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

TagContent
EnhancerAtlas ID
HS139-03180 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr1:150166150-150167860 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs6692738chr1150166773hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL1MA0477.1chr1:150166345-150166356GGTGACTCATG+6.62
JUNDMA0491.1chr1:150166345-150166356GGTGACTCATG+6.02
RARA(var.2)MA0730.1chr1:150167433-150167450TGGTCATGAGAAGGTCA+6.09
Twist2MA0633.1chr1:150167427-150167437AACATATGGT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr1150166670150167023
chr1150166245150166384
Number: 1             
IDChromosomeStartEnd
GH01I150193chr1150165894150167634
Enhancer Sequence
TGATCTCAAT CTCGACCTCG TGATCCGCCG CCTCGACCTC CCAAAGTGCT GGGATCATAG 60
GCGTAAGCCA TTGCGCCCGG CCAACTCCAG CCATTTTTAA GCTATACTTA AGATCTTTCT 120
GTCTTACATT TCTGTAATGA GACAGCTAAT CACAACTAAG CGGGTTGGTT ATAAAGATCT 180
AAACCGGCCG GGCGCGGTGA CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCGAGGTGG 240
GCGGATCACG AGGTCAGGAG ATCCAGACCA TCCTGGCTAA CAGTGAAACC CCGTCTCTAC 300
TGAAAATACA AAAAATTAGC CAGGCATGGT GGCGGACGCC TGTAGTCCCA GCTACTCGGG 360
AGGCTGAGGC AAGAGAATGG CATGAACCTG GAAGGCGGAG CTTGCAGTGA GCTGAGATCG 420
CACCACTGCA CTCCATCCTG GGCGACAGAG TGAGACTCCG TCTCAAAAAA AAAAAAAAAA 480
AAAAAAGACC TAAACCGACA TTGTAAGCAA GACAATGCTA CAAAATATGG AAGACACAAA 540
GAGAGTTCCT ACCCTCCAGA GAATTTCCCT GAGACGAGTA CTGCCTTTCA GTTTTCTCTG 600
TTGTGGGGAC AGAAAGAATA ATGGTAAGAG GCTGAGTAAT GGCTGCATCA TGAGGGTAGT 660
CTAGACAAGC AACCCATGGA TATGCAAGAG AAAGACTGTC TCCAGGGGTC CATGAAAGAG 720
ACTGCCTGAA GGTGGGTGGG ATCTTGATGA GATGGAAAAC CTTCCAGGCA GAGGGAAAAG 780
TGTGAGCAAA GACAGAGAGA TTTGTGTATT CATTTCCCAG GGCTGCTGGA ACAAGGTACC 840
ACAAACTGGG TGGCTTAAAA CAGCAGAAAT CTCTCACAGT TCTGAAGGCC AGAAGTCTGA 900
CATAGAGTTG TGGGTGGGGC AATACTTTCT CTGAAGGCTC TAAGAGAGGA TTTTCCTTGC 960
TGCTTCTTAG CTTCTGGTGG TTGCAGACAA TTCTTGGCAT TCTTTGGTTT GTAGACACAC 1020
ATCACTCCAA TCTCTGCCTC CACCGTGATA TGTTGTTTTC TTTATATGTC TCTCTGTTCA 1080
CATGCCCCCC AGCTCTGCGT CTGTATCTAT ATCTCCTCCT CTCATAGGTA CATAGCTTAT 1140
ACTGGATTAG AGCCCACCCA CCCACTAGGA CATCATCTTA ACTACATCTA CAATGACTCT 1200
ATCTCCAAAT AAGGTCACAT TCATAGGTAG GCATTAGAAC TTGAACATAT CTTTTTGAAG 1260
GACACAATTC AACCCACAAC ATATGGTCAT GAGAAGGTCA GTGTGGTCAG AAAGTAGAGT 1320
ATATCTAGGG AAAGAGTGGA AGTAACTCAG GAAGAAGGGG CTGGAGTATA GAGAACCTTG 1380
ATGAATAAGC AATGAGGGTG CACAGAATAT ATATATATAT TTTTTCGAGG CAGAGTTTCA 1440
CTCTTGTTGC CCAGCTGGAG TTGCAATGCA CGATCTTGGC TCACTGCAAC CTCTGCCTCC 1500
CGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCAAGTAGC TGGGATTACA GGCATGTGCC 1560
ACCACACCTG GCTAATTTTG TATTTTTAGT AGAGACAGGG TTTCTCCATG TTGGTCAGGC 1620
TAGTCTTGCA CTCCTGACCT CAGGTGATCT GCCTGCCTTG GCCTCCCAAA GTGCTGGGAT 1680
TACAGGCGTG AGCCACCACG CCCAGCCATT 1710