Variant report

Variant	nsv569005
Chromosome Location	chr15:34718594-35032856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4326)
CpG islands
(count:3237)
Chromatin interactive
region (count:155)
LncRNA
region (count:31)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:4326 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
2	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
3	ARID3A	chr15:34908827-34909205	K562	blood:	n/a	n/a
4	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
5	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
6	ARID3A	chr15:35000570-35000896	K562	blood:	n/a	n/a
7	ARID3A	chr15:34731584-34731600	K562	blood:	n/a	n/a
8	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
9	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
10	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
11	ARID3A	chr15:34781246-34781587	K562	blood:	n/a	n/a
12	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
13	ARID3A	chr15:34989159-34989187	K562	blood:	n/a	n/a
14	ARID3A	chr15:34902659-34902943	K562	blood:	n/a	n/a
15	ARID3A	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
16	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
17	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
18	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
19	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
20	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
21	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
22	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
23	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
24	ARID3A	chr15:34905532-34905838	K562	blood:	n/a	n/a
25	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
26	ATF1	chr15:34985696-34985896	K562	blood:	n/a	n/a
27	ATF1	chr15:35019827-35019831	K562	blood:	n/a	n/a
28	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
29	ATF1	chr15:34807442-34807640	K562	blood:	n/a	n/a
30	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
31	ATF1	chr15:35006704-35007397	K562	blood:	n/a	n/a
32	ATF1	chr15:34905714-34905797	K562	blood:	n/a	n/a
33	ATF1	chr15:35000572-35001097	K562	blood:	n/a	n/a
34	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
35	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
36	ATF1	chr15:34808283-34808324	K562	blood:	n/a	n/a
37	ATF1	chr15:34896856-34896884	K562	blood:	n/a	n/a
38	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
39	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
40	ATF1	chr15:34908847-34909148	K562	blood:	n/a	n/a
41	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
42	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
43	ATF1	chr15:34761374-34761389	K562	blood:	n/a	n/a
44	ATF2	chr15:34880089-34880894	GM12878	blood:	n/a	n/a
45	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
46	ATF2	chr15:34880257-34880906	GM12878	blood:	n/a	n/a
47	ATF2	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
48	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
49	ATF3	chr15:34781262-34781502	K562	blood:	n/a	n/a
50	ATF3	chr15:34908811-34909131	K562	blood:	n/a	n/a

(count:3237 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34812400-34812450	CMK	blood:	n/a
2	chr15:34876283-34876333	HCM	heart:	n/a
3	chr15:34806810-34806860	SAEC	small airway:	n/a
4	chr15:34786594-34786644	GM06990	blood:	n/a
5	chr15:34812400-34812450	CMK	blood:	n/a
6	chr15:34876283-34876333	HCM	heart:	n/a
7	chr15:34806810-34806860	SAEC	small airway:	n/a
8	chr15:34786594-34786644	GM06990	blood:	n/a
9	chr15:34876347-34876397	GM12892	blood:	n/a
10	chr15:34787920-34787970	NHDF-neo	bronchial:	n/a
11	chr15:34875117-34875167	SAEC	small airway:	n/a
12	chr15:34807221-34807271	SAEC	small airway:	n/a
13	chr15:34880284-34880334	AG04450	lung:	fetal
14	chr15:34877407-34877457	PrEC	prostate:	n/a
15	chr15:34875937-34875987	PrEC	prostate:	n/a
16	chr15:34876471-34876521	LNCaP	prostate:	n/a
17	chr15:35014229-35014279	H1-hESC	embryonic stem cell:	embryo
18	chr15:34812400-34812450	SAEC	small airway:	n/a
19	chr15:34807221-34807271	HPAEpiC	pulmonary alveolar:	n/a
20	chr15:34876471-34876521	HL-60	blood:	n/a
21	chr15:34788847-34788897	RPTEC	kidney:	n/a
22	chr15:34729310-34729360	U87	brain:	n/a
23	chr15:34875325-34875375	Caco-2	colon:	n/a
24	chr15:34781969-34782019	ProgFib	skin:	n/a
25	chr15:34872733-34872783	NT2-D1	testis:	n/a
26	chr15:34729115-34729165	AoSMC	blood vessel:	n/a
27	chr15:34874862-34874912	MCF10A-Er-Src	breast:	n/a
28	chr15:34806810-34806860	HEK293	kidney:	embryo
29	chr15:35014270-35014320	GM06990	blood:	n/a
30	chr15:34788017-34788067	SK-N-SH	brain:	n/a
31	chr15:34875138-34875188	HCPEpiC	choroid plexus:	n/a
32	chr15:34877407-34877457	Hela-S3	cervix:	n/a
33	chr15:34782167-34782217	Hepatocyte	liver:	n/a
34	chr15:34788017-34788067	HCM	heart:	n/a
35	chr15:34729310-34729360	BE2_C	brain:	n/a
36	chr15:34782820-34782870	HIPEpiC	eye:	n/a
37	chr15:34806592-34806642	SK-N-SH_RA	brain:	n/a
38	chr15:34988869-34988919	PrEC	prostate:	n/a
39	chr15:34782820-34782870	Hepatocyte	liver:	n/a
40	chr15:34876283-34876333	SK-N-MC	brain:	n/a
41	chr15:34787920-34787970	HIPEpiC	eye:	n/a
42	chr15:35001084-35001134	HMEC	breast:	n/a
43	chr15:34806810-34806860	NT2-D1	testis:	n/a
44	chr15:34807050-34807100	HRPEpiC	eye:	n/a
45	chr15:34782820-34782870	GM12892	blood:	n/a
46	chr15:34876295-34876345	HCF	heart:	n/a
47	chr15:34880284-34880334	Hepatocyte	liver:	n/a
48	chr15:34806810-34806860	HCT-116	colon:	n/a
49	chr15:35001084-35001134	BE2_C	brain:	n/a
50	chr15:34788847-34788897	CMK	blood:	n/a

