Variant report

Variant	nsv832965
Chromosome Location	chr15:34835996-35001160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2689)
CpG islands
(count:1281)
Chromatin interactive
region (count:104)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2689 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
2	ARID3A	chr15:34989159-34989187	K562	blood:	n/a	n/a
3	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
4	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
5	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
6	ARID3A	chr15:34902659-34902943	K562	blood:	n/a	n/a
7	ARID3A	chr15:34905532-34905838	K562	blood:	n/a	n/a
8	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
9	ARID3A	chr15:34908827-34909205	K562	blood:	n/a	n/a
10	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
11	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
12	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
13	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
14	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
15	ARID3A	chr15:35000570-35000896	K562	blood:	n/a	n/a
16	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
17	ARID3A	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
18	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
19	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
20	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
21	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
22	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
23	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
24	ATF1	chr15:34896856-34896884	K562	blood:	n/a	n/a
25	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
26	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
27	ATF1	chr15:34908847-34909148	K562	blood:	n/a	n/a
28	ATF1	chr15:34985696-34985896	K562	blood:	n/a	n/a
29	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
30	ATF1	chr15:34905714-34905797	K562	blood:	n/a	n/a
31	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
32	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
33	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
34	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
35	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
36	ATF1	chr15:35000572-35001097	K562	blood:	n/a	n/a
37	ATF2	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
39	ATF2	chr15:34880089-34880894	GM12878	blood:	n/a	n/a
40	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
41	ATF2	chr15:34880257-34880906	GM12878	blood:	n/a	n/a
42	ATF3	chr15:34908811-34909131	K562	blood:	n/a	n/a
43	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
44	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
45	BACH1	chr15:34876822-34876846	K562	blood:	n/a	n/a
46	BATF	chr15:34842337-34842744	GM12878	blood:	n/a	n/a
47	BATF	chr15:34841508-34841849	GM12878	blood:	n/a	n/a
48	BATF	chr15:34842238-34842949	GM12878	blood:	n/a	n/a
49	BATF	chr15:34841482-34841862	GM12878	blood:	n/a	n/a
50	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449

