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

TagContent
EnhancerAtlas ID
HS139-14434 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr13:26759880-26761070 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs509915chr1326759884hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr13:26760361-26760382AAAAGAGAAGTGAAAGCAAGC-6.18
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr132676020026760326
chr132676053126760858
Number: 1             
IDChromosomeStartEnd
GH13I026185chr132675959126762164
Enhancer Sequence
CTCAAAAAAA AGTTGTTACT TAAAGTAATG CATTGTCAAC AGAAGTGTAG AGGCCATGAT 60
TCTAAACTTG TGTTCTCTAC GCCTAACTAC GAACCTTGTG CCTTTCCAAA ACCAAAGGTC 120
ACACTTCTGG AAAGTTCCTT CCTCCCTCAC ATTCAATATC TATTTAGAGA ACACACACTA 180
TGTCCTAGCT TCTGCTAGGT TCTGAAAATA CAGTAAGAGG CAAAAGAGCC ATAGCCCCTC 240
CCACCCCGTG CCCTTATGAA ACTTGCAGTC TACATAAACA TAGATATGAA ACAAACACAA 300
AATGTATGTT TTAACCCTAA AATGCGATAG GGAAGCCAGT CAGACGATTT ACTCGGGAGT 360
AAGAATTCAG GTCATTCACC AAGGCGCCCA TGTCAAAGCT TCATCACCCG CCTCGCGGCC 420
CTAAAACGTG TCAGAGTCAT GATACACACA ACGCAGAGGA AAAGTTCAAA AACAGATCTT 480
AAAAAGAGAA GTGAAAGCAA GCGATCAAAA CATTTCTGGA AATCTGACAC ATCTGGAGTG 540
CCGTGTGGAG ACGCCAGGGC GCGTGGAGCT TTGAGCAGTT AAAAACCCAG ACCGGGAGGC 600
CAGTGCGTGT GTAAGACCGC GTTTCTCTGC AAGGCTGTCC CGCGGCAGGA ACGCGCTCGT 660
TGGGCCGCAG AGCAAGAGCG GGACGCGCCG GGGGGCGTCT GCGTGGCACG TGGGCCCCGC 720
AGCCAGTCGC GCTACCGACT GGCAGTCAGC GGAGACGCTT CGGAGCAGGT CTGTTAGGGC 780
GCGCGCACAC ACATGCACGT GCACGAGCGC ACGTACACGC GCACACCGCC AGCGCGGACC 840
CTGACGGGGC CGAGCCTCGG AATTGGGCCT CCTCGGCCGC CGTCGTCTTC TCAGCTCTCA 900
CAGGGCCCGC AGCGGCGCTA TACCTTCGGC CACAGGTAGC GCGTTCCTTC GCTGTGCTGA 960
CCGTCGATCC CGGGGGCGCT AGAGCGCCGG CTCCGGGGAG GGCAGGGAAG CGTCAGGGAC 1020
CTTTCTTCTT CTTTTTTTTT TTTTCTTTTT TTGAGACGGA GTCTCGTTCT GTCGCCCAGG 1080
CTGGAGTGTA GTGGCGCGAT CTCGGCTCAC TGCAATTTCC GCCTCCCAGG TTCACGCCAT 1140
TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ACTACAGGCG CCCGCCACCA 1190