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

TagContent
EnhancerAtlas ID
HS098-57197 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr9:37692890-37694100 
Target genes
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MSCMA0665.1chr9:37693441-37693451AACAGCTGTT+6.02
MSCMA0665.1chr9:37693441-37693451AACAGCTGTT-6.02
MYF6MA0667.1chr9:37693441-37693451AACAGCTGTT+6.02
MYF6MA0667.1chr9:37693441-37693451AACAGCTGTT-6.02
Myod1MA0499.1chr9:37693227-37693240AGCAGCTGTTCCT+7.22
Tcf12MA0521.1chr9:37693226-37693237CAGCAGCTGTT-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr93769391637693999
chr93769400037694050
Number: 1             
IDChromosomeStartEnd
GH09I037692chr93769224137693978
Enhancer Sequence
ATTTTGCTGG AGTGCTTTTC CCTGTACCCT ACCCCCAACA TGTACCTACA CACACACAGA 60
GACACCCCAA CTCACACACA CTTACAACAT TTACAAACAC ACTGACACAC AGACATACAC 120
ACAGAAATAC ACTCATACAT ACTCATACGC ACATGCATAT ACACTCTCTG GAGCACACAC 180
TCATACATAC ACTCTTTTGA TCTCTCTCTG ACACACACAC AGACACACAC ACACATAGAG 240
ACACACACCT CTTGTCTTAG TACTTGACAT GAAGGTCAGG TAATCTGCCG TTTATATTCT 300
TTCTGTGTCT TCTGTGTCTT TCTGTGTCTT CGTTTCCAGC AGCTGTTCCT TCCTTGCAGT 360
CCCTATGTCA TTCTAAACAA AATAAAATGA AATCAAATAC AGATCTGATT TGACTGCTAC 420
AGGAGAACTT TCAAATATGT TCTGTTTCGA AGCGTTCATT TTTGCTTGGA TTTCCCATCT 480
GGCCCTGCCA CAGAGATGAA ATATCACGTG TCAGGTGTTT CTGAGACACA CATTCTTCCA 540
AAGGAACTGG AAACAGCTGT TCTGCTGCTG AGTAATAAAC TTTGCTCAGG GCTCCACTGC 600
CCTGTGGCCA AGTTCTCTGA TCCTCACACA CCGAGGTCAG ATAAAATGGG GCTCCCTTTT 660
ACAGATGAAA CACCTAAGGC TCATAGAGTG ACTTGTTTAG GACCACTCTT ACCCAATGCT 720
CAGAAAGCTT GGATGGGTCC CCATTTATTA TAGGAGGAAG CTTAAACATT TTTGGTCTGA 780
CGTTTCAAGC TGCAATCCTT TCCAGCTATT TGTCTTACTA CTCTGCTTCC TTCACAGTAT 840
GCTCCAGCTA AAGGGAACAC TTATTATTCT ACTACAAGCA CCCTCTCTTC TCTTTCACCC 900
CTTGGACCTG GGCTCCTGGG CCATATCCCT TCCTCCCATC TCCATGTGGC CAGAACCCCC 960
CGCAGCTTAA GGCTTGGCTG AAGTGCTGGG TCTTCCATGA AGCCTTCCTC TGTCTAGAGT 1020
CAGGATGAAT TTCTCCATAG GACCCCGTAG TATTTTATTT GTAGCACTGG CATTGTGCTC 1080
CCCCTGGTGC ATTCAACTTT TCGAGCCCAT TCATTTCCTT TCTCCTAGAC CTGCCTTCTG 1140
TGAGGTCCAG GAAAGTATTG GCTTCATCTC TATGGCCCAG AAGTGATTGT CTTGCATGAG 1200
TGTTGTAGGT 1210