood:	n/a
31	chr14:19949555-19949605	HMEC	breast:	n/a
32	chr14:20012038-20012088	GM12892	blood:	n/a
33	chr14:19959522-19959572	T-47D	breast:	n/a
34	chr14:20136822-20136872	AG04449	skin:	fetal
35	chr14:20147187-20147237	AG09309	skin:	n/a
36	chr14:19747134-19747184	PrEC	prostate:	n/a
37	chr14:19925080-19925130	HL-60	blood:	n/a
38	chr14:19959522-19959572	K562	blood:	n/a
39	chr14:19932946-19932996	BE2_C	brain:	n/a
40	chr14:19858845-19858895	GM06990	blood:	n/a
41	chr14:20020024-20020074	NT2-D1	testis:	n/a
42	chr14:19641452-19641502	HMEC	breast:	n/a
43	chr14:19960976-19961026	SK-N-SH	brain:	n/a
44	chr14:19719837-19719887	GM12891	blood:	n/a
45	chr14:19686155-19686205	HCM	heart:	n/a
46	chr14:19614541-19614591	HEEpiC	esophagus:	n/a
47	chr14:19858845-19858895	H1-hESC	embryonic stem cell:	embryo
48	chr14:20139478-20139528	NH-A	brain:	n/a
49	chr14:19614829-19614879	AG04450	lung:	fetal
50	chr14:19829406-19829456	HCM	heart:	n/a

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

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

(count:224 , 50 per page) page: 1 2 3 4 5

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEG-4	chr14:19680595-19680685	ENSG00000225210
2	lnc-POTEM-2	chr14:19856964-19857070	NONHSAT035499
3	lnc-POTEG-3	chr14:19605328-19606529	NONHSAT035465
4	lnc-POTEG-4	chr14:19653908-19654004	ENSG00000225210
5	lnc-POTEM-7	chr14:19678513-19678600	ENSG00000228294
6	lnc-POTEG-4	chr14:19655734-19655871	NR_110526
7	lnc-POTEG-3	chr14:19606385-19606529	ENSG00000258314
8	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
9	lnc-POTEG-4	chr14:19680595-19680685	NONHSAT035478
10	lnc-OR4N2-4	chr14:19894369-19894691	XLOC_010749
11	lnc-POTEG-3	chr14:19646572-19646644	NONHSAT035469
12	lnc-POTEG-3	chr14:19619448-19619513	NONHSAT035465
13	lnc-POTEG-4	chr14:19653625-19653710	NONHSAT035478
14	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
15	lnc-POTEG-4	chr14:19656089-19656224	NR_110526
16	lnc-POTEM-7	chr14:19673473-19673623	ENSG00000228294
17	lnc-POTEG-4	chr14:19691355-19691404	NONHSAT035478
18	lnc-POTEG-4	chr14:19655734-19655871	ENSG00000225210
19	lnc-OR4N2-4	chr14:19896785-19896872	XLOC_010749
20	lnc-POTEM-2	chr14:19925240-19925294	NONHSAT035522
21	lnc-POTEG-4	chr14:19650061-19650126	ENSG00000225210
22	lnc-POTEG-3	chr14:19619448-19619513	ENSG00000258314
23	lnc-POTEG-4	chr14:19652244-19652358	ENSG00000225210
24	lnc-POTEG-4	chr14:19656089-19656210	ENSG00000225210
25	lnc-POTEM-7	chr14:19670480-19671105	ENSG00000228294
26	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT035521
27	lnc-POTEM-2	chr14:19894700-19894790	ENSG00000244306
28	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
29	lnc-POTEM-2	chr14:19919138-19919273	ENSG00000244306
30	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT140152
31	lnc-POTEG-4	chr14:19655758-19655871	ENSG00000225210
32	lnc-POTEG-4	chr14:19680595-19680685	ENSG00000225210
33	lnc-POTEG-5	chr14:19859457-19859970	ENSG00000258188.1
34	lnc-POTEG-4	chr14:19655782-19655871	ENSG00000225210
35	lnc-POTEM-2	chr14:19919492-19919629	NONHSAT035521
36	lnc-POTEG-4	chr14:19652244-19652354	ENSG00000225210
37	lnc-POTEM-1	chr14:19932012-19932316	ENSG00000257931.2
38	lnc-POTEM-2	chr14:19893856-19894790	ENSG00000244306
39	lnc-POTEM-12	chr14:19806437-19807415	NONHSAT035495
40	lnc-POTEM-2	chr14:19882464-19884029	ENSG00000244306
41	lnc-POTEG-4	chr14:19653893-19654004	NR_110526
42	lnc-POTEM-2	chr14:19925240-19925311	ENSG00000244306
43	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
44	lnc-POTEM-2	chr14:19925240-19925288	ENSG00000244306
45	lnc-POTEM-2	chr14:19880209-19884029	NONHSAT035503
46	lnc-POTEG-3	chr14:19643072-19643377	ENSG00000258314.2
47	lnc-POTEM-1	chr14:19932012-19932316	ENSG00000257931
48	lnc-POTEG-4	chr14:19650021-19650126	ENSG00000225210
49	lnc-POTEG-4	chr14:19653893-19654004	NONHSAT035478
50	lnc-POTEM-2	chr14:19892138-19892361	ENSG00000244306

