Variant report

Variant	nsv1046099
Chromosome Location	chr15:76444695-76490547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1236)
CpG islands
(count:1039)
Chromatin interactive
region (count:61)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1236 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76488758-76489089	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:76478041-76478258	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:76483064-76483427	HepG2	liver:	n/a	n/a
4	ATF2	chr15:76473823-76474454	GM12878	blood:	n/a	n/a
5	ATF2	chr15:76473954-76474425	GM12878	blood:	n/a	n/a
6	ATF2	chr15:76483089-76483813	GM12878	blood:	n/a	n/a
7	ATF3	chr15:76461359-76461682	GM12878	blood:	n/a	n/a
8	ATF3	chr15:76488695-76489271	A549	lung:	n/a	n/a
9	ATF3	chr15:76461499-76461617	GM12878	blood:	n/a	n/a
10	ATF3	chr15:76461375-76461737	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr15:76461421-76461690	K562	blood:	n/a	n/a
12	BACH1	chr15:76483297-76483365	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr15:76473865-76474455	GM12878	blood:	n/a	chr15:76474119-76474130
14	BATF	chr15:76473923-76474319	GM12878	blood:	n/a	chr15:76474119-76474130
15	BCL11A	chr15:76473914-76474363	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:76474032-76474320	GM12878	blood:	n/a	n/a
17	BCL3	chr15:76488403-76489359	A549	lung:	n/a	n/a
18	BCL3	chr15:76482892-76483810	A549	lung:	n/a	n/a
19	BCLAF1	chr15:76473788-76474517	GM12878	blood:	n/a	n/a
20	BCLAF1	chr15:76473905-76474445	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:76472787-76472910	K562	blood:	n/a	n/a
22	BHLHE40	chr15:76473924-76474330	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:76486297-76486653	K562	blood:	n/a	n/a
24	BHLHE40	chr15:76486294-76486734	HepG2	liver:	n/a	n/a
25	BHLHE40	chr15:76455772-76455880	K562	blood:	n/a	n/a
26	BHLHE40	chr15:76483122-76483431	K562	blood:	n/a	n/a
27	BHLHE40	chr15:76483088-76483437	GM12878	blood:	n/a	n/a
28	BHLHE40	chr15:76482536-76482865	K562	blood:	n/a	n/a
29	BHLHE40	chr15:76469949-76470149	A549	lung:	n/a	n/a
30	BHLHE40	chr15:76488854-76489227	K562	blood:	n/a	n/a
31	BHLHE40	chr15:76472876-76472910	HepG2	liver:	n/a	n/a
32	BRCA1	chr15:76483097-76483525	Hela-S3	cervix:	n/a	chr15:76483441-76483448
33	BRCA1	chr15:76490319-76490372	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr15:76483167-76483490	HepG2	liver:	n/a	chr15:76483441-76483448
35	BRCA1	chr15:76455813-76456207	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr15:76483134-76483378	H1-hESC	embryonic stem cell:	n/a	n/a
37	CBX3	chr15:76488727-76489226	K562	blood:	n/a	n/a
38	CBX3	chr15:76477995-76478351	K562	blood:	n/a	n/a
39	CEBPB	chr15:76455728-76456127	HepG2	liver:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
40	CEBPB	chr15:76455726-76456095	ECC-1	luminal epithelium:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
41	CEBPB	chr15:76455786-76456001	K562	blood:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
42	CEBPB	chr15:76455867-76455874	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr15:76455169-76456214	Hela-S3	cervix:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
44	CEBPB	chr15:76455706-76456096	HepG2	liver:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
45	CEBPB	chr15:76455731-76456075	A549	lung:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
46	CEBPB	chr15:76455634-76456132	A549	lung:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
47	CEBPB	chr15:76482803-76483407	MCF-7	breast:	n/a	n/a
48	CEBPB	chr15:76455735-76456003	K562	blood:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
49	CEBPB	chr15:76482808-76483429	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr15:76469800-76470434	Hela-S3	cervix:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76484473-76484523	HMEC	breast:	n/a
2	chr15:76483344-76483394	Hela-S3	cervix:	n/a
3	chr15:76484473-76484523	HMEC	breast:	n/a
4	chr15:76483344-76483394	Hela-S3	cervix:	n/a
5	chr15:76470979-76471029	HCT-116	colon:	n/a
6	chr15:76458365-76458415	HNPCEpiC	eye:	n/a
7	chr15:76483344-76483394	SK-N-SH	brain:	n/a
8	chr15:76458365-76458415	NB4	blood:	n/a
9	chr15:76470979-76471029	HCM	heart:	n/a
10	chr15:76484102-76484152	HAEpiC	amniotic membrane:	n/a
11	chr15:76470979-76471029	AG09309	skin:	n/a
12	chr15:76461960-76462010	ProgFib	skin:	n/a
13	chr15:76478102-76478152	BJ	skin:	n/a
14	chr15:76475969-76476019	GM12892	blood:	n/a
15	chr15:76483201-76483251	SK-N-SH	brain:	n/a
