Variant report

Variant	nsv569581
Chromosome Location	chr15:57635719-57775826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1340)
CpG islands
(count:1773)
Chromatin interactive
region (count:46)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1340 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:57769934-57770658	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:57673166-57673314	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:57698812-57699080	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:57709023-57709306	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57767593-57767849	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:57683674-57684095	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:57675122-57675478	K562	blood:	n/a	n/a
8	ATF1	chr15:57739082-57739221	K562	blood:	n/a	n/a
9	ATF1	chr15:57675232-57675432	K562	blood:	n/a	n/a
10	ATF2	chr15:57677951-57678684	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr15:57677879-57679030	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr15:57648804-57649568	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:57649168-57649224	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:57738064-57738618	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:57678068-57678736	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:57738124-57738415	K562	blood:	n/a	n/a
17	BACH1	chr15:57668896-57669038	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr15:57648928-57649135	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr15:57648891-57649186	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr15:57683205-57684026	HepG2	liver:	n/a	n/a
21	BHLHE40	chr15:57768791-57768792	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:57769828-57770706	HepG2	liver:	n/a	n/a
23	BHLHE40	chr15:57675229-57675611	K562	blood:	n/a	n/a
24	BRCA1	chr15:57649151-57649161	H1-hESC	embryonic stem cell:	n/a	n/a
25	CCNT2	chr15:57675201-57675501	K562	blood:	n/a	n/a
26	CEBPB	chr15:57644830-57645208	K562	blood:	n/a	chr15:57644878-57644889
27	CEBPB	chr15:57664474-57664663	HepG2	liver:	n/a	n/a
28	CEBPB	chr15:57719550-57719876	HepG2	liver:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
29	CEBPB	chr15:57645093-57645295	A549	lung:	n/a	n/a
30	CEBPB	chr15:57753700-57754104	MCF-7	breast:	n/a	n/a
31	CEBPB	chr15:57679152-57679246	K562	blood:	n/a	n/a
32	CEBPB	chr15:57719526-57719922	Hela-S3	cervix:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
33	CEBPB	chr15:57669158-57669538	HepG2	liver:	n/a	chr15:57669334-57669345
34	CEBPB	chr15:57644547-57645343	HepG2	liver:	n/a	chr15:57644878-57644889
35	CEBPB	chr15:57770322-57770596	HepG2	liver:	n/a	n/a
36	CEBPB	chr15:57669326-57669420	K562	blood:	n/a	chr15:57669334-57669345
37	CEBPB	chr15:57719546-57719910	IMR90	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
38	CEBPB	chr15:57664441-57664787	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr15:57698709-57699074	HepG2	liver:	n/a	chr15:57698876-57698887
40	CEBPB	chr15:57755183-57755257	K562	blood:	n/a	chr15:57755215-57755226
41	CEBPB	chr15:57669218-57669407	HepG2	liver:	n/a	chr15:57669334-57669345
42	CEBPB	chr15:57669119-57669538	HepG2	liver:	n/a	chr15:57669334-57669345
43	CEBPB	chr15:57688268-57688424	A549	lung:	n/a	n/a
44	CEBPB	chr15:57669187-57669508	H1-hESC	embryonic stem cell:	n/a	chr15:57669334-57669345
45	CEBPB	chr15:57645133-57645231	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr15:57759160-57759196	A549	lung:	n/a	n/a
47	CEBPB	chr15:57649017-57649179	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr15:57644775-57645006	HepG2	liver:	n/a	chr15:57644878-57644889
49	CEBPB	chr15:57644596-57645326	HepG2	liver:	n/a	chr15:57644878-57644889
50	CEBPB	chr15:57719370-57720131	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726

(count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57719252-57719302	SK-N-MC	brain:	n/a
2	chr15:57719252-57719302	HRE	kidney:	n/a
3	chr15:57729383-57729433	AG04450	lung:	fetal
4	chr15:57668039-57668089	HepG2	liver:	n/a
5	chr15:57719252-57719302	SK-N-MC	brain:	n/a
6	chr15:57719252-57719302	HRE	kidney:	n/a
7	chr15:57729383-57729433	AG04450	lung:	fetal
8	chr15:57668039-57668089	HepG2	liver:	n/a
9	chr15:57719252-57719302	HCM	heart:	n/a
10	chr15:57647657-57647707	SK-N-MC	brain:	n/a
11	chr15:57682357-57682407	GM12891	blood:	n/a
12	chr15:57668039-57668089	RPTEC	kidney:	n/a
13	chr15:57668895-57668945	PANC-1	pancreas:	n/a
14	chr15:57719252-57719302	K562	blood:	n/a
15	chr15:57668087-57668137	ProgFib	skin:	n/a
16	chr15:57737942-57737992	HEK293	kidney:	embryo
17	chr15:57668547-57668597	ProgFib	skin:	n/a
