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

TagContent
EnhancerAtlas ID
HS050-12253 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr11:61262940-61264370 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gfi1bMA0483.1chr11:61264314-61264325GGCTGTGATTT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr116126342761263971
Enhancer Sequence
GCATGTTGGC ACATGCCGGT AGTCCCAGCT ACTCGGGAGG CTGAAGTGGG AAGAGAGCTT 60
GAGGCCAGGA AGTTGAGGCT GTAGTGAGAC ATGTTCACAC CACTGTACTC TAGCCTGGGT 120
GACATACTGA GACCCTGTCT CAACAAAACA AAACAAAACC CTTCCCTGAG AGCAGCCCTC 180
CTCTCTATCA AGGGTGGGTG ATCACCTGCA CAGCCTGACC TGGAAGGCCT TGGCTGCCCT 240
TCCAGTGGTT TACTCCCACT TAAGCCCCCG TCCCTAAGTC CAGCTTCTGC CAGGCCCTCC 300
TGGCAGCTGC CTGCTTCTCC CTTCACCTGG TAACCAGGCT TTGGGTGTTC ACAGAGTCAG 360
TCCTTCTGGC AGGTGACATT GCAGTTGCTG CCAGAAGTTT CCTGCCCCCT CCTCAACGAA 420
TATTTTTAAA AACTTGCTGA GGTGTACAGG GATGATGATT AACCTTTATT AAGCCCCCAC 480
AGCCTGCGGG TGCTGAGAAT ATCCGTGGGC CTTCACCTTT CCAGCAAGAA CACAGAGGGG 540
CCTCCCTCTG GGGGAAGTTT AGGGACACAG GTGGGTGCGG CGCTGACGGC TTTGGTGTGG 600
GGGTGTGGAG CCTAGAGGGC TGACGGGACA GCAGGTGGGG TGGCTGCTGG GCGCCGTGAG 660
ATCAGACACG GCTTGTGACG CGTGTGGACG CGTGTGAGGT TGCTGTTTGT TCGTCATGGC 720
CTGGTGGCGG CTAATGTTGA CAGGTGCCAT CTGGCCTGAG TCACGTGGTA GCAGGCAGCA 780
CCACCGGCTC GTTGGCTTGA CAGCTGTCCA GCTGGGAACA CAGGGCTCCT GGGGGTGGGG 840
GCGGTTAGAG GCATCTGTCT TTGGGAACTG GAGGCCTGGG GGTGGTGGGA GGCCCTGCGT 900
GGGGAGGCTG AGGACGGGGG ATATGATACA CCCAGACAGA TGGAGTGTGT GAGGCTCTGA 960
ATCGGTTCCC CAGTCTCCTC TCTGACCATC TGGAGGGCCA CCCATTCCTG AGGAACTGTT 1020
CCCCGAACAA GCAAGTATGC AAGGGCAGAG GATGAATCAG ACCCAGCAGG TCCCACTGAG 1080
GGCCCCCGTT GAAGATCAGA GGGGTCTGGC AGGGCCTGTG GGACATCCCG CCATGCCTCG 1140
CTTCCTCCCC ACACTGCTGC AGACAGGCTC TGCCCAGGAC CTTTGTGATG GGCAGGTCAA 1200
CCTGACCAGA GGTGAGGCGA CCTGCCCAAA GCCATGCGGT GCCGGCCCCG TGAGCGCGCT 1260
CGCACTCTCT TCTGAATCCA AGCCTCTCCC CACCCCATCG CTTCCCTGGG GGTCTCGGAT 1320
GAGCAGGAAT GGGGCCTGGG AACTTCCTGG GAGAGCCAGG CAGTGATAGG GATGGGCTGT 1380
GATTTCTTTT GCTAAAGAGG TGAGTGCACT TGTGTGAGAG TGTGTGTGTG 1430