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

TagContent
EnhancerAtlas ID
HS180-01749 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:54751180-54754450 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:54753246-54753264GGAAGGAGGGAGGGAGGG+7.12
RUNX1MA0002.2chr1:54751331-54751342CTCTGTGGTTT+6.14
ZNF263MA0528.1chr1:54753243-54753264TGGGGAAGGAGGGAGGGAGGG+6.23
ZNF263MA0528.1chr1:54753247-54753268GAAGGAGGGAGGGAGGGATGC+6.37
ZNF263MA0528.1chr1:54753244-54753265GGGGAAGGAGGGAGGGAGGGA+6.61
ZNF740MA0753.2chr1:54754257-54754270GTGGGGGGGGGGA-6.3
Number of super-enhancer constituents: 27             
IDCoordinateTissue/cell
SE_01019chr1:54752247-54754319Adrenal_Gland
SE_01595chr1:54751203-54759655Aorta
SE_03451chr1:54752074-54754199Brain_Angular_Gyrus
SE_04187chr1:54751873-54754162Brain_Anterior_Caudate
SE_04901chr1:54751170-54754425Brain_Cingulate_Gyrus
SE_05919chr1:54750929-54759710Brain_Hippocampus_Middle
SE_07802chr1:54751293-54754608Brain_Inferior_Temporal_Lobe
SE_08904chr1:54752439-54752817Brain_Mid_Frontal_Lobe
SE_08904chr1:54752873-54753200Brain_Mid_Frontal_Lobe
SE_24580chr1:54752076-54754303Colon_Crypt_2
SE_25961chr1:54751204-54754577Duodenum_Smooth_Muscle
SE_26701chr1:54751969-54754451Esophagus
SE_28122chr1:54751720-54754452Fetal_Intestine
SE_29698chr1:54751486-54754587Fetal_Muscle
SE_31383chr1:54751291-54754337Gastric
SE_33414chr1:54751466-54754498H2171
SE_41585chr1:54752012-54752806LNCaP
SE_41585chr1:54752835-54753501LNCaP
SE_42582chr1:54751871-54754530Lung
SE_46626chr1:54752006-54752816Ovary
SE_46626chr1:54752831-54754462Ovary
SE_47967chr1:54752871-54753560Pancreas
SE_50141chr1:54750323-54754516Sigmoid_Colon
SE_52383chr1:54751201-54754495Small_Intestine
SE_54182chr1:54751464-54754325Spleen
SE_65414chr1:54751886-54754405Pancreatic_islets
SE_68686chr1:54751900-54754312H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr15475150854754190
Number: 1             
IDChromosomeStartEnd
GH01I054284chr15475047454757956
Enhancer Sequence
ACTTTAAAAT TATTATTATT ATAATTAGAG ACCTGGTCCC CAGGCTGGAA TGCAGTGGCC 60
CAATCATGAT TACTACGTGT ATAATTCAGA GACCTGCTCA AAGCTGACCG TCCAGAGCCA 120
GGCCTTTCCA GACTGCTAGG AATCGGCCTC CCTCTGTGGT TTCCAACTTT GAGCTGGAGC 180
TCCATTAAGG CGCTCAGCAA AGCGTCTCAT GAGTTTTCCC TAACAACACA AAACCAAAAC 240
CCCTGAAAAC CCCCATTATT CACTGAGGCC TACAGCATGC CAGGGCTGCA GTGGGTGCAT 300
GGGCTAGAAG TCCCCCACGG AAGAAGAGAG AAAAGAACAC TGGATTCAGA AGCTAGAGAT 360
CTCCTAGCTG GGAGCCCACG GACAGGCCCC TTTCTCGTTC TGGGACTCAG TTTCCCCATG 420
TGTCCAATGA TGGTGTTAGA GGAGATGACC ACTAAGGCTC TTCTTCCAAG CTGCTCTCCC 480
CAGCTAAGTC TACACACCAA GGGGAGCTAG GTCTGGAAAC AGCAGCTCTT CCATGAACAG 540
GACAGCAACC CTCTTTCCAG GGCACCTGGG TTTTAACTCT TCTCTGTTCA TTATAGGCCA 600
TTTTGTGATC AAAGATTAAA CACTACCGAG AGACCTGTTA TCTGAGCCCA CAGATAACAG 660
TGGGTGACAT TGGGTTCTAA CCGCCCAGGC CTTCCTTCCT CACCAATGCT TATCCACTTT 720
TTGGACTCAA GAAAGCCAAC TCAAACCACC CATGCAGTTT GGTAACATGC ACTTTAAAAA 780
