Variant report

Variant	esv33661
Chromosome Location	chr15:44016519-44064420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1261)
CpG islands
(count:919)
Chromatin interactive
region (count:49)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1261 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:44039196-44039219	K562	blood:	n/a	n/a
2	ATF1	chr15:44038419-44038682	K562	blood:	n/a	n/a
3	ATF2	chr15:44042010-44042390	GM12878	blood:	n/a	n/a
4	ATF2	chr15:44027183-44028065	GM12878	blood:	n/a	n/a
5	ATF2	chr15:44041865-44042432	GM12878	blood:	n/a	n/a
6	ATF2	chr15:44036163-44036572	GM12878	blood:	n/a	n/a
7	ATF2	chr15:44038444-44038755	GM12878	blood:	n/a	n/a
8	BATF	chr15:44038524-44038730	GM12878	blood:	n/a	n/a
9	BATF	chr15:44027667-44027975	GM12878	blood:	n/a	n/a
10	BATF	chr15:44027201-44028048	GM12878	blood:	n/a	chr15:44027328-44027338
11	BCL11A	chr15:44027233-44027533	GM12878	blood:	n/a	chr15:44027515-44027524
12	BCL11A	chr15:44027190-44027603	GM12878	blood:	n/a	chr15:44027515-44027524
13	BCL11A	chr15:44036222-44036455	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:44035850-44036211	GM12878	blood:	n/a	n/a
15	BCL3	chr15:44061161-44061729	K562	blood:	n/a	n/a
16	BCLAF1	chr15:44027614-44028044	GM12878	blood:	n/a	n/a
17	BCLAF1	chr15:44041944-44042449	GM12878	blood:	n/a	chr15:44042242-44042251
18	BCLAF1	chr15:44036122-44036511	GM12878	blood:	n/a	n/a
19	BHLHE40	chr15:44040684-44040879	K562	blood:	n/a	n/a
20	BHLHE40	chr15:44038444-44039446	K562	blood:	n/a	n/a
21	BHLHE40	chr15:44036123-44036507	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:44040586-44040919	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:44038317-44038684	GM12878	blood:	n/a	n/a
24	BHLHE40	chr15:44042043-44042401	GM12878	blood:	n/a	n/a
25	BRCA1	chr15:44061881-44062181	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr15:44038403-44039579	K562	blood:	n/a	n/a
27	CCNT2	chr15:44038282-44038852	K562	blood:	n/a	n/a
28	CEBPB	chr15:44054841-44055442	IMR90	lung:	n/a	chr15:44054989-44055002
29	CEBPB	chr15:44052234-44052414	HepG2	liver:	n/a	chr15:44052236-44052247
30	CEBPB	chr15:44017169-44017255	Hela-S3	cervix:	n/a	chr15:44017219-44017230
31	CEBPB	chr15:44041996-44042162	K562	blood:	n/a	n/a
32	CEBPB	chr15:44038463-44038682	Hela-S3	cervix:	n/a	chr15:44038558-44038566
33	CEBPB	chr15:44027117-44028063	GM12878	blood:	n/a	chr15:44027406-44027417
34	CEBPB	chr15:44017050-44017346	HepG2	liver:	n/a	chr15:44017219-44017230
35	CEBPB	chr15:44041813-44042490	GM12878	blood:	n/a	n/a
36	CEBPD	chr15:44038452-44038724	HepG2	liver:	n/a	n/a
37	CEBPD	chr15:44038386-44038846	K562	blood:	n/a	n/a
38	CEBPD	chr15:44038203-44038884	HepG2	liver:	n/a	n/a
39	CHD1	chr15:44039568-44039688	GM12878	blood:	n/a	n/a
40	CHD1	chr15:44038466-44038853	GM12878	blood:	n/a	n/a
41	CHD1	chr15:44038630-44039103	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr15:44038438-44038840	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr15:44038259-44038858	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr15:44038438-44038775	K562	blood:	n/a	n/a
45	CHD2	chr15:44038413-44038679	HepG2	liver:	n/a	n/a
46	CHD2	chr15:44036259-44036411	GM12878	blood:	n/a	n/a
47	CHD2	chr15:44038330-44038835	GM12878	blood:	n/a	n/a
48	CREB1	chr15:44038258-44038870	GM12878	blood:	n/a	n/a
49	CREB1	chr15:44041879-44042492	GM12878	blood:	n/a	n/a
50	CREB1	chr15:44038264-44038798	A549	lung:	n/a	n/a

(count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:44055560-44055610	HRPEpiC	eye:	n/a
2	chr15:44038307-44038357	HNPCEpiC	eye:	n/a
3	chr15:44038991-44039041	GM19239	blood:	n/a
4	chr15:44038991-44039041	Hela-S3	cervix:	n/a
5	chr15:44055560-44055610	HRPEpiC	eye:	n/a
6	chr15:44038307-44038357	HNPCEpiC	eye:	n/a
7	chr15:44038991-44039041	GM19239	blood:	n/a
8	chr15:44038991-44039041	Hela-S3	cervix:	n/a
9	chr15:44038386-44038436	AoSMC	blood vessel:	n/a
