EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS190-13243 
Organism
Homo sapiens 
Tissue/cell
Treg_cell 
Coordinate
chr9:134292320-134295150 
TF binding sites/motifs
Number: 6             
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
Stat6MA0520.1chr9:134294655-134294670GTCTTCCTGAGAATT+6.28
Tcf12MA0521.1chr9:134294062-134294073GACAGCTGCAG+6.14
ZNF263MA0528.1chr9:134292709-134292730CCTTTCCCCACCCCTTCCCCC-6.07
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00628chr9:134292148-134295588Adipose_Nuclei
SE_01026chr9:134292530-134294306Adrenal_Gland
SE_01026chr9:134294415-134295234Adrenal_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_24637chr9:134294698-134295020Colon_Crypt_2
SE_26264chr9:134293098-134294919Duodenum_Smooth_Muscle
SE_27033chr9:134292629-134295105Esophagus
SE_30040chr9:134292936-134295037Fetal_Muscle
SE_31919chr9:134292558-134294277Gastric
SE_31919chr9:134294513-134295136Gastric
SE_33613chr9:134292126-134295180H2171
SE_41398chr9:134292514-134295099Left_Ventricle
SE_41755chr9:134292378-134293781LNCaP
SE_41755chr9:134294610-134295616LNCaP
SE_42733chr9:134293003-134294323Lung
SE_42733chr9:134294418-134295345Lung
SE_44717chr9:134292572-134295021NHDF-Ad
SE_46497chr9:134292552-134295287Osteoblasts
SE_47717chr9:134293151-134294173Pancreas
SE_47717chr9:134294430-134294943Pancreas
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: 3             
ChromosomeStartEnd
chr9134293600134294400
chr9134294961134295076
chr9134292366134293574
Number: 1             
IDChromosomeStartEnd
GH09I131417chr9134292424134295430
Enhancer Sequence
TTATAATACA TATTTTTAAT CTTTGATCTC TGGCACTGTC TGTTTCCTCT GTTATTTTGT 60
CTATTTATTT GGTGTCTGTC TTTTAGTTGG TCATCTCTCA GATACCTGTG GTCTCGGGCA 120
CACAGCTGAT TGGAAACTGC ATGGACTCTT CAGAGTGGGT GCCTGGATGG GAGGCTGGCC 180
TTTTCATTTC TTGAATCCCA TGTTGGTGTA TATAGGTTTT CTTTCTCTGG GGCTGGTTTT 240
TCAAGAGAAG ACTCCCTTGT CTTTGCCTGA GGAGTGGAGG GTGGTGTGGT GTTTGTCTGC 300
TGCCCTCCTG TGAGGAGCAG CAGAAGTGGG GGGCCTGAAG CTTCTGAGGT TTGCCACTCA 360
GGTTCTCTCT TCACTTTTTT GGGGGGTCTC CTTTCCCCAC CCCTTCCCCC TCTGACCCTG 420
GTGTTCTCAA GTCTAGACTT CTCTTGTTTA ATGTATCCAG TGGGGGAGGG AAGGGGCCGT 480
AGGTGTCTAG CTGTTGCACT TGCAGCCTTC AGCCAGTCCC CCCACATCTG AGTTCCCACC 540
TTCCCCTTTC ATGCAAGGTG CCTGCCACCT CCTACGACCT CCTGAGCCTT CTGATATCCT 600
GGGTGAAGGG AGGTTTTCCC CTCTGCAGTC CTCATGTTGT GGCATCTTTC AGTCTGTGAA 660
ATCTGTTCAT ACTTTTGCCC CCTCCTTGCC AAAACTGTCC CTGTTGTTTG GGTTCTTCGC 720
TGTTTTCATT TTCGGGGGTT GGAAGGATGA GCTGTACAAG CCCTCAGTCT TTCTGCCATG 780
