EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS095-13339 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr17:79064090-79067370 
TF binding sites/motifs
Number: 14             
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
Nfe2l2MA0150.2chr17:79065868-79065883TGCTGTGTCATTGTC-6.21
PPARGMA0066.1chr17:79065259-79065279ATAGTTCACGGTGCCCCCTT+6.09
RREB1MA0073.1chr17:79064990-79065010ACCCCACCCCACCCCACCCC+6.22
RREB1MA0073.1chr17:79064986-79065006CCCCACCCCACCCCACCCCA+7.67
RREB1MA0073.1chr17:79064991-79065011CCCCACCCCACCCCACCCCA+7.67
ZNF263MA0528.1chr17:79064165-79064186TGCTCCTCCCCATCCGCCTCC-6.28
ZNF263MA0528.1chr17:79067259-79067280GGGGGAGGAGGGAGGTGAGGC+6.8
ZNF263MA0528.1chr17:79064168-79064189TCCTCCCCATCCGCCTCCTTC-7.46
ZfxMA0146.2chr17:79065692-79065706CTGGCCGGGGCCTG+6.08
ZfxMA0146.2chr17:79066092-79066106GAGGCCGAGGCCCC-6.31
Number of super-enhancer constituents: 16             
IDCoordinateTissue/cell
SE_25200chr17:79064331-79065001Colon_Crypt_3
SE_25200chr17:79065029-79066386Colon_Crypt_3
SE_25200chr17:79066404-79067110Colon_Crypt_3
SE_26560chr17:79058335-79072649Esophagus
SE_31420chr17:79063494-79065851Gastric
SE_31420chr17:79065869-79071978Gastric
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_65191chr17:79065995-79066845NHEK
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: 5             
ChromosomeStartEnd
chr177906467379065032
chr177906518779065373
chr177906567279066072
chr177906662679066874
chr177906728179067336
Number: 1             
IDChromosomeStartEnd
GH17I081089chr177906372979072490
Enhancer Sequence
GTAGAGCCAG GATGAGCCGA CATCAACCTT CTCACGGTGC CTGCGTGGGG GCTCTCCTGG 60
ACGGACCTCC GCCTCTGCTC CTCCCCATCC GCCTCCTTCC TCTGTCAATG GGAGACGGGG 120
CTTCAACTCT TAACCACACA GGTGTTTTAT TTTTGTGGTT TTTCCCAAGT CACCGAGTTT 180
CTTCAGGAAG GGCTAGGTCT CATTTCTCCT GCGTCCCACT TGGTGCCAAG CACAAGCTGG 240
TCACGCAGCA GATAGCTAGT AAGTGCTAAG TGGTTTCGAA ACAACATTTT GGGGTGGGAA 300
ACAGAGGGAG CCACACCCCG GTGTGCTTTC TGCTCCCCAG TGGCCTGGAA GCCCAGGAGG 360
CCAGGCCTCG GAGCCGTCAG CATCCCCAGC CCCACATCGG AGTTTGAGGG GGTGGGGCAC 420
TTGGTATGTG GCTGCGTACG CGCCCCCCGA GCTGCGGGGA GGCTGCGGCC ACCATCCTGG 480
GGTGAGTGCC ATGTGGCTGC CTGGCTGGGA TGTGCTGCCG GCCTCGCTGC TCCAGGCCCC 540
TTGCCCCACC CAGGGCTGTT CCTGCTGGTT CCCATTGCCT TTGCAAACCC GGCCAGCGGG 600
CTCTGTGGGA CTTCTACTTT AGGGTGTGGC CGCTGGGGGC CCAGCTGTTG CATGTCCTCT 660
CCACTTCTGA AGAGAGGAAG CACCCTGGGC TGGGGAACTG GGCTGGCTGG CCCCGCCTAC 720
TCATGTGCAG CCCCGCCCCT CCAGTGCATT CCACCCCGCC CCCACTTGTG TGGACCCGCC 780
CCCACTTGTG TGCCCCGACT TGTGTGGTGC AGGAGGCCCT GCCCTTGCTT GTGTGGCCCC 840
ACCCCTTGGT GCAGGAGGCC CCGTCCCTCC AGTGCACCCC ACCCCCATTT ATGTGGCCCC 900
ACCCCACCCC ACCCCACCCC ACAGGCCTCC TAGCTGTCCC TAACTCCTGG CTTGCCTCGC 960