(count:1281 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34876295-34876345	NT2-D1	testis:	n/a
2	chr15:34876283-34876333	AG09319	gingival:	n/a
3	chr15:35001084-35001134	HAEpiC	amniotic membrane:	n/a
4	chr15:34876295-34876345	GM12892	blood:	n/a
5	chr15:34880284-34880334	SK-N-SH	brain:	n/a
6	chr15:34875250-34875300	BJ	skin:	n/a
7	chr15:34875945-34875995	Hepatocyte	liver:	n/a
8	chr15:34875250-34875300	HMEC	breast:	n/a
9	chr15:34876471-34876521	PANC-1	pancreas:	n/a
10	chr15:34875891-34875941	HRPEpiC	eye:	n/a
11	chr15:34876283-34876333	K562	blood:	n/a
12	chr15:34874862-34874912	Hepatocyte	liver:	n/a
13	chr15:34872733-34872783	HIPEpiC	eye:	n/a
14	chr15:34875891-34875941	HEK293	kidney:	embryo
15	chr15:34875825-34875875	Jurkat	blood:	n/a
16	chr15:34876283-34876333	HepG2	liver:	n/a
17	chr15:34875138-34875188	T-47D	breast:	n/a
18	chr15:34875325-34875375	MCF-7	breast:	n/a
19	chr15:34875117-34875167	NT2-D1	testis:	n/a
20	chr15:34880284-34880334	K562	blood:	n/a
21	chr15:34875138-34875188	GM06990	blood:	n/a
22	chr15:34876347-34876397	T-47D	breast:	n/a
23	chr15:34872733-34872783	HRPEpiC	eye:	n/a
24	chr15:35001084-35001134	HRE	kidney:	n/a
25	chr15:34874862-34874912	HRE	kidney:	n/a
26	chr15:34876347-34876397	HL-60	blood:	n/a
27	chr15:34876283-34876333	HAEpiC	amniotic membrane:	n/a
28	chr15:34875325-34875375	ovcar-3	ovarian:	n/a
29	chr15:34875945-34875995	NHBE	bronchial:	n/a
30	chr15:34875825-34875875	Hela-S3	cervix:	n/a
31	chr15:34872733-34872783	AG09309	skin:	n/a
32	chr15:34875825-34875875	NHBE	bronchial:	n/a
33	chr15:34876295-34876345	AG09309	skin:	n/a
34	chr15:34875930-34875980	AG04450	lung:	fetal
35	chr15:34988869-34988919	NHDF-neo	bronchial:	n/a
36	chr15:34875825-34875875	ECC-1	luminal epithelium:	n/a
37	chr15:34877407-34877457	RPTEC	kidney:	n/a
38	chr15:34874183-34874233	HEK293	kidney:	embryo
39	chr15:34876295-34876345	AG09319	gingival:	n/a
40	chr15:34875825-34875875	SK-N-MC	brain:	n/a
41	chr15:34875945-34875995	GM06990	blood:	n/a
42	chr15:34875945-34875995	HMEC	breast:	n/a
43	chr15:34876396-34876446	GM06990	blood:	n/a
44	chr15:34880284-34880334	MCF10A-Er-Src	breast:	n/a
45	chr15:34874183-34874233	AG09309	skin:	n/a
46	chr15:34876347-34876397	NHDF-neo	bronchial:	n/a
47	chr15:34875825-34875875	GM06990	blood:	n/a
48	chr15:35001084-35001134	NH-A	brain:	n/a
49	chr15:35001084-35001134	AG09319	gingival:	n/a
50	chr15:34876295-34876345	HPAEpiC	pulmonary alveolar:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:34892499..34894333-chr15:34896967..34899231,2	K562	blood:
2	chr15:34949750..34952665-chr15:35241317..35244101,2	K562	blood:
3	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
4	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
5	chr15:34913918..34914531-chr15:35212584..35213285,2	MCF-7	breast:
6	chr15:34658082..34661057-chr15:34874863..34877414,3	MCF-7	breast:
7	chr15:34913751..34914597-chr15:35212096..35212867,7	K562	blood:
8	chr15:34876102..34877627-chr15:34879229..34881136,2	MCF-7	breast:
9	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
10	chr15:34949722..34952645-chr15:34986997..34989606,2	K562	blood:
11	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
12	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
13	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
14	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
15	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
16	chr15:34980841..34982732-chr15:34984201..34987180,2	K562	blood:
17	chr15:34330963..34332496-chr15:34876229..34877827,2	K562	blood:
18	chr15:34983650..34987842-chr15:34989482..34992979,5	K562	blood:
19	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
20	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
21	chr15:34659441..34662117-chr15:34875107..34877933,3	K562	blood:
22	chr15:34875152..34877762-chr15:34886558..34889393,2	MCF-7	breast:
23	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
24	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
25	chr15:34908560..34909558-chr15:35212164..35213076,4	K562	blood:
26	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
27	chr15:34983650..34987345-chr15:34990001..34992979,4	K562	blood:
28	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
29	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
30	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
31	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
32	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
33	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
34	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
35	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
36	chr15:34632776..34635331-chr15:34879472..34881728,2	K562	blood:
37	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
38	chr13:92448522..92450690-chr15:34895323..34897374,2	K562	blood:
39	chr15:34351759..34355755-chr15:34876768..34880095,3	K562	blood:
40	chr15:34988822..34991429-chr15:34996883..34999400,2	K562	blood:
41	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
42	chr15:34953489..34955951-chr15:35181219..35183157,2	K562	blood:
43	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
44	chr15:34908586..34909269-chr15:35212549..35213068,2	MCF-7	breast:
45	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
46	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
47	chr15:34989332..34992979-chr15:34995533..34998034,4	K562	blood:
48	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
49	chr15:34659566..34660339-chr15:34879136..34879733,2	MCF-7	breast:
50	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
2	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
3	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT041596
4	lnc-GJD2-4	chr15:34845096-34845292	NONHSAT140232
5	lnc-AC114546.1-12	chr15:34988228-34988460	NONHSAT041602
6	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
7	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
8	lnc-GJD2-3	chr15:34858091-34858674	NONHSAT041597
9	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
10	lnc-GJD2-4	chr15:34845174-34845292	NONHSAT041596
11	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT140232
12	lnc-GJD2-3	chr15:34874951-34875061	NONHSAT041597
13	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
14	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
15	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
16	lnc-GJD2-4	chr15:34873667-34873700	NONHSAT140232
17	lnc-GJD2-4	chr15:34875717-34875835	NONHSAT041596
18	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
19	lnc-GJD2-4	chr15:34867026-34867115	NONHSAT041596
20	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
21	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
22	lnc-GJD2-4	chr15:34843392-34843477	NONHSAT140232
23	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+

No data

Variant related genes	Relation type
ENSG00000261304	TF binding region
ENSG00000259892	TF binding region
GOLGA8A	TF binding region
ENSG00000252425	TF binding region
GOLGA8B	TF binding region
ENSG00000261304	CpG island
ENSG00000259892	CpG island
GOLGA8A	CpG island
ENSG00000252425	CpG island
GOLGA8B	CpG island
ENSG00000182117	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000259904	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000261304	chromatin interactions
NEK9	miRNA target sites
NEK7	miRNA target sites

