Variant report

Variant	nsv569110
Chromosome Location	chr15:34742839-34982384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3265)
CpG islands
(count:2506)
Chromatin interactive
region (count:111)
LncRNA
region (count:24)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:3265 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
2	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
3	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
4	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
5	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
6	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
7	ARID3A	chr15:34905532-34905838	K562	blood:	n/a	n/a
8	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
9	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
10	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:34902659-34902943	K562	blood:	n/a	n/a
12	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
13	ARID3A	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
14	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
15	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
16	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
17	ARID3A	chr15:34781246-34781587	K562	blood:	n/a	n/a
18	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
19	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
20	ARID3A	chr15:34908827-34909205	K562	blood:	n/a	n/a
21	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
22	ATF1	chr15:34808283-34808324	K562	blood:	n/a	n/a
23	ATF1	chr15:34908847-34909148	K562	blood:	n/a	n/a
24	ATF1	chr15:34905714-34905797	K562	blood:	n/a	n/a
25	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
26	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
27	ATF1	chr15:34807442-34807640	K562	blood:	n/a	n/a
28	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
29	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
30	ATF1	chr15:34896856-34896884	K562	blood:	n/a	n/a
31	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
32	ATF1	chr15:34761374-34761389	K562	blood:	n/a	n/a
33	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
34	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
35	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
36	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
37	ATF2	chr15:34880089-34880894	GM12878	blood:	n/a	n/a
38	ATF2	chr15:34880257-34880906	GM12878	blood:	n/a	n/a
39	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
40	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
41	ATF2	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF3	chr15:34908811-34909131	K562	blood:	n/a	n/a
43	ATF3	chr15:34781262-34781502	K562	blood:	n/a	n/a
44	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
45	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
46	BACH1	chr15:34806578-34807213	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr15:34876822-34876846	K562	blood:	n/a	n/a
48	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
49	BATF	chr15:34942288-34942693	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
50	BATF	chr15:34842337-34842744	GM12878	blood:	n/a	n/a

(count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34874862-34874912	SK-N-SH_RA	brain:	n/a
2	chr15:34786594-34786644	HL-60	blood:	n/a
3	chr15:34875825-34875875	HepG2	liver:	n/a
4	chr15:34880284-34880334	HNPCEpiC	eye:	n/a
5	chr15:34788017-34788067	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:34874862-34874912	SK-N-SH_RA	brain:	n/a
7	chr15:34786594-34786644	HL-60	blood:	n/a
8	chr15:34875825-34875875	HepG2	liver:	n/a
9	chr15:34880284-34880334	HNPCEpiC	eye:	n/a
10	chr15:34788017-34788067	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:34875945-34875995	BJ	skin:	n/a
12	chr15:34806349-34806399	LNCaP	prostate:	n/a
13	chr15:34876396-34876446	MCF10A-Er-Src	breast:	n/a
14	chr15:34877407-34877457	GM12892	blood:	n/a
15	chr15:34781969-34782019	SK-N-SH_RA	brain:	n/a
16	chr15:34781891-34781941	SK-N-SH	brain:	n/a
17	chr15:34788017-34788067	RPTEC	kidney:	n/a
18	chr15:34876347-34876397	PrEC	prostate:	n/a
19	chr15:34787920-34787970	AoSMC	blood vessel:	n/a
20	chr15:34876347-34876397	HEEpiC	esophagus:	n/a
21	chr15:34875250-34875300	HEEpiC	esophagus:	n/a
22	chr15:34877407-34877457	SK-N-SH_RA	brain:	n/a
23	chr15:34876471-34876521	HNPCEpiC	eye:	n/a
24	chr15:34874183-34874233	PFSK-1	brain:	n/a
25	chr15:34787420-34787470	MCF10A-Er-Src	breast:	n/a
26	chr15:34876283-34876333	MCF-7	breast:	n/a
27	chr15:34807679-34807729	SKMC	muscle:	n/a
28	chr15:34880284-34880334	PANC-1	pancreas:	n/a
29	chr15:34874183-34874233	Caco-2	colon:	n/a
30	chr15:34876396-34876446	HCPEpiC	choroid plexus:	n/a
31	chr15:34875250-34875300	PrEC	prostate:	n/a
32	chr15:34781705-34781755	NH-A	brain:	n/a
33	chr15:34876347-34876397	SKMC	muscle:	n/a
34	chr15:34787400-34787450	AoSMC	blood vessel:	n/a
35	chr15:34781969-34782019	HRPEpiC	eye:	n/a
36	chr15:34812400-34812450	IMR90	lung:	fetal
37	chr15:34806349-34806399	NH-A	brain:	n/a
38	chr15:34875945-34875995	HCM	heart:	n/a
39	chr15:34876295-34876345	AoSMC	blood vessel:	n/a
40	chr15:34806592-34806642	Hepatocyte	liver:	n/a
41	chr15:34788847-34788897	AG09319	gingival:	n/a
42	chr15:34876283-34876333	GM12892	blood:	n/a
43	chr15:34807050-34807100	HEK293	kidney:	embryo
44	chr15:34781891-34781941	SK-N-SH_RA	brain:	n/a
45	chr15:34782167-34782217	GM12891	blood:	n/a
46	chr15:34880284-34880334	MCF-7	breast:	n/a
47	chr15:34817982-34818032	HRCEpiC	kidney:	n/a
48	chr15:34875945-34875995	HAEpiC	amniotic membrane:	n/a
49	chr15:34872733-34872783	PrEC	prostate:	n/a
50	chr15:34807143-34807193	HPAEpiC	pulmonary alveolar:	n/a

