EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS087-05645 
Organism
Homo sapiens 
Tissue/cell
HEK293T 
Coordinate
chr12:133021600-133023180 
TF binding sites/motifs
Number: 26             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ATF3MA0605.2chr12:133022695-133022707GATGACGTCACC+6.74
ATF3MA0605.2chr12:133022796-133022808GATGACGTCACC+6.74
ATF3MA0605.2chr12:133022847-133022859GATGACGTCACC+6.74
ATF3MA0605.2chr12:133022897-133022909GATGACGTCACC+6.74
ATF3MA0605.2chr12:133022695-133022707GATGACGTCACC-6.92
ATF3MA0605.2chr12:133022796-133022808GATGACGTCACC-6.92
ATF3MA0605.2chr12:133022847-133022859GATGACGTCACC-6.92
ATF3MA0605.2chr12:133022897-133022909GATGACGTCACC-6.92
CREB1MA0018.3chr12:133022644-133022656TATGACGTCACC+6.02
CREB1MA0018.3chr12:133022745-133022757TATGACGTCACC+6.02
CREB1MA0018.3chr12:133022644-133022656TATGACGTCACC-6.02
CREB1MA0018.3chr12:133022745-133022757TATGACGTCACC-6.02
CREB1MA0018.3chr12:133022695-133022707GATGACGTCACC+6.74
CREB1MA0018.3chr12:133022796-133022808GATGACGTCACC+6.74
CREB1MA0018.3chr12:133022847-133022859GATGACGTCACC+6.74
CREB1MA0018.3chr12:133022897-133022909GATGACGTCACC+6.74
CREB1MA0018.3chr12:133022695-133022707GATGACGTCACC-6.74
CREB1MA0018.3chr12:133022796-133022808GATGACGTCACC-6.74
CREB1MA0018.3chr12:133022847-133022859GATGACGTCACC-6.74
CREB1MA0018.3chr12:133022897-133022909GATGACGTCACC-6.74
JDP2(var.2)MA0656.1chr12:133022644-133022656TATGACGTCACC+6.14
JDP2(var.2)MA0656.1chr12:133022745-133022757TATGACGTCACC+6.14
JDP2(var.2)MA0656.1chr12:133022695-133022707GATGACGTCACC+6.92
JDP2(var.2)MA0656.1chr12:133022796-133022808GATGACGTCACC+6.92
JDP2(var.2)MA0656.1chr12:133022847-133022859GATGACGTCACC+6.92
JDP2(var.2)MA0656.1chr12:133022897-133022909GATGACGTCACC+6.92
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_10775chr12:133020028-133023469CD19_Primary
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12133021781133022391
Number: 1             
IDChromosomeStartEnd
GH12I132443chr12133020139133023744
Enhancer Sequence
GCAGAAGGGG GAACCGGGTG CAGGCCCAAC GCCGGTCTCT CAGTGTGGCA GCCTTGCGCG 60
CGAGCAGAAG CAGAAGGCCT AGTTCCTACT CTGCAGCCTT GGCTGCCGGG CACGGAGAAC 120
GTTTTAGCAG AAACACCTCT GCAAAACCAC TTCCTGGCCC GGGCCCAGCC AAACACCATC 180
TTCTCCTCCA CCCCAGGGCT CCGCCCCCAT CTCCAGGCTC AGCCCAGCAC CCCCACCCCC 240
GAAACCCCCA GCCCCACTGC ATCTGCCCTG GCCATCTGCC TCCGCCCTGC CTCGCTAACA 300
CAGTTATTAA TGAGCAATTT TCCTGTAATT ACAACGCAGT TATGCCAGTT ACCCCGACCT 360
GCTGACAGAG AGCATTCACT TCCATGTGGC ACTAGCCCCC AGGCCTGAGA GGACGCAAAC 420
ACTTGCCCCT CATTCGCTGC CCCCACCCCC ACTCTGCCAG CCAGCACCAC CCTCCACCCA 480
CTCTAGGCCC TTAAGAAAGG AGGGAAGGGC CGCGGGGAGG AGCTCTCAGA TCCCGAGGCC 540
CCACTCCCCC TGCAAGGAAG GCTGTGAGCT CGGCCCCAGC CCACCTGCCA GCTCCCCAAA 600
CACCTCCCAC CTCCCTCCGC CGCCTCCTGA AGGGACTACA CTCCCCTGGC TCCTCCAAAA 660
TCCGCTAATG AACAGCAGGC GCAGAGGCTC CGCCACCGGC GTGCTCCTGG CCTCAGCCCT 720
CCCTGTTCTG AAACCGCCTT TGCTAAGACG GTAGTAGTGA GGAATCACGA CAGTGGCAGA 780
GGCCAACCTG ACCCGCTCCA CCTGCCTCCA CCCCAACCCG CCCGGCTGCT TCCTGAGCGT 840
GGGCCAAACT AACTTTGACA GGAACTTAGT TTACAGTTTA AGTTGGGAAC AAAAAGGATA 900
ACAGCCCCTC CCCAAAACAG ATTCCCTCCT CGCTTGGGGG GACCAGTCCC GTTGTAAAAC 960
CGACAAATAA CAGCAGGATT AGGAATTCCG GCTCAGGATT CACGCAGCCA GACGCCACAG 1020
GACTCCTCCC CAGCCGCTCC TGTATATGAC GTCACCGCCG TAAGACCACA GGACACCGCC 1080
CCAGCCGCGC CTGTAGATGA CGTCACCATC GTAAGACCAC AGGACCCTTC CCAGCCGCTC 1140
CTGTATATGA CGTCACCGCC GTAAGACCAC AAGTCACCGC CCCAGCCGCT CCTGTAGATG 1200
ACGTCACCAC AGTAAGACCA CAGGATACCG CCCCAGCCGC GCCTGTAGAT GACGTCACCA 1260
TCGTAGGCCC ACAGGACCCT TCCCAGCCGC TCCTGTGGAT GACGTCACCG CCGTAGGACC 1320
TAAGATTGAT GCTGGAGAGG TTCTTCAGAC CCTGCGTTCT GACGGCTCCG CTGGCACCAC 1380
CCAGACGGGT AAACTAGCTC TTCCGGTCTG TGGCCCTCAC AGGAACCGAC TCGGTGCAGG 1440
AGGACAGCTT CAGCCCCTGT GATTTCATCC CCGACCAACC AGCCAGCACT CCCCACTCCC 1500
TAGCCCCCTG CCTGCCAAAC TATCTTTTAA AAAACTCCAG TTTCCAAATT TTCAGGGAGG 1560
CTGATTTGAG TAATAATAAA 1580