| Tag | Content |
|---|
EnhancerAtlas ID | HS050-12409 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr11:63897780-63898860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr11:63898275-63898287 | GCAAAGTAAACA | - | 6.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTAAAAAGCT CCTGCTCAAA TGAGAGAGAG AGAGTGGGTG ATACCTACCC CTCCATGGCT 60
GCTTTCCTGT ACCTGGAAAC TGCCCTTACC TGGCTACCAC TGGGTTCTGG AAGCTTCCCT 120
TCTCCTGCCC CTACTTCCCA GGAGGGGTCT CTGGCCTCAC CGAGCAACCT GAAGAAGAGG 180
CGTCGGAACC TGGGAGGGGT CTAACACCCC AGGCCACACC CCCACACCCA AGTTCTGTGG 240
CTGAGTCTTA TCACCCAGCC TAGGAGGGTC CCGGACGCAT GGGAGGGCAC CCAGCTGGCC 300
CTGAAATTCT GCCTCCGTGG GTCTGACATT GGCTCATCCA CTTTCAGGCA CCCCAAATAA 360
GGCATGCTTC CAGGACCCCC CCACACATGC CGCTGCCTCC CCGCCGCCGC ACCCACGTCA 420
CCTTCCAGTG CTGACACTGC CACCTCCCCA CCCGCCACCC TGTCCAGCAC CTCCAGAGGA 480
CCTTCTCCTC CTGCGGCAAA GTAAACAGGC TCTCTGGAGT GCTAACTGAC AGCACAAATG 540
AAATCCTGCA CTCCCTCCCT CTAAGATTTA CAGGGGAAGT GAAATCTTAT TTGCAATGCT 600
GCCAAGCCTG GGACGAGATG AAATTATGCC TCAAGAAGAG AACTGGCCGG CCCGGCGAGG 660
AAGCACTGCA TCGGAGATGG GCTTATTAAA ACCACAGTGG CCACATTTCA ACCTGTTTCA 720
GGTGTTAAGT AATTTACTGC CACCCAGAAT TCAGTGGCAG GTTTTTATCA TTTTTATTCT 780
TGTGATGCAG GCGAGTGCCC CAGGAGGTCC CTGTGCAGGG AGCTGCGGGT CTAAATGCTC 840
CCTGTCACCC CCGCCCCAGG CACTGCAGAG GGAAATGGGG GCCAGCTGCC TGAAGCGGGT 900
GAGGACACCC TGACTCTCTC CAGGGTTACA CCCAGCTTGG CCATAGCTCA GAGTGACGGG 960
GAGGGCAGGC TTTAAGACCC TCACCCCACC CACGTGTGGG GGCTCCATGA TCCCTCAAAG 1020
ACCCTCGGGA CGTTTTCTTT TTTTTGATGG AGTCTCGCTC TGTCACCCAG GCTGGTGTAC 1080
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