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

TagContent
EnhancerAtlas ID
HS135-01518 
Organism
Homo sapiens 
Tissue/cell
MM1S 
Coordinate
chr20:30295640-30297290 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Myod1MA0499.1chr20:30295800-30295813AGGAGCAGCTGCT-6.11
Number of super-enhancer constituents: 57             
IDCoordinateTissue/cell
SE_00546chr20:30293974-30296822Adipose_Nuclei
SE_01656chr20:30295753-30297464Aorta
SE_03109chr20:30295668-30296248Bladder
SE_03156chr20:30295499-30297228Brain_Angular_Gyrus
SE_03894chr20:30293076-30297376Brain_Anterior_Caudate
SE_04818chr20:30291888-30312530Brain_Cingulate_Gyrus
SE_05813chr20:30291812-30312465Brain_Hippocampus_Middle
SE_06739chr20:30292005-30297574Brain_Hippocampus_Middle_150
SE_07749chr20:30292115-30312408Brain_Inferior_Temporal_Lobe
SE_08789chr20:30295651-30295825Brain_Mid_Frontal_Lobe
SE_08789chr20:30296331-30296936Brain_Mid_Frontal_Lobe
SE_13448chr20:30295550-30297154CD34_Primary_RO01536
SE_14426chr20:30292092-30297225CD4_Memory_Primary_7pool
SE_18483chr20:30295500-30297239CD4p_CD25-_Il17-_PMAstim_Th
SE_19226chr20:30295673-30296770CD4p_CD25-_Il17p_PMAstim_Th17
SE_22440chr20:30295774-30296556CD8_primiary
SE_23622chr20:30295644-30297320Colon_Crypt_1
SE_25330chr20:30291945-30297378DND41
SE_25933chr20:30295533-30297299Duodenum_Smooth_Muscle
SE_26879chr20:30295600-30297395Esophagus
SE_27731chr20:30291257-30297421Fetal_Intestine
SE_28698chr20:30291565-30297515Fetal_Intestine_Large
SE_30903chr20:30292078-30302768Fetal_Thymus
SE_31430chr20:30295525-30297479Gastric
SE_33407chr20:30292055-30302718H2171
SE_34309chr20:30291576-30306320HCT-116
SE_34643chr20:30295497-30297120HeLa
SE_35852chr20:30295533-30296546HMEC
SE_36989chr20:30295237-30297458HSMMtube
SE_39443chr20:30295619-30296905Jurkat
SE_39853chr20:30295594-30296586K562
SE_40644chr20:30295475-30297500Left_Ventricle
SE_41648chr20:30295850-30297257LNCaP
SE_42121chr20:30295482-30306315Lung
SE_43515chr20:30291879-30312193MM1S
SE_47264chr20:30295479-30296870Panc1
SE_47861chr20:30295737-30297223Pancreas
SE_48182chr20:30295496-30302360Psoas_Muscle
SE_48890chr20:30295793-30297174Right_Atrium
SE_49886chr20:30295531-30297118RPMI-8402
SE_50155chr20:30295533-30297457Sigmoid_Colon
SE_51509chr20:30293396-30302434Skeletal_Muscle
SE_52373chr20:30295497-30297438Small_Intestine
SE_55108chr20:30295622-30297363Thymus
SE_56767chr20:30295601-30297377VACO_400
SE_57375chr20:30295642-30297287VACO_503
SE_57919chr20:30295614-30297374VACO_9m
