EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS112-04070 
Organism
Homo sapiens 
Tissue/cell
KELLY 
Coordinate
chr12:133021140-133023490 
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
AGGCCGGGGC TAGGAAACTG TGAGCCCCGC CTTGTCTGTG TCTTTCTCAG GGATTCTCGT 60
CCTTTCCAAC CTGGTGCCCG ATGTCCGGAA GCACCTCTTC TGTGTTTTCA AATGGGAGAG 120
CGAATCCAGT CCTTTTCACT CCATTTTGGC CAGAAACAGA AGTCCTCCGT GATTTATATT 180
TTTACTAGAA TCTTTTAAAG GGGCACAAAT GGGGGTGTTT TGCAGGCATA CAGAAGCCCC 240
CGTCACTCCT CCCGCCTTGT CTCTGAACCG CTGTGGGGTG GGGAGGGGTC TCTTCTCTCT 300
CCAACCCACA TCACTTTCAC CCCCCGCCGG CCAAGGCTGC GTTTCCCTCG CCCCCACCCC 360
AGTCCCCCGC GTTGGTAGTG GGATCGGTTT GGTATTCTGA GGCTTCTCTC ATTTCTCCTT 420
TATCACCATC TGCCCCACAG CAGGCAGGCC CGGAGCCTCT GCAGAAGGGG GAACCGGGTG 480
CAGGCCCAAC GCCGGTCTCT CAGTGTGGCA GCCTTGCGCG CGAGCAGAAG CAGAAGGCCT 540
AGTTCCTACT CTGCAGCCTT GGCTGCCGGG CACGGAGAAC GTTTTAGCAG AAACACCTCT 600
GCAAAACCAC TTCCTGGCCC GGGCCCAGCC AAACACCATC TTCTCCTCCA CCCCAGGGCT 660
CCGCCCCCAT CTCCAGGCTC AGCCCAGCAC CCCCACCCCC GAAACCCCCA GCCCCACTGC 720
ATCTGCCCTG GCCATCTGCC TCCGCCCTGC CTCGCTAACA CAGTTATTAA TGAGCAATTT 780
TCCTGTAATT ACAACGCAGT TATGCCAGTT ACCCCGACCT GCTGACAGAG AGCATTCACT 840
TCCATGTGGC ACTAGCCCCC AGGCCTGAGA GGACGCAAAC ACTTGCCCCT CATTCGCTGC 900
CCCCACCCCC ACTCTGCCAG CCAGCACCAC CCTCCACCCA CTCTAGGCCC TTAAGAAAGG 960
AGGGAAGGGC CGCGGGGAGG AGCTCTCAGA TCCCGAGGCC CCACTCCCCC TGCAAGGAAG 1020
GCTGTGAGCT CGGCCCCAGC CCACCTGCCA GCTCCCCAAA CACCTCCCAC CTCCCTCCGC 1080
CGCCTCCTGA AGGGACTACA CTCCCCTGGC TCCTCCAAAA TCCGCTAATG AACAGCAGGC 1140
GCAGAGGCTC CGCCACCGGC GTGCTCCTGG CCTCAGCCCT CCCTGTTCTG AAACCGCCTT 1200
TGCTAAGACG GTAGTAGTGA GGAATCACGA CAGTGGCAGA GGCCAACCTG ACCCGCTCCA 1260
CCTGCCTCCA CCCCAACCCG CCCGGCTGCT TCCTGAGCGT GGGCCAAACT AACTTTGACA 1320
GGAACTTAGT TTACAGTTTA AGTTGGGAAC AAAAAGGATA ACAGCCCCTC CCCAAAACAG 1380
ATTCCCTCCT CGCTTGGGGG GACCAGTCCC GTTGTAAAAC CGACAAATAA CAGCAGGATT 1440
AGGAATTCCG GCTCAGGATT CACGCAGCCA GACGCCACAG GACTCCTCCC CAGCCGCTCC 1500
TGTATATGAC GTCACCGCCG TAAGACCACA GGACACCGCC CCAGCCGCGC CTGTAGATGA 1560
CGTCACCATC GTAAGACCAC AGGACCCTTC CCAGCCGCTC CTGTATATGA CGTCACCGCC 1620
GTAAGACCAC AAGTCACCGC CCCAGCCGCT CCTGTAGATG ACGTCACCAC AGTAAGACCA 1680
CAGGATACCG CCCCAGCCGC GCCTGTAGAT GACGTCACCA TCGTAGGCCC ACAGGACCCT 1740
TCCCAGCCGC TCCTGTGGAT GACGTCACCG CCGTAGGACC TAAGATTGAT GCTGGAGAGG 1800
TTCTTCAGAC CCTGCGTTCT GACGGCTCCG CTGGCACCAC CCAGACGGGT AAACTAGCTC 1860
TTCCGGTCTG TGGCCCTCAC AGGAACCGAC TCGGTGCAGG AGGACAGCTT CAGCCCCTGT 1920
GATTTCATCC CCGACCAACC AGCCAGCACT CCCCACTCCC TAGCCCCCTG CCTGCCAAAC 1980
TATCTTTTAA AAAACTCCAG TTTCCAAATT TTCAGGGAGG CTGATTTGAG TAATAATAAA 2040
ACTCCAGTCT CCTGCTAGCT GGCTCTGGAT GCACTAGACT CTATTGCAAT TCTCCTGTCC 2100
TGATAAATCG GCTGTCAGGC AAGAAGAACC CGTTGGGTGG TTACAGTTTC AAGGCTATAT 2160
TCAGAGAACT ATCCACTAAT AAAATCTCTG TTTATGCAGT AGGTCCCACC CCACACCCTC 2220
CCTGCTCAAA CTGCTGCAAT CCCGGCACAG CTTTGTTGAC AATGTACCCA TCAGCCAACA 2280
AAATGTAACA AAATGCACTT TCTTTTAGTT ATCTCCTGCT ACGTAATAAA CTTCCCCGGG 2340
AGGTGGAGGT 2350