Variant report

Variant	nsv1043041
Chromosome Location	chr15:58744505-58876327
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2557)
CpG islands
(count:857)
Chromatin interactive
region (count:136)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2557 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58755905-58756780	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:58865349-58865801	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:58761980-58762558	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:58843760-58844405	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:58759096-58761393	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:58844004-58844144	K562	blood:	n/a	n/a
7	ARID3A	chr15:58767778-58769308	HepG2	liver:	n/a	n/a
8	ARID3A	chr15:58785240-58785433	K562	blood:	n/a	n/a
9	ARID3A	chr15:58812778-58814188	K562	blood:	n/a	n/a
10	ARID3A	chr15:58749976-58750707	HepG2	liver:	n/a	n/a
11	ARID3A	chr15:58820207-58820855	HepG2	liver:	n/a	n/a
12	ARID3A	chr15:58838842-58839281	K562	blood:	n/a	n/a
13	ARID3A	chr15:58747156-58747675	HepG2	liver:	n/a	n/a
14	ARID3A	chr15:58843627-58843679	K562	blood:	n/a	n/a
15	ATF1	chr15:58813645-58814435	K562	blood:	n/a	n/a
16	ATF1	chr15:58762340-58762460	K562	blood:	n/a	n/a
17	ATF1	chr15:58843838-58844224	K562	blood:	n/a	n/a
18	ATF1	chr15:58759466-58759852	K562	blood:	n/a	n/a
19	ATF1	chr15:58763625-58763852	K562	blood:	n/a	n/a
20	ATF1	chr15:58749705-58749952	K562	blood:	n/a	n/a
21	ATF1	chr15:58838759-58839354	K562	blood:	n/a	n/a
22	ATF1	chr15:58808004-58808383	K562	blood:	n/a	n/a
23	ATF1	chr15:58837601-58837928	K562	blood:	n/a	n/a
24	ATF1	chr15:58810309-58810725	K562	blood:	n/a	n/a
25	ATF1	chr15:58760148-58760226	K562	blood:	n/a	n/a
26	ATF2	chr15:58765955-58766385	GM12878	blood:	n/a	n/a
27	ATF2	chr15:58810025-58810912	GM12878	blood:	n/a	n/a
28	ATF2	chr15:58749559-58750757	GM12878	blood:	n/a	n/a
29	ATF2	chr15:58746536-58747070	GM12878	blood:	n/a	n/a
30	ATF2	chr15:58765953-58766459	GM12878	blood:	n/a	n/a
31	ATF2	chr15:58807914-58808407	GM12878	blood:	n/a	n/a
32	ATF2	chr15:58807930-58808408	GM12878	blood:	n/a	n/a
33	ATF2	chr15:58749604-58750667	GM12878	blood:	n/a	n/a
34	ATF2	chr15:58746518-58747031	GM12878	blood:	n/a	n/a
35	ATF2	chr15:58813644-58814121	GM12878	blood:	n/a	n/a
36	ATF2	chr15:58809964-58810730	GM12878	blood:	n/a	n/a
37	ATF3	chr15:58761860-58762588	A549	lung:	n/a	n/a
38	ATF3	chr15:58813670-58814130	K562	blood:	n/a	n/a
39	ATF3	chr15:58838727-58839898	A549	lung:	n/a	n/a
40	ATF3	chr15:58813620-58813978	K562	blood:	n/a	n/a
41	ATF3	chr15:58761953-58762623	A549	lung:	n/a	n/a
42	ATF3	chr15:58762213-58762548	K562	blood:	n/a	n/a
43	ATF3	chr15:58838774-58839929	A549	lung:	n/a	n/a
44	ATF3	chr15:58838821-58839124	K562	blood:	n/a	n/a
45	ATF3	chr15:58820176-58820772	A549	lung:	n/a	n/a
46	ATF3	chr15:58762307-58762508	K562	blood:	n/a	n/a
47	BACH1	chr15:58759449-58759476	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr15:58785186-58785562	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr15:58785153-58785591	K562	blood:	n/a	n/a
50	BACH1	chr15:58813395-58813427	K562	blood:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58839555-58839605	HRPEpiC	eye:	n/a
2	chr15:58791257-58791307	BJ	skin:	n/a
3	chr15:58782688-58782738	AG10803	skin:	n/a
4	chr15:58839555-58839605	HRPEpiC	eye:	n/a
5	chr15:58791257-58791307	BJ	skin:	n/a
6	chr15:58782688-58782738	AG10803	skin:	n/a
7	chr15:58840596-58840646	HNPCEpiC	eye:	n/a
8	chr15:58791257-58791307	HUVEC	blood vessel:	n/a
9	chr15:58844359-58844409	HPAEpiC	pulmonary alveolar:	n/a
10	chr15:58797839-58797889	HNPCEpiC	eye:	n/a
11	chr15:58844583-58844633	Jurkat	blood:	n/a
12	chr15:58791257-58791307	IMR90	lung:	fetal
13	chr15:58791257-58791307	K562	blood:	n/a
14	chr15:58758468-58758518	HRE	kidney:	n/a
15	chr15:58782685-58782735	Hepatocyte	liver:	n/a
16	chr15:58840596-58840646	NB4	blood:	n/a
17	chr15:58782688-58782738	K562	blood:	n/a
18	chr15:58791257-58791307	CMK	blood:	n/a
19	chr15:58839555-58839605	HRE	kidney:	n/a
20	chr15:58844500-58844550	HRE	kidney:	n/a
21	chr15:58853142-58853192	AG09319	gingival:	n/a
22	chr15:58766885-58766935	PrEC	prostate:	n/a
23	chr15:58844583-58844633	K562	blood:	n/a
24	chr15:58844359-58844409	HCPEpiC	choroid plexus:	n/a
25	chr15:58844500-58844550	A549	lung:	n/a
26	chr15:58766885-58766935	HCM	heart:	n/a
27	chr15:58812960-58813010	HCPEpiC	choroid plexus:	n/a
28	chr15:58782685-58782735	HAEpiC	amniotic membrane:	n/a
29	chr15:58844500-58844550	MCF-7	breast:	n/a
30	chr15:58844583-58844633	NHBE	bronchial:	n/a