16	chr15:76478102-76478152	HMEC	breast:	n/a
17	chr15:76484473-76484523	HRE	kidney:	n/a
18	chr15:76483201-76483251	AG09319	gingival:	n/a
19	chr15:76458279-76458329	IMR90	lung:	fetal
20	chr15:76461960-76462010	HRE	kidney:	n/a
21	chr15:76484102-76484152	HL-60	blood:	n/a
22	chr15:76458279-76458329	MCF-7	breast:	n/a
23	chr15:76483201-76483251	NHBE	bronchial:	n/a
24	chr15:76480434-76480484	HCPEpiC	choroid plexus:	n/a
25	chr15:76483344-76483394	MCF10A-Er-Src	breast:	n/a
26	chr15:76484473-76484523	HL-60	blood:	n/a
27	chr15:76458279-76458329	ovcar-3	ovarian:	n/a
28	chr15:76480434-76480484	SK-N-SH	brain:	n/a
29	chr15:76484102-76484152	Jurkat	blood:	n/a
30	chr15:76462821-76462871	Hela-S3	cervix:	n/a
31	chr15:76475969-76476019	U87	brain:	n/a
32	chr15:76458372-76458422	AoSMC	blood vessel:	n/a
33	chr15:76478102-76478152	Hela-S3	cervix:	n/a
34	chr15:76483344-76483394	HPAEpiC	pulmonary alveolar:	n/a
35	chr15:76483281-76483331	SK-N-SH_RA	brain:	n/a
36	chr15:76470979-76471029	PANC-1	pancreas:	n/a
37	chr15:76470979-76471029	GM12878	blood:	n/a
38	chr15:76484379-76484429	A549	lung:	n/a
39	chr15:76458279-76458329	HRPEpiC	eye:	n/a
40	chr15:76475969-76476019	SK-N-SH_RA	brain:	n/a
41	chr15:76462821-76462871	LNCaP	prostate:	n/a
42	chr15:76455848-76455898	ECC-1	luminal epithelium:	n/a
43	chr15:76458365-76458415	A549	lung:	n/a
44	chr15:76484102-76484152	NB4	blood:	n/a
45	chr15:76483281-76483331	HUVEC	blood vessel:	n/a
46	chr15:76484102-76484152	U87	brain:	n/a
47	chr15:76484473-76484523	CMK	blood:	n/a
48	chr15:76455848-76455898	HMEC	breast:	n/a
49	chr15:76462821-76462871	ECC-1	luminal epithelium:	n/a
50	chr15:76462821-76462871	Caco-2	colon:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
2	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
3	chr15:76484853..76487491-chr15:76488798..76492049,5	K562	blood:
4	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
5	chr15:76478115..76478633-chr15:76622409..76623267,2	MCF-7	breast:
6	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
7	chr15:76482420..76485297-chr15:76485451..76488299,2	K562	blood:
8	chr15:76483246..76483790-chr15:77158830..77159724,2	K562	blood:
9	chr15:76489835..76492594-chr15:76628976..76630921,2	K562	blood:
10	chr15:76486525..76491130-chr15:76491292..76495169,6	MCF-7	breast:
11	chr15:76482740..76483457-chr15:76626133..76626814,2	MCF-7	breast:
12	chr15:76483018..76483722-chr15:76622624..76623279,3	K562	blood:
13	chr15:76482820..76483740-chr15:76577311..76578273,3	K562	blood:
14	chr15:76489717..76491571-chr15:76503812..76506764,2	K562	blood:
15	chr15:76487373..76491413-chr15:76492592..76495149,4	K562	blood:
16	chr15:76442105..76446396-chr15:76447199..76450761,5	MCF-7	breast:
17	chr15:76483023..76483731-chr15:76527305..76528242,4	MCF-7	breast:
18	chr15:76477747..76478594-chr15:76625784..76626375,2	MCF-7	breast:
19	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
20	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
21	chr15:76490388..76492553-chr15:76494551..76496076,2	MCF-7	breast:
22	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
23	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
24	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
25	chr15:76483216..76483808-chr15:76625887..76626857,3	K562	blood:
26	chr15:76484065..76486868-chr15:76602060..76604082,2	MCF-7	breast:
27	chr15:76457780..76460448-chr15:76461142..76462656,2	K562	blood:
28	chr15:76489752..76492594-chr15:76628754..76630476,2	K562	blood:
29	chr15:76488936..76490866-chr15:76603480..76605348,2	MCF-7	breast:
30	chr15:76457780..76460448-chr15:76461142..76462656,2	K562	blood:
31	chr15:76482846..76483696-chr15:76577399..76578194,4	MCF-7	breast:
32	chr15:76461088..76462629-chr15:76483253..76485151,2	K562	blood:
33	chr15:76482924..76483751-chr15:76625816..76626899,5	MCF-7	breast:
34	chr15:76484853..76487491-chr15:76488798..76492049,5	K562	blood:
35	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
36	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
37	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:
38	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
39	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
40	chr15:76482829..76483665-chr15:77158796..77159907,4	MCF-7	breast:
41	chr15:76481529..76484202-chr15:76633877..76636476,2	K562	blood:
42	chr15:76487953..76490483-chr15:76500123..76503783,3	K562	blood:
43	chr15:76488844..76490782-chr15:76625306..76628294,2	K562	blood:
44	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
45	chr15:76482702..76486394-chr15:76633656..76636389,3	K562	blood:
46	chr15:76478027..76479862-chr15:76483019..76485634,3	MCF-7	breast:
47	chr15:76478149..76479732-chr15:76481760..76484387,3	K562	blood:
48	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:
49	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
50	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000259422	TF binding region
C15orf27	TF binding region
ENSG00000259422	CpG island
C15orf27	CpG island
ENSG00000270036	chromatin interactions
ENSG00000159556	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000169758	chromatin interactions
ENSG00000259514	chromatin interactions
ENSG00000259422	chromatin interactions

Extended variants
information (count: 1834 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1834 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2959862	chr15:76444695-76444696	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559745899	chr15:76444711-76444712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs28455920	chr15:76444756-76444757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34780709	chr15:76444862-76444863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111863586	chr15:76444866-76444867	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs527819916	chr15:76444867-76444868	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs377064089	chr15:76444872-76444873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561050093	chr15:76444881-76444882	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs2955747	chr15:76444883-76444884	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs549992475	chr15:76444904-76444905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550690646	chr15:76444934-76444935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116098146	chr15:76444955-76444956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142530032	chr15:76444972-76444973	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188181888	chr15:76444987-76444988	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547691328	chr15:76445035-76445036	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs66945281	chr15:76445038-76445039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs565951698	chr15:76445066-76445067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs116390164	chr15:76445095-76445096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs118041938	chr15:76445120-76445121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115714718	chr15:76445131-76445132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537943094	chr15:76445144-76445145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562838846	chr15:76445155-76445156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146425330	chr15:76445212-76445213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577792733	chr15:76445219-76445220	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs545167102	chr15:76445233-76445234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554057335	chr15:76445248-76445249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140852423	chr15:76445255-76445256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542607584	chr15:76445306-76445307	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191076796	chr15:76445321-76445322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536010997	chr15:76445343-76445344	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56853800	chr15:76445350-76445351	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs868577	chr15:76445359-76445360	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs144694817	chr15:76445383-76445384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532370093	chr15:76445416-76445417	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs547581377	chr15:76445421-76445422	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs147310067	chr15:76445426-76445427	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs565974450	chr15:76445429-76445430	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs529900709	chr15:76445430-76445431	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs549398919	chr15:76445433-76445434	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs540245258	chr15:76445475-76445476	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs5813821	chr15:76445476-76445477	