Variant report

Variant	nsv569131
Chromosome Location	chr15:34871296-35020391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2701)
CpG islands
(count:1527)
Chromatin interactive
region (count:113)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2701 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34902659-34902943	K562	blood:	n/a	n/a
2	ARID3A	chr15:34905532-34905838	K562	blood:	n/a	n/a
3	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
4	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
5	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
6	ARID3A	chr15:35000570-35000896	K562	blood:	n/a	n/a
7	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
8	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
9	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
10	ARID3A	chr15:34989159-34989187	K562	blood:	n/a	n/a
11	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
12	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
13	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
14	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
15	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
16	ARID3A	chr15:34908827-34909205	K562	blood:	n/a	n/a
17	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
18	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
19	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
20	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
21	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
22	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
23	ATF1	chr15:34985696-34985896	K562	blood:	n/a	n/a
24	ATF1	chr15:34905714-34905797	K562	blood:	n/a	n/a
25	ATF1	chr15:35000572-35001097	K562	blood:	n/a	n/a
26	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
27	ATF1	chr15:34896856-34896884	K562	blood:	n/a	n/a
28	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
29	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
30	ATF1	chr15:35006704-35007397	K562	blood:	n/a	n/a
31	ATF1	chr15:34908847-34909148	K562	blood:	n/a	n/a
32	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
33	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
34	ATF1	chr15:35019827-35019831	K562	blood:	n/a	n/a
35	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
36	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
37	ATF2	chr15:34880257-34880906	GM12878	blood:	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	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr15:34942319-34942566	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	chr15:34876822-34876846	K562	blood:	n/a	n/a
45	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
46	BATF	chr15:34942288-34942693	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
47	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
48	BCL11A	chr15:34942342-34942649	GM12878	blood:	n/a	n/a
49	BCL11A	chr15:34942273-34942696	GM12878	blood:	n/a	n/a
50	BCL11A	chr15:34875680-34875925	GM12878	blood:	n/a	chr15:34875720-34875733 chr15:34875761-34875774