31	chr15:58797839-58797889	AG04450	lung:	fetal
32	chr15:58791257-58791307	SK-N-SH_RA	brain:	n/a
33	chr15:58812960-58813010	GM12891	blood:	n/a
34	chr15:58844359-58844409	A549	lung:	n/a
35	chr15:58766885-58766935	SK-N-SH_RA	brain:	n/a
36	chr15:58840678-58840728	HAEpiC	amniotic membrane:	n/a
37	chr15:58840678-58840728	HUVEC	blood vessel:	n/a
38	chr15:58766885-58766935	HIPEpiC	eye:	n/a
39	chr15:58782688-58782738	HUVEC	blood vessel:	n/a
40	chr15:58758468-58758518	HCF	heart:	n/a
41	chr15:58853142-58853192	IMR90	lung:	fetal
42	chr15:58797839-58797889	HEK293	kidney:	embryo
43	chr15:58853142-58853192	HAEpiC	amniotic membrane:	n/a
44	chr15:58844583-58844633	HIPEpiC	eye:	n/a
45	chr15:58812960-58813010	RPTEC	kidney:	n/a
46	chr15:58844583-58844633	IMR90	lung:	fetal
47	chr15:58839555-58839605	GM12892	blood:	n/a
48	chr15:58797839-58797889	HUVEC	blood vessel:	n/a
49	chr15:58791257-58791307	HRPEpiC	eye:	n/a
50	chr15:58758468-58758518	SK-N-MC	brain:	n/a

(count:136 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:58800669..58805424-chr15:58807712..58810883,4	K562	blood:
2	chr15:58800980..58802725-chr15:58817478..58819244,2	K562	blood:
3	chr15:58843959..58845583-chr15:58846564..58848827,2	K562	blood:
4	chr15:58816638..58820223-chr15:58821126..58823355,3	K562	blood:
5	chr15:58769989..58771899-chr15:58773674..58776005,2	K562	blood:
6	chr15:58826844..58829894-chr15:58830653..58832935,3	MCF-7	breast:
7	chr15:58797460..58800451-chr15:58803881..58805523,2	K562	blood:
8	chr15:58810857..58816650-chr15:58835363..58842392,10	K562	blood:
9	chr15:58855055..58857360-chr15:58858745..58860281,2	K562	blood:
10	chr15:58836656..58842196-chr15:58843431..58849915,8	K562	blood:
11	chr15:58623181..58625459-chr15:58764481..58766715,2	MCF-7	breast:
12	chr15:58821339..58824324-chr15:58827495..58830002,2	K562	blood:
13	chr15:58819551..58822537-chr15:58827877..58830479,4	MCF-7	breast:
14	chr15:58720668..58723820-chr15:58759148..58762580,3	K562	blood:
15	chr15:58814659..58816490-chr15:58819397..58821413,2	MCF-7	breast:
16	chr15:58819426..58821702-chr15:58824237..58826443,2	K562	blood:
17	chr15:58840975..58843014-chr15:59224464..59226714,2	MCF-7	breast:
18	chr15:58778802..58780678-chr15:58783257..58786951,3	K562	blood:
19	chr15:58850686..58852786-chr15:58855873..58857553,2	K562	blood:
20	chr15:58731963..58734945-chr15:58743116..58746394,3	K562	blood:
21	chr15:58805398..58807499-chr15:58809534..58812404,4	MCF-7	breast:
22	chr15:58839847..58842164-chr15:59040340..59041855,2	MCF-7	breast:
23	chr15:58730575..58732285-chr15:58839559..58842370,2	K562	blood:
24	chr15:58778802..58780678-chr15:58783257..58786951,3	K562	blood:
25	chr15:58797035..58800948-chr15:58803702..58808140,4	K562	blood:
26	chr15:58841673..58842595-chr20:49248753..49249599,2	MCF-7	breast:
27	chr15:58800669..58805424-chr15:58807712..58810883,4	K562	blood:
28	chr15:58818144..58821107-chr15:58827941..58830725,2	K562	blood:
29	chr15:58846252..58850551-chr15:58852253..58854849,4	MCF-7	breast:
30	chr15:58855055..58857360-chr15:58858745..58860281,2	K562	blood:
31	chr15:58815750..58818981-chr15:58825032..58827694,3	K562	blood:
32	chr15:58841936..58843699-chr15:59035411..59037859,2	MCF-7	breast:
33	chr15:58868577..58870503-chr15:58875385..58877365,2	K562	blood:
34	chr15:58767751..58769658-chr15:58771265..58773299,2	MCF-7	breast:
35	chr15:58844000..58845908-chr15:58853129..58855286,2	K562	blood:
36	chr15:58811000..58814506-chr15:58833587..58836863,3	K562	blood:
37	chr15:58860633..58862696-chr15:58874289..58877097,2	MCF-7	breast:
38	chr15:58742210..58745056-chr15:58745443..58748993,3	K562	blood:
39	chr15:58841313..58844294-chr15:58848370..58850226,2	K562	blood:
40	chr15:58791633..58793802-chr15:58794935..58797234,3	K562	blood:
41	chr15:58801519..58805506-chr15:58811166..58813986,3	K562	blood:
42	chr15:58812962..58815052-chr15:58815681..58818546,2	K562	blood:
43	chr15:58758547..58760128-chr15:58777523..58780209,2	MCF-7	breast:
44	chr15:58767133..58770014-chr15:58770584..58772843,2	MCF-7	breast:
45	chr15:58831032..58833136-chr15:58839307..58841040,2	MCF-7	breast:
46	chr15:58728810..58730578-chr15:58760180..58761799,2	MCF-7	breast:
47	chr15:58742210..58745056-chr15:58745443..58748993,3	K562	blood:
48	chr15:58819551..58822537-chr15:58827877..58830479,4	MCF-7	breast:
49	chr15:58815750..58818981-chr15:58825032..58827694,3	K562	blood:
50	chr15:58860633..58862696-chr15:58874289..58877097,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM10-9	chr15:58789916-58790065	NONHSAT044093
