Variant report

Variant	nsv904147
Chromosome Location	chr15:43309429-43403955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:755)
CpG islands
(count:735)
Chromatin interactive
region (count:59)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:43397648-43398773	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:43386853-43387247	K562	blood:	n/a	n/a
3	ARID3A	chr15:43398251-43398659	K562	blood:	n/a	n/a
4	ARID3A	chr15:43397368-43397887	K562	blood:	n/a	n/a
5	ARID3A	chr15:43388218-43388264	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:43387449-43387830	K562	blood:	n/a	n/a
7	ATF1	chr15:43398151-43398528	K562	blood:	n/a	n/a
8	ATF1	chr15:43387460-43387755	K562	blood:	n/a	n/a
9	ATF1	chr15:43386875-43387161	K562	blood:	n/a	n/a
10	ATF2	chr15:43378722-43379113	GM12878	blood:	n/a	n/a
11	ATF2	chr15:43397991-43398451	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr15:43397682-43398573	GM12878	blood:	n/a	n/a
13	ATF3	chr15:43398126-43398472	K562	blood:	n/a	n/a
14	ATF3	chr15:43398097-43398441	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr15:43398117-43398486	HepG2	liver:	n/a	n/a
16	BACH1	chr15:43397593-43397889	K562	blood:	n/a	n/a
17	BATF	chr15:43378759-43379062	GM12878	blood:	n/a	n/a
18	BATF	chr15:43317398-43317616	GM12878	blood:	n/a	chr15:43317546-43317557
19	BATF	chr15:43359977-43360156	GM12878	blood:	n/a	n/a
20	BATF	chr15:43388203-43388457	GM12878	blood:	n/a	n/a
21	BATF	chr15:43317425-43317631	GM12878	blood:	n/a	chr15:43317546-43317557
22	BATF	chr15:43378535-43379134	GM12878	blood:	n/a	n/a
23	BATF	chr15:43359931-43360160	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:43368163-43368349	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:43397997-43398637	GM12878	blood:	n/a	n/a
26	BCLAF1	chr15:43397552-43398686	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:43382873-43382875	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:43397656-43398507	K562	blood:	n/a	n/a
29	BHLHE40	chr15:43397805-43398668	GM12878	blood:	n/a	n/a
30	BRCA1	chr15:43398031-43398634	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr15:43396304-43396666	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr15:43397993-43398585	K562	blood:	n/a	n/a
33	CBX3	chr15:43399955-43400320	K562	blood:	n/a	n/a
34	CCNT2	chr15:43386885-43387085	K562	blood:	n/a	n/a
35	CCNT2	chr15:43398119-43398840	K562	blood:	n/a	n/a
36	CEBPB	chr15:43396241-43396513	MCF-7	breast:	n/a	chr15:43396333-43396346 chr15:43396335-43396346 chr15:43396314-43396325 chr15:43396312-43396323 chr15:43396314-43396323 chr15:43396312-43396325
37	CEBPB	chr15:43387520-43388382	IMR90	lung:	n/a	n/a
38	CEBPB	chr15:43395846-43396462	K562	blood:	n/a	chr15:43396333-43396346 chr15:43396335-43396346 chr15:43396314-43396325 chr15:43396312-43396323 chr15:43396314-43396323 chr15:43396312-43396325
39	CEBPB	chr15:43396243-43396459	A549	lung:	n/a	chr15:43396333-43396346 chr15:43396335-43396346 chr15:43396314-43396325 chr15:43396312-43396323 chr15:43396314-43396323 chr15:43396312-43396325
40	CEBPB	chr15:43381521-43381833	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr15:43360281-43360994	K562	blood:	n/a	n/a
42	CEBPB	chr15:43391418-43391790	IMR90	lung:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
43	CEBPB	chr15:43391418-43391785	HepG2	liver:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
44	CEBPB	chr15:43386312-43386463	K562	blood:	n/a	n/a
45	CEBPB	chr15:43391414-43391809	K562	blood:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
46	CEBPB	chr15:43366074-43366271	A549	lung:	n/a	chr15:43366175-43366186
47	CEBPB	chr15:43366110-43366257	HepG2	liver:	n/a	chr15:43366175-43366186
48	CEBPB	chr15:43395862-43396480	HepG2	liver:	n/a	chr15:43396333-43396346 chr15:43396335-43396346 chr15:43396314-43396325 chr15:43396312-43396323 chr15:43396314-43396323 chr15:43396312-43396325
49	CEBPB	chr15:43391438-43391791	K562	blood:	n/a	chr15:43391596-43391609 chr15:43391598-43391607 chr15:43391596-43391607 chr15:43391598-43391607 chr15:43391598-43391607
50	CEBPB	chr15:43374726-43375076	IMR90	lung:	n/a	chr15:43374901-43374912

(count:735 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:43387679-43387729	PrEC	prostate:	n/a
2	chr15:43399625-43399675	K562	blood:	n/a
3	chr15:43398826-43398876	PFSK-1	brain:	n/a
4	chr15:43387679-43387729	PrEC	prostate:	n/a
5	chr15:43399625-43399675	K562	blood:	n/a
6	chr15:43398826-43398876	PFSK-1	brain:	n/a
7	chr15:43398435-43398485	NHDF-neo	bronchial:	n/a
8	chr15:43398365-43398415	SK-N-MC	brain:	n/a
9	chr15:43398270-43398320	T-47D	breast:	n/a
10	chr15:43398173-43398223	LNCaP	prostate:	n/a
11	chr15:43398270-43398320	LNCaP	prostate:	n/a
12	chr15:43398581-43398631	HIPEpiC	eye:	n/a
13	chr15:43398270-43398320	RPTEC	kidney:	n/a