10	chr15:44039223-44039273	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:44038332-44038382	CMK	blood:	n/a
12	chr15:44038307-44038357	HEK293	kidney:	embryo
13	chr15:44038421-44038471	IMR90	lung:	fetal
14	chr15:44038390-44038440	ovcar-3	ovarian:	n/a
15	chr15:44038991-44039041	ProgFib	skin:	n/a
16	chr15:44038414-44038464	NB4	blood:	n/a
17	chr15:44039223-44039273	AoSMC	blood vessel:	n/a
18	chr15:44038332-44038382	GM12878	blood:	n/a
19	chr15:44063940-44063990	HRCEpiC	kidney:	n/a
20	chr15:44038307-44038357	HEEpiC	esophagus:	n/a
21	chr15:44035561-44035611	HCT-116	colon:	n/a
22	chr15:44039223-44039273	HAEpiC	amniotic membrane:	n/a
23	chr15:44038386-44038436	NH-A	brain:	n/a
24	chr15:44041928-44041978	AG10803	skin:	n/a
25	chr15:44038414-44038464	AG04449	skin:	fetal
26	chr15:44038390-44038440	SK-N-MC	brain:	n/a
27	chr15:44063940-44063990	MCF10A-Er-Src	breast:	n/a
28	chr15:44035561-44035611	NHDF-neo	bronchial:	n/a
29	chr15:44041928-44041978	GM06990	blood:	n/a
30	chr15:44038332-44038382	SK-N-SH_RA	brain:	n/a
31	chr15:44038386-44038436	HCM	heart:	n/a
32	chr15:44039223-44039273	SK-N-SH	brain:	n/a
33	chr15:44039057-44039107	AG04449	skin:	fetal
34	chr15:44038871-44038921	Jurkat	blood:	n/a
35	chr15:44038871-44038921	HL-60	blood:	n/a
36	chr15:44038390-44038440	BJ	skin:	n/a
37	chr15:44038390-44038440	GM12891	blood:	n/a
38	chr15:44038414-44038464	Caco-2	colon:	n/a
39	chr15:44038414-44038464	NHDF-neo	bronchial:	n/a
40	chr15:44038991-44039041	H1-hESC	embryonic stem cell:	embryo
41	chr15:44038307-44038357	GM12878	blood:	n/a
42	chr15:44039223-44039273	NB4	blood:	n/a
43	chr15:44038871-44038921	A549	lung:	n/a
44	chr15:44038812-44038862	ProgFib	skin:	n/a
45	chr15:44041928-44041978	Jurkat	blood:	n/a
46	chr15:44038307-44038357	Hela-S3	cervix:	n/a
47	chr15:44038991-44039041	T-47D	breast:	n/a
48	chr15:44038332-44038382	HEK293	kidney:	embryo
49	chr15:44038307-44038357	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:44038386-44038436	CMK	blood:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:44063293..44066887-chr15:44068416..44071024,5	K562	blood:
2	chr15:44040936..44043692-chr15:44068997..44071077,2	K562	blood:
3	15:43792489-43802874..15:44015129-44020909	GM12878	blood:
4	chr15:44054384..44056100-chr15:44068549..44070083,2	K562	blood:
5	chr15:44038510..44041452-chr15:44052653..44054615,2	MCF-7	breast:
6	chr15:44030932..44033144-chr15:44084781..44086406,2	K562	blood:
7	chr15:44056082..44057916-chr15:44089069..44091952,2	K562	blood:
8	chr15:44036049..44038671-chr15:44067430..44069245,2	K562	blood:
9	15:43782117-43785993..15:44015129-44020909	GM12878	blood:
10	chr15:44060722..44063228-chr15:44091472..44093558,2	K562	blood:
11	chr15:44057941..44060272-chr15:44063922..44065523,2	K562	blood:
12	chr15:44038791..44041212-chr15:44089540..44091517,2	MCF-7	breast:
13	chr15:44059089..44061936-chr15:44091048..44093575,2	MCF-7	breast:
14	chr15:44036424..44040091-chr15:44116705..44119319,4	K562	blood:
15	chr15:44052411..44054206-chr15:44056852..44059319,2	MCF-7	breast:
16	chr15:44037042..44038971-chr15:44059434..44062055,2	K562	blood:
17	chr15:44056082..44057709-chr15:44089290..44091952,2	K562	blood:
18	chr15:44056557..44058823-chr15:44066923..44069715,2	K562	blood:
19	chr15:44057941..44060272-chr15:44063922..44065523,2	K562	blood:
20	chr15:44038318..44039268-chr6:109703161..109703718,2	Hela-S3	cervix:
21	chr15:44060005..44061672-chr15:44083950..44086890,2	K562	blood:
22	chr15:44038515..44039093-chr16:56965918..56966473,2	Hela-S3	cervix:
23	chr15:44052819..44056366-chr15:44062691..44065082,4	K562	blood:
24	15:43792489-43802874..15:44044200-44049293	Hela-S3	cervix:
25	chr15:44044384..44046194-chr15:44067431..44070081,2	MCF-7	breast:
26	chr15:44060550..44065898-chr15:44066868..44071265,7	MCF-7	breast:
27	chr11:62608635..62609223-chr15:44058695..44059277,2	NB4	blood:
