EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS048-38264 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr9:134292400-134294580 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:134293887-134293905GGAAGGTGGGGAGGAATG+6.31
Myod1MA0499.1chr9:134294059-134294072AGGGACAGCTGCA-7.82
MyogMA0500.1chr9:134294062-134294073GACAGCTGCAG+6.62
Tcf12MA0521.1chr9:134294062-134294073GACAGCTGCAG+6.14
ZNF263MA0528.1chr9:134292709-134292730CCTTTCCCCACCCCTTCCCCC-6.07
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00628chr9:134292148-134295588Adipose_Nuclei
SE_01026chr9:134292530-134294306Adrenal_Gland
SE_03526chr9:134292763-134295058Brain_Angular_Gyrus
SE_04347chr9:134292201-134295834Brain_Anterior_Caudate
SE_05517chr9:134292123-134295829Brain_Cingulate_Gyrus
SE_06360chr9:134292038-134299680Brain_Hippocampus_Middle
SE_07571chr9:134292259-134295628Brain_Hippocampus_Middle_150
SE_08249chr9:134292283-134299455Brain_Inferior_Temporal_Lobe
SE_24637chr9:134292684-134293046Colon_Crypt_2
SE_24637chr9:134293305-134293822Colon_Crypt_2
SE_24637chr9:134293837-134294151Colon_Crypt_2
SE_26264chr9:134293098-134294919Duodenum_Smooth_Muscle
SE_27033chr9:134292629-134295105Esophagus
SE_30040chr9:134292936-134295037Fetal_Muscle
SE_31919chr9:134292558-134294277Gastric
SE_33613chr9:134292126-134295180H2171
SE_41398chr9:134292514-134295099Left_Ventricle
SE_41755chr9:134292378-134293781LNCaP
SE_42733chr9:134293003-134294323Lung
SE_44717chr9:134292572-134295021NHDF-Ad
SE_46497chr9:134292552-134295287Osteoblasts
SE_47717chr9:134293151-134294173Pancreas
SE_49107chr9:134292429-134294217Right_Atrium
SE_50633chr9:134292531-134295195Sigmoid_Colon
SE_53163chr9:134292426-134295143Small_Intestine
SE_54201chr9:134292903-134294232Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9134293600134294400
Number: 1             
IDChromosomeStartEnd
GH09I131417chr9134292424134295430
Enhancer Sequence
TTTTAGTTGG TCATCTCTCA GATACCTGTG GTCTCGGGCA CACAGCTGAT TGGAAACTGC 60
ATGGACTCTT CAGAGTGGGT GCCTGGATGG GAGGCTGGCC TTTTCATTTC TTGAATCCCA 120
TGTTGGTGTA TATAGGTTTT CTTTCTCTGG GGCTGGTTTT TCAAGAGAAG ACTCCCTTGT 180
CTTTGCCTGA GGAGTGGAGG GTGGTGTGGT GTTTGTCTGC TGCCCTCCTG TGAGGAGCAG 240
CAGAAGTGGG GGGCCTGAAG CTTCTGAGGT TTGCCACTCA GGTTCTCTCT TCACTTTTTT 300
