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

TagContent
EnhancerAtlas ID
HS101-00518 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr1:17889710-17893440 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr1:17891101-17891116TGGGTTCAAAGGCCA+6.53
MYCNMA0104.4chr1:17891089-17891101AGCCACGTGGCC+6.37
MYCNMA0104.4chr1:17891089-17891101AGCCACGTGGCC-6.37
ZBTB18MA0698.1chr1:17893199-17893212AGTCCAGATGTTC+6.11
ZNF263MA0528.1chr1:17891863-17891884TTCCCTTCTCCCTCCTGCTTA-6.14
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00612chr1:17885040-17898127Adipose_Nuclei
SE_01537chr1:17887238-17903710Aorta
SE_03096chr1:17890604-17891914Bladder
SE_06186chr1:17884729-17903611Brain_Hippocampus_Middle
SE_23081chr1:17890473-17892557Colon_Crypt_1
SE_23081chr1:17892959-17893832Colon_Crypt_1
SE_23747chr1:17890421-17891202Colon_Crypt_2
SE_23747chr1:17891217-17891794Colon_Crypt_2
SE_24767chr1:17890329-17891818Colon_Crypt_3
SE_26139chr1:17891743-17893168Duodenum_Smooth_Muscle
SE_26573chr1:17889896-17898099Esophagus
SE_31687chr1:17890278-17892487Gastric
SE_34117chr1:17890518-17891819HCC1954
SE_40808chr1:17889889-17894001Left_Ventricle
SE_43031chr1:17890076-17897872Lung
SE_46963chr1:17890621-17891038Ovary
SE_46963chr1:17891953-17892681Ovary
SE_46963chr1:17892689-17893219Ovary
SE_47562chr1:17890635-17891305Pancreas
SE_47562chr1:17891307-17891921Pancreas
SE_47562chr1:17891929-17892571Pancreas
SE_50079chr1:17890152-17892462Sigmoid_Colon
SE_52601chr1:17890706-17892409Small_Intestine
SE_52601chr1:17892839-17893981Small_Intestine
SE_54767chr1:17885171-17898261Stomach_Smooth_Muscle
SE_65277chr1:17890222-17891588Pancreatic_islets
SE_65277chr1:17891654-17892888Pancreatic_islets
SE_68684chr1:17890304-17893069H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr11789045017890600
chr11789240017893024
Number: 2             
IDChromosomeStartEnd
GH01I017566chr11789269017893219
GH01I017564chr11789052917892478
Enhancer Sequence
GCTTTGTCAG AGAGCCCTTT TCTTTTTTTT TTTTTTTGAG ACAGGGTCTC GTTCCATTGC 60
CCAGGGTGGA GCGCAGTGGC GCCATCTTGG CTCACTGCAC CCTCGACCTC CCAGGCTCAA 120
GTGATCCTCC CACTTTAGCC TCCTGAGTAG CTGGGACTAC AGGCGTGTAC CACCATGCCT 180
