Variant report

Variant	esv2761873
Chromosome Location	chr15:57643653-57779035
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1332)
CpG islands
(count:1832)
Chromatin interactive
region (count:39)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1332 , 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	chr15:57675122-57675478	K562	blood:	n/a	n/a
2	ARID3A	chr15:57769934-57770658	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:57709023-57709306	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:57683674-57684095	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57698812-57699080	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:57778069-57778326	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:57767593-57767849	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:57673166-57673314	HepG2	liver:	n/a	n/a
9	ATF1	chr15:57675232-57675432	K562	blood:	n/a	n/a
10	ATF1	chr15:57739082-57739221	K562	blood:	n/a	n/a
11	ATF2	chr15:57677951-57678684	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	chr15:57677879-57679030	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr15:57777927-57778577	HCT-116	colon:	n/a	n/a
15	ATF3	chr15:57777946-57778537	A549	lung:	n/a	n/a
16	BACH1	chr15:57738064-57738618	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:57668896-57669038	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:57678068-57678736	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:57778042-57778485	H1-hESC	embryonic stem cell:	n/a	chr15:57778256-57778270
20	BACH1	chr15:57738124-57738415	K562	blood:	n/a	n/a
21	BACH1	chr15:57649168-57649224	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	chr15:57769828-57770706	HepG2	liver:	n/a	n/a
25	BHLHE40	chr15:57768791-57768792	GM12878	blood:	n/a	n/a
26	BHLHE40	chr15:57675229-57675611	K562	blood:	n/a	n/a
27	BHLHE40	chr15:57778087-57778398	HepG2	liver:	n/a	n/a
28	BHLHE40	chr15:57683205-57684026	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	chr15:57669187-57669508	H1-hESC	embryonic stem cell:	n/a	chr15:57669334-57669345
32	CEBPB	chr15:57719462-57720034	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
33	CEBPB	chr15:57669119-57669538	HepG2	liver:	n/a	chr15:57669334-57669345
34	CEBPB	chr15:57679152-57679246	K562	blood:	n/a	n/a
35	CEBPB	chr15:57759160-57759196	A549	lung:	n/a	n/a
36	CEBPB	chr15:57644830-57645208	K562	blood:	n/a	chr15:57644878-57644889
37	CEBPB	chr15:57645093-57645295	A549	lung:	n/a	n/a
38	CEBPB	chr15:57719531-57719898	MCF-7	breast:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
39	CEBPB	chr15:57664420-57664754	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:57664474-57664663	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:57719546-57719910	IMR90	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
42	CEBPB	chr15:57669326-57669420	K562	blood:	n/a	chr15:57669334-57669345
43	CEBPB	chr15:57669133-57669500	HepG2	liver:	n/a	chr15:57669334-57669345
44	CEBPB	chr15:57698709-57699074	HepG2	liver:	n/a	chr15:57698876-57698887
45	CEBPB	chr15:57683760-57684057	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:57753678-57754168	MCF-7	breast:	n/a	n/a
47	CEBPB	chr15:57770322-57770596	HepG2	liver:	n/a	n/a
48	CEBPB	chr15:57664441-57664787	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr15:57755183-57755257	K562	blood:	n/a	chr15:57755215-57755226
50	CEBPB	chr15:57719550-57719876	HepG2	liver:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57668895-57668945	Jurkat	blood:	n/a
2	chr15:57664490-57664540	HRPEpiC	eye:	n/a
3	chr15:57668895-57668945	Jurkat	blood:	n/a
4	chr15:57664490-57664540	HRPEpiC	eye:	n/a
5	chr15:57719922-57719972	IMR90	lung:	fetal
6	chr15:57695943-57695993	NH-A	brain:	n/a
7	chr15:57669179-57669229	SKMC	muscle:	n/a
8	chr15:57668539-57668589	HNPCEpiC	eye:	n/a
9	chr15:57668039-57668089	SK-N-MC	brain:	n/a
10	chr15:57731055-57731105	Hela-S3	cervix:	n/a
11	chr15:57680479-57680529	HRCEpiC	kidney:	n/a
12	chr15:57778278-57778328	K562	blood:	n/a
13	chr15:57668539-57668589	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:57731648-57731698	SAEC	small airway:	n/a
15	chr15:57669165-57669215	NB4	blood:	n/a
16	chr15:57731108-57731158	HAEpiC	amniotic membrane:	n/a
17	chr15:57669179-57669229	NHDF-neo	bronchial:	n/a
18	chr15:57668539-57668589	MCF10A-Er-Src	breast:	n/a
19	chr15:57731648-57731698	GM19239	blood:	n/a
20	chr15:57669179-57669229	U87	brain:	n/a
21	chr15:57668247-57668297	AG09319	gingival:	n/a
22	chr15:57668087-57668137	H1-hESC	embryonic stem cell:	embryo
23	chr15:57668552-57668602	SK-N-SH	brain:	n/a
24	chr15:57682357-57682407	HRPEpiC	eye:	n/a
25	chr15:57769667-57769717	HAEpiC	amniotic membrane:	n/a
26	chr15:57668261-57668311	ProgFib	skin:	n/a
27	chr15:57655799-57655849	LNCaP	prostate:	n/a
28	chr15:57669165-57669215	T-47D	breast:	n/a
29	chr15:57729383-57729433	AG04450	lung:	fetal
30	chr15:57682357-57682407	Jurkat	blood:	n/a
31	chr15:57680479-57680529	BE2_C	brain:	n/a
32	chr15:57668552-57668602	MCF10A-Er-Src	breast:	n/a
