EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS101-09079 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr11:118503810-118506110 
Target genes
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr11:118505632-118505651CGACCAGGAGAGGGCGGAG+6.03
Klf12MA0742.1chr11:118504258-118504273GTTGTGGGCGTGGTC-6.44
SP1MA0079.4chr11:118504260-118504275TGTGGGCGTGGTCTT-6.46
SP3MA0746.2chr11:118504260-118504273TGTGGGCGTGGTC-6.21
SP4MA0685.1chr11:118504258-118504275GTTGTGGGCGTGGTCTT-6.01
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00080chr11:118471872-118521952Adipose_Nuclei
SE_01233chr11:118504769-118506582Adrenal_Gland
SE_01769chr11:118503614-118507080Aorta
SE_03266chr11:118504102-118505600Brain_Angular_Gyrus
SE_03940chr11:118500747-118507464Brain_Anterior_Caudate
SE_04898chr11:118497416-118507949Brain_Cingulate_Gyrus
SE_05853chr11:118495088-118516368Brain_Hippocampus_Middle
SE_06817chr11:118501829-118506885Brain_Hippocampus_Middle_150
SE_07848chr11:118502589-118507837Brain_Inferior_Temporal_Lobe
SE_26284chr11:118504786-118505605Duodenum_Smooth_Muscle
SE_29845chr11:118504812-118506509Fetal_Muscle
SE_32447chr11:118504162-118504885Gastric
SE_32447chr11:118504938-118506425Gastric
SE_33210chr11:118504727-118506496H1
SE_40907chr11:118503657-118507013Left_Ventricle
SE_42414chr11:118503664-118507977Lung
SE_44245chr11:118504110-118505710NHDF-Ad
SE_44828chr11:118504230-118504819NHLF
SE_44828chr11:118504871-118505760NHLF
SE_45888chr11:118503422-118505676Osteoblasts
SE_46702chr11:118504403-118504793Ovary
SE_46702chr11:118504851-118506333Ovary
SE_47945chr11:118505197-118506435Pancreas
SE_48825chr11:118504302-118506807Right_Atrium
SE_50429chr11:118503974-118507146Sigmoid_Colon
SE_51626chr11:118503992-118506884Skeletal_Muscle
SE_55031chr11:118503313-118506914Stomach_Smooth_Muscle
SE_63206chr11:118491155-118513415GLC16
SE_69185chr11:118504318-118507131H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11118504730118505063
Number: 1             
IDChromosomeStartEnd
GH11I118633chr11118504281118507887
Enhancer Sequence
CCCTTCTAAT CACTGACTTG GGCTTTCCGC ATGCCCCTAA CTGCCAGTGC CACCCAGGTA 60
GGGCTGAGCC ATGCCCGCTT TTGCACTAAC TCAGTGGGTG CCTCTGTGCC CCTGGCCTCT 120
CTCCTCTAAT GCTGCCTCCT TCTTTTCTTG GTGTGGGACC CCAGAGTTTT TATATGAAAG 180
GAATTGGCAG GAGGATTGGT AGCTCAACTT TACTCAAGGG GGCATTGGCA GGAGGGGTAT 240
GAGGGTGGGG GAAATGCTTG GCTGTGGAGC TGCTCAGACT GAAGAGTTCT TTCCATTGGA 300