(count:111 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:34351759..34355755-chr15:34876768..34880095,3	K562	blood:
2	chr15:34513565..34517614-chr15:34877827..34881077,3	K562	blood:
3	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
4	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
5	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
6	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
7	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
8	chr15:34770080..34772217-chr15:34772786..34775252,2	K562	blood:
9	chr15:34949722..34952645-chr15:34986997..34989606,2	K562	blood:
10	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
11	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
12	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
13	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
14	chr15:34728066..34730668-chr15:34791069..34792682,2	K562	blood:
15	chr15:34875152..34877762-chr15:34886558..34889393,2	MCF-7	breast:
16	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
17	chr15:34761476..34764376-chr15:34768521..34770931,2	K562	blood:
18	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
19	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
20	chr15:34628679..34631455-chr15:34874185..34875808,2	K562	blood:
21	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
22	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
23	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
24	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
25	chr15:34658082..34661057-chr15:34874863..34877414,3	MCF-7	breast:
26	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
27	chr15:34659441..34662117-chr15:34875107..34877933,3	K562	blood:
28	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
29	chr15:34762215..34765168-chr15:34878877..34880750,2	K562	blood:
30	chr15:34658214..34660711-chr15:34806608..34809602,2	K562	blood:
31	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
32	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
33	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
34	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
35	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
36	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
37	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
38	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
39	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
40	chr15:34913751..34914597-chr15:35212096..35212867,7	K562	blood:
41	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
42	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
43	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
44	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
45	chr15:34632776..34635331-chr15:34879472..34881728,2	K562	blood:
46	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
47	chr15:34908560..34909558-chr15:35212164..35213076,4	K562	blood:
48	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
49	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
50	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJD2-3	chr15:34874951-34875061	NONHSAT041597
2	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
3	lnc-C15orf55-4	chr15:34752685-34752950	uc_384_+
4	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
5	lnc-GOLGA8B-1	chr15:34752685-34752950	uc_384_-
6	lnc-GJD2-4	chr15:34843392-34843477	NONHSAT140232
7	lnc-GJD2-3	chr15:34858091-34858674	NONHSAT041597
8	lnc-GJD2-4	chr15:34867026-34867115	NONHSAT041596
9	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
10	lnc-GJD2-4	chr15:34875717-34875835	NONHSAT041596
11	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
12	lnc-GJD2-4	chr15:34873667-34873700	NONHSAT140232
13	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
14	lnc-GJD2-4	chr15:34845096-34845292	NONHSAT140232
15	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
16	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
17	lnc-GJD2-4	chr15:34845174-34845292	NONHSAT041596
18	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
19	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT041596
20	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
21	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
22	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT140232
23	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
24	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1233-3p	chr15:34820491-34820510	MIMAT0005588_1
hsa-miR-1233-5p	chr15:34820548-34820569	MIMAT0022943_1

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA8B	hsa-miR-15a-5p	chr15:34817527-34817548
2	GOLGA8B	hsa-miR-32-5p	chr15:34818291-34818311

Variant related genes	Relation type
ENSG00000261304	TF binding region
ENSG00000261559	TF binding region
MIR1233-2	TF binding region
ENSG00000259892	TF binding region
GOLGA8A	TF binding region
HNRNPLP2	TF binding region
ENSG00000252425	TF binding region
GOLGA8B	TF binding region
ENSG00000261304	CpG island
ENSG00000261559	CpG island
MIR1233-2	CpG island
ENSG00000259892	CpG island
GOLGA8A	CpG island
HNRNPLP2	CpG island
ENSG00000252425	CpG island
GOLGA8B	CpG island
ENSG00000169857	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000259904	chromatin interactions
NEK7	miRNA target sites
NEK9	miRNA target sites