33	chr15:57729383-57729433	HUVEC	blood vessel:	n/a
34	chr15:57668039-57668089	CMK	blood:	n/a
35	chr15:57769667-57769717	HL-60	blood:	n/a
36	chr15:57671034-57671084	HRCEpiC	kidney:	n/a
37	chr15:57668247-57668297	BE2_C	brain:	n/a
38	chr15:57680479-57680529	AoSMC	blood vessel:	n/a
39	chr15:57668261-57668311	GM06990	blood:	n/a
40	chr15:57669165-57669215	U87	brain:	n/a
41	chr15:57719922-57719972	K562	blood:	n/a
42	chr15:57719252-57719302	HEK293	kidney:	embryo
43	chr15:57668895-57668945	RPTEC	kidney:	n/a
44	chr15:57719922-57719972	AG10803	skin:	n/a
45	chr15:57668552-57668602	NH-A	brain:	n/a
46	chr15:57668895-57668945	ECC-1	luminal epithelium:	n/a
47	chr15:57731166-57731216	ECC-1	luminal epithelium:	n/a
48	chr15:57682357-57682407	HEEpiC	esophagus:	n/a
49	chr15:57778278-57778328	LNCaP	prostate:	n/a
50	chr15:57647657-57647707	HNPCEpiC	eye:	n/a

(count:39 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGNL1-2	chr15:57690539-57690628	NONHSAT044073
2	lnc-CGNL1-2	chr15:57730183-57730215	NONHSAT044072
3	lnc-CGNL1-2	chr15:57669124-57669363	NONHSAT044072
4	lnc-CGNL1-2	chr15:57669344-57669363	NONHSAT044073
5	lnc-CGNL1-2	chr15:57694859-57694912	NONHSAT044073
6	lnc-CGNL1-2	chr15:57694217-57694236	NONHSAT044073
7	lnc-ALDH1A2-4	chr15:57769682-57769812	ENSG00000261489.1
8	lnc-ALDH1A2-4	chr15:57770404-57770527	ENSG00000261489.1
9	lnc-CGNL1-2	chr15:57686151-57686289	NONHSAT044073
10	lnc-CGNL1-2	chr15:57689122-57689304	NONHSAT044073
11	lnc-CGNL1-2	chr15:57699171-57699474	NONHSAT044073
12	lnc-CGNL1-2	chr15:57668165-57668468	NONHSAT044072
13	lnc-ALDH1A2-6	chr15:57741444-57741697	expReg_chr15_4576_-
14	lnc-CGNL1-2	chr15:57698164-57698262	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
ENSG00000128849	chromatin interactions
ENSG00000261489	chromatin interactions
ENSG00000261265	chromatin interactions

Extended variants
information (count: 6210 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6210 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4238324	chr15:57643653-57643654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140523127	chr15:57643661-57643662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377657089	chr15:57643733-57643734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531629722	chr15:57643740-57643741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551651109	chr15:57643744-57643745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs541920625	chr15:57643799-57643800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs571448983	chr15:57643817-57643818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539956436	chr15:57643821-57643822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2440945	chr15:57643863-57643864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546795777	chr15:57643864-57643865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548518244	chr15:57643880-57643881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568540404	chr15:57643881-57643882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2921421	chr15:57643886-57643887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555331539	chr15:57643891-57643892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150426533	chr15:57643963-57643964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs188469489	chr15:57643990-57643991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551887140	chr15:57643991-57643992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578119243	chr15:57644024-57644025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369072081	chr15:57644032-57644033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565646766	chr15:57644033-57644034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34165818	chr15:57644048-57644049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374547545	chr15:57644049-57644050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs386383112	chr15:57644051-57644052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs398070672	chr15:57644052-57644053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2440946	chr15:57644070-57644071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573639251	chr15:57644113-57644114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180969442	chr15:57644129-57644130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562467213	chr15:57644136-57644137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs377303721	chr15:57644150-57644151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531667454	chr15:57644169-57644170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561804478	chr15:57644173-57644174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79520775	chr15:57644178-57644179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145370762	chr15:57644181-57644182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527516540	chr15:57644185-57644186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547524604	