Variant report

Variant	nsv563609
Chromosome Location	chr14:19344858-19612853
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:915)
CpG islands
(count:915)
Chromatin interactive
region (count:0)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:19450073-19450214	K562	blood:	n/a	n/a
2	ATF1	chr14:19610591-19610826	K562	blood:	n/a	n/a
3	ATF1	chr14:19461425-19461537	K562	blood:	n/a	n/a
4	ATF1	chr14:19609027-19609227	K562	blood:	n/a	n/a
5	ATF1	chr14:19436953-19437483	K562	blood:	n/a	n/a
6	ATF1	chr14:19464826-19465023	K562	blood:	n/a	n/a
7	ATF1	chr14:19462190-19462538	K562	blood:	n/a	n/a
8	BACH1	chr14:19464051-19464239	K562	blood:	n/a	n/a
9	BACH1	chr14:19608951-19609223	K562	blood:	n/a	n/a
10	BACH1	chr14:19462184-19462510	K562	blood:	n/a	n/a
11	BACH1	chr14:19438368-19438886	K562	blood:	n/a	n/a
12	BATF	chr14:19541408-19541756	GM12878	blood:	n/a	n/a
13	BATF	chr14:19586478-19586681	GM12878	blood:	n/a	n/a
14	BATF	chr14:19487460-19487744	GM12878	blood:	n/a	n/a
15	BATF	chr14:19548036-19548546	GM12878	blood:	n/a	n/a
16	BATF	chr14:19546952-19547321	GM12878	blood:	n/a	n/a
17	BATF	chr14:19541484-19541694	GM12878	blood:	n/a	n/a
18	BATF	chr14:19548118-19548363	GM12878	blood:	n/a	n/a
19	BCL11A	chr14:19488926-19489115	GM12878	blood:	n/a	n/a
20	BCL11A	chr14:19352644-19352904	GM12878	blood:	n/a	n/a
21	BCL11A	chr14:19548084-19548501	GM12878	blood:	n/a	chr14:19548252-19548261
22	BHLHE40	chr14:19458927-19459003	K562	blood:	n/a	n/a
23	BHLHE40	chr14:19457659-19457916	K562	blood:	n/a	chr14:19457829-19457838
24	BHLHE40	chr14:19597673-19597903	HepG2	liver:	n/a	n/a
25	BHLHE40	chr14:19594736-19594966	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:19461190-19461447	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:19489607-19489939	K562	blood:	n/a	n/a
28	CEBPB	chr14:19489602-19489933	IMR90	lung:	n/a	n/a
29	CEBPB	chr14:19491543-19491896	K562	blood:	n/a	chr14:19491752-19491761 chr14:19491752-19491761 chr14:19491752-19491761
30	CEBPB	chr14:19489600-19489962	A549	lung:	n/a	n/a
31	CTCF	chr14:19562844-19562904	Lung_OC	lung:	n/a	n/a
32	CTCF	chr14:19363353-19363445	Pancreas_OC	pancreas:	n/a	n/a
33	CTCF	chr14:19422635-19423093	K562	blood:	n/a	n/a
34	CTCF	chr14:19400940-19401090	GM12869	blood:	n/a	n/a
35	CTCF	chr14:19393162-19393281	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr14:19360012-19360088	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr14:19408475-19408480	GM10248	blood:	n/a	n/a
38	CTCF	chr14:19601480-19601630	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr14:19360020-19360111	GM10248	blood:	n/a	n/a
40	CTCF	chr14:19445000-19445150	HEK293	kidney:	n/a	n/a
41	CTCF	chr14:19421674-19421788	MCF-7	breast:	n/a	chr14:19421768-19421786 chr14:19421768-19421781 chr14:19421769-19421785 chr14:19421771-19421784
42	CTCF	chr14:19601373-19601694	A549	lung:	n/a	n/a
43	CTCF	chr14:19503380-19503886	K562	blood:	n/a	chr14:19503599-19503612
44	CTCF	chr14:19567660-19567810	GM12864	blood:	n/a	n/a
45	CTCF	chr14:19393052-19393293	K562	blood:	n/a	n/a
46	CTCF	chr14:19552360-19552510	HepG2	liver:	n/a	chr14:19552377-19552386
47	CTCF	chr14:19404984-19404999	Medullo	brain:	n/a	n/a
48	CTCF	chr14:19379050-19379121	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr14:19360050-19360132	GM20000	blood:	n/a	n/a
50	CTCF	chr14:19597476-19598004	K562	blood:	n/a	chr14:19597769-19597785

