EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS161-10844 
Organism
Homo sapiens 
Tissue/cell
PC3 
Coordinate
chr22:50340400-50344140 
Target genes
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr22:50341971-50341981GCCCCGCCCC+6.02
PLAG1MA0163.1chr22:50340609-50340623GAGGCCCAAAGGGG+6.37
PLAG1MA0163.1chr22:50341608-50341622GGGGGCCACGGGGG+7.1
ZEB1MA0103.3chr22:50343784-50343795CGCACCTGCCC+6.02
ZNF263MA0528.1chr22:50343322-50343343CCCCCACCCTGCTCCTCCACC-6.47
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_03028chr22:50341487-50344026Bladder
SE_17545chr22:50337358-50341301CD4p_CD25-_CD45RAp_Naive
SE_17909chr22:50337253-50340777CD4p_CD25-_CD45ROp_Memory
SE_23129chr22:50340142-50347336Colon_Crypt_1
SE_23738chr22:50340192-50347293Colon_Crypt_2
SE_24687chr22:50340156-50348528Colon_Crypt_3
SE_26808chr22:50341423-50346477Esophagus
SE_28169chr22:50340100-50347261Fetal_Intestine
SE_29459chr22:50340194-50347426Fetal_Intestine_Large
SE_31381chr22:50340030-50364844Gastric
SE_34375chr22:50340613-50344021HCT-116
SE_35007chr22:50341530-50344029HeLa
SE_35554chr22:50341650-50344088HepG2
SE_41617chr22:50341850-50344223LNCaP
SE_42159chr22:50339996-50364887Lung
SE_47471chr22:50340157-50349301Pancreas
SE_50117chr22:50339205-50347666Sigmoid_Colon
SE_52469chr22:50340730-50346981Small_Intestine
SE_56937chr22:50340142-50346911VACO_400
SE_57421chr22:50341953-50344030VACO_503
SE_58096chr22:50340895-50342014VACO_9m
SE_58096chr22:50342032-50347148VACO_9m
SE_61206chr22:50315437-50364432HBL1
SE_61985chr22:50315627-50364432Toledo
SE_62450chr22:50318672-50364388Tonsil
SE_65335chr22:50340176-50344048Pancreatic_islets
SE_68380chr22:50327316-50364640TC32
SE_68381chr22:50327316-50364640TC32
SE_68382chr22:50327316-50364640TC32
SE_69071chr22:50340249-50341775H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr225034180750343620
chr225034385650343984
chr225034370750343853
Number: 1             
IDChromosomeStartEnd
GH22I049942chr225033615950349619
Enhancer Sequence
CCTGACCTGC TCCACACCCC CGCAGGCCCG CAGGGGAGGG CAGAACTAGA AGGGACCAGC 60
GCATAGGGAC CTGGGGGTGC TGGCACTGAG GTCTCTGGGC CTGGGATGCT GACCTTCCCG 120
