EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-38110 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr18:74825240-74827420 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr18:74827130-74827147AGGGTCAACATGACCCC+6.95
Gata1MA0035.3chr18:74826925-74826936TCCTTATCTGT+6.14
SOX10MA0442.2chr18:74826365-74826376AAAACAAAGCA+6.02
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_02611chr18:74826281-74827197Astrocytes
SE_09139chr18:74806175-74829571CD14
SE_11015chr18:74825798-74828579CD20
SE_12122chr18:74826636-74828283CD3
SE_12973chr18:74825728-74828255CD34_Primary_RO01480
SE_13574chr18:74825324-74829325CD34_Primary_RO01536
SE_14365chr18:74825724-74828924CD34_Primary_RO01549
SE_15148chr18:74826909-74828307CD4_Memory_Primary_7pool
SE_17992chr18:74825815-74828687CD4p_CD25-_CD45ROp_Memory
SE_18533chr18:74825547-74828795CD4p_CD25-_Il17-_PMAstim_Th
SE_19370chr18:74826505-74829277CD4p_CD25-_Il17p_PMAstim_Th17
SE_19981chr18:74825094-74829885CD56
SE_22307chr18:74808493-74829791CD8_primiary
SE_25341chr18:74808379-74829893DND41
SE_25885chr18:74825339-74828776Duodenum_Smooth_Muscle
SE_26884chr18:74825543-74828334Esophagus
SE_30168chr18:74825906-74826552Fetal_Muscle
SE_30168chr18:74826553-74827620Fetal_Muscle
SE_31917chr18:74825145-74826085Gastric
SE_31917chr18:74826200-74828693Gastric
SE_36043chr18:74825624-74828115HMEC
SE_37921chr18:74825645-74827997HSMMtube
SE_39556chr18:74825781-74828802Jurkat
SE_41189chr18:74825046-74828357Left_Ventricle
SE_42218chr18:74825053-74828585Lung
SE_44218chr18:74825138-74828320NHDF-Ad
SE_47137chr18:74808444-74829846Panc1
SE_48227chr18:74824993-74828500Psoas_Muscle
SE_49182chr18:74825077-74828060Right_Atrium
SE_50555chr18:74825062-74828772Sigmoid_Colon
SE_51089chr18:74822823-74828788Skeletal_Muscle
SE_52417chr18:74824043-74828503Small_Intestine
SE_53332chr18:74825337-74828320Spleen
SE_58547chr18:74756065-74865317Ly1
SE_62520chr18:74808577-74846347Tonsil
SE_64359chr18:74825590-74828088NHEK
SE_65574chr18:74822755-74829090Pancreatic_islets
SE_66494chr18:74825781-74828802Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr187482607174826200
Number: 1             
IDChromosomeStartEnd
GH18I077094chr187480680074829611
Enhancer Sequence
GGAGAAACAC CACATGACAA TGGAGGCAGA GATTTGGAAT GACATGGCTA CAAGGCCAGG 60
GACACCAGGG ATTGCCGCAG CCACCAGAAG CTGGAAGAGG TGAAGACAGA GCCTCCTGCA 120
GAGCTCCCAC TCTGCCAACG CCTTGACTTT GCACTTCTGG CCTCCAGGAC TGTGTGTGTG 180
