EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS113-37069 
Organism
Homo sapiens 
Tissue/cell
Keratinocyte 
Coordinate
chr8:144300230-144301960 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs56960668chr8144300760hg19
TF binding sites/motifs
Number: 36             
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
RREB1MA0073.1chr8:144300249-144300269CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300273-144300293CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300285-144300305CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300309-144300329CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300355-144300375CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300401-144300421CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300423-144300443CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300512-144300532CCCAACACCACCCCCAACAC+6.08
RREB1MA0073.1chr8:144300422-144300442ACCCAACACCACCCCCAACA+6.09
RREB1MA0073.1chr8:144300238-144300258CCCAACACCACCCCAACACC+6.11
RREB1MA0073.1chr8:144300413-144300433CCCAACACCACCCAACACCA+6.11
RREB1MA0073.1chr8:144300535-144300555CTCCACACCACCCCCAACAC+6.14
RREB1MA0073.1chr8:144300235-144300255ACCCCCAACACCACCCCAAC+6.18
RREB1MA0073.1chr8:144300321-144300341CCCAACACCACCCCCACACT+6.27
RREB1MA0073.1chr8:144300243-144300263CACCACCCCAACACCACCCC+6.29
RREB1MA0073.1chr8:144300343-144300363CCCCACACCAGCCCCAACAC+6.33
RREB1MA0073.1chr8:144300465-144300485CCCCAACACCACCACCAACA+6.39
RREB1MA0073.1chr8:144300282-144300302ACCCCCAACACCACCCCCAA+6.4
RREB1MA0073.1chr8:144300318-144300338ACCCCCAACACCACCCCCAC+6.4
RREB1MA0073.1chr8:144300420-144300440CCACCCAACACCACCCCCAA+6.4
RREB1MA0073.1chr8:144300509-144300529ACCCCCAACACCACCCCCAA+6.4
RREB1MA0073.1chr8:144300248-144300268CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300272-144300292CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300284-144300304CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300308-144300328CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300354-144300374CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300400-144300420CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300511-144300531CCCCAACACCACCCCCAACA+6.6
RREB1MA0073.1chr8:144300463-144300483CCCCCCAACACCACCACCAA+6.81
RREB1MA0073.1chr8:144300417-144300437ACACCACCCAACACCACCCC+6.82
RREB1MA0073.1chr8:144300410-144300430ACCCCCAACACCACCCAACA+6.98
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
ACACCACCCC CAACACCACC CCAACACCAC CCCCAACACC ATCCCCAACA CCACCCCCAA 60
CACCACCCCC AACACCATCC CCAACACCAC CCCCAACACC ACCCCCACAC TGCCCCCACA 120
CCAGCCCCAA CACCACCCCC AACACCAGCC CCAACACCAC CCCAATACCT CCCCAACACC 180
ACCCCCAACA CCACCCAACA CCACCCCCAA CACCATCCCC AACACCCCAA TAACCCCCCA 240
ACACCACCAC CAACACCACC CAACACCATG CCCCACACCA CCCCCAACAC CACCCCCAAC 300
ACCACCTCCA CACCACCCCC AACACCACCC TAACACCACC TCACACCATC CCCAACACCA 360
CTCCCAGCAG CTCACAGAGG GCTTTCTCCT GGCACCCACT CAGGCTCTGA GCAGGAAGAG 420
AGGGTATCGT GCTTAGCTGT CTACGGTGGG CCCTGTCACA GCCCCCCGAG GTACGAAAGC 480
CTGCAGCTGC GACATGAGGC TCGAGCTCAA GGTCACACAG CTGGGCGGTG CAGATCCAGG 540
ATCCAGTCCC CGGGCTTCCT GCCAACCGCA CCCAGCTTCC CAGAGGTGTC CCAGGCTCCA 600
GGACGCCTCA GCTGGGGAGG AGCTGGATGT CAGCCAAGAG CCAGCCAGAT TCCCAGGCCA 660
AGTCGAGTCT GAGCCAGGCA AGTCAGCGGT GCCAACGGGC GGATGGTCAC AGCCAAGACA 720
CCCTGGGCCC CGTCTCAGAG CCCAACGCAT GCTGTCAGTC TCAAGAGTGA ACATAGAGGG 780
ACCTCCCTTT CTCATCCAGC CCAGCAGCAG GGAGACTGGG GGCTGGGGGG CTGGGCAGGG 840
AGGGGGCAGG GCCCTGGCCC AAGAACCCAT GTCCCTCTGT ACCAGTTTCC CAGGGCTGCC 900
ATAACAAATC ACCACGAACC TAGTGACTTA ACACAAGTTC ATGCTGTGGC TCTGGAGGTC 960
AGAAGTTCAC GTCAGGGCTC TGGCTGGGCT GCGTTTTCTT GGGAGAGAAT CCACCCCCGC 1020
CCTCTCAGCT TCAAGAGGCC ACCTGCTCTC CTTGGCTCAT GGCCCTTCCT CCACCTTCGA 1080
AGCCGCTCCA ACCACTGCTC CCTCACCAGC TTCCCGAGTC AGCTCTCCCT CGGCCTCCTT 1140
CTTACAGGGA TCCTGTGACC ACAGTTAGGA CTCGCCTGGA GAATCCGGAG CCATCTCCCA 1200
TCTCAGATCC TCCGCTTCCT CATGGCTGCA AAGTCCCTTT TGCCATAGAA GGCACATTCA 1260
CAGGCTTGAG GATTTGAACC TGGGTATGTC AAAGACCTTT CCTGAGCCCA CATCAGCCCT 1320
TCCCTGGACA CCTGCTCCGA GACTAGCTGT GCTCTGGAAG CCACGGTCCT GGGGAGGATA 1380
AAGCCCAGCT CCCTGGCTCA AGGGGGCCAC AGTCCCAGGA AGGAGGCCTT GCCGGGCCCC 1440
TGGTGGCCAC AGTCCAGAAG TCAGTCCCAC AGTGGTCTCT TCCTGCCCCA GAAGAATTCA 1500
GGCCCCTTCG CCTGTGCTCA TCACGAGAAG CCGGGCAGAG GCTTGTTCTC ACTCTGTCTC 1560
TCCCGCACCC CTTGGGTCTG CCCACACCCA GGTCTCCCCG CCATCAAAAC TGACCAAGAC 1620
CAGGGTGCAG TGCCTGACTC ACTCATGGGA CAAACCCTAA CCACGCCTCC CTCCTGACTC 1680
AACTCATGGG ACAGACCCTA ACCACGCCTC CCTCCTGACT CAACTCATCG 1730