2	lnc-FAM63B-2	chr15:58814150-58815568	ENSG00000249011
3	lnc-FAM63B-2	chr15:58813510-58813845	ENSG00000259476.1
4	lnc-ADAM10-9	chr15:58765830-58765959	NONHSAT044093
5	lnc-ALDH1A2-1	chr15:58786972-58787082	ENSG00000259293.1
6	lnc-FAM63B-2	chr15:58813510-58813845	ENSG00000249011
7	lnc-FAM63B-2	chr15:58814150-58815570	ENSG00000259476.1
8	lnc-ALDH1A2-1	chr15:58790838-58790934	ENSG00000259293.1

No data

Variant related genes	Relation type
LIPC	TF binding region
ENSG00000259476	TF binding region
ENSG00000259250	TF binding region
ENSG00000259293	TF binding region
ALDH1A2	TF binding region
LIPC	CpG island
ENSG00000259476	CpG island
ENSG00000259250	CpG island
ENSG00000259293	CpG island
ALDH1A2	CpG island
ENSG00000166035	chromatin interactions
ENSG00000259293	chromatin interactions
ENSG00000137776	chromatin interactions
ENSG00000128918	chromatin interactions
ENSG00000259250	chromatin interactions
ENSG00000137845	chromatin interactions
ENSG00000259476	chromatin interactions
RAB14	miRNA target sites

Extended variants
information (count: 5882 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:5882 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148468516	chr15:58744505-58744506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs367571966	chr15:58744508-58744509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186003556	chr15:58744525-58744526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555074285	chr15:58744527-58744528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs575249824	chr15:58744564-58744565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142606327	chr15:58744576-58744577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs146527524	chr15:58744581-58744582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs577100973	chr15:58744640-58744641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370093284	chr15:58744642-58744643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546008771	chr15:58744644-58744645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75828665	chr15:58744689-58744690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139978831	chr15:58744715-58744716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190909506	chr15:58744754-58744755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562038543	chr15:58744755-58744756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372370257	chr15:58744758-58744759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530973261	chr15:58744764-58744765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113701682	chr15:58744769-58744770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs35543273	chr15:58744779-58744780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs111477460	chr15:58744870-58744871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564397144	chr15:58744883-58744884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533232238	chr15:58744913-58744914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546829533	chr15:58744935-58744936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143451569	chr15:58744944-58744945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11071383	chr15:58744970-58744971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569027815	chr15:58744981-58744982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568845064	chr15:58744987-58744988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74399293	chr15:58745036-58745037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557303564	chr15:58745048-58745049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182542186	chr15:58745061-58745062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113390721	chr15:58745117-58745118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs116365823	chr15:58745125-58745126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185776246	chr15:58745141-58745142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537683537	chr15:58745172-58745173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553153896	chr15:58745199-58745200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145749514	chr15:58745269-58745270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs112341099	chr15:58745273-58745274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs28593360	chr15:58745274-58745275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs111288227	chr15:58745284-58745285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373068953	