28	chr15:44060010..44065607-chr15:44066577..44070669,7	K562	blood:
29	chr15:44054982..44059641-chr15:44059790..44066522,8	MCF-7	breast:
30	chr15:44062113..44074982-chr15:44088756..44097846,29	MCF-7	breast:
31	chr15:44052411..44054206-chr15:44056852..44059319,2	MCF-7	breast:
32	chr15:44032763..44036308-chr15:44037158..44039814,5	K562	blood:
33	chr15:44062639..44065303-chr15:44085346..44088406,3	MCF-7	breast:
34	chr1:167191880..167192380-chr15:44037569..44038070,2	Hela-S3	cervix:
35	chr15:44053208..44055542-chr15:44063582..44065145,2	K562	blood:
36	chr15:44045694..44048584-chr15:44091714..44093995,2	MCF-7	breast:
37	chr15:44036424..44040091-chr15:44115436..44119319,5	K562	blood:
38	chr15:44052819..44056366-chr15:44062691..44065082,4	K562	blood:
39	chr15:44038048..44038553-chr17:80415569..80416490,2	Hela-S3	cervix:
40	chr15:44034068..44036503-chr15:44037132..44039251,3	K562	blood:
41	chr15:44061265..44064131-chr15:44066362..44068342,4	K562	blood:
42	chr15:44038318..44039246-chr17:41465388..41466312,2	Hela-S3	cervix:
43	chr11:76494689..76495371-chr15:44038517..44039029,2	Hela-S3	cervix:
44	chr15:44022701..44024388-chr15:44037503..44040006,2	K562	blood:
45	chr15:44036863..44039388-chr15:44043033..44046484,4	MCF-7	breast:
46	chr15:44053208..44055542-chr15:44063582..44065145,2	K562	blood:
47	chr15:44037743..44040701-chr15:44068299..44070156,3	MCF-7	breast:
48	chr15:44044631..44046288-chr15:44091287..44093017,2	K562	blood:
49	15:43924442-43930824..15:44015129-44020909	GM12878	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STRC-1	chr15:44037220-44037368	NONHSAT042116
2	lnc-STRC-1	chr15:44038246-44038425	NONHSAT042116
3	lnc-STRC-1	chr15:44036469-44036766	NONHSAT042116
4	lnc-STRC-1	chr15:44036593-44036766	NONHSAT042113
5	lnc-SERF2-2	chr15:44063303-44063743	NONHSAT042121
6	lnc-STRC-1	chr15:44028996-44029206	NONHSAT042113
7	lnc-STRC-1	chr15:44038729-44039292	NONHSAT042114
8	lnc-SERF2-3	chr15:44038608-44038904	NONHSAT042119
9	lnc-STRC-1	chr15:44036011-44036766	NONHSAT042114
10	lnc-STRC-1	chr15:44037220-44037365	NONHSAT042115
11	lnc-SERF2-2	chr15:44062481-44062778	NONHSAT042121
12	lnc-STRC-1	chr15:44036593-44036766	NONHSAT042115
13	lnc-STRC-1	chr15:44037220-44037365	NONHSAT042114
14	lnc-STRC-1	chr15:44038246-44038359	NONHSAT042115
15	lnc-STRC-1	chr15:44036349-44036417	NONHSAT042115
16	lnc-STRC-1	chr15:44037220-44037365	NONHSAT042113
17	lnc-SERF2-3	chr15:44048847-44048923	NONHSAT042119
18	lnc-STRC-1	chr15:44038412-44038483	NONHSAT042113

No data

Variant related genes	Relation type
CATSPER2P1	TF binding region
RNU6-354P	TF binding region
SERF2	TF binding region
PDIA3	TF binding region
CATSPER2P1	CpG island
RNU6-354P	CpG island
SERF2	CpG island
PDIA3	CpG island
ENSG00000140259	chromatin interactions
ENSG00000206991	chromatin interactions
ENSG00000184716	chromatin interactions
ENSG00000166762	chromatin interactions
ENSG00000141562	chromatin interactions
ENSG00000242028	chromatin interactions
ENSG00000167004	chromatin interactions
ENSG00000140264	chromatin interactions
ENSG00000182704	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000205771	chromatin interactions
ENSG00000067369	chromatin interactions
ENSG00000051108	chromatin interactions
ENSG00000265458	chromatin interactions
ENSG00000135535	chromatin interactions
ENSG00000128886	chromatin interactions
ENSG00000092470	chromatin interactions
ENSG00000221792	chromatin interactions

Extended variants
