Variant report

Variant	nsv457206
Chromosome Location	chr15:76971456-77121196
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:548)
CpG islands
(count:123)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77097607-77097795	K562	blood:	n/a	n/a
2	ATF1	chr15:77116459-77116462	K562	blood:	n/a	n/a
3	ATF2	chr15:77003716-77004122	GM12878	blood:	n/a	n/a
4	ATF2	chr15:77003703-77004047	GM12878	blood:	n/a	n/a
5	BACH1	chr15:77097486-77097858	K562	blood:	n/a	n/a
6	BACH1	chr15:77097576-77097776	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr15:77092170-77092438	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr15:76996451-76996676	GM12878	blood:	n/a	n/a
9	BATF	chr15:76996436-76996655	GM12878	blood:	n/a	n/a
10	BCL11A	chr15:77003618-77004150	GM12878	blood:	n/a	n/a
11	BCL11A	chr15:77003630-77004113	GM12878	blood:	n/a	n/a
12	BCLAF1	chr15:77003650-77004026	GM12878	blood:	n/a	n/a
13	BHLHE40	chr15:77003580-77004137	GM12878	blood:	n/a	n/a
14	CBX3	chr15:77069395-77069686	K562	blood:	n/a	n/a
15	CBX3	chr15:77055892-77056260	K562	blood:	n/a	n/a
16	CBX3	chr15:77055938-77056220	K562	blood:	n/a	n/a
17	CBX3	chr15:77069334-77069671	K562	blood:	n/a	n/a
18	CEBPB	chr15:77092170-77092370	K562	blood:	n/a	n/a
19	CEBPB	chr15:77048788-77049111	IMR90	lung:	n/a	n/a
20	CEBPB	chr15:77052043-77052208	A549	lung:	n/a	n/a
21	CEBPB	chr15:77092175-77092446	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr15:77092195-77092457	MCF-7	breast:	n/a	n/a
23	CEBPB	chr15:77092148-77092465	A549	lung:	n/a	n/a
24	CEBPB	chr15:77028334-77028569	A549	lung:	n/a	n/a
25	CEBPB	chr15:77092177-77092463	A549	lung:	n/a	n/a
26	CEBPB	chr15:76996796-76997148	HepG2	liver:	n/a	n/a
27	CEBPB	chr15:76996894-76997016	HepG2	liver:	n/a	n/a
28	CEBPB	chr15:76996963-76996987	A549	lung:	n/a	n/a
29	CEBPB	chr15:77092102-77092498	IMR90	lung:	n/a	n/a
30	CHD1	chr15:77003681-77004001	GM12878	blood:	n/a	n/a
31	CHD2	chr15:77003655-77004118	GM12878	blood:	n/a	n/a
32	CTCF	chr15:76974060-76974210	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr15:77024760-77024910	AG10803	skin:	n/a	n/a
34	CTCF	chr15:77024860-77025010	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr15:77024756-77024961	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr15:77024780-77024930	GM12866	blood:	n/a	n/a
37	CTCF	chr15:77024750-77024986	MCF-7	breast:	n/a	n/a
38	CTCF	chr15:77024840-77024990	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr15:77024766-77024960	ProgFib	skin:	n/a	n/a
40	CTCF	chr15:77024600-77025014	K562	blood:	n/a	n/a
41	CTCF	chr15:77056747-77056845	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:77024800-77024950	HVMF	connective:	n/a	n/a
43	CTCF	chr15:77024800-77024950	AG09319	gingival:	n/a	n/a
44	CTCF	chr15:77024840-77024990	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr15:77024760-77024910	Caco-2	colon:	n/a	n/a
46	CTCF	chr15:77024792-77024917	LNCaP	prostate:	n/a	n/a
47	CTCF	chr15:76995580-76995730	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr15:77024800-77024950	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr15:77024800-77024950	HPF	lung:	n/a	n/a
50	CTCF	chr15:77024840-77024990	HUVEC	blood vessel:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77085390-77085440	HCT-116	colon:	n/a
2	chr15:77085390-77085440	HCT-116	colon:	n/a
3	chr15:77085390-77085440	HRE	kidney:	n/a
4	chr15:77085390-77085440	HPAEpiC	pulmonary alveolar:	n/a
5	chr15:77095150-77095200	NHDF-neo	bronchial:	n/a
6	chr15:77085390-77085440	HRPEpiC	eye:	n/a
7	chr15:77085390-77085440	Hepatocyte	liver:	n/a
8	chr15:77085390-77085440	MCF-7	breast:	n/a
9	chr15:77095150-77095200	SK-N-SH	brain:	n/a
10	chr15:77085390-77085440	AG09319	gingival:	n/a
