Variant report

Variant	nsv1053730
Chromosome Location	chr15:34862247-35033073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2823)
CpG islands
(count:1527)
Chromatin interactive
region (count:120)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2823 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:34908827-34909205	K562	blood:	n/a	n/a
3	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
5	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
6	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
7	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
8	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
9	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
10	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
11	ARID3A	chr15:34905532-34905838	K562	blood:	n/a	n/a
12	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
13	ARID3A	chr15:34902659-34902943	K562	blood:	n/a	n/a
14	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
15	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
16	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
17	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
18	ARID3A	chr15:34989159-34989187	K562	blood:	n/a	n/a
19	ARID3A	chr15:35000570-35000896	K562	blood:	n/a	n/a
20	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
21	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
22	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
23	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
24	ATF1	chr15:35006704-35007397	K562	blood:	n/a	n/a
25	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
26	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
27	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
28	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
29	ATF1	chr15:35000572-35001097	K562	blood:	n/a	n/a
30	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
31	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
32	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
33	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
34	ATF1	chr15:34896856-34896884	K562	blood:	n/a	n/a
35	ATF1	chr15:34985696-34985896	K562	blood:	n/a	n/a
36	ATF1	chr15:34908847-34909148	K562	blood:	n/a	n/a
37	ATF1	chr15:35019827-35019831	K562	blood:	n/a	n/a
38	ATF1	chr15:34905714-34905797	K562	blood:	n/a	n/a
39	ATF2	chr15:34880257-34880906	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	ATF2	chr15:34880089-34880894	GM12878	blood:	n/a	n/a
43	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
44	ATF3	chr15:34908811-34909131	K562	blood:	n/a	n/a
45	BACH1	chr15:34876822-34876846	K562	blood:	n/a	n/a
46	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
47	BACH1	chr15:35032729-35032741	K562	blood:	n/a	n/a
48	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
49	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
50	BATF	chr15:34942288-34942693	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:35014270-35014320	SKMC	muscle:	n/a
2	chr15:34880284-34880334	HMEC	breast:	n/a
3	chr15:35014270-35014320	SKMC	muscle:	n/a
4	chr15:34880284-34880334	HMEC	breast:	n/a
5	chr15:34874183-34874233	HCT-116	colon:	n/a
6	chr15:34875825-34875875	HIPEpiC	eye:	n/a
7	chr15:34877407-34877457	NHDF-neo	bronchial:	n/a
8	chr15:35017944-35017994	SAEC	small airway:	n/a
9	chr15:34876396-34876446	BJ	skin:	n/a
10	chr15:35014270-35014320	HAEpiC	amniotic membrane:	n/a
11	chr15:34875937-34875987	HCPEpiC	choroid plexus:	n/a
12	chr15:34877407-34877457	H1-hESC	embryonic stem cell:	embryo
13	chr15:34875937-34875987	H1-hESC	embryonic stem cell:	embryo
14	chr15:34874862-34874912	BJ	skin:	n/a
15	chr15:35001084-35001134	HCT-116	colon:	n/a
16	chr15:34875930-34875980	SK-N-MC	brain:	n/a
17	chr15:34874183-34874233	PFSK-1	brain:	n/a
18	chr15:34874862-34874912	ProgFib	skin:	n/a
19	chr15:34876471-34876521	PFSK-1	brain:	n/a
20	chr15:34874183-34874233	AG04450	lung:	fetal
21	chr15:34875325-34875375	SK-N-SH	brain:	n/a
22	chr15:34876471-34876521	Jurkat	blood:	n/a
23	chr15:34875930-34875980	Caco-2	colon:	n/a
24	chr15:34880284-34880334	HRPEpiC	eye:	n/a
25	chr15:35017944-35017994	Caco-2	colon:	n/a
26	chr15:34876471-34876521	H1-hESC	embryonic stem cell:	embryo
27	chr15:34874862-34874912	AG09319	gingival:	n/a
28	chr15:34875325-34875375	Caco-2	colon:	n/a
29	chr15:34875891-34875941	T-47D	breast:	n/a
30	chr15:34875138-34875188	U87	brain:	n/a
31	chr15:34875891-34875941	HUVEC	blood vessel:	n/a
32	chr15:35017944-35017994	BJ	skin:	n/a
33	chr15:34876347-34876397	NH-A	brain:	n/a
34	chr15:35017944-35017994	AG09319	gingival:	n/a
35	chr15:35010826-35010876	HUVEC	blood vessel:	n/a
36	chr15:34874183-34874233	Caco-2	colon:	n/a
37	chr15:35001084-35001134	BE2_C	brain:	n/a
38	chr15:35017944-35017994	HL-60	blood:	n/a
39	chr15:34880284-34880334	LNCaP	prostate:	n/a
40	chr15:34875325-34875375	HRCEpiC	kidney:	n/a
41	chr15:34877407-34877457	ECC-1	luminal epithelium:	n/a
42	chr15:34875325-34875375	AG04449	skin:	fetal
43	chr15:34875117-34875167	LNCaP	prostate:	n/a
44	chr15:34874183-34874233	HCM	heart:	n/a
45	chr15:34876283-34876333	Hepatocyte	liver:	n/a
46	chr15:35017944-35017994	HNPCEpiC	eye:	n/a
47	chr15:35014270-35014320	RPTEC	kidney:	n/a
48	chr15:34875937-34875987	NHDF-neo	bronchial:	n/a
49	chr15:34875891-34875941	MCF10A-Er-Src	breast:	n/a
50	chr15:35001084-35001134	MCF-7	breast:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
2	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
3	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
4	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
5	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
6	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
7	chr15:35005678..35008340-chr15:35281317..35283659,2	K562	blood:
8	chr15:34351759..34355755-chr15:34876768..34880095,3	K562	blood:
9	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
10	chr15:34988822..34991429-chr15:34996883..34999400,2	K562	blood:
11	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
