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

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EnhancerAtlas ID
HS053-25942 
Organism
Homo sapiens 
Tissue/cell
Foreskin_keratinocyte 
Coordinate
chr22:39630920-39631780 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr22:39631638-39631649TGGGTGTGGCC-6.62
PLAG1MA0163.1chr22:39631071-39631085GGGGCCCAACGGGG+6.59
ZNF263MA0528.1chr22:39631507-39631528ACCTTCTCCCCGCCCTCCCTC-6.27
ZNF263MA0528.1chr22:39631511-39631532TCTCCCCGCCCTCCCTCCTCC-8.37
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_30056chr22:39628747-39634686Fetal_Muscle
SE_32163chr22:39629962-39634400Gastric
SE_38289chr22:39629153-39634033HUVEC
SE_41218chr22:39628660-39642490Left_Ventricle
SE_42330chr22:39628660-39642412Lung
SE_47425chr22:39630056-39638428Panc1
SE_48326chr22:39628720-39642328Psoas_Muscle
SE_48924chr22:39628682-39643679Right_Atrium
SE_49743chr22:39629800-39633271Right_Ventricle
SE_51377chr22:39628592-39638387Skeletal_Muscle
SE_65688chr22:39629876-39631974Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr223963124439631333
Enhancer Sequence
GTCGGGCATA GGGTGGGGGT TGTGGGAGAC ATCGGGTGGG GGCCCTGGCG AACAATAGGT 60
GGGCCCAGCT GGGGCCCCCT CCTGCCTGCC TCACCGCCCC CCAGCACAGG CGGGATTGAA 120
AGGGCCCGGG AATGCTTTTG AGAGGGAGCC AGGGGCCCAA CGGGGAGAGG AAACAAAGGC 180
AGGAAATGCT GTTCCCCCGT AGATAGCGTC TGGGCAAGGA TTACAAAGTG ACAAAGAGAC 240
AGAACCCCAG AGGGAAGGGG ACCTGGGGGT GCAGGGGGGC TGCTGACCAG GGCTCCAGGG 300
AACAGGCCAG AGGTTAGAAT AGAATGGAAT TTGCTCTGAA GACAGCGTTT ATAAATACAT 360
TGTCAATCCA GCCCGCCAGC CCCGCCACGT GTGTGCCACC GAGCACGTGC CCATTCGCTG 420
AGTGAGCTCT GGGGCACGGG CAGGGCTGCC TGCTGGTCGA GGCCAGGTGT CCCCAGGGGA 480
CCTCACAGAC CGGGCCCCTA GCCAGAGGGG CGGGGAGATG ACTCCTCCAG TGCCACCCTC 540
CCTGGCTGGG CCCACACCTG GAGACATACT CGGCAGATGC CCTGGGCACC TTCTCCCCGC 600
CCTCCCTCCT CCTGGCACCC CACCCTTGGC ACCAAGCCGG AGCCACACGT GGGTGCTTCT 660
CCTGCCACAC CCCAAGTCCC AGGTACCAAC CCGCCTGCTG ACTCGGCCCT GCCCTGGATG 720
GGTGTGGCCA CGCTCTCTCT GGGCTGCCAT GGGCCTCTAG TTCTCCAGAC GTCAAGAAGG 780
AGGGATGCCT CCTGTCCTGC CCCTCCCAGA TCTCTTAAAG TCTCCTCGGA GGGCCGGAGC 840
GCGGGGCGAG GATTCCATTT 860