| Tag | Content |
|---|
EnhancerAtlas ID | HS050-35518 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:20570950-20571860 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Pou2f3 | MA0627.1 | chr2:20571329-20571345 | ACAAATTTGCATAAAA | - | 6.7 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTCCAAGAA CTTATTAACA ACTTTAAGTG AGGACTCACT GTATATAAAA ATAGAGTCAT 60
GTATACATTG AGCAGTCGAG GGACACATTG TAGTGGTCAT TTACTTTTTT AAGCATCATT 120
TAGCCTTTTT CAGTAACAGA CCCTGCTTGA ATCAAGCTAA GCCACCCTCA TGACATAAGG 180
ATTTATCCAA AAGACAAGCA CATAAACCAA GTTAATTCAA GTGGAATAAT TCCACAGGAT 240
TTTTTTCAAA CTGAAGTTGG GAGAGGAAAG CCCCTCTTCT CTGTCTTACA AACTGTAATG 300
ATCTGAGCCA AGAGCTCCCA GTAGTCATCA TTATACTTTT GTGGGAGAGA GCCAGCCTAA 360
GAGAGGAACG CTAACATACA CAAATTTGCA TAAAAGAGAG ACCAAAAGAG AAAGCTAGTT 420
GCGGACTGGG AGAGAAAGAG AGAGGGAGAG AGGAAGGAAA AGAAGGGTTT ACCCCAACCT 480
CCTTGCTGTT TGGTTGTGAT CCAATACAAT ATCTATCTGG CTGTCTGTGT CAGGCCAGTT 540
TTTGCATCTC TATAAAGAAA TGCTTGAATC TGAGGAATTT ATAAAGAAAA GAGGTTTAAT 600
TGGCTCATGT TCTTCAGGCT GTACAGGAAG TGTGGTGCTG GCATCTGCTT CTGGCAAGGG 660
CCCCAAGAAG CTTACAGTCA TGGCAGAAGG TGGAGAGGAA ACAGGCATGT CATATGGCGA 720
AAGGGAGCAA GAGAGAGTGA GGACGAGGAG CCAGACTCCT TTAAACAACC AGCTCTCAAG 780
TGAGCTAACA GACTCACTCA TAATAAGAAC TCACTCATTA CCATGGGGAA GGCAGCAAAC 840
CGTTGGTGAA AGATTCACCC CCATGATCCA ATGGGCCTTC CACTATACCC CACCTCCAAG 900
ATTGGAGGTC 910
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