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

TagContent
EnhancerAtlas ID
HS145-05144 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr11:130051560-130052300 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr11:130052084-130052095AATGAGTCACA-6.62
Number of super-enhancer constituents: 19             
IDCoordinateTissue/cell
SE_23084chr11:130047397-130052721Colon_Crypt_1
SE_23752chr11:130050721-130051652Colon_Crypt_2
SE_23752chr11:130051656-130052123Colon_Crypt_2
SE_23752chr11:130052207-130052565Colon_Crypt_2
SE_24749chr11:130047721-130052693Colon_Crypt_3
SE_27111chr11:130047544-130052738Esophagus
SE_27706chr11:130047367-130053339Fetal_Intestine
SE_28552chr11:130047102-130055375Fetal_Intestine_Large
SE_41707chr11:130048078-130052166LNCaP
SE_50138chr11:130047351-130052790Sigmoid_Colon
SE_52428chr11:130047377-130052939Small_Intestine
SE_57437chr11:130050712-130052138VACO_503
SE_57437chr11:130052187-130052576VACO_503
SE_58103chr11:130051720-130052212VACO_9m
SE_58103chr11:130052214-130052575VACO_9m
SE_58488chr11:129985075-130060331Ly1
SE_60756chr11:130015852-130052711DHL6
SE_61683chr11:129986883-130083431Toledo
SE_65550chr11:130050703-130052770Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr11130051825130052120
Number: 1             
IDChromosomeStartEnd
GH11I130177chr11130047463130054066
Enhancer Sequence
TTAAAAGAGC TTTGCTGCTT CACTGACTTT ATTAACTTTG TGACCTTGGA CAGGCCACTC 60
CCTCTCTTTC ATCCTCAGTG TTCTTATCAA TAAAACGATG GGATTATGCA ACAGTATCTC 120
TGTTACACCT GAAAATGGAG CCAAGAGCTA AGGTTATAAA AGGAAGCAGC CCAGTTACTG 180
ATTAGACAGC ACTTTTAGGC TGGGTGGAGC CACAGAACTC ACACTGCAGG GAGGACAGAG 240
GACCCACCAT TGAGCTAGCG CCACTGCTGA CAGCCTCGCT CCGTGGCAGA GTCTGGGGTG 300
ACCCCTGAGT CAATGCCCTC AGCCACCTTA CCCCTTCTCA TGGGAGTCTC TGTCTTCTGT 360
TTCCCTGAAT CCTTGCTCCC AGAATTCTGG AACCTAACCA CACTGGGAGG CAGTAAACCA 420
GGACCAGATT CTGGATCTGC CACCAAGTAC TGGGTGACCT TGCAAAATCA GCATTCTTCC 480
CTGCCTTCTT TATATAACAC GGGTGATAGC ACCAGCCAGT CTTGAATGAG TCACAGGACT 540
GTCATGAAGA TCCAGTAAGA AAATGGTTGT GAAATTACCC TGTGAATTGG ATATACATCT 600
AAACATGATA AATTATTATT TCATTACATT TCTTTTTTTC TTTGTTTCTT TCTTTCCTTT 660
TTTTTTTTGA GATGAGGTTT TGCTGTCTCT GTCTCGCCCA GGCAGGAGGG CAGTGGCATG 720
ACTATGGCTC ACTGCAGCCT 740