| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00092 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:2021120-2022240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:2021431-2021445 | CCGGGCCAGGCCTG | + | 6.23 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAGGATTTC AGCGTGTGAA TTCGGTGGGA CGTAAACACT CAGGTCACAG TGCTGGGGCC 60
GCTGTAGCAA CGTACCACAG ATGGCGGCTC ACACGGCAGA ACTCAATTCT CTCTCAGCTT 120
GTGTGGTGAT CCCAGCTACT CCGGAGGCTG CGGTGGGAGG ACCTCTTGAG TGCAGGAGTT 180
TGAATGTAGC CAGGGCAACA TAGCGAGATC CCATTAAAAA AAATCCAAAC AAAAAGCTTT 240
ATTCTCTGTC TGGAGACCAG CGTCTGAGAG CTGGGTTTCG GCAGGGCTGG TTCCCGGAGG 300
CCGTGAGGAG CCCGGGCCAG GCCTGTCCCC TTGGCTGGTG GAGCCGTCTC TTCTTCACCC 360
GGGCCCTTCC TCCCCGTGCG GCCGTGTCCA CGTTACCCTC TGTTATGAGA ACAGCAGTTG 420
TTTTGGATCT AAGTCTGCTG TAATGACCTC ACTCACTTAA CTGATTACAT CTGCAGTGTC 480
CTATGTGTAA ATAAGGGCAT GTTCTGAGCT CCTGGGGGTC AGGACGGCAG CTTGGATTCC 540
GAGGGGATTC AGTTGCACTC ATGCAGAGGC CCTGGGGGCT GCACCTTGGC AAGGGGTTCC 600
CATGGCCTGG CCGGTCTGCA GTCCTTGTAG TCAGCTGCAC CCAGCCCTCC CGCAGAAGGG 660
GCCCGTGCAC CCATGGTTTT GTAGCCGTCA GGGAGCACCT GTTCAGAGGG CCCTGCTGAC 720
CGAGGGGCGT GGGCTCAGCA CTGCCAGGGC CCGTGCCCTG TGTCCCCACA GGATGGTGCT 780
GGCCGTCTCA CCACTGAGGG GATGCCCCCC AGCCCCCTCA CCCTCAGCTG CTCCTTCCAG 840
GAGCTTAAGG CCCCTAAAGT CTGCCCCGGT CCCTGGGGTC AGAGCCCACC CTGGGCTGGT 900
TTTGAAGAAA CACCAGTGCT TCTCCAAGGA GGCCCCGTGC ACATGTAGGA ATGAAGCCCT 960
CGTCCTCCCA CAGCCGCGTG CCCCTCCTGC GCTGCGTGTG TGGTTTTGCT CATGGCACCT 1020
GGCGTGGGCG CCCTGGGAGC GGCAGCCGGG GGCGTCTCGG AGAGAGCCAG TGCAGGGGGG 1080
ACCCCACAAT CTGGGAGGCC ATGGATCCTG GTTGTGGGTT 1120
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