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

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EnhancerAtlas ID
HS095-19774 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr22:39630750-39631780 
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
CACATGGTTG CCTTGAAACA GGCCTGCTAT TGAAACCTCA TCTCCAAGAT CCCGACCCCC 60
ACCAGGGGTG TGGAGGGGCC GTCTGAGGGT GGGGGTGTAA AGGCTTGGAA AGAAATGGTA 120
GAAAGGCTAA ATTTGGAAGT TGCCCCATTG TGTGTGGCCA GGGGCGGCCA GTCGGGCATA 180
GGGTGGGGGT TGTGGGAGAC ATCGGGTGGG GGCCCTGGCG AACAATAGGT GGGCCCAGCT 240
GGGGCCCCCT CCTGCCTGCC TCACCGCCCC CCAGCACAGG CGGGATTGAA AGGGCCCGGG 300
AATGCTTTTG AGAGGGAGCC AGGGGCCCAA CGGGGAGAGG AAACAAAGGC AGGAAATGCT 360
GTTCCCCCGT AGATAGCGTC TGGGCAAGGA TTACAAAGTG ACAAAGAGAC AGAACCCCAG 420
AGGGAAGGGG ACCTGGGGGT GCAGGGGGGC TGCTGACCAG GGCTCCAGGG AACAGGCCAG 480
AGGTTAGAAT AGAATGGAAT TTGCTCTGAA GACAGCGTTT ATAAATACAT TGTCAATCCA 540
GCCCGCCAGC CCCGCCACGT GTGTGCCACC GAGCACGTGC CCATTCGCTG AGTGAGCTCT 600
GGGGCACGGG CAGGGCTGCC TGCTGGTCGA GGCCAGGTGT CCCCAGGGGA CCTCACAGAC 660
CGGGCCCCTA GCCAGAGGGG CGGGGAGATG ACTCCTCCAG TGCCACCCTC CCTGGCTGGG 720
CCCACACCTG GAGACATACT CGGCAGATGC CCTGGGCACC TTCTCCCCGC CCTCCCTCCT 780
CCTGGCACCC CACCCTTGGC ACCAAGCCGG AGCCACACGT GGGTGCTTCT CCTGCCACAC 840
CCCAAGTCCC AGGTACCAAC CCGCCTGCTG ACTCGGCCCT GCCCTGGATG GGTGTGGCCA 900
CGCTCTCTCT GGGCTGCCAT GGGCCTCTAG TTCTCCAGAC GTCAAGAAGG AGGGATGCCT 960
CCTGTCCTGC CCCTCCCAGA TCTCTTAAAG TCTCCTCGGA GGGCCGGAGC GCGGGGCGAG 1020
GATTCCATTT 1030