GGCTAATTTT TGTATTTTTT GTAGACATGG GGTTTCCCCA TGTTGCCCGG GATGGTCTTG 240
AACTCCTGAG CTCAAGGAAT CTGCCTGTCT CGGCCTCCCA AAGTGCTGGA GTTACAGGCA 300
TGAGCCACTG TGCCCAGGCC CTTTTTCTTT TCTGTTTGTT CACTGATGTG TCCCAAGTAC 360
TCAGAACAGG ACTTGGCTCA TGGAGGTGCT TAATAAATGT GGGTTGAATG AATGAATGGT 420
TGGATGAATG AATGAATATT ACCTAATTGG GTCTCAGGAG TGTCATGACA CCCAGTTTGC 480
AGATGAATAA ACTGAGGCTT AGGGAGGTTA AGTTGCACAT TTGCTAGGTT GTGGAGCTGG 540
GATTTGGAGT CCCCACTGTC TGACTCCAGA GCCGGTGCAC AGACCCACCC ATCTATTAGG 600
ATCCTCAAGG AGGAATTCTT TCTGTGGCTG ACAGGTTGGA TTTCAACCTC TCAAAGACCC 660
CTCCGTCGTC TGAGAGCGTC TGATTGTGGG AAGAAACAAA ATGACCCAGA CAACAGCTGG 720
GTCAGTGCTG CAAGTGACAG CAGATGGCTC CTGCCACTAA CTCCTGTTCT GATCAGTGGG 780
TGCCCTTTCA AGGAGCCAGG TTGGGAGAGA GATGGATGCT GCCAGCCCCA AGGAGGCCCT 840
TCCAGGCTTG GTCTGACATC ATCGTTATCC TCAGCCACAG AGCGGGAGGG TGCTGGCTCT 900
GGCACAGCTG GCACATAGTG CTTGCTCTGG CCTGCACAGT GGGGCCCGTG TCTCAGGTCA 960
CCCCTGCCTG GGTGCATCTC CAGGGTGGTG GCTAGATGGC CTGGGTGAAT CCCAGGTGTT 1020
CACGGGGACA TGTGCCTGCC CTCAGCCCCC AGGTGGTTCT GGACCAGAAT GCCCAGGAGC 1080
TTAGGGCTGG GACCCAGAGA GACTTGGAGG GGGGCTGCTT TGAGAGGCTC TGTTAGGGGC 1140
AGTGCCGCTG CAACACTTCA GGGGGGCCAC TGGTCTTGGG CACTTGATCT GAGTCCCCCA 1200
AGTTCTCCTC CTGATGTGCT GTCCCACTGG GGCCCTGTCC TACTTGCTCC CATGGGTGGA 1260
GGCTTCATGG TCCCACCTGA GTGTACCCCA GCAGCACAGG AGCCCAGCTG ACTGGTGGCT 1320
GGCTCGTGGC TGAGGTTTTA ACCTGTAAAT ACTGTAGGGG CTCAAGACAC AGGCTCTGCA 1380
GCCACGTGGC CTGGGTTCAA AGGCCAGCGC TCTCATTTAT TGACTATGTG ACCTCGAGCA 1440
ATTTTCTGAA CCTCTCTATG CCTCTATTTC CTAACCTGTA AAAGGGAATG AGAGTGGCCC 1500
CTGTCTCAGA GGGTTTTTAG GAGGAAATTA TAGGAGCTGT AGGAGTAAAG GGCTTGGATT 1560
AGCACTGGGC CCTTAGCACG CAGTTAACAC GTGTTCGGTG TCTGATGTTG ATTTTGGCAC 1620
TGACATTGGG CAACCCAAGG AGCCACTGCA TTTCTGCTGT GCCCTGTGGC TGGCACCTGG 1680
ATTCCACTTC CTCAGTAATG CTTGTCATGA ATGGGCCAGG TCAGCAGGGA CAAGAAGAGC 1740
AAAGGCAGCA CCCGGGCACT TCACTCCCAC CCAAGGCCCC ATTCGGGCAG CTGTAACGAA 1800
ATGCCGTGAC TCTTACCAGC AACAGGCAGT TATTTCTCAA AGTTCTGAAG GCTGGAAGCC 1860
CATGATCAAG GCAACAGCAG ATTCGGTGTC TGGTGAGGGC CTGTTCCTTA TAGATGGTAC 1920
