Variant report

Variant	nsv1047539
Chromosome Location	chr15:76435640-76485966
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1618)
CpG islands
(count:1346)
Chromatin interactive
region (count:66)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1618 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:76443358-76443550	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	ARID3A	chr15:76443498-76443553	K562	blood:	n/a	n/a
5	ATF2	chr15:76483089-76483813	GM12878	blood:	n/a	n/a
6	ATF2	chr15:76473954-76474425	GM12878	blood:	n/a	n/a
7	ATF2	chr15:76473823-76474454	GM12878	blood:	n/a	n/a
8	ATF2	chr15:76443272-76443758	GM12878	blood:	n/a	n/a
9	ATF2	chr15:76443260-76443649	H1-hESC	embryonic stem cell:	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	ATF3	chr15:76461499-76461617	GM12878	blood:	n/a	n/a
13	ATF3	chr15:76461359-76461682	GM12878	blood:	n/a	n/a
14	BACH1	chr15:76483297-76483365	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr15:76443332-76443766	GM12878	blood:	n/a	chr15:76443610-76443620
16	BATF	chr15:76443394-76443743	GM12878	blood:	n/a	chr15:76443610-76443620
17	BATF	chr15:76473923-76474319	GM12878	blood:	n/a	chr15:76474119-76474130
18	BATF	chr15:76473865-76474455	GM12878	blood:	n/a	chr15:76474119-76474130
19	BCL11A	chr15:76443407-76443717	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:76443382-76443708	GM12878	blood:	n/a	n/a
21	BCL11A	chr15:76473914-76474363	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:76474032-76474320	GM12878	blood:	n/a	n/a
23	BCL3	chr15:76482892-76483810	A549	lung:	n/a	n/a
24	BCLAF1	chr15:76473905-76474445	GM12878	blood:	n/a	n/a
25	BCLAF1	chr15:76443247-76443763	GM12878	blood:	n/a	n/a
26	BCLAF1	chr15:76473788-76474517	GM12878	blood:	n/a	n/a
27	BHLHE40	chr15:76483122-76483431	K562	blood:	n/a	n/a
28	BHLHE40	chr15:76443352-76443674	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:76482536-76482865	K562	blood:	n/a	n/a
30	BHLHE40	chr15:76473924-76474330	GM12878	blood:	n/a	n/a
31	BHLHE40	chr15:76472787-76472910	K562	blood:	n/a	n/a
32	BHLHE40	chr15:76440299-76440592	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:76472876-76472910	HepG2	liver:	n/a	n/a
34	BHLHE40	chr15:76443337-76443588	K562	blood:	n/a	n/a
35	BHLHE40	chr15:76483088-76483437	GM12878	blood:	n/a	n/a
36	BHLHE40	chr15:76455772-76455880	K562	blood:	n/a	n/a
37	BHLHE40	chr15:76469949-76470149	A549	lung:	n/a	n/a
38	BRCA1	chr15:76483097-76483525	Hela-S3	cervix:	n/a	chr15:76483441-76483448
39	BRCA1	chr15:76455813-76456207	Hela-S3	cervix:	n/a	n/a
40	BRCA1	chr15:76483167-76483490	HepG2	liver:	n/a	chr15:76483441-76483448
41	BRCA1	chr15:76440353-76440459	HepG2	liver:	n/a	n/a
42	BRCA1	chr15:76483134-76483378	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr15:76477995-76478351	K562	blood:	n/a	n/a
44	CEBPB	chr15:76482949-76483412	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr15:76482803-76483407	MCF-7	breast:	n/a	n/a
46	CEBPB	chr15:76455736-76456063	K562	blood:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
47	CEBPB	chr15:76455793-76455960	HepG2	liver:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
48	CEBPB	chr15:76443302-76443706	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr15:76455726-76456095	ECC-1	luminal epithelium:	n/a	chr15:76455897-76455908 chr15:76455897-76455908
50	CEBPB	chr15:76470121-76470486	HepG2	liver:	n/a	n/a

(count:1346 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:76484473-76484523	H1-hESC	embryonic stem cell:	embryo
2	chr15:76484625-76484675	NHDF-neo	bronchial:	n/a
3	chr15:76475969-76476019	BJ	skin:	n/a
4	chr15:76440443-76440493	HEEpiC	esophagus:	n/a
5	chr15:76484473-76484523	H1-hESC	embryonic stem cell:	embryo
6	chr15:76484625-76484675	NHDF-neo	bronchial:	n/a
7	chr15:76475969-76476019	BJ	skin:	n/a
8	chr15:76440443-76440493	HEEpiC	esophagus:	n/a
9	chr15:76455848-76455898	H1-hESC	embryonic stem cell:	embryo
10	chr15:76470979-76471029	RPTEC	kidney:	n/a
11	chr15:76470979-76471029	GM12892	blood:	n/a
12	chr15:76440448-76440498	MCF-7	breast:	n/a
13	chr15:76470979-76471029	BE2_C	brain:	n/a
14	chr15:76475969-76476019	AG09319	gingival:	n/a
15	chr15:76483344-76483394	ProgFib	skin:	n/a
16	chr15:76484102-76484152	LNCaP	prostate:	n/a
17	chr15:76442477-76442527	HRE	kidney:	n/a
18	chr15:76470979-76471029	ProgFib	skin:	n/a
19	chr15:76475969-76476019	NB4	blood:	n/a
20	chr15:76458365-76458415	Jurkat	blood:	n/a
21	chr15:76462821-76462871	SKMC	muscle:	n/a
22	chr15:76458365-76458415	AG09309	skin:	n/a
