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

TagContent
EnhancerAtlas ID
HS139-15881 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr13:113768640-113769970 
Target genes
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs569557chr13113769917hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF2MA0051.1chr13:113769636-113769654ATTGGACTTTCACTTTCC-6.03
ZNF263MA0528.1chr13:113769291-113769312GGAGGAGGCTGAAGAGAGAGG+6.62
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr13113769612113769662
Enhancer Sequence
GGTTTGTTTT TTTTTTAACC ATCTGAATAT TAAATTATCA CAAAGTTTGA GGCCCCCAAC 60
CTCCCTTGGG TTCAGTAATT CACTAGAAGG ACTCATAGAA TCCACTGAAG TGGATACACT 120
CACAGGTACC GTTTATTACA GCAAAGGATG CAGGCTTAAG TCTGCAGAGG GACCAGGCAC 180
AAGCTTCCCC TTGTCCTCTC CCTGTGGGGT CATGTGGACA GTCCTTAATT CTCCCAGAAT 240
GACGTGTGAC GAGACGTGGG AAGTACTGCC AACTTGGGAA GCTCTACGAG CCCCGGTGTC 300
CAGAGGTTTT ATCAGGGCTC AATCACATAG ACCCAGCTGA CCACCCGCAT GGCTGACCTC 360
AGTCTCAGCC CCTCCAGAGG CTACGCCGAT AGTGCGGCCC AAGGCCCCAC CATACATCAC 420
ATTGTCAGCT AGACCATCCA GCATGGCTCA AGGCCCAGGT AAACACCAAC ATTCCCTCAG 480
GCAAGACCTT CCAAGGGCTT AGCGGTCATT TCCCAGGAGC CAAGGCAAAG GCTACCCTTT 540
CTCTGGCACA GCAGTTCATC CTTGACCACC CAAGACCACA TTCTTACACT GAATGAGCTC 600
TCCTGTGCAG CAGCCATTTT CTTCTCTAAG CAGAAGAGAG CCCAGCAAGC TGGAGGAGGC 660
TGAAGAGAGA GGCTTCCTGC TGGTCATCTG GGTCCAGAAT GCCTGGAGAT CTCTGCTCAG 720
CCCTGGTGCC CAGCAGCCCT GGTGTGCATC CTGCAGGGCA GGCCTTCCCG CCGGAGTCCT 780
GGACTTGCTC AGGGCCACTC CCCTTGCCCA TGTCAACCAA AGTCAGGCTG CCGGTTCTGC 840
TTCTTCTGTC TGAGCCCATG ACCAGTGCTG GGACTAACTG TCCCCAGGCG GGCTCACGGT 900
GGTACGAGGC CAGCTTGGAG AACTGTCTCA GCTCTCTGGT CCTCTCGTCA GTTGGGTCTC 960
TGATTGGAAA GTCCCTTGGA CACTTTTACC ATCCCCATTG GACTTTCACT TTCCCCCAGG 1020
CTCCCATCAG CTGCTCGGAA GAGTGGTCAC CCTGGAGGCC ACTGCCCACC AGCCAGGCAC 1080
CCCCCAAATG CAACCGCAGC CAGCACTGCC AGCCACTGGC AAGGCTGTTC AGACATGTGG 1140
CTCCTCTGAT CCACGCCTTG TCCTTTGGAT CAGTCCACGG AGCAGGTGGT GCCAAGCTCA 1200
GGCTCTGTCA CCCACAGCTC AGTGCCACCT TCCAGGCAGA ACACCACTGC TGACCCAGGG 1260
CATGGCCACC CCGGGGGCTG GCTCTCGCTG ACCCCCAGAA GCCCCTCTCA GGGTGTCCCC 1320
TTCCTGTCCC 1330