EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS161-04214 
Organism
Homo sapiens 
Tissue/cell
PC3 
Coordinate
chr12:133020720-133023740 
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
CATTCCTGCA CCTTTTTCTG GCGTGCGGTT CAGTTACATG GAAAAGGTTT GGCCTCTCAG 60
GTCTTATTTT AAAGTGGCCG TCAGGGCCGA ATGTTCTGCC CATTTTGTCC ACACTAATTA 120
TCCCTCTTTG GGGAGCAAGA CCCTTGTGAG ATGCCACCGC CACCCTCGGG AGGCCTCCAG 180
GCTGGGGGAC GGGCACTGTG GGCTGCTGGT GTAGGGCCGG ACGCTCTCTG ACAGTGTTGC 240
CCCTGGCCTC CGGCGGCTTC CTCCCAAGCT GGGTTGGGGC TCTTCTGAAC GCTCCCCTCC 300
ATGCCCTGTC CTGGGAACTT TAACCCTCTG GGCCTCCCGG AGCCCTCTGT CTCCCCTGTC 360
CCAGGGGGTC TGCTGGGCTC CACCGGGCCC CGCCCTGAAT GCAGCCTGGA GCAACGCTGG 420
AGGCCGGGGC TAGGAAACTG TGAGCCCCGC CTTGTCTGTG TCTTTCTCAG GGATTCTCGT 480
CCTTTCCAAC CTGGTGCCCG ATGTCCGGAA GCACCTCTTC TGTGTTTTCA AATGGGAGAG 540
CGAATCCAGT CCTTTTCACT CCATTTTGGC CAGAAACAGA AGTCCTCCGT GATTTATATT 600
TTTACTAGAA TCTTTTAAAG GGGCACAAAT GGGGGTGTTT TGCAGGCATA CAGAAGCCCC 660
CGTCACTCCT CCCGCCTTGT CTCTGAACCG CTGTGGGGTG GGGAGGGGTC TCTTCTCTCT 720
CCAACCCACA TCACTTTCAC CCCCCGCCGG CCAAGGCTGC GTTTCCCTCG CCCCCACCCC 780
AGTCCCCCGC GTTGGTAGTG GGATCGGTTT GGTATTCTGA GGCTTCTCTC ATTTCTCCTT 840
TATCACCATC TGCCCCACAG CAGGCAGGCC CGGAGCCTCT GCAGAAGGGG GAACCGGGTG 900
CAGGCCCAAC GCCGGTCTCT CAGTGTGGCA GCCTTGCGCG CGAGCAGAAG CAGAAGGCCT 960
AGTTCCTACT CTGCAGCCTT GGCTGCCGGG CACGGAGAAC GTTTTAGCAG AAACACCTCT 1020
GCAAAACCAC TTCCTGGCCC GGGCCCAGCC AAACACCATC TTCTCCTCCA CCCCAGGGCT 1080
CCGCCCCCAT CTCCAGGCTC AGCCCAGCAC CCCCACCCCC GAAACCCCCA GCCCCACTGC 1140
ATCTGCCCTG GCCATCTGCC TCCGCCCTGC CTCGCTAACA CAGTTATTAA TGAGCAATTT 1200
TCCTGTAATT ACAACGCAGT TATGCCAGTT ACCCCGACCT GCTGACAGAG AGCATTCACT 1260
TCCATGTGGC ACTAGCCCCC AGGCCTGAGA GGACGCAAAC ACTTGCCCCT CATTCGCTGC 1320
CCCCACCCCC ACTCTGCCAG CCAGCACCAC CCTCCACCCA CTCTAGGCCC TTAAGAAAGG 1380
AGGGAAGGGC CGCGGGGAGG AGCTCTCAGA TCCCGAGGCC CCACTCCCCC TGCAAGGAAG 1440
