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

TagContent
EnhancerAtlas ID
HS044-09226 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr3:124553460-124554880 
TF binding sites/motifs
Number: 24             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr3:124553468-124553486GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr3:124553506-124553524GGAGGGAGGGGAGGGAGG+6.09
EWSR1-FLI1MA0149.1chr3:124553510-124553528GGAGGGGAGGGAGGAAAG+6.42
EWSR1-FLI1MA0149.1chr3:124553514-124553532GGGAGGGAGGAAAGAAGG+6.84
EWSR1-FLI1MA0149.1chr3:124553472-124553490GGAGGGAGGGAGGGAAGG+6.94
EWSR1-FLI1MA0149.1chr3:124553476-124553494GGAGGGAGGGAAGGACGG+6.95
EWSR1-FLI1MA0149.1chr3:124553534-124553552GGAAGGAAGCAAGCAAGC+7.54
EWSR1-FLI1MA0149.1chr3:124553518-124553536GGGAGGAAAGAAGGAAGG+7.87
EWSR1-FLI1MA0149.1chr3:124553526-124553544AGAAGGAAGGAAGGAAGC+8.2
EWSR1-FLI1MA0149.1chr3:124553530-124553548GGAAGGAAGGAAGCAAGC+8.73
EWSR1-FLI1MA0149.1chr3:124553522-124553540GGAAAGAAGGAAGGAAGG+9.47
MyogMA0500.1chr3:124554071-124554082CAGCAGCTGTC-6.14
Tcf12MA0521.1chr3:124554071-124554082CAGCAGCTGTC-6.02
ZNF263MA0528.1chr3:124553498-124553519GAGGAAGGGGAGGGAGGGGAG+6.19
ZNF263MA0528.1chr3:124553473-124553494GAGGGAGGGAGGGAAGGACGG+6.24
ZNF263MA0528.1chr3:124553519-124553540GGAGGAAAGAAGGAAGGAAGG+6.35
ZNF263MA0528.1chr3:124553485-124553506GAAGGACGGACAGGAGGAAGG+6.48
ZNF263MA0528.1chr3:124553516-124553537GAGGGAGGAAAGAAGGAAGGA+6.49
ZNF263MA0528.1chr3:124553512-124553533AGGGGAGGGAGGAAAGAAGGA+6.77
ZNF263MA0528.1chr3:124553465-124553486TGGGGAGGGAGGGAGGGAGGG+7.27
ZNF263MA0528.1chr3:124553507-124553528GAGGGAGGGGAGGGAGGAAAG+7.41
ZNF263MA0528.1chr3:124553469-124553490GAGGGAGGGAGGGAGGGAAGG+7.63
ZNF263MA0528.1chr3:124553503-124553524AGGGGAGGGAGGGGAGGGAGG+7.8
ZNF263MA0528.1chr3:124553497-124553518GGAGGAAGGGGAGGGAGGGGA+8.13
Number of super-enhancer constituents: 13             
IDCoordinateTissue/cell
SE_00134chr3:124547020-124559577Adipose_Nuclei
SE_01601chr3:124553540-124555288Aorta
SE_26511chr3:124553515-124557575Duodenum_Smooth_Muscle
SE_28222chr3:124550200-124559533Fetal_Intestine
SE_28829chr3:124549713-124559644Fetal_Intestine_Large
SE_36977chr3:124550125-124557910HSMMtube
SE_40878chr3:124553479-124557049Left_Ventricle
SE_42485chr3:124553498-124557009Lung
SE_44477chr3:124546810-124557600NHDF-Ad
SE_45642chr3:124549904-124560226Osteoblasts
SE_47296chr3:124553454-124559365Panc1
SE_51707chr3:124553448-124555305Skeletal_Muscle_Myoblast
SE_63495chr3:124553375-124555297HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr3124553626124554125
Number: 1             
IDChromosomeStartEnd
GH03I124831chr3124549953124559456
Enhancer Sequence
AAGGATGGGG AGGGAGGGAG GGAGGGAAGG ACGGACAGGA GGAAGGGGAG GGAGGGGAGG 60
GAGGAAAGAA GGAAGGAAGG AAGCAAGCAA GCAAACCAGG AATACAGGGA AGTAGTATCA 120
AAGAAAACCA GGAATACAGG AATGGAGTAT CCAAACAGAG GAAACAACAC ATGCAAAGGC 180
CTTGCCTGAG TCAGAGTAAC GCACTCCAGG TCACTGTGGC TGGAATGCAG AGGCCACAGG 240
TAGAGGCCAC AGGCAGAGAG CCTTGCAACA GGAGCCCAAG AGCAAATTCC TGTCTCCTTT 300
CATCTTTGCT CAGTGGACAT TCCAAGCAAG AAGGAGCCTC TGACTTAAAA TAAAAAATTG 360
ACATTCTCAC CTGGTATGAA AACAGAGCCC CAGCCATCAA AGGGGCCTCC TACCCTTTCC 420
CCAGGATGAT TATTCCCTGC CTTGGTCAGT GAAGGGAGCC ACCAGCACGT GTAGACACCT 480
CCTAAGCACA GGTGCAAGGC AGGCACGTGA CTTGTTTACA CTAGAGGGCA AAAAGAAACG 540
CAAACTCTCC CACGTGCCCT GTTCACGATA CTGAGTTATG ACTCAGCCAG TTCCCACCGC 600
TCAACCCAGA ACAGCAGCTG TCGGTGGGGC TGCGGAGCCC ACAACACAGC TCACAGCAGA 660
AGGCAGAGCC AGGAAACCAC GGAGTCCTGC ACTTGGGATG TCGCCTCAGA GACCAAAACA 720
GTAGAAGGAT TCAGAAGTGC ACATGAAACC ACTGCCGTCT GCCACATAGA AAGCCAAGGG 780
GAAGCTGCGC CACACCTGTC TGACAACAAC CCTACAGGGC AGAGGGTCTG CACACCTGCA 840
TGCGCAATGC CCAGAGAAAT CCAATACTTT AATGGTGCTT CCCCAAAGAC ACGGCAGCAC 900
AGGAAGAGCA GGCAGCCTGG CGCTGGATCA AGCCCCGGAA ACCTGTGGTG CGATCTGCTA 960
GCAGAAGCAG CTCACACATG CTGAGACAGA CAACGCAGAC AGCTGGGAAG CAGAACATGT 1020
GGCGGGTCCC TCTCTTCAGG TGGTGCAGAG GTTTGAGGAG TGGGGGGATG CCTTCCTTGA 1080
GGAAAGAAAG GCAATTTCCT GTATTTCTCA ACTCATGCTT GGAAAAGTGA CACAAGTCTG 1140
AGGTCTAAAA GAAATCAGGC AATAAGTCAA AAGAAAGCGA GTCAATTCTG CAGGAACTGG 1200
GAGCTGGGAG GGAGCAAGAG GAAACCCTGA CAAAGTTGTG CCTGACTCTG GGACTGGGGA 1260
ATTTTCCACA TTTTACAGGT GTCTGCAGCA GCCTCTACTG GGTCTGAGGC TTAAGCCTGA 1320
GCCAGAAGAG ACAAAAAAGC AAAATCAAAG GCCTTGAGCA AAGGAGACAG GGCTGTGACC 1380
AAGTCCTCTG CGAGAAGTGG CACTGGCTGG CACAGATGGA 1420