EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS129-37896 
Organism
Homo sapiens 
Tissue/cell
MCF10A 
Coordinate
chr9:127058250-127060970 
Target genes
Number: 7             
NameEnsembl ID
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr9:127060468-127060486CATCCCTTCCTTTCTCCC-6.11
EWSR1-FLI1MA0149.1chr9:127060464-127060482CCCTCATCCCTTCCTTTC-6.1
EWSR1-FLI1MA0149.1chr9:127060472-127060490CCTTCCTTTCTCCCTTCC-8
ZNF263MA0528.1chr9:127060479-127060500TTCTCCCTTCCTCCTTCCCCC-6.49
ZNF263MA0528.1chr9:127060472-127060493CCTTCCTTTCTCCCTTCCTCC-7.17
ZNF263MA0528.1chr9:127060475-127060496TCCTTTCTCCCTTCCTCCTTC-7.79
Number of super-enhancer constituents: 24             
IDCoordinateTissue/cell
SE_02294chr9:127058747-127061147Astrocytes
SE_04593chr9:127059062-127060101Brain_Anterior_Caudate
SE_06625chr9:127056677-127060591Brain_Hippocampus_Middle
SE_09789chr9:127057746-127058767CD14
SE_26169chr9:127059447-127060785Duodenum_Smooth_Muscle
SE_27460chr9:127058134-127058841Esophagus
SE_27460chr9:127059031-127060840Esophagus
SE_29975chr9:127058299-127060583Fetal_Muscle
SE_31765chr9:127059185-127060283Gastric
SE_36996chr9:127057100-127061544HSMMtube
SE_38009chr9:127053913-127061502HUVEC
SE_38868chr9:127057550-127060966IMR90
SE_42506chr9:127056765-127061114Lung
SE_44293chr9:127057605-127061041NHDF-Ad
SE_44809chr9:127058896-127060886NHLF
SE_45648chr9:127057560-127065055Osteoblasts
SE_47283chr9:127057060-127064535Panc1
SE_47557chr9:127057925-127058759Pancreas
SE_47557chr9:127059253-127060282Pancreas
SE_49326chr9:127057754-127060918Right_Atrium
SE_50283chr9:127056709-127060042Sigmoid_Colon
SE_51779chr9:127058092-127060961Skeletal_Muscle_Myoblast
SE_63558chr9:127058095-127060961HSMM
SE_65907chr9:127057785-127058835Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9127059573127060376
chr9127059067127059561
Enhancer Sequence
AGATGCCGTT TCACCCGTGG ATGTTGGCTG ATGTTGAAGT TGGTCCGGCC TTGACCCAGC 60
CAGTGGCCAG TGCAGTGAGC TGTCCTTGCC GGGCCTCCGA TCTTCAGCTC CCTGGGGCAT 120
GTGTCGGGCA GTGGAGCCTC TGCAGGCTGG CTGAAGGCCC CAGGCAGTGG GCATCCATCC 180
TCGGCTTCTG CCACCAGGAG CCAGCTGGAC CAACAGACAT CACCCCTGGT GCTGGCACTG 240
GTGCTGCCAG TACCATTCGC TCGGGGCGGA GAGAAAGCTG TGTGTGCCTG AGTGTGAAGC 300
CACAGGGACG GCTTCCTGCT TTAGGGAAAA CAACCTGTGA AGCTGTGCCC TCGGCTGGAG 360
GCACAGAGGA GGGGCCTTGC TCAGGGAAAC TGGAGAGGGG AGTACAGTGT CTGGCCAAGG 420
CTGACCTCCA AGGCCAGGAG TGGGTTCTCC CTGGGCTTGG CAACACCTGT CAGTCTGGGA 480
GCCACAACTG CCTTTGCCAC GTCTACCCTC TGCTTCAGTG GACAGAACGA GCCTGGTGGA 540
CATTAGATGA CCCCTGATCA TGCCTGTGCA CGTGCACACA CAGGAGCAGA AGAGGCAGGC 600