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19562827-19562877	HUVEC	blood vessel:	n/a
2	chr14:19413192-19413242	HCM	heart:	n/a
3	chr14:19360878-19360928	SK-N-SH_RA	brain:	n/a
4	chr14:19360878-19360928	Hepatocyte	liver:	n/a
5	chr14:19413192-19413242	ovcar-3	ovarian:	n/a
6	chr14:19602149-19602199	H1-hESC	embryonic stem cell:	embryo
7	chr14:19597077-19597127	HCM	heart:	n/a
8	chr14:19377109-19377159	Hela-S3	cervix:	n/a
9	chr14:19413192-19413242	GM12892	blood:	n/a
10	chr14:19602149-19602199	HRPEpiC	eye:	n/a
11	chr14:19602855-19602905	Hela-S3	cervix:	n/a
12	chr14:19597077-19597127	Jurkat	blood:	n/a
13	chr14:19360878-19360928	Jurkat	blood:	n/a
14	chr14:19413192-19413242	HRE	kidney:	n/a
15	chr14:19402845-19402895	NHBE	bronchial:	n/a
16	chr14:19360467-19360517	RPTEC	kidney:	n/a
17	chr14:19402845-19402895	PFSK-1	brain:	n/a
18	chr14:19360878-19360928	AG04449	skin:	fetal
19	chr14:19422337-19422387	HNPCEpiC	eye:	n/a
20	chr14:19360467-19360517	SKMC	muscle:	n/a
21	chr14:19413192-19413242	HRPEpiC	eye:	n/a
22	chr14:19600442-19600492	NHBE	bronchial:	n/a
23	chr14:19360467-19360517	HUVEC	blood vessel:	n/a
24	chr14:19413192-19413242	Jurkat	blood:	n/a
25	chr14:19585143-19585193	GM12878	blood:	n/a
26	chr14:19602855-19602905	AG09319	gingival:	n/a
27	chr14:19600442-19600492	H1-hESC	embryonic stem cell:	embryo
28	chr14:19597077-19597127	HUVEC	blood vessel:	n/a
29	chr14:19422337-19422387	NT2-D1	testis:	n/a
30	chr14:19602149-19602199	HepG2	liver:	n/a
31	chr14:19413192-19413242	MCF10A-Er-Src	breast:	n/a
32	chr14:19422337-19422387	AG04449	skin:	fetal
33	chr14:19402845-19402895	BE2_C	brain:	n/a
34	chr14:19597077-19597127	HL-60	blood:	n/a
35	chr14:19422337-19422387	LNCaP	prostate:	n/a
36	chr14:19422337-19422387	HCT-116	colon:	n/a
37	chr14:19377109-19377159	SAEC	small airway:	n/a
38	chr14:19421688-19421738	AoSMC	blood vessel:	n/a
39	chr14:19597077-19597127	GM12878	blood:	n/a
40	chr14:19597077-19597127	K562	blood:	n/a
41	chr14:19360878-19360928	RPTEC	kidney:	n/a
42	chr14:19553612-19553662	HepG2	liver:	n/a
43	chr14:19421688-19421738	HNPCEpiC	eye:	n/a
44	chr14:19585143-19585193	PrEC	prostate:	n/a
45	chr14:19600442-19600492	Hepatocyte	liver:	n/a
46	chr14:19377109-19377159	HNPCEpiC	eye:	n/a
47	chr14:19600442-19600492	HCPEpiC	choroid plexus:	n/a
48	chr14:19553612-19553662	AG04450	lung:	fetal
49	chr14:19594171-19594221	NHDF-neo	bronchial:	n/a
50	chr14:19360467-19360517	MCF10A-Er-Src	breast:	n/a

