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

TagContent
EnhancerAtlas ID
HS047-35118 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr9:132646670-132649460 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CREB3MA0638.1chr9:132649278-132649292ATTCCACGTCACCA+6.51
EWSR1-FLI1MA0149.1chr9:132647332-132647350CCTCCATTCCTTCCTTCG-6.49
ZNF263MA0528.1chr9:132649142-132649163TTCACCACCTCCTCCTGCCCC-6.05
Number of super-enhancer constituents: 29             
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_39649chr9:132646947-132651663Jurkat
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_66269chr9:132646947-132651663Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9132648080132648314
chr9132648304132649200
Enhancer Sequence
GAAATAGGTA CCAATTTGCC TTAAAACGTT TCTTTTAAAA TACCTGGCTT TTAAGGAGTT 60
CAGACTGAGA TGCCAAGATC TGAAGTCTGT GCTTGATTAC TGAGCAGGGA CAGGAAGTGC 120
TCGGTGACTG GGGAGGCGGG GCTCAGGCCT CGCTCCCCAC GGTGCCCCAC GGTGGCTCCT 180
CCTCCGCGCT AAGCCAGGGC GTGGCTTCAG CAGCGCTTCT TAGAGGAGCC GGAAAGGCGC 240
CCCTGCACCG TGGGGGAGGC TGCAGGAGAC CTGCCGCCTG CCTGTGGTTC TGTCGGCCAT 300
GGCGCTGCTC ACAAACCTGC ATCCGAATAC ATTTGCAAGG CGCAGCCACC CAAAAAGTGT 360
AGTTCCTACC TTTGTTCTGT TTTAAATTCA GTGCAAACAT AAATTATCCT GAGGGTCTTA 420
ATGCTACCTA ATTTTGAGCC CCAGAGAGCC TTGGGGGAAG TGAGCAGAGG TTTCGGAATC 480
ACAGCCCCCT CTGGCTCGTC CCTTCTGCAA CTTCACCTAC ACAGAGAGAC ACCTGCTACC 540
TGGACGGAGC AAGGGTGAGC TGGGCGCAGA AGAAACACAC GCCTTTGGGG AAAGCTAGGA 600
GCAGTAGACA GCCTAGGCAA TGTATGTTCT GGAAGGGTGT CCCAGGGTTT CTCAGGGTGC 660
AGCCTCCATT CCTTCCTTCG ATTTGACCCG GGACCAGCCT AGATGAGGGG GCCTGTGGAG 720
AGCTGGAACT GGAAACAGGT TCTCAAGGGC AGGGCTCGGC ACAGCGTGGC AGCCAGGGGC 780
TGTGCGGACT GAAGGGATGC GGCCCTGTCC TAGGCTGAGA CGTCCGTCCA GCAGGTGCCG 840
CAGGGAGGAA GGGAGCCTTC CCCATCCCCG ACGGGGACAG TGGGTCCGTG TTTCCTCCCA 900
CAGCTTTCGG CCCCTTAGCT CTGAGGACAA GGATAGGGTC CTTCCTCTGC TTCTTCTGTA 960
CCTTTTGTGG TCCGGAGATG TCCCCGGCGG AGGTCACTAT ACCATCTGGA GGTCTAACGG 1020
GAGGCAGGAG TGCTCAAGTC AAGGCCGAAT GGGCACTCAG TGGGACCCTG GAGAAGCAGC 1080
TGACACACCA AGGGGCTGCC ACGTGCCTGC TGGCAGCCTT CACACGCTCA TCCCGGGTCT 1140
CAGAGGGCGC TGGCAACACA GATCCCTGCC TCCCCTATCG GGAAAGCGTT TTAGGACCAG 1200
GGAAAAGGAG GCCTCCCCCA GGCGAGTGCG CAGAGCCAGG GAACCCGTCT GGATGGTGGC 1260
TCTTTCCCAC CATCCTTCTC TGGCAGCAGC AGTTCAAAGT GGAGCTTCCA GGCTGTCCCA 1320
TACATTTCAC GATTTCTGAG TCTTTCGCTT CAATTTAAAA AAAGCTGGGG GCACGACCGA 1380
ATCCTGCCTC TGTCCACCGC CATCTCGTTC CTCATCGCAG GGGGCCCTTC TTGCTCCCTC 1440
CACTGCTGCG CTCTGCCGTC TGCTCCCGCC AGGGGTCCCC ACCACCTCTG CGGACGGAGG 1500
AGCCGCCTCC CAGGCCCGGG CGTGCCCAGG GCGGGTGGAG GGCGTGGGGC GGGCCGGTAT 1560
TTCCTGACCC GCTGGAGGAG CCGGCCCCAC AGGCTTGTGG CCTCCCCGGA GCCGGTGAGT 1620
CAGGAACTTC CTACTTCAAG AGGCTTCCCC AGTGCAGCAG AAAACAAACT AGTCGCCCCC 1680
AATGCTCCCG ACCTCTGTGA TGTCCACACC CGCGGAAATG GGGGCCCCAA ACCAGCAGGC 1740
TCTGTTCTAG GCTTCTCAGC GCTGGTGCGG CTCTTGGAGA AGGCTCGGCA GGGGCGGGTG 1800
GGGCATGGGG GGGTTCACAG GTGGAGACAG CCCGTCTCCG CCCCACAGAC GGCTGGGCGC 1860
AGTCCCGAAA TATTCTTCCC AAGTGGACTT TTTTGCTGAC AACCTAGAGG AGAGGGTTTC 1920
GGGTAGGATA ACAGTAGATC CACCTTGTTC CCTTGTGCCA CACTGTGTCA CACTGGGAAC 1980
CAGCAATTCT CAATGGTGCC TTGAAGCCAA CTGCACGCAC TTGTGGTTAG AGGTTACCAA 2040
TGGCCCCATA TTGGTGCCCT CACCTCCTGC CCTCCGCAAG TGAGGATGCT TGGCATCAGC 2100
AGAGCTGCCA GGTCTGCACT TGGTGTAGCT GCGAATATGT CATTTCCTGG ACAACTGTTT 2160
TCCTAAAACA GTGCTAAAAA AAAAAAAAAA AAAACCCTTG GGACACAGAG AAGTGTGGGC 2220
ACAAACCAAT CCTATCTTCC CCCAAAAGGC CAGGGTGAAA TTTTCAAAGC TGGCTGTGGA 2280
AACGGGGCCT CCCACTGCAC ATGTCCAGCC AGTGCCAGGC ACAAGGCTGC TGCCCTTTCG 2340
AGTTGTCCAC GTGAAACAGC TCCGCACTGC CTGCAGCTTC ACAGAAACTA GTGATTCCAG 2400
CCACGCCACC AGGAGTACCG GCTTGAGCAC TGGTGATACC AGATAAATAA TGAAACTCAG 2460
GTGTGCCCTC ATTTCACCAC CTCCTCCTGC CCCAGCCCCA AGCAATGAGG TCCCCAAAGA 2520
GCTAGAGCAG CAACCAGTTG AATGTGCATG CAAAAAATAC TCCTGGCCAT AAGCAGCCTC 2580
TCGCAATCCT CGCACTACAT CAGCCCGAAT TCCACGTCAC CACGGTCTGA GAGCCTCCCC 2640
CTCCACCGTG GATGGGGGTG GAACTGAGAG CTATCTAGGT CTCCAGCTCC TCCCAGGGGC 2700
CAGCTCCCCA GCCCAGGGGG CTTCCAATGA CACCAGGCTG CTTCCACAAC TAGGGTCATA 2760
TCTTCATGCA ACAAAACAGT CCCGTGACAC 2790