EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-26592 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr18:74825680-74827230 
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
GCACTCATGG GGGGATTGGG GGAGTGACTT AGACCACGCA CACAGACAAT GTTCTTCACC 60
CGTTTTGAAC AGTGAGTCAA TTCTGCCCAT GAGCAAGTCT TCCAGACTGT TGGGCCCTAG 120
ACGAAGAACG ACCTGCAAGC CGGGAATTCT CTGCAAAGGA CAATGTCAAA ACTCATCTGA 180
GGCATCCATG TCTGTCCTAC AGCAAGCTTC CCCGTGACAC TGGAGGGACC TAGGCTCCCG 240
GCAGTTTTCA GGAGCCAGCC CTGGGCTAGG GGCTCCACAG TACTTGCAAA CAAAGAGTTC 300
CAAAAACCCA ATTTGCATTC ACCCATGTAA GAAGTGCCTG ATAAGGAAGT AGCGTCTCTA 360
TTTCCTGGGA TGGGGATTTT TGCTCTGGGG TATCAGATAA TATTATTTGT AAGCTAGTCA 420
TCACCATCCT TCGTTTTCTT CTGCCTTAGC AGATTCAGGT AGATTTATGG CACTGACTAT 480
CACTGCTTTA AAGTTATCAA AAATCACTTT AAAAGAAAAT GACGAGATTG CAGAAAAGTG 540
GAGTTTATTG AAAATCTGAC TGTGGTCCCT TGAAGTTACT GCTTACAGGA TCAGCTGACT 600
TTGGAGAGAA AGCCATTATC AGAATCAAGC AGCAAATTAC TGGCCCCAGA GTTCCTAGCT 660
TGCTACAATA TCAGCTGTCT AAACCAAAAC AAAGCATTTT GTTGAAGCGG GGAAAAAAAG 720
GCAGATCAAA GAGTAGCTCA TCCACGTGTC AGTTAGATTA GCATTTGAAA TTCCTTGTGA 780
ATGTATCCAC ATGTTTATGA CAGGCATGGT GTTCAGCTTT AGCAGCATTA TGGGGAGTTA 840
CGAAATTCTC TGTGTAAAAA TAGCGAGGTC ATGAGGAAAC CACTCTTGCT GTGTAAGTCC 900
TGACAAGCCA TGCCAACACC GTCACGCTGG GACTGGCCTT CGGATGGCAC GGGGAGGGCA 960
GAGTCACGCA GGCACACGTG ACACGCCCTT GCTCTGCGGC CGGTGGGATC CCTGGTAGCT 1020
TCGCAGTCAT GTGGGGCTTA GTCACAGGAG CATAGGTCAG GTCCTGCTGA GCCCCCTTTC 1080
CAAGTGTGCG GTGCGCAAGC CGCCCAACCC AGGGGCCGGC AGCTGGGACA GGGCGAGCAG 1140
TGGGCTGCAG GGAGGAAGTG GGGAAGGCCT GGGGGCAGAC GTGCCTGGGC GAGGGCCTTC 1200
CTATTCCTGC TCTCCCTGTC TGCTCTGAGG ATGTGGGCCC TGACCTCCTT ATCTGTAAAG 1260
CCCTGATGGT GGATGCAGCT TCCTGGAGCT GCTGTGGAAA CCACTGGTTA ATATTTTACA 1320
GGTCGCTGGG TTACAAACTG TCAAGTCAGA GGAACACTAC ACGCTGGCAC CAGCTGCTCC 1380
TCTGTAGCCA CCCGTATGTC CCTCCTGAGC CGTGGCAGGG AGTGACACCT TTGCCAATAC 1440
CACCATCCAC AGGGTCAACA TGACCCCGGG CCCTGGTCTT AGTAACTAGA GGAAACACAC 1500
CGACTTCAGG CATTGCTCAC AGCCAGAGCT GGTGTTAACT GAAGAATGTT 1550