Variant report

Variant	nsv1040110
Chromosome Location	chr14:19382197-20105479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4167)
CpG islands
(count:3357)
Chromatin interactive
region (count:0)
LncRNA
region (count:254)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:4167 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

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	chr14:19436953-19437483	K562	blood:	n/a	n/a
3	ATF1	chr14:19461425-19461537	K562	blood:	n/a	n/a
4	ATF1	chr14:19610591-19610826	K562	blood:	n/a	n/a
5	ATF1	chr14:19450073-19450214	K562	blood:	n/a	n/a
6	ATF1	chr14:19609027-19609227	K562	blood:	n/a	n/a
7	ATF1	chr14:19619825-19620010	K562	blood:	n/a	n/a
8	ATF1	chr14:19795048-19796237	K562	blood:	n/a	n/a
9	ATF1	chr14:19462190-19462538	K562	blood:	n/a	n/a
10	ATF1	chr14:19614523-19614771	K562	blood:	n/a	n/a
11	ATF1	chr14:19697695-19697910	K562	blood:	n/a	n/a
12	ATF1	chr14:19792967-19794009	K562	blood:	n/a	n/a
13	ATF1	chr14:19464826-19465023	K562	blood:	n/a	n/a
14	ATF3	chr14:19614578-19614850	K562	blood:	n/a	n/a
15	BACH1	chr14:19438368-19438886	K562	blood:	n/a	n/a
16	BACH1	chr14:19614506-19614753	K562	blood:	n/a	n/a
17	BACH1	chr14:19608951-19609223	K562	blood:	n/a	n/a
18	BACH1	chr14:19464051-19464239	K562	blood:	n/a	n/a
19	BACH1	chr14:19795663-19796213	K562	blood:	n/a	n/a
20	BACH1	chr14:19462184-19462510	K562	blood:	n/a	n/a
21	BATF	chr14:19748478-19748726	GM12878	blood:	n/a	n/a
22	BATF	chr14:19637509-19637829	GM12878	blood:	n/a	chr14:19637679-19637690
23	BATF	chr14:20031700-20032016	GM12878	blood:	n/a	n/a
24	BATF	chr14:19937525-19937845	GM12878	blood:	n/a	chr14:19937698-19937709
25	BATF	chr14:19653590-19653843	GM12878	blood:	n/a	n/a
26	BATF	chr14:19548118-19548363	GM12878	blood:	n/a	n/a
27	BATF	chr14:19586478-19586681	GM12878	blood:	n/a	n/a
28	BATF	chr14:19546952-19547321	GM12878	blood:	n/a	n/a
29	BATF	chr14:19541408-19541756	GM12878	blood:	n/a	n/a
30	BATF	chr14:19827024-19827305	GM12878	blood:	n/a	n/a
31	BATF	chr14:20025214-20025459	GM12878	blood:	n/a	n/a
32	BATF	chr14:19986920-19987123	GM12878	blood:	n/a	n/a
33	BATF	chr14:19637495-19637851	GM12878	blood:	n/a	chr14:19637679-19637690
34	BATF	chr14:20025031-20025541	GM12878	blood:	n/a	n/a
35	BATF	chr14:19541484-19541694	GM12878	blood:	n/a	n/a
36	BATF	chr14:19921485-19921738	GM12878	blood:	n/a	n/a
37	BATF	chr14:19548036-19548546	GM12878	blood:	n/a	n/a
38	BATF	chr14:19937503-19937859	GM12878	blood:	n/a	chr14:19937698-19937709
39	BATF	chr14:20026256-20026650	GM12878	blood:	n/a	n/a
40	BATF	chr14:20085953-20086237	GM12878	blood:	n/a	n/a
41	BATF	chr14:19487460-19487744	GM12878	blood:	n/a	n/a
42	BCL11A	chr14:19637542-19637751	GM12878	blood:	n/a	n/a
43	BCL11A	chr14:19488926-19489115	GM12878	blood:	n/a	n/a
44	BCL11A	chr14:19826657-19827003	GM12878	blood:	n/a	n/a
45	BCL11A	chr14:19920793-19920958	GM12878	blood:	n/a	n/a
46	BCL11A	chr14:19776347-19776520	GM12878	blood:	n/a	n/a
47	BCL11A	chr14:20025076-20025493	GM12878	blood:	n/a	chr14:20025351-20025360
48	BCL11A	chr14:19637480-19637880	GM12878	blood:	n/a	n/a
49	BCL11A	chr14:19819837-19820033	GM12878	blood:	n/a	n/a
50	BCL11A	chr14:19747489-19747677	GM12878	blood:	n/a	n/a

