EnhancerDB

Chrom.	Start	End	Enhancer ID	TSS of gene	Distance between enhancer and TSS	Tissues that enhancer appears
chr11	63954598	63954956	vista10558	64052176	97220	VISTA
chr11	63954905	63959675	enh13986	64052176	92501	Muscle (A673) Placenta
chr11	63978965	63986575	enh1817	64052176	65601	Muscle (A673) Blood (Karpas-422)
chr11	64004385	64012595	enh1818	64052176	39581	Blood (Karpas-422)
chr11	64075545	64081044	enh13987	64052176	23369	Skin (Keratinocyte) Liver (HepG2) Esophagus Placenta Colon (HCT116)
chr11	64090889	64094911	enh86072	64052176	38713	Colon (HCT116)
chr11	64095085	64101829	enh1819	64052176	42909	Bone Marrow (K562) Prostate (PC-3) Cervix (HeLa-S3) Epithelial (MCF-7) Prostate (RWPE1) Esophagus Stomach Colon (HCT116) Thyroid Blood (Karpas-422) Lung (PC-9) Pancreas Pancreas (Panc1) Blood (T-cell) Heart
chr11	64102702	64102834	vista10559	64052176	50526	VISTA
chr11	64125464	64125650	vista10560	64052176	73288	VISTA
chr11	64140304	64140795	vista10561	64052176	88128	VISTA
chr11	64144045	64148195	enh87883	64052176	91869	Pancreas Adrenal
chr11	64146714	64147096	vista10562	64052176	94538	VISTA
chr11	64147622	64147982	vista10563	64052176	95446	VISTA
chr11	64149145	64156115	enh13988	64052176	96969	Placenta Epithelial (MCF-7)

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
chr11	64780912	rs6591868	G	A	728736	Esophagus	0.203587	2043125
chr11	64004008	rs7128979	A	C	33294	Heart	4.10183e-08	2038965
chr11	64368664	rs117280820	C	A	316488	Ovary	0.396374	2041221
chr11	65040436	rs601310	C	T	988260	Lung	0.270895	2044503
chr11	63856635	rs12805664	A	G	180667	Adrenal	0.0416026	2037950

Genomic Location	chr11:64037302-64052176[-]
TSS	64052176
Gene Name	BAD
Ensembl ID	ENSG00000002330.9
ENTREZID	572
Uniprot
	Q92934
	A0A024R562
Protein Name
	isoform CRA_c
	BCL2-antagonist of cell death
	Bcl2-associated agonist of cell death