No data

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
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
OR4M1	TF binding region
BMS1P17	TF binding region
ENSG00000258781	TF binding region
OR11K2P	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
OR4H12P	TF binding region
ENSG00000257931	TF binding region
OR4K6P	TF binding region
ENSG00000225210	TF binding region
ENSG00000257310	TF binding region
GRAMD4P4	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
DUXAP10	TF binding region
ENSG00000259016	CpG island
OR4K5	CpG island
GRAMD4P3	CpG island
ENSG00000244306	CpG island
ENSG00000257142	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
OR4M1	CpG island
BMS1P17	CpG island
ENSG00000258781	CpG island
OR11K2P	CpG island
ENSG00000257395	CpG island
OR4N1P	CpG island
ENSG00000257493	CpG island
OR4Q3	CpG island
ENSG00000258276	CpG island
ENSG00000271632	CpG island
OR4H12P	CpG island
ENSG00000257931	CpG island
OR4K6P	CpG island
ENSG00000225210	CpG island
ENSG00000257310	CpG island
GRAMD4P4	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
DUXAP10	CpG island
ENSG00000176290	chromatin interactions

Extended variants
information (count: 9365 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:9365 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532865440	chr14:19602828-19602829	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs146640808	chr14:19602840-19602841	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs544164214	chr14:19602863-19602864	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs370621817	chr14:19602871-19602872	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs562525880	chr14:19602922-19602923	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs371205400	chr14:19603229-19603230	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs376175431	chr14:19603241-19603242	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs201450749	chr14:19603269-19603270	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs555905212	chr14:19605365-19605366	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs564285358	chr14:19605397-19605398	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs199970343	chr14:19605400-19605401	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs145678576	chr14:19605411-19605412	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs200937803	chr14:19605424-19605425	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs201617389	chr14:19605435-19605436	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs556645397	chr14:19605484-19605485	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs56196262	chr14:19605486-19605487	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs202007559	chr14:19605495-19605496	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs372051547	chr14:19605501-19605502	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs531584900	chr14:19605622-19605623	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs550091432	chr14:19605633-19605634	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs568375297	chr14:19605647-19605648	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs200272346	chr14:19605682-19605683	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs535396003	chr14:19605707-19605708	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs547393943	chr14:19605708-19605709	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs77474668	chr14:19605709-19605710	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs367548838	chr14:19605721-19605722	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs565607476	chr14:19605745-19605746	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs144508852	chr14:19605791-19605792	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs374821368	chr14:19605798-19605799	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs539501766	chr14:19605805-19605806	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs557594234	chr14:19605817-19605818	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs577362708	chr14:19605849-19605850	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs28469010	chr14:19605908-19605909	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs538088958	chr14:19605921-19605922	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs556398087	chr14:19605936-19605937	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs574793440	chr14:19605961-19605962	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs541791975	chr14:19605964-19605965	