Variant report

Variant	nsv1037633
Chromosome Location	chr14:19273613-19852821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2866)
CpG islands
(count:2138)
Chromatin interactive
region (count:0)
LncRNA
region (count:137)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2866 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:19614565-19614964	K562	blood:	n/a	n/a
2	ATF1	chr14:19609027-19609227	K562	blood:	n/a	n/a
3	ATF1	chr14:19464826-19465023	K562	blood:	n/a	n/a
4	ATF1	chr14:19795048-19796237	K562	blood:	n/a	n/a
5	ATF1	chr14:19461425-19461537	K562	blood:	n/a	n/a
6	ATF1	chr14:19614523-19614771	K562	blood:	n/a	n/a
7	ATF1	chr14:19462190-19462538	K562	blood:	n/a	n/a
8	ATF1	chr14:19619825-19620010	K562	blood:	n/a	n/a
9	ATF1	chr14:19792967-19794009	K562	blood:	n/a	n/a
10	ATF1	chr14:19436953-19437483	K562	blood:	n/a	n/a
11	ATF1	chr14:19697695-19697910	K562	blood:	n/a	n/a
12	ATF1	chr14:19610591-19610826	K562	blood:	n/a	n/a
13	ATF1	chr14:19450073-19450214	K562	blood:	n/a	n/a
14	ATF3	chr14:19614578-19614850	K562	blood:	n/a	n/a
15	BACH1	chr14:19795663-19796213	K562	blood:	n/a	n/a
16	BACH1	chr14:19614506-19614753	K562	blood:	n/a	n/a
17	BACH1	chr14:19438368-19438886	K562	blood:	n/a	n/a
18	BACH1	chr14:19608951-19609223	K562	blood:	n/a	n/a
19	BACH1	chr14:19462184-19462510	K562	blood:	n/a	n/a
20	BACH1	chr14:19464051-19464239	K562	blood:	n/a	n/a
21	BATF	chr14:19546952-19547321	GM12878	blood:	n/a	n/a
22	BATF	chr14:19653590-19653843	GM12878	blood:	n/a	n/a
23	BATF	chr14:19487460-19487744	GM12878	blood:	n/a	n/a
24	BATF	chr14:19637509-19637829	GM12878	blood:	n/a	chr14:19637679-19637690
25	BATF	chr14:19827024-19827305	GM12878	blood:	n/a	n/a
26	BATF	chr14:19548036-19548546	GM12878	blood:	n/a	n/a
27	BATF	chr14:19548118-19548363	GM12878	blood:	n/a	n/a
28	BATF	chr14:19586478-19586681	GM12878	blood:	n/a	n/a
29	BATF	chr14:19541408-19541756	GM12878	blood:	n/a	n/a
30	BATF	chr14:19637495-19637851	GM12878	blood:	n/a	chr14:19637679-19637690
31	BATF	chr14:19748478-19748726	GM12878	blood:	n/a	n/a
32	BATF	chr14:19541484-19541694	GM12878	blood:	n/a	n/a
33	BCL11A	chr14:19637542-19637751	GM12878	blood:	n/a	n/a
34	BCL11A	chr14:19748843-19749025	GM12878	blood:	n/a	n/a
35	BCL11A	chr14:19821581-19821893	GM12878	blood:	n/a	n/a
36	BCL11A	chr14:19747489-19747677	GM12878	blood:	n/a	n/a
37	BCL11A	chr14:19819837-19820033	GM12878	blood:	n/a	n/a
38	BCL11A	chr14:19653966-19654150	GM12878	blood:	n/a	n/a
39	BCL11A	chr14:19753894-19754206	GM12878	blood:	n/a	n/a
40	BCL11A	chr14:19746165-19746357	GM12878	blood:	n/a	n/a
41	BCL11A	chr14:19748407-19748711	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:19826657-19827003	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:19637480-19637880	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:19548084-19548501	GM12878	blood:	n/a	chr14:19548252-19548261
