EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS157-04032 
Organism
Homo sapiens 
Tissue/cell
PANC-1 
Coordinate
chr12:133021300-133024090 
TF binding sites/motifs
Number: 28             
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
KLF4MA0039.3chr12:133023350-133023361CCACACCCTCC+6.32
PRDM1MA0508.2chr12:133021450-133021460TCACTTTCAC+6.02
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: 3             
ChromosomeStartEnd
chr12133021598133021727
chr12133021781133022391
chr12133021534133022956
Number: 1             
IDChromosomeStartEnd
GH12I132443chr12133020139133023744
Enhancer Sequence
AGTCCTCCGT GATTTATATT TTTACTAGAA TCTTTTAAAG GGGCACAAAT GGGGGTGTTT 60
TGCAGGCATA CAGAAGCCCC CGTCACTCCT CCCGCCTTGT CTCTGAACCG CTGTGGGGTG 120
GGGAGGGGTC TCTTCTCTCT CCAACCCACA TCACTTTCAC CCCCCGCCGG CCAAGGCTGC 180
GTTTCCCTCG CCCCCACCCC AGTCCCCCGC GTTGGTAGTG GGATCGGTTT GGTATTCTGA 240
GGCTTCTCTC ATTTCTCCTT TATCACCATC TGCCCCACAG CAGGCAGGCC CGGAGCCTCT 300
GCAGAAGGGG GAACCGGGTG CAGGCCCAAC GCCGGTCTCT CAGTGTGGCA GCCTTGCGCG 360
CGAGCAGAAG CAGAAGGCCT AGTTCCTACT CTGCAGCCTT GGCTGCCGGG CACGGAGAAC 420
GTTTTAGCAG AAACACCTCT GCAAAACCAC TTCCTGGCCC GGGCCCAGCC AAACACCATC 480
TTCTCCTCCA CCCCAGGGCT CCGCCCCCAT CTCCAGGCTC AGCCCAGCAC CCCCACCCCC 540
GAAACCCCCA GCCCCACTGC ATCTGCCCTG GCCATCTGCC TCCGCCCTGC CTCGCTAACA 600
CAGTTATTAA TGAGCAATTT TCCTGTAATT ACAACGCAGT TATGCCAGTT ACCCCGACCT 660
GCTGACAGAG AGCATTCACT TCCATGTGGC ACTAGCCCCC AGGCCTGAGA GGACGCAAAC 720
ACTTGCCCCT CATTCGCTGC CCCCACCCCC ACTCTGCCAG CCAGCACCAC CCTCCACCCA 780
CTCTAGGCCC TTAAGAAAGG AGGGAAGGGC CGCGGGGAGG AGCTCTCAGA TCCCGAGGCC 840
CCACTCCCCC TGCAAGGAAG GCTGTGAGCT CGGCCCCAGC CCACCTGCCA GCTCCCCAAA 900
CACCTCCCAC CTCCCTCCGC CGCCTCCTGA AGGGACTACA CTCCCCTGGC TCCTCCAAAA 960
TCCGCTAATG AACAGCAGGC GCAGAGGCTC CGCCACCGGC GTGCTCCTGG CCTCAGCCCT 1020
CCCTGTTCTG AAACCGCCTT TGCTAAGACG GTAGTAGTGA GGAATCACGA CAGTGGCAGA 1080
GGCCAACCTG ACCCGCTCCA CCTGCCTCCA CCCCAACCCG CCCGGCTGCT TCCTGAGCGT 1140
GGGCCAAACT AACTTTGACA GGAACTTAGT TTACAGTTTA AGTTGGGAAC AAAAAGGATA 1200
ACAGCCCCTC CCCAAAACAG ATTCCCTCCT CGCTTGGGGG GACCAGTCCC GTTGTAAAAC 1260
CGACAAATAA CAGCAGGATT AGGAATTCCG GCTCAGGATT CACGCAGCCA GACGCCACAG 1320
GACTCCTCCC CAGCCGCTCC TGTATATGAC GTCACCGCCG TAAGACCACA GGACACCGCC 1380
CCAGCCGCGC CTGTAGATGA CGTCACCATC GTAAGACCAC AGGACCCTTC CCAGCCGCTC 1440
CTGTATATGA CGTCACCGCC GTAAGACCAC AAGTCACCGC CCCAGCCGCT CCTGTAGATG 1500
ACGTCACCAC AGTAAGACCA CAGGATACCG CCCCAGCCGC GCCTGTAGAT GACGTCACCA 1560
TCGTAGGCCC ACAGGACCCT TCCCAGCCGC TCCTGTGGAT GACGTCACCG CCGTAGGACC 1620
TAAGATTGAT GCTGGAGAGG TTCTTCAGAC CCTGCGTTCT GACGGCTCCG CTGGCACCAC 1680
CCAGACGGGT AAACTAGCTC TTCCGGTCTG TGGCCCTCAC AGGAACCGAC TCGGTGCAGG 1740
AGGACAGCTT CAGCCCCTGT GATTTCATCC CCGACCAACC AGCCAGCACT CCCCACTCCC 1800
TAGCCCCCTG CCTGCCAAAC TATCTTTTAA AAAACTCCAG TTTCCAAATT TTCAGGGAGG 1860
CTGATTTGAG TAATAATAAA ACTCCAGTCT CCTGCTAGCT GGCTCTGGAT GCACTAGACT 1920
CTATTGCAAT TCTCCTGTCC TGATAAATCG GCTGTCAGGC AAGAAGAACC CGTTGGGTGG 1980
TTACAGTTTC AAGGCTATAT TCAGAGAACT ATCCACTAAT AAAATCTCTG TTTATGCAGT 2040
AGGTCCCACC CCACACCCTC CCTGCTCAAA CTGCTGCAAT CCCGGCACAG CTTTGTTGAC 2100
AATGTACCCA TCAGCCAACA AAATGTAACA AAATGCACTT TCTTTTAGTT ATCTCCTGCT 2160
ACGTAATAAA CTTCCCCGGG AGGTGGAGGT TGCCATGAGC CGAGATTGCA CCATTGCACT 2220
CCAGCCTGGG CAACAAGAGC AAGACTCCGT CTCAAAAATA AATAAATAAA TAAATAAATA 2280
AGCCTCCCCG GAGCTTGATG GCCTAAATAG CAATCTACCG TGAGTGCTCA GGGCTCTGGA 2340
GTTGACTGGG CTGCGCTGGG TGCTTCCTGC CTAGGGTCTC CAGTGTGGTT GCAGCAAATG 2400
CAGGCTGGAG CTGTCCAGCA TCTCTTTCTG AGTAGCCTCT CCACGCTCAG CTTGGACCCC 2460
CTCACAGCAT GGCTGCCAGG GTCATCAAGC TTCTTGGCAG GCAGCTGGCC TCCCCTAGGA 2520
CAAATCCCAC AAAGCTGAGG CAGGAGTTCC AGGGCTACTA AGACGCCGTC TCAGAGTCAC 2580
AGTCTGCCAC CTCCAGCTCA TGCCACTGGC TACACAGGCC CAGAGTCCGT GCGTCTGGGG 2640
AGGCACCATC CTGAGAAGCC ATCTTACGAG TGAGAAGTGG GTGCCAGGAA ATGGGGTGCC 2700
ACCATGATTA GCACCCCAAA TATGTGCTGT CACCTTTGGA GTCACGCAGA ACCTGGGGGC 2760
CTCCAGGAGT CTACGGGGGA TGGTGGGAAG 2790