Extended variants
information (count: 6650 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:6650 , 50 per page) page: 1 2 3 4 5 6 7 ... 133

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62008329	chr15:34749207-34749208	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs28414761	chr15:34749244-34749245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147949156	chr15:34749254-34749255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs386782909	chr15:34749267-34749268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201475112	chr15:34749268-34749269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199692653	chr15:34749269-34749270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372092700	chr15:34749283-34749284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547063600	chr15:34749287-34749288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565720350	chr15:34749312-34749313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539538503	chr15:34749330-34749331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551451368	chr15:34749334-34749335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148985200	chr15:34749364-34749365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74007841	chr15:34749367-34749368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs183553253	chr15:34749382-34749383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs563132133	chr15:34749413-34749414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114303571	chr15:34749479-34749480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs4525461	chr15:34749482-34749483	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs4561436	chr15:34749549-34749550	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs4534805	chr15:34749554-34749555	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs4534806	chr15:34749584-34749585	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs563406240	chr15:34749596-34749597	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35871294	chr15:34749647-34749648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575713554	chr15:34749680-34749681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561573302	chr15:34749703-34749704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201206272	chr15:34749741-34749742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34699440	chr15:34749742-34749743	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs7495533	chr15:34749743-34749744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs529166797	chr15:34749755-34749756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188036862	chr15:34749762-34749763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs113132143	chr15:34749769-34749770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559692449	chr15:34749790-34749791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192832789	chr15:34749861-34749862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75051616	chr15:34749883-34749884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74722741	chr15:34749899-34749900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139718654	chr15:34749921-34749922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74873021	chr15:34749924-34749925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202233757	chr15:34749926-34749927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs74007842	chr15:34749928-34749929	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs73378065	chr15:34750037-34750038	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs534906447	chr15:34750040-34750041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78436894	chr15:34750055-34750056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79359798	chr15:34750068-34750069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73378066	chr15:34750092-34750093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs113046326	chr15:34750104-34750105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544591768	chr15:34750116-34750117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74007845	chr15:34750130-34750131	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs62008330	chr15:34750138-34750139	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs543149040	chr15:34750154-34750155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs16973668	chr15:34750181-34750182	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs560726677	chr15:34750182-34750183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1882 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34749200-34749600	Enhancers	Fetal Lung	lung
2	chr15:34749600-34750400	Weak transcription	Fetal Lung	lung
3	chr15:34750400-34750600	Enhancers	Fetal Lung	lung
4	chr15:34750600-34750800	Weak transcription	Fetal Lung	lung
5	chr15:34753600-34754200	Enhancers	HepG2	liver
6	chr15:34753800-34754000	Enhancers	Fetal Lung	lung
7	chr15:34759000-34759400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:34761000-34762800	Enhancers	HepG2	liver
9	chr15:34768400-34769000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr15:34772600-34773200	Enhancers	Fetal Brain Male	brain
11	chr15:34773200-34775000	Weak transcription	Fetal Brain Male	brain
12	chr15:34775200-34775400	Enhancers	Fetal Brain Male	brain
13	chr15:34780400-34781600	Active TSS	K562	blood
14	chr15:34780800-34781600	Bivalent/Poised TSS	A549	lung
15	chr15:34781000-34781600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr15:34781600-34781800	Flanking Active TSS	K562	blood
17	chr15:34782000-34786600	Weak transcription	Right Ventricle	heart
18	chr15:34782200-34783200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
19	chr15:34782400-34782600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr15:34782400-34782600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
21	chr15:34782400-34782800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:34782400-34783000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr15:34782400-34783200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
24	chr15:34782400-34783200	Active TSS	H9 Cell Line	embryonic stem cell
25	chr15:34782400-34783200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
26	chr15:34782400-34783400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
27	chr15:34782600-34783000	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:34782600-34783200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr15:34782800-34783000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
30	chr15:34782800-34783000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr15:34782800-34783000	Bivalent/Poised TSS	HSMM	muscle
32	chr15:34782800-34783200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr15:34782800-34783200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr15:34782800-34783200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
35	chr15:34782800-34783200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:34782800-34783200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr15:34782800-34783400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr15:34783000-34783200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
39	chr15:34783000-34783200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr15:34783000-34783200	Bivalent Enhancer	Fetal Heart	heart
41	chr15:34783000-34783400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr15:34783000-34783400	Bivalent Enhancer	Fetal Lung	lung
43	chr15:34783200-34783400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
44	chr15:34783200-34783400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr15:34783200-34783400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
46	chr15:34783600-34783800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
47	chr15:34784200-34784400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
48	chr15:34786200-34786400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
49	chr15:34786200-34786400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
50	chr15:34786200-34787000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

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