14	chr15:43399625-43399675	HL-60	blood:	n/a
15	chr15:43398435-43398485	MCF-7	breast:	n/a
16	chr15:43399625-43399675	Jurkat	blood:	n/a
17	chr15:43398302-43398352	Hela-S3	cervix:	n/a
18	chr15:43398302-43398352	RPTEC	kidney:	n/a
19	chr15:43398435-43398485	HL-60	blood:	n/a
20	chr15:43398346-43398396	SK-N-SH	brain:	n/a
21	chr15:43398270-43398320	BJ	skin:	n/a
22	chr15:43398346-43398396	HEEpiC	esophagus:	n/a
23	chr15:43398826-43398876	NHBE	bronchial:	n/a
24	chr15:43398173-43398223	RPTEC	kidney:	n/a
25	chr15:43398338-43398388	PrEC	prostate:	n/a
26	chr15:43398101-43398151	HCM	heart:	n/a
27	chr15:43399625-43399675	AG04449	skin:	fetal
28	chr15:43398270-43398320	HCM	heart:	n/a
29	chr15:43398435-43398485	NT2-D1	testis:	n/a
30	chr15:43398826-43398876	AG10803	skin:	n/a
31	chr15:43398365-43398415	HCF	heart:	n/a
32	chr15:43398302-43398352	ECC-1	luminal epithelium:	n/a
33	chr15:43398302-43398352	HUVEC	blood vessel:	n/a
34	chr15:43399625-43399675	ECC-1	luminal epithelium:	n/a
35	chr15:43398581-43398631	SK-N-SH_RA	brain:	n/a
36	chr15:43398365-43398415	HCM	heart:	n/a
37	chr15:43398346-43398396	AG09309	skin:	n/a
38	chr15:43398270-43398320	A549	lung:	n/a
39	chr15:43387679-43387729	AG09319	gingival:	n/a
40	chr15:43398826-43398876	HRCEpiC	kidney:	n/a
41	chr15:43398365-43398415	HNPCEpiC	eye:	n/a
42	chr15:43398173-43398223	T-47D	breast:	n/a
43	chr15:43398270-43398320	H1-hESC	embryonic stem cell:	embryo
44	chr15:43398346-43398396	T-47D	breast:	n/a
45	chr15:43398270-43398320	SAEC	small airway:	n/a
46	chr15:43398302-43398352	HEK293	kidney:	embryo
47	chr15:43398435-43398485	AG04450	lung:	fetal
48	chr15:43398173-43398223	HRE	kidney:	n/a
49	chr15:43398302-43398352	HCF	heart:	n/a
50	chr15:43398365-43398415	HUVEC	blood vessel:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:43380437..43382771-chr15:43396547..43398200,2	K562	blood:
2	chr15:43398347..43398933-chr15:43477332..43478080,2	NB4	blood:
3	chr15:43398098..43400146-chr15:43707936..43709689,2	K562	blood:
4	chr15:43398288..43398793-chr19:2050787..2051312,2	NB4	blood:
5	chr15:43375936..43379231-chr15:43382227..43385005,3	K562	blood:
6	chr15:43356222..43358202-chr15:43362263..43364733,2	MCF-7	breast:
7	chr15:43346995..43348533-chr15:43350036..43351977,2	K562	blood:
8	chr15:43360392..43362682-chr15:43423469..43425924,2	K562	blood:
9	chr15:43394707..43396213-chr15:43401061..43403612,2	K562	blood:
10	chr15:43380004..43382980-chr15:43386018..43388996,5	K562	blood:
11	chr15:43388815..43390634-chr15:43391926..43394516,2	K562	blood:
12	chr15:43318855..43320896-chr15:43323404..43325415,2	K562	blood:
13	chr15:43389228..43391104-chr15:43396856..43399270,2	K562	blood:
14	chr15:43383221..43388610-chr15:43389653..43393489,4	K562	blood:
15	chr15:43397628..43400398-chr15:43414771..43418048,4	MCF-7	breast:
16	chr1:156698639..156699343-chr15:43397712..43398533,2	Hela-S3	cervix:
17	chr15:43383221..43385892-chr15:43389653..43392510,3	K562	blood:
18	chr15:43368519..43371458-chr15:43478469..43480102,2	K562	blood:
19	chr15:43397435..43400079-chr15:43619938..43624138,3	K562	blood:
20	chr15:43354633..43356543-chr15:43359222..43361458,2	K562	blood:
21	chr15:43390055..43391666-chr15:43396242..43397765,2	MCF-7	breast:
22	chr15:43390055..43391666-chr15:43396242..43397765,2	MCF-7	breast:
23	chr15:43380437..43382771-chr15:43396547..43398200,2	K562	blood:
24	chr15:43397688..43398582-chr8:41909391..41910087,2	Hela-S3	cervix:
25	chr15:43402075..43404958-chr15:43407508..43410226,3	K562	blood:
26	chr15:43395932..43399418-chr15:43425897..43428585,4	K562	blood:
27	chr15:43336054..43338771-chr15:43342997..43344575,2	MCF-7	breast:
28	chr15:43375936..43379231-chr15:43382227..43385005,3	K562	blood:
29	chr15:43356222..43358202-chr15:43362263..43364733,2	MCF-7	breast:
30	chr15:43337776..43340565-chr15:43396734..43398497,2	K562	blood:
31	chr15:43392059..43394941-chr15:43396768..43399559,3	K562	blood:
32	chr15:43327543..43330321-chr15:43334414..43337253,2	MCF-7	breast:
33	chr15:43306847..43311067-chr15:43312226..43316473,3	K562	blood:
34	chr15:43388815..43390634-chr15:43391926..43394516,2	K562	blood:
35	chr15:43394707..43396213-chr15:43401061..43403612,2	K562	blood:
36	chr15:43346995..43348533-chr15:43350036..43351977,2	K562	blood:
37	chr15:43360121..43362777-chr15:43399326..43401275,2	MCF-7	breast:
38	chr15:43383221..43388610-chr15:43389653..43393489,4	K562	blood:
39	chr15:43336054..43338771-chr15:43342997..43344575,2	MCF-7	breast:
40	chr15:43325373..43328292-chr15:43334536..43336063,2	K562	blood:
41	chr15:43392607..43394491-chr15:43442865..43444779,2	K562	blood:
42	chr1:145382743..145383443-chr15:43397728..43398383,2	Hela-S3	cervix:
43	chr15:43397983..43399514-chr15:43421683..43423629,2	K562	blood:
44	chr15:43385287..43387946-chr15:43396303..43398701,2	K562	blood:
45	chr15:43360121..43362777-chr15:43399326..43401275,2	MCF-7	breast:
46	chr15:43392028..43394734-chr15:43397894..43400122,2	MCF-7	breast:
47	chr15:43380004..43382980-chr15:43386018..43388996,5	K562	blood:
48	chr15:43326792..43329076-chr15:43333977..43336036,2	K562	blood:
49	chr15:43397022..43400041-chr15:43403163..43407004,5	K562	blood:
50	chr15:43379754..43382277-chr15:43415120..43416972,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPB42-2	chr15:43398423-43398493	NONHSAT042053
2	lnc-EPB42-2	chr15:43398666-43398735	NONHSAT042053
3	lnc-EPB42-2	chr15:43401117-43401168	NONHSAT042053

No data

Variant related genes	Relation type
UBR1	TF binding region
UBR1	CpG island
ENSG00000168806	chromatin interactions
ENSG00000143303	chromatin interactions
ENSG00000138834	chromatin interactions
ENSG00000083168	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000099875	chromatin interactions
ENSG00000166946	chromatin interactions
ENSG00000261687	chromatin interactions
ENSG00000159459	chromatin interactions
ENSG00000205871	chromatin interactions
ENSG00000260928	chromatin interactions
ENSG00000168803	chromatin interactions
ENSG00000137842	chromatin interactions

Extended variants
information (count: 3167 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3167 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7182063	chr15:43309429-43309430	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs58941543	chr15:43309469-43309470	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530528488	chr15:43309512-43309513	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs75539088	chr15:43309524-43309525	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs563130802	chr15:43309537-43309538	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs376889799	chr15:43309555-43309556	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs549913183	chr15:43309570-43309571	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs531919410	chr15:43309591-43309592	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs542585785	chr15:43309658-43309659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77619714	chr15:43309668-43309669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs531273106	chr15:43309677-43309678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs527285024	chr15:43309689-43309690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534506842	chr15:43309715-43309716	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76476161	chr15:43309742-43309743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs36054626	chr15:43309765-43309766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs34209024	chr15:43309790-43309791	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs533080286	chr15:43309817-43309818	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112882183	chr15:43309889-43309890	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs187809103	chr15:43309908-43309909	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs62020739	chr15:43309921-43309922	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs527261640	chr15:43309934-43309935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7497930	chr15:43309968-43309969	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191965105	chr15:43309999-43310000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs140878686	chr15:43310061-43310062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11630595	chr15:43310121-43310122	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs182890731	chr15:43310141-43310142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186858232	chr15:43310157-43310158	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554102960	chr15:43310158-43310159	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577154031	chr15:43310209-43310210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116991451	chr15:43310240-43310241	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs111720761	chr15:43310254-43310255	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs192893839	chr15:43310272-43310273	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs542395152	chr15:43310286-43310287	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs562387867	chr15:43310348-43310349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144615319	chr15:43310349-43310350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541345489	chr15:43310358-43310359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564134401	chr15:43310361-43310362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532785690	chr15:43310362-43310363	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549891636	