(count:3357 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:19613906-19613956	T-47D	breast:	n/a
2	chr14:19402845-19402895	AG04449	skin:	fetal
3	chr14:19613906-19613956	T-47D	breast:	n/a
4	chr14:19402845-19402895	AG04449	skin:	fetal
5	chr14:19625154-19625204	PANC-1	pancreas:	n/a
6	chr14:20020668-20020718	ovcar-3	ovarian:	n/a
7	chr14:19600442-19600492	HEK293	kidney:	embryo
8	chr14:19746900-19746950	SAEC	small airway:	n/a
9	chr14:19964024-19964074	GM12878	blood:	n/a
10	chr14:19950047-19950097	HNPCEpiC	eye:	n/a
11	chr14:19625820-19625870	RPTEC	kidney:	n/a
12	chr14:19888629-19888679	GM19239	blood:	n/a
13	chr14:19855384-19855434	HAEpiC	amniotic membrane:	n/a
14	chr14:19855384-19855434	ECC-1	luminal epithelium:	n/a
15	chr14:19625154-19625204	Hela-S3	cervix:	n/a
16	chr14:19888629-19888679	BJ	skin:	n/a
17	chr14:19553612-19553662	A549	lung:	n/a
18	chr14:19562827-19562877	NB4	blood:	n/a
19	chr14:19855384-19855434	NT2-D1	testis:	n/a
20	chr14:20020024-20020074	Jurkat	blood:	n/a
21	chr14:19964024-19964074	K562	blood:	n/a
22	chr14:19960920-19960970	SK-N-SH_RA	brain:	n/a
23	chr14:19686155-19686205	HMEC	breast:	n/a
24	chr14:20012038-20012088	GM06990	blood:	n/a
25	chr14:19602149-19602199	PFSK-1	brain:	n/a
26	chr14:19887082-19887132	BE2_C	brain:	n/a
27	chr14:19747134-19747184	GM12891	blood:	n/a
28	chr14:19888327-19888377	HCM	heart:	n/a
29	chr14:19959522-19959572	PrEC	prostate:	n/a
30	chr14:19602149-19602199	NH-A	brain:	n/a
31	chr14:19614829-19614879	MCF-7	breast:	n/a
32	chr14:19625154-19625204	SK-N-SH_RA	brain:	n/a
33	chr14:19829406-19829456	HCPEpiC	choroid plexus:	n/a
34	chr14:19625820-19625870	NB4	blood:	n/a
35	chr14:19888327-19888377	NB4	blood:	n/a
36	chr14:19932946-19932996	HUVEC	blood vessel:	n/a
37	chr14:19887082-19887132	HCM	heart:	n/a
38	chr14:19855384-19855434	SAEC	small airway:	n/a
39	chr14:19890087-19890137	NHDF-neo	bronchial:	n/a
40	chr14:19597077-19597127	AG04449	skin:	fetal
41	chr14:19585143-19585193	SAEC	small airway:	n/a
42	chr14:20020024-20020074	HCPEpiC	choroid plexus:	n/a
43	chr14:19686155-19686205	U87	brain:	n/a
44	chr14:19602855-19602905	BJ	skin:	n/a
45	chr14:19585143-19585193	HEK293	kidney:	embryo
46	chr14:19858845-19858895	PFSK-1	brain:	n/a
47	chr14:20020024-20020074	Hela-S3	cervix:	n/a
48	chr14:19959522-19959572	HL-60	blood:	n/a
49	chr14:19600442-19600492	AG10803	skin:	n/a
50	chr14:19413192-19413242	GM12891	blood:	n/a

