Tag | Content |
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EnhancerAtlas ID | HS050-72384 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chrX:135332380-135333440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chrX:135332395-135332409 | CAATCGTAAACAAT | + | 6.92 | HINFP | MA0131.2 | chrX:135333167-135333179 | CCGCGTCCGCGG | + | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAACATATAG CTTCCCAATC GTAAACAATC TAACTTTTTA ATTGCAAATG CAAAAAAACC 60 CCTAAGAAAT TCAATTAAAA TTAATAAAAT CGTTTTATTC GCGCTCATAG CAGAGGGAAC 120 TAGTCTAACA GGCTAAAAGC AACCTCCTGA AAGGAAGAAA TCCTATCTCA GGTAGTGGAG 180 CAGTCTCCTG GACCAAGCAA TGTGCTGTCA AATTGTATAA GATTAACGGT TTTCGAGGAG 240 GGAAAAACGT TTTGGCGATG GGACTAGTTG AGGAAAAAGC ACTCTGAAGT GCTGATTCCC 300 GTTCAGTTCA GCCTAGAGAC TGCAAGATGT CCCACAGAAG ATGACATCTT GTTGAAGTCA 360 TGTGCTACAG CAGGCAAATC AGGAGATGCA AAGAGCCAAG TTTCATCCCA ACTTTTAAAG 420 CAACTTTTAA GCATCCCCAC CCTCACCCAG CTTCCTCCCT GGACCTTGAC CGGGAGGGTG 480 CAGGAGGTAA GCCTTTGGGA GAGGCAAGGA CTGCGACAGT AAAAGCGCCT AAACTCGCCC 540 ACGACCCGGG CTGGGGGATA ACTCAAACTT TCCGTGCCTG GAAAGGCTGC CTGGCGGCGG 600 AGGCGGCGCC GGCGCGCGGA GTCCCTGCGG GCGCCCGCAC ATCCCAGGCA GCTGTGCGTT 660 CGTTGGGGCG GTTGCGCGGG CGGCCACCGC CCCCCAAGGG CAGATGGGGC ACGGGGCGGT 720 CCGCGGGGTC CGGCTTCCAG CCGCCCCCGC CCCGCCCGTC GAAGCAGAGC CCGTGAGTTG 780 CCTCGCGCCG CGTCCGCGGG GCTCAGACCG TTGGCAGCGG CAGTTCGACC GTTGGCGGCG 840 GGACTCAGGC GGCTCGCGGC GTCGGCTGAC AATTTCAACC CCCCGCCCCC GCCCCTGTCC 900 CATCCCAGGG CACTCCGGCG GGGGTGAGGG GAGGACCAGA TAGCACGAGG CGACTCCAGG 960 GAAAAGTTTT GTGGCGCCCG CTGCGCCGCT CCGACGGCCC GGGGACTGCG GGAACCCTGC 1020 CTCCCACGCG GGCCCGAACC ACCCCCGGGA GCCACCCGCC 1060
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