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

TagContent
EnhancerAtlas ID
HS139-57418 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr9:132646330-132649160 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:132647332-132647350CCTCCATTCCTTCCTTCG-6.49
FOXP2MA0593.1chr9:132646532-132646543TTTGTTTACAT-6.14
Number of super-enhancer constituents: 31             
IDCoordinateTissue/cell
SE_09183chr9:132645771-132653823CD14
SE_12013chr9:132645967-132655908CD3
SE_13645chr9:132645606-132652474CD34_Primary_RO01536
SE_14403chr9:132645514-132655765CD4_Memory_Primary_7pool
SE_15436chr9:132646020-132654964CD4_Memory_Primary_8pool
SE_15844chr9:132646003-132653664CD4_Naive_Primary_7pool
SE_16321chr9:132645767-132654772CD4_Naive_Primary_8pool
SE_16884chr9:132645926-132655747CD4p_CD225int_CD127p_Tmem
SE_17318chr9:132645781-132659831CD4p_CD25-_CD45RAp_Naive
SE_17810chr9:132645517-132659442CD4p_CD25-_CD45ROp_Memory
SE_18802chr9:132645510-132655979CD4p_CD25-_Il17-_PMAstim_Th
SE_19281chr9:132645830-132658747CD4p_CD25-_Il17p_PMAstim_Th17
SE_20293chr9:132645787-132655078CD56
SE_20770chr9:132643424-132655006CD8_Memory_7pool
SE_21500chr9:132645995-132654502CD8_Naive_7pool
SE_21929chr9:132645944-132655003CD8_Naive_8pool
SE_22497chr9:132645857-132655701CD8_primiary
SE_25537chr9:132645898-132661500DND41
SE_30927chr9:132645834-132656055Fetal_Thymus
SE_39649chr9:132645924-132646772Jurkat
SE_39649chr9:132646947-132651663Jurkat
SE_39887chr9:132645817-132651357K562
SE_43960chr9:132646193-132652488MM1S
SE_51016chr9:132645842-132653277Sigmoid_Colon
SE_54159chr9:132645919-132653916Spleen
SE_55115chr9:132645857-132654103Thymus
SE_59885chr9:132645831-132658813Ly4
SE_61843chr9:132645962-132663709Toledo
SE_62799chr9:132645749-132664038Tonsil
SE_66269chr9:132645924-132646772Jurkat
SE_66269chr9:132646947-132651663Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9132648080132648314
chr9132646480132646964
Enhancer Sequence
CAGTTTCCCA ATCTTGGTAT AAAGGTAAAC GATTCTCTTC CCAGGGGTTC GGGCCGGCCT 60
AGTGCTGTTA GAGGCTGTAT TCTAGGAAAG CCTATGACGG TTTGGGAAAC TGGGCCATGC 120
TGAGTGCCTG TAGACAGCGT TCCCGGAAGA GGAAAAAGCA ACCTTTGTCT TTATGTGGGA 180
ATCTCTAAGC AATATTTTTG GCTTTGTTTA CATTTGAAGG TTAGATATGT GTCAATCCAC 240
GTGATTGACA TTGAACATGG AAAATGAGAA TGAAAGTTTT GTCTGGAAGA TTTATTTAGG 300
AGGTTTGGAG ACAGTTCTTG CACTACAGAA AGGTGGGCTG GAAATAGGTA CCAATTTGCC 360
TTAAAACGTT TCTTTTAAAA TACCTGGCTT TTAAGGAGTT CAGACTGAGA TGCCAAGATC 420
TGAAGTCTGT GCTTGATTAC TGAGCAGGGA CAGGAAGTGC TCGGTGACTG GGGAGGCGGG 480
GCTCAGGCCT CGCTCCCCAC GGTGCCCCAC GGTGGCTCCT CCTCCGCGCT AAGCCAGGGC 540
GTGGCTTCAG CAGCGCTTCT TAGAGGAGCC GGAAAGGCGC CCCTGCACCG TGGGGGAGGC 600