chr15:43310389-43310390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184964148	chr15:43310399-43310400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529058892	chr15:43310402-43310403	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548740605	chr15:43310421-43310422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs28620443	chr15:43310442-43310443	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs189369094	chr15:43310489-43310490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192463089	chr15:43310504-43310505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570871010	chr15:43310505-43310506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568010815	chr15:43310530-43310531	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539410865	chr15:43310540-43310541	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs57801418	chr15:43310573-43310574	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs150364366	chr15:43310578-43310579	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Intellectual disability	21811512	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:3015 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43232000-43362800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:43248000-43320600	Weak transcription	Stomach Mucosa	stomach
3	chr15:43267200-43323000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr15:43269000-43312800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr15:43269200-43397200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr15:43269800-43314800	Weak transcription	Fetal Brain Male	brain
7	chr15:43269800-43335200	Weak transcription	Small Intestine	intestine
8	chr15:43287400-43346000	Weak transcription	A549	lung
9	chr15:43292000-43316000	Weak transcription	Fetal Heart	heart
10	chr15:43296200-43312800	Weak transcription	HMEC	breast
11	chr15:43297400-43309800	Strong transcription	Fetal Muscle Leg	muscle
12	chr15:43297400-43348000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr15:43298600-43346200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr15:43298800-43346000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:43299000-43312800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr15:43299400-43346000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr15:43299600-43313400	Weak transcription	NHDF-Ad	bronchial
18	chr15:43300800-43312400	Weak transcription	Brain Angular Gyrus	brain
19	chr15:43301400-43313400	Weak transcription	K562	blood
20	chr15:43301400-43314800	Weak transcription	HepG2	liver
21	chr15:43301600-43312400	Weak transcription	Brain Substantia Nigra	brain
22	chr15:43301600-43321400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr15:43301800-43310200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr15:43301800-43311000	Strong transcription	Cortex derived primary cultured neurospheres	brain
25	chr15:43301800-43312200	Weak transcription	Right Ventricle	heart
26	chr15:43301800-43318800	Strong transcription	Fetal Muscle Trunk	muscle
27	chr15:43301800-43343800	Weak transcription	Psoas Muscle	Psoas
28	chr15:43301800-43345800	Weak transcription	Colonic Mucosa	Colon
29	chr15:43301800-43345800	Weak transcription	Pancreas	Pancrea
30	chr15:43301800-43385800	Weak transcription	Gastric	stomach
31	chr15:43302000-43309600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr15:43302000-43309800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr15:43302000-43310400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr15:43302000-43310800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr15:43302000-43312600	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr15:43302000-43312800	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr15:43302200-43312000	Weak transcription	HSMM	muscle
38	chr15:43302200-43312600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr15:43302800-43312600	Weak transcription	Fetal Kidney	kidney
40	chr15:43303400-43312600	Weak transcription	Ovary	ovary
41	chr15:43303400-43316000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr15:43303400-43345800	Weak transcription	Aorta	Aorta
43	chr15:43303400-43397400	Weak transcription	Esophagus	oesophagus
44	chr15:43304000-43312000	Weak transcription	Fetal Thymus	thymus
45	chr15:43304600-43318200	Strong transcription	Placenta	Placenta
46	chr15:43305600-43318600	Strong transcription	Fetal Brain Female	brain
47	chr15:43306000-43312600	Weak transcription	Brain Anterior Caudate	brain
48	chr15:43306000-43312600	Weak transcription	Rectal Smooth Muscle	rectum
49	chr15:43306000-43313000	Strong transcription	Fetal Stomach	stomach
50	chr15:43306400-43309800	Strong transcription	Primary neutrophils fromperipheralblood	blood

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