GCTGTGAGCT CGGCCCCAGC CCACCTGCCA GCTCCCCAAA CACCTCCCAC CTCCCTCCGC 1500
CGCCTCCTGA AGGGACTACA CTCCCCTGGC TCCTCCAAAA TCCGCTAATG AACAGCAGGC 1560
GCAGAGGCTC CGCCACCGGC GTGCTCCTGG CCTCAGCCCT CCCTGTTCTG AAACCGCCTT 1620
TGCTAAGACG GTAGTAGTGA GGAATCACGA CAGTGGCAGA GGCCAACCTG ACCCGCTCCA 1680
CCTGCCTCCA CCCCAACCCG CCCGGCTGCT TCCTGAGCGT GGGCCAAACT AACTTTGACA 1740
GGAACTTAGT TTACAGTTTA AGTTGGGAAC AAAAAGGATA ACAGCCCCTC CCCAAAACAG 1800
ATTCCCTCCT CGCTTGGGGG GACCAGTCCC GTTGTAAAAC CGACAAATAA CAGCAGGATT 1860
AGGAATTCCG GCTCAGGATT CACGCAGCCA GACGCCACAG GACTCCTCCC CAGCCGCTCC 1920
TGTATATGAC GTCACCGCCG TAAGACCACA GGACACCGCC CCAGCCGCGC CTGTAGATGA 1980
CGTCACCATC GTAAGACCAC AGGACCCTTC CCAGCCGCTC CTGTATATGA CGTCACCGCC 2040
GTAAGACCAC AAGTCACCGC CCCAGCCGCT CCTGTAGATG ACGTCACCAC AGTAAGACCA 2100
CAGGATACCG CCCCAGCCGC GCCTGTAGAT GACGTCACCA TCGTAGGCCC ACAGGACCCT 2160
TCCCAGCCGC TCCTGTGGAT GACGTCACCG CCGTAGGACC TAAGATTGAT GCTGGAGAGG 2220
TTCTTCAGAC CCTGCGTTCT GACGGCTCCG CTGGCACCAC CCAGACGGGT AAACTAGCTC 2280
TTCCGGTCTG TGGCCCTCAC AGGAACCGAC TCGGTGCAGG AGGACAGCTT CAGCCCCTGT 2340
GATTTCATCC CCGACCAACC AGCCAGCACT CCCCACTCCC TAGCCCCCTG CCTGCCAAAC 2400
TATCTTTTAA AAAACTCCAG TTTCCAAATT TTCAGGGAGG CTGATTTGAG TAATAATAAA 2460
ACTCCAGTCT CCTGCTAGCT GGCTCTGGAT GCACTAGACT CTATTGCAAT TCTCCTGTCC 2520
TGATAAATCG GCTGTCAGGC AAGAAGAACC CGTTGGGTGG TTACAGTTTC AAGGCTATAT 2580
TCAGAGAACT ATCCACTAAT AAAATCTCTG TTTATGCAGT AGGTCCCACC CCACACCCTC 2640
CCTGCTCAAA CTGCTGCAAT CCCGGCACAG CTTTGTTGAC AATGTACCCA TCAGCCAACA 2700
AAATGTAACA AAATGCACTT TCTTTTAGTT ATCTCCTGCT ACGTAATAAA CTTCCCCGGG 2760
AGGTGGAGGT TGCCATGAGC CGAGATTGCA CCATTGCACT CCAGCCTGGG CAACAAGAGC 2820
AAGACTCCGT CTCAAAAATA AATAAATAAA TAAATAAATA AGCCTCCCCG GAGCTTGATG 2880
GCCTAAATAG CAATCTACCG TGAGTGCTCA GGGCTCTGGA GTTGACTGGG CTGCGCTGGG 2940
TGCTTCCTGC CTAGGGTCTC CAGTGTGGTT GCAGCAAATG CAGGCTGGAG CTGTCCAGCA 3000
TCTCTTTCTG AGTAGCCTCT 3020