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

TagContent
EnhancerAtlas ID
HS052-31104 
Organism
Homo sapiens 
Tissue/cell
Fibroblast_foreskin 
Coordinate
chr5:138897160-138898590 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr5:138898206-138898218GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr5:138898210-138898222GTTTGTTTGTTT+6.32
NHLH1MA0048.2chr5:138897574-138897584CGCAGCTGCG+6.02
NHLH1MA0048.2chr5:138897574-138897584CGCAGCTGCG-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5138897527138897822
Number: 1             
IDChromosomeStartEnd
GH05I139517chr5138896810138898710
Enhancer Sequence
TAAATAAATT TCCTTCCTCC AGCTGCAGGG CAAAAAATGG GTTGAAGAGC CGGACTGGTG 60
GTAACTGGTG TGGCCATCCA GCCTGGAGTC GATGTTGGCA TGAATGAAGA CACAGGCAGT 120
TGGGACAGAG AGAAGCGAGT GGGATGTGGA GGTGACCCGA TGAAATACTG GCCCGGAGAT 180
ATGAGGCATG AGGCGGGGAG CACGAGGGTG TCGAAGGGCC AAAATGTGGT AAGAGAAGCC 240
GGAGGAGTGT GAGGACAGGT GGAAGGGATC CAATGTGGGA TCTAAGGGGT CTGAGACCAC 300
CGTGGCCGCG GGAGGCAGGA GAAGGTACCG CAGAGCTCCC GGTGATGTGT CAGGAGGCCC 360
TACACTCGCG CGTGCACTGG CTCGCAGTTT GGACAGAGAC CCTACAGGCC AGGCCGCAGC 420
TGCGCCCAGA CCACCCCCAG CGGGTGAAGA CTGCCGCGGC GGCGCAGTTC CCGGCATGCC 480
TCCGGCCGGT GACTTCATCC GGCCCGGGGC CAAGGCCCGG CCTCCGCTAG AGGGCGCTGC 540
TCTCAGCAGC CGCGCCGCCC GGATGGACTC GCGCCAGAGT AGGACAAGAG AGGCAGGCGG 600
CGGCTGCTCC GTGCGGCTCC CACGCCTCTC GGGCGGCAGG TCCTGCCTCG GACCTGGGAC 660
CACTGGCTGG CGCCTGTGGC TCACATCTCC ACGCCTTTGC CCGCTCCTCC CAGGAGCCCG 720
AGTCAGAAAC CTGTGCTTCA CCCTCGAGAG CGCTGCCATC CTCCCCCTCA ACCAGACGGG 780
CATGGCGTCT GGTTGTCCGT CCTGTCTTCT CATCGTCTCA GAGCCCTTCC CTGACCCCTA 840
CCCTCTCTCA GACCAACAGG ATGATGACAG GAAGAGGATC CAGGACCAAC TCCTAGCGGT 900
GACCTTGAGA AAACAATCTC ATACCCCAGT TTCCCTTACA ATGCAATGGA AATAATACTA 960
ACAACCCTGG AAGAGTGTTG GAAGGACTAA ACGAAATCAT CTTTTTCAGT ACTAAGCAGA 1020
GGCTCAGTGA GCATCAGCGT TTTTTTGTTT GTTTGTTTGT TTTCTTGAAA CTGGTTGGAG 1080
CCCAGGCTGG AGTGCAGTGG CATGATCTTG GCCCACTTGA GCCTCAATTG CCTGGGCTCA 1140
AGCCATTCTT CCTCCTCAGC CTCTGGAGTA GCTGGGACCA CAGTTGCATG CCACCACGAC 1200
TGGCTACTTT TGTTCATTTT TTTTGTAGAG TTGGGGTCTC TCTAAATGGT CTTGAACTAC 1260
TGGACTCAAG CGATCCTCCC ACCTCGGCTT CCCAAAGCAC TGGGATTACA GGCATGAGCC 1320
ACTGTCCCCG GCCAACATCA GCTATTTTAA CACTTCTCTC TGTTGCTGGA ATGTACTCAC 1380
TGGCCCCAAA CTCTTCAGTG GCTTCTGACT GCCCTCAGGA TCAGTCCACA 1430