Variant report

Variant	nsv1038144
Chromosome Location	chr15:57642065-57778324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1315)
CpG islands
(count:1833)
Chromatin interactive
region (count:39)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1315 , 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	chr15:57683674-57684095	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:57673166-57673314	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	chr15:57675122-57675478	K562	blood:	n/a	n/a
6	ARID3A	chr15:57769934-57770658	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:57709023-57709306	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:57767593-57767849	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	chr15:57777927-57778577	HCT-116	colon:	n/a	n/a
15	ATF3	chr15:57777946-57778537	A549	lung:	n/a	n/a
16	BACH1	chr15:57778042-57778485	H1-hESC	embryonic stem cell:	n/a	chr15:57778256-57778270
17	BACH1	chr15:57678068-57678736	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:57738124-57738415	K562	blood:	n/a	n/a
19	BACH1	chr15:57668896-57669038	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	chr15:57649168-57649224	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL11A	chr15:57648928-57649135	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr15:57648891-57649186	H1-hESC	embryonic stem cell:	n/a	n/a
24	BHLHE40	chr15:57675229-57675611	K562	blood:	n/a	n/a
25	BHLHE40	chr15:57769828-57770706	HepG2	liver:	n/a	n/a
26	BHLHE40	chr15:57683205-57684026	HepG2	liver:	n/a	n/a
27	BHLHE40	chr15:57768791-57768792	GM12878	blood:	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	chr15:57669218-57669407	HepG2	liver:	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	chr15:57669133-57669500	HepG2	liver:	n/a	chr15:57669334-57669345
34	CEBPB	chr15:57719370-57720131	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
35	CEBPB	chr15:57669119-57669538	HepG2	liver:	n/a	chr15:57669334-57669345
36	CEBPB	chr15:57755052-57755277	HepG2	liver:	n/a	chr15:57755215-57755226
37	CEBPB	chr15:57645093-57645295	A549	lung:	n/a	n/a
38	CEBPB	chr15:57770322-57770596	HepG2	liver:	n/a	n/a
39	CEBPB	chr15:57664442-57664743	A549	lung:	n/a	n/a
40	CEBPB	chr15:57644830-57645208	K562	blood:	n/a	chr15:57644878-57644889
41	CEBPB	chr15:57645104-57645259	HepG2	liver:	n/a	n/a
42	CEBPB	chr15:57645133-57645231	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr15:57767622-57767921	HepG2	liver:	n/a	n/a
44	CEBPB	chr15:57719526-57719922	Hela-S3	cervix:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
45	CEBPB	chr15:57719550-57719876	HepG2	liver:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
46	CEBPB	chr15:57719531-57719898	MCF-7	breast:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
47	CEBPB	chr15:57683760-57684057	HepG2	liver:	n/a	n/a
48	CEBPB	chr15:57675162-57675437	K562	blood:	n/a	n/a
49	CEBPB	chr15:57669187-57669508	H1-hESC	embryonic stem cell:	n/a	chr15:57669334-57669345
50	CEBPB	chr15:57719529-57719914	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726

(count:1833 , 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	AG04450	lung:	fetal
2	chr15:57737942-57737992	GM12878	blood:	n/a
3	chr15:57778278-57778328	HL-60	blood:	n/a
4	chr15:57668895-57668945	AG04450	lung:	fetal
5	chr15:57737942-57737992	GM12878	blood:	n/a
6	chr15:57778278-57778328	HL-60	blood:	n/a
7	chr15:57737942-57737992	BJ	skin:	n/a
8	chr15:57719922-57719972	Hela-S3	cervix:	n/a
9	chr15:57724857-57724907	ovcar-3	ovarian:	n/a
10	chr15:57724857-57724907	T-47D	breast:	n/a
11	chr15:57724857-57724907	SK-N-SH	brain:	n/a
12	chr15:57668547-57668597	HEEpiC	esophagus:	n/a
13	chr15:57778278-57778328	SKMC	muscle:	n/a
14	chr15:57677507-57677557	GM19239	blood:	n/a
15	chr15:57724857-57724907	Caco-2	colon:	n/a
16	chr15:57669165-57669215	BJ	skin:	n/a
17	chr15:57669165-57669215	HMEC	breast:	n/a
18	chr15:57778278-57778328	GM12878	blood:	n/a
19	chr15:57769667-57769717	AG09319	gingival:	n/a
20	chr15:57664490-57664540	RPTEC	kidney:	n/a
21	chr15:57669179-57669229	HEEpiC	esophagus:	n/a
22	chr15:57737942-57737992	IMR90	lung:	fetal
23	chr15:57680479-57680529	HepG2	liver:	n/a
24	chr15:57668552-57668602	HRE	kidney:	n/a
25	chr15:57695943-57695993	GM06990	blood:	n/a
26	chr15:57724857-57724907	SK-N-SH_RA	brain:	n/a
27	chr15:57731055-57731105	GM19239	blood:	n/a
28	chr15:57668087-57668137	U87	brain:	n/a
29	chr15:57668812-57668862	BE2_C	brain:	n/a
30	chr15:57668087-57668137	BJ	skin:	n/a
31	chr15:57719922-57719972	HepG2	liver:	n/a
32	chr15:57682357-57682407	HCT-116	colon:	n/a
33	chr15:57668539-57668589	ECC-1	luminal epithelium:	n/a
34	chr15:57778278-57778328	Caco-2	colon:	n/a
35	chr15:57731108-57731158	GM12892	blood:	n/a
36	chr15:57668547-57668597	Hepatocyte	liver:	n/a
37	chr15:57695943-57695993	MCF10A-Er-Src	breast:	n/a
38	chr15:57655799-57655849	ProgFib	skin:	n/a
39	chr15:57680479-57680529	RPTEC	kidney:	n/a
40	chr15:57668547-57668597	SK-N-SH	brain:	n/a
41	chr15:57719922-57719972	HEEpiC	esophagus:	n/a
42	chr15:57737942-57737992	SAEC	small airway:	n/a
43	chr15:57668547-57668597	PFSK-1	brain:	n/a
44	chr15:57655799-57655849	SK-N-MC	brain:	n/a
45	chr15:57671034-57671084	BE2_C	brain:	n/a
46	chr15:57668547-57668597	PrEC	prostate:	n/a
47	chr15:57729383-57729433	ovcar-3	ovarian:	n/a
48	chr15:57668895-57668945	HMEC	breast:	n/a
49	chr15:57668812-57668862	HCF	heart:	n/a
50	chr15:57731055-57731105	IMR90	lung:	fetal