chr15:58745285-58745286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546154839	chr15:58745286-58745287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140424203	chr15:58745320-58745321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564774988	chr15:58745355-58745356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564436704	chr15:58745364-58745365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533270939	chr15:58745392-58745393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540582775	chr15:58745397-58745398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182007	chr15:58745398-58745399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs78229996	chr15:58745415-58745416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548884038	chr15:58745420-58745421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs629700	chr15:58745433-58745434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555463053	chr15:58745469-58745470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Chronic lymphocytic leukemia	21546498	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
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2809 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58730400-58746200	Weak transcription	GM12878-XiMat	blood
2	chr15:58736600-58746200	Weak transcription	Spleen	Spleen
3	chr15:58737400-58749800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr15:58737400-58761800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:58737800-58746600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr15:58737800-58748200	Weak transcription	Left Ventricle	heart
7	chr15:58739600-58749600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr15:58740000-58745000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr15:58740000-58745000	Weak transcription	HSMMtube	muscle
10	chr15:58740400-58748800	Weak transcription	NHLF	lung
11	chr15:58740400-58749800	Weak transcription	Adipose Nuclei	Adipose
12	chr15:58740600-58746400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr15:58740600-58749600	Weak transcription	Small Intestine	intestine
14	chr15:58740800-58745200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr15:58740800-58749600	Weak transcription	Liver	Liver
16	chr15:58740800-58749600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr15:58741000-58746200	Weak transcription	HepG2	liver
18	chr15:58741200-58744600	Weak transcription	Thymus	Thymus
19	chr15:58741400-58745000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:58741600-58746200	Weak transcription	Pancreas	Pancrea
21	chr15:58741600-58748000	Weak transcription	Gastric	stomach
22	chr15:58743600-58745200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr15:58743800-58744600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr15:58743800-58770400	Enhancers	Fetal Thymus	thymus
25	chr15:58744000-58746000	Weak transcription	HSMM	muscle
26	chr15:58744200-58751800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr15:58744400-58745400	Weak transcription	Dnd41	blood
28	chr15:58744600-58747800	Enhancers	Thymus	Thymus
29	chr15:58745000-58745800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr15:58745000-58746200	Enhancers	HSMMtube	muscle
31	chr15:58745000-58747200	Enhancers	Fetal Muscle Trunk	muscle
32	chr15:58745000-58748400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr15:58745000-58748600	Enhancers	Fetal Muscle Leg	muscle
34	chr15:58745200-58747600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:58745200-58751400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:58745400-58747800	Enhancers	Dnd41	blood
37	chr15:58745800-58746200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr15:58746000-58748200	Enhancers	HSMM	muscle
39	chr15:58746200-58746600	Enhancers	Lung	lung
40	chr15:58746200-58746800	Enhancers	Spleen	Spleen
41	chr15:58746200-58746800	Flanking Active TSS	HSMMtube	muscle
42	chr15:58746200-58747000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:58746200-58747000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr15:58746200-58747000	Enhancers	Pancreas	Pancrea
45	chr15:58746200-58748400	Enhancers	HepG2	liver
46	chr15:58746200-58749800	Enhancers	GM12878-XiMat	blood
47	chr15:58746400-58747400	Enhancers	Primary hematopoietic stem cells short term culture	blood
48	chr15:58746400-58747600	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr15:58746400-58747600	Enhancers	K562	blood
50	chr15:58746400-58747800	Enhancers	Muscle Satellite Cultured Cells	--

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