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs77713581	chr14:19605967-19605968	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs201674005	chr14:19605986-19605987	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs554151968	chr14:19606004-19606005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs28455991	chr14:19606039-19606040	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs546275491	chr14:19606040-19606041	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs187762149	chr14:19606042-19606043	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs192475236	chr14:19606054-19606055	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs376405730	chr14:19606058-19606059	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs200107260	chr14:19606086-19606087	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs2716302	chr14:19606099-19606100	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs369637062	chr14:19606128-19606129	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs202115756	chr14:19606153-19606154	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs201363241	chr14:19606162-19606163	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Urothelial carcinoma	21177765	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	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
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	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:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19607400-19609600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr14:19608600-19609200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr14:19610800-19612800	Weak transcription	Fetal Lung	lung
4	chr14:19611000-19611200	Enhancers	Lung	lung
5	chr14:19611200-19612800	Weak transcription	Lung	lung
6	chr14:19612600-19615200	Weak transcription	Right Atrium	heart
7	chr14:19612800-19613400	ZNF genes & repeats	Fetal Kidney	kidney
8	chr14:19612800-19613400	ZNF genes & repeats	Fetal Lung	lung
9	chr14:19612800-19613400	ZNF genes & repeats	Lung	lung
10	chr14:19613000-19613200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:19613000-19613200	ZNF genes & repeats	Gastric	stomach
12	chr14:19613000-19613200	Bivalent Enhancer	K562	blood
13	chr14:19613000-19613400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr14:19613000-19613400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
15	chr14:19613000-19613400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr14:19613000-19613400	ZNF genes & repeats	Fetal Brain Male	brain
17	chr14:19613000-19613400	ZNF genes & repeats	Pancreas	Pancrea
18	chr14:19613000-19615000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:19613400-19614200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr14:19613400-19614400	Weak transcription	Pancreas	Pancrea
21	chr14:19613400-19614600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr14:19613400-19616200	Weak transcription	Fetal Lung	lung
23	chr14:19613600-19614200	Weak transcription	Lung	lung
24	chr14:19614200-19614800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:19614200-19614800	Active TSS	K562	blood
26	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:19614400-19614800	Bivalent Enhancer	Lung	lung
29	chr14:19614400-19614800	ZNF genes & repeats	Pancreas	Pancrea
30	chr14:19614400-19615000	Bivalent/Poised TSS	A549	lung
31	chr14:19614600-19614800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr14:19614600-19614800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
33	chr14:19614600-19614800	Bivalent Enhancer	Right Ventricle	heart
34	chr14:19614800-19616000	Weak transcription	Pancreas	Pancrea
35	chr14:19619800-19620000	Bivalent Enhancer	A549	lung
36	chr14:19641200-19641400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr14:19641200-19641400	Enhancers	K562	blood
38	chr14:19641200-19641600	Active TSS	A549	lung
39	chr14:19641200-19641600	Active TSS	HepG2	liver
40	chr14:19641600-19642800	Weak transcription	HepG2	liver
41	chr14:19641600-19643000	Weak transcription	A549	lung
42	chr14:19642800-19643200	Enhancers	HepG2	liver
43	chr14:19643000-19643200	Enhancers	K562	blood
44	chr14:19643000-19643400	Enhancers	A549	lung
45	chr14:19649600-19650000	Active TSS	A549	lung
46	chr14:19686600-19686800	Enhancers	Placenta	Placenta
47	chr14:19761400-19761600	Enhancers	Dnd41	blood
48	chr14:19763800-19764600	Weak transcription	Dnd41	blood
49	chr14:19764600-19764800	Enhancers	Dnd41	blood
50	chr14:19764800-19766400	Weak transcription	Dnd41	blood

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