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

TagContent
EnhancerAtlas ID
HS041-22342 
Organism
Homo sapiens 
Tissue/cell
EWS502 
Coordinate
chr9:135994340-135996290 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs59449333chr9135995304hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF740MA0753.2chr9:135995814-135995827ACCCCCCCCCCAC+6.32
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00682chr9:135992529-135999630Adipose_Nuclei
SE_00941chr9:135987489-135999300Adrenal_Gland
SE_03180chr9:135991932-135996409Brain_Angular_Gyrus
SE_03904chr9:135987523-136000869Brain_Anterior_Caudate
SE_04821chr9:135987134-136024535Brain_Cingulate_Gyrus
SE_05796chr9:135975584-136025980Brain_Hippocampus_Middle
SE_06709chr9:135987770-135999285Brain_Hippocampus_Middle_150
SE_07782chr9:135987299-136019128Brain_Inferior_Temporal_Lobe
SE_08796chr9:135993925-135994590Brain_Mid_Frontal_Lobe
SE_08796chr9:135994706-135995671Brain_Mid_Frontal_Lobe
SE_08796chr9:135995838-135996326Brain_Mid_Frontal_Lobe
SE_11572chr9:135995475-135998687CD20
SE_14394chr9:135994483-136011929CD4_Memory_Primary_7pool
SE_16859chr9:135995865-135998028CD4p_CD225int_CD127p_Tmem
SE_17482chr9:135995498-135999468CD4p_CD25-_CD45RAp_Naive
SE_17768chr9:135995422-136025692CD4p_CD25-_CD45ROp_Memory
SE_18626chr9:135995731-135998323CD4p_CD25-_Il17-_PMAstim_Th
SE_19123chr9:135995631-135998216CD4p_CD25-_Il17p_PMAstim_Th17
SE_19979chr9:135995661-135996602CD56
SE_20743chr9:135995422-136000873CD8_Memory_7pool
SE_23083chr9:135994779-135996675Colon_Crypt_1
SE_23731chr9:135994789-135995227Colon_Crypt_2
SE_23731chr9:135995289-135996712Colon_Crypt_2
SE_24697chr9:135994813-135998026Colon_Crypt_3
SE_26484chr9:135994314-135996614Duodenum_Smooth_Muscle
SE_26644chr9:135987567-135999307Esophagus
SE_29849chr9:135993682-135996573Fetal_Muscle
SE_31496chr9:135992120-135999153Gastric
SE_33626chr9:135992796-135997831H2171
SE_34626chr9:135994676-136005394HeLa
SE_40917chr9:135987525-135999450Left_Ventricle
SE_41634chr9:135987722-135996589LNCaP
SE_42210chr9:135987263-136000526Lung
SE_47570chr9:135994870-135995348Pancreas
SE_47570chr9:135995842-135996609Pancreas
SE_48127chr9:135986843-135999277Psoas_Muscle
SE_48745chr9:135992130-135996703Right_Atrium
SE_49539chr9:135994784-135995649Right_Ventricle
SE_49539chr9:135995837-135996604Right_Ventricle
SE_50127chr9:135987674-136000960Sigmoid_Colon
SE_51366chr9:135987756-135999305Skeletal_Muscle
SE_52380chr9:135987803-136000487Small_Intestine
SE_53581chr9:135992724-135999186Spleen