GAGCCCTGAG CTGGGCCAGG ACGAGGTCTT CCCATCAGAC TTGCCGCTGG CTAGGTGACC 180
GGCCTGTCTC ACAGATGAAA ATATATTCTG AGGCCCAAAG GGGGCCCAGA CCCTGACTTT 240
GTGGCCCAGA GCCAGGTTCT CCCCATAACC AGCAGGCTTC TTTACCCACA GGCCACTGTC 300
CACCCAAGCC CCGCAGGCAG GAACCCTTGG TATTGGGTGG CCCTGAGCTT GGGATTTGCC 360
GCTGGCTGTG TGGCCCTTCG GAGCCAGTCC GGCACACCCG CAGGCACACA CACATGCGCA 420
CTCGCATACA GCCACAGATT ACACAGGCAC CAGCTTCCCG GGAATCCATT TGTCATGCAA 480
ATGCCCCTCC TGGGGCCCCT TGCCTCCCCA GAGCTGTGTC TGTCCAGGGT GGGGCCCAGG 540
TCCGTGGAGT CCTGCAGTTT CCTGGCCACA GCTATTGGCA ACTGAGGGAT GTCTCTCCAA 600
AGAGGACCCA GATCCACGTC CAGGCTTGCC TGGGACCCGA TCCCTGCCCA GTGCGGGGGC 660
TGCAGCCTCA AGGCCCAGTC TGGCCACCGC CAAGTCCACT GGGAGCCAAG TGTGGGTTCA 720
TTCCCTCGTG GCTTCTGGTG CACCAGTGGG GTGGGGGGCC AGGCCTCTTT CCCTCCTTGG 780
CTGCCTCAAA GCAAGAGGGA GGGACTCTCA GCCCTGTGCC CACCGACAGG CCCAGTCTCC 840
ATTCCTCCTA AAGCCCCTCT ATGGCCCCCC AGCCCTTGGA GCTGAGCTTG TGAGAGCCGT 900
CCCCTACAGG GTGGGCTCGG GAGGCAGAGC TGTGAGCCTG CTCCCCGCCC ACCCAGAGCC 960
CAGCTGGGGC AGACCCAGGC ATCCAGGCCG GCAGGGTGAG CCTGTGCCCA GGTTGGGCAG 1020
CCCCCTATGC TGGGGGTGGC CAGGCTCTGG GCCTAAGTGC TGCCGGGAGA CAGGGTGGCT 1080
GGGCTCTGGG ATGCTGGCTG AGGGACACAG GCTCCCTCCT GTCCTCCGGG GCCAGTGGAC 1140
CCTGGGGCAG CCCCCATGCC TGCTGTCCTG TCCCCACACA GCCTGTGAAG CAGGCTCCAG 1200
GCACACATGG GGGCCACGGG GGCAGGTGGT CCAGACGGCT CTCAAGGCAA AGCTGGGAAC 1260
ACTGTCCCAT CCCTCTGGAA CCCGCCCTGG TGAGGGGTGC AGGGGCCCTC AGTGGCCACC 1320
TTATAGGACC GGGCACCGGG CACTTCATGA GGCTGTCTGC TCGGCCACAG CAGCCCTGCT 1380
GATGGAAGCC AGCCCTGGGC CCACTGCAGC TGAGCCACCC AGGGGCCTGG CCACCCAGAG 1440
CTTCCCTGAT AGGCTGCGCT GTGCCCGGAG CCCCCCAGTG ACTGTCTCCT GCCCAGCCAG 1500
GTCCCAGACC CAGGGCAGCC TGCAGGACCC CAGGCCTCCA CTCCCGCCAC CTGAGTGTCT 1560
GTTCTGCATC TGCCCCGCCC CTGCCTACTG GCAGCCGCAG CCCTGGGCGG GCCTCAGCCG 1620
TCGGCTTTCT CAGGGTGTCT GGGTTGGGGC GGGCAGAGCT GCCCTCTGGG GGTTCCCGTG 1680
GTCCCCTAGA GGGTGGGCTC AGCGGCATCA GCTGCCAGAG AGGCTGACCG GCCCTCATGG 1740
CTCTTGACGG TATGTGCAAG AGTTTGCCTG GCGTGGTGGG GGGTGTTGCT GGCCAGGAAC 1800
TTTCTTGCCA TCGTCTTTCT TGGTGTCTGT CTCCCCTGGG TTCTCTGGAC CCTGTCAAGC 1860
CTGTATGCTG AGGGTATGCT GTTACCAGGT GGCAAGGTGT CTCAGGCACT CCTTCAGGGT 1920
