EnhancerDB

Chrom.	Start	End	Enhancer ID	TSS of gene	Distance between enhancer and TSS	Tissues that enhancer appears
chr13	113856100	113861895	enh30709	113951556	89661	Astrocyte Colon (HCT116) Heart
chr13	113868485	113873239	enh30710	113951556	78317	Bone Marrow (K562) Prostate (PC-3) Liver (HepG2) Epithelial (MCF-7) Cervix (HeLa-S3) Large Intestine Esophagus Astrocyte Lung Stomach Muscle (A673) Colon (HCT116) Adrenal Lung (PC-9) Neural Stem Cells (H9) Heart
chr13	113870568	113870732	vista17147	113951556	80824	VISTA
chr13	113876905	113881055	enh51727	113951556	70501	Large Intestine
chr13	113925325	113932010	enh3023	113951556	19546	Bone Marrow (K562) Skin (Keratinocyte) Prostate (PC-3) Prostate (RWPE1) Astrocyte Bone (Osteoblast) Placenta Blood (Karpas-422)
chr13	113926958	113927400	vista17148	113951556	24156	VISTA
chr13	113928164	113928348	vista17149	113951556	23208	VISTA
chr13	113928610	113928824	vista17150	113951556	22732	VISTA
chr13	113941305	113945455	enh103951	113951556	6101	Peripheral Blood (MM.1S)
chr13	113946276	113946648	vista17151	113951556	4908	VISTA
chr13	113965761	113972535	enh86170	113951556	14205	Colon (HCT116) Epithelial (MCF-7)
chr13	113982391	113982456	vista17152	113951556	30835	VISTA
chr13	113983805	113988375	enh96468	113951556	32249	Lung (PC-9) Epithelial (MCF-7)
chr13	114032425	114037670	enh92503	113951556	80869	Liver (HepG2)
chr13	114043565	114053055	enh3024	113951556	92009	Large Intestine Liver (HepG2) Neural Stem Cells (H9) Blood (Karpas-422)

Chrom.	Start	End	TF name	Source	Predicted site?	Tissue	TSS of gene	Distance between TFBS and gene	id
chr13	113945919	113947706	TCF7L2	GTRD	no	Colon (HCT116)	113951556	3850	108091099
chr13	113945937	113948135	ZNF143	GTRD	no	Epithelial (MCF-7)	113951556	3421	108091100
chr13	113946171	113948395	TCF7L2	GTRD	no	Colon (HCT116)	113951556	3161	108091102
chr13	113946235	113946849	ZNF143	GTRD	no	Epithelial (MCF-7)	113951556	4707	108091103
chr13	113946335	113947515	TCF7L2	GTRD	no	Colon (HCT116)	113951556	4041	108091104
chr13	113946410	113946668	EGR1	UCSC Txn Factor	no	Conserved	113951556	4888	108091105
chr13	113946410	113946668	ZNF274	ENCODE Uniform TFBS	no	Bone Marrow (K562)	113951556	4888	108091106
chr13	113946461	113946622	ZNF143	ENCODE Uniform TFBS	no	Embryonic Stem Cell Line (H1-hESC)	113951556	4934	108091108
chr13	113946546	113946558	HINFP	JASPAR	yes		113951556	4998	19347697
chr13	113946598	113946619	ZNF263	JASPAR	yes		113951556	4937	19347698
chr13	113946606	113946620	SPI1	JASPAR	yes		113951556	4936	19347699
chr13	113946606	113946620	SPIC	JASPAR	yes		113951556	4936	19347700
chr13	113946607	113946615	EHF	JASPAR	yes		113951556	4941	19347701
chr13	113946640	113946646	LEF1	TRANSFAC	yes		113951556	4910	19347702
chr13	113946640	113946646	SOX10	JASPAR	yes		113951556	4910	19347703

Chrom.	Position	dbSNP ID	Reference Allele	Alternative Allele	Distance between TSS and SNP	Tissue	q Value	id
chr13	114611528	rs7489888	C	T	633541	Esophagus	0.297901	3413855
chr13	114909364	rs4883658	G	A	931377	Heart	0.26391	3416211
chr13	113514014	rs57337881	G	A	437542	Heart	0.231254	3407249
chr13	113554910	rs72660087	G	C	396646	Pancreas	0.315105	3407365
chr13	113927208	rs9604045	G	T	24348	Spleen	4.36728e-05	3409201
chr13	113558220	rs1317395	G	A	393336	Thyroid	0.0493578	3407415
chr13	114127141	rs2258798	C	T	149154	Liver	0.288046	3410866
chr13	113927208	rs9604045	G	T	24348	Lung	1.07458e-10	3409201

Genomic Location	chr13:113951556-113977987[+]
TSS	113951556
Gene Name	LAMP1
Ensembl ID	ENSG00000185896.9
ENTREZID	3916
Uniprot
	P11279
	A0A024RDY3
Protein Name
	isoform CRA_a
	Lysosomal-associated membrane protein 1
	Lysosome-associated membrane glycoprotein 1