No data

(count:45 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEG-6	chr14:19558991-19559164	NR_027480
2	lnc-POTEM-8	chr14:19566286-19566680	NR_046571
3	lnc-POTEG-7	chr14:19603658-19603689	NONHSAT035463
4	lnc-POTEM-9	chr14:19409573-19409681	ENSG00000257504
5	lnc-POTEM-10	chr14:19372736-19372787	ENSG00000257959.1
6	lnc-POTEG-6	chr14:19563404-19563541	NR_027480
7	lnc-POTEG-6	chr14:19584597-19584942	NR_027480
8	lnc-POTEG-1	chr14:19529958-19530169	ENSG00000258265.1
9	lnc-POTEM-9	chr14:19409942-19410111	ENSG00000257504
10	lnc-POTEG-6	chr14:19566012-19566082	NR_027480
11	lnc-POTEG-3	chr14:19605328-19606529	NONHSAT035465
12	lnc-POTEG-6	chr14:19582971-19583089	NR_027480
13	lnc-OR11H12.1-1	chr14:19413561-19413898	ENSG00000258364.1
14	lnc-POTEM-9	chr14:19406795-19408008	ENSG00000257504
15	lnc-POTEM-8	chr14:19562689-19564808	ENSG00000258252
16	lnc-POTEG-7	chr14:19595933-19596023	NONHSAT035463
17	lnc-POTEG-6	chr14:19553365-19553937	NR_027480
18	lnc-POTEG-1	chr14:19530730-19530898	ENSG00000258265.1
19	lnc-POTEG-6	chr14:19573100-19573144	NR_027480
20	lnc-POTEG-7	chr14:19603204-19603279	NONHSAT035463
21	lnc-POTEG-6	chr14:19561994-19562100	NR_027480
22	lnc-POTEG-3	chr14:19611695-19611964	ENSG00000258314
23	lnc-POTEG-6	chr14:19571348-19571418	NR_027480
24	lnc-POTEM-15	chr14:19459200-19459267	NONHSAT035446
25	lnc-POTEM-8	chr14:19563712-19564808	NR_046571
26	lnc-POTEG-2	chr14:19515341-19515613	ENSG00000257891.1
27	lnc-POTEM-8	chr14:19566286-19566680	NR_110504
28	lnc-OR11H12.1-2	chr14:19345173-19345267	NONHSAT035436
29	lnc-POTEG-7	chr14:19597285-19597388	NONHSAT035463
30	lnc-POTEG-6	chr14:19558717-19558831	NR_027480
31	lnc-OR11H12.1-1	chr14:19412520-19412744	ENSG00000258364.1
32	lnc-POTEG-3	chr14:19606385-19606529	ENSG00000258314
33	lnc-POTEM-8	chr14:19563122-19564808	NR_110504
34	lnc-POTEM-8	chr14:19566286-19566731	ENSG00000258252
35	lnc-POTEM-9	chr14:19409573-19409681	NR_046104
36	lnc-POTEG-6	chr14:19574186-19574352	NR_027480
37	lnc-POTEG-2	chr14:19517501-19517607	ENSG00000257891.1
38	lnc-POTEG-2	chr14:19519800-19519837	ENSG00000257891.1
39	lnc-POTEM-9	chr14:19409942-19410111	NR_046104
40	lnc-POTEG-7	chr14:19602828-19602942	NONHSAT035463
41	lnc-POTEG-6	chr14:19578325-19578373	NR_027480
42	lnc-POTEG-9	chr14:19468509-19468885	NONHSAT035447
43	lnc-POTEG-3	chr14:19611768-19611964	ENSG00000258314.2
44	lnc-POTEM-9	chr14:19407015-19408008	NR_046104
45	lnc-POTEM-15	chr14:19458358-19458713	NONHSAT035446

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
ENSG00000258265	TF binding region
ENSG00000257558	TF binding region
ENSG00000258364	TF binding region
ENSG00000257504	TF binding region
ENSG00000257175	TF binding region
ARHGAP42P5	TF binding region
ENSG00000258314	TF binding region
ENSG00000257731	TF binding region
RNU6-1239P	TF binding region
ENSG00000258252	TF binding region
NF1P4	TF binding region
ENSG00000257825	TF binding region
ENSG00000257891	TF binding region
ENSG00000257959	TF binding region
ENSG00000258076	TF binding region
MED15P1	TF binding region
ENSG00000257635	TF binding region
ENSG00000257672	TF binding region
ENSG00000239200	TF binding region
ENSG00000257224	TF binding region
ENSG00000257644	TF binding region
OR11H12	TF binding region
POTEG	TF binding region
ENSG00000258265	CpG island
ENSG00000257558	CpG island
ENSG00000258364	CpG island
ENSG00000257504	CpG island
ENSG00000257175	CpG island
ARHGAP42P5	CpG island
ENSG00000258314	CpG island
ENSG00000257731	CpG island
RNU6-1239P	CpG island
ENSG00000258252	CpG island
NF1P4	CpG island
ENSG00000257825	CpG island
ENSG00000257891	CpG island
ENSG00000257959	CpG island
ENSG00000258076	CpG island
MED15P1	CpG island
ENSG00000257635	CpG island
ENSG00000257672	CpG island
ENSG00000239200	CpG island
ENSG00000257224	CpG island
ENSG00000257644	CpG island
OR11H12	CpG island
POTEG	CpG island