No data

(count:254 , 50 per page) page: 1 2 3 4 5 6

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POTEM-2	chr14:19880059-19884029	ENSG00000244306
2	lnc-POTEG-4	chr14:19680595-19680685	ENSG00000225210
3	lnc-POTEG-4	chr14:19652244-19652354	NONHSAT035478
4	lnc-POTEG-4	chr14:19653893-19654004	ENSG00000225210
5	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
6	lnc-POTEG-7	chr14:19595933-19596023	NONHSAT035463
7	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT035520
8	lnc-POTEM-2	chr14:19880596-19880882	ENSG00000244306
9	lnc-POTEG-4	chr14:19653893-19654004	NONHSAT035478
10	lnc-POTEG-1	chr14:19529958-19530169	ENSG00000258265.1
11	lnc-POTEG-7	chr14:19597285-19597388	NONHSAT035463
12	lnc-POTEG-4	chr14:19718326-19718379	NONHSAT035478
13	lnc-POTEM-2	chr14:19894700-19894790	ENSG00000244306
14	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
15	lnc-POTEM-2	chr14:19925240-19925311	ENSG00000244306
16	lnc-POTEM-2	chr14:19919138-19919273	NR_110526
17	lnc-OR4N2-3	chr14:20008836-20010956	NR_110505
18	lnc-POTEM-2	chr14:19921591-19921738	ENSG00000244306
19	lnc-POTEM-2	chr14:19921591-19921738	NONHSAT035503
20	lnc-POTEM-2	chr14:19881070-19881410	ucscGeneNc_uc001vxa_1
21	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT035521
22	lnc-POTEM-2	chr14:19891517-19892052	ENSG00000244306
23	lnc-POTEG-4	chr14:19680595-19680685	ENSG00000225210
24	lnc-OR4N2-3	chr14:20006913-20007358	ENSG00000258276
25	lnc-POTEG-4	chr14:19680595-19680685	NONHSAT035478
26	lnc-POTEM-1	chr14:19944559-19944820	ENSG00000257931
27	lnc-POTEG-4	chr14:19690487-19690609	ENSG00000225210
28	lnc-POTEM-2	chr14:19925240-19925345	ENSG00000244306
29	lnc-POTEG-3	chr14:19611695-19611964	ENSG00000258314
30	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
31	lnc-POTEG-4	chr14:19655782-19655871	ENSG00000225210
32	lnc-POTEM-2	chr14:19921591-19921738	ENSG00000244306
33	lnc-POTEM-1	chr14:19932012-19932316	ENSG00000257931.2
34	lnc-OR4N2-4	chr14:19896785-19896872	XLOC_010749
35	lnc-POTEG-3	chr14:19643072-19643377	ENSG00000258314.2
36	lnc-POTEM-2	chr14:19925240-19925333	NONHSAT035503
37	lnc-POTEG-4	chr14:19650060-19650126	ENSG00000225210
38	lnc-POTEM-2	chr14:19919492-19919629	ENSG00000244306
39	lnc-POTEM-2	chr14:19919492-19919581	ENSG00000244306
40	lnc-POTEM-1	chr14:19955880-19955945	ENSG00000257931
41	lnc-POTEG-4	chr14:19656089-19656224	ENSG00000225210
42	lnc-POTEM-2	chr14:19921359-19921470	ENSG00000244306
43	lnc-POTEM-7	chr14:19678513-19678600	XLOC_010962
44	lnc-POTEG-2	chr14:19517501-19517607	ENSG00000257891.1
45	lnc-POTEM-6	chr14:19837830-19837836	ENSG00000257898.1
46	lnc-POTEM-7	chr14:19670792-19671105	ENSG00000228294
47	lnc-OR4N2-3	chr14:20006913-20007358	NR_110505
48	lnc-POTEM-8	chr14:19562689-19564808	ENSG00000258252
49	lnc-POTEM-2	chr14:19921359-19921470	NONHSAT140152
50	lnc-POTEM-2	chr14:19894700-19894790	NONHSAT035503

