Variant report

Variant	nsv1051027
Chromosome Location	chr15:57647132-57766519
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1032)
CpG islands
(count:1711)
Chromatin interactive
region (count:36)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

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	chr15:57683674-57684095	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:57709023-57709306	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:57698812-57699080	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57673166-57673314	HepG2	liver:	n/a	n/a
6	ATF1	chr15:57675232-57675432	K562	blood:	n/a	n/a
7	ATF1	chr15:57739082-57739221	K562	blood:	n/a	n/a
8	ATF2	chr15:57677951-57678684	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:57677879-57679030	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr15:57648804-57649568	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:57649168-57649224	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:57668896-57669038	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:57678068-57678736	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:57738124-57738415	K562	blood:	n/a	n/a
15	BACH1	chr15:57738064-57738618	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL11A	chr15:57648891-57649186	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr15:57648928-57649135	H1-hESC	embryonic stem cell:	n/a	n/a
18	BHLHE40	chr15:57675229-57675611	K562	blood:	n/a	n/a
19	BHLHE40	chr15:57683205-57684026	HepG2	liver:	n/a	n/a
20	BRCA1	chr15:57649151-57649161	H1-hESC	embryonic stem cell:	n/a	n/a
21	CCNT2	chr15:57675201-57675501	K562	blood:	n/a	n/a
22	CEBPB	chr15:57719546-57719910	IMR90	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
23	CEBPB	chr15:57669218-57669407	HepG2	liver:	n/a	chr15:57669334-57669345
24	CEBPB	chr15:57755052-57755277	HepG2	liver:	n/a	chr15:57755215-57755226
25	CEBPB	chr15:57669326-57669420	K562	blood:	n/a	chr15:57669334-57669345
26	CEBPB	chr15:57719550-57719876	HepG2	liver:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
27	CEBPB	chr15:57664441-57664787	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr15:57679152-57679246	K562	blood:	n/a	n/a
29	CEBPB	chr15:57719462-57720034	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
30	CEBPB	chr15:57755183-57755257	K562	blood:	n/a	chr15:57755215-57755226
31	CEBPB	chr15:57753678-57754168	MCF-7	breast:	n/a	n/a
32	CEBPB	chr15:57669119-57669538	HepG2	liver:	n/a	chr15:57669334-57669345
33	CEBPB	chr15:57719529-57719914	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
34	CEBPB	chr15:57759160-57759196	A549	lung:	n/a	n/a
35	CEBPB	chr15:57719526-57719922	Hela-S3	cervix:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
36	CEBPB	chr15:57683760-57684057	HepG2	liver:	n/a	n/a
37	CEBPB	chr15:57664442-57664743	A549	lung:	n/a	n/a
38	CEBPB	chr15:57669133-57669500	HepG2	liver:	n/a	chr15:57669334-57669345
39	CEBPB	chr15:57664420-57664754	HepG2	liver:	n/a	n/a
40	CEBPB	chr15:57719370-57720131	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
