EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS101-06130 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr10:112617080-112618560 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EBF1MA0154.3chr10:112617678-112617692GGTCCCAGGGGACT-6.08
EsrraMA0592.2chr10:112618484-112618495CTCAAGGTCAT+6.02
EsrrgMA0643.1chr10:112618485-112618495TCAAGGTCAT+6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_09857chr10:112616857-112628549CD14
SE_11277chr10:112616945-112648557CD20
SE_11975chr10:112616888-112626992CD3
SE_12542chr10:112617663-112617913CD34_adult
SE_12542chr10:112617937-112618091CD34_adult
SE_12797chr10:112617081-112617317CD34_fetal
SE_12797chr10:112617684-112618019CD34_fetal
SE_14999chr10:112616784-112621466CD4_Memory_Primary_7pool
SE_16975chr10:112616940-112617714CD4p_CD225int_CD127p_Tmem
SE_17344chr10:112616862-112644426CD4p_CD25-_CD45RAp_Naive
SE_17953chr10:112616923-112635127CD4p_CD25-_CD45ROp_Memory
SE_19062chr10:112616858-112636764CD4p_CD25-_Il17-_PMAstim_Th
SE_20267chr10:112616888-112634225CD56
SE_22432chr10:112616807-112641171CD8_primiary
SE_23151chr10:112616959-112618632Colon_Crypt_1
SE_24035chr10:112617068-112618237Colon_Crypt_2
SE_25029chr10:112616950-112618632Colon_Crypt_3
SE_25873chr10:112616959-112621627Duodenum_Smooth_Muscle
SE_26657chr10:112616944-112618393Esophagus
SE_27704chr10:112616886-112621676Fetal_Intestine
SE_28632chr10:112616586-112621854Fetal_Intestine_Large
SE_29988chr10:112616981-112618179Fetal_Muscle
SE_30992chr10:112616631-112627071Fetal_Thymus
SE_31444chr10:112616885-112618795Gastric
SE_32525chr10:112616908-112622157GM12878
SE_33439chr10:112616622-112618766H2171
SE_43605chr10:112616823-112628738MM1S
SE_47589chr10:112617072-112617501Pancreas
SE_47589chr10:112617520-112618291Pancreas
SE_50110chr10:112616857-112618704Sigmoid_Colon
SE_52404chr10:112616970-112621458Small_Intestine
SE_55285chr10:112616961-112618777Thymus
SE_58452chr10:112593100-112642895Ly1
SE_59745chr10:112593531-112634215Ly4
SE_60671chr10:112600128-112635801DHL6
SE_60982chr10:112552689-112654127HBL1
SE_61666chr10:112600053-112634910Toledo
SE_62307chr10:112592977-112644561Tonsil
SE_67012chr10:112616622-112618766H2171
SE_67382chr10:112616823-112628738MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10112617518112617573
Enhancer Sequence
TTTCACACTG ATGTGGTTTT ACTGCACTAG CTCCATTTTA CGGATGGGGA CATGGATGCC 60
AATAAGACAA GATGACTCAG TCAAGGCCAC ATGGCAAGTG AGTGGGTGTC TTCCTCCATC 120
CATGGCCCTG TCAGTTTTGG CTTGGATGAG CCAAGTGGTA GAAGCGTGAC TGGGGCAAAG 180
CTCACCAGCA CCTCTCCTGG ACTTTTCTTC AGAAGAGAGG GTCAGCAGTA GCCCCTCTGG 240
GAGGTTTAAA CAACTCCATG ATACACCTGG ATCCCTTCTG CTAATGCAGC AGGCCCCTTC 300
ATTTCCAGAA ATTAGAGCTT GCCAAACAGC TGTGTTTACA TTCAGAGCCG TAGTTTATCG 360
CTGCTGGTCC TGGAAGGGAT TGTTCAAGCT TATCTTCTCT AGATAGCAAC GTGCTGAGGG 420
TTGCACAATT CTGACCTAGA TTGAAATCAG CTGCAAAACA CCTAGTCCTG AACACACACA 480
CGCACACGTC TCAGGAGACT CAAGGCACTG CAACTCACTG ACACATTCTC TCCTCAACAG 540
GCCAACTCTC TCCCATAATC CTGGGACCTG GGCCAAGGCA AGGCGGTACG GCAGCAAAGG 600
TCCCAGGGGA CTTTGTTGAG GCAGGACTGT TTCCCTGAGC TGGGTGCCGG CCTCCTGCCC 660
CATGTGCCTC ATTCTCTTGT CTTTCATGCA GGGAGACAGC TGGGTGAGAG GGCACAGAGA 720
AGAAAGACAG TAGGCATCAT GCTGCAGAAG ATTCAGGGCC AGAACAAAGG GCAGCCATTG 780
ACAGCTGCAC ATTTTATGCA AATCTTGAAC GGTTTCATCC AGGGAACAAA ACCCTTGTGA 840
AAATGGTGGA AAAGGGCCCT TTCCCTTTTA GAAATTCTAC GGTCTGACTA CTCCAGATGG 900
TAGAAGACTA ACAAAAAGCT CCAGCCCCCA TGGCTCTGAT CTGCCCACTG CCTGGTCAGA 960
AACCTTTAAG AGCTTTCAAC AGTTGGCCCT ATAAAGTCCA AACTCATTCA AGACTCTTTA 1020
TGGACTGGCC ACATCTTTAG CTCCCTCCCA GCCCAGAGTC ACCCTCTGCC TGCTCTCAAC 1080
CTTCCTGGTC TTTTATCTGT ACCCCTCCTT GTGCACTTAT CACTTTCCAC TATGTACAAT 1140
GGTTGTTTTT ATGAGTCTTA TCATTCCTGC TGGCCTAGTC TATCAGTTCC TTAAGGGCAG 1200
GGCCTATGCT TGTTTATCTT TGTACGTTGA AGCTTTAGTA TGGTATGCAT TATGGGGTGC 1260
CCAATAAAAT TTATTGAATT AAACCAGGGA CTCTCCCACA GGGATGAACT TACCTTGAGA 1320
AAGACATCTA AATTCCTCAC TGAACCCAGG AGCAGGAAGG ACACCTTCAC CCCAGCCTGC 1380
ATAGGAAGTG TTTCAGATAG TAATCTCAAG GTCATGTGGT CCAACTCTTC TATTTCAGGA 1440
GATGAAGAGA CTGAGATCCA AGTGTTGGGC TAGGGACAGT 1480