CTTCTCACTG TGTCCCTGCG TGGTGGGAGG GCCTAGCCGG GGCCTTGTTT ACAAGGATAC 1980
TAATCCCATT CACGAGGGCT CTACCCTCAT GACCTGATTA CCTCCCCAAA GCCCCACTGC 2040
CTAATCCATC ACCTTGGGGG TGAGGTTTCC GCATAGGAAT TTTAGGGGGA TAAAAACATG 2100
CAAATACTGT GGGGCTCAAG GCACAGGCCC TGGAAGCCCT CATTTCTACC TTCTTCCCTT 2160
CTCCCTCCTG CTTAACATTT GCTCCTTGCT GCTGCATCCC AGGCATTGCA GACGAACTAT 2220
CCATGCTTTT GGTCACCCTT TCAAGGAGCA CTAACTGGTG GACGGCCCCC CTCCAACTCC 2280
TCATTGCCTG AATCTAGGCT CAAGTCTGCT CTCAGGAGTT TCTGCAGCCC CCAGGTCTCC 2340
CGAAGGGAAG CCCAGCTGCT ATTGTCAACA CTGTTCAGTT CTCCTTCCCC TTCTGGACCG 2400
CCAGTGGCTG TGTCTTTCTC ACCACAGCAG GGGATACTTG ATGAATATGC ATAGAGGGTT 2460
GAGCCATGCG CTAGGCTCCG GGACACAGGG CAGGAGGGTG CAGCTCCTGG CCTCGGAGAG 2520
CTCGGCAGTC TGGTTGTTTA TTTACTAACT CGGGTACCAG GACCGTGGCT GGGCACTGAG 2580
GACATGGAGA GGCAAAAGAT GCAGTCCCAC CTTAAAGAGG CGGCTGTACA TATTCCCCCT 2640
CCCTCCCTGG CTGCCTCCTC TCCCCACCTC CTGTATTGCG GATGCTGGGC CAGGTGGTGC 2700
AGATACAGAC ACAAGTAGGT CGTGGTCTCT GCCCCCACAG TCTAGCGGGG AGAGGCACAA 2760
AAACAAGTAC TGTAGCAGAA TGCAGTTTCT TTAGATACTT GTAGCCTGGT GTTTGTCTGC 2820
CATGGAAACC AGTGGCAATG GCTTTGGTCT TTGTATTCCT GTGACTAGTA ATGGTGACAC 2880
AACCCTGCAT TAACAGGCCA GCGTCTGCTA TAGATCCCCA GAGGACTTCA CCAATGCCCT 2940
CTGATCCGGG TTTCCCAACC TCGATCCATT GACATTTGGG CTGGATCATT CTTTGTGTTG 3000
GGGCTGTCCT GTGCCCTAAA GGATGTTTAG CGGCTTCCCT GGCTTCCACC CACCAGATGC 3060
CAGTAGTGTC CCCCCTCCCC ACCTAGTGTG GCAACCAAAG TGTCTACTGC CATTGCCAAA 3120
TGTCCCTTGG GGGACACAAC AGCCCCTGGT TGAGAACCAT GGCCTCCCAT AGATCTGTAA 3180
AGCTGTAACT ATAAATCAAG GTGGGATGGA AATTTTGAAA TCCAATACTG TCTCCCTCCC 3240
CAACATCCCA TGTACCTTGG GAGCATCAGT GATCTGGTTT GGCATAAAAC ACAAACATCT 3300
TCTGGGATGT GGAGGGGCCC TTGGAGGCTG TGCACCTTGC CCAGGCCACA GAGAAGCAGG 3360
GCCCCTGGCG GAATGAACTG GATCATTGCC AGGTGTTCAT GTGCCCTGTT CTGTGTGGAT 3420
GCAGTGTTGG GCCGGTCATC ACATGGCCAC ATGGAGTATG CAGGGCCAGT ATCAGACCTG 3480
GGAGAGTTGA GTCCAGATGT TCAACTGTCC TCTTGAATCT CAGTTCAGCC CCGGTATTCT 3540
CCTTCACCTC ACAGCACCTA TGACCAGGGG ACCAAGTGCT CATCAGCAAA CCCCATAACC 3600
TCGAGTGCTT CCTGGGGCAC AATAAAGATT TGCTGAATGA GCAAGGGGGG GTTGTTGGAT 3660
GGCAGAGGGA TGCCAAGGGA TGCAGACTGG CTTTTCTGTC ACCCTCTCGA ATGCCGTTGA 3720
ACTTAAAAGT 3730