45	BCL11A	chr14:19827491-19827723	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:19488926-19489115	GM12878	blood:	n/a	n/a
47	BCL11A	chr14:19827039-19827376	GM12878	blood:	n/a	n/a
48	BCL11A	chr14:19824315-19824574	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:19352644-19352904	GM12878	blood:	n/a	n/a
50	BCL11A	chr14:19747728-19747905	GM12878	blood:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19614541-19614591	ProgFib	skin:	n/a
2	chr14:19360878-19360928	MCF-7	breast:	n/a
3	chr14:19829406-19829456	AG10803	skin:	n/a
4	chr14:19614541-19614591	ProgFib	skin:	n/a
5	chr14:19360878-19360928	MCF-7	breast:	n/a
6	chr14:19829406-19829456	AG10803	skin:	n/a
7	chr14:19614556-19614606	GM12891	blood:	n/a
8	chr14:19402845-19402895	PFSK-1	brain:	n/a
9	chr14:19647166-19647216	HEEpiC	esophagus:	n/a
10	chr14:19377109-19377159	GM12891	blood:	n/a
11	chr14:19647166-19647216	ovcar-3	ovarian:	n/a
12	chr14:19585143-19585193	PrEC	prostate:	n/a
13	chr14:19585143-19585193	AG04450	lung:	fetal
14	chr14:19829406-19829456	SAEC	small airway:	n/a
15	chr14:19597077-19597127	HUVEC	blood vessel:	n/a
16	chr14:19641452-19641502	T-47D	breast:	n/a
17	chr14:19641452-19641502	HCM	heart:	n/a
18	chr14:19829406-19829456	HRPEpiC	eye:	n/a
19	chr14:19614541-19614591	HEK293	kidney:	embryo
20	chr14:19626001-19626051	MCF10A-Er-Src	breast:	n/a
21	chr14:19647166-19647216	HUVEC	blood vessel:	n/a
22	chr14:19626001-19626051	PANC-1	pancreas:	n/a
23	chr14:19421688-19421738	NB4	blood:	n/a
24	chr14:19719837-19719887	SAEC	small airway:	n/a
25	chr14:19585143-19585193	AoSMC	blood vessel:	n/a
26	chr14:19360467-19360517	HRE	kidney:	n/a
27	chr14:19828288-19828338	GM06990	blood:	n/a
28	chr14:19562827-19562877	AoSMC	blood vessel:	n/a
29	chr14:19594171-19594221	ECC-1	luminal epithelium:	n/a
30	chr14:19413192-19413242	ECC-1	luminal epithelium:	n/a
31	chr14:19745841-19745891	AG09309	skin:	n/a
32	chr14:19626001-19626051	CMK	blood:	n/a
33	chr14:19594171-19594221	HCF	heart:	n/a
34	chr14:19360467-19360517	NHBE	bronchial:	n/a
35	chr14:19600442-19600492	AoSMC	blood vessel:	n/a
36	chr14:19625154-19625204	SK-N-MC	brain:	n/a
37	chr14:19643599-19643649	ECC-1	luminal epithelium:	n/a
38	chr14:19686155-19686205	IMR90	lung:	fetal
39	chr14:19643599-19643649	NH-A	brain:	n/a
40	chr14:19828288-19828338	GM12892	blood:	n/a
41	chr14:19614556-19614606	HRCEpiC	kidney:	n/a
42	chr14:19597077-19597127	ovcar-3	ovarian:	n/a
43	chr14:19602855-19602905	CMK	blood:	n/a
44	chr14:19746900-19746950	HCPEpiC	choroid plexus:	n/a
45	chr14:19626001-19626051	SKMC	muscle:	n/a
46	chr14:19602855-19602905	HL-60	blood:	n/a
47	chr14:19602149-19602199	NHDF-neo	bronchial:	n/a
48	chr14:19597077-19597127	SK-N-SH_RA	brain:	n/a
49	chr14:19647166-19647216	AG09309	skin:	n/a
50	chr14:19828288-19828338	PrEC	prostate:	n/a