12	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
13	chr15:35001097..35003090-chr15:35007070..35008790,2	K562	blood:
14	chr15:34659566..34660339-chr15:34879136..34879733,2	MCF-7	breast:
15	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
16	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
17	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
18	chr15:34518743..34520763-chr15:34876016..34878611,2	MCF-7	breast:
19	chr15:34628679..34631455-chr15:34874185..34875808,2	K562	blood:
20	chr15:35020981..35022904-chr15:35025559..35027089,2	K562	blood:
21	chr15:34983650..34987842-chr15:34989482..34992979,5	K562	blood:
22	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
23	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
24	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
25	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
26	chr15:35014688..35016306-chr15:35021250..35023169,2	K562	blood:
27	chr15:34913751..34914597-chr15:35212096..35212867,7	K562	blood:
28	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
29	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
30	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
31	chr15:34664329..34667047-chr15:34894143..34895743,2	MCF-7	breast:
32	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
33	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
34	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
35	chr15:34727885..34731466-chr15:34878887..34881950,4	K562	blood:
36	chr15:35014688..35016306-chr15:35021250..35023169,2	K562	blood:
37	chr15:34727095..34731466-chr15:34878887..34881950,4	K562	blood:
38	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
39	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
40	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
41	chr15:34988822..34991429-chr15:34996883..34999400,2	K562	blood:
42	chr10:75006642..75007633-chr15:35013735..35014638,2	Hela-S3	cervix:
43	chr15:34934825..34936603-chr15:34945044..34948146,4	K562	blood:
44	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
45	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
46	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
47	chr15:34908560..34909558-chr15:35212164..35213076,4	K562	blood:
48	chr15:34913918..34914531-chr15:35212584..35213285,2	MCF-7	breast:
49	chr15:34945476..34948299-chr15:35000578..35003258,2	K562	blood:
50	chr15:35010787..35013754-chr15:35014491..35016542,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
2	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
3	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
4	lnc-GJD2-3	chr15:34874951-34875061	NONHSAT041597
5	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
6	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
7	lnc-GJD2-4	chr15:34875717-34875835	NONHSAT041596
8	lnc-GJD2-4	chr15:34867026-34867115	NONHSAT041596
9	lnc-AC114546.1-4	chr15:35015735-35016108	XLOC_011205
10	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
11	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
12	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
13	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
14	lnc-AC114546.1-4	chr15:35014395-35014438	NONHSAT041604
15	lnc-AC114546.1-12	chr15:34988228-34988460	NONHSAT041602
16	lnc-AC114546.1-4	chr15:35014273-35014438	XLOC_011205
17	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
18	lnc-AC114546.1-4	chr15:35015809-35016397	NONHSAT041604
19	lnc-GJD2-4	chr15:34873667-34873700	NONHSAT140232
20	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
21	lnc-GJD2-1	chr15:35012518-35012708	XLOC_011422
22	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421

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
ENSG00000197846	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000259904	chromatin interactions
ENSG00000236756	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000128463	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000215252	chromatin interactions
NEK9	miRNA target sites
NEK7	miRNA target sites

Extended variants
information (count: 6237 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:6237 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376381880	chr15:34862263-34862264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538703619	chr15:34862265-34862266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs397843028	chr15:34862269-34862270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114468443	chr15:34862308-34862309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113454992	chr15:34862329-34862330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538616690	chr15:34862344-34862345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373146008	chr15:34862360-34862361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184948300	chr15:34862372-34862373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs138999067	chr15:34862416-34862417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs377169538	chr15:34862427-34862428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536550659	chr15:34862454-34862455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146578938	chr15:34862488-34862489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148740634	chr15:34862496-34862497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573453357	chr15:34862505-34862506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113930097	chr15:34862519-34862520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs142418024	chr15:34862529-34862530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558491159	chr15:34862536-34862537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576949386	chr15:34862616-34862617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112687757	chr15:34862619-34862620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs544256230	chr15:34862655-34862656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563346964	