chr15:57644210-57644211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79496494	chr15:57644211-57644212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185139273	chr15:57644212-57644213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188046490	chr15:57644217-57644218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs536846925	chr15:57644261-57644262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs141337650	chr15:57644265-57644266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs935322	chr15:57644267-57644268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376791176	chr15:57644272-57644273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78595815	chr15:57644309-57644310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539689938	chr15:57644375-57644376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534137125	chr15:57644400-57644401	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs554335892	chr15:57644409-57644410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs935321	chr15:57644412-57644413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs542724950	chr15:57644421-57644422	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs199515226	chr15:57644422-57644423	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs935320	chr15:57644442-57644443	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:2655 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57627600-57668200	Weak transcription	Right Atrium	heart
2	chr15:57636200-57647200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:57638400-57645000	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr15:57638400-57645600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr15:57638600-57644000	Weak transcription	HepG2	liver
6	chr15:57638600-57645200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:57638600-57647200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr15:57642200-57644600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr15:57643600-57645400	Enhancers	Fetal Muscle Trunk	muscle
10	chr15:57643600-57646000	Enhancers	Fetal Muscle Leg	muscle
11	chr15:57643600-57646400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr15:57644000-57644400	Enhancers	HepG2	liver
13	chr15:57644000-57645000	Weak transcription	Fetal Kidney	kidney
14	chr15:57644200-57644400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr15:57644200-57647800	Enhancers	Fetal Heart	heart
16	chr15:57644400-57644600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:57644400-57645200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr15:57644400-57645400	Flanking Active TSS	HepG2	liver
19	chr15:57644400-57646000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr15:57644400-57649800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr15:57644600-57644800	Enhancers	H1 Cell Line	embryonic stem cell
22	chr15:57644600-57646200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr15:57644600-57646200	Enhancers	Placenta	Placenta
24	chr15:57644800-57645600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr15:57645000-57645200	Enhancers	Fetal Kidney	kidney
26	chr15:57645000-57645400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr15:57645000-57645400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr15:57645200-57645400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr15:57645200-57645600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr15:57645200-57646000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr15:57645200-57646200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr15:57645200-57646200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr15:57645200-57646200	Enhancers	Fetal Stomach	stomach
34	chr15:57645200-57646400	Weak transcription	Fetal Kidney	kidney
35	chr15:57645200-57646600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:57645400-57646000	Flanking Bivalent TSS/Enh	HepG2	liver
37	chr15:57645400-57646200	Enhancers	Fetal Intestine Small	intestine
38	chr15:57645400-57646400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr15:57645400-57648000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr15:57645400-57648200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr15:57645600-57645800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr15:57645600-57646000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr15:57645600-57646200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr15:57645600-57646600	Enhancers	H1 Cell Line	embryonic stem cell
45	chr15:57645800-57646000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr15:57645800-57646400	Enhancers	Fetal Intestine Large	intestine
47	chr15:57645800-57646800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr15:57646000-57646200	Bivalent Enhancer	Fetal Muscle Leg	muscle
49	chr15:57646000-57646400	Bivalent Enhancer	HepG2	liver
50	chr15:57646000-57647000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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