information (count: 1866 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1866 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115942644	chr15:44016522-44016523	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs183117139	chr15:44016594-44016595	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs187802599	chr15:44016621-44016622	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs372520927	chr15:44016628-44016629	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs376058426	chr15:44016651-44016652	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs558552614	chr15:44016653-44016654	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs575486721	chr15:44016662-44016663	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs554032103	chr15:44016679-44016680	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs369363078	chr15:44016682-44016683	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs561314262	chr15:44016785-44016786	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs139195421	chr15:44016821-44016822	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs114599776	chr15:44016848-44016849	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs558238154	chr15:44016867-44016868	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs28504496	chr15:44016883-44016884	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs115958045	chr15:44016896-44016897	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs191608612	chr15:44016902-44016903	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs370501037	chr15:44016908-44016909	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs374492332	chr15:44016930-44016931	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs566875574	chr15:44016942-44016943	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs374976586	chr15:44016974-44016975	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs28743004	chr15:44016983-44016984	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
22	rs373432352	chr15:44016987-44016988	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs28361392	chr15:44016990-44016991	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
24	rs201817369	chr15:44016991-44016992	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs28505059	chr15:44017005-44017006	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
26	rs548501437	chr15:44017054-44017055	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs568156446	chr15:44017067-44017068	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs527517676	chr15:44017091-44017092	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs547292768	chr15:44017095-44017096	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs537568989	chr15:44017143-44017144	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs566930979	chr15:44017165-44017166	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs149146615	chr15:44017190-44017191	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs555803560	chr15:44017202-44017203	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs2467411	chr15:44017232-44017233	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs142365050	chr15:44017250-44017251	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs568953308	chr15:44017263-44017264	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs11070407	chr15:44017276-44017277	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs2447201	chr15:44017343-44017344	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs142006113	chr15:44017401-44017402	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs149233033	chr15:44017554-44017555	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs553685203	chr15:44017559-44017560	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs574918878	chr15:44017596-44017597	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs144447143	chr15:44017704-44017705	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs148413778	chr15:44017756-44017757	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs147608923	chr15:44017936-44017937	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs572349355	chr15:44017986-44017987	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs542519293	chr15:44018009-44018010	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs540786314	chr15:44018099-44018100	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs554091771	chr15:44018100-44018101	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs576964585	chr15:44018212-44018213	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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	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