AATGCCTAGG CTGCTGTCTT AGGCTACTGT CTGAGGACAG CATGAGATAA CCCAAGGAAG 360
CTTCCTGGCA GCTTCCTGCA CAGCAGAGTA GGCTGTCTTC CACCTATTCC CCTGCCTGCC 420
CTCTGGAGCC AAGGAGTAAG GAGGCCCAGT TGTGGGCGTG GTCTTGGAGG GCTTGAACAG 480
GACCTCTCTG CCAACATAGT GGCTACCCTT CCTAGCTTTC CCTTGGGGCT TCCCAAATTC 540
AGATACCCAT CAGAGGTTGG TAATGGGTAG CCCCTACTCT TCTCCTCACT CCTGAGCCAC 600
CTATAACACA GGGTATTTTA AAGGCTGAGT CCAAGGATGA GGAAGCACCT AGACCCCAGG 660
AACTGGCCTG ATTAGGTCCT CCTCTCTGGG GATGGGTAGA TGAGTTGGGT AGAGGGATGG 720
GAGTGACTGG GTTCAGCATA GGGCCTCACT CCCAGGGATA AAGCTCAGCA TTTCAGAAGG 780
AACCTGCCTA ACCTCATTTC CCACTGACCT GGAGTTTTTT GGAGGCCTAG ACTTCGCTTT 840
CTCTGTGGGG AAGAGAGGTT ATTCGAGGCT GTGGTAGTGA TGGTGGTGGT GGTGATGGTG 900
GTAGTGATGG CAATGGTGTG GAGGGTTCAC TTGGCTTCCC TCCCCTGCCC TCAGCCCATG 960
GCTCCACTCT GGCTTTGGAA TCAGTAACCA CAGTTTCTCC TCTGCCTGTC CTTTGAGGGG 1020
TGACTCACCA AACCCTCCCC TCGTCCCCCT TCCCACCCTC AGAGGTGTCA TCTCACCCCA 1080
GAAAGAACCG TCCACCCCCT CTGTACCCAC TCCTGGGACT CATTACCATG GAAACAGCCC 1140
GAACTAATTG CAACCCTCAT CCCTGAAGTT CAGCCTGCAG GGCCAACACC CCACCCCGAC 1200
CCTGGGCAGG AGGGGAGGGA GGCCAAGGGT GTTGGGTTGG GGTCCCCTCT GCCACACTGC 1260
TTTAACATCC TCAGCTCCTG ATTGACGCCC AACCCTGGAT TTAACCCTCA CCATCACTAC 1320
CCTTTTTCCC TGGGTTAAAT TTTGGTCTCT GGGCTGTAGT AGAAGGGGAG GGATGAGAGC 1380
TGGAGGCTCT GTGATGCAGA ACCAGCCTTG ACTGGTTTGG AGAGAAAACA GAGGGCCTTT 1440
TCTCGAGACC TACCCAACAA TTTCAGTTCA AGGGACTTCA GGAGACCAAA ATCTGTGCCC 1500
TGCCCCCACA CCTCTGCCTG TGTTACCTCA TCCCCTGCAC CTCTGACTGC CGTGTTACCT 1560
TCAGCTCCTG GCCTTGGGCC CTCTCCCTCT TCACCTCTTT CCCTCCTCAC TTTCCCTTTC 1620
TGCCCTTTTC TTTCTCCTCG CCTGGTTATT CTCCTCTTTG ATTCTAGCCT TTTTTTCTCC 1680
TCTCTCAACC CCCATTGCCG ACCCCCATTC TGTCCCGCCC TGGCCGCCCT CCCGCGCTCC 1740
CCTCCCGCCG CTGCCGGGCC GGAGTTGAGG AGTGTGTGTT CTGTTTCTCC CCTGTGCCCC 1800
GCCCTCTCCC TCGCCCTCCC GCCGACCAGG AGAGGGCGGA GCTGGCCGCG GGACGGAGGC 1860
ACCTGGTAGG CCCGCCAGGC GCTCTACGCC GAGCTCCAGA CGCAGCTCGA TAACTGCCCC 1920
GAGTCAGTGC GGGAACAGTT ACAGGAGCAG CTGAGAAGGG TCAGTTCCAC CGCCCCCCCT 1980
CCCCCGGCCC CGCGGGCCAC GCCCCAGAAG GAAGAGAGGA GAGCGGTGGG ACGGGACCAC 2040
CTGGCCTCTG CAGTACCTGC CGGACACCAG GGTCGGTGCT GCGGTTTGGA GGGAACCGGG 2100
AAGGTTGGGG AATCAGCGCT CCAGGCCATG ATGCCCGCAA AAGGGCAAGG CCAAGTACAG 2160
CGGGAGCTGG GGGGAGGCAG GTTTCTTACC CAATTTCCCC GGGTCCAGCC CCATACAACG 2220
CATGCCCCTG TGGCCTGGTC TTCCAGGCCC AGAGTGGCAT TGCAAGCACC ACCCAACCCC 2280
CTTTGTCACT GTCGTTGAAG 2300