EnhancerDB

Chrom.	Start	End	Enhancer ID	TSS of gene	Distance between enhancer and TSS	Tissues that enhancer appears
chr13	111275345	111284355	enh30703	111365083	80728	Astrocyte Blood (T-cell) Stomach
chr13	111278486	111278706	vista17069	111365083	86377	VISTA
chr13	111289528	111293778	enh115564	111365083	71305	Brain (SK-N-SH)
chr13	111307965	111314590	enh3018	111365083	50493	Blood (Karpas-422) Blood (GM12878)
chr13	111312907	111313086	vista17070	111365083	51997	VISTA
chr13	111335145	111339915	enh51725	111365083	25168	Large Intestine Stomach
chr13	111376625	111382575	enh107580	111365083	11542	Blood (T-cell)
chr13	111406825	111414462	enh30704	111365083	41742	Cervix (HeLa-S3) Astrocyte Bone (Osteoblast) Lung (A549) Neural Stem Cells (H9)
chr13	111410023	111410076	vista17071	111365083	44940	VISTA
chr13	111421645	111425815	enh94229	111365083	56562	Spleen
chr13	111429465	111433615	enh112283	111365083	64382	Brain (SK-N-MC)
chr13	111449605	111454455	enh15503	111365083	84522	Pancreas Placenta Uterus
chr13	111460271	111465494	enh68638	111365083	95188	Neural Stem Cells (H9) Embryonic Stem Cell Line (H1-hESC) Epithelial (MCF-7)
chr13	111464605	111464817	vista17072	111365083	99522	VISTA

Chrom.	Start	End	TF name	Source	Predicted site?	Tissue	TSS of gene	Distance between TFBS and gene	id	More

Chrom.	Position	dbSNP ID	Reference Allele	Alternative Allele	Distance between TSS and SNP	Tissue	q Value	id
chr13	110708480	rs61749314	T	C	656603	Esophagus	0.0872629	3390399
chr13	111720076	rs9583579	A	G	346655	Esophagus	0.973467	3399874
chr13	111658947	rs9588326	C	G,T	285526	Heart	0.239015	3399414
chr13	110981837	rs112522662	C	T	383246	Liver	0.32105	3393138
chr13	110655030	rs148376449	G	T	710053	Stomach	0.261688	3389694
chr13	111157480	rs113771884	A	G,T	207603	Adrenal	0.144502	3395226