EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS116-05278 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr10:114846760-114847650 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxo1MA0480.1chr10:114847321-114847332TCCTGTTTACA+6.62
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_00015chr10:114842925-114850682Adipose_Nuclei
SE_01749chr10:114846677-114847678Aorta
SE_23518chr10:114846586-114847803Colon_Crypt_1
SE_26340chr10:114845822-114848182Duodenum_Smooth_Muscle
SE_27908chr10:114844345-114850525Fetal_Intestine
SE_28766chr10:114843640-114850341Fetal_Intestine_Large
SE_32011chr10:114846599-114847835Gastric
SE_34581chr10:114844667-114848652HCT-116
SE_35111chr10:114845148-114848512HeLa
SE_38797chr10:114845297-114848257HUVEC
SE_46188chr10:114845504-114848507Osteoblasts
SE_47203chr10:114842176-114857398Panc1
SE_50693chr10:114845127-114850063Sigmoid_Colon
SE_53049chr10:114845046-114847855Small_Intestine
SE_57588chr10:114846557-114847228VACO_503
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10114847181114847492
Number: 1             
IDChromosomeStartEnd
GH10I113083chr10114843580114850476
Enhancer Sequence
ACAAGAAAAA AAAAAGGGCA ATAAGTGTAG CCCAGTAACA TAAGGTGGGG AATAAGGTTA 60
GGGGTAAGGT TAATTCTACA AGTTCAAAGC CAGTAGCCCC TGATGCGCTG TTGGACGTGA 120
ACTATAAATT TGGCTCTGAG GTTCCCAGGC ATGGAAGAAT ATCTAGATCT GTACAGAGAG 180
GTTGTGTGTG TGTTTAACAT TTCCATAATG TACAATTTCC TCTAAGAGTA AAGGCCATGA 240
GGAAATGCCC GTGGAAGATA AAGGAGACCA TGTGGTCTGT GGCAACCATG GATACATTTC 300
TTTCCCAACG CATTCTCTGA GGCACTTTGG TAACTCTGCC TCTTTGCTCT CAGCATTGTG 360
TTAGAAAATA AAGCCAGCAG ACAAGGATTA AACCCTCATG TTGCTGGGTT CCTTCTAGAA 420
ACAATTGGAG GGCTAACCAA GTCACCTTTG GTGGAAGGCA GTAAGGTGAG TCATTGCTGT 480
GGCTGGACTG AATAGGATAG CCTTAGCTGT AAAATTGGGC TGATCTTTCA AATGGACTCA 540
TGCTTGCCGA ATGACTCACG CTCCTGTTTA CAAATCAGCT CTGTGAAGAA ATGCAGAGTG 600
GGAGGCTCTG CTTGCCAGAC GGAGACCTTA GACCTCCAGG GGTGGAGAAC GGAGTACTTC 660
CTCTGGTGCT CGGCTTCCCT TCCTGGGGGC AGATCTCTCA GCTTCTGGTT GGTGGCTCTC 720
AAAATCCAGA CACAAGGTCA GCTGCAGCCA GCGTGGGCCC TGGAGTAGCT CCAGTTATGG 780
GGCAGCAATG GCCCCCTCTC ATTTTGAGAG CTCACTTTGC CTGTGGATGG TTTTAATCCA 840
TCTGGATAAA CTTGAGGCCC ATGGGAATAC CATATACTAT GGTAACCATG 890