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

TagContent
EnhancerAtlas ID
HS047-05876 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr11:46413990-46415060 
TF binding sites/motifs
Number: 10             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR1MA0162.3chr11:46414518-46414532ATTGCGGGGGCGGC-6.05
EGR3MA0732.1chr11:46414518-46414533ATTGCGGGGGCGGCG-6.22
EHFMA0598.2chr11:46414628-46414640AACCCGGAAGTG+6.74
ELF1MA0473.2chr11:46414628-46414640AACCCGGAAGTG+7.22
ELF3MA0640.1chr11:46414628-46414641AACCCGGAAGTGG+6.87
ELF4MA0641.1chr11:46414628-46414640AACCCGGAAGTG+7.22
ELF5MA0136.2chr11:46414629-46414640ACCCGGAAGTG+6.32
GabpaMA0062.2chr11:46414631-46414642CCGGAAGTGGA+6.32
RESTMA0138.2chr11:46414264-46414285TTCAGCACCTCGGAGAGCTCC+9.64
ZBTB7AMA0750.2chr11:46414629-46414642ACCCGGAAGTGGA+6.42
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr114641422446414324
Number: 1             
IDChromosomeStartEnd
GH11I046387chr114640898646415190
Enhancer Sequence
CGCTCGGCTG CCTGCTCAGC GTTCCGGGCC GGGGAAGGGG CGCGCCCCTG CTCTCCCAGC 60
CCTGGGATGG GACGCGCCGC CAGTCCAGGC GCAGCCTGGA CCGCCAGTTC ACCGCCGCCT 120
GTGAGGGACA GTCGGTTGCC CAAGGTCGCC GGGGCCGGAG CCCGGGACAA GATCCCGGAG 180
AGCGGGCAGC CAATCTCAGA GGTCGCTGGG AACCGCACGG GCCGTAGCCT CAGGACTCCG 240
GGCCTCGCCC AGGCTGGGCG GACCTTGGGG CGGCTTCAGC ACCTCGGAGA GCTCCCCGCG 300
CCCTGGCCCA GCAGCCTCGC CTGCCTGATT CCGCTCCAGC GCTTGTCTCC CTCCGAGAGC 360
GCCCTTCCGG GGGACCGCCG GGGTCGGACG CTCCCCACTG CGCCCAGGAC CGAGGCCTGT 420
AACCCCAAAT TCTGATCGCA AACATTTGAT TAAGCTTAAG ACGTCTGATT TCTTCTCTCG 480
GGGAAACAAC TCAAGACCCT CCCCCGAGGG CCGGAGGTGG TGAGGGCGAT TGCGGGGGCG 540
GCGGTGGAGG AGAGGCAGGA GCCTCTTGGC AGAGAATGGG AGGGAACTCG AGTAGAAGCC 600
AGCGCTGCGG GGCTCTTGGT GTGGGGTTCT CCGCGCGGAA CCCGGAAGTG GAGTTCGGGT 660
CCCCAGAGCT CGCGAGCGCG ACGGCTGGGG TTGGTCGGAA TTGGGAACTT CAGGGCTGGG 720
GTTGGTTGGC TAGAGTAGGA AGCCATCTTC TGTTGTTACA TGAATGATCG GGTCTCCCAA 780
GACCTCATAA CTGGGGGTGA AAGAAGCACT ACTCTTCTTG CCCCACTTCA CAAATAAGGA 840
AAGTTGGTTC ATAAGACCCT AAGACGGCAC TCCTGCACTT CTTCCACTTT GCCATATCCT 900
TCCCAGGGCA CAGAAGAGTG TGATACTCCT AAGAGGAGGT GGGGGTTGTG GAGGAGGAAG 960
GCAGATAGAT CCTTAAAACA GTCAGATGAG AAAACAAGCA AGGCCAAGGG CGGGAGGCTG 1020
CATACACAAG ACACGCCTCC AGCTACTGAC CCCAGCTCTT CCAGAAGCTG 1070