Tag | Content |
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EnhancerAtlas ID | HS050-72249 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chrX:122318500-122319270 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chrX:122318643-122318654 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chrX:122318644-122318654 | GGGGCGGGGC | - | 6.02 | RREB1 | MA0073.1 | chrX:122319023-122319043 | GCGTTGGTGGTGGATGGGGT | - | 6.14 | SP3 | MA0746.2 | chrX:122318642-122318655 | GGGGGGCGGGGCG | - | 6.11 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCGCAAGCGA GCCAGCCGTC GGTCCAGGCT CTCCCTCACC CGAGACCACT GCCCCGGCAA 60 GGCTTTCCCT GCGGTGGGTC CCTGTCCTGC GTGGCCTGGG AACTGGGACT GGGGCCGGGA 120 CCGGGCAGAG ATGGTGCGGG GCGGGGGGCG GGGCGGGGGG AATCTGAGCC TCAACGAGGT 180 GGCTGGTCTG AAGAGCCTCT GGGACAAGAG AGGGGTCTCC TGGGGCTAGT GGGGGTGAAC 240 TGCTAGGTTT TCCGAGCCGA GAGGAGCACC GGAGGCGAGC AGGAGGCTGG GATGCTGCAA 300 GGGGGTGAAG AGTCGAGGCT TTTCGGCTCG CTGCTCTGGA CTTTGCCATG GCGTGCGTGC 360 AGCTCCTGGA AGTTGTCCCA GGGTGATGCC GACTGTCTGG CCGCGCCAGG GCGCATAACC 420 CGGGCCCGGG GTGCTCAGTC CGTGGTCTCC GGCTGTCGGG AGACAGGCTG GTGCTGGGGG 480 AGGTGGAGCC CACTTTGGAT CTCCCAGACC CGGGCAGCAG CAGGCGTTGG TGGTGGATGG 540 GGTAGGAGGC GGGGGTGAGA CTAGGAGCTG AGCGGGCAAG CGGCGAAGTC ACGCAGACCA 600 CGAATTCATG AATTGCCGCT GTGTCTGTCT GGAGCCCGGC TCCTGGGCGC CTGGAGGGAG 660 TTATCTTGGC TTCTGTCGTA TTTACAAGTC TAGAAGTTAG AATTTTTGCC ATTACTGAAC 720 CAACCCCCTG TATTGTCACG GGGGAGGGTG GCTATGGGGA ACGGGTTGGG 770
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