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

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

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

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

No data

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

Extended variants
information (count: 6274 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6274 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142319520	chr15:57642170-57642171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532881054	chr15:57642193-57642194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs115017499	chr15:57642221-57642222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116815540	chr15:57642225-57642226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559759533	chr15:57642236-57642237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145973779	chr15:57642268-57642269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548448237	chr15:57642301-57642302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs139492610	chr15:57642386-57642387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149299286	chr15:57642425-57642426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs72736077	chr15:57642525-57642526	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs200885209	chr15:57642533-57642534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs535584867	chr15:57642546-57642547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs67851561	chr15:57642548-57642549	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs560157760	chr15:57642553-57642554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538249753	chr15:57642568-57642569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535619031	chr15:57642575-57642576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573006159	chr15:57642644-57642645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs5812886	chr15:57642663-57642664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs33967286	chr15:57642664-57642665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568253798	chr15:57642667-57642668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56013622	chr15:57642668-57642669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs202068563	chr15:57642669-57642670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146354520	chr15:57642670-57642671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs3889450	chr15:57642671-57642672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139826034	chr15:57642672-57642673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201171322	chr15:57642673-57642674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs55893168	chr15:57642688-57642689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535647307	chr15:57642693-57642694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs180836814	chr15:57642701-57642702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148453532	chr15:57642715-57642716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558657778	chr15:57642727-57642728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543910466	chr15:57642733-57642734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186393669	chr15:57642734-57642735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190833543	chr15:57642735-57642736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546190228	chr15:57642743-57642744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183914680	chr15:57642745-57642746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs565787555	chr15:57642763-57642764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528741415	chr15:57642769-57642770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548807655	chr15:57642782-57642783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562152220	chr15:57642860-57642861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562142844	chr15:57642862-57642863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188468880	chr15:57642866-57642867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550245939	chr15:57642868-57642869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191646498	chr15:57642893-57642894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534681071	chr15:57642947-57642948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs550807591	chr15:57642948-57642949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs145316123	chr15:57642957-57642958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574671287	chr15:57643001-57643002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs183040586	chr15:57643034-57643035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555562635	chr15:57643046-57643047	Weak transcription	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:2629 , 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	chr15:57636200-57647200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:57636800-57643600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr15:57638400-57645000	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr15:57638400-57645600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr15:57638600-57644000	Weak transcription	HepG2	liver
7	chr15:57638600-57645200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:57638600-57647200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr15:57642000-57642200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr15:57642200-57644600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr15:57643600-57645400	Enhancers	Fetal Muscle Trunk	muscle
12	chr15:57643600-57646000	Enhancers	Fetal Muscle Leg	muscle
13	chr15:57643600-57646400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr15:57644000-57644400	Enhancers	HepG2	liver
15	chr15:57644000-57645000	Weak transcription	Fetal Kidney	kidney
16	chr15:57644200-57644400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr15:57644200-57647800	Enhancers	Fetal Heart	heart
18	chr15:57644400-57644600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr15:57644400-57645200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr15:57644400-57645400	Flanking Active TSS	HepG2	liver
21	chr15:57644400-57646000	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr15:57644400-57649800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr15:57644600-57644800	Enhancers	H1 Cell Line	embryonic stem cell
24	chr15:57644600-57646200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:57644600-57646200	Enhancers	Placenta	Placenta
26	chr15:57644800-57645600	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr15:57645000-57645200	Enhancers	Fetal Kidney	kidney
28	chr15:57645000-57645400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr15:57645000-57645400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr15:57645200-57645400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr15:57645200-57645600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr15:57645200-57646000	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr15:57645200-57646200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr15:57645200-57646200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr15:57645200-57646200	Enhancers	Fetal Stomach	stomach
36	chr15:57645200-57646400	Weak transcription	Fetal Kidney	kidney
37	chr15:57645200-57646600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr15:57645400-57646000	Flanking Bivalent TSS/Enh	HepG2	liver
39	chr15:57645400-57646200	Enhancers	Fetal Intestine Small	intestine
40	chr15:57645400-57646400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr15:57645400-57648000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr15:57645400-57648200	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr15:57645600-57645800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr15:57645600-57646000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr15:57645600-57646200	Enhancers	H9 Cell Line	embryonic stem cell
46	chr15:57645600-57646600	Enhancers	H1 Cell Line	embryonic stem cell
47	chr15:57645800-57646000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr15:57645800-57646400	Enhancers	Fetal Intestine Large	intestine
49	chr15:57645800-57646800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr15:57646000-57646200	Bivalent Enhancer	Fetal Muscle Leg	muscle

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