(count:155 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
2	chr15:34869058..34871895-chr15:34873883..34875893,3	K562	blood:
3	chr15:35029315..35031883-chr15:35048194..35050280,2	K562	blood:
4	chr15:34997005..34998827-chr15:34999088..35001652,2	K562	blood:
5	chr15:34934825..34936603-chr15:34945044..34948146,4	K562	blood:
6	chr15:34518743..34520763-chr15:34876016..34878611,2	MCF-7	breast:
7	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
8	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
9	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
10	chr15:34330963..34332496-chr15:34876229..34877827,2	K562	blood:
11	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
12	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
13	chr15:34759701..34761289-chr15:34761464..34762969,2	K562	blood:
14	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
15	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
16	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
17	chr15:34762215..34765168-chr15:34878877..34880750,2	K562	blood:
18	chr15:34728066..34730668-chr15:34791069..34792682,2	K562	blood:
19	chr15:34659566..34660339-chr15:34879136..34879733,2	MCF-7	breast:
20	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
21	chr15:34870217..34872096-chr15:35279333..35281998,2	K562	blood:
22	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
23	chr15:34727581..34729084-chr15:34874171..34876472,2	MCF-7	breast:
24	chr15:34879223..34881623-chr15:34893177..34895546,2	K562	blood:
25	chr15:35020981..35022904-chr15:35025559..35027089,2	K562	blood:
26	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
27	chr15:35010890..35011778-chr17:59321038..59321843,2	MCF-7	breast:
28	chr15:34658082..34661057-chr15:34874863..34877414,3	MCF-7	breast:
29	chr15:34351759..34355755-chr15:34876768..34880095,3	K562	blood:
30	chr15:34983650..34987345-chr15:34990001..34992979,4	K562	blood:
31	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
32	chr15:34783968..34786265-chr15:34799018..34801586,2	K562	blood:
33	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
34	chr15:35012152..35014532-chr15:35016625..35018343,2	MCF-7	breast:
35	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
36	chr15:34989332..34992979-chr15:34995533..34998034,4	K562	blood:
37	chr15:34988822..34991429-chr15:34996883..34999400,2	K562	blood:
38	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
39	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
40	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
41	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
42	chr15:34628679..34631455-chr15:34874185..34875808,2	K562	blood:
43	chr15:35001097..35003090-chr15:35007070..35008790,2	K562	blood:
44	chr15:34989332..34992979-chr15:34995533..34998034,4	K562	blood:
45	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
46	chr15:34988822..34991429-chr15:34996883..34999400,2	K562	blood:
47	chr15:34913918..34914531-chr15:35212584..35213285,2	MCF-7	breast:
48	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
49	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
50	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT041596
2	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
3	lnc-AC114546.1-4	chr15:35014273-35014438	XLOC_011205
4	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
5	lnc-AC114546.1-4	chr15:35014395-35014438	NONHSAT041604
6	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
7	lnc-AC114546.1-4	chr15:35015809-35016397	NONHSAT041604
8	lnc-GJD2-3	chr15:34858091-34858674	NONHSAT041597
9	lnc-GJD2-4	chr15:34845096-34845292	NONHSAT140232
10	lnc-GJD2-4	chr15:34873667-34873700	NONHSAT140232
11	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
12	lnc-GJD2-4	chr15:34843392-34843477	NONHSAT140232
13	lnc-GJD2-1	chr15:35012518-35012708	XLOC_011422
14	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
15	lnc-GJD2-4	chr15:34867026-34867115	NONHSAT041596
16	lnc-GJD2-4	chr15:34845174-34845292	NONHSAT041596
17	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
18	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
19	lnc-GJD2-4	chr15:34875717-34875835	NONHSAT041596
20	lnc-AC114546.1-4	chr15:35015735-35016108	XLOC_011205
21	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
22	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
23	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
24	lnc-GOLGA8B-1	chr15:34752685-34752950	uc_384_-
25	lnc-C15orf55-4	chr15:34752685-34752950	uc_384_+
26	lnc-AC114546.1-12	chr15:34988228-34988460	NONHSAT041602
27	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
28	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT140232
29	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
30	lnc-LPCAT4-1	chr15:34720816-34721126	NONHSAT041586
31	lnc-GJD2-3	chr15:34874951-34875061	NONHSAT041597