18	chr15:57769667-57769717	HCM	heart:	n/a
19	chr15:57731166-57731216	NT2-D1	testis:	n/a
20	chr15:57668895-57668945	GM12891	blood:	n/a
21	chr15:57668087-57668137	SKMC	muscle:	n/a
22	chr15:57719922-57719972	SK-N-MC	brain:	n/a
23	chr15:57668039-57668089	NH-A	brain:	n/a
24	chr15:57724857-57724907	AG10803	skin:	n/a
25	chr15:57682357-57682407	ECC-1	luminal epithelium:	n/a
26	chr15:57731108-57731158	AoSMC	blood vessel:	n/a
27	chr15:57677507-57677557	HNPCEpiC	eye:	n/a
28	chr15:57719252-57719302	HIPEpiC	eye:	n/a
29	chr15:57724857-57724907	HIPEpiC	eye:	n/a
30	chr15:57668039-57668089	CMK	blood:	n/a
31	chr15:57680479-57680529	HEK293	kidney:	embryo
32	chr15:57719252-57719302	AG09319	gingival:	n/a
33	chr15:57737942-57737992	HCPEpiC	choroid plexus:	n/a
34	chr15:57737942-57737992	GM06990	blood:	n/a
35	chr15:57668539-57668589	PrEC	prostate:	n/a
36	chr15:57668261-57668311	NHDF-neo	bronchial:	n/a
37	chr15:57671034-57671084	GM06990	blood:	n/a
38	chr15:57668087-57668137	PANC-1	pancreas:	n/a
39	chr15:57677507-57677557	HIPEpiC	eye:	n/a
40	chr15:57719922-57719972	Hepatocyte	liver:	n/a
41	chr15:57695943-57695993	HRPEpiC	eye:	n/a
42	chr15:57655799-57655849	NT2-D1	testis:	n/a
43	chr15:57737942-57737992	Hepatocyte	liver:	n/a
44	chr15:57668895-57668945	HAEpiC	amniotic membrane:	n/a
45	chr15:57731055-57731105	GM12878	blood:	n/a
46	chr15:57719252-57719302	ovcar-3	ovarian:	n/a
47	chr15:57668812-57668862	AG09309	skin:	n/a
48	chr15:57668261-57668311	HEEpiC	esophagus:	n/a
49	chr15:57719922-57719972	NT2-D1	testis:	n/a
50	chr15:57677507-57677557	AoSMC	blood vessel:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
2	chr1:121483186..121485028-chr15:57701904..57703998,2	MCF-7	breast:
3	chr15:57703606..57706122-chr15:57710560..57712105,2	MCF-7	breast:
4	chr15:57632854..57634984-chr15:57638024..57640746,3	K562	blood:
5	chr15:57637767..57638513-chr15:57664087..57664757,2	MCF-7	breast:
6	chr15:57668102..57670225-chr15:57677163..57679480,2	MCF-7	breast:
7	chr15:57637959..57638490-chr15:57834171..57834725,2	MCF-7	breast:
8	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
9	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
10	chr15:57637629..57639520-chr15:57818149..57819741,2	MCF-7	breast:
11	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
12	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
13	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
14	chr15:57769251..57771985-chr15:57775808..57777973,2	K562	blood:
15	chr15:57637767..57638513-chr15:57664087..57664757,2	MCF-7	breast:
16	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
17	chr15:57669468..57670026-chr15:57819642..57820286,2	MCF-7	breast:
18	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
19	chr15:57636178..57637065-chr15:57819415..57820032,2	MCF-7	breast:
20	chr15:57750506..57752282-chr15:57753554..57755712,2	K562	blood:
21	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
22	chr15:57767857..57770751-chr15:57775808..57778592,2	K562	blood:
23	chr15:57667871..57669464-chr15:57819823..57821848,2	MCF-7	breast:
24	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
25	chr15:57750506..57752282-chr15:57753554..57755712,2	K562	blood:
26	chr15:57667349..57669479-chr15:57681702..57683974,2	K562	blood:
27	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
28	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:
29	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
30	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:
31	chr15:57703606..57706122-chr15:57710560..57712105,2	MCF-7	breast:
32	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
33	chr15:57720476..57722936-chr15:57724611..57727742,3	K562	blood:
34	chr15:57633114..57634635-chr15:57634661..57636364,2	K562	blood:
35	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
36	chr15:57745679..57747449-chr15:57751511..57754366,2	MCF-7	breast:
37	chr15:57720476..57722936-chr15:57724611..57727742,3	K562	blood:
38	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:
39	chr15:57637995..57638567-chr15:57798058..57798880,2	MCF-7	breast:
40	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
41	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
42	chr15:57745679..57747449-chr15:57751511..57754366,2	MCF-7	breast:
43	chr15:57662175..57664160-chr15:57665608..57668558,2	K562	blood:
44	chr15:57668435..57670141-chr15:57674647..57676838,2	MCF-7	breast:
45	chr15:57614506..57616256-chr15:57638929..57640760,2	K562	blood:
46	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGNL1-2	chr15:57730183-57730215	NONHSAT044072
2	lnc-ALDH1A2-6	chr15:57741444-57741697	expReg_chr15_4576_-
