Variant report

Variant	nsv569589
Chromosome Location	chr15:57648012-57782249
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1308)
CpG islands
(count:1774)
Chromatin interactive
region (count:42)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1308 , 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	chr15:57709023-57709306	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:57769934-57770658	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:57778069-57778326	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:57698812-57699080	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57683674-57684095	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:57767593-57767849	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:57675122-57675478	K562	blood:	n/a	n/a
8	ARID3A	chr15:57673166-57673314	HepG2	liver:	n/a	n/a
9	ATF1	chr15:57739082-57739221	K562	blood:	n/a	n/a
10	ATF1	chr15:57675232-57675432	K562	blood:	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	ATF2	chr15:57677951-57678684	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr15:57777946-57778537	A549	lung:	n/a	n/a
15	ATF3	chr15:57777927-57778577	HCT-116	colon:	n/a	n/a
16	BACH1	chr15:57649168-57649224	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:57738124-57738415	K562	blood:	n/a	n/a
18	BACH1	chr15:57778042-57778485	H1-hESC	embryonic stem cell:	n/a	chr15:57778256-57778270
19	BACH1	chr15:57678068-57678736	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:57738064-57738618	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:57668896-57669038	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr15:57648891-57649186	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr15:57648928-57649135	H1-hESC	embryonic stem cell:	n/a	n/a
24	BHLHE40	chr15:57768791-57768792	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:57769828-57770706	HepG2	liver:	n/a	n/a
26	BHLHE40	chr15:57675229-57675611	K562	blood:	n/a	n/a
27	BHLHE40	chr15:57683205-57684026	HepG2	liver:	n/a	n/a
28	BHLHE40	chr15:57778087-57778398	HepG2	liver:	n/a	n/a
29	BRCA1	chr15:57649151-57649161	H1-hESC	embryonic stem cell:	n/a	n/a
30	CCNT2	chr15:57675201-57675501	K562	blood:	n/a	n/a
31	CEBPB	chr15:57649017-57649179	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr15:57675162-57675437	K562	blood:	n/a	n/a
33	CEBPB	chr15:57779041-57779081	K562	blood:	n/a	n/a
34	CEBPB	chr15:57688268-57688424	A549	lung:	n/a	n/a
35	CEBPB	chr15:57669218-57669407	HepG2	liver:	n/a	chr15:57669334-57669345
36	CEBPB	chr15:57753678-57754168	MCF-7	breast:	n/a	n/a
37	CEBPB	chr15:57679152-57679246	K562	blood:	n/a	n/a
38	CEBPB	chr15:57698709-57699074	HepG2	liver:	n/a	chr15:57698876-57698887
39	CEBPB	chr15:57719370-57720131	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
40	CEBPB	chr15:57664474-57664663	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:57719550-57719876	HepG2	liver:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
42	CEBPB	chr15:57669133-57669500	HepG2	liver:	n/a	chr15:57669334-57669345
43	CEBPB	chr15:57768816-57769016	IMR90	lung:	n/a	n/a
44	CEBPB	chr15:57753700-57754104	MCF-7	breast:	n/a	n/a
45	CEBPB	chr15:57669187-57669508	H1-hESC	embryonic stem cell:	n/a	chr15:57669334-57669345
46	CEBPB	chr15:57737280-57737551	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:57767622-57767921	HepG2	liver:	n/a	n/a
48	CEBPB	chr15:57755183-57755257	K562	blood:	n/a	chr15:57755215-57755226
49	CEBPB	chr15:57719531-57719898	MCF-7	breast:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
50	CEBPB	chr15:57759160-57759196	A549	lung:	n/a	n/a