23	chr15:76484379-76484429	HRE	kidney:	n/a
24	chr15:76440443-76440493	AG04450	lung:	fetal
25	chr15:76484473-76484523	HEEpiC	esophagus:	n/a
26	chr15:76484625-76484675	HPAEpiC	pulmonary alveolar:	n/a
27	chr15:76440443-76440493	HCPEpiC	choroid plexus:	n/a
28	chr15:76484102-76484152	PFSK-1	brain:	n/a
29	chr15:76442477-76442527	Hepatocyte	liver:	n/a
30	chr15:76442477-76442527	HMEC	breast:	n/a
31	chr15:76484625-76484675	CMK	blood:	n/a
32	chr15:76458365-76458415	AoSMC	blood vessel:	n/a
33	chr15:76462821-76462871	NH-A	brain:	n/a
34	chr15:76444525-76444575	HMEC	breast:	n/a
35	chr15:76483281-76483331	HCT-116	colon:	n/a
36	chr15:76484625-76484675	HCT-116	colon:	n/a
37	chr15:76440448-76440498	Jurkat	blood:	n/a
38	chr15:76440405-76440455	HAEpiC	amniotic membrane:	n/a
39	chr15:76440448-76440498	MCF10A-Er-Src	breast:	n/a
40	chr15:76483344-76483394	ECC-1	luminal epithelium:	n/a
41	chr15:76462821-76462871	T-47D	breast:	n/a
42	chr15:76484625-76484675	HUVEC	blood vessel:	n/a
43	chr15:76484473-76484523	LNCaP	prostate:	n/a
44	chr15:76442477-76442527	HAEpiC	amniotic membrane:	n/a
45	chr15:76478102-76478152	HIPEpiC	eye:	n/a
46	chr15:76458279-76458329	GM12878	blood:	n/a
47	chr15:76470979-76471029	HMEC	breast:	n/a
48	chr15:76455848-76455898	HEEpiC	esophagus:	n/a
49	chr15:76480434-76480484	HL-60	blood:	n/a
50	chr15:76440405-76440455	PrEC	prostate:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:76221299..76222193-chr15:76443491..76444002,2	MCF-7	breast:
2	chr15:76484853..76487491-chr15:76488798..76492049,5	K562	blood:
3	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
4	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:
5	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
6	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
7	chr15:76478115..76478633-chr15:76622409..76623267,2	MCF-7	breast:
8	chr15:76349917..76350459-chr15:76440383..76440942,2	K562	blood:
9	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
10	chr15:76435308..76437788-chr15:76443138..76445810,3	K562	blood:
11	chr15:76478027..76479862-chr15:76483019..76485634,3	MCF-7	breast:
12	chr15:76452837..76455028-chr15:76460465..76463193,2	K562	blood:
13	chr15:76431477..76432448-chr15:76439936..76440516,2	K562	blood:
14	chr15:76482420..76485297-chr15:76485451..76488299,2	K562	blood:
15	chr15:76483023..76483731-chr15:76527305..76528242,4	MCF-7	breast:
16	chr15:76484065..76486868-chr15:76602060..76604082,2	MCF-7	breast:
17	chr15:76431446..76432246-chr15:76440422..76441109,2	MCF-7	breast:
18	chr15:76436435..76439411-chr15:76454805..76456724,2	K562	blood:
19	chr15:76482840..76483720-chr15:77132911..77133894,4	MCF-7	breast:
20	chr15:76442105..76446396-chr15:76447199..76450761,5	MCF-7	breast:
21	chr15:76481529..76484202-chr15:76633877..76636476,2	K562	blood:
22	chr15:76436435..76439411-chr15:76454805..76456724,2	K562	blood:
23	chr15:76453448..76455028-chr15:76460465..76463377,2	K562	blood:
24	chr15:76467419..76469629-chr15:76476906..76478729,2	MCF-7	breast:
25	chr15:76439768..76440654-chr15:77152468..77153214,2	K562	blood:
26	chr15:76440836..76444169-chr15:76451014..76453553,3	MCF-7	breast:
27	chr15:76472338..76474227-chr15:76482406..76484297,2	K562	blood:
28	chr15:76435308..76438673-chr15:76443082..76445810,3	K562	blood:
29	chr15:76476723..76478991-chr15:76480313..76482582,2	K562	blood:
30	chr15:76482829..76483665-chr15:77158796..77159907,4	MCF-7	breast:
31	chr15:76440174..76440912-chr15:76625983..76626603,2	MCF-7	breast:
32	chr15:76482924..76483751-chr15:76625816..76626899,5	MCF-7	breast:
33	chr15:76455415..76457030-chr15:76460537..76462743,2	K562	blood:
34	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
35	chr15:76460346..76463407-chr15:76465556..76467922,3	MCF-7	breast:
36	chr15:76482702..76486394-chr15:76633656..76636389,3	K562	blood:
37	chr15:76442105..76446396-chr15:76447199..76450761,5	MCF-7	breast:
38	chr15:76478149..76479732-chr15:76481760..76484387,3	K562	blood:
39	chr15:76441645..76443484-chr15:76650484..76652153,2	K562	blood:
40	chr15:76453204..76454747-chr15:76459797..76461438,2	MCF-7	breast:
41	chr15:76460184..76462752-chr15:76465404..76467904,2	K562	blood:
42	chr15:76482820..76483740-chr15:76577311..76578273,3	K562	blood:
43	chr15:76452254..76455049-chr15:76455599..76457140,2	K562	blood:
44	chr15:76436946..76439521-chr3:195163273..195165269,2	MCF-7	breast:
45	chr15:76435308..76437788-chr15:76443138..76445810,3	K562	blood:
46	chr15:76482689..76486583-chr15:76628039..76631365,3	K562	blood:
47	chr15:76349477..76350031-chr15:76443009..76443529,2	K562	blood:
48	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:
49	chr15:76483246..76483790-chr15:77158830..77159724,2	K562	blood:
50	chr15:76446927..76448705-chr15:76450684..76453682,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000259422	TF binding region
C15orf27	TF binding region
ENSG00000259422	CpG island
C15orf27	CpG island
ENSG00000259422	chromatin interactions
ENSG00000259514	chromatin interactions
ENSG00000169752	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000140374	chromatin interactions
ENSG00000270036	chromatin interactions
ENSG00000169758	chromatin interactions
ENSG00000159556	chromatin interactions

Extended variants
information (count: 2003 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2955726	chr15:76435640-76435641	Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs12591302	chr15:76435654-76435655	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs568858565	chr15:76435677-76435678	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs369793216	chr15:76435705-76435706	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs539337980	chr15:76435722-76435723	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs562664625	chr15:76435748-76435749	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs58823470	chr15:76435792-76435793	Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs192510495	chr15:76435822-76435823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564293656	chr15:76435823-76435824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564460723	chr15:76435856-76435857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557725944	chr15:76435893-76435894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533104996	chr15:76435972-76435973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547105438	chr15:76436001-76436002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562300217	chr15:76436012-76436013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529487098	chr15:76436039-76436040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551126148	chr15:76436084-76436085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569464562	chr15:76436109-76436110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540084413	chr15:76436201-76436202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376164292	chr15:76436218-76436219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185655099	chr15:76436227-76436228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2955725	chr15:76436248-76436249	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs150077398	chr15:76436323-76436324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79030373	chr15:76436391-76436392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2955724	chr15:76436509-76436510	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs59798822	chr15:76436551-76436552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142872583	chr15:76436558-76436559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs3065684	chr15:76436561-76436562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs386785474	chr15:76436562-76436563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199596754	chr15:76436563-76436564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs372837343	chr15:76436564-76436565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs57628019	chr15:76436565-76436566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs199710235	chr15:76436566-76436567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200768013	chr15:76436567-76436568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs3065686	chr15:76436568-76436569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2959864	chr15:76436581-76436582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs577864432	chr15:76436586-76436587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545282899	chr15:76436630-76436631	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35980406	chr15:76436648-76436649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12905758	chr15:76436661-76436662	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs200892233	chr15:76436671-76436672	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115849339	chr15:76436673-76436674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550920364	chr15:76436700-76436701	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74963212	