TTTAACCAGA AGCCCCCTGT ATTCTAAATA GTGTGTCTGT GAGTTGGATG GAATTGAATT 840
AAGGGCCATC TGTGGGATGT GTGTGCGTGG AGATGCGTGC ACAGCCCTCT TTATGTACAC 900
GGGTGTGGGA GTATTTTTGT CCGAGCACCA CTCGACTGCC TTTTCCCCAT GATCGAGCAT 960
GACTCTCTTT TTGTGTCAGA ACCTCAAGAA CTGCCATTTG CTGTGGTCGC TACAGAGCAT 1020
GGTGAGGCCC AGAGGTAAGG CTGGTTTTGA TGTCTGGTCA TTGGCACAAC CTTCTTACAC 1080
ATATGGAGGG TGAACTTCTC TGTCCTTCCC TCCAGACGCC TTGAGAAAGG GAGTCCAAAG 1140
CCCCGGAGGC AGAGAGTTCA GCCAGCTGCA GGGGGTGATG GTGTCACCAC CACTATCTGC 1200
TGAACTCCTC TGTGCCAAGG AGCATTGCAT CAGGGTGCTG GTGGCACACC TGGGGATCAT 1260
CATCTCTTCC TTCTAAAGCA GCTGTCTGTC TCCACTTTGT CACTGAGAAA ACAGTAAGTG 1320
CAGGAGGTGA CATTTGGCCC CTGGCCCCCT CTTCCTTCTG GAAACTTGTG TGTAGAGAGA 1380
GAGCTACTGC CTGCAAAGGG GGTTCATCCT CTATAGGGAG TGTTTGCCCC AGAGAGTGTT 1440
TACCTAGAGG TTAGGTGGGA GTTTAGATTC AGCGTTGGTT ATTATTTGGG GGATGATAGA 1500
ACCAATCTTG GTTTTTTTTA CCCCCCTGTG TTTTTTTCTG TGAGTCTCTG TGAGGACATA 1560
GGGTTTAGGA AGGTGGGGAG GAATGCTTTC TCCTGGGCTG AAGGAAGTCA CTTGCTGCCA 1620
GAGACAGGCC AGCCTGATTT GTCTTCTTCT TTTGTGCCCA GATTCCAGCT TGCTCCAGGT 1680
GACATCATTC CTACAGGGGA AAGGCTTTGG GTGTAAACAA TGGCACTGCC GGGCAAGCCA 1740
GGGACAGCTG CAGCTGGCTG GGACGTGGCC TTCCTCCTCG GTGTGTGTGT GCTCAGCTCA 1800
GCCTTTCTGC CATCCTGAGT TTTCTTTAAA ATTATCTTCA TAGTTTTAAA AAACAAATAG 1860
CAAATCTGTT TGGAATTAAT ACACAGTGTT TTATGACCCT TACTGCTGAA TTCTTTTGAA 1920
ATGGGAAGTC AAAACACAGT AGAACACGGG CGAGGCAGAT GATTAGTATT GCAGCGTGAC 1980
AGCACCTGGA ATTTAAGTGG CTCATGCTGG TGAAGAGAGA TCCAGGGATC TAATCTGGGA 2040
GCTGGTTTAG GGATGATACT TTTCTGTAAT TTTTTTTAAG ATTTACAGTT TTTCTGTATC 2100
AAGCGTATAT TTCTTTTGTT ACTAAAAATG TGATGGAGAA ATAAATGAGC AGTACTGGGA 2160
TTATCCACTT CCATAAGGCC ATCTATTGTA ACATCAGAGG GTGACTGCAG TAAATAGCTA 2220
CGTTTATTGC CCCAAAGTGG GAAGCCTTGA AACTGGGGCA GTTTAGTGTG GTTTAAATTA 2280
GTCACAGTAG AGTGTTTATC TCAAGAGGGT TTTCTGAGAA TCTCCCTGCA TCTCTGTCTT 2340
CCTGAGAATT AAAGGGGTCC ACTAGCAGAT CCTAAACACC TGGGAGTTTG TCCTCATGGT 2400
GTTTGAAGGT CTGCTCTCTG TACCAGCACC CTTAAACTGT GACACTTAAA CTGTGACACA 2460
CCAACGTGGG GACGGGTCCC CAGTGCACAG GAGGAGGTAG AAGCACAGGT GCCTGGTCTA 2520
CCCAGCACCA CCCAGAGCAG CCCTGCTGGG GAACGGAGGC TTCCCTGGCT GCATAGGAGT 2580
CTGGAGAGAT GAGCACTGTC AAAAGCTGAT AATTGGGTGG GCTGGAGAGA GAACAAGAGC 2640
AGAACCACGG TGAGGTGACA GCCGCCATTG GTCGAGTGCC TGCTGAGGAC AAGTGCTGGG 2700
TCAAGTGCGG GGGTCTTTGT TCTCTTGTTT ATTCCTTACA GCAGACCTGG GAGGTGGGAG 2760
ATTAACATGG TATGTTCATC TTAATCCACG AGGAAATAGA CCTCAAGTCA CAGTGTGGAG 2820
TGGAGGCGAG 2830