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs397785764	chr15:76445486-76445487	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs138641664	chr15:76445498-76445499	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs538362666	chr15:76445551-76445552	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs556258780	chr15:76445647-76445648	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs868576	chr15:76445689-76445690	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs538854491	chr15:76445690-76445691	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs553898032	chr15:76445708-76445709	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs77322678	chr15:76445718-76445719	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs554586996	chr15:76445779-76445780	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:1210 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76433000-76452800	Weak transcription	Right Atrium	heart
2	chr15:76440400-76445000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr15:76440400-76447000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr15:76440800-76445200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr15:76440800-76445600	Weak transcription	Spleen	Spleen
6	chr15:76442400-76445400	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr15:76442600-76446400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:76442600-76446400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:76442800-76444800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr15:76442800-76445000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr15:76442800-76446400	Enhancers	H1 Cell Line	embryonic stem cell
12	chr15:76443000-76453800	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr15:76443200-76444800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr15:76443200-76447200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:76443200-76447200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr15:76443200-76483000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr15:76443400-76445800	Weak transcription	Fetal Brain Male	brain
18	chr15:76443400-76466000	Weak transcription	Brain Angular Gyrus	brain
19	chr15:76443600-76445800	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr15:76443600-76446000	Weak transcription	Fetal Brain Female	brain
21	chr15:76444000-76445200	Weak transcription	Psoas Muscle	Psoas
22	chr15:76444200-76447800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr15:76444200-76447800	Weak transcription	HSMM	muscle
24	chr15:76444400-76447600	Weak transcription	NHDF-Ad	bronchial
25	chr15:76444400-76452800	Weak transcription	HMEC	breast
26	chr15:76444600-76445200	Enhancers	Fetal Muscle Trunk	muscle
27	chr15:76444600-76446400	Enhancers	Pancreas	Pancrea
28	chr15:76444600-76448800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr15:76444600-76448800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr15:76444800-76453400	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr15:76445000-76445400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:76445000-76447600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:76445200-76446200	Enhancers	Psoas Muscle	Psoas
34	chr15:76445200-76446400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr15:76445400-76446000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr15:76445400-76446200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr15:76445600-76445800	Enhancers	Spleen	Spleen
38	chr15:76445600-76446200	Enhancers	Fetal Muscle Leg	muscle
39	chr15:76445600-76446600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr15:76445800-76446400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr15:76445800-76446800	Enhancers	Fetal Brain Male	brain
42	chr15:76445800-76453400	Weak transcription	Spleen	Spleen
43	chr15:76446000-76446400	Enhancers	Fetal Brain Female	brain
44	chr15:76446200-76446400	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr15:76446200-76446800	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr15:76446400-76446800	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr15:76446400-76451800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr15:76446800-76452800	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr15:76446800-76453600	Weak transcription	Fetal Brain Male	brain
50	chr15:76447000-76448000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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