Variant report

Variant	nsv570159
Chromosome Location	chr15:78008843-78022087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr15:78008726-78009098	GM12878	blood:	n/a	n/a
2	BCL3	chr15:78011949-78012314	GM12878	blood:	n/a	n/a
3	BCL3	chr15:78008746-78009107	GM12878	blood:	n/a	n/a
4	CEBPB	chr15:78015519-78015716	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr15:78015108-78015464	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
6	CTCF	chr15:78015118-78015491	H1-hESC	embryonic stem cell:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
7	CTCF	chr15:78015200-78015350	A549	lung:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
8	CTCF	chr15:78009420-78009570	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr15:78015083-78015483	H1-hESC	embryonic stem cell:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
10	CTCF	chr15:78015109-78015429	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
11	CTCF	chr15:78015120-78015270	GM12874	blood:	n/a	n/a
12	CTCF	chr15:78015260-78015410	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
13	CTCF	chr15:78015240-78015390	GM12873	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
14	CTCF	chr15:78015220-78015370	GM12866	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
15	CTCF	chr15:78015180-78015330	HFF-Myc	foreskin:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
16	CTCF	chr15:78009740-78009890	GM12873	blood:	n/a	n/a
17	CTCF	chr15:78015237-78015372	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
18	CTCF	chr15:78009413-78009483	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr15:78011914-78011934	Lung_OC	lung:	n/a	n/a
20	CTCF	chr15:78015220-78015370	GM06990	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
21	CTCF	chr15:78015180-78015330	Caco-2	colon:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
22	CTCF	chr15:78015240-78015390	GM12871	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
23	CTCF	chr15:78015260-78015410	HepG2	liver:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
24	CTCF	chr15:78015040-78015190	A549	lung:	n/a	n/a
25	CTCF	chr15:78015160-78015310	HCT-116	colon:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
26	CTCF	chr15:78015234-78015363	HepG2	liver:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
27	CTCF	chr15:78015200-78015350	NB4	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
28	CTCF	chr15:78015200-78015350	GM06990	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
29	CTCF	chr15:78015209-78015399	H1-hESC	embryonic stem cell:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
30	CTCF	chr15:78015163-78015379	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
31	CTCF	chr15:78011840-78011904	K562	blood:	n/a	n/a
32	CTCF	chr15:78015166-78015359	K562	blood:	n/a	chr15:78015300-78015309 chr15:78015265-78015278
33	EGR1	chr15:78016098-78016281	K562	blood:	n/a	chr15:78016221-78016234 chr15:78016221-78016235 chr15:78016220-78016235 chr15:78016224-78016234 chr15:78016221-78016234 chr15:78016223-78016233 chr15:78016221-78016234 chr15:78016221-78016234 chr15:78016224-78016233
34	EGR1	chr15:78014959-78015151	K562	blood:	n/a	n/a
35	EGR1	chr15:78014954-78015201	K562	blood:	n/a	n/a
36	FOS	chr15:78014713-78014851	MCF10A-Er-Src	breast:	n/a	n/a
37	GATA2	chr15:78021834-78022132	SH-SY5Y	brain:	n/a	n/a
38	HMGN3	chr15:78015083-78015283	K562	blood:	n/a	n/a
39	JUND	chr15:78013187-78013191	K562	blood:	n/a	n/a
40	JUND	chr15:78018267-78018550	K562	blood:	n/a	n/a
41	MAFF	chr15:78014376-78014670	K562	blood:	n/a	n/a
42	MAFF	chr15:78014370-78014678	HepG2	liver:	n/a	n/a
43	MAFK	chr15:78014376-78014663	HepG2	liver:	n/a	chr15:78014539-78014554
44	MAFK	chr15:78014354-78014684	K562	blood:	n/a	chr15:78014539-78014554
45	MAFK	chr15:78014253-78014691	HepG2	liver:	n/a	chr15:78014290-78014301 chr15:78014290-78014306 chr15:78014291-78014302 chr15:78014290-78014301 chr15:78014289-78014303 chr15:78014539-78014554 chr15:78014291-78014302
46	MAFK	chr15:78014409-78014609	Hela-S3	cervix:	n/a	chr15:78014539-78014554
47	MAFK	chr15:78014365-78014668	IMR90	lung:	n/a	chr15:78014539-78014554
48	MAX	chr15:78012611-78012796	K562	blood:	n/a	chr15:78012731-78012740
49	MAZ	chr15:78013288-78013301	K562	blood:	n/a	n/a
50	MYC	chr15:78010695-78010797	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78015279-78015329	HNPCEpiC	eye:	n/a
2	chr15:78015279-78015329	HNPCEpiC	eye:	n/a
3	chr15:78015279-78015329	ProgFib	skin:	n/a
4	chr15:78015279-78015329	AG04449	skin:	fetal
5	chr15:78015279-78015329	HPAEpiC	pulmonary alveolar:	n/a
6	chr15:78015279-78015329	BE2_C	brain:	n/a
7	chr15:78015279-78015329	GM19239	blood:	n/a
8	chr15:78015279-78015329	HepG2	liver:	n/a
9	chr15:78015279-78015329	NHBE	bronchial:	n/a
10	chr15:78015279-78015329	NB4	blood:	n/a
11	chr15:78015279-78015329	ECC-1	luminal epithelium:	n/a
12	chr15:78015279-78015329	Hepatocyte	liver:	n/a
13	chr15:78015279-78015329	BJ	skin:	n/a
14	chr15:78015279-78015329	HRPEpiC	eye:	n/a
15	chr15:78015279-78015329	GM12892	blood:	n/a
16	chr15:78015279-78015329	NH-A	brain:	n/a
17	chr15:78015279-78015329	PrEC	prostate:	n/a
18	chr15:78015279-78015329	ovcar-3	ovarian:	n/a
19	chr15:78015279-78015329	HIPEpiC	eye:	n/a
20	chr15:78015279-78015329	NT2-D1	testis:	n/a