ACAACAACAA AAACAACAAA TAAAGCTAAT TTAAAATTCT TTTCTAAACA GCAAACAGGC 840
CTTAAACAGG GTGATGAGGC CCATTCCAGC CAGGTGCCTC CTCTAAACCT ACAGTCAACT 900
TGAAAAGCCC GAAGTGCTTT CCCAGAGCAC TGCCTGAAGT TTGCCGTTCA CAGCCAGGGA 960
GACTTGTGAA GAGGACTGAT CCCACAGCTC CATCTCTAAA GAGCAGGGTT TCTTGATGAT 1020
CCCAGGATGG GTACACAGCC ATGGGGCTCA GGGACTACCC CTGCCTCTGC CCTATCCATG 1080
CTCCAACGGG ACAGACACAT GCCACTGCAA CCAGAGATCC TCAGCAATCC CACTCCGTAA 1140
GGACACCTGA AAACCTCACC ACCAGTCCCA CCCTAGGAGA TGGATATTCC CCCTCTAACC 1200
TCCAGGGTGG AGAAGCAGGG TTCAAACAGG GGGCCTCAGA GCGGTGCTTC CAAGAGAAAG 1260
CGCCTTGGAA GCCAGGCTAA GGAATGGAAC TTTCTGCTCT GGGCAATGGC GGAGCGGGGG 1320
GACATCTACT GCCCCACCTC ACCCTGTGCC GGGCATAGGG ACCTTTCATG CTCACTCAAC 1380
AAATCCCAAT ACCACCAGAG TACCCCAAAT TCCAGGAGCA AGTGGACTTG ACGAGTCCCC 1440
ACATTCCCAG AGGCCTCTCA TCCCACCCTG AGAGAGAAGC ATCTCAGAGT AGGCAACAGT 1500
GTTGATGCTT TTCCTTCAAG AAGCAATGGT CCAGGGGCAT TCCCTGCAAG ATACTATCTT 1560
CTGGCCTCAT TTCAAGAACC CCAGCTATCC TCACTCACAA ACTAGCCTGA GACCCCCGCT 1620
CCAACCCTCT CTTTAAAATT AGTTCTAGGC ACAGGAAGCT CCTGGAAAAC TGAATAAAAA 1680
CAAATGCTCA GAGGGAAATG TGGGACTCCT GCCAGGTCGG CCAACCCCTC CTGACTGATT 1740
TACAAGGCTG CAAAATGGTA CTTTGTTCTG CAAATCCCCT CCCCTCCTTG CCCCGCCCTA 1800
ATACTCAGGC CTTGGCGTGC AGCAGCTTGG GGGCCACATG CAGAACCGCA TGTGCAGACG 1860
ACTTCCTTGA CTGAAACTCA ACACAGGCTG CGTGGCCCAG GGCCCAAAAC ACCAGGGGGT 1920
GGGAGGTGTG TGCTGAGGGT GGAGCCATGT GCTCAAAGCT GGGAAATGGA GGTCACTCAA 1980
GGGAGCTTGG GGCACTCCTG TGATGACTAC ATACAGAGGG CAAGTGAGAC AGGAAGCCTC 2040
CAAGTGACGC CTGTCTGGTG GCCTGGGGAA GGAGGGAGGG AGGGATGCTG GCACTGGTTT 2100
CAGCAAGACA GGGGCTTCTG TGCAAACTAT GGAGTAACCC GGGTCCCTCT GGGGCCAGGT 2160
TTCCCAGAGG GAATTTCAGC AGCAACAACA AACTAAAGAT ATAAATCAGG AATGGAAGCG 2220
ACCGGGGGAA TGTCATCACC CAGATGGAAA GGCCAAGACA GACAGAACTG GGGTTCAAAG 2280
AAGGGAAGGG GACAGGAAGA GGATTCCTGG TTTCATATGC AGACCACAGA ACAGAATCAG 2340
TTTTGGAGAA CAGGGGCTCT AATTGTGCAG TTTAGAGAAA ACAGAGCTGT TGCTACGTGA 2400
AGAGGCAGAA CCAGCTGACG TTAAAAATAG GTTTGGATGA CACACAGGAG TGACACAAGA 2460
TCCCTGCCTT CAAATAGTCA GGGGGCCATC GTGTGGGAGG AGGGATGGAT GTGTCTCCCG 2520
GCACCAATGG ACGGCCCTGG GTCCAACAGT AGATGCCCCA AGCTACAAAA AGCTTCTTGG 2580
CTGCCTCAGA AGGGGGCGGG CTGTGATAAT TTGGGGTCGC TCCCAGCGGA GACATGGCAC 2640
AAACCATATT AAAAAAGGAT TGCCATAGGA CCCACCACCG CCTGGGCCTG GGGATTATTA 2700
AGACAAAAGA GTCCTGCACT GAGGGTCCCA GGATCAGGAT TCCAGCTCTG GCGGCAAACC 2760
ACCTACTGTG TGATCTGATC AGGCCTTCCT GCCCCGGGCC CTGGACTCCA CACAAGGCAG 2820
CTGATGTCCT GCTGCTCCAG TGACACTGTG GATGTCCAAG GAGCTCTTCA GCAAGCGACC 2880
TGAAAAGGGC CACGTATAGA CAACAAAAGC CTCAACCTGT CAGGGCCAGG CCATCAGACC 2940
CAAATGAGGG TGGTCTTGAT ACCTGAGCTT ATTTTACTAA GTCCCAGCTC ATGTCTGCCA 3000
CCTGGGTATG ACCCTGGAAT GCAAGAGGGG CTGGAGAAGT GCCTGCCTTT TCATTTTGAT 3060
CCCATACATC AGCAGGGGTG GGGGGGGGGA GGGTAGTATT TATTCCCCAA CATCGCTGGG 3120
AAGATGTCAT TTCTGTTTTC CTGGTAAGGA AACTGAGGCA CAGAGAGCTG TACTATCTCA 3180
AGGTCAGGCA GCTAAGTGGC TCTAACATTA GTCCCTCTGT GCCTCCACCT TTTATCTTGG 3240
GTTCAAAAAA CAAAACCACA GTCCACTCTG 3270