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
ENSG00000244306	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
BMS1P18	TF binding region
ENSG00000257357	TF binding region
ENSG00000257868	TF binding region
ENSG00000258314	TF binding region
OR11H13P	TF binding region
ENSG00000257731	TF binding region
ENSG00000258027	TF binding region
ENSG00000258198	TF binding region
MED15P6	TF binding region
RNU6-1239P	TF binding region
BMS1P17	TF binding region
ENSG00000258781	TF binding region
ENSG00000258252	TF binding region
NF1P4	TF binding region
ENSG00000257891	TF binding region
ENSG00000258076	TF binding region
ENSG00000258276	TF binding region
ENSG00000271632	TF binding region
MED15P1	TF binding region
ENSG00000257931	TF binding region
ENSG00000257635	TF binding region
ENSG00000257672	TF binding region
ENSG00000239200	TF binding region
ENSG00000225210	TF binding region
ENSG00000257310	TF binding region
GRAMD4P4	TF binding region
ENSG00000257224	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
ENSG00000257644	TF binding region
POTEG	TF binding region
DUXAP10	TF binding region
GRAMD4P3	CpG island
ENSG00000244306	CpG island
ENSG00000258265	CpG island
ENSG00000257558	CpG island
ENSG00000258364	CpG island
ENSG00000257504	CpG island
ENSG00000257175	CpG island
ENSG00000257573	CpG island
ARHGAP42P5	CpG island
BMS1P18	CpG island
ENSG00000257357	CpG island
ENSG00000257868	CpG island
ENSG00000258314	CpG island
OR11H13P	CpG island
ENSG00000257731	CpG island
ENSG00000258027	CpG island
ENSG00000258198	CpG island
MED15P6	CpG island
RNU6-1239P	CpG island
BMS1P17	CpG island
ENSG00000258781	CpG island
ENSG00000258252	CpG island
NF1P4	CpG island
ENSG00000257891	CpG island
ENSG00000258076	CpG island
ENSG00000258276	CpG island
ENSG00000271632	CpG island
MED15P1	CpG island
ENSG00000257931	CpG island
ENSG00000257635	CpG island
ENSG00000257672	CpG island
ENSG00000239200	CpG island
ENSG00000225210	CpG island
ENSG00000257310	CpG island
GRAMD4P4	CpG island
ENSG00000257224	CpG island
RNU6-1268P	CpG island
ENSG00000257749	CpG island
ENSG00000258188	CpG island
ENSG00000257977	CpG island
ENSG00000257432	CpG island
POTEM	CpG island
ENSG00000257644	CpG island
POTEG	CpG island
DUXAP10	CpG island

Extended variants
information (count: 5227 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5227 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200075830	chr14:19389307-19389308	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs572276773	chr14:19389450-19389451	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs61969997	chr14:19389462-19389463	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs539695307	chr14:19389480-19389481	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs61969998	chr14:19389487-19389488	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs199576637	chr14:19389729-19389730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs200610431	chr14:19389738-19389739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs573626430	chr14:19390774-19390775	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs74580404	chr14:19390824-19390825	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs541135598	chr14:19390842-19390843	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77704721	chr14:19390843-19390844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs201890645	chr14:19390848-19390849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs527876486	chr14:19390849-19390850	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs200646044	chr14:19403090-19403091	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs537628062	chr14:19403094-19403095	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs201499575	chr14:19403169-19403170	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs199559481	chr14:19403206-19403207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs556345784	chr14:19403246-19403247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs111668312	chr14:19403314-19403315	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs61970029	chr14:19403330-19403331	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs61970030	chr14:19403351-19403352	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs564128162	chr14:19406950-19406951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs199790270	chr14:19406968-19406969	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs576017576	chr14:19407045-19407046	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs543512210	chr14:19407049-19407050	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs562891113	chr14:19407070-19407071	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs530227441	chr14:19407075-19407076	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs548413310	chr14:19407108-19407109	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs560398137	chr14:19407128-19407129	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs199742475	chr14:19407206-19407207	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs200566280	chr14:19407317-19407318	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs61970053	chr14:19407538-19407539	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs528006000	chr14:19407692-19407693	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs375201155	chr14:19407714-19407715	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
35	rs570834517	chr14:19407725-19407726	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs368081818	chr14:19407726-19407727	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs537906403	chr14:19407740-19407741	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs550246359	chr14:19407747-19407748	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs568503854	chr14:19407792-19407793	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs61970054	chr14:19407819-19407820	Inactive region	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs535631669	chr14:19407911-19407912	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs554040400	chr14:19407924-19407925	Inactive region	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs565949825	chr14:19408014-19408015	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs539757761	chr14:19408030-19408031	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs557427171	chr14:19408110-19408111	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs2027638	chr14:19409171-19409172	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs200578081	chr14:19409239-19409240	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201026949	chr14:19409666-19409667	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs371531146	chr14:19409970-19409971	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs568548118	chr14:19410001-19410002	Inactive region	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
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
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	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
Breast cancer	21509527	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:165 , 50 per page) page: 1 2 3 4

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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