No data

(count:137 , 50 per page) page: 1 2 3

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEG-4	chr14:19655734-19655871	NR_110526
2	lnc-POTEG-4	chr14:19653940-19654004	ENSG00000225210
3	lnc-POTEG-4	chr14:19656089-19656224	ENSG00000225210
4	lnc-POTEG-4	chr14:19652244-19652354	NR_110526
5	lnc-POTEM-7	chr14:19678513-19678600	XLOC_010962
6	lnc-POTEG-7	chr14:19603204-19603279	NONHSAT035463
7	lnc-POTEG-7	chr14:19597285-19597388	NONHSAT035463
8	lnc-POTEG-4	chr14:19653893-19654004	NONHSAT035478
9	lnc-POTEG-4	chr14:19691355-19692916	NR_110526
10	lnc-OR11H12.1-2	chr14:19340299-19340388	NONHSAT035436
11	lnc-POTEG-4	chr14:19680595-19681593	ENSG00000225210
12	lnc-POTEG-4	chr14:19656089-19656224	NR_110526
13	lnc-POTEM-8	chr14:19563122-19564808	NR_110504
14	lnc-POTEG-4	chr14:19656700-19656886	ENSG00000225210
15	lnc-POTEG-4	chr14:19650021-19650126	ENSG00000225210
16	lnc-POTEG-4	chr14:19691355-19691404	NONHSAT035478
17	lnc-POTEG-6	chr14:19573100-19573144	NR_027480
18	lnc-OR11H12.1-1	chr14:19412520-19412744	ENSG00000258364.1
19	lnc-POTEG-4	chr14:19680595-19681519	ENSG00000225210
20	lnc-POTEG-4	chr14:19683027-19683250	ENSG00000225210
21	lnc-POTEG-5	chr14:19812176-19812247	ENSG00000258188.1
22	lnc-POTEM-15	chr14:19458358-19458713	NONHSAT035446
23	lnc-POTEG-4	chr14:19683692-19684834	ENSG00000225210
24	lnc-POTEM-8	chr14:19563712-19564808	NR_046571
25	lnc-POTEG-4	chr14:19650061-19650126	ENSG00000225210
26	lnc-POTEG-3	chr14:19619448-19619513	NONHSAT035465
27	lnc-POTEG-4	chr14:19655758-19655871	ENSG00000225210
28	lnc-POTEG-3	chr14:19643072-19643377	ENSG00000258314.2
29	lnc-POTEG-4	chr14:19650061-19650126	ENSG00000225210
30	lnc-POTEG-2	chr14:19515341-19515613	ENSG00000257891.1
31	lnc-POTEG-4	chr14:19656089-19656224	ENSG00000225210
32	lnc-POTEG-4	chr14:19653893-19654004	NR_110526
33	lnc-POTEG-2	chr14:19517501-19517607	ENSG00000257891.1
34	lnc-POTEM-9	chr14:19406795-19408008	ENSG00000257504
35	lnc-POTEG-2	chr14:19519800-19519837	ENSG00000257891.1
36	lnc-POTEG-6	chr14:19584597-19584942	NR_027480
37	lnc-POTEG-4	chr14:19680591-19680685	ENSG00000225210
38	lnc-POTEG-4	chr14:19650060-19650126	ENSG00000225210
39	lnc-POTEG-4	chr14:19653625-19653772	ENSG00000225210
40	lnc-POTEG-6	chr14:19578325-19578373	NR_027480
41	lnc-POTEG-4	chr14:19655734-19655871	ENSG00000225210
42	lnc-POTEG-6	chr14:19571348-19571418	NR_027480
43	lnc-POTEG-6	chr14:19563404-19563541	NR_027480
44	lnc-POTEM-7	chr14:19670792-19671105	ENSG00000228294
45	lnc-POTEG-7	chr14:19602828-19602942	NONHSAT035463
46	lnc-POTEG-4	chr14:19650066-19650126	ENSG00000225210
47	lnc-POTEG-4	chr14:19680595-19680685	ENSG00000225210
48	lnc-POTEG-3	chr14:19606385-19606529	ENSG00000258314
49	lnc-OR11H12.1-2	chr14:19341921-19341993	NONHSAT035436
50	lnc-POTEG-4	chr14:19650032-19650126	NR_110526

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
GRAMD4P3	TF binding region
ENSG00000258265	TF binding region
ENSG00000257558	TF binding region
ENSG00000258364	TF binding region
ENSG00000257504	TF binding region
ENSG00000257175	TF binding region
ENSG00000257573	TF binding region
ARHGAP42P5	TF binding region
ENSG00000258314	TF binding region
OR11H13P	TF binding region
ENSG00000257731	TF binding region
ENSG00000258198	TF binding region
RNU6-1239P	TF binding region
BMS1P17	TF binding region
ENSG00000258781	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
ENSG00000271632	TF binding region
MED15P1	TF binding region
ENSG00000257635	TF binding region
ENSG00000257672	TF binding region
ENSG00000239200	TF binding region
ENSG00000225210	TF binding region
ENSG00000257310	TF binding region
ENSG00000257224	TF binding region
ENSG00000258188	TF binding region
ENSG00000258367	TF binding region
ENSG00000257721	TF binding region
ENSG00000257644	TF binding region
OR11H12	TF binding region
POTEG	TF binding region
DUXAP10	TF binding region
GRAMD4P3	CpG island
ENSG00000258265	CpG island
ENSG00000257558	CpG island
ENSG00000258364	CpG island
ENSG00000257504	CpG island
ENSG00000257175	CpG island
ENSG00000257573	CpG island
ARHGAP42P5	CpG island
ENSG00000258314	CpG island
OR11H13P	CpG island
ENSG00000257731	CpG island
ENSG00000258198	CpG island
RNU6-1239P	CpG island
BMS1P17	CpG island
ENSG00000258781	CpG island
ENSG00000258252	CpG island
NF1P4	CpG island
ENSG00000257825	CpG island
ENSG00000257891	CpG island
ENSG00000257959	CpG island
ENSG00000258076	CpG island
ENSG00000271632	CpG island
MED15P1	CpG island
ENSG00000257635	CpG island
ENSG00000257672	CpG island
ENSG00000239200	CpG island
ENSG00000225210	CpG island
ENSG00000257310	CpG island
ENSG00000257224	CpG island
ENSG00000258188	CpG island
ENSG00000258367	CpG island
ENSG00000257721	CpG island
ENSG00000257644	CpG island
OR11H12	CpG island
POTEG	CpG island
DUXAP10	CpG island

