Variant report

Variant	nsv525433
Chromosome Location	chr15:73766072-73833600
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	ARID3A	chr15:73832546-73832746	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:73797135-73797723	K562	blood:	n/a	n/a
3	ARID3A	chr15:73766927-73767688	K562	blood:	n/a	n/a
4	ATF1	chr15:73767051-73767702	K562	blood:	n/a	n/a
5	ATF1	chr15:73797339-73797510	K562	blood:	n/a	n/a
6	ATF1	chr15:73768211-73768425	K562	blood:	n/a	n/a
7	ATF3	chr15:73767079-73767484	K562	blood:	n/a	n/a
8	BACH1	chr15:73766993-73767427	K562	blood:	n/a	n/a
9	BHLHE40	chr15:73767066-73767583	K562	blood:	n/a	n/a
10	BHLHE40	chr15:73797289-73797531	K562	blood:	n/a	n/a
11	BRCA1	chr15:73823153-73823264	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr15:73777778-73778493	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr15:73767095-73767538	K562	blood:	n/a	n/a
14	CCNT2	chr15:73767115-73767482	K562	blood:	n/a	chr15:73767310-73767330
15	CEBPB	chr15:73797286-73797709	K562	blood:	n/a	n/a
16	CEBPB	chr15:73832602-73832854	IMR90	lung:	n/a	chr15:73832806-73832817 chr15:73832806-73832817
17	CEBPB	chr15:73823045-73823282	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr15:73778116-73778570	A549	lung:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
19	CEBPB	chr15:73778160-73778568	MCF-7	breast:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
20	CEBPB	chr15:73832570-73832900	HepG2	liver:	n/a	chr15:73832806-73832817 chr15:73832806-73832817
21	CEBPB	chr15:73777815-73778657	K562	blood:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
22	CEBPB	chr15:73767103-73767547	K562	blood:	n/a	n/a
23	CEBPB	chr15:73797231-73797552	K562	blood:	n/a	n/a
24	CEBPB	chr15:73778253-73778476	HepG2	liver:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
25	CEBPB	chr15:73767145-73767556	K562	blood:	n/a	n/a
26	CEBPB	chr15:73778162-73778558	MCF-7	breast:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
27	CEBPB	chr15:73787582-73787966	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr15:73778172-73778659	IMR90	lung:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
29	CEBPB	chr15:73778279-73778593	H1-hESC	embryonic stem cell:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
30	CEBPB	chr15:73811799-73812019	A549	lung:	n/a	n/a
31	CEBPB	chr15:73778110-73778566	K562	blood:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
32	CEBPB	chr15:73778291-73778518	K562	blood:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
33	CEBPB	chr15:73832452-73833011	A549	lung:	n/a	chr15:73832806-73832817 chr15:73832806-73832817 chr15:73832499-73832510
34	CEBPB	chr15:73832544-73832905	A549	lung:	n/a	chr15:73832806-73832817 chr15:73832806-73832817
35	CEBPB	chr15:73832579-73832942	A549	lung:	n/a	chr15:73832806-73832817 chr15:73832806-73832817
36	CEBPB	chr15:73777771-73778941	Hela-S3	cervix:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
37	CEBPB	chr15:73831577-73832199	A549	lung:	n/a	chr15:73832125-73832138
38	CEBPB	chr15:73778272-73778503	HepG2	liver:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
39	CEBPB	chr15:73811801-73811904	K562	blood:	n/a	n/a
40	CEBPB	chr15:73832644-73832836	K562	blood:	n/a	chr15:73832806-73832817 chr15:73832806-73832817
41	CEBPB	chr15:73778181-73778637	A549	lung:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
42	CEBPB	chr15:73797290-73797305	A549	lung:	n/a	n/a
43	CEBPB	chr15:73778249-73778553	ECC-1	luminal epithelium:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
44	CEBPB	chr15:73778145-73778550	A549	lung:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
45	CEBPB	chr15:73778182-73778637	HepG2	liver:	n/a	chr15:73778361-73778372 chr15:73778360-73778373
46	CEBPB	chr15:73786263-73786658	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:73831321-73832904	Hela-S3	cervix:	n/a	chr15:73832806-73832817 chr15:73832806-73832817 chr15:73832499-73832510 chr15:73832125-73832138
48	CEBPD	chr15:73797257-73797673	K562	blood:	n/a	n/a
49	CEBPD	chr15:73767064-73767572	K562	blood:	n/a	n/a
50	CEBPD	chr15:73767030-73767609	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:73809957-73810007	SAEC	small airway:	n/a
2	chr15:73776842-73776892	MCF10A-Er-Src	breast:	n/a
3	chr15:73776842-73776892	ovcar-3	ovarian:	n/a
4	chr15:73776842-73776892	HRCEpiC	kidney:	n/a
5	chr15:73800308-73800358	Jurkat	blood:	n/a
6	chr15:73776842-73776892	AoSMC	blood vessel:	n/a
7	chr15:73800308-73800358	MCF10A-Er-Src	breast:	n/a
8	chr15:73800308-73800358	HepG2	liver:	n/a
9	chr15:73800308-73800358	LNCaP	prostate:	n/a
10	chr15:73809957-73810007	IMR90	lung:	fetal
11	chr15:73809957-73810007	NHBE	bronchial:	n/a
12	chr15:73800308-73800358	GM12891	blood:	n/a
13	chr15:73800308-73800358	Hepatocyte	liver:	n/a
14	chr15:73776842-73776892	IMR90	lung:	fetal
15	chr15:73800308-73800358	HIPEpiC	eye:	n/a
16	chr15:73800308-73800358	MCF-7	breast:	n/a
17	chr15:73776842-73776892	K562	blood:	n/a
18	chr15:73776842-73776892	AG10803	skin:	n/a
19	chr15:73809957-73810007	CMK	blood:	n/a
20	chr15:73809957-73810007	HEK293	kidney:	embryo
21	chr15:73800308-73800358	SAEC	small airway:	n/a
22	chr15:73809957-73810007	HCM	heart:	n/a
23	chr15:73809957-73810007	AoSMC	blood vessel:	n/a
24	chr15:73776842-73776892	ECC-1	luminal epithelium:	n/a
25	chr15:73776842-73776892	HRE	kidney:	n/a
