EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-14759 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr17:79063100-79065780 
TF binding sites/motifs
Number: 13             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELK4MA0076.2chr17:79065502-79065513GCCGGAAGTGG-6.62
GabpaMA0062.2chr17:79065503-79065514CCGGAAGTGGA+6.32
KLF5MA0599.1chr17:79064819-79064829GCCCCGCCCC+6.02
Klf1MA0493.1chr17:79064710-79064721AGGGTGTGGCC-6.32
Myod1MA0499.1chr17:79063856-79063869TGCAGCTGCTCCT+6.15
PPARGMA0066.1chr17:79065259-79065279ATAGTTCACGGTGCCCCCTT+6.09
RREB1MA0073.1chr17:79064990-79065010ACCCCACCCCACCCCACCCC+6.22
RREB1MA0073.1chr17:79064986-79065006CCCCACCCCACCCCACCCCA+7.67
RREB1MA0073.1chr17:79064991-79065011CCCCACCCCACCCCACCCCA+7.67
ZNF263MA0528.1chr17:79063429-79063450GGCGGAGGGGGAGAGGGAGGG+6.09
ZNF263MA0528.1chr17:79064165-79064186TGCTCCTCCCCATCCGCCTCC-6.28
ZNF263MA0528.1chr17:79064168-79064189TCCTCCCCATCCGCCTCCTTC-7.46
ZfxMA0146.2chr17:79065692-79065706CTGGCCGGGGCCTG+6.08
Number of super-enhancer constituents: 15             
IDCoordinateTissue/cell
SE_25200chr17:79063035-79063867Colon_Crypt_3
SE_25200chr17:79064331-79065001Colon_Crypt_3
SE_25200chr17:79065029-79066386Colon_Crypt_3
SE_26560chr17:79058335-79072649Esophagus
SE_31420chr17:79063494-79065851Gastric
SE_34261chr17:79063419-79064965HCT-116
SE_34261chr17:79065007-79076982HCT-116
SE_42160chr17:79063291-79067388Lung
SE_57453chr17:79063873-79064697VACO_503
SE_65191chr17:79063513-79064752NHEK
SE_65191chr17:79064909-79065712NHEK
SE_65309chr17:79063459-79064237Pancreatic_islets
SE_65309chr17:79064249-79064829Pancreatic_islets
SE_65309chr17:79065152-79072658Pancreatic_islets
SE_69007chr17:79064121-79066191H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr177906327279063545
chr177906467379065032
chr177906518779065373
Number: 1             
IDChromosomeStartEnd
GH17I081089chr177906372979072490
Enhancer Sequence
GTGCCTCGGT GGACCCTTCG TTGACTGGCC CAAGGGTCAC CTGATTCGCA GCCACAGGGG 60
GCTGGACCTG GCGGTGACTC GAGGGGCCTT GGCCCTGCCT CAGTGCTGTG GTCCACGGTC 120
TGGGCAAGGG GCCGCTGCTG GGTGCCCCAG GGGCTGACTG AACCATTTGG CAACAGAACT 180
AAGGTGGCTG GTGGCTGGGC CCGTCCTGGG GCCCCTTGAG TGCCCTTTCG TGGTAAGCCA 240
GGTGACCCAG TTTTGGGAGT AAGCCACAGC ACCTGTTTCC CAACGGCTGC CACAGTCGTC 300
ACAAAGCCCC CCTCGTCCGC AGGAGGGCAG GCGGAGGGGG AGAGGGAGGG GGTCGTGGCC 360
TTACAGGCTG TCTGCGTCCT GATGGGCCAG ACCCCGGAGC CCGGCAGGGT CAGGAATGAG 420
GGCAGCATTC CCATCTGTGG CTGCTAGTTG CCGAGGCAAA TGGTCCCCCT AGCACCTGTG 480
AGTGGGTCTG GGCGGGGACC ATGTGGGCGG AGAGGGCAGG CAGGGCCCCG AAGCGCATGG 540