AGGACACACA CCGTTACCAC CTCCAGGGTT CAGAGCAAGG AGAGGTGTAA GATCCAGTAT 660
ATGAATGCAC TTCCATGCAT GGACCCCAGT ACACATGGAC CCTTGCAAGC TCATGCCCCC 720
AAACCTGCTC CAAGCAGGGT CCTTGGACAG AGCCCTCCTG GTGTCTGAGG TCGTGCTTCA 780
CTGGCCGGGC CACGATGAGC CACCAGTCTC CATGAAGTGT GGCATTTGAC AGGAGGCACA 840
GGAATGACTT CCCCCTAGGT GAAGTTTCCA AAAATTCAGA GGCAAGGGCC CAATGACAGC 900
CTTGGTCAGA AAGGCCACTT GGAACCTCAG AGCCAGCCCA TTACAGCAGC CGATCCCTTC 960
CAGCAGGTGC CTGGATTAAA ACCAAGCGCT CATGTCTCCC TAGGGTCACA GCCCACATTA 1020
GTGAGAGCCT CATCCATGGC CGGGCAGGGT GCGGCACAGC AGCTGGCTTT GCAGAGGCAG 1080
CCACGGCTCA CGTAGATGAT GAAGACGTTT GCTCCAGAGC AGTCCTAAAG AGGCCATGCT 1140
GCGTAGGACA TAGAGCAGCA ATCTTGGGTC CAACAGCCCC AGCTGTGTCA TTTACCAGCT 1200
GTGTTACCTG GGGCAGGGAT GACCCTGGGC AAGTCCCTGC CTCAGGCCCC ATGTCTGTCA 1260
CATGGAGGTG ATCACGCCTC CATTGTACAA GTGAGGGTTA GCTTCAATAG CTAAATAGCC 1320
TCATAGCTAA AGCCTCAGAG GTCCCTTCCC ATGTGCCAGG CTCTGTGCTA AGGAGTTTAC 1380
AGTGACCCTA AGAGGAAGAT CTGACTGTTA GCCCATTTTC CAGATGAAGA AACTGAGACG 1440
CAGCATGGTT AGATGAAACC GGGCCAGGAC CTGGACTCCT GCAGTCCAGC TCCCCGCCAG 1500
CCTCACTGAA CCCTGAGGCT TCTCCCAATC TGGTCCCTCG GTGCCTGGGG ACACACAGCA 1560
CACGGCAGCC TAAAGCCAGG AACCTGAGCT GGGAAGCCTC ACTGTGCAGC TATCCACAGT 1620
GTTTTGCAAA TGTAGGGCCC TTGCTTGAGG CAGAAGAAAA GCCCTCTTTG AGGTGGTGTT 1680
CAGTGTGGCC TGCAGCTCTG GGTCTTGCAT TCCATGGATT TTTGGCCCCT GACTTGGGCT 1740
TGGCAGCTAC TACCTCATTG TTCTGCAACT TGGCAGGAGC CGCGGGATCC CGGGGACGGG 1800
CAGTCCTCAG TGTTACCCCG AGGTGCCTGC ACGCATGTGC TAAGGGTCTT TTCCCTGCTC 1860
CGTGTGGCTC GTCCTTCCAC GTCCCCTTTG CCTTGGCCTT TCTGCATCTG AACCCCCTAA 1920
GAAGCAGTTT CTGACAGGAA TTTCCAGAGC ACAGGGCTTG GGTTTCTGTT GGGGTGTGGA 1980
CCAATAGAAC AAAATGCCCT AAAATCCAAT ACCCATGGAG AGCCCCAAGA GGCAGTAGAT 2040
TCCTTGGAAC AAAGAGGGAG TTTAGAGTCA CTGAGATCTG GATTTGAATC CTTTCTCTGC 2100
AGCTTATCAG CCTAATGGCA TCGAGCCTCT TCCTCTGAGC CTCGGTTTCC CCATCTATAA 2160
AATGGGTCTA CCAATAGCCC CGAGGGTGAA TGGGAAAGAC CTGGCCCACA GGAACCCTCA 2220
TCCCTTCCTT TCTCCCTTCC TCCTTCCCCC TCGCGCCTCC CCACCTCCTT CCCCTCAGCA 2280
GGGACCCTCT CTGGCTCTCG GTGGGTAGGG GCTTGCAGAG TCCTCCGTGG CTGCTGCTTT 2340
CCTAGAACAG GGAACATCAA CACCTGCCGG CTCCTCCCTG GAGGCTAACG GTGCCGCAGG 2400
TTCCATTAGG TTCTGAACAG AGCAGCTCGT AATGACTGGG GTTTGGCAGC AAAGGCACCA 2460
CTGGGGTAGA CAGTGGTGCT GCATCAGCTT GCTGTGGTCA GTGGGGCAGA GTCTCCGGGG 2520
GCTCCTGCCC CTGGGGACCC TGTGGAGGAA ATGGGCCCTT GTGGTCCGCC AGCCCTGAGA 2580
TCACCCCTGT GCATCAGCAG CACAGGCCCC ATTCTCAAGT GGAGAGAGGG CCCATTCGGG 2640
GTGGAGCCAG CTGGAGAGAT GATGGTGTTG CTGTGTAAGA ACCTGTGGGG AGTGCAGTAC 2700
CGTAGTTTTG GACAAATATG 2720