EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS086-05792 
Organism
Homo sapiens 
Tissue/cell
HEK293 
Coordinate
chr17:76348600-76350060 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr17:76349309-76349320GGGGGCGGGGC-6.02
KLF16MA0741.1chr17:76349045-76349056GGGGGCGTGGC-6.62
KLF16MA0741.1chr17:76349056-76349067GGGGGCGTGGC-6.62
KLF16MA0741.1chr17:76349067-76349078GGGGGCGTGGC-6.62
KLF5MA0599.1chr17:76349310-76349320GGGGCGGGGC-6.02
ZNF263MA0528.1chr17:76348909-76348930TCTCCTCCCTCTCCCGCCCCC-6.18
ZNF263MA0528.1chr17:76349546-76349567GCCTCCTTCCCCCCCTCCCCC-7.83
Number of super-enhancer constituents: 43             
IDCoordinateTissue/cell
SE_00808chr17:76349389-76349603Adipose_Tissue
SE_00808chr17:76349781-76349944Adipose_Tissue
SE_02705chr17:76347502-76349020Astrocytes
SE_02705chr17:76349075-76350356Astrocytes
SE_06650chr17:76346825-76352412Brain_Hippocampus_Middle
SE_17289chr17:76348319-76350228CD4p_CD225int_CD127p_Tmem
SE_17631chr17:76348133-76357695CD4p_CD25-_CD45RAp_Naive
SE_19096chr17:76348317-76357839CD4p_CD25-_Il17-_PMAstim_Th
SE_19802chr17:76348354-76350502CD4p_CD25-_Il17p_PMAstim_Th17
SE_26074chr17:76347359-76349099Duodenum_Smooth_Muscle
SE_26074chr17:76349185-76350720Duodenum_Smooth_Muscle
SE_26825chr17:76347289-76350782Esophagus
SE_29662chr17:76347102-76350489Fetal_Muscle
SE_31461chr17:76347308-76350758Gastric
SE_32794chr17:76348585-76349878H1
SE_34272chr17:76347393-76350499HCT-116
SE_34704chr17:76347260-76357731HeLa
SE_36965chr17:76347183-76350755HSMMtube
SE_38941chr17:76347119-76349047IMR90
SE_38941chr17:76349071-76351453IMR90
SE_40802chr17:76347230-76350705Left_Ventricle
SE_42104chr17:76347251-76352834Lung
SE_44143chr17:76345560-76356228NHDF-Ad
SE_44765chr17:76346950-76351514NHLF
SE_45620chr17:76347079-76357119Osteoblasts
SE_46745chr17:76347749-76348991Ovary
SE_46745chr17:76349065-76350276Ovary
SE_47352chr17:76346822-76356405Panc1
SE_48690chr17:76347278-76350510Right_Atrium
SE_50089chr17:76347130-76352877Sigmoid_Colon
SE_51088chr17:76345601-76358088Skeletal_Muscle
SE_51835chr17:76349183-76350131Skeletal_Muscle_Myoblast
SE_52389chr17:76347145-76350785Small_Intestine
SE_53327chr17:76347102-76357950Spleen
SE_55689chr17:76347044-76350617u87
SE_58926chr17:76309354-76389031Ly3
SE_61360chr17:76309626-76357699HBL1
SE_62409chr17:76309367-76385525Tonsil
SE_63627chr17:76347742-76348975HSMM
SE_63627chr17:76349150-76350131HSMM
SE_65603chr17:76347223-76350252Pancreatic_islets
SE_67525chr17:76347044-76350617u87
SE_68712chr17:76347245-76350535H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr177634896476349371
Enhancer Sequence
ACCGTGGGAT GTGTTCCACA GAGATTTGCT GAATGAATGA ACGAGTGAAT GAATGAGTGA 60
CTAGAAGGGG AGAGGGCTGA GGCTCCAAGA ACAGGCTCCC TGAATAGAGC GTGTGTTGGG 120
GGTGGGTTTG CTCCGCTGAC CTGAAGGGGG TTCTCGGCTC CCCTGGGACA AGAAAACTTG 180
ACCCACTCAC GGCCGGGAAA GAGTCCAGGC TTTCTGAGCA GCCGCCCCTG GGAGGGGTCA 240
GTGACCCCCG GTGACGAACG CCTGACTCCC CCCTTCCCCC ACGCGCCCAG CGCGGCCTGG 300
TCCACCCTGT CTCCTCCCTC TCCCGCCCCC CACCCCAGGG AGGTGCGCCT GGCAGCCTCC 360
CGGCCGAATT TCCTGGCACT GGGCTGAGAA TAAACAGCGC TCTCCGCCCG TAATCCCGTT 420
GCCCCGGCGA CCGCGCTCCG CGGGCGGGGG CGTGGCGGGG GCGTGGCGGG GGCGTGGCGT 480
GGCGGGGCCG TACCCGAGGC GCAAGCTCTG CAGGGCGCAG CGGCGGCTGC GGCCGCGGCG 540
ATGCGGGCCC GGGAGGTGCC ACCCCCCGTA CTCGGCGCGG ACATTCTTCG CATAGCTCCG 600
CCAGGGCTCC CGCGGTGTCC GGGAAGTGAC TCTTCCTGGC AGAGGGCGGC CTCGAGGCGA 660
CGCGCCTGCC CGCCCGCCAG CCCGGCGGCC GCCAGATCTG GAGGGGAGTG GGGGCGGGGC 720
GCAAGAAGGT GCTCCCAGCC CTGGGGCTCC TGTCACCCTC GGCCTCGATC ATCCCGCCCC 780
GCGCTCCTGG GACCGGAGTC CCTTACTCCC ATAGACTCTC GACTGCCTCT CCGCCCAACC 840
CCCGCCCGGT ACCCTTGCGG TGCCCCCTCC CAAACATCCT TACTCATTCC TAAGACTAGG 900
ACACATCGTG CAGGCTGATT TTCCATCGCT GGCTCCCCTG TCTGAGGCCT CCTTCCCCCC 960
CTCCCCCAGA GCAGGACTTA GATTTCCCAT TCTTGGCTCT AGCCTCAGGA GGCCTGCCCT 1020
AAAACAGCAC CACCGGAGAG AGGATAGGGC CTCTTGGGGT GGAGTCTTAC AGCTCTAGAA 1080
GCAAGGTAAT AGGGCACAGG GCTGGGAGCG GGGATTTCTC CCCTTTCTGT TGGCCGGGGA 1140
CCCTCAGCCT TGTTTTTAAC CAGGCCGAGG CACGAGTGCC TGCCCAAGCC AGGAGAAGCT 1200
GCCCACTGCC TGCAGGACAC TTGTCAGCAC ATCTGGGAGC CAGGAATACC CCTCCTCCCC 1260
CAGCCAGGCC AGAGGGCCCC CGACTAAGTC CCTTAGAGGA GGGTGTCTTC CCTTCTGAGG 1320
ATTGAGAAGT GCAGAAAGAC TTCTGTTATG GGGTATGGGA TGAGGAGAGA AGGGAGCCGG 1380
TGCTGAGCAG AGTCATCTGG GGGAGAGATT CTTTCCTGGC CTTCCCAGCA GCTTGTTGTG 1440
TGGGCTTGAG CATGTTGCTT 1460