Extended variants
information (count: 1515 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:1515 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535318111	chr14:19345194-19345195	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs553995257	chr14:19345209-19345210	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs200024567	chr14:19345235-19345236	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs573417657	chr14:19345262-19345263	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs200759451	chr14:19364816-19364817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs552997087	chr14:19364936-19364937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs138515461	chr14:19364959-19364960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs577917815	chr14:19364995-19364996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs544670246	chr14:19364996-19364997	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs201672812	chr14:19365003-19365004	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs563330805	chr14:19365006-19365007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs140120645	chr14:19365010-19365011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs542334613	chr14:19365022-19365023	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs561911701	chr14:19365133-19365134	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs529453669	chr14:19365218-19365219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs548021258	chr14:19365252-19365253	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs566238440	chr14:19365381-19365382	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs200309239	chr14:19365393-19365394	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs78188837	chr14:19365450-19365451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs61969138	chr14:19365467-19365468	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533718534	chr14:19365485-19365486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs551466576	chr14:19365492-19365493	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570090448	chr14:19365496-19365497	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs369740322	chr14:19365503-19365504	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs537511493	chr14:19365504-19365505	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs549510842	chr14:19365509-19365510	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs567424381	chr14:19365515-19365516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs185939991	chr14:19365534-19365535	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs553173879	chr14:19365535-19365536	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs577845667	chr14:19365537-19365538	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs538952611	chr14:19365545-19365546	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs556655299	chr14:19365550-19365551	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs574909063	chr14:19365551-19365552	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542273312	chr14:19365560-19365561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs541254273	chr14:19365804-19365805	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs559928539	chr14:19365858-19365859	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533434333	chr14:19365948-19365949	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs375905170	chr14:19366337-19366338	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs369297293	chr14:19366358-19366359	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs372424608	chr14:19366364-19366365	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs552069494	chr14:19366383-19366384	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs200873213	chr14:19366398-19366399	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373551295	chr14:19367505-19367506	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs371094568	chr14:19367523-19367524	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs528550407	chr14:19367530-19367531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs547086624	chr14:19367533-19367534	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs199770506	chr14:19373645-19373646	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs61969148	chr14:19373916-19373917	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs145459725	chr14:19373981-19373982	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs140080877	chr14:19373992-19373993	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Lung cancer	18438408	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
Breast cancer	20932292	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
Ependymoma	20639864	CNVD
Williams Syndrome	20824207	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21668985	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:19433200-19433800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
2	chr14:19433600-19433800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr14:19435400-19439200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr14:19444400-19444800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr14:19444400-19445200	ZNF genes & repeats	Fetal Lung	lung
6	chr14:19444400-19445800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
7	chr14:19444400-19446000	Active TSS	Fetal Heart	heart
8	chr14:19445000-19445200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr14:19462400-19462800	ZNF genes & repeats	Fetal Kidney	kidney
10	chr14:19500000-19500200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:19597000-19597600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr14:19597200-19597600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:19607400-19609600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr14:19608600-19609200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr14:19610800-19612800	Weak transcription	Fetal Lung	lung
16	chr14:19611000-19611200	Enhancers	Lung	lung
17	chr14:19611200-19612800	Weak transcription	Lung	lung
18	chr14:19612600-19615200	Weak transcription	Right Atrium	heart
19	chr14:19612800-19613400	ZNF genes & repeats	Fetal Kidney	kidney
20	chr14:19612800-19613400	ZNF genes & repeats	Fetal Lung	lung
21	chr14:19612800-19613400	ZNF genes & repeats	Lung	lung

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