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

TagContent
EnhancerAtlas ID
HS007-03869 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr12:57666140-57667130 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MyogMA0500.1chr12:57666619-57666630CTGCAGCTGTT-6.02
RREB1MA0073.1chr12:57666394-57666414GGGGGTGGGGTGGGGGGGGG-7.32
Tcf12MA0521.1chr12:57666619-57666630CTGCAGCTGTT-6.62
ZNF263MA0528.1chr12:57666394-57666415GGGGGTGGGGTGGGGGGGGGG+6.24
ZNF740MA0753.2chr12:57666403-57666416GTGGGGGGGGGGT-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr125766649957667011
Number: 1             
IDChromosomeStartEnd
GH12I057272chr125766605957667725
Enhancer Sequence
CAACATGCTT ACAAGGCCAT CACAGACTGA CCCAGACATA CCTACAGATA CAGGCCACAC 60
ATGAACAAGA CAAAAAGGGG GAATGGAGTT TATACCATGT TGTACTGCTG GGGCGGAGAG 120
ACTGGCAGAA GGACTTGGGG ACAGGAGCTT GGAGAGAACT GAACAGGCTG CGGAGAGGGC 180
TGCAGAGCCG GGACTGGCTG TGGGCCAGCA GAGAGGCATG TGGAAAAGGG AAGAGAAAAG 240
AGAGGTGGGA AGCGGGGGGT GGGGTGGGGG GGGGGTGCGG GCAGAGATGG GGAGGGAAAG 300
GGAAGGAACA ATAAGGTTAA TAATCATAGA AGAAATTTCA CATGAGTAGC ACGACTGCTG 360
AGCAGGTAGG TGACCAAGCC CGGGACAGCT TGAAGATTTA ACATCTCTTT GACAAACAGG 420
CAATCTCTCT TATCAGGGGA GACCTGCTGC ACTCCCTTCC CCATTAGCCA TTCAGAACTC 480
TGCAGCTGTT GTGAGCAATC TGAGGACTCT CAGGGTCAGG GTCTGCTGTC TGATTCCAAA 540
TACAGCTTTT CCCAAAGCAG TTTTTCTGAA CACACAATTC CTGGGGAGCA TGATCATAAC 600
CCTCCTTGAC TGCCCACTTG AGAAGAGATT CCTGTCTGCA CTGCTGCACT GCTTCTGCAG 660
GAAGGGTCAT CCAAGGTCTG GCTCAGCTGC TCCTGATTTC ACACCACAGC TCTCCTAGAG 720
GAAATACTCA TTCACAAGGA TCATCTCCCT CCCAAGGGCA GAGAAGGAAA AAACACCCAA 780
GATCATGCCT GCTTCTGGCT ACTTCCTTCC ACTCCATGAT TGCTCCTCCA GGCTGTGACA 840
GCAATATGAA AAATCCACCT CCACCCCCCA AGCAAACAGG AAGGATTTAG GAATAAAATA 900
TAAATAGCTT AGCTTTAGTT TTTGTCCCTT CAGTCCCCCT TCACTAGCCT CAAGCAGGAG 960
GATTTGTTTA CTAGGAACAT AGAGTGTTCT 990