SE_58612chr20:30249012-30312162Ly1
SE_59155chr20:30248900-30312556Ly3
SE_61228chr20:30249013-30312452HBL1
SE_61455chr20:30248898-30312277Toledo
SE_62770chr20:30248811-30312352Tonsil
SE_63330chr20:30279572-30311864NCI-H82
SE_65412chr20:30295708-30297841Pancreatic_islets
SE_66334chr20:30295619-30296905Jurkat
SE_66898chr20:30292055-30302718H2171
SE_67146chr20:30291879-30312193MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr203029568830297247
Number: 1             
IDChromosomeStartEnd
GH20I031702chr203029062130297397
Enhancer Sequence
ACATGAGGAA ACTAAGGCTG GGAAAGATTA AGTATTTGCC AAGGATAACT ATTAAGCAAG 60
TGAGACTCAC CAACTCAACA ACGGTTTGTC AAATTTCGTA CCTGACTCTT AACAACGATG 120
GAATTTCTCC CAAGGAGGCA AGGCAGACAC CAGGAATACC AGGAGCAGCT GCTGCCTGAG 180
AGAGTGGGGG GCCTCCAGAG CCCCCAGAAG AGTCTTCCTA ACCTCTTTCC ATCAGGTTTT 240
AACATCACAC TGAGATGGGG AGGTAAGGAA AGAATGGTTA GGTGTGCTCA ATCTATCCTT 300
AGGGCAACAA GGGTCTGGCC CTCTTTGTTG ACCCTCAAGG GAAGAAGTTT GTGACTTCCC 360
ATTTGTCACT CACCAACCCT CTAGAGAGAA ACAGAAGGGG GCAAGGGCAT GGGAGTATTT 420
TCTCCCTGGG GTTGGGGGGC ACACACAAGG GAAGAAGCAG CAGCCTTACT GGCTCTTTCC 480
TCCCCTGGGC AAGAAGCCTG TACATGTGAT ACAGTGTATG TCATTCACAT GGAACCCCCT 540
TGGGGAAATG CCAAGGTACC TTTTGGACCC AAGAAGCCTC AGAGAGGAGA GACTGGCAAA 600
GCCCTGAACT GCAAGCTAAG CTGACAATTT CTAAGCATTG TAACTAGGTC ATCAGGTTCC 660
TGGAGAAGCC AGCTGTGGCT GGGGGATGGG GAGGAAAATT TTGCAGCCTA CCAAGATCCC 720
TACTTCCCTT TAGGCCCCAC CCTCCCTGAA ATCTGCACCT GCTCCCAAAC TGACCCCTCC 780
CCCCAGCTGA GCCCAGCTGT CAACGGCTCC CAATGCCCCG CCCTGCCTTC CTTAGGCCAG 840
AACCATGGGG GCCTCTTGGG CAGGAGGTAC CTGATTGCCA CCTGAGCTTT GCAGAGAAGG 900
AGCTGTGGGG CAGGGAAGGA TTGGCCTCTC CTAGAAGATA TTTCTTGCTC CACCAGGGCA 960
GCAAGAAAGT TAGGCCCCTT TGGGCCTACC TAGGGTACCC TTCCTGGCAT TGTCACTGCA 1020
GGTGGCAGGA GACAGGTGAT GTTTACCCTG CTGAGGCCAG AGTTGCCAAA AGGCTTCAAT 1080
CAATCCTTTG AATCTGCACC TGGCCCTGAG TCCCAAAATA ACAACCAGGG CAGCTTACCT 1140
GATCTGCAGG TTGCAGGTGC CTCTGGCTTT TCTCTCCCTG CAGCTCTGCC TGCTGAGCCC 1200
TGGCTGGCAA GAGATTCTTT TTCTTAGGGG TTACTGAGAC CTAACTGCAT CCCACAGGTG 1260
CTCTGGGCCT CTCCCCATTA GGCCCACCTC TACCATCAAC CATCCCTCTG TCCAGAGGCC 1320
TCTGTCATCA GCCACCTGGT TTCTTCCCTG ACCAACTTTA TTGCTGACAC AGACCATCTT 1380
TGGCTCTAGC CAGTCTGCCT CCTCATGATC TCTCAAATGC TTCATACATA CTCCACCCTC 1440
CAGTTCTGTC TGGGTGGTTC TTACCCGTCT GGCCTGCTCG TGTGTGTGTG TGCGCGCGTG 1500
CACGCGTGTG TAACTAGCCT GATCTTTTTG GTGTGTGTGT GTGTGGCAGA GTCTCCCTCT 1560
GTCGCCCAAG CTGGAGTGCA ATGGCATGAT TTCAGCTCAC TGCAACCTCC ATTTCCCGGC 1620
CTCAAGTGAT TCTCCTGACT CAGCCTCCCA 1650