41	CEBPB	chr15:57649017-57649179	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr15:57669158-57669538	HepG2	liver:	n/a	chr15:57669334-57669345
43	CEBPB	chr15:57698709-57699074	HepG2	liver:	n/a	chr15:57698876-57698887
44	CEBPB	chr15:57675162-57675437	K562	blood:	n/a	n/a
45	CEBPB	chr15:57753700-57754104	MCF-7	breast:	n/a	n/a
46	CEBPB	chr15:57737280-57737551	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:57669187-57669508	H1-hESC	embryonic stem cell:	n/a	chr15:57669334-57669345
48	CEBPB	chr15:57719531-57719898	MCF-7	breast:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
49	CEBPB	chr15:57664474-57664663	HepG2	liver:	n/a	n/a
50	CEBPB	chr15:57688268-57688424	A549	lung:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57668261-57668311	Hela-S3	cervix:	n/a
2	chr15:57668895-57668945	GM12878	blood:	n/a
3	chr15:57695943-57695993	AG04449	skin:	fetal
4	chr15:57668261-57668311	Hela-S3	cervix:	n/a
5	chr15:57668895-57668945	GM12878	blood:	n/a
6	chr15:57695943-57695993	AG04449	skin:	fetal
7	chr15:57731648-57731698	HNPCEpiC	eye:	n/a
8	chr15:57731055-57731105	Hela-S3	cervix:	n/a
9	chr15:57731108-57731158	IMR90	lung:	fetal
10	chr15:57677507-57677557	HEEpiC	esophagus:	n/a
11	chr15:57664490-57664540	HNPCEpiC	eye:	n/a
12	chr15:57729383-57729433	MCF10A-Er-Src	breast:	n/a
13	chr15:57729383-57729433	HUVEC	blood vessel:	n/a
14	chr15:57731055-57731105	HIPEpiC	eye:	n/a
15	chr15:57668247-57668297	H1-hESC	embryonic stem cell:	embryo
16	chr15:57719922-57719972	RPTEC	kidney:	n/a
17	chr15:57668087-57668137	BJ	skin:	n/a
18	chr15:57677507-57677557	AG10803	skin:	n/a
19	chr15:57668539-57668589	HIPEpiC	eye:	n/a
20	chr15:57719252-57719302	AG09319	gingival:	n/a
21	chr15:57719252-57719302	PANC-1	pancreas:	n/a
22	chr15:57680479-57680529	PFSK-1	brain:	n/a
23	chr15:57668552-57668602	AG04449	skin:	fetal
24	chr15:57731166-57731216	U87	brain:	n/a
25	chr15:57668539-57668589	NHBE	bronchial:	n/a
26	chr15:57668547-57668597	HCF	heart:	n/a
27	chr15:57668539-57668589	NHDF-neo	bronchial:	n/a
28	chr15:57677507-57677557	GM06990	blood:	n/a
29	chr15:57668087-57668137	HRCEpiC	kidney:	n/a
30	chr15:57680479-57680529	IMR90	lung:	fetal
31	chr15:57664490-57664540	AG10803	skin:	n/a
32	chr15:57731108-57731158	HL-60	blood:	n/a
33	chr15:57668812-57668862	AoSMC	blood vessel:	n/a
34	chr15:57677507-57677557	GM12891	blood:	n/a
35	chr15:57664490-57664540	K562	blood:	n/a
36	chr15:57668552-57668602	IMR90	lung:	fetal
37	chr15:57719252-57719302	Hela-S3	cervix:	n/a
38	chr15:57669179-57669229	NHBE	bronchial:	n/a
39	chr15:57669165-57669215	HCT-116	colon:	n/a
40	chr15:57731166-57731216	A549	lung:	n/a
41	chr15:57731648-57731698	SAEC	small airway:	n/a
42	chr15:57647657-57647707	NB4	blood:	n/a
43	chr15:57724857-57724907	SKMC	muscle:	n/a
44	chr15:57668247-57668297	BJ	skin:	n/a
45	chr15:57719922-57719972	T-47D	breast:	n/a
46	chr15:57655799-57655849	HPAEpiC	pulmonary alveolar:	n/a
47	chr15:57668552-57668602	LNCaP	prostate:	n/a
48	chr15:57729383-57729433	PFSK-1	brain:	n/a
49	chr15:57668039-57668089	PrEC	prostate:	n/a
50	chr15:57664490-57664540	HRPEpiC	eye:	n/a

