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

TagContent
EnhancerAtlas ID
HS139-00384 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr1:11399340-11400790 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
LBX2MA0699.1chr1:11399704-11399714GCTAATTGGC-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11139954611400529
Number: 1             
IDChromosomeStartEnd
GH01I011339chr11139926811400731
Enhancer Sequence
CAATCGCCAA TGAACAATGA GACAGCGTGG GGGTGAGACG GGAGGACACA CCGGGAGGGG 60
CGCAAGAAAT GCCAGAGGCA GGAGACAGAT GGGTCCAAGG GCCAGAGAGC CTGCTCCAGT 120
GGCTCCTCGG AGTGAGATGG GTCAGAGAGG GAGGCAGGAG ACCAGAAAAT ACCAAGGAAG 180
AAAAATCTAA GGTAAGGGAG ACCAAGAAAG AAAGAAGAAG GAGTCAGACG TGCAGCTGCA 240
GGGACAAAGA CACATAAACC GGGGGTGAGA GAGACAGAGT GAGAGTTGCC TCCAGCTGGG 300
GCTGGGTGGG GAACTTAGTT CCCACCAGGG TTGTGGACTT GGGAGCTTGC TTGCGGGGAG 360
GAGGGCTAAT TGGCGATTTC ATCCAGGTCC TCCAGAACGT CTGCAGAAAA ACAAACCCGC 420
TAAACATCTC TCACCGTCTG TCATCTTCAT TTTGCTTTTG TCTTCAGAAT AAAGAGAATC 480
TGAAACTCCC TAGGAGAAGC GGCTCCAGCG GCTCTCAGGC TGTCTCCCGT TCTGCTCCTT 540
CTTCATGCTT TTCTGGTTGG AGTCTTTGTT CCGCAGCTTC TTGCCCTGGT TCAGGCTGGC 600
GGCTGCTCTG ACCCGGCGTG CTGGGGTCTC CATCCCCATC TCTGTCACAC TGTGGTCTGG 660
AGTGTCTGGG TCTCTTGCTC CCCTCCCCCT CCCCCCAGGC TCAGCCTGAG CCACCCCACC 720
CCCCTTGGCC CGCGTGGCCG CTGCTGATCC TTGCTACTCC CAGCTGTCTC CGTGGCTCAG 780
CCTGCAGATT GACAGGGCCC ATAAATCACC GTGGCAAGGC AGGGCCCTGG GAAAGGAACA 840
CGGGGCCAGG TGCTGACAGG GCTGGCCTTG GGAGCTGGGG CTTTCGGCTT TCTGGTGAAT 900
CGCTGGGGCG TGGAGCCTGT GGCTTCTCTC CCAGCTAAAT GGAGCATTTT GGTTGCAGTG 960
CCTGTGTCTC CTGCCGATTT TCTCCAGCTC CCTGGAAGGT GGGACAAGAA GAAATAGGTT 1020
GAATGTGAAG CAAGTGGGAT TCGGGTTAGA CTGAAAAGAA GAATTTGCAG TGATGAGGCT 1080
TAACTTTGGA AAGAGGAAAC ACTGGGATGG GAAATGGTGA AACCCCTTGG CAAGGAGTTG 1140
GTAAAATCTG GATGGATTCT GTCTGATGAT TTATAGTGCT GCCTGGAGAC AGGGGAATGA 1200
AACATATGAT CCACTCGACA CAGAAGCCTT TGCTTTGTTT GAGGGGAGCC CGGGGGCCAG 1260
GAGAGCAAAG AAGTTACCAG TGGGGGCTTG GGGAACATGC AGCTCCCCTC CTGACCTGCT 1320
GTGTGATCCT GAGCAAGTGA CTCAACCTGG CTGGTCTCTA TCTGTAAAAT GGGGATAGTC 1380
CCACTTCGTA GACTTACCAT GAAGCTTAAA GGGCAGTGTA TGCAAAGGGC TCTGCACAGT 1440
GCTTGGCACA 1450