GGGGGGTCTC CTTTCCCCAC CCCTTCCCCC TCTGACCCTG GTGTTCTCAA GTCTAGACTT 360
CTCTTGTTTA ATGTATCCAG TGGGGGAGGG AAGGGGCCGT AGGTGTCTAG CTGTTGCACT 420
TGCAGCCTTC AGCCAGTCCC CCCACATCTG AGTTCCCACC TTCCCCTTTC ATGCAAGGTG 480
CCTGCCACCT CCTACGACCT CCTGAGCCTT CTGATATCCT GGGTGAAGGG AGGTTTTCCC 540
CTCTGCAGTC CTCATGTTGT GGCATCTTTC AGTCTGTGAA ATCTGTTCAT ACTTTTGCCC 600
CCTCCTTGCC AAAACTGTCC CTGTTGTTTG GGTTCTTCGC TGTTTTCATT TTCGGGGGTT 660
GGAAGGATGA GCTGTACAAG CCCTCAGTCT TTCTGCCATG TTTAACCAGA AGCCCCCTGT 720
ATTCTAAATA GTGTGTCTGT GAGTTGGATG GAATTGAATT AAGGGCCATC TGTGGGATGT 780
GTGTGCGTGG AGATGCGTGC ACAGCCCTCT TTATGTACAC GGGTGTGGGA GTATTTTTGT 840
CCGAGCACCA CTCGACTGCC TTTTCCCCAT GATCGAGCAT GACTCTCTTT TTGTGTCAGA 900
ACCTCAAGAA CTGCCATTTG CTGTGGTCGC TACAGAGCAT GGTGAGGCCC AGAGGTAAGG 960
CTGGTTTTGA TGTCTGGTCA TTGGCACAAC CTTCTTACAC ATATGGAGGG TGAACTTCTC 1020
TGTCCTTCCC TCCAGACGCC TTGAGAAAGG GAGTCCAAAG CCCCGGAGGC AGAGAGTTCA 1080
GCCAGCTGCA GGGGGTGATG GTGTCACCAC CACTATCTGC TGAACTCCTC TGTGCCAAGG 1140
AGCATTGCAT CAGGGTGCTG GTGGCACACC TGGGGATCAT CATCTCTTCC TTCTAAAGCA 1200
GCTGTCTGTC TCCACTTTGT CACTGAGAAA ACAGTAAGTG CAGGAGGTGA CATTTGGCCC 1260
CTGGCCCCCT CTTCCTTCTG GAAACTTGTG TGTAGAGAGA GAGCTACTGC CTGCAAAGGG 1320
GGTTCATCCT CTATAGGGAG TGTTTGCCCC AGAGAGTGTT TACCTAGAGG TTAGGTGGGA 1380
GTTTAGATTC AGCGTTGGTT ATTATTTGGG GGATGATAGA ACCAATCTTG GTTTTTTTTA 1440
CCCCCCTGTG TTTTTTTCTG TGAGTCTCTG TGAGGACATA GGGTTTAGGA AGGTGGGGAG 1500
GAATGCTTTC TCCTGGGCTG AAGGAAGTCA CTTGCTGCCA GAGACAGGCC AGCCTGATTT 1560
GTCTTCTTCT TTTGTGCCCA GATTCCAGCT TGCTCCAGGT GACATCATTC CTACAGGGGA 1620
AAGGCTTTGG GTGTAAACAA TGGCACTGCC GGGCAAGCCA GGGACAGCTG CAGCTGGCTG 1680
GGACGTGGCC TTCCTCCTCG GTGTGTGTGT GCTCAGCTCA GCCTTTCTGC CATCCTGAGT 1740
TTTCTTTAAA ATTATCTTCA TAGTTTTAAA AAACAAATAG CAAATCTGTT TGGAATTAAT 1800
ACACAGTGTT TTATGACCCT TACTGCTGAA TTCTTTTGAA ATGGGAAGTC AAAACACAGT 1860
AGAACACGGG CGAGGCAGAT GATTAGTATT GCAGCGTGAC AGCACCTGGA ATTTAAGTGG 1920
CTCATGCTGG TGAAGAGAGA TCCAGGGATC TAATCTGGGA GCTGGTTTAG GGATGATACT 1980
TTTCTGTAAT TTTTTTTAAG ATTTACAGTT TTTCTGTATC AAGCGTATAT TTCTTTTGTT 2040
ACTAAAAATG TGATGGAGAA ATAAATGAGC AGTACTGGGA TTATCCACTT CCATAAGGCC 2100
ATCTATTGTA ACATCAGAGG GTGACTGCAG TAAATAGCTA CGTTTATTGC CCCAAAGTGG 2160
GAAGCCTTGA AACTGGGGCA 2180