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

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EnhancerAtlas ID
HS091-24203 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:44006440-44008050 
Target genes
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
GATA2MA0036.3chr19:44006601-44006612TTCTTATCTTT+6.62
KLF14MA0740.1chr19:44006444-44006458AGGGGGGCGTGGTT-6.46
KLF16MA0741.1chr19:44006446-44006457GGGGGCGTGGT-6.14
SP1MA0079.4chr19:44006445-44006460GGGGGGCGTGGTTAA-7
SP3MA0746.2chr19:44006445-44006458GGGGGGCGTGGTT-6.27
SP4MA0685.1chr19:44006443-44006460GAGGGGGGCGTGGTTAA-6.96
SP8MA0747.1chr19:44006445-44006457GGGGGGCGTGGT-6.18
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194400677544007016
Number: 1             
IDChromosomeStartEnd
GH19I043501chr194400553344006743
Enhancer Sequence
GTTGAGGGGG GCGTGGTTAA GTGGAGATGC CTCGCCCCCT GCAATCACTA AGTAGGTCTG 60
GTCCCCACCC AACATCACCC TCTGCGGGTC TCAGTCCATC AGTCCACTTA CCTAACACAA 120
CCACCACTCC CATAATCTGT CGCAGGCTCT TTTCTTTTTC TTTCTTATCT TTTTTTTTTT 180
TTTGTCCTGA GATAGGGTCT CACTGGCTGG AGTGCAGTGG CGCGATTACG GCTCACTGCA 240
GCATCGACCT CCCTCGCTCA AGCGATTCTT CTGCCTCATC CTCCTAGGTA GCTGTGACTA 300
CAGGCGCGCA CCGCCACGCC AAGCTCTTTT TTTTTTTTTT TTTTTTTGGC AGAGAGGGGG 360
CGATGCTATG TTGCCCAGGC TGGTCTCAAA CTCCTAGGCT CAAGGGATTC TCCCACCTCG 420
GCCTCCCAAA GTGCTACGAT TACAGGCATA AGCCACCGCG CCCGGCCTCA GACCCCTGTA 480
TTTAAGGTCG GAGTGGGGGA GGGTGCAAGT CCCGTGACCA CCCAACCACA CGGACCACAG 540
AGGCTTGCAG TACCGTATGG AGGGTGAGCA GGTGTAAAGC CGACTTATGA AAGGTGTTTC 600
TTTTTCTCTA TCAGGTCCTA TTCTCTTGGC GTCACTTTCT TGTAGTGCCT GGATCTGTCT 660
CTGTCTCTCC ACCTGACCCC AGTCTCTCAG ATTCGGTATC TGTCCACTAG ATCTGTCCAC 720
TAGAATCACT AGATCTTTCT TCCTCGGAGT ATGTCCCTCT CTCGAGGTTT TTGTCTATTT 780
GTTTCTCTGA GCATCTCTGC CATTTATTTC TGGGTTTCCC TCTGTCTCGA TTCCCCTCTC 840
TCTGACTCTA GTCTCACTGT GTCTCTGTCT TTTTGGGGTC TTTGTCTCTC AGTCTCCATG 900
TCTCTGGGTC TCTGTCTGGC TTCTTGATCT CTCTGCATCT CTTACTCGTT TGGTTCTCTC 960
TGTTCTGTAG TCTCTCCTGT CTGTCTATCT GGTCTCTCTC TCTCTCTCTC TCTCTCTCTC 1020
TCTCTCTCAT TTTTAGAGAT AGGTTCTGCT TTGTCCCAGG CTGGGGTGCA GTGGCGCAGT 1080
CATAGTTCAC CGCAGCCTAC AACTCCTGGG CTCAAGCGAT CCTCCTGCCT CAGCCTCCCG 1140
AGTAGCTGGG ATTACAGGCA CGCGGCACTG CGCTTGGACA ATTTTTGTAT TTTTTTTTTC 1200
TCTAGAGACA GGGATTTGCT ATGTTGCCCA GACTTGTCTC GAACTCCTGG GCTTAAGCAA 1260
TCCTCCCCTC GGCCTCCCCA AGTGCTGGGA TTACAGGCGT GAGCCACCTA TCTGGTTCCT 1320
CTATACTAGT CTCTCTGTCT CTGTCGCCCG TTTGGGTCTA TCTCCGTTCT TGGGGCCTCC 1380
CCGTGGCTCT ATCTGGTTTC TGTCTCTGTA TCTGGTTTCT GTCTGTCTGT GCCTCTGCCT 1440
CTCTGGCTCC GTGTCCTGGT GTATCTCTCT CTCAGTAGTC TCTGCTATCA CTCGGTCTCT 1500
CTCCCTGTCT CCGGGTCTCT GTCTTTCTGG TTTCCCTCTA CCTGTCTACC TGTCTGGCCA 1560
CCTGTTTGGG TCCCCGTCGG TCCAAGCCCC CCGCGCTGTC GCCCTCGGGC 1610