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

TagContent
EnhancerAtlas ID
HS192-09089 
Organism
Homo sapiens 
Tissue/cell
U2OS 
Coordinate
chr20:60971650-60973120 
Target genes
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ArMA0007.3chr20:60972209-60972226TGGAACATTCTGTTCCT-6.36
NR3C1MA0113.3chr20:60972209-60972226TGGAACATTCTGTTCCT+6.1
NR3C1MA0113.3chr20:60972209-60972226TGGAACATTCTGTTCCT-6.57
NR3C2MA0727.1chr20:60972209-60972226TGGAACATTCTGTTCCT+6.14
NR3C2MA0727.1chr20:60972209-60972226TGGAACATTCTGTTCCT-6.49
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr206097285960972909
Enhancer Sequence
GCAAGATGAC AATGGAGCCT CAAAACAGGC CACCAGCCCG GGTGCCGCCT TTGTGGCCAG 60
AAACCGAGTG CCGCCCGCTG TGCAGGGAAG GGCCACTCTC CAGCCCAGCG GCGCACCCAT 120
GGGCCGAGGG GCTTCCAGAG CCCATGCAGA CTGAGGCGGG GAGGAGGGGC ACCTCCTGCC 180
TTGAGAGGTT CCTGTTTTGG AGGCACTGAG CTCTTCTCTG GGGACCAGCA GCCCTGGGGG 240
ACAGGCTCCT CAGGCATAGG ATAGCACAGC ACAGCACAGC ACGCCAACCT GCCCTGCCCA 300
CCGAGGGTCG CTCGGCCCCA AGCAACACCC TGCTGGGGGC ACCACCAACT CTGACAGGCC 360
CATCCCACCC AGCGCTGCCT GAGACTGGTG CTGCCTGCCC CTCCCTGAAG CACAGCTGGG 420
CATTGGGGCA CCATGGCATG GGCAGGCGGG GTGGGCACCG GGCACCCCTT GCTCTCAGGC 480
CACCTTCCCC TGGCTTGCAG CTCCCTGCAC CAGCCACAAC CTCCCACCTC AGTGCCGTCA 540
CGGGGGCTGC TCCTCCGTCT GGAACATTCT GTTCCTGCTC TTCCAGTGGC CACCTCTTTC 600
TGAACTTTTT GGCTCATAGG TGGCCCGCTG AGGGAGGCTG CCCGGATCCT GCTATTCTGT 660
GACTTGCTCA AGGCACTGGT CACTACAGGA AGGAGGCATC CCTGCCTCAC CACCCACCTG 720
CCGTCTGCCT CCCCTTCCAG AGTGCCGGCC CCATGGATGG GGCAGGGTCT GTCCCCACTC 780
ACTGCTGTCC TTAGTGCCTG CCCTCCTGCC TGGACTTCAG GAGTCTCCCA GGTGTTTCCC 840
ATAAGCGAAA CGTGCAGGCA AATATTTGTT GGCTGAATGA CTGTACAACG CACTTCCTTG 900
AAGACCCCTC AGGGCACAAT GCCCACTGCT CCTCAGACCC TCAACACTCG GGACCAAGCG 960
AGGCCATCCT GATGCGGAGA CATGACGTGG TTCAGTAACT CTCAGGGTCA CGCAACTCCA 1020
AGTGCAGAGC TGGGTCTTGA ACCCAGGTCT GTCGGGGACT CCAAAGCTTT GTTCTCTCCC 1080
TTATACCGGG AGCCATGAAT GTGTGCCTGA GCACCAAGGC ATTCCAAAAG CACAGCTTAG 1140
GAGATAAGGT CCCATGCCAG TTGATACAAC GTTGCAGTAT TGGAAAACCA CTCCAATTGC 1200
GATGACAATG ATGGGCGATG TGGCGTGGCA CGTCTGAGGA TCCTGCCTGC CCTGCAGGGC 1260
TGTTGGCCCC CAGAAGGGAG CAGTTGGTGG TGGTGATGGC GGTGGTGGTG ATGGTGATGG 1320
CAGTGGTGAT GGTGGTGGTG GTGATGGTGG TGACGGTAGT GGTGGTGATG GTGGTGACAG 1380
TGGTGATGGC GGTGGTGGTG ATGATGGTGA TGGTTATGGC GGTGGTGGTG GTGGTGACAG 1440
TGATGGTGAT GGTGGTGATG GCGATGGTGG 1470