EnhancerDB

Chrom.	Start	End	Enhancer ID	TSS of gene	Distance between enhancer and TSS	Tissues that enhancer appears
chr2	74276054	74276330	vista32071	74375121	98791	VISTA
chr2	74276685	74283460	enh5647	74375121	91661	Blood (T-cell) Esophagus Placenta Blood (Karpas-422) Neural Stem Cells (H9) Thymus Epithelial (MCF-7)
chr2	74288725	74296175	enh76302	74375121	78946	Stomach Muscle (A673) Epithelial (MCF-7)
chr2	74297420	74297667	vista32072	74375121	77454	VISTA
chr2	74298270	74298885	vista32073	74375121	76236	VISTA
chr2	74300965	74307015	enh91281	74375121	68106	Bone Marrow (K562)
chr2	74320865	74325435	enh109873	74375121	49686	Stomach
chr2	74345042	74349808	enh99681	74375121	25313	Pancreas (Panc1) Uterus
chr2	74400165	74404315	enh5648	74375121	25044	Blood (Karpas-422)
chr2	74406905	74413235	enh5649	74375121	31784	Blood (Karpas-422)
chr2	74408934	74409182	vista32074	74375121	33813	VISTA
chr2	74412696	74412729	vista32075	74375121	37575	VISTA
chr2	74424305	74431575	enh88468	74375121	49184	Pancreas Uterus Bone (Osteoblast)
chr2	74446656	74447054	vista32076	74375121	71535	VISTA
chr2	74461925	74466155	enh110964	74375121	86804	Cervix (HeLa-S3) Brain (SK-N-MC)

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
chr2	74347666	rs1667618	T	G	14859	Esophagus	0.182087	5851355
chr2	74191417	rs3923991	A	C	171108	Esophagus	0.333969	5850299
chr2	74305565	rs61000685	C	A,G	56960	Esophagus	0.0630534	5851213
chr2	73913941	rs115615197	G	T	448584	Pancreas	0.368564	5849438
chr2	73907643	rs72485387	T	C	454882	Spleen	0.238952	5849378
chr2	74859165	rs13386693	T	C	484044	Ovary	0.373198	5852963
chr2	74258087	rs556008427	A	AT	104438	Uterus	0.000193189	5850805
chr2	75374435	rs144255633	C	T	999314	Liver	0.310034	5856400
chr2	74191155	rs36203866	AGCCAACTTCGACTTTCTC	A	171370	Stomach	0.359141	5850295