EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS041-00783 
Organism
Homo sapiens 
Tissue/cell
EWS502 
Coordinate
chr1:27903080-27904560 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:27903181-27903199GCTTCCCTCCTCCCTTTC-6.19
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00527chr1:27902382-27904230Adipose_Nuclei
SE_00861chr1:27886075-27904718Adrenal_Gland
SE_01588chr1:27886149-27904879Aorta
SE_02913chr1:27903002-27903825Bladder
SE_03261chr1:27902998-27903917Brain_Angular_Gyrus
SE_03939chr1:27902441-27904040Brain_Anterior_Caudate
SE_05478chr1:27897313-27904233Brain_Cingulate_Gyrus
SE_05814chr1:27902415-27904734Brain_Hippocampus_Middle
SE_06945chr1:27896906-27903953Brain_Hippocampus_Middle_150
SE_07770chr1:27902330-27904310Brain_Inferior_Temporal_Lobe
SE_08953chr1:27903462-27903801Brain_Mid_Frontal_Lobe
SE_23479chr1:27902429-27903538Colon_Crypt_1
SE_25901chr1:27902420-27904188Duodenum_Smooth_Muscle
SE_26518chr1:27885702-27904919Esophagus
SE_27625chr1:27902211-27904001Fetal_Intestine
SE_28547chr1:27903163-27904086Fetal_Intestine_Large
SE_29557chr1:27886726-27904956Fetal_Muscle
SE_31394chr1:27886081-27904513Gastric
SE_33503chr1:27886818-27904912H2171
SE_36974chr1:27887536-27905229HSMMtube
SE_40593chr1:27885841-27904966Left_Ventricle
SE_42106chr1:27886079-27904957Lung
SE_46630chr1:27903048-27903978Ovary
SE_46630chr1:27904038-27904684Ovary
SE_47670chr1:27903148-27903731Pancreas
SE_48058chr1:27885887-27904727Psoas_Muscle
SE_48567chr1:27886102-27904727Right_Atrium
SE_50130chr1:27900347-27904001Sigmoid_Colon
SE_51091chr1:27886184-27904991Skeletal_Muscle
SE_53892chr1:27886040-27904947Spleen
SE_54527chr1:27885939-27904929Stomach_Smooth_Muscle
SE_65253chr1:27900425-27904808Pancreatic_islets
SE_68682chr1:27900020-27903843H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12790421727904495
Number: 1             
IDChromosomeStartEnd
GH01I027559chr12788613127905256
Enhancer Sequence
TCACACAATG TCAGAGCCTA AAGTCAGAAA AACTCTGGTT CCAGAACCCG TTAACCACTG 60
AACACAGTGT TCACCCTGAC ACAGGCAGGA CAAGCATTGC TGCTTCCCTC CTCCCTTTCA 120
GGCAGTCCCT GGGGACCCCT TCTGCTCTGG TCCCAGTTCC AGGCATGAGG GGCTGTTCTC 180
AACAGCTCCA CTGGGGCCAT TCCCACCTCC ATCTACCCGT AGGGACATGG GGGGATCACA 240
CCAGTGTCAC CCTTACAACA GTGGAGGCTG CTTTTGGGCA TGTGGTGACC CGTGACCCTG 300
GCCCTGTCTA GGCACTGGCC ATCCTGAGTC TAGCACCTCA CACACACACA TATATACAGT 360
GCATCCCAGT GCTCACCGCC TGCCCACACC CCCCAACGCC AGCACCCACC GTCATGACAT 420
GAACACAGAG ACCAGTACCC TACCTTGCAC TGGTGACAGC GCCCCTGTCA CAAAGCCAGC 480
AGCTTCAGAC AGCATCCCTC AACATTCTTC CTGGCTACTC TGTCCCTGTC CCTCACTCCC 540
TCTCCAGTAG CTCACAGTCC AAATCCCACA ACGGATGGGG AAGCTTAGGC CCAAGAGGAA 600
GGGATGGGAG GACACAGTCA TCCCTCCTGA GACCCGGGGA TAGGATCATA AATGAGGAAA 660
GAAAATTGCC TTTGGCCAGT GAATGACAGA CGTGGGCATC CAATACAAAT CATTCAGCTC 720
CTGGTCGGTT GCCCCACTGC AGCCCTCTGA ATCTGTTCAG CTCCTGCCGT GCGGCAGCTA 780
GAGGGGCCCC CAGGACAGGA TTCTAGAAAT GGGCACCAAG CTGGGACCAG AGTCCTAAGG 840
ACCACTCTCT GCTCCCAAGT GTCAGTCCCA GACTATGGGC CCCTAGGTTT CACTAATCCA 900
TCAAATTCTA GACTCAGCCT AGCCTCAGAG CCATGGGGGC AGGGGCATCT GGGGGTGAGG 960
GGAGATGGCA TACAGGGGGA ACAGCCTAGG ACAGGGCTTG GAGCTGCTTC CTGCTCCCCC 1020
CACTCCCAAG CAAGGAAGCA CAAAGACTGG CAGGCCCCCC ACTCCGCCCC GGAAACCTGG 1080
CAGTTTATTT CTGTCTCTGG GCCCCCTGTT TCCACAGAGT CAGTCCAGGA AGGCTGGCAG 1140
CAGCTGGCTC GGAGGGGTGG AGCTCCTGCT CTCTCAAGGG TCCAGCTGCC ACCCTGCTCC 1200
CCTCCCCCTG ACCTGCCAGG CCAGACAAGA CTGAGGTGAC ACTGGGATAA GGGACAGGAA 1260
CTGGGGGCCA GTGCTCAGAG GTGATACTGA ATACCCTGAG AGGCCAGAGC CCCAACAGAG 1320
ATTCCACCTG AGGCCAGGGA GTTAAGACTC CAGGGGAGGG AACCCCTGAC TCCCCAGCCC 1380
ACAGCCCAGA TGTTCTCCCA GGCAGTCAGA CTACACCCAG TTCAAGTCTG CTAAGGGTGT 1440
AACCTCTGGC GAGTACAACC CTACTTGTTC CAGATTATTC 1480