chr15:34862662-34862663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530775055	chr15:34862737-34862738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201877593	chr15:34862867-34862868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542455929	chr15:34862869-34862870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561265877	chr15:34862871-34862872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs151295575	chr15:34862928-34862929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528378478	chr15:34862969-34862970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546633836	chr15:34862980-34862981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571233718	chr15:34863000-34863001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554473647	chr15:34863003-34863004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200487005	chr15:34863014-34863015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532248316	chr15:34863016-34863017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575788750	chr15:34863098-34863099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550607578	chr15:34863153-34863154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201424829	chr15:34863176-34863177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536896778	chr15:34863214-34863215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs202166887	chr15:34863231-34863232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200573678	chr15:34863250-34863251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375949112	chr15:34863313-34863314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548481646	chr15:34863354-34863355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558596194	chr15:34863396-34863397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397833439	chr15:34863399-34863400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566841897	chr15:34863401-34863402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534196742	chr15:34863409-34863410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558534306	chr15:34863458-34863459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147838618	chr15:34863462-34863463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141344186	chr15:34863463-34863464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2455923	chr15:34863468-34863469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs62006251	chr15:34863495-34863496	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs2455924	chr15:34863523-34863524	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:1801 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

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	chr15:34857000-34867000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr15:34857000-34873000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:34857200-34872400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr15:34857400-34873000	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr15:34859000-34872600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr15:34860400-34869800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr15:34861400-34862400	Enhancers	Fetal Muscle Trunk	muscle
12	chr15:34861600-34862600	Enhancers	Left Ventricle	heart
13	chr15:34861600-34862600	Enhancers	Pancreas	Pancrea
14	chr15:34861600-34862600	Enhancers	Right Ventricle	heart
15	chr15:34861800-34862600	Enhancers	Spleen	Spleen
16	chr15:34861800-34873000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr15:34862000-34862400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr15:34862000-34862400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr15:34862000-34862400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr15:34862000-34862400	Enhancers	Fetal Muscle Leg	muscle
21	chr15:34862000-34862600	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr15:34862200-34862600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr15:34862400-34870400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr15:34862400-34874000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
25	chr15:34862400-34874600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr15:34862600-34866600	Weak transcription	Pancreas	Pancrea
27	chr15:34862600-34870600	Weak transcription	Right Ventricle	heart
28	chr15:34862600-34873000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr15:34862600-34873800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:34862600-34874000	Weak transcription	Spleen	Spleen
31	chr15:34863000-34868800	Weak transcription	Aorta	Aorta
32	chr15:34864200-34864600	Active TSS	Brain Hippocampus Middle	brain
33	chr15:34864200-34866600	Enhancers	HepG2	liver
34	chr15:34864400-34864800	Enhancers	Liver	Liver
35	chr15:34864400-34864800	Active TSS	Brain Angular Gyrus	brain
36	chr15:34864800-34873000	Weak transcription	Brain Angular Gyrus	brain
37	chr15:34866200-34867000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr15:34866400-34866600	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr15:34866600-34867200	Genic enhancers	Pancreas	Pancrea
40	chr15:34866600-34869600	Weak transcription	HepG2	liver
41	chr15:34866600-34873000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr15:34866800-34867000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr15:34867000-34867200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr15:34867000-34868400	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr15:34867000-34870400	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr15:34867000-34872800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr15:34867200-34868000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr15:34867200-34868000	Weak transcription	Pancreas	Pancrea
49	chr15:34867200-34874000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr15:34867400-34870400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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