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34875937-34875987	AG09309	skin:	n/a
2	chr15:34875825-34875875	AG04450	lung:	fetal
3	chr15:34875937-34875987	AG09309	skin:	n/a
4	chr15:34875825-34875875	AG04450	lung:	fetal
5	chr15:34880284-34880334	AG04449	skin:	fetal
6	chr15:34875937-34875987	ProgFib	skin:	n/a
7	chr15:34874862-34874912	AG09309	skin:	n/a
8	chr15:34875945-34875995	NT2-D1	testis:	n/a
9	chr15:34875250-34875300	GM12891	blood:	n/a
10	chr15:34988869-34988919	H1-hESC	embryonic stem cell:	embryo
11	chr15:35014229-35014279	HRPEpiC	eye:	n/a
12	chr15:34875325-34875375	NB4	blood:	n/a
13	chr15:34875891-34875941	CMK	blood:	n/a
14	chr15:34874862-34874912	AG09319	gingival:	n/a
15	chr15:34875945-34875995	H1-hESC	embryonic stem cell:	embryo
16	chr15:35017944-35017994	Jurkat	blood:	n/a
17	chr15:34876283-34876333	HCM	heart:	n/a
18	chr15:34875945-34875995	RPTEC	kidney:	n/a
19	chr15:34876396-34876446	H1-hESC	embryonic stem cell:	embryo
20	chr15:34876283-34876333	HRE	kidney:	n/a
21	chr15:34875325-34875375	HNPCEpiC	eye:	n/a
22	chr15:34872733-34872783	HCF	heart:	n/a
23	chr15:34875825-34875875	Jurkat	blood:	n/a
24	chr15:34874862-34874912	LNCaP	prostate:	n/a
25	chr15:34875325-34875375	HCPEpiC	choroid plexus:	n/a
26	chr15:34875945-34875995	GM12878	blood:	n/a
27	chr15:34877407-34877457	T-47D	breast:	n/a
28	chr15:34875937-34875987	HUVEC	blood vessel:	n/a
29	chr15:34875891-34875941	HRCEpiC	kidney:	n/a
30	chr15:34876283-34876333	Jurkat	blood:	n/a
31	chr15:34876295-34876345	K562	blood:	n/a
32	chr15:34875825-34875875	AoSMC	blood vessel:	n/a
33	chr15:34876471-34876521	CMK	blood:	n/a
34	chr15:34876295-34876345	GM12891	blood:	n/a
35	chr15:35001084-35001134	LNCaP	prostate:	n/a
36	chr15:34876347-34876397	HCT-116	colon:	n/a
37	chr15:34874862-34874912	T-47D	breast:	n/a
38	chr15:34875325-34875375	AG09319	gingival:	n/a
39	chr15:34880284-34880334	ECC-1	luminal epithelium:	n/a
40	chr15:34875930-34875980	AG09309	skin:	n/a
41	chr15:34875250-34875300	AG09319	gingival:	n/a
42	chr15:35014229-35014279	HEK293	kidney:	embryo
43	chr15:34875937-34875987	Jurkat	blood:	n/a
44	chr15:34876471-34876521	MCF-7	breast:	n/a
45	chr15:35010826-35010876	HCT-116	colon:	n/a
46	chr15:34875250-34875300	SK-N-SH	brain:	n/a
47	chr15:34988869-34988919	Jurkat	blood:	n/a
48	chr15:34875825-34875875	GM12892	blood:	n/a
49	chr15:34875325-34875375	HCT-116	colon:	n/a
50	chr15:34875825-34875875	LNCaP	prostate:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:35005678..35008340-chr15:35281317..35283659,2	K562	blood:
2	chr15:34953489..34955951-chr15:35181219..35183157,2	K562	blood:
3	chr15:35001097..35003090-chr15:35007070..35008790,2	K562	blood:
4	chr15:34876102..34877627-chr15:34879229..34881136,2	MCF-7	breast:
5	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
6	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
7	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
8	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
9	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
10	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
11	chr13:92448522..92450690-chr15:34895323..34897374,2	K562	blood:
12	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
13	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
14	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
15	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
16	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
17	chr15:35010787..35013754-chr15:35014491..35016542,2	K562	blood:
18	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
19	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
20	chr15:34330963..34332496-chr15:34876229..34877827,2	K562	blood:
21	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
22	chr15:34628679..34631455-chr15:34874185..34875808,2	K562	blood:
23	chr15:35010787..35013754-chr15:35014491..35016542,2	K562	blood:
24	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
25	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
26	chr15:34513565..34517614-chr15:34877827..34881077,3	K562	blood:
27	chr15:34908560..34909558-chr15:35212164..35213076,4	K562	blood:
28	chr15:34892499..34894333-chr15:34896967..34899231,2	K562	blood:
29	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
30	chr15:34988822..34991429-chr15:34996883..34999400,2	K562	blood:
31	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
32	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
33	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
34	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
35	chr15:35010890..35011778-chr17:59321038..59321843,2	MCF-7	breast:
36	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
37	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
38	chr15:34875152..34877762-chr15:34886558..34889393,2	MCF-7	breast:
39	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
40	chr15:34913751..34914597-chr15:35212096..35212867,7	K562	blood:
41	chr15:34913918..34914531-chr15:35212584..35213285,2	MCF-7	breast:
42	chr15:35001097..35003090-chr15:35007070..35008790,2	K562	blood:
43	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
44	chr15:34632776..34635331-chr15:34879472..34881728,2	K562	blood:
45	chr15:35012152..35014532-chr15:35016625..35018343,2	MCF-7	breast:
46	chr15:34908586..34909269-chr15:35212549..35213068,2	MCF-7	breast:
47	chr15:35012152..35014532-chr15:35016625..35018343,2	MCF-7	breast:
48	chr15:34980841..34982732-chr15:34984201..34987180,2	K562	blood:
49	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
50	chr15:34983650..34987842-chr15:34989482..34992979,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC114546.1-4	chr15:35015809-35016397	NONHSAT041604
2	lnc-GJD2-4	chr15:34875717-34875835	NONHSAT041596
3	lnc-GJD2-3	chr15:34874951-34875061	NONHSAT041597
4	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
5	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
6	lnc-AC114546.1-12	chr15:34988228-34988460	NONHSAT041602
7	lnc-GJD2-4	chr15:34873667-34873700	NONHSAT140232
8	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
9	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
10	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
11	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
12	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
13	lnc-AC114546.1-4	chr15:35014273-35014438	XLOC_011205
14	lnc-GJD2-1	chr15:35012518-35012708	XLOC_011422
15	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
16	lnc-AC114546.1-4	chr15:35014395-35014438	NONHSAT041604
17	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
18	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
19	lnc-AC114546.1-4	chr15:35015735-35016108	XLOC_011205
20	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
21	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1

No data

Variant related genes	Relation type
ENSG00000261304	TF binding region
GOLGA8A	TF binding region
ENSG00000252425	TF binding region
GOLGA8B	TF binding region
ENSG00000261304	CpG island
GOLGA8A	CpG island
ENSG00000252425	CpG island
GOLGA8B	CpG island
ENSG00000140199	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000236756	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000259904	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000197409	chromatin interactions
NEK9	miRNA target sites
NEK7	miRNA target sites

