EnhancerDB

Chrom.	Start	End	Enhancer ID	TSS of gene	Distance between enhancer and TSS	Tissues that enhancer appears
chr19	7605825	7613055	enh109824	7694451	81396	Cervix (HeLa-S3) Stomach
chr19	7608551	7608716	vista28486	7694451	85735	VISTA
chr19	7609600	7609849	vista28487	7694451	84602	VISTA
chr19	7633848	7638338	enh58843	7694451	56113	Skin (Keratinocyte)
chr19	7638372	7642668	enh86298	7694451	51783	Colon (HCT116)
chr19	7665007	7665263	vista28488	7694451	29188	VISTA
chr19	7665558	7669955	enh86299	7694451	24496	Pancreas Thyroid Colon (HCT116) Stomach
chr19	7701239	7701460	vista28489	7694451	6788	VISTA
chr19	7714356	7714558	vista28490	7694451	19905	VISTA
chr19	7715085	7725515	enh17894	7694451	20634	Bone Marrow (K562) Cervix (HeLa-S3) Blood (T-cell) Stomach Placenta Lung (PC-9) Pancreas Thymus Epithelial (MCF-7)
chr19	7720323	7720877	vista28491	7694451	25872	VISTA
chr19	7723326	7723586	vista28492	7694451	28875	VISTA
chr19	7739294	7739517	vista28493	7694451	44843	VISTA
chr19	7746304	7746484	vista28494	7694451	51853	VISTA
chr19	7754625	7759935	enh107752	7694451	60174	Blood (T-cell)
chr19	7756040	7757119	vista28495	7694451	61589	VISTA
chr19	7770608	7770891	vista28496	7694451	76157	VISTA
chr19	7771510	7771603	vista28497	7694451	77059	VISTA
chr19	7771927	7772280	vista28498	7694451	77476	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
chr19	8681865	rs10426805	T	A	987414	Spleen	0.1666	5429839
chr19	7490524	rs2878344	C	T	193887	Uterus	0.872298	5422220
chr19	7714951	rs794069	G	C	20500	Thyroid	0.00872273	5423491
chr19	7637746	rs397859614	GT	G	46665	Liver	0.256637	5422950
chr19	7694393	rs4134809	G	A,T	0	Stomach	0.000980989	5423243