11	chr15:77085390-77085440	AG04449	skin:	fetal
12	chr15:77095150-77095200	HNPCEpiC	eye:	n/a
13	chr15:77095150-77095200	GM12891	blood:	n/a
14	chr15:77085390-77085440	H1-hESC	embryonic stem cell:	embryo
15	chr15:77095150-77095200	SK-N-MC	brain:	n/a
16	chr15:77095150-77095200	AG04449	skin:	fetal
17	chr15:77085390-77085440	AG09309	skin:	n/a
18	chr15:77095150-77095200	AG09309	skin:	n/a
19	chr15:77095150-77095200	U87	brain:	n/a
20	chr15:77085390-77085440	ECC-1	luminal epithelium:	n/a
21	chr15:77095150-77095200	MCF-7	breast:	n/a
22	chr15:77095150-77095200	HCF	heart:	n/a
23	chr15:77095150-77095200	RPTEC	kidney:	n/a
24	chr15:77085390-77085440	CMK	blood:	n/a
25	chr15:77095150-77095200	MCF10A-Er-Src	breast:	n/a
26	chr15:77085390-77085440	NT2-D1	testis:	n/a
27	chr15:77085390-77085440	HNPCEpiC	eye:	n/a
28	chr15:77095150-77095200	HRCEpiC	kidney:	n/a
29	chr15:77095150-77095200	ovcar-3	ovarian:	n/a
30	chr15:77085390-77085440	LNCaP	prostate:	n/a
31	chr15:77095150-77095200	AoSMC	blood vessel:	n/a
32	chr15:77085390-77085440	HL-60	blood:	n/a
33	chr15:77085390-77085440	U87	brain:	n/a
34	chr15:77095150-77095200	AG09319	gingival:	n/a
35	chr15:77085390-77085440	HCPEpiC	choroid plexus:	n/a
36	chr15:77095150-77095200	HCM	heart:	n/a
37	chr15:77085390-77085440	GM12892	blood:	n/a
38	chr15:77085390-77085440	HMEC	breast:	n/a
39	chr15:77085390-77085440	ProgFib	skin:	n/a
40	chr15:77095150-77095200	HUVEC	blood vessel:	n/a
41	chr15:77085390-77085440	HepG2	liver:	n/a
42	chr15:77095150-77095200	NB4	blood:	n/a
43	chr15:77085390-77085440	AG10803	skin:	n/a
44	chr15:77095150-77095200	BJ	skin:	n/a
45	chr15:77095150-77095200	PFSK-1	brain:	n/a
46	chr15:77085390-77085440	RPTEC	kidney:	n/a
47	chr15:77085390-77085440	AoSMC	blood vessel:	n/a
48	chr15:77085390-77085440	NH-A	brain:	n/a
49	chr15:77095150-77095200	K562	blood:	n/a
50	chr15:77095150-77095200	Hela-S3	cervix:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:77083317..77084988-chr15:77087176..77089675,2	K562	blood:
2	chr15:77092193..77094695-chr15:77097938..77099629,2	K562	blood:
3	chr15:76964455..76968844-chr15:76969640..76972722,4	K562	blood:
4	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:
5	chr15:77044758..77046845-chr15:77050241..77052508,2	MCF-7	breast:
6	chr15:77017797..77020777-chr8:43093705..43096561,2	K562	blood:
7	chr15:77118239..77119838-chr15:77122177..77123804,2	K562	blood:
8	chr15:77044758..77046845-chr15:77050241..77052508,2	MCF-7	breast:
9	chr15:77024348..77024882-chr15:77132939..77133789,2	MCF-7	breast:
10	chr15:77051074..77052943-chr15:77058188..77061067,2	K562	blood:
11	chr15:77085685..77088111-chr15:77091340..77093808,2	K562	blood:
12	chr15:77119804..77122749-chr15:77124403..77126200,2	K562	blood:
13	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
14	chr15:76997314..76998845-chr15:77007470..77009179,2	MCF-7	breast:
15	chr10:94276542..94277057-chr15:77040784..77041284,2	MCF-7	breast:
16	chr15:77052021..77055015-chr15:77055082..77056903,3	K562	blood:
17	chr15:77051074..77052943-chr15:77058188..77061067,2	K562	blood:
18	chr15:76967596..76970375-chr15:76976896..76979262,2	K562	blood:
19	chr15:76978559..76980160-chr15:76982250..76984451,2	MCF-7	breast:
20	chr15:77052021..77055015-chr15:77055082..77056903,3	K562	blood:
21	chr15:76482009..76484403-chr15:77035735..77037455,2	MCF-7	breast:
22	chr15:77022336..77024619-chr15:77130860..77133173,2	MCF-7	breast:
23	chr15:76969596..76972550-chr15:76979737..76981959,2	MCF-7	breast:
24	chr15:76997314..76998845-chr15:77007470..77009179,2	MCF-7	breast:
25	chr15:77083317..77084988-chr15:77087176..77089675,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RCN2-1	chr15:77028982-77029321	NONHSAT047408