26	chr15:73800308-73800358	NH-A	brain:	n/a
27	chr15:73776842-73776892	NHBE	bronchial:	n/a
28	chr15:73776842-73776892	SK-N-SH_RA	brain:	n/a
29	chr15:73809957-73810007	HCT-116	colon:	n/a
30	chr15:73809957-73810007	MCF10A-Er-Src	breast:	n/a
31	chr15:73776842-73776892	HCPEpiC	choroid plexus:	n/a
32	chr15:73800308-73800358	RPTEC	kidney:	n/a
33	chr15:73800308-73800358	HEEpiC	esophagus:	n/a
34	chr15:73809957-73810007	ECC-1	luminal epithelium:	n/a
35	chr15:73800308-73800358	AG04449	skin:	fetal
36	chr15:73776842-73776892	Hepatocyte	liver:	n/a
37	chr15:73809957-73810007	HMEC	breast:	n/a
38	chr15:73800308-73800358	SK-N-SH	brain:	n/a
39	chr15:73809957-73810007	HNPCEpiC	eye:	n/a
40	chr15:73800308-73800358	HCM	heart:	n/a
41	chr15:73809957-73810007	HRPEpiC	eye:	n/a
42	chr15:73809957-73810007	HL-60	blood:	n/a
43	chr15:73776842-73776892	SK-N-SH	brain:	n/a
44	chr15:73809957-73810007	MCF-7	breast:	n/a
45	chr15:73776842-73776892	SAEC	small airway:	n/a
46	chr15:73776842-73776892	HRPEpiC	eye:	n/a
47	chr15:73800308-73800358	PFSK-1	brain:	n/a
48	chr15:73776842-73776892	SKMC	muscle:	n/a
49	chr15:73809957-73810007	AG04449	skin:	fetal
50	chr15:73800308-73800358	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:73759900..73762156-chr15:73764346..73766091,2	MCF-7	breast:
2	chr15:73793807..73796662-chr15:73797098..73799823,2	MCF-7	breast:
3	chr15:73783487..73784303-chr3:28967494..28967994,2	MCF-7	breast:
4	chr15:73598394..73598898-chr15:73823428..73824292,2	K562	blood:
5	chr15:73778746..73780698-chr15:73793082..73795138,2	MCF-7	breast:
6	chr15:73793807..73796662-chr15:73797098..73799823,2	MCF-7	breast:
7	chr15:73757019..73759384-chr15:73766067..73769375,3	K562	blood:
8	chr15:73777860..73779711-chr15:73796678..73798817,2	K562	blood:
9	chr15:73833100..73835017-chr15:73835234..73837594,2	MCF-7	breast:
10	chr15:73775861..73777735-chr15:73790397..73792808,2	K562	blood:
11	chr15:73598023..73598791-chr15:73831624..73832277,2	MCF-7	breast:
12	chr15:73778746..73780698-chr15:73793082..73795138,2	MCF-7	breast:
13	chr15:73791240..73791905-chr15:79437462..79438211,2	MCF-7	breast:
14	chr15:73777860..73779711-chr15:73796678..73798817,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPTN-1	chr15:73807066-73809830	ucscGeneNc_uc002bay_1
2	lnc-NPTN-1	chr15:73817783-73818019	ucscGeneNc_uc002bay_1
3	lnc-NPTN-1	chr15:73811363-73811548	ucscGeneNc_uc002bay_1

Variant related genes	Relation type
MRPS15P1	TF binding region
MRPS15P1	CpG island
ENSG00000259186	chromatin interactions

Extended variants
information (count: 1530 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138028941	chr15:73766401-73766402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531222757	chr15:73766442-73766443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190045462	chr15:73766450-73766451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570937491	chr15:73766457-73766458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs182196243	chr15:73766508-73766509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538890665	chr15:73766533-73766534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7163253	chr15:73766542-73766543	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs79555328	chr15:73766562-73766563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535845226	chr15:73766624-73766625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143509385	chr15:73766658-73766659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs116221626	chr15:73766659-73766660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543309286	chr15:73766661-73766662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547953655	chr15:73766750-73766751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535697989	chr15:73766761-73766762	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555543471	chr15:73766766-73766767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115441769	chr15:73766832-73766833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537960165	chr15:73766877-73766878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145798317	chr15:73766918-73766919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs187336501	chr15:73766930-73766931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189294377	chr15:73766947-73766948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530176882	chr15:73766991-73766992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542285147	chr15:73767048-73767049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563670452	chr15:73767102-73767103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138376095	chr15:73767103-73767104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149234100	chr15:73767161-73767162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566240319	chr15:73767208-73767209	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs533893484	chr15:73767239-73767240	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs571094157	chr15:73767240-73767241	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs180876707	chr15:73767258-73767259	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs144841350	chr15:73767298-73767299	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs372305212	chr15:73767317-73767318	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs565645767	