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

TagContent
EnhancerAtlas ID
HS007-16996 
Organism
Homo sapiens 
Tissue/cell
BE2C 
Coordinate
chr8:144300440-144301340 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56960668chr8144300760hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr8:144301184-144301199GAGGTCAGAAGTTCA+6.38
Nr5a2MA0505.1chr8:144300732-144300747GAGCTCAAGGTCACA+6.38
RARAMA0729.1chr8:144301184-144301202GAGGTCAGAAGTTCACGT+7.2
RREB1MA0073.1chr8:144300453-144300473ACCCCAATAACCCCCCAACA+6.02
RREB1MA0073.1chr8:144300512-144300532CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300535-144300555CTCCACACCACCCCCAACAC+6.14
RREB1MA0073.1chr8:144300465-144300485CCCCAACACCACCACCAACA+6.39
RREB1MA0073.1chr8:144300509-144300529ACCCCCAACACCACCCCCAA+6.4
RREB1MA0073.1chr8:144300511-144300531CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300463-144300483CCCCCCAACACCACCACCAA+6.81
RREB1MA0073.1chr8:144300500-144300520CCCCACACCACCCCCAACAC+7.87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8144300689144301200
Number: 1             
IDChromosomeStartEnd
GH08I143217chr8144299859144303931
Enhancer Sequence
CACCATCCCC AACACCCCAA TAACCCCCCA ACACCACCAC CAACACCACC CAACACCATG 60
CCCCACACCA CCCCCAACAC CACCCCCAAC ACCACCTCCA CACCACCCCC AACACCACCC 120
TAACACCACC TCACACCATC CCCAACACCA CTCCCAGCAG CTCACAGAGG GCTTTCTCCT 180
GGCACCCACT CAGGCTCTGA GCAGGAAGAG AGGGTATCGT GCTTAGCTGT CTACGGTGGG 240
CCCTGTCACA GCCCCCCGAG GTACGAAAGC CTGCAGCTGC GACATGAGGC TCGAGCTCAA 300
GGTCACACAG CTGGGCGGTG CAGATCCAGG ATCCAGTCCC CGGGCTTCCT GCCAACCGCA 360
CCCAGCTTCC CAGAGGTGTC CCAGGCTCCA GGACGCCTCA GCTGGGGAGG AGCTGGATGT 420
CAGCCAAGAG CCAGCCAGAT TCCCAGGCCA AGTCGAGTCT GAGCCAGGCA AGTCAGCGGT 480
GCCAACGGGC GGATGGTCAC AGCCAAGACA CCCTGGGCCC CGTCTCAGAG CCCAACGCAT 540
GCTGTCAGTC TCAAGAGTGA ACATAGAGGG ACCTCCCTTT CTCATCCAGC CCAGCAGCAG 600
GGAGACTGGG GGCTGGGGGG CTGGGCAGGG AGGGGGCAGG GCCCTGGCCC AAGAACCCAT 660
GTCCCTCTGT ACCAGTTTCC CAGGGCTGCC ATAACAAATC ACCACGAACC TAGTGACTTA 720
ACACAAGTTC ATGCTGTGGC TCTGGAGGTC AGAAGTTCAC GTCAGGGCTC TGGCTGGGCT 780
GCGTTTTCTT GGGAGAGAAT CCACCCCCGC CCTCTCAGCT TCAAGAGGCC ACCTGCTCTC 840
CTTGGCTCAT GGCCCTTCCT CCACCTTCGA AGCCGCTCCA ACCACTGCTC CCTCACCAGC 900