EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS145-06382 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr12:133021320-133023790 
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
TTTACTAGAA TCTTTTAAAG GGGCACAAAT GGGGGTGTTT TGCAGGCATA CAGAAGCCCC 60
CGTCACTCCT CCCGCCTTGT CTCTGAACCG CTGTGGGGTG GGGAGGGGTC TCTTCTCTCT 120
CCAACCCACA TCACTTTCAC CCCCCGCCGG CCAAGGCTGC GTTTCCCTCG CCCCCACCCC 180
AGTCCCCCGC GTTGGTAGTG GGATCGGTTT GGTATTCTGA GGCTTCTCTC ATTTCTCCTT 240
TATCACCATC TGCCCCACAG CAGGCAGGCC CGGAGCCTCT GCAGAAGGGG GAACCGGGTG 300
CAGGCCCAAC GCCGGTCTCT CAGTGTGGCA GCCTTGCGCG CGAGCAGAAG CAGAAGGCCT 360
AGTTCCTACT CTGCAGCCTT GGCTGCCGGG CACGGAGAAC GTTTTAGCAG AAACACCTCT 420
GCAAAACCAC TTCCTGGCCC GGGCCCAGCC AAACACCATC TTCTCCTCCA CCCCAGGGCT 480
CCGCCCCCAT CTCCAGGCTC AGCCCAGCAC CCCCACCCCC GAAACCCCCA GCCCCACTGC 540
ATCTGCCCTG GCCATCTGCC TCCGCCCTGC CTCGCTAACA CAGTTATTAA TGAGCAATTT 600
TCCTGTAATT ACAACGCAGT TATGCCAGTT ACCCCGACCT GCTGACAGAG AGCATTCACT 660
TCCATGTGGC ACTAGCCCCC AGGCCTGAGA GGACGCAAAC ACTTGCCCCT CATTCGCTGC 720
CCCCACCCCC ACTCTGCCAG CCAGCACCAC CCTCCACCCA CTCTAGGCCC TTAAGAAAGG 780
AGGGAAGGGC CGCGGGGAGG AGCTCTCAGA TCCCGAGGCC CCACTCCCCC TGCAAGGAAG 840
GCTGTGAGCT CGGCCCCAGC CCACCTGCCA GCTCCCCAAA CACCTCCCAC CTCCCTCCGC 900
CGCCTCCTGA AGGGACTACA CTCCCCTGGC TCCTCCAAAA TCCGCTAATG AACAGCAGGC 960
GCAGAGGCTC CGCCACCGGC GTGCTCCTGG CCTCAGCCCT CCCTGTTCTG AAACCGCCTT 1020
TGCTAAGACG GTAGTAGTGA GGAATCACGA CAGTGGCAGA GGCCAACCTG ACCCGCTCCA 1080
CCTGCCTCCA CCCCAACCCG CCCGGCTGCT TCCTGAGCGT GGGCCAAACT AACTTTGACA 1140
GGAACTTAGT TTACAGTTTA AGTTGGGAAC AAAAAGGATA ACAGCCCCTC CCCAAAACAG 1200
ATTCCCTCCT CGCTTGGGGG GACCAGTCCC GTTGTAAAAC CGACAAATAA CAGCAGGATT 1260
AGGAATTCCG GCTCAGGATT CACGCAGCCA GACGCCACAG GACTCCTCCC CAGCCGCTCC 1320
TGTATATGAC GTCACCGCCG TAAGACCACA GGACACCGCC CCAGCCGCGC CTGTAGATGA 1380
CGTCACCATC GTAAGACCAC AGGACCCTTC CCAGCCGCTC CTGTATATGA CGTCACCGCC 1440
GTAAGACCAC AAGTCACCGC CCCAGCCGCT CCTGTAGATG ACGTCACCAC AGTAAGACCA 1500
CAGGATACCG CCCCAGCCGC GCCTGTAGAT GACGTCACCA TCGTAGGCCC ACAGGACCCT 1560
TCCCAGCCGC TCCTGTGGAT GACGTCACCG CCGTAGGACC TAAGATTGAT GCTGGAGAGG 1620
TTCTTCAGAC CCTGCGTTCT GACGGCTCCG CTGGCACCAC CCAGACGGGT AAACTAGCTC 1680
TTCCGGTCTG TGGCCCTCAC AGGAACCGAC TCGGTGCAGG AGGACAGCTT CAGCCCCTGT 1740
GATTTCATCC CCGACCAACC AGCCAGCACT CCCCACTCCC TAGCCCCCTG CCTGCCAAAC 1800
TATCTTTTAA AAAACTCCAG TTTCCAAATT TTCAGGGAGG CTGATTTGAG TAATAATAAA 1860
ACTCCAGTCT CCTGCTAGCT GGCTCTGGAT GCACTAGACT CTATTGCAAT TCTCCTGTCC 1920
TGATAAATCG GCTGTCAGGC AAGAAGAACC CGTTGGGTGG TTACAGTTTC AAGGCTATAT 1980
TCAGAGAACT ATCCACTAAT AAAATCTCTG TTTATGCAGT AGGTCCCACC CCACACCCTC 2040
CCTGCTCAAA CTGCTGCAAT CCCGGCACAG CTTTGTTGAC AATGTACCCA TCAGCCAACA 2100
AAATGTAACA AAATGCACTT TCTTTTAGTT ATCTCCTGCT ACGTAATAAA CTTCCCCGGG 2160
AGGTGGAGGT TGCCATGAGC CGAGATTGCA CCATTGCACT CCAGCCTGGG CAACAAGAGC 2220
AAGACTCCGT CTCAAAAATA AATAAATAAA TAAATAAATA AGCCTCCCCG GAGCTTGATG 2280
GCCTAAATAG CAATCTACCG TGAGTGCTCA GGGCTCTGGA GTTGACTGGG CTGCGCTGGG 2340
TGCTTCCTGC CTAGGGTCTC CAGTGTGGTT GCAGCAAATG CAGGCTGGAG CTGTCCAGCA 2400
TCTCTTTCTG AGTAGCCTCT CCACGCTCAG CTTGGACCCC CTCACAGCAT GGCTGCCAGG 2460
GTCATCAAGC 2470