TAGGTGGAGG TTGCAGTGGG TGTGAGGTGA GGGTGGCCCA GCAGCCCCCT TGGAAAGGCC 600
TCTGCCACCC GGTACAGAGA CGCTTGGCGA GCCTCATCTT CTCGGCCTCC CAGGGCCCCT 660
CCTGGGAGAT GTGTGGTGCT GGTCTTTCTT CCCAGGTCCC AGGGGCCCTG CTGTGGCTCC 720
CCAGCCCTGG CTGAGCAGCC TCCTTTCTCT AGAACTTGCA GCTGCTCCTC CCCACTCACC 780
AGGGGACCTG TGGGTGGCCC CAGGCTGGAC TGTCCCCACC TGGGCACAGC CTCAAGGCCC 840
TGGTGTCAGG CTTAGGCTTG GATCTGGCTC TGTCCCTTAT GGGTCATGTG GCCGCAGCAA 900
GCCCCAGAGC TTCTCTGAGC CTCAGTTTCC CCATTTGTGA GGGGGAATAT CCTGGCTTTC 960
TCCCTCTTCT GAGCACTGAC GGGAAGGGCT GTAGAGCCAG GATGAGCCGA CATCAACCTT 1020
CTCACGGTGC CTGCGTGGGG GCTCTCCTGG ACGGACCTCC GCCTCTGCTC CTCCCCATCC 1080
GCCTCCTTCC TCTGTCAATG GGAGACGGGG CTTCAACTCT TAACCACACA GGTGTTTTAT 1140
TTTTGTGGTT TTTCCCAAGT CACCGAGTTT CTTCAGGAAG GGCTAGGTCT CATTTCTCCT 1200
GCGTCCCACT TGGTGCCAAG CACAAGCTGG TCACGCAGCA GATAGCTAGT AAGTGCTAAG 1260
TGGTTTCGAA ACAACATTTT GGGGTGGGAA ACAGAGGGAG CCACACCCCG GTGTGCTTTC 1320
TGCTCCCCAG TGGCCTGGAA GCCCAGGAGG CCAGGCCTCG GAGCCGTCAG CATCCCCAGC 1380
CCCACATCGG AGTTTGAGGG GGTGGGGCAC TTGGTATGTG GCTGCGTACG CGCCCCCCGA 1440
GCTGCGGGGA GGCTGCGGCC ACCATCCTGG GGTGAGTGCC ATGTGGCTGC CTGGCTGGGA 1500
TGTGCTGCCG GCCTCGCTGC TCCAGGCCCC TTGCCCCACC CAGGGCTGTT CCTGCTGGTT 1560
CCCATTGCCT TTGCAAACCC GGCCAGCGGG CTCTGTGGGA CTTCTACTTT AGGGTGTGGC 1620
CGCTGGGGGC CCAGCTGTTG CATGTCCTCT CCACTTCTGA AGAGAGGAAG CACCCTGGGC 1680
TGGGGAACTG GGCTGGCTGG CCCCGCCTAC TCATGTGCAG CCCCGCCCCT CCAGTGCATT 1740
CCACCCCGCC CCCACTTGTG TGGACCCGCC CCCACTTGTG TGCCCCGACT TGTGTGGTGC 1800
AGGAGGCCCT GCCCTTGCTT GTGTGGCCCC ACCCCTTGGT GCAGGAGGCC CCGTCCCTCC 1860
AGTGCACCCC ACCCCCATTT ATGTGGCCCC ACCCCACCCC ACCCCACCCC ACAGGCCTCC 1920
TAGCTGTCCC TAACTCCTGG CTTGCCTCGC GGGGTCTACT GTCCTGGGGC CTAGGTTGTC 1980
AGCGAAGTCC TGCTGGTTGC AGGGAAAGGG CCTGCTGGAA GTACTCTTGG GGGAAGCAGA 2040
GACCTCTTCA CCGGCCTCTC CATTCCTAAA GCGGTTGGTT GCTTCCCAGC TGTTCTACAG 2100
ACCAGCCCAG CAGCTGCACC CTATGCTGGG GGCAGCCCGG GGGTGTCTAC GCAGAGAGTA 2160
TAGTTCACGG TGCCCCCTTG AGATCCCTGC CTCGGTCCCT GGACCTGCCT GCCCCCAGCT 2220
CTTCTAGCTG TCTCCAGTGT ATGCCCTGTG GGGTCACTGG CGACCATAGC AGTTGTCCCC 2280
AATCCTGAAG ACCCTGAGAG AGGCAGGTGT GCCCACACGT CGTTGGAGTG CAGGGCAGGA 2340
GTCTGGCCCA TTCGGGCTCC TGGGGCTGCT TTCTTGAGCG GGCAGGAGGG GGCTGCCGGA 2400
CTGCCGGAAG TGGAAGTGAC CCCACGCAAG GGTGGCCTGA AGCCAGTGTC CAGCCAGGGG 2460
CGTGAGTAGC AGAGAAGCAG ATGCCTCCCT GCGGTTCCCA AGCTGCCCCT GCCACAGAGG 2520
CCTTTCCCTT GGAGACCCTT TAGTGCCTCT GGGGTCTCTG GCCCTGCATG TCCCTCACCT 2580
GGCAGCCTAG AGCTGGCCGG GGCCTGGCTG GTGGTGCAGC CATGTGGGTG GTGCATGCAG 2640
GTGGAGGCTG TTCAGGCAGC TCCACGGGCT GGACGGGCGC 2680