3	lnc-CGNL1-2	chr15:57694859-57694912	NONHSAT044073
4	lnc-CGNL1-2	chr15:57699171-57699474	NONHSAT044073
5	lnc-CGNL1-2	chr15:57694217-57694236	NONHSAT044073
6	lnc-CGNL1-2	chr15:57686151-57686289	NONHSAT044073
7	lnc-CGNL1-2	chr15:57668165-57668468	NONHSAT044072
8	lnc-CGNL1-2	chr15:57669124-57669363	NONHSAT044072
9	lnc-ALDH1A2-4	chr15:57770404-57770527	ENSG00000261489.1
10	lnc-CGNL1-2	chr15:57689122-57689304	NONHSAT044073
11	lnc-ALDH1A2-4	chr15:57769682-57769812	ENSG00000261489.1
12	lnc-CGNL1-2	chr15:57669344-57669363	NONHSAT044073
13	lnc-CGNL1-2	chr15:57698164-57698262	NONHSAT044073
14	lnc-CGNL1-2	chr15:57690539-57690628	NONHSAT044073

No data

Variant related genes	Relation type
RNU6-844P	TF binding region
CGNL1	TF binding region
ENSG00000261489	TF binding region
RNU6-844P	CpG island
CGNL1	CpG island
ENSG00000261489	CpG island
ENSG00000261265	chromatin interactions
ENSG00000128849	chromatin interactions
ENSG00000261489	chromatin interactions

Extended variants
information (count: 6453 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6453 , 50 per page) page: 1 2 3 4 5 6 7 ... 130

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4774257	chr15:57635719-57635720	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549948150	chr15:57635740-57635741	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs570029432	chr15:57635748-57635749	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs187395319	chr15:57635759-57635760	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs552887092	chr15:57635780-57635781	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs74016163	chr15:57635799-57635800	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs375109682	chr15:57635800-57635801	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs535251504	chr15:57635808-57635809	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs191924690	chr15:57635839-57635840	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs568075135	chr15:57635840-57635841	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs184141449	chr15:57635856-57635857	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs556730866	chr15:57635862-57635863	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs576752367	chr15:57635941-57635942	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs8026926	chr15:57635951-57635952	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147285933	chr15:57635954-57635955	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs572773269	chr15:57636050-57636051	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs35711718	chr15:57636084-57636085	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs372938410	chr15:57636085-57636086	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs139238082	chr15:57636089-57636090	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs189569222	chr15:57636104-57636105	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs530180415	chr15:57636107-57636108	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs534961524	chr15:57636139-57636140	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs553370458	chr15:57636176-57636177	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs573286660	chr15:57636217-57636218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs543875192	chr15:57636229-57636230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs563565812	chr15:57636234-57636235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542342630	chr15:57636275-57636276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs149441435	chr15:57636338-57636339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1079052	chr15:57636401-57636402	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs528380033	chr15:57636425-57636426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs80300558	chr15:57636431-57636432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545196968	chr15:57636432-57636433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548541844	chr15:57636441-57636442	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552644425	chr15:57636443-57636444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs374991670	chr15:57636461-57636462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs78447664	chr15:57636476-57636477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527605290	chr15:57636514-57636515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557004358	chr15:57636586-57636587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375024393	chr15:57636604-57636605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs116307404	