Extended variants
information (count: 5118 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:5118 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2879515	chr15:34871296-34871297	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533470575	chr15:34871314-34871315	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs200649443	chr15:34871331-34871332	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs549552618	chr15:34871332-34871333	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs77431455	chr15:34871338-34871339	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs187701248	chr15:34871404-34871405	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs529121830	chr15:34871406-34871407	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs2339594	chr15:34871413-34871414	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs372193124	chr15:34871428-34871429	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs150755693	chr15:34871441-34871442	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs565627772	chr15:34871449-34871450	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs140208218	chr15:34871451-34871452	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs539053178	chr15:34871455-34871456	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs140317873	chr15:34871459-34871460	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs7180148	chr15:34871473-34871474	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs147506445	chr15:34871477-34871478	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs373759950	chr15:34871478-34871479	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs569628183	chr15:34871481-34871482	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs139672084	chr15:34871482-34871483	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs369470571	chr15:34871488-34871489	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs144621267	chr15:34871498-34871499	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs182779841	chr15:34871534-34871535	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs149095905	chr15:34871537-34871538	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs375129928	chr15:34871542-34871543	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs111241422	chr15:34871554-34871555	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs112379566	chr15:34871555-34871556	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs138119978	chr15:34871560-34871561	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs187024939	chr15:34871583-34871584	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs553381888	chr15:34871588-34871589	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs3964611	chr15:34871609-34871610	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs369108003	chr15:34871640-34871641	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs545053655	chr15:34871641-34871642	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs34861720	chr15:34871652-34871653	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs79642675	chr15:34871660-34871661	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs77157276	chr15:34871664-34871665	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs77571247	chr15:34871687-34871688	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs4923707	chr15:34871690-34871691	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs74475075	chr15:34871734-34871735	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs74407991	chr15:34871741-34871742	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs4924042	chr15:34871743-34871744	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs78111834	chr15:34871745-34871746	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs77828532	chr15:34871756-34871757	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs201196743	chr15:34871766-34871767	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs74193858	chr15:34871768-34871769	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs7179402	chr15:34871785-34871786	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs549964287	chr15:34871809-34871810	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs150738118	chr15:34871812-34871813	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs373368920	chr15:34871814-34871815	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs74510946	chr15:34871820-34871821	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs113047879	chr15:34871827-34871828	Weak transcription Enhancers	Chromatin interactive region	3 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:1654 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34848400-34874600	Weak transcription	Esophagus	oesophagus
2	chr15:34854600-34873600	Weak transcription	GM12878-XiMat	blood
3	chr15:34856400-34872600	Weak transcription	Gastric	stomach
4	chr15:34856600-34873200	Weak transcription	Ovary	ovary
5	chr15:34857000-34873000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr15:34857200-34872400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:34857400-34873000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr15:34859000-34872600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr15:34861800-34873000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:34862400-34874000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr15:34862400-34874600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr15:34862600-34873000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr15:34862600-34873800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr15:34862600-34874000	Weak transcription	Spleen	Spleen
15	chr15:34864800-34873000	Weak transcription	Brain Angular Gyrus	brain
16	chr15:34866600-34873000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr15:34867000-34872800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr15:34867200-34874000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr15:34867400-34874400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr15:34867800-34872800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr15:34869000-34871800	Weak transcription	Right Atrium	heart
22	chr15:34869200-34871800	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr15:34869200-34872400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr15:34869200-34874000	Weak transcription	Colonic Mucosa	Colon
25	chr15:34869200-34874200	Weak transcription	Aorta	Aorta
26	chr15:34869400-34873000	Weak transcription	Left Ventricle	heart
27	chr15:34869600-34873000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr15:34869800-34871800	Weak transcription	Fetal Heart	heart
29	chr15:34870000-34871400	Weak transcription	Fetal Muscle Leg	muscle
30	chr15:34870000-34872400	Weak transcription	HSMM	muscle
31	chr15:34870000-34873000	Weak transcription	HSMMtube	muscle
32	chr15:34870400-34872600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr15:34870400-34872800	Enhancers	Pancreas	Pancrea
34	chr15:34870400-34874200	Weak transcription	NHLF	lung
35	chr15:34870600-34871800	Weak transcription	Fetal Brain Female	brain
36	chr15:34870600-34872600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr15:34870600-34872800	Weak transcription	Lung	lung
38	chr15:34870600-34873800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr15:34870600-34873800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr15:34870600-34873800	Weak transcription	Hela-S3	cervix
41	chr15:34870600-34874000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr15:34870600-34874600	Weak transcription	NHDF-Ad	bronchial
43	chr15:34870800-34871400	Weak transcription	Right Ventricle	heart
44	chr15:34870800-34872000	Weak transcription	Fetal Brain Male	brain
45	chr15:34870800-34872400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr15:34870800-34872600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr15:34870800-34873000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr15:34870800-34873000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr15:34870800-34873400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr15:34870800-34873800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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