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

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EnhancerAtlas ID
HS012-18149 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr3:58034830-58035660 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12494328chr358035497hg19
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_00762chr3:58032174-58039716Adipose_Nuclei
SE_01957chr3:58034706-58035838Aorta
SE_23194chr3:58034815-58035733Colon_Crypt_1
SE_26498chr3:58033363-58039459Duodenum_Smooth_Muscle
SE_27681chr3:58033703-58037597Fetal_Intestine
SE_29426chr3:58033550-58039244Fetal_Intestine_Large
SE_30574chr3:58034058-58035832Fetal_Muscle
SE_36024chr3:58033449-58039332HMEC
SE_37989chr3:58025669-58040227HUVEC
SE_41579chr3:58034780-58035730LNCaP
SE_45969chr3:58032377-58039419Osteoblasts
SE_47269chr3:58019885-58040171Panc1
SE_56289chr3:58032310-58039346u87
SE_64106chr3:58033450-58035902HSMM
SE_65730chr3:58034390-58037100Pancreatic_islets
SE_67942chr3:58032310-58039346u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr35803500658035314
Number: 1             
IDChromosomeStartEnd
GH03I058046chr35803243758041425
Enhancer Sequence
GTTCCAAGTG TGGCAGACAG CTCTCACAAG TTACAAGTCG TTGCGTAGGA CATACCTATG 60
CTAAACGATT TGATGTTTAT CTAAATTAAT ATGTAACTGA TATCTTGTAT TTTTATTTGT 120
ACGATCTTCC AAGCCCACGT CCCACCGCCT TCTCGGGGAT GGCCACCATT TGTGTTTGCT 180
GCCTGGTGGT GTTTGCAGCT GCGAGAAGGG CCTTGGAGGA GGAGCAAAGT GTAGTGGTAT 240
CTCCGTGCTG TGGCCTTGGG CACTGGGGTG GGGGTTAGAT GAGTAATTAG CTGAATATGA 300
CCTCACCCAT GAAGAATGTG CCCTTGCTAG GTATTAGCAG AGGTTTAGGC TCCAGGGAGC 360
CATTGTCAGA AGCTTGTCAG TGATGTCATC AGCTGGAAGG GCCAGCTTTC AGGCCTCAGG 420
AAAAAGCTTG AAAGTCAGGG CTCCAGTTTT GGTAATAAAT GGGAATGGAG TTTCACAGGT 480
AGGGTGTGGA GGAATTTATT GTGACAGGAA GCCTGATGGA GCCTCTTGCC TGTGTGCAGC 540
CCCCAGCCAG GTTTCTGAGT TCTGATGAAC TACCAGAAAC TTCCACCACG GCCTGTGATT 600
ACACTGTTGG CCCAATGCCC TGGAAAAATT GGCTTGCTCT CGGGGAACAC TCCAGGAGCT 660
GCAAAGGGGG TGTCAGGACT GTTGTGCAGC TCCCCTTAAA TTGGGGAGGA GGGGTGGCTG 720
ATGTGGAAAC TGTTCATTAG ACTGCTCAGG GTAGTGTGAG AAAACGTGTA ATCTGTGGGC 780
ATCTACCCCT AGCTGCCCCT CTGATCTCAC CCACTACTGT GGGAGGACCC 830