(count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57668039-57668089	PFSK-1	brain:	n/a
2	chr15:57668039-57668089	HIPEpiC	eye:	n/a
3	chr15:57719252-57719302	AG04450	lung:	fetal
4	chr15:57682357-57682407	GM19239	blood:	n/a
5	chr15:57668539-57668589	U87	brain:	n/a
6	chr15:57668039-57668089	PFSK-1	brain:	n/a
7	chr15:57668039-57668089	HIPEpiC	eye:	n/a
8	chr15:57719252-57719302	AG04450	lung:	fetal
9	chr15:57682357-57682407	GM19239	blood:	n/a
10	chr15:57668539-57668589	U87	brain:	n/a
11	chr15:57769667-57769717	GM12892	blood:	n/a
12	chr15:57682357-57682407	ProgFib	skin:	n/a
13	chr15:57724857-57724907	CMK	blood:	n/a
14	chr15:57677507-57677557	NH-A	brain:	n/a
15	chr15:57769667-57769717	NH-A	brain:	n/a
16	chr15:57668039-57668089	ProgFib	skin:	n/a
17	chr15:57729383-57729433	HCT-116	colon:	n/a
18	chr15:57695943-57695993	GM12891	blood:	n/a
19	chr15:57778278-57778328	RPTEC	kidney:	n/a
20	chr15:57731108-57731158	HRCEpiC	kidney:	n/a
21	chr15:57668261-57668311	U87	brain:	n/a
22	chr15:57668261-57668311	PFSK-1	brain:	n/a
23	chr15:57669165-57669215	HCM	heart:	n/a
24	chr15:57668261-57668311	NHDF-neo	bronchial:	n/a
25	chr15:57669165-57669215	HCPEpiC	choroid plexus:	n/a
26	chr15:57778278-57778328	AG09319	gingival:	n/a
27	chr15:57668087-57668137	MCF-7	breast:	n/a
28	chr15:57680479-57680529	U87	brain:	n/a
29	chr15:57668247-57668297	NH-A	brain:	n/a
30	chr15:57731055-57731105	HRE	kidney:	n/a
31	chr15:57682357-57682407	Hela-S3	cervix:	n/a
32	chr15:57737942-57737992	HEEpiC	esophagus:	n/a
33	chr15:57737942-57737992	HCF	heart:	n/a
34	chr15:57682357-57682407	GM06990	blood:	n/a
35	chr15:57769667-57769717	HIPEpiC	eye:	n/a
36	chr15:57682357-57682407	SK-N-SH_RA	brain:	n/a
37	chr15:57731108-57731158	HAEpiC	amniotic membrane:	n/a
38	chr15:57664490-57664540	NHBE	bronchial:	n/a
39	chr15:57778278-57778328	NB4	blood:	n/a
40	chr15:57668247-57668297	HRPEpiC	eye:	n/a
41	chr15:57668539-57668589	HCF	heart:	n/a
42	chr15:57668812-57668862	HRCEpiC	kidney:	n/a
43	chr15:57655799-57655849	HRCEpiC	kidney:	n/a
44	chr15:57677507-57677557	HUVEC	blood vessel:	n/a
45	chr15:57668552-57668602	HL-60	blood:	n/a
46	chr15:57655799-57655849	HEK293	kidney:	embryo
47	chr15:57668087-57668137	BJ	skin:	n/a
48	chr15:57668039-57668089	GM12892	blood:	n/a
49	chr15:57769667-57769717	AG09309	skin:	n/a
50	chr15:57668895-57668945	HRCEpiC	kidney:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
2	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
3	chr15:57769251..57771985-chr15:57775808..57777973,2	K562	blood:
4	chr15:57720476..57722936-chr15:57724611..57727742,3	K562	blood:
5	chr15:57745679..57747449-chr15:57751511..57754366,2	MCF-7	breast:
6	chr15:57703606..57706122-chr15:57710560..57712105,2	MCF-7	breast:
7	chr15:57782161..57783961-chr15:57796230..57798996,2	K562	blood:
8	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
9	chr15:57669468..57670026-chr15:57819642..57820286,2	MCF-7	breast:
10	chr15:57703606..57706122-chr15:57710560..57712105,2	MCF-7	breast:
11	chr15:57750506..57752282-chr15:57753554..57755712,2	K562	blood:
12	chr15:57780102..57781680-chr15:57834323..57835869,2	K562	blood:
13	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
14	chr15:57780555..57782783-chr15:57783060..57786197,3	K562	blood:
15	chr15:57668102..57670225-chr15:57677163..57679480,2	MCF-7	breast:
16	chr15:57720476..57722936-chr15:57724611..57727742,3	K562	blood:
17	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
18	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
19	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
20	chr15:57767857..57770751-chr15:57775808..57778592,2	K562	blood:
21	chr15:57777677..57780127-chr15:57786834..57789579,2	K562	blood:
22	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:
23	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:
24	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
25	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:
26	chr15:57667349..57669479-chr15:57681702..57683974,2	K562	blood:
27	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
28	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:
29	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
30	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
31	chr15:57668435..57670141-chr15:57674647..57676838,2	MCF-7	breast:
32	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
33	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
34	chr15:57750506..57752282-chr15:57753554..57755712,2	K562	blood:
35	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
36	chr15:57637767..57638513-chr15:57664087..57664757,2	MCF-7	breast:
37	chr15:57745679..57747449-chr15:57751511..57754366,2	MCF-7	breast:
38	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
39	chr1:121483186..121485028-chr15:57701904..57703998,2	MCF-7	breast:
40	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
41	chr15:57667871..57669464-chr15:57819823..57821848,2	MCF-7	breast:
42	chr15:57662175..57664160-chr15:57665608..57668558,2	K562	blood:

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

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

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
ENSG00000261489	chromatin interactions
ENSG00000128849	chromatin interactions

Extended variants
information (count: 6114 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6114 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs734489	chr15:57648012-57648013	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577691725	chr15:57648055-57648056	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs191773183	chr15:57648059-57648060	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs17239637	chr15:57648077-57648078	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563597916	chr15:57648109-57648110	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs116004647	chr15:57648118-57648119	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs376541880	chr15:57648129-57648130	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs562782445	chr15:57648389-57648390	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs148818632	chr15:57648395-57648396	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs57490143	chr15:57648477-57648478	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs61650990	chr15:57648503-57648504	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs112693784	chr15:57648526-57648527	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs528240554	chr15:57648548-57648549	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs551194372	chr15:57648572-57648573	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs183816171	chr15:57648583-57648584	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs58358937	chr15:57648593-57648594	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs548954498	chr15:57648660-57648661	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs569253993	chr15:57648685-57648686	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs538506614	chr15:57648709-57648710	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs2440952	chr15:57648710-57648711	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs571827634	chr15:57648767-57648768	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs534103015	chr15:57648778-57648779	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs553907518	chr15:57648845-57648846	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs573739405	chr15:57648849-57648850	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs542686258	chr15:57648876-57648877	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs556192377	chr15:57648948-57648949	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs189212840	chr15:57648983-57648984	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs545274915	chr15:57648986-57648987	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs565000771	chr15:57648994-57648995	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs527505214	chr15:57649014-57649015	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs137977008	chr15:57649055-57649056	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs180851971	chr15:57649103-57649104	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs143638873	chr15:57649106-57649107	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs116585125	chr15:57649107-57649108	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs147180439	chr15:57649110-57649111	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs568894756	chr15:57649152-57649153	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs566906850	chr15:57649194-57649195	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs531571328	chr15:57649239-57649240	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs79529118	chr15:57649247-57649248	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs187406070	chr15:57649250-57649251	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs138819037	chr15:57649251-57649252	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs2440953	chr15:57649259-57649260	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs567416613	chr15:57649260-57649261	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs566145473	chr15:57649309-57649310	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs78053087	chr15:57649359-57649360	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs569202934	chr15:57649370-57649371	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs535179500	chr15:57649375-57649376	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs112121543	chr15:57649387-57649388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs142929191	chr15:57649390-57649391	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs376100523	chr15:57649391-57649392	Enhancers Weak transcription Flanking Active TSS	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:2617 , 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	chr15:57644400-57649800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:57645400-57648200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr15:57646200-57648600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr15:57646200-57648600	Weak transcription	Placenta	Placenta
6	chr15:57646200-57649400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:57646800-57648400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:57646800-57649400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr15:57647000-57648200	Weak transcription	Fetal Kidney	kidney
10	chr15:57647000-57649200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:57647000-57649400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr15:57647200-57648400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:57647200-57649400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr15:57647200-57649400	Enhancers	HSMMtube	muscle
15	chr15:57647200-57650400	Enhancers	Fetal Stomach	stomach
16	chr15:57647400-57649400	Enhancers	HSMM	muscle
17	chr15:57647600-57650000	Enhancers	Stomach Smooth Muscle	stomach
18	chr15:57647800-57648400	Flanking Active TSS	Fetal Heart	heart
19	chr15:57647800-57649400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr15:57647800-57649400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr15:57647800-57649600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr15:57647800-57649600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr15:57647800-57649600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr15:57648000-57648400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr15:57648000-57648600	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr15:57648000-57649800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr15:57648000-57649800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr15:57648000-57650400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr15:57648200-57649000	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr15:57648200-57649000	Bivalent Enhancer	Fetal Muscle Leg	muscle
31	chr15:57648200-57649400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr15:57648200-57649400	Enhancers	Fetal Kidney	kidney
33	chr15:57648200-57649600	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr15:57648200-57649600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:57648200-57649600	Enhancers	NH-A	brain
36	chr15:57648200-57649600	Enhancers	Osteobl	bone
37	chr15:57648400-57648800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr15:57648400-57649200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr15:57648400-57649400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr15:57648400-57649400	Enhancers	Fetal Heart	heart
41	chr15:57648400-57649400	Enhancers	HMEC	breast
42	chr15:57648400-57649600	Enhancers	NHEK	skin
43	chr15:57648600-57649000	Enhancers	Placenta	Placenta
44	chr15:57648600-57649400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr15:57648600-57649400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:57648600-57649400	Enhancers	HUVEC	blood vessel
47	chr15:57648600-57649400	Enhancers	NHDF-Ad	bronchial
48	chr15:57648600-57649600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr15:57648800-57649000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr15:57648800-57649000	Weak transcription	HepG2	liver

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