TGGGGGGCTG CTTCTGCTGT TTCAGGACGC CCACCTGTGG TGCCGCCTTG CAGCAGCCCT 240
ACAGGGTAAC ATGCAGGGAA GTGGGAAGTA AGTGGAGACT TGCAGGATGC AGAAGGTGCA 300
GGTGAAGGTG CTGAGGAGGG AAACAGCGTT CTGGGCAGAG GGCACGGCTG TGCAAAGGCC 360
CTGTTGCACA GACACTGTGA GTGGAGTTTG AGTGTGGCAT GAAGTGACCT AATAGAACAG 420
AATCTGCGAA TGCACGGGGT GCACTCATGG GGGGATTGGG GGAGTGACTT AGACCACGCA 480
CACAGACAAT GTTCTTCACC CGTTTTGAAC AGTGAGTCAA TTCTGCCCAT GAGCAAGTCT 540
TCCAGACTGT TGGGCCCTAG ACGAAGAACG ACCTGCAAGC CGGGAATTCT CTGCAAAGGA 600
CAATGTCAAA ACTCATCTGA GGCATCCATG TCTGTCCTAC AGCAAGCTTC CCCGTGACAC 660
TGGAGGGACC TAGGCTCCCG GCAGTTTTCA GGAGCCAGCC CTGGGCTAGG GGCTCCACAG 720
TACTTGCAAA CAAAGAGTTC CAAAAACCCA ATTTGCATTC ACCCATGTAA GAAGTGCCTG 780
ATAAGGAAGT AGCGTCTCTA TTTCCTGGGA TGGGGATTTT TGCTCTGGGG TATCAGATAA 840
TATTATTTGT AAGCTAGTCA TCACCATCCT TCGTTTTCTT CTGCCTTAGC AGATTCAGGT 900
AGATTTATGG CACTGACTAT CACTGCTTTA AAGTTATCAA AAATCACTTT AAAAGAAAAT 960
GACGAGATTG CAGAAAAGTG GAGTTTATTG AAAATCTGAC TGTGGTCCCT TGAAGTTACT 1020
GCTTACAGGA TCAGCTGACT TTGGAGAGAA AGCCATTATC AGAATCAAGC AGCAAATTAC 1080
TGGCCCCAGA GTTCCTAGCT TGCTACAATA TCAGCTGTCT AAACCAAAAC AAAGCATTTT 1140
GTTGAAGCGG GGAAAAAAAG GCAGATCAAA GAGTAGCTCA TCCACGTGTC AGTTAGATTA 1200
GCATTTGAAA TTCCTTGTGA ATGTATCCAC ATGTTTATGA CAGGCATGGT GTTCAGCTTT 1260
AGCAGCATTA TGGGGAGTTA CGAAATTCTC TGTGTAAAAA TAGCGAGGTC ATGAGGAAAC 1320
CACTCTTGCT GTGTAAGTCC TGACAAGCCA TGCCAACACC GTCACGCTGG GACTGGCCTT 1380
CGGATGGCAC GGGGAGGGCA GAGTCACGCA GGCACACGTG ACACGCCCTT GCTCTGCGGC 1440
CGGTGGGATC CCTGGTAGCT TCGCAGTCAT GTGGGGCTTA GTCACAGGAG CATAGGTCAG 1500
GTCCTGCTGA GCCCCCTTTC CAAGTGTGCG GTGCGCAAGC CGCCCAACCC AGGGGCCGGC 1560
AGCTGGGACA GGGCGAGCAG TGGGCTGCAG GGAGGAAGTG GGGAAGGCCT GGGGGCAGAC 1620
GTGCCTGGGC GAGGGCCTTC CTATTCCTGC TCTCCCTGTC TGCTCTGAGG ATGTGGGCCC 1680
TGACCTCCTT ATCTGTAAAG CCCTGATGGT GGATGCAGCT TCCTGGAGCT GCTGTGGAAA 1740
CCACTGGTTA ATATTTTACA GGTCGCTGGG TTACAAACTG TCAAGTCAGA GGAACACTAC 1800
ACGCTGGCAC CAGCTGCTCC TCTGTAGCCA CCCGTATGTC CCTCCTGAGC CGTGGCAGGG 1860
AGTGACACCT TTGCCAATAC CACCATCCAC AGGGTCAACA TGACCCCGGG CCCTGGTCTT 1920
AGTAACTAGA GGAAACACAC CGACTTCAGG CATTGCTCAC AGCCAGAGCT GGTGTTAACT 1980
GAAGAATGTT TTAATTCACC TGCCGAGGAA CTCACACATT CCTTGCCAGC AGGCACAATG 2040
GCTCTTGATA GCCTGTGTGC AGGGAACAAA TGTGTTGGCC CCATGCTCAG GCCATGCGTA 2100
CACATAAGAG CTGTCGTCTG GGTCTTGGCT AAAATAAACT GAATCTTCCC GAAAACACAG 2160
GTTCCTATTA CGGAGTCCAT 2180