(count:36 , 50 per page) page: 1

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

(count:12 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 5477 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:5477 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2431039	chr15:57647132-57647133	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs575025717	chr15:57647137-57647138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs36140884	chr15:57647225-57647226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs144700821	chr15:57647243-57647244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148503687	chr15:57647256-57647257	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142885257	chr15:57647295-57647296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs546532693	chr15:57647315-57647316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560225750	chr15:57647316-57647317	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146787191	chr15:57647326-57647327	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs66943178	chr15:57647327-57647328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs386383113	chr15:57647328-57647329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs397732740	chr15:57647331-57647332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529198791	chr15:57647338-57647339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192964817	chr15:57647340-57647341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs569054863	chr15:57647341-57647342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534489187	chr15:57647384-57647385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550818275	chr15:57647388-57647389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs570878932	chr15:57647411-57647412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs539459883	chr15:57647414-57647415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs151055222	chr15:57647415-57647416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs76374984	chr15:57647426-57647427	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535728009	chr15:57647432-57647433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143756099	chr15:57647472-57647473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146878377	chr15:57647495-57647496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs367775967	chr15:57647528-57647529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544742357	chr15:57647529-57647530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs35511598	chr15:57647562-57647563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540842625	chr15:57647574-57647575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554362875	chr15:57647609-57647610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs564034073	chr15:57647624-57647625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs74016165	chr15:57647638-57647639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139060911	chr15:57647642-57647643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs370464560	chr15:57647643-57647644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140748604	chr15:57647654-57647655	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560071791	chr15:57647657-57647658	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555667958	chr15:57647658-57647659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373435910	chr15:57647661-57647662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529239358	chr15:57647664-57647665	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs734490	chr15:57647707-57647708	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs562742848	chr15:57647759-57647760	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150481234	chr15:57647804-57647805	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs551513497	chr15:57647805-57647806	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs79260567	chr15:57647807-57647808	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138409868	chr15:57647826-57647827	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs188808311	chr15:57647853-57647854	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs566513696	chr15:57647877-57647878	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs117602897	chr15:57647926-57647927	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs555641412	chr15:57647944-57647945	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs569165661	chr15:57647992-57647993	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs538092854	chr15:57648010-57648011	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:2347 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

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	chr15:57638600-57647200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr15:57644200-57647800	Enhancers	Fetal Heart	heart
5	chr15:57644400-57649800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:57645400-57648000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr15:57645400-57648200	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr15:57646000-57647800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr15:57646000-57647800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr15:57646000-57647800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr15:57646200-57647200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr15:57646200-57647200	Weak transcription	Fetal Stomach	stomach
13	chr15:57646200-57647800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr15:57646200-57648600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr15:57646200-57648600	Weak transcription	Placenta	Placenta
16	chr15:57646200-57649400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:57646800-57648400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:57646800-57649400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr15:57647000-57647600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:57647000-57648200	Weak transcription	Fetal Kidney	kidney
21	chr15:57647000-57649200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:57647000-57649400	Enhancers	H1 Cell Line	embryonic stem cell
23	chr15:57647200-57647400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr15:57647200-57648400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr15:57647200-57649400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr15:57647200-57649400	Enhancers	HSMMtube	muscle
27	chr15:57647200-57650400	Enhancers	Fetal Stomach	stomach
28	chr15:57647400-57647800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr15:57647400-57649400	Enhancers	HSMM	muscle
30	chr15:57647600-57648000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr15:57647600-57650000	Enhancers	Stomach Smooth Muscle	stomach
32	chr15:57647800-57648400	Flanking Active TSS	Fetal Heart	heart
33	chr15:57647800-57649400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr15:57647800-57649400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr15:57647800-57649600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr15:57647800-57649600	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr15:57647800-57649600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr15:57648000-57648400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr15:57648000-57648600	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr15:57648000-57649800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr15:57648000-57649800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr15:57648000-57650400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr15:57648200-57649000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr15:57648200-57649000	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr15:57648200-57649400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr15:57648200-57649400	Enhancers	Fetal Kidney	kidney
47	chr15:57648200-57649600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr15:57648200-57649600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:57648200-57649600	Enhancers	NH-A	brain
50	chr15:57648200-57649600	Enhancers	Osteobl	bone

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