No data

Variant related genes	Relation type
SCAPER	TF binding region
RN7SKP217	TF binding region
SCAPER	CpG island
RN7SKP217	CpG island
ENSG00000169758	chromatin interactions
ENSG00000140386	chromatin interactions

Extended variants
information (count: 5489 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5489 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4886825	chr15:76971456-76971457	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs528402080	chr15:76971461-76971462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546887249	chr15:76971464-76971465	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs55856713	chr15:76971474-76971475	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs535645340	chr15:76971485-76971486	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550973913	chr15:76971488-76971489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182703547	chr15:76971505-76971506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570206813	chr15:76971579-76971580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76968909	chr15:76971588-76971589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543723940	chr15:76971632-76971633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148108189	chr15:76971661-76971662	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115426925	chr15:76971752-76971753	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564818925	chr15:76971829-76971830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534973526	chr15:76971872-76971873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553651441	chr15:76971926-76971927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574894458	chr15:76971971-76971972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533544113	chr15:76971997-76971998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186603821	chr15:76972029-76972030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370173125	chr15:76972035-76972036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563039394	chr15:76972068-76972069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575021809	chr15:76972081-76972082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189923014	chr15:76972082-76972083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs60146084	chr15:76972087-76972088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs397977818	chr15:76972089-76972090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563701605	chr15:76972098-76972099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372702603	chr15:76972104-76972105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542365119	chr15:76972109-76972110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528095756	chr15:76972120-76972121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546528237	chr15:76972165-76972166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115834092	chr15:76972250-76972251	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs562449977	chr15:76972295-76972296	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs377149715	chr15:76972297-76972298	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs183259042	chr15:76972326-76972327	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs570145083	chr15:76972344-76972345	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs140305304	chr15:76972392-76972393	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs188910909	chr15:76972457-76972458	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs540821680	chr15:76972506-76972507	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs570831152	chr15:76972535-76972536	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs535026717	chr15:76972613-76972614	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs373630873	chr15:76972640-76972641	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs575122526	chr15:76972695-76972696	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs193066040	chr15:76972740-76972741	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs201552282	chr15:76972753-76972754	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs141541121	chr15:76972755-76972756	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs201228004	chr15:76972758-76972759	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs398027999	chr15:76972792-76972793	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs185350433	chr15:76972804-76972805	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs188222932	chr15:76972910-76972911	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs556604659	chr15:76972931-76972932	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs73461327	chr15:76972938-76972939	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:61)

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
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:76882200-76991400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr15:76898400-76981000	Weak transcription	Pancreas	Pancrea
3	chr15:76902600-76992000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:76911400-76990800	Weak transcription	Placenta	Placenta
5	chr15:76926600-76974600	Weak transcription	Esophagus	oesophagus
6	chr15:76933200-76974800	Weak transcription	Thymus	Thymus
7	chr15:76936600-76991800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr15:76940200-76991800	Weak transcription	Left Ventricle	heart
9	chr15:76941400-76991600	Weak transcription	Stomach Smooth Muscle	stomach
10	chr15:76941800-76974200	Weak transcription	Fetal Stomach	stomach
11	chr15:76941800-76976200	Weak transcription	Fetal Muscle Leg	muscle
12	chr15:76942400-76991800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr15:76944600-76973800	Weak transcription	Fetal Intestine Small	intestine
14	chr15:76947400-76991600	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr15:76947400-76991600	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr15:76952000-76974600	Weak transcription	Right Ventricle	heart
17	chr15:76952800-76972200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr15:76952800-76972800	Weak transcription	Primary B cells from cord blood	blood
19	chr15:76954200-76992000	Weak transcription	Rectal Smooth Muscle	rectum
20	chr15:76956200-76975800	Weak transcription	Fetal Intestine Large	intestine
21	chr15:76957600-76991600	Weak transcription	Liver	Liver
22	chr15:76957800-76991200	Weak transcription	Primary T cells from cord blood	blood
23	chr15:76958000-76974600	Weak transcription	Adipose Nuclei	Adipose
24	chr15:76958200-76973800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr15:76961200-76992000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr15:76970600-76971800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr15:76970800-76971600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:76970800-76971600	Enhancers	NHDF-Ad	bronchial
29	chr15:76970800-76971800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr15:76971000-76971800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr15:76971000-76971800	Enhancers	Osteobl	bone
32	chr15:76972200-76972600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr15:76972400-76973200	ZNF genes & repeats	Aorta	Aorta
34	chr15:76972400-76991400	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr15:76972600-76991600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr15:76972600-76991800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:76972800-76973200	Strong transcription	Primary B cells from cord blood	blood
38	chr15:76973000-76974400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr15:76973200-76991600	Weak transcription	Primary B cells from cord blood	blood
40	chr15:76973200-76991800	Weak transcription	Aorta	Aorta
41	chr15:76973600-76973800	Weak transcription	Lung	lung
42	chr15:76973800-76974000	Enhancers	Lung	lung
43	chr15:76973800-76974200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:76973800-76974400	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr15:76973800-76975000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr15:76974000-76974400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr15:76974000-76974400	Genic enhancers	Lung	lung
48	chr15:76974200-76974600	Enhancers	Spleen	Spleen
49	chr15:76974200-76974800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr15:76974200-76975200	ZNF genes & repeats	Fetal Stomach	stomach

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