GAGCAGTCAG CTCCTGCTGC TGCCAGGGCA GAGGTGCAGA GAGCGGGGAG CAGCTGGTGG 1980
TGCCGGAACC CACAGCAAAC CCCCCGCCCT CCAGCCCTGC CCCTGACACA CCCCCGATGG 2040
CCTGGCGGAG CATCCCACCA GCCCAGCAAG AGGGCTCCTC TCCTCACCTG CCCAGGTCCC 2100
CTGGGGGAGG GGCCGTCCCT GTCCCCGCTG TCCCCCAGCC CTGGCCAGGG CTGTCCTCAG 2160
GGTGGGGAAG GCAGGCCCCC GCCACCCTCT CAGGGCCTCA GGCCTGGGGC AGGCCAGAGG 2220
GCTGGGTGAG GAGCCCTAGC AGGGCCCACC TGCAACTCCC ACTGGCGCCC CAGAGAGACT 2280
CCGCACCTAG GAAGGGCCTC GGCAGGGACC AGAGCCAAGC CCTGCCCGCT TGGCCTCTGC 2340
CCCAACCCAG ATGTACTGAG AAAGCCCAGG GCTGAGGCCC GTCTAGGGCT GCACCCGCCT 2400
GTGGACAAGG GCGGGGCAGA TGCAGGACAG GCACTCAGGT GGTGGGAGTG GAGGCCTGGA 2460
GTCCTGCAGG CTGTCCTGGG CCTGGGGCGT GGCTGGGCAG GAGAGGAGTC GCCAGCAGGG 2520
CCGGGCAGAG TAAGCCGCTC TCCCTGACGG GGCTCCTTGG GTGGACTTGG TGGGGTTGCC 2580
AAGGGGGTGG CCAGGGCACG AGTGCCACAC CCAGGCTGCA GCAGGGACAG CTCCACATGG 2640
AGGCCCATGG GCACTGGAAC CCCTGGGCGC GTGCCCTGGC CTCGCAGCCA CCCTCCCGGC 2700
TGGCCCCCAC ACCACGGCCG CGTCCCAGGA CACGGTGTGC AGCTGGGAAC AGGGCGTGTA 2760
TTTGCTTAGG GCGCCCAGGA GCTGCGGCCT GTAGGACAAG GGCCCATTGT GTGCCCAGCT 2820
GCCCCACCCC CGGGCCTCTC CACGCCCCTC GAACCCCGTC CACACGGCCC CCCACACATG 2880
ACACCCTCCG CCAACCCTGC TACCCAGCCC TCTTGGCCTG TGCCCCCACC CTGCTCCTCC 2940
ACCATCGCCC CTGCCTGCGT CCCCGCAGCC AGTCCTCCAT GTTTCCTCAC TTCCCACCCT 3000
GACACCCCTC CACCCACCAG GACCCAGGTT CTCCGAGCAG AGGATCAGAT TTCCGGCATT 3060
GCTGCCCGGG CTCCACGCAT CCGGGCCTCG CTCACGGGTC TCTCTATACA CGGGTCTCCA 3120
CTATACAGAA GGCCGATCAG TGGCCCCTGC CCCTGGAGCA GAGCCCCTCA ACCGGCAGGG 3180
ACACAGGCTT CCCACTGGAG GGGCCCTGGG GAGAAGTCCT TGGCTGGAGA GGGGGGTGGG 3240
CCGTCAGAAA CTCCCCAGGC GGGTCCAGCA TGCTGGGGGG CAGCACAGGC CCAGGGCTGG 3300
GACCCTCTGC AGTGTGGGTC TCGCAGTGTC CCCCCGCTGG CCAGAGGTGA GGCCTCAGGT 3360
GTGGCGGGCA CAGGCCATGA GAGCCGCACC TGCCCGAGGG CCCTGGCTGT TGGACTTTCC 3420
ACTCTAGAGG GGCTCAGGGG AGGCTCTGAC ACCAAGGGAG CTGGACCTCC TGCACCGTCC 3480
TGGGGACCCA GGCCCTCAGG TCCGCCAGAC AAGCCCGGCA CAGCCACTGC AGGGCCTCAT 3540
GTCAGGCACA CCCCTCCCGC CCTGCAGTAG CACAGGGGGA TTGGGGTCAC CATCAACCAC 3600
GGGGAAGCAC AGAGGGGTGG GGGGATGTGG GGGACAGGGG GGTATAGCGG GGGGAGGCGG 3660
GCATGGGGCC TGGGCCAGGC TGTGTTATGG GGGAGCCGGT GCAGGGGGTG GGGCCTGGGC 3720
CAGGCTGTGT TGTTGGGGGT 3740