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

TagContent
EnhancerAtlas ID
HS050-70013 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr9:116384830-116385960 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFYAMA0060.3chr9:116385369-116385380GGCCAATCAGA+6.02
NFYBMA0502.1chr9:116385364-116385379ACCTGGGCCAATCAG+6.93
Number of super-enhancer constituents: 12             
IDCoordinateTissue/cell
SE_00715chr9:116381849-116384978Adipose_Nuclei
SE_01545chr9:116384980-116386578Aorta
SE_02292chr9:116381830-116386777Astrocytes
SE_29700chr9:116380789-116385875Fetal_Muscle
SE_37366chr9:116381946-116388389HSMMtube
SE_38013chr9:116380995-116386367HUVEC
SE_44306chr9:116381993-116386918NHDF-Ad
SE_45031chr9:116382269-116385987NHLF
SE_45799chr9:116381711-116388595Osteoblasts
SE_55765chr9:116381308-116390127u87
SE_65476chr9:116385248-116386339Pancreatic_islets
SE_67932chr9:116381308-116390127u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9116385277116385518
Number: 1             
IDChromosomeStartEnd
GH09I113619chr9116381352116386641
Enhancer Sequence
CCAAAACTCA CTGTGCCTGA ACTATGAATG TCCCCCAAGC TGCTTAGCCC TTGTGTCTGC 60
TTTTAAAAGT TCTGCTTTGC TTCTATATTT TTAAAGATTT CTTCCTCATG AGATATCAGC 120
AGTTACTTCT CACCACGTTA TCATGACTCC TTTGGATGAA AAACCAATAA CCAGTGTGTA 180
TCAGGATTGT CTGTAGTGTA AGAGTTCATA ATCAATGAAT GAGAGGACTC TCTGATGAGT 240
CAGGGATGTG GATTTTTGAC ATTTGTTTTG GCAGCTGAGA ATAAGGGGTA GTTTTTTTCT 300
TTCTAATTTT CACCCCAATA GCAGCTGCTT TCTGAGAGTT TTCTAGATAA ATGTGAAATG 360
AGTGTAGATC GATTTTTCCA TGTAACTAAT TTACATTCTG GGTGAACTCA TTTTGCTTCT 420
GACTTAGAGG TGCTTTCATT TCCTTCTCAT CTGCACCCTG TTCTTGGAGA AGCTGCTCCA 480
CCCCTAGCCC ATGATACATG ATGCATGACC CAGCCCACTG GGCCCCCTGA TGCCACCTGG 540
GCCAATCAGA TTTTCCAGTC AGGAAATTTG CAATTGAGAT TCAGAGCTGG AAAGAGTCAC 600
CTGCTCTGAT GGGAGCTGCA TTTGTGGACT GTGACTCAGA GGCTGAGGCC CCAGGGAGCC 660
GACCCCATGG GCCCTGGGCA AGCCCAGAGT GAATGTGGAA GCCGGGCTGT GGAGGTTCCC 720
TGAGCAGACA GTCCGGGTGT GTGTGCGTGT GTTTGTCTGT GTGTGTGCGC ACATGCTGGA 780
GGATGGGGCA GAACGTAGGG TCCCAAGCCC CTGAGGGAGG GGCTTGTCCT AATCAAGTCA 840
CAGAAATCAG GGCAGGGAGA GCATGAAAGA GTCTTGTTCC CCTCTCTGCA TTTGGGAGAT 900
TCAGGCCCCG GGGAGAGGAG AGACTGACCC ATGATCATCC AGAGGGGACT TGGTTAAGCT 960
GGTCCTGAGC TCTGCCATGC ATGTTCTGTT TTCCTACCCT GGCAGCTGGC TCAGAGCATG 1020
GATAGGCCTT GTCTCTCTTT TCTTTCTTTC TGCCAAATTC TTTTCTGTTG GGAATCTGAA 1080
CAGCGGGTAG ATGCAGTCAT GGCATGATTT GCTCCAAATA TCTCCCCAAC 1130