EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS012-13615 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr15:67442090-67443320 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs17293632chr1567442596hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxd3MA0041.1chr15:67443036-67443048AATTGTTTGTTT+6.22
SP2MA0516.2chr15:67442662-67442679CCAACCCCCGCCCCCAG+6.12
STAT1MA0137.3chr15:67442805-67442816TTTCCAGGAAA+6.62
Stat4MA0518.1chr15:67442805-67442819TTTCCAGGAAAAAA+6.02
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00035chr15:67436757-67445463Adipose_Nuclei
SE_02258chr15:67434429-67443726Astrocytes
SE_02918chr15:67441987-67442963Bladder
SE_09181chr15:67436431-67443849CD14
SE_10875chr15:67436777-67443225CD20
SE_14469chr15:67441694-67443321CD4_Memory_Primary_7pool
SE_17822chr15:67438131-67443611CD4p_CD25-_CD45ROp_Memory
SE_18371chr15:67441444-67443356CD4p_CD25-_Il17-_PMAstim_Th
SE_19163chr15:67438237-67443338CD4p_CD25-_Il17p_PMAstim_Th17
SE_20091chr15:67441765-67443150CD56
SE_23212chr15:67438436-67443079Colon_Crypt_1
SE_25827chr15:67440940-67443576Duodenum_Smooth_Muscle
SE_26536chr15:67436749-67443276Esophagus
SE_28551chr15:67441761-67443508Fetal_Intestine_Large
SE_31411chr15:67440403-67443154Gastric
SE_35122chr15:67438336-67444036HeLa
SE_35858chr15:67437440-67443735HMEC
SE_36917chr15:67432472-67444892HSMMtube
SE_37941chr15:67424014-67445333HUVEC
SE_38858chr15:67432374-67443213IMR90
SE_40854chr15:67440475-67443283Left_Ventricle
SE_42172chr15:67436843-67443113Lung
SE_44149chr15:67433529-67443310NHDF-Ad
SE_44749chr15:67432338-67443689NHLF
SE_45534chr15:67405577-67448068Osteoblasts
SE_47100chr15:67357928-67475420Panc1
SE_47566chr15:67442362-67443080Pancreas
SE_48052chr15:67436792-67443191Psoas_Muscle
SE_48704chr15:67440533-67443140Right_Atrium
SE_50064chr15:67436770-67443203Sigmoid_Colon
SE_51081chr15:67436595-67443592Skeletal_Muscle
SE_51859chr15:67436149-67443786Skeletal_Muscle_Myoblast
SE_52344chr15:67436796-67443154Small_Intestine
SE_53518chr15:67441740-67443198Spleen
SE_55348chr15:67442328-67442692Thymus
SE_55686chr15:67433900-67443259u87
SE_58377chr15:67342858-67447290Ly1
SE_62286chr15:67356723-67443338Tonsil
SE_63642chr15:67434343-67443975HSMM
SE_64236chr15:67438078-67443807NHEK
SE_65752chr15:67440920-67442299Pancreatic_islets
SE_65752chr15:67442449-67443748Pancreatic_islets
SE_67502chr15:67433900-67443259u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr156744234767443164
Enhancer Sequence
AGGGCACCCA TTCTTTGTTA CCATTTGGGA TGGAAACTGC TTATATAAGC TTGTAAAGCT 60
TTGGTTCAGA AAGCAAGAGA ATGTGTATGG AACGTTAGCA ATTGCTGTCA TGCAAATGCT 120
GCATTTTTTG CATGTAAAGG TACCTCTTTA CCTCCATGGT CCTTAAACTA ACTTTTTCAA 180
GAAACATGGT CATTTCCCAC CCTTCCTTTA CTTCCAGCTC CCCATTCATA CCCAACAGTG 240
GCTAACTGAA AGGTTTGCAA ATCCTGAAGG CTTTGGGGCT TCTTTTAAAA AGAAGAGACT 300
GAGTTGTAAA TGTCATAAGA CTGAGATGGT TGTAAATGTC CCAACCATAC TGTGTGACAT 360
TTGCTAGGAA TTGTTGTAAA ATCACTGGAG TGAGCGCTTG TCCTGAGGCA CTGCCTCTCC 420
GCGTGAATGT CACTGAGTCG CCCGGTTGAC CCGTTGCATG TTATGCAGCA CTTGTGACAT 480
TGTTTTATCT CTCTAGCCGG TGACTCATAA TTAAGGAAGT CAAAACTGTG CAATTAACAC 540
AAAACCTCCT CATTTGCCCT CTTCACCTCT CCCCAACCCC CGCCCCCAGT CAGGAATGCC 600
CGCCTGACAT TTTCTCTAAG TCTTTGGAAA CTTTAAGATT TGTTTTGATA GAACAAGGCC 660
GCCAGTTATC ATCGCCTGGT TCCACTTGTT TTACCCCAAA AGTCTGTGAG AATCTTTTCC 720
AGGAAAAAAA AGAAAGAAAG AAAGAAAGTA AATCCCACCC CCAAGCGTGC AGTCTGCCCA 780
CAGGAAGTGA TTCATGGTGC TCCGATTCGG GCAGACCTGA CTGCAGGAGG CGGGAGGCTG 840
GGAACCAGGT CTGGGAAAAG AGGGCAGAGA GAGGATACCC AGACCTAATG GCTTCTGCTC 900
TGTGGAAGAA AGTGAAAAAC AGAATGACTA AGAGTCCTGT AATAAGAATT GTTTGTTTTG 960
TGAAGTTGAA CTAATAGTGA GGTTTGCCGG CAGATAAGAC TTGAGAAATT GCAGTTGTCA 1020
GGGGAGGGGA CTTTTCCATG TCCTGCTTTT TTTTTTTTTT TTTTTTTATT AAGAGAGCAA 1080
AGCTATTTCT CAGTCTTTTT TTTTTTTTTT TTTTTTTTTT TGAGATGGAG TCTCTCTCTG 1140
TCGCCCAGGC TAGAGTGCAG TGGCACAATC TCGGCTCACT GCAACCTCCA CCTCCCAGGT 1200
TCAAGTGATT CTCTTGCCTC AGCCTCCCCA 1230