EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS042-11907 
Organism
Homo sapiens 
Tissue/cell
Fetal_brain 
Coordinate
chr12:133020710-133023380 
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
TATGTGGAAA CATTCCTGCA CCTTTTTCTG GCGTGCGGTT CAGTTACATG GAAAAGGTTT 60
GGCCTCTCAG GTCTTATTTT AAAGTGGCCG TCAGGGCCGA ATGTTCTGCC CATTTTGTCC 120
ACACTAATTA TCCCTCTTTG GGGAGCAAGA CCCTTGTGAG ATGCCACCGC CACCCTCGGG 180
AGGCCTCCAG GCTGGGGGAC GGGCACTGTG GGCTGCTGGT GTAGGGCCGG ACGCTCTCTG 240
ACAGTGTTGC CCCTGGCCTC CGGCGGCTTC CTCCCAAGCT GGGTTGGGGC TCTTCTGAAC 300
GCTCCCCTCC ATGCCCTGTC CTGGGAACTT TAACCCTCTG GGCCTCCCGG AGCCCTCTGT 360
CTCCCCTGTC CCAGGGGGTC TGCTGGGCTC CACCGGGCCC CGCCCTGAAT GCAGCCTGGA 420
GCAACGCTGG AGGCCGGGGC TAGGAAACTG TGAGCCCCGC CTTGTCTGTG TCTTTCTCAG 480
GGATTCTCGT CCTTTCCAAC CTGGTGCCCG ATGTCCGGAA GCACCTCTTC TGTGTTTTCA 540
AATGGGAGAG CGAATCCAGT CCTTTTCACT CCATTTTGGC CAGAAACAGA AGTCCTCCGT 600
GATTTATATT TTTACTAGAA TCTTTTAAAG GGGCACAAAT GGGGGTGTTT TGCAGGCATA 660
CAGAAGCCCC CGTCACTCCT CCCGCCTTGT CTCTGAACCG CTGTGGGGTG GGGAGGGGTC 720
TCTTCTCTCT CCAACCCACA TCACTTTCAC CCCCCGCCGG CCAAGGCTGC GTTTCCCTCG 780
CCCCCACCCC AGTCCCCCGC GTTGGTAGTG GGATCGGTTT GGTATTCTGA GGCTTCTCTC 840
ATTTCTCCTT TATCACCATC TGCCCCACAG CAGGCAGGCC CGGAGCCTCT GCAGAAGGGG 900
GAACCGGGTG CAGGCCCAAC GCCGGTCTCT CAGTGTGGCA GCCTTGCGCG CGAGCAGAAG 960
CAGAAGGCCT AGTTCCTACT CTGCAGCCTT GGCTGCCGGG CACGGAGAAC GTTTTAGCAG 1020
AAACACCTCT GCAAAACCAC TTCCTGGCCC GGGCCCAGCC AAACACCATC TTCTCCTCCA 1080
CCCCAGGGCT CCGCCCCCAT CTCCAGGCTC AGCCCAGCAC CCCCACCCCC GAAACCCCCA 1140
GCCCCACTGC ATCTGCCCTG GCCATCTGCC TCCGCCCTGC CTCGCTAACA CAGTTATTAA 1200
TGAGCAATTT TCCTGTAATT ACAACGCAGT TATGCCAGTT ACCCCGACCT GCTGACAGAG 1260
AGCATTCACT TCCATGTGGC ACTAGCCCCC AGGCCTGAGA GGACGCAAAC ACTTGCCCCT 1320
CATTCGCTGC CCCCACCCCC ACTCTGCCAG CCAGCACCAC CCTCCACCCA CTCTAGGCCC 1380
TTAAGAAAGG AGGGAAGGGC CGCGGGGAGG AGCTCTCAGA TCCCGAGGCC CCACTCCCCC 1440
TGCAAGGAAG GCTGTGAGCT CGGCCCCAGC CCACCTGCCA GCTCCCCAAA CACCTCCCAC 1500
CTCCCTCCGC CGCCTCCTGA AGGGACTACA CTCCCCTGGC TCCTCCAAAA TCCGCTAATG 1560
AACAGCAGGC GCAGAGGCTC CGCCACCGGC GTGCTCCTGG CCTCAGCCCT CCCTGTTCTG 1620
AAACCGCCTT TGCTAAGACG GTAGTAGTGA GGAATCACGA CAGTGGCAGA GGCCAACCTG 1680
ACCCGCTCCA CCTGCCTCCA CCCCAACCCG CCCGGCTGCT TCCTGAGCGT GGGCCAAACT 1740
AACTTTGACA GGAACTTAGT TTACAGTTTA AGTTGGGAAC AAAAAGGATA ACAGCCCCTC 1800
CCCAAAACAG ATTCCCTCCT CGCTTGGGGG GACCAGTCCC GTTGTAAAAC CGACAAATAA 1860
CAGCAGGATT AGGAATTCCG GCTCAGGATT CACGCAGCCA GACGCCACAG GACTCCTCCC 1920
CAGCCGCTCC TGTATATGAC GTCACCGCCG TAAGACCACA GGACACCGCC CCAGCCGCGC 1980
CTGTAGATGA CGTCACCATC GTAAGACCAC AGGACCCTTC CCAGCCGCTC CTGTATATGA 2040
CGTCACCGCC GTAAGACCAC AAGTCACCGC CCCAGCCGCT CCTGTAGATG ACGTCACCAC 2100
AGTAAGACCA CAGGATACCG CCCCAGCCGC GCCTGTAGAT GACGTCACCA TCGTAGGCCC 2160
ACAGGACCCT TCCCAGCCGC TCCTGTGGAT GACGTCACCG CCGTAGGACC TAAGATTGAT 2220
GCTGGAGAGG TTCTTCAGAC CCTGCGTTCT GACGGCTCCG CTGGCACCAC CCAGACGGGT 2280
AAACTAGCTC TTCCGGTCTG TGGCCCTCAC AGGAACCGAC TCGGTGCAGG AGGACAGCTT 2340
CAGCCCCTGT GATTTCATCC CCGACCAACC AGCCAGCACT CCCCACTCCC TAGCCCCCTG 2400
CCTGCCAAAC TATCTTTTAA AAAACTCCAG TTTCCAAATT TTCAGGGAGG CTGATTTGAG 2460
TAATAATAAA ACTCCAGTCT CCTGCTAGCT GGCTCTGGAT GCACTAGACT CTATTGCAAT 2520
TCTCCTGTCC TGATAAATCG GCTGTCAGGC AAGAAGAACC CGTTGGGTGG TTACAGTTTC 2580
AAGGCTATAT TCAGAGAACT ATCCACTAAT AAAATCTCTG TTTATGCAGT AGGTCCCACC 2640
CCACACCCTC CCTGCTCAAA CTGCTGCAAT 2670