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

TagContent
EnhancerAtlas ID
HS043-16900 
Organism
Homo sapiens 
Tissue/cell
Fetal_heart 
Coordinate
chr16:84088250-84089600 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr16:84088664-84088678AAGGGGGCGTGGCG-6.88
KLF16MA0741.1chr16:84088666-84088677GGGGGCGTGGC-6.62
Nfe2l2MA0150.2chr16:84089568-84089583CAGGATGACTGAGCA+6.5
SP3MA0746.2chr16:84088665-84088678AGGGGGCGTGGCG-6.82
SP4MA0685.1chr16:84088663-84088680AAAGGGGGCGTGGCGGA-6.16
SP8MA0747.1chr16:84088665-84088677AGGGGGCGTGGC-6.92
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr168408905584089327
Number: 1             
IDChromosomeStartEnd
GH16I084055chr168408892184089607
Enhancer Sequence
CTGTAAGAGG ACAGCCGGTT GAACAGGCAG GAACGCCACA GAGCTACCAT GACGGCCTTT 60
TTCTATGACG GCTGGATTCA TCAGAAACTA AATGCGAGCT AATTTCACTA GCTGGGCTTG 120
CAGGGCATAC ATCATTTTTA AGCCTTAGCT AAAGTAACCC AGGCTATTAA TAAAGAGTGG 180
ATGAGAGCAA AGAGCAGCCA CTTCCTGTGG GGTGGAGGCT CGGTGGATCT CTGCTGCCCT 240
TCCTCCCTGG GATCCCCGCA GACGGATGAT CAGGCCCAGC TATGCTTCTG TCACAACCTA 300
CCGAAGGGAG GCCCAGAGGC GCTCTGTGTT TCTCTAAACA CAAGGGAAGA TGGGCACGTC 360
TCTATCCAGG GGAGAAGGAG GGGCCTGTGG TTCCAGCTGA GTGGGAGGAG GAGAAAGGGG 420
GCGTGGCGGA AGAAGCACCG CTGGCAGTGC CCCGCCTCTG GGAAAGCCCT TCATGGAGGG 480
GACGTGTGGC TGAAAGCCAG GAGAGGCCAT CAGAGGACCC TGGTTCAGAA TGTCAATACG 540
ACTGGGCAAG GCCAAGGGCT CTGGAATTTA CCTTCAGCGC ACCCCGTGAC CTATGCGCAA 600
GGCCCTCAGG ACCCTGGCAC CACCACGTGG TGTCCAGGGC TGGACTGCAC AGACAGGGGT 660
GCCCCTTCCT GATCCCATTT CTGGACAATT CCTGGAACCC AGAGAAACTC CTCTTGGTAG 720
CTATAAACTC TTTGGAAGAG TACAGGGGAC TCTAGAGCAA AAGAACTGCC CAGGCTCGGC 780
TGGAAAGGCC TGGTACCAAT TGCCTTGGGT AGTGGAGAAG AACCTGCCCT AGGCAGTCTA 840
TGTAGCCAGT CAGGATCCCT GGAGAGACAG ACAGGATGAG ACCACCTAAG GGACACACCC 900
CAGCTCAGTC AAGTCCCTCC CAGGGGGGCA GGGCAGAGAA CTGAAGGGGC CTTCTGGGCT 960
GAGGGCTGGG AGCCAGGGCG GCTGCTGCCA TTGGCTGGGA CCCAAACCAG CAGACAGGCA 1020
TCCTGTAAGG GACGTTAATA GGTGGCTGGC AGAACTTTCA TAAAGAGCGT GCAAGTTACT 1080
TTGAACATGT TTAAGTAGAT CACCCAGCCG TTGTAAAATA AATTCAAATG TGAAAATCTA 1140
GGTAGCATTT TCTAAGGGAA ACAACAATCT CTTAATCTGT CAGGCCTGCC CTTGCTCATG 1200
CTGGTTTGTG CCACAAAAGA AGCCAAGAGC CAAGGCCACC ACAGCTCCCA GGAAGGCAGA 1260
GACAGGGAGA GTCTGGCCCG CCTCCTGGGG AGGGAGGGAG ACTCCTTTGA ACAAAATACA 1320
GGATGACTGA GCACAATCAC AAAGCAGCCG 1350