SE_62626chr9:135987373-136020779Tonsil
SE_65763chr9:135986901-135996538Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9135994562135994927
chr9135995063135995322
Enhancer Sequence
CACAACCTGC ACTTTTTGTC TGGCCAAAGC AACAGCCTGT CCAGAGATGG GGGCACGGAC 60
CAGGTCACCT CCAGAAAGCA AGAACTGTGC AGGCCAAGCT GGGTCATTGG TGGCTTGGCT 120
TAGAATCGGG AAGATAAGCG GAAGCCCAGA TGTGAGGAGA TCTGGCAGCC CAGAGGGAAG 180
CACCGGGTGG AAGCTAGGTA GGGAAACAGG GATGCGGGGG AAGGCAGAAA CTGTCTGGTG 240
GTTTCCAGAG AGGACAGGGA CCAAGTGCGC AGCGTCAGCT CTGGCAGGCC ACATAGACAC 300
CAGGAAACCA GCCCCAGGAC GGGGGGTGTT GGCAGGAGGG ACAGGGACTT CCCCGCCCCC 360
TCCCTTGGGC CCTTGGTAAA TGGTCATTGT GTTCAGTTTC CGGCAGTGGC CTCCTCTCCT 420
GCCAGGATCC TGGTTTTCCT GACCCAGCCA GAAGCTTCCC CTTTGATTTC TAAATAGCAG 480
TCGAGGTCTG GATCTCAGTG CTGAGGCTGG GCAAGGAGCG CCAGGGCCAG AGAGAGGGAA 540
GACAAGACCC CCAGGCAGGG GTGGGGCTCA GCTCTGCCTC TCCCTCAGTT CCTCAGGGAC 600
GGAGAGAGGG AACCTGCACG GCCACTGTGA GCGCTCCGCC GGACCCTCCC AGCACACAAA 660
GCCCGAGCTG CTGCCAGAGG TAATGAAAGC CAGATGAGCG CTGGGCTGGT GTCAGCCTCC 720
CACCCCCACC CTCCCAGGGG TCCCTCTCCA GCCGCCAATG AGGACCAGAG CCCTGGATAG 780
ATGAGGGTTG AGGGAACACG TCTGGTCCGG CCATCTGCCA AGCTCAGGAG GAAAGGGTCT 840
CTCAGGCGTG TGGTGTTCCC CCACCAAGAG CTCTGCCCAA CACTGGGCGG AGAAACAAGT 900
CGCATCCAGG CCCTGTCTAG GTACCGGGAC ACCAAGAGGC ACGAGACTCA GGCTAACAAT 960
CGCCAGCAAT CACAACGCGC CACAGTCTAA AGCCATGAAG CGACTGGAGA CGCAGCAAGG 1020
CAACACGATG CCGCACGGGG ACTCAGGAGG TTCACTGTGA AGGCTGCAGC CCAGCCAAAG 1080
CTCTGATGGG CCCTGAGCCC CCGATCCAGG AATGGCCTCT GTGCAGGCCC TGTGCCCAGG 1140
CAGAGCAGGG CGAGGGGGGC ATCTCTGGAT TCCACTCCCT CTGCTGTGTA GTCAGCAGCA 1200
GTCAGGTGGG AGGCAGATGG CACCACCCAG AGACCCAGGG CACACGAGAA ACAAGCCCCC 1260
GCCCTCACCT AGTCACCCTC CCCTCCATCC ATCACAGGTA CACCACTCCC TTCTCTGAAT 1320
CCTACCCAGT CCTTACCGAT TCAGGGTGTT GGCACTCTTT CCAGTTAAGC AGAAACAAGT 1380
CTTGCCCGCC CTGGGCCTGG GCCACCCTCC TCCCCTCACC ACCAGGACAT CTGGTCCCAC 1440
GTGTTGGAGG CCTGCTGCTC CACCCCATCC CCCGACCCCC CCCCCACCCC GCTCTGAGCA 1500
GCCCCGATGT CCCTGGTCAC CAGATCCACA TCTGCCCCAA GTAGGGTCTG TCTGGAAGGC 1560
CCCTATGGTC TCATCACCTC TGAGGATTCT AGGATTTGGC CTTCCCGACC ACTTGTTCCA 1620
CACCTGCATC GTAAAGGCTA ACGACGCGCT GCGGGCCCTG GGTGGGAACT GAGTGAAATA 1680
AGGCACAGGC CACCGATGTA AACAGGGACA GTGCCGCAGA AAAAGGTCCA CCTGGGCTGC 1740
AGCGGCCTTG GTGACAGCAG GCCCTGGAAC GGTATTGAGG GGCGCAAAAC CCCAGCCGTG 1800
GTCCCTACTG TTGGACGGGG CGCGGCGGCA GCCCCCACTG CCCACCCTGC TGGCTGATTT 1860
CTGCAGAAGG CCCCGACCCC CACCTATGGA GGAGAGAGGA GGGAGGCGGC CCGCTGGGAT 1920
CGCCCGGCCC CGTCCGGGGC TCGCCCCGAC 1950