TGCAGGAGAC CTGCCGCCTG CCTGTGGTTC TGTCGGCCAT GGCGCTGCTC ACAAACCTGC 660
ATCCGAATAC ATTTGCAAGG CGCAGCCACC CAAAAAGTGT AGTTCCTACC TTTGTTCTGT 720
TTTAAATTCA GTGCAAACAT AAATTATCCT GAGGGTCTTA ATGCTACCTA ATTTTGAGCC 780
CCAGAGAGCC TTGGGGGAAG TGAGCAGAGG TTTCGGAATC ACAGCCCCCT CTGGCTCGTC 840
CCTTCTGCAA CTTCACCTAC ACAGAGAGAC ACCTGCTACC TGGACGGAGC AAGGGTGAGC 900
TGGGCGCAGA AGAAACACAC GCCTTTGGGG AAAGCTAGGA GCAGTAGACA GCCTAGGCAA 960
TGTATGTTCT GGAAGGGTGT CCCAGGGTTT CTCAGGGTGC AGCCTCCATT CCTTCCTTCG 1020
ATTTGACCCG GGACCAGCCT AGATGAGGGG GCCTGTGGAG AGCTGGAACT GGAAACAGGT 1080
TCTCAAGGGC AGGGCTCGGC ACAGCGTGGC AGCCAGGGGC TGTGCGGACT GAAGGGATGC 1140
GGCCCTGTCC TAGGCTGAGA CGTCCGTCCA GCAGGTGCCG CAGGGAGGAA GGGAGCCTTC 1200
CCCATCCCCG ACGGGGACAG TGGGTCCGTG TTTCCTCCCA CAGCTTTCGG CCCCTTAGCT 1260
CTGAGGACAA GGATAGGGTC CTTCCTCTGC TTCTTCTGTA CCTTTTGTGG TCCGGAGATG 1320
TCCCCGGCGG AGGTCACTAT ACCATCTGGA GGTCTAACGG GAGGCAGGAG TGCTCAAGTC 1380
AAGGCCGAAT GGGCACTCAG TGGGACCCTG GAGAAGCAGC TGACACACCA AGGGGCTGCC 1440
ACGTGCCTGC TGGCAGCCTT CACACGCTCA TCCCGGGTCT CAGAGGGCGC TGGCAACACA 1500
GATCCCTGCC TCCCCTATCG GGAAAGCGTT TTAGGACCAG GGAAAAGGAG GCCTCCCCCA 1560
GGCGAGTGCG CAGAGCCAGG GAACCCGTCT GGATGGTGGC TCTTTCCCAC CATCCTTCTC 1620
TGGCAGCAGC AGTTCAAAGT GGAGCTTCCA GGCTGTCCCA TACATTTCAC GATTTCTGAG 1680
TCTTTCGCTT CAATTTAAAA AAAGCTGGGG GCACGACCGA ATCCTGCCTC TGTCCACCGC 1740
CATCTCGTTC CTCATCGCAG GGGGCCCTTC TTGCTCCCTC CACTGCTGCG CTCTGCCGTC 1800
TGCTCCCGCC AGGGGTCCCC ACCACCTCTG CGGACGGAGG AGCCGCCTCC CAGGCCCGGG 1860
CGTGCCCAGG GCGGGTGGAG GGCGTGGGGC GGGCCGGTAT TTCCTGACCC GCTGGAGGAG 1920
CCGGCCCCAC AGGCTTGTGG CCTCCCCGGA GCCGGTGAGT CAGGAACTTC CTACTTCAAG 1980
AGGCTTCCCC AGTGCAGCAG AAAACAAACT AGTCGCCCCC AATGCTCCCG ACCTCTGTGA 2040
TGTCCACACC CGCGGAAATG GGGGCCCCAA ACCAGCAGGC TCTGTTCTAG GCTTCTCAGC 2100
GCTGGTGCGG CTCTTGGAGA AGGCTCGGCA GGGGCGGGTG GGGCATGGGG GGGTTCACAG 2160
GTGGAGACAG CCCGTCTCCG CCCCACAGAC GGCTGGGCGC AGTCCCGAAA TATTCTTCCC 2220
AAGTGGACTT TTTTGCTGAC AACCTAGAGG AGAGGGTTTC GGGTAGGATA ACAGTAGATC 2280
CACCTTGTTC CCTTGTGCCA CACTGTGTCA CACTGGGAAC CAGCAATTCT CAATGGTGCC 2340
TTGAAGCCAA CTGCACGCAC TTGTGGTTAG AGGTTACCAA TGGCCCCATA TTGGTGCCCT 2400
CACCTCCTGC CCTCCGCAAG TGAGGATGCT TGGCATCAGC AGAGCTGCCA GGTCTGCACT 2460
TGGTGTAGCT GCGAATATGT CATTTCCTGG ACAACTGTTT TCCTAAAACA GTGCTAAAAA 2520
AAAAAAAAAA AAAACCCTTG GGACACAGAG AAGTGTGGGC ACAAACCAAT CCTATCTTCC 2580
CCCAAAAGGC CAGGGTGAAA TTTTCAAAGC TGGCTGTGGA AACGGGGCCT CCCACTGCAC 2640
ATGTCCAGCC AGTGCCAGGC ACAAGGCTGC TGCCCTTTCG AGTTGTCCAC GTGAAACAGC 2700
TCCGCACTGC CTGCAGCTTC ACAGAAACTA GTGATTCCAG CCACGCCACC AGGAGTACCG 2760
GCTTGAGCAC TGGTGATACC AGATAAATAA TGAAACTCAG GTGTGCCCTC ATTTCACCAC 2820
CTCCTCCTGC 2830