Extended variants
information (count: 4118 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4118 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539593447	chr14:19332182-19332183	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs561033056	chr14:19332252-19332253	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs557834962	chr14:19332486-19332487	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs569778895	chr14:19332508-19332509	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs537067324	chr14:19332522-19332523	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs555319639	chr14:19332537-19332538	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs574285353	chr14:19332581-19332582	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs569842234	chr14:19334122-19334123	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs562859976	chr14:19337474-19337475	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs200380175	chr14:19337476-19337477	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530471953	chr14:19337513-19337514	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs565664800	chr14:19339183-19339184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs532907990	chr14:19339224-19339225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs558048246	chr14:19339417-19339418	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs576302716	chr14:19339418-19339419	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs543685890	chr14:19339436-19339437	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs562294917	chr14:19339438-19339439	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs529023683	chr14:19339504-19339505	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs541121515	chr14:19339506-19339507	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs113680245	chr14:19339512-19339513	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs559448191	chr14:19339534-19339535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs374943822	chr14:19339542-19339543	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs190077115	chr14:19339550-19339551	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs544090426	chr14:19340300-19340301	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs555735370	chr14:19340332-19340333	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs574184084	chr14:19340347-19340348	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs541228290	chr14:19340371-19340372	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs535318111	chr14:19345194-19345195	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs553995257	chr14:19345209-19345210	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs200024567	chr14:19345235-19345236	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs573417657	chr14:19345262-19345263	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs200759451	chr14:19364816-19364817	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs552997087	chr14:19364936-19364937	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs138515461	chr14:19364959-19364960	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577917815	chr14:19364995-19364996	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs544670246	chr14:19364996-19364997	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs201672812	chr14:19365003-19365004	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs563330805	chr14:19365006-19365007	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs140120645	chr14:19365010-19365011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs542334613	chr14:19365022-19365023	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs561911701	chr14:19365133-19365134	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs529453669	chr14:19365218-19365219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs548021258	chr14:19365252-19365253	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs566238440	chr14:19365381-19365382	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200309239	chr14:19365393-19365394	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs78188837	chr14:19365450-19365451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs61969138	chr14:19365467-19365468	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs533718534	chr14:19365485-19365486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs551466576	chr14:19365492-19365493	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs570090448	chr14:19365496-19365497	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	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
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

Chromatin state (count:117 , 50 per page) page: 1 2 3

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
22	chr14:19613000-19613200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr14:19613000-19613200	ZNF genes & repeats	Gastric	stomach
24	chr14:19613000-19613200	Bivalent Enhancer	K562	blood
25	chr14:19613000-19613400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr14:19613000-19613400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
27	chr14:19613000-19613400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr14:19613000-19613400	ZNF genes & repeats	Fetal Brain Male	brain
29	chr14:19613000-19613400	ZNF genes & repeats	Pancreas	Pancrea
30	chr14:19613000-19615000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr14:19613400-19614200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr14:19613400-19614400	Weak transcription	Pancreas	Pancrea
33	chr14:19613400-19614600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr14:19613400-19616200	Weak transcription	Fetal Lung	lung
35	chr14:19613600-19614200	Weak transcription	Lung	lung
36	chr14:19614200-19614800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr14:19614200-19614800	Active TSS	K562	blood
38	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr14:19614400-19614800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:19614400-19614800	Bivalent Enhancer	Lung	lung
41	chr14:19614400-19614800	ZNF genes & repeats	Pancreas	Pancrea
42	chr14:19614400-19615000	Bivalent/Poised TSS	A549	lung
43	chr14:19614600-19614800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr14:19614600-19614800	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
45	chr14:19614600-19614800	Bivalent Enhancer	Right Ventricle	heart
46	chr14:19614800-19616000	Weak transcription	Pancreas	Pancrea
47	chr14:19619800-19620000	Bivalent Enhancer	A549	lung
48	chr14:19641200-19641400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr14:19641200-19641400	Enhancers	K562	blood
50	chr14:19641200-19641600	Active TSS	A549	lung

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