chr15:73767407-73767408	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs535930873	chr15:73767413-73767414	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs185864748	chr15:73767444-73767445	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs569287247	chr15:73767462-73767463	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs536982393	chr15:73767480-73767481	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs558593157	chr15:73767490-73767491	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs375587834	chr15:73767491-73767492	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs60688200	chr15:73767506-73767507	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs577020753	chr15:73767522-73767523	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs558109558	chr15:73767532-73767533	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs190286389	chr15:73767548-73767549	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs577592343	chr15:73767596-73767597	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs540215852	chr15:73767603-73767604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs75718920	chr15:73767606-73767607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541702208	chr15:73767621-73767622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542323580	chr15:73767706-73767707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs554158478	chr15:73767712-73767713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182510454	chr15:73767759-73767760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142970282	chr15:73767907-73767908	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
Lung cancer	18438408	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
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:164 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73766400-73767200	Enhancers	K562	blood
2	chr15:73767200-73767600	Flanking Active TSS	K562	blood
3	chr15:73767600-73768400	Enhancers	K562	blood
4	chr15:73773800-73775400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr15:73774200-73774400	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr15:73774200-73775200	Enhancers	K562	blood
7	chr15:73774400-73774800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr15:73774800-73775000	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr15:73775000-73777200	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr15:73775200-73775600	Weak transcription	K562	blood
11	chr15:73775200-73776400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr15:73775400-73777800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr15:73775600-73776800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:73775600-73778600	Enhancers	K562	blood
15	chr15:73776200-73776800	Enhancers	Right Ventricle	heart
16	chr15:73776400-73777400	Enhancers	Fetal Heart	heart
17	chr15:73776600-73776800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:73776600-73777200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr15:73777000-73777800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr15:73777200-73779000	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr15:73777800-73778200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr15:73777800-73778400	Bivalent Enhancer	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr15:73777800-73778800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr15:73777800-73778800	Enhancers	Hela-S3	cervix
25	chr15:73777800-73779200	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr15:73778000-73778400	Enhancers	Liver	Liver
27	chr15:73778800-73780400	Weak transcription	Hela-S3	cervix
28	chr15:73780400-73780600	Enhancers	Hela-S3	cervix
29	chr15:73787400-73787800	Enhancers	Fetal Lung	lung
30	chr15:73791200-73793800	Enhancers	Fetal Heart	heart
31	chr15:73793400-73793800	Enhancers	K562	blood
32	chr15:73793800-73796600	Weak transcription	K562	blood
33	chr15:73796600-73798400	Enhancers	K562	blood
34	chr15:73805600-73809200	Weak transcription	Right Atrium	heart
35	chr15:73806200-73806400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr15:73806400-73806600	Active TSS	H1 Cell Line	embryonic stem cell
37	chr15:73806400-73806800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
38	chr15:73806400-73806800	Active TSS	H9 Cell Line	embryonic stem cell
39	chr15:73806400-73806800	Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr15:73806400-73806800	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr15:73806400-73806800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr15:73806400-73807000	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr15:73806400-73807000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
44	chr15:73806400-73807000	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr15:73806600-73806800	Flanking Active TSS	H1 Cell Line	embryonic stem cell
46	chr15:73806800-73807000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr15:73806800-73807200	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr15:73806800-73807200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr15:73806800-73807400	Enhancers	H1 Cell Line	embryonic stem cell
50	chr15:73806800-73807600	Enhancers	HUES64 Cell Line	embryonic stem cell

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