chr15:76436753-76436754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76843349	chr15:76436785-76436786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4886773	chr15:76436823-76436824	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs553664248	chr15:76436849-76436850	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533497207	chr15:76436884-76436885	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs552036883	chr15:76436885-76436886	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566159361	chr15:76436895-76436896	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566875332	chr15:76436898-76436899	Weak transcription Enhancers Strong transcription	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:1288 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76429400-76442800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr15:76429600-76442800	Weak transcription	Brain Angular Gyrus	brain
3	chr15:76432400-76440400	Weak transcription	Pancreas	Pancrea
4	chr15:76432400-76442800	Weak transcription	Gastric	stomach
5	chr15:76432600-76440400	Weak transcription	Placenta	Placenta
6	chr15:76432600-76442800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr15:76433000-76436600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr15:76433000-76437000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr15:76433000-76437400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr15:76433000-76439600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr15:76433000-76440400	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr15:76433000-76442800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr15:76433000-76452800	Weak transcription	Right Atrium	heart
14	chr15:76433200-76440600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr15:76433600-76439800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr15:76433600-76440400	Weak transcription	Spleen	Spleen
17	chr15:76435400-76435800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr15:76436600-76438200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr15:76436800-76438400	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr15:76437000-76437200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:76437200-76439200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:76437400-76437800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr15:76437400-76437800	Enhancers	Primary hematopoietic stem cells	blood
24	chr15:76437400-76437800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr15:76437400-76438000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr15:76437800-76438000	Flanking Active TSS	GM12878-XiMat	blood
27	chr15:76437800-76440400	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr15:76438000-76438200	Enhancers	GM12878-XiMat	blood
29	chr15:76438200-76440400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr15:76438200-76442400	Weak transcription	GM12878-XiMat	blood
31	chr15:76438400-76439200	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr15:76439000-76439200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:76439000-76439400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:76439000-76439800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr15:76439200-76439600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr15:76439200-76439800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr15:76439200-76439800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr15:76439200-76440200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr15:76439200-76441400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr15:76439400-76439600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr15:76439400-76439600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr15:76439400-76439600	Enhancers	HMEC	breast
43	chr15:76439400-76440400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr15:76439600-76439800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr15:76439600-76440200	Weak transcription	HMEC	breast
46	chr15:76439600-76440400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr15:76439800-76440200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:76439800-76440200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr15:76439800-76440800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr15:76439800-76442800	Weak transcription	H1 Cell Line	embryonic stem cell

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