GGGGTCTACT GTCCTGGGGC CTAGGTTGTC AGCGAAGTCC TGCTGGTTGC AGGGAAAGGG 1020
CCTGCTGGAA GTACTCTTGG GGGAAGCAGA GACCTCTTCA CCGGCCTCTC CATTCCTAAA 1080
GCGGTTGGTT GCTTCCCAGC TGTTCTACAG ACCAGCCCAG CAGCTGCACC CTATGCTGGG 1140
GGCAGCCCGG GGGTGTCTAC GCAGAGAGTA TAGTTCACGG TGCCCCCTTG AGATCCCTGC 1200
CTCGGTCCCT GGACCTGCCT GCCCCCAGCT CTTCTAGCTG TCTCCAGTGT ATGCCCTGTG 1260
GGGTCACTGG CGACCATAGC AGTTGTCCCC AATCCTGAAG ACCCTGAGAG AGGCAGGTGT 1320
GCCCACACGT CGTTGGAGTG CAGGGCAGGA GTCTGGCCCA TTCGGGCTCC TGGGGCTGCT 1380
TTCTTGAGCG GGCAGGAGGG GGCTGCCGGA CTGCCGGAAG TGGAAGTGAC CCCACGCAAG 1440
GGTGGCCTGA AGCCAGTGTC CAGCCAGGGG CGTGAGTAGC AGAGAAGCAG ATGCCTCCCT 1500
GCGGTTCCCA AGCTGCCCCT GCCACAGAGG CCTTTCCCTT GGAGACCCTT TAGTGCCTCT 1560
GGGGTCTCTG GCCCTGCATG TCCCTCACCT GGCAGCCTAG AGCTGGCCGG GGCCTGGCTG 1620
GTGGTGCAGC CATGTGGGTG GTGCATGCAG GTGGAGGCTG TTCAGGCAGC TCCACGGGCT 1680
GGACGGGCGC CCCCATCTAC AGGGCCCCCC ACCTCAGCTG CCGCTGATGA AGGGGAGGTG 1740
GTGGCTGGTG CCTGACTCTG GTCTTTGGGG GTGTAGCATG CTGTGTCATT GTCAGATGTG 1800
GGTTCCCTCA GCGACCCAAG AGCTGGGTGT CTCGAAGTGA TTGCCGGGGT CTCCAGTGGG 1860
CTCAGAAACC TGGCGCCAGC TGCACCCCAC CTGAGCTGCA TGTATGCGGA GCACCAGGCT 1920
CCTGGGAGCT GTGAGGCTGC TGGGCAGCGA GGCTGGGCCC ATGGCACGTG TGAGGGGCGG 1980
CTTCATGCTC CAGGGTGCCT ACGAGGCCGA GGCCCCCGAT GCGCACTGCC CGCCTCCACT 2040
GCCGGGCTCA TTGTGTGGCA GCGGCCAGGC CTTCAGCCTG AGCTGAAACA GGGACACACC 2100
ACACCAGGCC CTGGGGGCAG AGGTGGGGCT GCAGGGAGGG GTGGGCGTGA GGTTGGCCAG 2160
GCCCTGCCCC AGAGAGGCAG GCAGAGTGGA TTTCTCTGTC TGCCTGCCAG GGTGCCCTTG 2220
AGCGGGGCTG GGCCCGGGGG CCTCCTGTTG TTCAAGAACT GCTTGTAATT GAGATGGTGT 2280
TTTGGGATTT CCATGAAAAG AAGTAATTTT AGTTATAGGT CAGGGCACTG GGGCTAGGAA 2340
GCATTTGGGG TGTTTGTTAA CTAGGACGGG AGAGCTTTAC GTAAGGGGCC CGGCCCGGAG 2400
CACCGCCCTG ACGGCCTTGG GCAGCGGCAC CTTCACTCCC CAGGACCGTG GTCGTTGCCA 2460
CATTTGCTGG GCCAGGTGCT GACAGACGTG CCCGTCTGCC TGGAGGGAAT GTTCTCCACA 2520
CCACGCGGGG CACGGTGGAC ATGCTGGGGC AGGGGACACC TTCTCTGTGG GTTTATCAGT 2580
GTGTCCGCGG GGCGTGGTCA CAGCCTGGTC CAGCTCCTCC TTAGAACAGA GGGGTGTGGC 2640
TGTGTCCACA GGGCCCGGAA TGGGGCTGAG AGCAGAGCCC AGCCTGTGCC CACCGCTCGG 2700
GGGCAGGGAG CAGGGCCCGG GGGACGTGTC CACATGCCCC ATCCTGCATC TGGAACCCAG 2760
GGTGGGAGGC GAGTGGCCCA CCCACTCCCT GGGCTGGGCT GGGCTGGGCT GGGCTGGGCT 2820
GGGCTGGGCT GGGCTGGGCT GTGGGCACGA GGACCTGAGT GTGAGGAGGG AGCCCCGGCC 2880
CGCTGGATGC AACTTGTCCT TCCTAACCCA TGTGCACTGA GGGTGGGGCA GCCGGGCCCC 2940
TGCTCAGAAT CGCACTGGGC ATGGGCTCGA CTTGCTGGCC CTGGGACGAC CCTGCTCAGC 3000
CAGCTCTGGA GGCTTCCTCA GCGGCCTGAA ACTCCTGCTG CAGAGGAGGG TAGCATTGCC 3060
CTGTCCACTC ACCACCTCCT GGGGCTTTTC TGGACAGAGA TGCCCGGGGC TACAAGGAGA 3120
GCCAGGGTTT CTGCTGGGTT ACCTTCCCCT GTTCCCTTTC TGAGATGATG GGGGAGGAGG 3180
GAGGTGAGGC AGGTGCAGCC CTCGCTGGCC GGTCGTGAGT GAGGAGGGAG AGATGGCCCC 3240
GCATCCCTGG GGATGCTGCC TCCCAGAGAC CATGGGGGCT 3280