21	chr15:78015279-78015329	T-47D	breast:	n/a
22	chr15:78015279-78015329	HRCEpiC	kidney:	n/a
23	chr15:78015279-78015329	HCF	heart:	n/a
24	chr15:78015279-78015329	MCF-7	breast:	n/a
25	chr15:78015279-78015329	HAEpiC	amniotic membrane:	n/a
26	chr15:78015279-78015329	HMEC	breast:	n/a
27	chr15:78015279-78015329	HCPEpiC	choroid plexus:	n/a
28	chr15:78015279-78015329	SAEC	small airway:	n/a
29	chr15:78015279-78015329	IMR90	lung:	fetal
30	chr15:78015279-78015329	HEK293	kidney:	embryo
31	chr15:78015279-78015329	HCM	heart:	n/a
32	chr15:78015279-78015329	RPTEC	kidney:	n/a
33	chr15:78015279-78015329	LNCaP	prostate:	n/a
34	chr15:78015279-78015329	SKMC	muscle:	n/a
35	chr15:78015279-78015329	HCT-116	colon:	n/a
36	chr15:78015279-78015329	U87	brain:	n/a
37	chr15:78015279-78015329	SK-N-MC	brain:	n/a
38	chr15:78015279-78015329	HUVEC	blood vessel:	n/a
39	chr15:78015279-78015329	AG10803	skin:	n/a
40	chr15:78015279-78015329	MCF10A-Er-Src	breast:	n/a
41	chr15:78015279-78015329	CMK	blood:	n/a
42	chr15:78015279-78015329	GM12878	blood:	n/a
43	chr15:78015279-78015329	AoSMC	blood vessel:	n/a
44	chr15:78015279-78015329	Jurkat	blood:	n/a
45	chr15:78015279-78015329	SK-N-SH	brain:	n/a
46	chr15:78015279-78015329	HRE	kidney:	n/a
47	chr15:78015279-78015329	GM12891	blood:	n/a
48	chr15:78015279-78015329	PFSK-1	brain:	n/a
49	chr15:78015279-78015329	A549	lung:	n/a
50	chr15:78015279-78015329	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr15:78021356..78025369-chr15:78027266..78032240,6	K562	blood:
2	chr15:77996121..77999450-chr15:78013163..78015366,3	K562	blood:
3	chr15:77993820..77996463-chr15:78016040..78017926,2	MCF-7	breast:
4	chr15:78009070..78011036-chr15:78012914..78014777,2	K562	blood:
5	chr15:78008270..78009842-chr15:78011273..78013230,2	MCF-7	breast:
6	chr15:78006781..78008736-chr15:78010587..78012816,2	K562	blood:
7	chr15:78006143..78008281-chr15:78009901..78012087,2	K562	blood:
8	chr15:78021486..78023162-chr15:78023634..78026490,2	K562	blood:
9	chr15:73923669..73926089-chr15:78010481..78013463,2	K562	blood:
10	chr15:78008224..78009963-chr15:78011351..78014041,3	MCF-7	breast:

Variant related genes	Relation type
LINGO1	TF binding region
LINGO1	CpG island
ENSG00000169783	chromatin interactions
ENSG00000156642	chromatin interactions

Extended variants
information (count: 578 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11855821	chr15:78008843-78008844	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs563380130	chr15:78008871-78008872	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552028564	chr15:78008880-78008881	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs114540731	chr15:78008910-78008911	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150835389	chr15:78008911-78008912	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs74407398	chr15:78009037-78009038	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532797363	chr15:78009085-78009086	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs35723803	chr15:78009088-78009089	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139251071	chr15:78009239-78009240	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555292398	chr15:78009252-78009253	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201672507	chr15:78009267-78009268	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs74025399	chr15:78009292-78009293	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146564642	chr15:78009309-78009310	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186322780	chr15:78009326-78009327	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536872335	chr15:78009385-78009386	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558686228	chr15:78009386-78009387	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577074251	chr15:78009413-78009414	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534645168	chr15:78009414-78009415	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs71462545	chr15:78009418-78009419	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs34968270	chr15:78009424-78009425	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs397854430	chr15:78009425-78009426	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574129384	chr15:78009441-78009442	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs4569231	chr15:78009448-78009449	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs563257989	chr15:78009450-78009451	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527706348	chr15:78009547-78009548	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575262680	chr15:78009558-78009559	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543661727	chr15:78009570-78009571	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140142185	chr15:78009588-78009589	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532752166	chr15:78009597-78009598	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143831320	chr15:78009610-78009611	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs560076149	chr15:78009658-78009659	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145806675	chr15:78009688-78009689	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182893808	chr15:78009696-78009697	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570068788	