Mental retardation	17124404	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44013400-44037400	Weak transcription	Fetal Intestine Small	intestine
2	chr15:44015400-44016600	Weak transcription	Placenta	Placenta
3	chr15:44016600-44016800	Enhancers	Placenta	Placenta
4	chr15:44019800-44021200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr15:44020000-44021400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr15:44020000-44038000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr15:44020400-44021200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr15:44020400-44021200	Enhancers	HSMMtube	muscle
9	chr15:44020400-44021200	Enhancers	Osteobl	bone
10	chr15:44020400-44021400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr15:44020400-44021400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr15:44020400-44021400	Enhancers	HSMM	muscle
13	chr15:44020600-44021000	Enhancers	HMEC	breast
14	chr15:44020600-44021200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr15:44020800-44021200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr15:44020800-44021200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr15:44020800-44021200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:44020800-44021200	Enhancers	Aorta	Aorta
19	chr15:44020800-44021200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr15:44027200-44027400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr15:44027200-44027400	Flanking Active TSS	GM12878-XiMat	blood
22	chr15:44027200-44028000	Enhancers	Primary B cells from peripheral blood	blood
23	chr15:44027400-44027600	Active TSS	GM12878-XiMat	blood
24	chr15:44027400-44027800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:44027400-44027800	Enhancers	Small Intestine	intestine
26	chr15:44027600-44027800	Enhancers	Gastric	stomach
27	chr15:44027600-44027800	Enhancers	Osteobl	bone
28	chr15:44027600-44028000	Flanking Active TSS	GM12878-XiMat	blood
29	chr15:44027600-44028000	Enhancers	HSMMtube	muscle
30	chr15:44027800-44028000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:44028000-44028800	Enhancers	GM12878-XiMat	blood
32	chr15:44028000-44038000	Weak transcription	HSMMtube	muscle
33	chr15:44028800-44029000	Weak transcription	GM12878-XiMat	blood
34	chr15:44032600-44032800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr15:44032600-44037800	Weak transcription	Liver	Liver
36	chr15:44032800-44038000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr15:44033800-44035000	Enhancers	K562	blood
38	chr15:44033800-44037800	Weak transcription	Right Ventricle	heart
39	chr15:44034400-44037800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:44035000-44037200	Weak transcription	K562	blood
41	chr15:44035400-44036400	Enhancers	GM12878-XiMat	blood
42	chr15:44035800-44037800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr15:44036000-44036200	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr15:44036000-44037200	Enhancers	Primary B cells from peripheral blood	blood
45	chr15:44036200-44036400	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr15:44036200-44036400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr15:44036200-44036400	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr15:44036200-44037000	Enhancers	Primary B cells from cord blood	blood
49	chr15:44036400-44037000	Flanking Active TSS	GM12878-XiMat	blood
50	chr15:44036400-44037800	Weak transcription	Primary neutrophils fromperipheralblood	blood

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