chr15:57636627-57636628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539068760	chr15:57636629-57636630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192772404	chr15:57636659-57636660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184260728	chr15:57636664-57636665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541718132	chr15:57636669-57636670	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555300458	chr15:57636730-57636731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs2004972	chr15:57636772-57636773	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs35042095	chr15:57636775-57636776	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530093247	chr15:57636810-57636811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563824976	chr15:57636892-57636893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs139149223	chr15:57636899-57636900	Weak transcription Enhancers	n/a	n/a	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
Gastrointestinal stromal cancer	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57627600-57668200	Weak transcription	Right Atrium	heart
2	chr15:57629600-57638000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:57631200-57638000	Weak transcription	Fetal Intestine Small	intestine
4	chr15:57633400-57638000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr15:57634800-57636000	Bivalent Enhancer	HepG2	liver
6	chr15:57634800-57637800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:57635200-57636200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr15:57635400-57635800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr15:57635400-57636000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:57635400-57636200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr15:57635400-57636600	Enhancers	Fetal Heart	heart
12	chr15:57635400-57636800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr15:57635600-57636000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr15:57635600-57636200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr15:57635600-57636200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr15:57635600-57638000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr15:57636000-57636600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:57636000-57637000	Enhancers	HepG2	liver
19	chr15:57636000-57638200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr15:57636200-57647200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:57636600-57636800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:57636600-57637800	Weak transcription	Fetal Heart	heart
23	chr15:57636800-57637800	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr15:57636800-57643600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:57637000-57637400	Weak transcription	HepG2	liver
26	chr15:57637400-57637800	Weak transcription	Fetal Kidney	kidney
27	chr15:57637400-57637800	Enhancers	HepG2	liver
28	chr15:57637800-57638200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr15:57637800-57638200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:57637800-57638400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr15:57637800-57638400	Flanking Active TSS	HepG2	liver
32	chr15:57637800-57638600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr15:57637800-57638600	Enhancers	Fetal Heart	heart
34	chr15:57638000-57638200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr15:57638000-57638400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr15:57638000-57638400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr15:57638000-57638400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr15:57638000-57638400	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr15:57638000-57638600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr15:57638000-57638600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr15:57638000-57638600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr15:57638200-57638400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr15:57638200-57639200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr15:57638400-57638600	Enhancers	HepG2	liver
45	chr15:57638400-57639200	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr15:57638400-57645000	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr15:57638400-57645600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr15:57638600-57644000	Weak transcription	HepG2	liver
49	chr15:57638600-57645200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:57638600-57647200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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