Extended variants
information (count: 5518 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5518 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs348323	chr15:34836521-34836522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs574638613	chr15:34836548-34836549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541768672	chr15:34836581-34836582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560438510	chr15:34836616-34836617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551028684	chr15:34836718-34836719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200393765	chr15:34841726-34841727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202124390	chr15:34841780-34841781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544509117	chr15:34841809-34841810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200636269	chr15:34841908-34841909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs537484348	chr15:34841943-34841944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs549395913	chr15:34841982-34841983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536209110	chr15:34842150-34842151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112457515	chr15:34842376-34842377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2615363	chr15:34842923-34842924	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368220976	chr15:34842925-34842926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs199813402	chr15:34842977-34842978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567788497	chr15:34842987-34842988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534791759	chr15:34843003-34843004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553947123	chr15:34843093-34843094	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs565708496	chr15:34843107-34843108	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs2615364	chr15:34843121-34843122	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539720929	chr15:34843129-34843130	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs557587961	chr15:34843174-34843175	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs369606606	chr15:34843330-34843331	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs575919055	chr15:34843411-34843412	Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs200797971	chr15:34843597-34843598	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs543058460	chr15:34843834-34843835	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs138594282	chr15:34843867-34843868	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs554930233	chr15:34843888-34843889	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs573698681	chr15:34843925-34843926	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs540743716	chr15:34843926-34843927	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201744117	chr15:34844078-34844079	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs559902178	chr15:34844145-34844146	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372587486	chr15:34844149-34844150	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs533324625	chr15:34844157-34844158	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs545609342	chr15:34844237-34844238	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs564017431	chr15:34844244-34844245	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs531208147	chr15:34844326-34844327	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs549433130	chr15:34844327-34844328	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs567517537	chr15:34844381-34844382	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs74007860	chr15:34844388-34844389	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs138705460	chr15:34844389-34844390	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs554945965	chr15:34844408-34844409	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs76506208	chr15:34844420-34844421	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs113956598	chr15:34844434-34844435	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs147838853	chr15:34844442-34844443	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs150176079	chr15:34844466-34844467	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs201978944	chr15:34844501-34844502	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs76374677	chr15:34844573-34844574	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs149396148	chr15:34844577-34844578	Weak transcription	TF binding region	1 gene(s)	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:1383 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34836400-34836800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr15:34836400-34836800	Enhancers	HUVEC	blood vessel
3	chr15:34841600-34862000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr15:34841800-34844200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr15:34842400-34849200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:34842800-34843200	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr15:34842800-34843200	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr15:34842800-34843200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr15:34842800-34843200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr15:34842800-34843200	Enhancers	GM12878-XiMat	blood
11	chr15:34848400-34874600	Weak transcription	Esophagus	oesophagus
12	chr15:34854200-34862000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr15:34854600-34873600	Weak transcription	GM12878-XiMat	blood
14	chr15:34856000-34856800	Weak transcription	Lung	lung
15	chr15:34856400-34872600	Weak transcription	Gastric	stomach
16	chr15:34856600-34873200	Weak transcription	Ovary	ovary
17	chr15:34856800-34857000	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr15:34856800-34857200	ZNF genes & repeats	Lung	lung
19	chr15:34856800-34857200	Enhancers	Spleen	Spleen
20	chr15:34857000-34857200	ZNF genes & repeats	Aorta	Aorta
21	chr15:34857000-34857200	Enhancers	Left Ventricle	heart
22	chr15:34857000-34857200	Enhancers	Pancreas	Pancrea
23	chr15:34857000-34857400	Enhancers	Primary T cells fromperipheralblood	blood
24	chr15:34857000-34857400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr15:34857000-34867000	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr15:34857000-34873000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr15:34857200-34857600	Weak transcription	Aorta	Aorta
28	chr15:34857200-34861600	Weak transcription	Pancreas	Pancrea
29	chr15:34857200-34861800	Weak transcription	Spleen	Spleen
30	chr15:34857200-34872400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr15:34857400-34873000	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr15:34858800-34861600	Weak transcription	Right Ventricle	heart
33	chr15:34859000-34862000	Weak transcription	Fetal Muscle Leg	muscle
34	chr15:34859000-34872600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:34859600-34860000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr15:34860000-34860200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
37	chr15:34860400-34869800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr15:34861400-34862400	Enhancers	Fetal Muscle Trunk	muscle
39	chr15:34861600-34861800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:34861600-34862600	Enhancers	Left Ventricle	heart
41	chr15:34861600-34862600	Enhancers	Pancreas	Pancrea
42	chr15:34861600-34862600	Enhancers	Right Ventricle	heart
43	chr15:34861800-34862600	Enhancers	Spleen	Spleen
44	chr15:34861800-34873000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr15:34862000-34862400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr15:34862000-34862400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
47	chr15:34862000-34862400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr15:34862000-34862400	Enhancers	Fetal Muscle Leg	muscle
49	chr15:34862000-34862600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr15:34862200-34862600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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