chr15:78009706-78009707	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537512687	chr15:78009743-78009744	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149018275	chr15:78009745-78009746	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547330343	chr15:78009767-78009768	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570665214	chr15:78009781-78009782	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534492397	chr15:78009782-78009783	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143817293	chr15:78009787-78009788	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574361977	chr15:78009788-78009789	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs535094399	chr15:78009819-78009820	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150932232	chr15:78009855-78009856	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs141921958	chr15:78009881-78009882	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs545928792	chr15:78009944-78009945	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs564017935	chr15:78009980-78009981	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577550808	chr15:78009984-78009985	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs58398016	chr15:78010005-78010006	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs560113767	chr15:78010024-78010025	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530382781	chr15:78010043-78010044	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
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
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
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78003400-78009600	Weak transcription	Brain Germinal Matrix	brain
2	chr15:78004000-78009800	Weak transcription	Fetal Brain Female	brain
3	chr15:78004600-78012000	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr15:78006400-78013000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:78007000-78016600	Weak transcription	Brain Angular Gyrus	brain
6	chr15:78008800-78009400	Enhancers	H1 Cell Line	embryonic stem cell
7	chr15:78008800-78010000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr15:78009200-78010000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr15:78009200-78010000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr15:78009200-78012000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr15:78009400-78010000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
12	chr15:78009400-78010000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr15:78009400-78010000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
14	chr15:78009400-78010200	Bivalent Enhancer	Fetal Muscle Leg	muscle
15	chr15:78009400-78011800	Enhancers	Fetal Brain Male	brain
16	chr15:78009400-78015200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr15:78009600-78009800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr15:78009600-78009800	Enhancers	Brain Germinal Matrix	brain
19	chr15:78009800-78010000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chr15:78009800-78010200	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr15:78009800-78010200	Enhancers	Fetal Brain Female	brain
22	chr15:78009800-78012200	Weak transcription	Brain Germinal Matrix	brain
23	chr15:78010000-78010200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr15:78010000-78015200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:78010000-78015800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr15:78010200-78012200	Weak transcription	Fetal Brain Female	brain
27	chr15:78011800-78012000	Bivalent Enhancer	Fetal Brain Male	brain
28	chr15:78012000-78012200	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
29	chr15:78012000-78012200	Bivalent Enhancer	Fetal Kidney	kidney
30	chr15:78012000-78012400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr15:78012000-78015800	Weak transcription	Fetal Heart	heart
32	chr15:78012200-78012400	Bivalent Enhancer	Fetal Brain Male	brain
33	chr15:78012200-78013000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
34	chr15:78012200-78013000	Enhancers	Fetal Brain Female	brain
35	chr15:78012200-78013400	Enhancers	Brain Germinal Matrix	brain
36	chr15:78012400-78012600	Enhancers	Spleen	Spleen
37	chr15:78012400-78012800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr15:78012400-78013400	Enhancers	Fetal Brain Male	brain
39	chr15:78012400-78016000	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr15:78012600-78013200	Weak transcription	Spleen	Spleen
41	chr15:78012600-78013600	Enhancers	Fetal Muscle Trunk	muscle
42	chr15:78012600-78013600	Enhancers	Fetal Muscle Leg	muscle
43	chr15:78012800-78013200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr15:78012800-78013600	Enhancers	Placenta Amnion	Placenta Amnion
45	chr15:78013000-78013200	Enhancers	K562	blood
46	chr15:78013000-78013400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr15:78013000-78031200	Weak transcription	Fetal Brain Female	brain
48	chr15:78013200-78013400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr15:78013200-78013400	Enhancers	Spleen	Spleen
50	chr15:78013200-78015200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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