| Tag | Content |
|---|
EnhancerAtlas ID | HS050-67771 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr8:144697680-144698270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr8:144697813-144697827 | CACCACGCCCCCTT | + | 6.39 | | KLF16 | MA0741.1 | chr8:144697814-144697825 | ACCACGCCCCC | + | 6.14 | | SP1 | MA0079.4 | chr8:144697811-144697826 | TACACCACGCCCCCT | + | 6.07 | | SP3 | MA0746.2 | chr8:144697813-144697826 | CACCACGCCCCCT | + | 6.29 | | SP4 | MA0685.1 | chr8:144697811-144697828 | TACACCACGCCCCCTTC | + | 6.39 | | SP8 | MA0747.1 | chr8:144697814-144697826 | ACCACGCCCCCT | + | 6.52 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCAGAATCT CCTCTGAGCC TCTGCTCACG CTAGTGCCTC CTACGCTTAG CAAAGCCAGC 60
TAAGGCAAGG CTGCTGCCCA GTGACTGGTG GGGCCAACCC TCCGGAACAC AGCTAGCCAC 120
GGCAGGGCCC TTACACCACG CCCCCTTCCC CCAGACACAG GCAGCAGATG CACAGAGCGC 180
GGTTCACACC CCTGCACCCC AGAGTGTGTG GTGGGCCCGG CTAAGGGGAG CTGGGCCAGC 240
ACAGTCCTGG GAGCCAGAGG CTCCAGAGGC CCTGGGGACT CAGGGGGCAG GAACCAGCTC 300
CCAGTCCCAC GTGGCCGCTG GCTCTTTTCA GCCTCCCAAT GCTGCAAGTC AGCTCCACAG 360
CTTTGCCTAC TGGGCCAAGT GCCTCCAGGC CCCCTGCATG GCCCTCTGTC CACAGCACCA 420
AGTGTGAGTG ACTGGGGGTC CCTCAGGGGC TGCCCCCACC AGGCTGTGCC AAGCCCTGAT 480
CCTCAGGGAC TTCCTGGGGT GGGAATGTGG GCCTGTGAGA GTGGGAAGCC CGCCAGGAAG 540
TTCCCAGAAC CTGGGATCCT GGTTTCCAGT GCTTGCTGGG GCCACCCTCA 590
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