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

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EnhancerAtlas ID
HS048-23986 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr21:47414870-47416100 
Target genes
Number: 2             
NameEnsembl ID
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr21:47415452-47415463CCACACCCTGC+6.62
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_27212chr21:47411500-47415028Esophagus
SE_27212chr21:47415085-47416577Esophagus
SE_44233chr21:47414737-47416588NHDF-Ad
SE_46629chr21:47414671-47415058Ovary
SE_46629chr21:47415846-47416157Ovary
SE_54696chr21:47409788-47417445Stomach_Smooth_Muscle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr214741515947415200
chr214741520047415303
Number: 1             
IDChromosomeStartEnd
GH21I045994chr214741469047416297
Enhancer Sequence
CAGCTGCCCA CACACCGAGC ACAAGGCCAG ACCCTGGGCA CGGCAGCTGT CTCAGACGTC 60
CAGCAAGATG GGGCCTCAGA CCCAGGGAGA TGGGAGAGGC CGTCCCAGTG CAAGTCACAT 120
TTGTATTTCT GTGCACGAGG TGAAATCGTG CTTTTGTGGT GCCAACGGGT GTTACACAGC 180
TGTTAAAAAT ACCTGTGTCA TAGATGAGGA CCAGGGCAGG GCTTGGCAGG CGGGGTCTGG 240
GCCGTTCGTC CACCTGGTCC TGCGTGCCGC TCACGGCAGG GGCAGAAAGG GCTCCCGACA 300
CCTTCCTGGG GAAGTGCACG GCCTCAGTCT CTGATCCTCT TTGCTCTTTG AGCTCCCGGG 360
GCTCCAGCCC TGAGGATGAT CTGACCTCCC ATGTGGTCAC CCAGGACAGG GCCAGGTGCA 420
GGGCACAGTG CGTGGAAGAG GCCATGCAGC CAGTGGCAGA TTGTGGGGAG GGGACGGCCC 480
AGGGCCACGT TCCAGGCTTG GGAGGCTGCT CCAGACCTTG GTAGCTGAAA GTCTCAGTGG 540
GAATGAGCGT TCAGAGGCCA GGACTTGCTC GGAGAATTCT AACCACACCC TGCCTGTTTT 600
ATATGTTCAG TTTTCAAAGT AATCAATAGC CACTATAAGA AAAAAACAAA GCCACTTTCA 660
AAGGGTTGTG GTAAGAGGCA GTCCTGTGAG CAGGCCGGCT GCAGGGCCTC CAGGGCTGTG 720
GGGCAGGCTG CACAGGGGCT GGTGGGTCCC ATGCCTGGGG GTCTGGGAAT AGTCTCTAGG 780
CTGCTGTCCT GGAGGAGGTT TCCCCCAACG CCTGAGACCA GGGCACCATG TGACCCATGA 840
CTCACAGTTG CCTGGCTGAG GCAGGCACTT GTTCACCTGG AGCCTCCCTG GGGCCTTTCG 900
GGGCCCGGGG GTGTGGATAG GTGGCTTTGG AGCCACATTT GTCCATCGGG ACGTTGGGCT 960
CCCAGCTGGC CTTCCGGGCT TTCCCTGCTC CCAGAACCTC CCTGCTCAGC CCTTGCCAGC 1020
CTTACCCCTC CCCTCCACCC TGCCCAGCAT GGGGCTCTCC CTGTGTGGAT GCCAGAAGCA 1080
GTTGGGCCCT CAGGGCTGGT CCCAGGAGGT GCCCCCAGTG AGGTGCTCTG CAGAAACTGC 1140
CCAGTCTGGC CTCCTGCTGT CTGTGGCACA GTCTGACTGT GTGTGGTGAG GTCCAGGCCT 1200
TCTGCCTCCC ACTTACCTGG CCCAGGGCAC 1230