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1233-5p	chr15:34820548-34820569	MIMAT0022943_1
hsa-miR-1233-3p	chr15:34820491-34820510	MIMAT0005588_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
ENSG00000197409	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000259917	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000171421	chromatin interactions
ENSG00000236756	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000184507	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000259904	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000176454	chromatin interactions
NEK9	miRNA target sites
NEK7	miRNA target sites

Extended variants
information (count: 9902 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:9902 , 50 per page) page: 1 2 3 4 5 6 7 ... 199

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3894644	chr15:34718594-34718595	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183840350	chr15:34718595-34718596	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs3894643	chr15:34718597-34718598	Weak transcription Strong transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11351323	chr15:34718607-34718608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs151024399	chr15:34718617-34718618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200246847	chr15:34718652-34718653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201602462	chr15:34718658-34718659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs559875574	chr15:34718688-34718689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs4924717	chr15:34718710-34718711	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs140988185	chr15:34718731-34718732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370926997	chr15:34718737-34718738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376188718	chr15:34718743-34718744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113573777	chr15:34718759-34718760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112464429	chr15:34718761-34718762	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368387205	chr15:34718779-34718780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146700380	chr15:34718785-34718786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs540340705	chr15:34718795-34718796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2554787	chr15:34718805-34718806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188111645	chr15:34718813-34718814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371333097	chr15:34718816-34718817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs566979810	chr15:34718820-34718821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs148687709	chr15:34718826-34718827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111384118	chr15:34718868-34718869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112165968	chr15:34718869-34718870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112965049	chr15:34718870-34718871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141115138	chr15:34718876-34718877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146898154	chr15:34718884-34718885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2261586	chr15:34718898-34718899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs75845309	chr15:34718905-34718906	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527749815	chr15:34718913-34718914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549720050	chr15:34718928-34718929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201947054	chr15:34718929-34718930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370942972	chr15:34718934-34718935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377531345	chr15:34718963-34718964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370621919	chr15:34718979-34718980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553715834	chr15:34718996-34718997	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572205079	chr15:34719010-34719011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536784906	chr15:34719016-34719017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs555110122	chr15:34719023-34719024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374317378	chr15:34719030-34719031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs367720728	chr15:34719086-34719087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191424081	chr15:34719098-34719099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs147498577	chr15:34719143-34719144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374834433	chr15:34719175-34719176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs374728005	chr15:34719211-34719212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569218701	chr15:34719220-34719221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138220980	chr15:34719256-34719257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554573577	chr15:34719261-34719262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs76358577	chr15:34719271-34719272	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
50	rs144255525	chr15:34719272-34719273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3042 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34662800-34723600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr15:34695200-34722600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr15:34706800-34724200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr15:34709000-34721800	Weak transcription	GM12878-XiMat	blood
5	chr15:34709000-34724200	Weak transcription	Fetal Stomach	stomach
6	chr15:34709200-34721800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr15:34709400-34720200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr15:34709600-34724200	Weak transcription	Hela-S3	cervix
9	chr15:34709600-34728000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr15:34709800-34728600	Weak transcription	Gastric	stomach
11	chr15:34710400-34724400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:34711000-34720200	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr15:34711000-34722000	Weak transcription	Primary T cells from cord blood	blood
14	chr15:34711000-34723800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr15:34711000-34724400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr15:34711000-34726800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr15:34711200-34721800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr15:34711200-34724000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:34711200-34727800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr15:34711600-34728600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr15:34711800-34724400	Weak transcription	HSMMtube	muscle
22	chr15:34712000-34722000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr15:34712000-34727800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr15:34712200-34722400	Weak transcription	K562	blood
25	chr15:34712600-34727800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr15:34712800-34723600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr15:34714000-34722600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr15:34714400-34726200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr15:34714400-34727800	Weak transcription	HSMM	muscle
30	chr15:34714800-34728000	Weak transcription	Fetal Intestine Small	intestine
31	chr15:34715800-34724200	Weak transcription	Ovary	ovary
32	chr15:34716000-34720600	Weak transcription	Spleen	Spleen
33	chr15:34716000-34721800	Weak transcription	Lung	lung
34	chr15:34716200-34721800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:34716200-34724400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr15:34716200-34726400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr15:34716200-34728400	Weak transcription	Right Atrium	heart
38	chr15:34716400-34722000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:34716800-34728600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr15:34717000-34727800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr15:34717200-34718600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr15:34717200-34727800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr15:34717400-34724200	Weak transcription	Primary T helper cells fromperipheralblood	blood
44	chr15:34717600-34728400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr15:34718000-34718600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
46	chr15:34718200-34718600	Active TSS	Brain Angular Gyrus	brain
47	chr15:34718200-34718600	Active TSS	Brain Anterior Caudate	brain
48	chr15:34718200-34718600	Active TSS	Brain Cingulate Gyrus	brain
49	chr15:34718200-34718600	Active TSS	Brain Hippocampus Middle	brain
50	chr15:34718200-34718600	Active TSS	Brain Inferior Temporal Lobe	brain

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